| geneid | 55819 |
|---|---|
| ensemblid | ENSG00000113269.14 |
| hgncid | 18280 |
| symbol | RNF130 |
| name | ring finger protein 130 |
| refseq_nuc | NM_018434.6 |
| refseq_prot | NP_060904.2 |
| ensembl_nuc | ENST00000521389.6 |
| ensembl_prot | ENSP00000430237.1 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 179955067 |
| end | 180071759 |
| strand | - |
| ver | v1.2 |
| region | chr5:179955067-180071759 |
| region5000 | chr5:179950067-180076759 |
| regionname0 | RNF130_chr5_179955067_180071759 |
| regionname5000 | RNF130_chr5_179950067_180076759 |
| 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 | 419 | 336 | 95 | 71 | 127 | 14 | 27 | 97 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| a0002 | 0/0 | 419 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| a0003 | 0/0 | 419 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| a0004 | 0/0 | 419 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| a0005 | 0/0 | 419 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| 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 | 1260 | 138 | 68 | 18 | 41 | 4 | 6 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| c0002 | 0/1 | 1260 | 123 | 11 | 27 | 63 | 7 | 14 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| c0003 | 0/0 | 1260 | 53 | 12 | 21 | 12 | 3 | 5 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| c0004 | 0/0 | 1260 | 12 | 0 | 1 | 10 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| c0005 | 0/0 | 1260 | 4 | 4 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| c0006 | 0/0 | 1260 | 3 | 0 | 3 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| c0007 | 0/0 | 1260 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| c0008 | 0/0 | 1260 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| c0009 | 0/0 | 1260 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| c0010 | 0/0 | 1260 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| c0011 | 0/0 | 1260 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| c0012 | 0/0 | 1260 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| c0013 | 0/0 | 1260 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| 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 | 1/1 | 645 | 328 | 87 | 72 | 125 | 14 | 28 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| t0002 | 0/0 | 643 | 6 | 6 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| t0003 | 0/0 | 645 | 3 | 3 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| t0004 | 0/0 | 645 | 2 | 0 | 0 | 2 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| t0005 | 0/0 | 645 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| 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 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0002 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0014 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0282 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| 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 | 1260 | 138 | 68 | 18 | 41 | 4 | 6 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| a0001c0002 | 0/1 | 1260 | 123 | 11 | 27 | 63 | 7 | 14 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| a0001c0003 | 0/0 | 1260 | 53 | 12 | 21 | 12 | 3 | 5 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| a0001c0004 | 0/0 | 1260 | 12 | 0 | 1 | 10 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| a0001c0005 | 0/0 | 1260 | 4 | 4 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| a0001c0006 | 0/0 | 1260 | 3 | 0 | 3 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| a0001c0007 | 0/0 | 1260 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| a0001c0011 | 0/0 | 1260 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| a0001c0012 | 0/0 | 1260 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| a0002c0008 | 0/0 | 1260 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| a0003c0009 | 0/0 | 1260 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| a0004c0010 | 0/0 | 1260 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| a0005c0013 | 0/0 | 1260 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1904 | 137 | 67 | 18 | 41 | 4 | 6 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| a0001c0001t0002 | 0/0 | 1902 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| a0001c0002t0001 | 0/1 | 1904 | 121 | 10 | 27 | 62 | 7 | 14 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| a0001c0002t0002 | 0/0 | 1902 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| a0001c0002t0004 | 0/0 | 1904 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| a0001c0003t0001 | 0/0 | 1904 | 49 | 8 | 21 | 12 | 3 | 5 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| a0001c0003t0002 | 0/0 | 1902 | 4 | 4 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| a0001c0004t0001 | 0/0 | 1904 | 10 | 0 | 1 | 8 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| a0001c0004t0004 | 0/0 | 1904 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| a0001c0004t0005 | 0/0 | 1904 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| a0001c0005t0001 | 0/0 | 1904 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| a0001c0005t0003 | 0/0 | 1904 | 3 | 3 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| a0001c0006t0001 | 0/0 | 1904 | 3 | 0 | 3 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| a0001c0007t0001 | 0/0 | 1904 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| a0001c0011t0001 | 0/0 | 1904 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| a0001c0012t0001 | 0/0 | 1904 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| a0002c0008t0001 | 0/0 | 1904 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| a0003c0009t0001 | 0/0 | 1904 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| a0004c0010t0001 | 0/0 | 1904 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| a0005c0013t0001 | 0/0 | 1904 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | copy fasta | chr5 | 179950067 | 180076759 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0282 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0014 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0002 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0004t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0004t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0004t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0004t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0004t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0004t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0004t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0004t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0004t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0004t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0004t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0004t0005g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0005t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0005t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0005t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0005t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0006t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0006t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0006t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0007t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0011t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0012t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0002c0008t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0003c0009t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0004c0010t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0005c0013t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0048 | EUR | GBR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0118 | EUR | GBR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0303 | EUR | GBR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0017 | EUR | GBR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0258 | EUR | FIN | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00280 | hp2 | a0001 | c0003 | t0001 | g0166 | EUR | FIN | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0262 | EUR | FIN | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0060 | EUR | FIN | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | CHS | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00408 | hp2 | a0001 | c0003 | t0001 | g0152 | EAS | CHS | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0088 | EAS | CHS | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | CHS | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | CHS | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | CHS | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | CHS | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00558 | hp2 | a0001 | c0003 | t0001 | g0180 | EAS | CHS | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0057 | EAS | CHS | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | CHS | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00642 | hp1 | a0001 | c0003 | t0001 | g0162 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0119 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | CHS | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0105 | EAS | CHS | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0286 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00733 | hp2 | a0001 | c0003 | t0001 | g0163 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0046 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0113 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0049 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0333 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01069 | hp1 | a0001 | c0003 | t0001 | g0186 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0052 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01071 | hp1 | a0001 | c0003 | t0001 | g0002 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01074 | hp1 | a0001 | c0003 | t0001 | g0164 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0073 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01081 | hp1 | a0001 | c0003 | t0001 | g0171 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0097 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0065 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01168 | hp1 | a0001 | c0003 | t0001 | g0169 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0051 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01169 | hp1 | a0001 | c0003 | t0001 | g0170 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0324 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01175 | hp1 | a0001 | c0003 | t0001 | g0151 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0066 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0120 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01243 | hp1 | a0001 | c0003 | t0001 | g0189 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01243 | hp2 | a0004 | c0010 | t0001 | g0027 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0041 | AMR | CLM | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0068 | AMR | CLM | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01256 | hp1 | a0001 | c0003 | t0001 | g0182 | AMR | CLM | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0042 | AMR | CLM | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01257 | hp1 | a0001 | c0003 | t0001 | g0184 | AMR | CLM | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0080 | AMR | CLM | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0064 | AMR | CLM | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01258 | hp2 | a0001 | c0003 | t0001 | g0003 | AMR | CLM | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01261 | hp1 | a0001 | c0003 | t0001 | g0193 | AMR | CLM | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01261 | hp2 | a0001 | c0003 | t0001 | g0144 | AMR | CLM | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | CLM | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | CLM | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0116 | AMR | CLM | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01361 | hp2 | a0001 | c0006 | t0001 | g0196 | AMR | CLM | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01433 | hp1 | a0001 | c0003 | t0001 | g0003 | AMR | CLM | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01433 | hp2 | a0001 | c0012 | t0001 | g0289 | AMR | CLM | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0053 | AMR | CLM | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01496 | hp2 | a0001 | c0003 | t0001 | g0145 | AMR | CLM | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0016 | EUR | IBS | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01516 | hp2 | a0001 | c0003 | t0001 | g0147 | EUR | IBS | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0011 | EUR | IBS | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01517 | hp2 | a0001 | c0003 | t0001 | g0148 | EUR | IBS | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ACB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01884 | hp2 | a0001 | c0003 | t0002 | g0154 | AFR | ACB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0013 | AFR | ACB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | ACB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01928 | hp1 | a0001 | c0003 | t0001 | g0175 | AMR | PEL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | PEL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01934 | hp1 | a0001 | c0006 | t0001 | g0197 | AMR | PEL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0114 | AMR | PEL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01943 | hp1 | a0001 | c0003 | t0001 | g0172 | AMR | PEL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0043 | AMR | PEL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PEL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01952 | hp2 | a0001 | c0003 | t0001 | g0146 | AMR | PEL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0078 | AMR | PEL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01975 | hp2 | a0001 | c0006 | t0001 | g0195 | AMR | PEL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PEL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0089 | AMR | PEL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0079 | AMR | PEL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | PEL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0067 | AMR | PEL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0074 | AMR | PEL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0117 | AMR | PEL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02004 | hp2 | a0001 | c0003 | t0001 | g0174 | AMR | PEL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0110 | EAS | KHV | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0036 | EAS | KHV | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02055 | hp1 | a0005 | c0013 | t0001 | g0208 | AFR | ACB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | ACB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02056 | hp1 | a0001 | c0003 | t0001 | g0183 | EAS | KHV | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | KHV | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | KHV | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02074 | hp2 | a0001 | c0002 | t0004 | g0084 | EAS | KHV | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0109 | EAS | KHV | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0121 | EAS | KHV | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | KHV | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | KHV | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | KHV | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0115 | AFR | ACB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | CDX | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | CDX | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | CDX | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | CDX | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0054 | AFR | ACB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | ACB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0336 | AFR | ACB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0122 | AFR | ACB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | ACB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02280 | hp2 | a0001 | c0003 | t0001 | g0155 | AFR | ACB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0090 | AMR | PEL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02293 | hp2 | a0001 | c0004 | t0001 | g0135 | AMR | PEL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02451 | hp1 | a0001 | c0003 | t0002 | g0157 | AFR | ACB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02572 | hp1 | a0001 | c0005 | t0003 | g0190 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02602 | hp1 | a0001 | c0003 | t0001 | g0160 | SAS | PJL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02602 | hp2 | a0003 | c0009 | t0001 | g0010 | SAS | PJL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0045 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02622 | hp2 | a0001 | c0003 | t0001 | g0188 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02630 | hp2 | a0001 | c0005 | t0003 | g0161 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0108 | SAS | PJL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0091 | SAS | PJL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0059 | SAS | PJL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0329 | SAS | PJL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02717 | hp2 | a0001 | c0002 | t0002 | g0128 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0129 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0006 | SAS | PJL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0279 | SAS | PJL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0332 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | ESN | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | ESN | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0295 | AFR | ESN | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | ESN | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | ESN | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | ESN | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | ESN | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | ESN | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0082 | SAS | PJL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03017 | hp2 | a0001 | c0003 | t0001 | g0002 | SAS | PJL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03041 | hp1 | a0001 | c0003 | t0001 | g0158 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03098 | hp1 | a0001 | c0003 | t0001 | g0187 | AFR | MSL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | MSL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ESN | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03139 | hp2 | a0001 | c0003 | t0001 | g0156 | AFR | ESN | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0331 | AFR | ESN | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | ESN | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | MSL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | MSL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | MSL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | MSL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03453 | hp1 | a0001 | c0003 | t0001 | g0192 | AFR | MSL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | MSL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | MSL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0335 | AFR | MSL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0055 | SAS | PJL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0305 | SAS | PJL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0070 | SAS | PJL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0304 | SAS | PJL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ESN | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ESN | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0330 | AFR | MSL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | MSL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0285 | SAS | PJL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0326 | SAS | PJL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03704 | hp1 | a0001 | c0003 | t0001 | g0168 | SAS | PJL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0083 | SAS | PJL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0050 | SAS | PJL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0056 | SAS | PJL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0093 | SAS | BEB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03834 | hp2 | a0001 | c0004 | t0001 | g0138 | SAS | BEB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG04184 | hp1 | a0001 | c0003 | t0001 | g0150 | SAS | BEB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0028 | SAS | BEB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0112 | SAS | STU | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0012 | SAS | STU | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG04228 | hp1 | a0001 | c0003 | t0001 | g0181 | SAS | STU | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG04228 | hp2 | a0001 | c0007 | t0001 | g0004 | SAS | STU | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | YRI | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | YRI | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18612 | hp1 | a0001 | c0003 | t0001 | g0178 | EAS | CHB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0062 | EAS | CHB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | YRI | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0242 | AFR | YRI | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18939 | hp1 | a0001 | c0003 | t0001 | g0179 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0126 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18942 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18943 | hp1 | a0001 | c0003 | t0001 | g0185 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18948 | hp1 | a0001 | c0003 | t0001 | g0176 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18951 | hp1 | a0001 | c0004 | t0001 | g0141 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0104 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0127 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18962 | hp1 | a0001 | c0004 | t0001 | g0136 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18971 | hp1 | a0001 | c0003 | t0001 | g0177 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18971 | hp2 | a0002 | c0008 | t0001 | g0124 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18974 | hp2 | a0001 | c0004 | t0001 | g0132 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18987 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19004 | hp1 | a0001 | c0004 | t0001 | g0131 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19006 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19006 | hp2 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19030 | hp1 | a0001 | c0005 | t0001 | g0194 | AFR | LWK | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0130 | AFR | LWK | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | LWK | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19043 | hp2 | a0001 | c0003 | t0002 | g0153 | AFR | LWK | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19055 | hp1 | a0001 | c0004 | t0001 | g0134 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19055 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19056 | hp1 | a0001 | c0003 | t0001 | g0173 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19057 | hp2 | a0001 | c0011 | t0001 | g0143 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19065 | hp1 | a0001 | c0003 | t0001 | g0149 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19068 | hp1 | a0001 | c0004 | t0001 | g0137 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19070 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19080 | hp2 | a0001 | c0004 | t0001 | g0139 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19083 | hp2 | a0001 | c0004 | t0004 | g0142 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19086 | hp2 | a0001 | c0004 | t0001 | g0133 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19091 | hp2 | a0001 | c0004 | t0005 | g0140 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19240 | hp1 | a0001 | c0005 | t0003 | g0191 | AFR | YRI | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | YRI | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA20129 | hp1 | a0001 | c0003 | t0001 | g0159 | AFR | ASW | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0015 | AFR | ASW | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0261 | EUR | TSI | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0047 | EUR | TSI | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0309 | AMR | CLM | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | ACB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | ACB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0123 | AFR | ACB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | ACB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02559 | hp2 | a0001 | c0003 | t0001 | g0165 | AFR | ACB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0297 | AFR | MSL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0026 | AFR | MSL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0334 | AFR | USA | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | USA | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | USA | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | USA | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA21309 | hp1 | a0001 | c0003 | t0002 | g0167 | AFR | LWK | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | LWK | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0014 | REF | REF | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0282 | REF | REF | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:179966923
|
C | T | 1 | a0004 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.1033G>A | p.Asp345Asn | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 7/9 | 1090/1904 | 1033/1260 | 345/419 | chr5 | 179966923 | ||
| chr5:179966926
|
C | T | 1 | a0005 | 1 | HG02055.hp1 | missense_variant | MODERATE | c.1030G>A | p.Gly344Ser | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 7/9 | 1087/1904 | 1030/1260 | 344/419 | chr5 | 179966926 | ||
| chr5:180013203
|
C | T | 1 | a0003 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.551G>A | p.Arg184Gln | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/9 | 608/1904 | 551/1260 | 184/419 | chr5 | 180013203 | ||
| chr5:180040533
|
C | T | 1 | a0002 | 1 | NA18971.hp2 | missense_variant | MODERATE | c.362G>A | p.Arg121Gln | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/9 | 419/1904 | 362/1260 | 121/419 | chr5 | 180040533 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:179966867
|
T | C | 1 | a0001c0005 | 4 | HG02572.hp1 HG02630.hp2 NA19030.hp1 others(1): Show |
synonymous_variant | LOW | c.1089A>G | p.Ser363Ser | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 7/9 | 1146/1904 | 1089/1260 | 363/419 | chr5 | 179966867 | ||
| chr5:180040553
|
C | T | 1 | a0001c0012 | 1 | HG01433.hp2 | synonymous_variant | LOW | c.342G>A | p.Thr114Thr | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/9 | 399/1904 | 342/1260 | 114/419 | chr5 | 180040553 | ||
| chr5:180071529
|
G | A | 1 | a0001c0006 | 3 | HG01361.hp2 HG01934.hp1 HG01975.hp2 |
synonymous_variant | LOW | c.174C>T | p.Arg58Arg | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/9 | 231/1904 | 174/1260 | 58/419 | chr5 | 180071529 | ||
| chr5:180071592
|
C | T | 1 | a0001c0007 | 1 | HG04228.hp2 | synonymous_variant | LOW | c.111G>A | p.Ala37Ala | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/9 | 168/1904 | 111/1260 | 37/419 | chr5 | 180071592 | ||
| chr5:180071595
|
C | T | 8 | a0001c0002a0001c0003a0001c0005others(5): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(184): Show |
synonymous_variant | LOW | c.108G>A | p.Thr36Thr | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/9 | 165/1904 | 108/1260 | 36/419 | chr5 | 180071595 | ||
| chr5:180071652
|
C | T | 1 | a0001c0011 | 1 | NA19057.hp2 | synonymous_variant | LOW | c.51G>A | p.Leu17Leu | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/9 | 108/1904 | 51/1260 | 17/419 | chr5 | 180071652 | ||
| chr5:180071658
|
G | T | 6 | a0001c0002a0001c0004a0001c0007others(3): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(136): Show |
synonymous_variant | LOW | c.45C>A | p.Leu15Leu | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/9 | 102/1904 | 45/1260 | 15/419 | chr5 | 180071658 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:179955136
|
G | A | 1 | a0001c0004t0005 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*518C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 9/9 | 518 | chr5 | 179955136 | |||||
| chr5:179955152
|
A | C | 2 | a0001c0002t0004a0001c0004t0004 | 2 | HG02074.hp2 NA19083.hp2 |
3_prime_UTR_variant | MODIFIER | c.*502T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 9/9 | 502 | chr5 | 179955152 | |||||
| chr5:179955215
|
TCA | T | 3 | a0001c0001t0002a0001c0002t0002a0001c0003t0002 | 6 | HG01884.hp2 HG02451.hp1 HG02717.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*437_*438delTG | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 9/9 | 437 | chr5 | 179955215 | |||||
| chr5:179955594
|
C | T | 1 | a0001c0005t0003 | 3 | HG02572.hp1 HG02630.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*60G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 9/9 | 60 | chr5 | 179955594 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:179955920
|
G | A | 3 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256 | 3 | HG03209.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1245-251C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179955920 | ||||||
| chr5:179956531
|
C | T | 3 | a0001c0001t0001g0276a0001c0001t0001g0280a0001c0002t0001g0120 | 3 | HG01192.hp2 HG01928.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.1245-862G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179956531 | ||||||
| chr5:179956575
|
C | T | 4 | a0001c0003t0001g0174a0001c0005t0003g0161a0001c0005t0003g0190others(1): Show | 4 | HG02004.hp2 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1245-906G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179956575 | ||||||
| chr5:179956634
|
C | T | 1 | a0001c0002t0001g0110 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1245-965G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179956634 | ||||||
| chr5:179956757
|
C | T | 3 | a0001c0002t0001g0098a0001c0002t0001g0099a0001c0002t0001g0100 | 3 | NA18979.hp1 NA19079.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1245-1088G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179956757 | ||||||
| chr5:179956815
|
T | C | 194 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(191): Show | 197 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.1245-1146A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179956815 | ||||||
| chr5:179957222
|
G | A | 1 | a0001c0003t0001g0178 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1245-1553C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179957222 | ||||||
| chr5:179957356
|
G | A | 1 | a0001c0001t0001g0293 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1245-1687C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179957356 | ||||||
| chr5:179957626
|
G | T | 1 | a0001c0001t0001g0287 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1245-1957C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179957626 | ||||||
| chr5:179957696
|
T | C | 2 | a0001c0001t0001g0269a0001c0002t0001g0088 | 2 | HG00438.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1245-2027A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179957696 | ||||||
| chr5:179957881
|
CT | C | 214 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(211): Show | 217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.1245-2213delA | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179957881 | ||||||
| chr5:179957904
|
G | A | 5 | a0001c0001t0001g0314a0001c0003t0001g0002a0001c0003t0001g0169others(2): Show | 6 | HG01069.hp1 HG01071.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.1245-2235C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179957904 | ||||||
| chr5:179957945
|
T | C | 7 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(4): Show | 7 | HG02572.hp2 HG02818.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1245-2276A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179957945 | ||||||
| chr5:179957965
|
C | T | 2 | a0001c0001t0001g0293a0001c0001t0001g0296 | 2 | HG02486.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1245-2296G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179957965 | ||||||
| chr5:179957982
|
A | G | 7 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(4): Show | 7 | HG02572.hp2 HG02818.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1245-2313T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179957982 | ||||||
| chr5:179957999
|
T | G | 3 | a0001c0005t0003g0161a0001c0005t0003g0190a0001c0005t0003g0191 | 3 | HG02572.hp1 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1245-2330A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179957999 | ||||||
| chr5:179958022
|
C | T | 1 | a0001c0003t0001g0151 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1245-2353G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179958022 | ||||||
| chr5:179958090
|
G | A | 1 | a0001c0003t0001g0183 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1245-2421C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179958090 | ||||||
| chr5:179958131
|
T | C | 213 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(210): Show | 216 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.1245-2462A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179958131 | ||||||
| chr5:179958152
|
T | C | 2 | a0001c0001t0001g0265a0001c0002t0001g0020 | 2 | HG02155.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.1245-2483A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179958152 | ||||||
| chr5:179958493
|
G | A | 5 | a0001c0002t0001g0043a0001c0002t0001g0046a0001c0003t0001g0144others(2): Show | 5 | HG00735.hp1 HG01261.hp2 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.1245-2824C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179958493 | ||||||
| chr5:179958672
|
A | C | 145 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0213others(142): Show | 148 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.1245-3003T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179958672 | ||||||
| chr5:179958919
|
G | A | 1 | a0001c0002t0001g0061 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1245-3250C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179958919 | ||||||
| chr5:179959443
|
C | T | 216 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(213): Show | 219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.1245-3774G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179959443 | ||||||
| chr5:179960005
|
C | G | 1 | a0001c0002t0001g0120 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1244+3466G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179960005 | ||||||
| chr5:179960027
|
A | G | 1 | a0001c0002t0001g0130 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1244+3444T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179960027 | ||||||
| chr5:179960190
|
C | T | 2 | a0001c0003t0001g0147a0001c0003t0001g0148 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1244+3281G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179960190 | ||||||
| chr5:179960366
|
G | A | 10 | a0001c0001t0001g0203a0001c0001t0001g0210a0001c0001t0001g0211others(7): Show | 10 | HG02717.hp1 HG02723.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1244+3105C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179960366 | ||||||
| chr5:179960369
|
C | T | 31 | a0001c0001t0001g0199a0001c0001t0001g0273a0001c0001t0001g0304others(28): Show | 31 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.1244+3102G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179960369 | ||||||
| chr5:179960479
|
G | C | 2 | a0001c0002t0001g0026a0001c0002t0001g0129 | 2 | HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1244+2992C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179960479 | ||||||
| chr5:179960632
|
G | A | 1 | a0001c0003t0001g0155 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1244+2839C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179960632 | ||||||
| chr5:179960845
|
GA | G | 202 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(199): Show | 205 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.1244+2625delT | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179960845 | ||||||
| chr5:179960882
|
T | C | 8 | a0001c0001t0001g0236a0001c0001t0001g0243a0001c0001t0001g0244others(5): Show | 8 | HG02055.hp2 HG02280.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1244+2589A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179960882 | ||||||
| chr5:179960894
|
G | A | 1 | a0001c0005t0001g0194 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1244+2577C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179960894 | ||||||
| chr5:179960916
|
T | C | 2 | a0001c0001t0001g0246a0001c0001t0001g0248 | 2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1244+2555A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179960916 | ||||||
| chr5:179961061
|
G | A | 2 | a0001c0001t0001g0246a0001c0001t0001g0248 | 2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1244+2410C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179961061 | ||||||
| chr5:179961111
|
T | TA | 22 | a0001c0001t0001g0202a0001c0001t0001g0212a0001c0001t0001g0215others(19): Show | 22 | HG01243.hp2 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.1244+2359dupT | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179961111 | ||||||
| chr5:179961156
|
G | A | 2 | a0001c0001t0001g0246a0001c0001t0001g0248 | 2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1244+2315C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179961156 | ||||||
| chr5:179961212
|
G | A | 2 | a0001c0001t0001g0287a0001c0001t0001g0288 | 2 | HG01358.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1244+2259C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179961212 | ||||||
| chr5:179961249
|
A | C | 1 | a0001c0002t0001g0054 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1244+2222T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179961249 | ||||||
| chr5:179961363
|
C | T | 9 | a0001c0001t0001g0275a0001c0002t0001g0040a0001c0002t0001g0077others(6): Show | 9 | NA18942.hp1 NA18943.hp2 NA18950.hp2 others(6): Show |
intron_variant | MODIFIER | c.1244+2108G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179961363 | ||||||
| chr5:179961586
|
C | T | 24 | a0001c0001t0001g0199a0001c0001t0001g0273a0001c0001t0001g0304others(21): Show | 24 | HG00408.hp2 HG00609.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.1244+1885G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179961586 | ||||||
| chr5:179961664
|
T | C | 1 | a0001c0002t0001g0061 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1244+1807A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179961664 | ||||||
| chr5:179961714
|
A | C | 1 | a0001c0002t0001g0069 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1244+1757T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179961714 | ||||||
| chr5:179961857
|
G | T | 1 | a0001c0002t0001g0026 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1244+1614C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179961857 | ||||||
| chr5:179961859
|
C | T | 1 | a0001c0001t0001g0293 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1244+1612G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179961859 | ||||||
| chr5:179961875
|
G | A | 2 | a0001c0001t0001g0244a0001c0003t0001g0156 | 2 | HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1244+1596C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179961875 | ||||||
| chr5:179961947
|
T | C | 7 | a0001c0001t0001g0236a0001c0001t0001g0243a0001c0001t0001g0244others(4): Show | 7 | HG02055.hp2 HG02896.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1244+1524A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179961947 | ||||||
| chr5:179961964
|
A | C | 1 | a0001c0002t0001g0060 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1244+1507T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179961964 | ||||||
| chr5:179962124
|
T | C | 1 | a0001c0003t0002g0153 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1244+1347A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179962124 | ||||||
| chr5:179962294
|
C | T | 1 | a0001c0002t0001g0021 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1244+1177G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179962294 | ||||||
| chr5:179962391
|
A | T | 7 | a0001c0001t0001g0236a0001c0001t0001g0243a0001c0001t0001g0244others(4): Show | 7 | HG02055.hp2 HG02896.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1244+1080T>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179962391 | ||||||
| chr5:179962475
|
T | C | 1 | a0001c0002t0001g0095 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1244+996A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179962475 | ||||||
| chr5:179962539
|
C | T | 1 | a0001c0001t0001g0262 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1244+932G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179962539 | ||||||
| chr5:179962649
|
A | G | 1 | a0001c0001t0001g0285 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1244+822T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179962649 | ||||||
| chr5:179962717
|
C | T | 1 | a0001c0002t0001g0112 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1244+754G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179962717 | ||||||
| chr5:179962801
|
C | T | 1 | a0001c0002t0001g0041 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1244+670G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179962801 | ||||||
| chr5:179962836
|
G | A | 3 | a0001c0005t0003g0161a0001c0005t0003g0190a0001c0005t0003g0191 | 3 | HG02572.hp1 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1244+635C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179962836 | ||||||
| chr5:179962879
|
C | G | 8 | a0001c0001t0001g0236a0001c0001t0001g0243a0001c0001t0001g0244others(5): Show | 8 | HG02055.hp2 HG02280.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1244+592G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179962879 | ||||||
| chr5:179963003
|
A | C | 147 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0213others(144): Show | 150 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.1244+468T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179963003 | ||||||
| chr5:179963116
|
G | A | 2 | a0001c0001t0001g0211a0001c0001t0001g0218 | 2 | HG03098.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1244+355C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179963116 | ||||||
| chr5:179963682
|
G | C | 1 | a0001c0001t0001g0279 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1151-118C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 7/8 | chr5 | 179963682 | ||||||
| chr5:179963995
|
G | A | 1 | a0001c0005t0001g0194 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1151-431C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 7/8 | chr5 | 179963995 | ||||||
| chr5:179964061
|
T | C | 1 | a0001c0003t0001g0151 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1151-497A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 7/8 | chr5 | 179964061 | ||||||
| chr5:179964192
|
G | A | 1 | a0001c0003t0001g0159 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1151-628C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 7/8 | chr5 | 179964192 | ||||||
| chr5:179964584
|
C | T | 4 | a0001c0005t0001g0194a0001c0005t0003g0161a0001c0005t0003g0190others(1): Show | 4 | HG02572.hp1 HG02630.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1151-1020G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 7/8 | chr5 | 179964584 | ||||||
| chr5:179964811
|
A | G | 31 | a0001c0001t0001g0199a0001c0001t0001g0273a0001c0001t0001g0304others(28): Show | 31 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.1151-1247T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 7/8 | chr5 | 179964811 | ||||||
| chr5:179965075
|
G | C | 3 | a0001c0005t0003g0161a0001c0005t0003g0190a0001c0005t0003g0191 | 3 | HG02572.hp1 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1151-1511C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 7/8 | chr5 | 179965075 | ||||||
| chr5:179965081
|
C | T | 1 | a0001c0001t0001g0297 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1151-1517G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 7/8 | chr5 | 179965081 | ||||||
| chr5:179965120
|
G | A | 1 | a0001c0001t0001g0330 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1151-1556C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 7/8 | chr5 | 179965120 | ||||||
| chr5:179965303
|
G | A | 6 | a0001c0001t0002g0242a0001c0002t0002g0128a0001c0003t0002g0153others(3): Show | 6 | HG01884.hp2 HG02451.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1150+1503C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 7/8 | chr5 | 179965303 | ||||||
| chr5:179965313
|
C | T | 217 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(214): Show | 220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.1150+1493G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 7/8 | chr5 | 179965313 | ||||||
| chr5:179965325
|
C | T | 3 | a0001c0005t0003g0161a0001c0005t0003g0190a0001c0005t0003g0191 | 3 | HG02572.hp1 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1150+1481G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 7/8 | chr5 | 179965325 | ||||||
| chr5:179965358
|
A | G | 1 | a0001c0005t0001g0194 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1150+1448T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 7/8 | chr5 | 179965358 | ||||||
| chr5:179965379
|
C | T | 3 | a0001c0001t0001g0237a0001c0003t0001g0158a0001c0003t0001g0159 | 3 | HG03041.hp1 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1150+1427G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 7/8 | chr5 | 179965379 | ||||||
| chr5:179965728
|
A | G | 4 | a0001c0005t0001g0194a0001c0005t0003g0161a0001c0005t0003g0190others(1): Show | 4 | HG02572.hp1 HG02630.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1150+1078T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 7/8 | chr5 | 179965728 | ||||||
| chr5:179965961
|
G | A | 1 | a0001c0002t0001g0093 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1150+845C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 7/8 | chr5 | 179965961 | ||||||
| chr5:179966440
|
G | A | 3 | a0001c0005t0003g0161a0001c0005t0003g0190a0001c0005t0003g0191 | 3 | HG02572.hp1 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1150+366C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 7/8 | chr5 | 179966440 | ||||||
| chr5:179966461
|
A | G | 1 | a0001c0001t0001g0297 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1150+345T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 7/8 | chr5 | 179966461 | ||||||
| chr5:179966739
|
C | T | 1 | a0001c0002t0001g0108 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1150+67G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 7/8 | chr5 | 179966739 | ||||||
| chr5:179966790
|
G | A | 1 | a0001c0001t0001g0329 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1150+16C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 7/8 | chr5 | 179966790 | ||||||
| chr5:179967027
|
G | A | 12 | a0001c0001t0001g0198a0001c0001t0001g0261a0001c0001t0001g0265others(9): Show | 12 | HG00735.hp2 HG01071.hp2 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.946-17C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179967027 | ||||||
| chr5:179967096
|
C | T | 1 | a0001c0005t0001g0194 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.946-86G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179967096 | ||||||
| chr5:179967249
|
T | C | 12 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(9): Show | 12 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.946-239A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179967249 | ||||||
| chr5:179967343
|
T | C | 1 | a0001c0012t0001g0289 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.946-333A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179967343 | ||||||
| chr5:179967438
|
ATCTGGTA others(18): Show |
A | 2 | a0001c0002t0001g0025a0001c0002t0001g0102 | 2 | NA18983.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.946-453_946-429del others(25): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179967438 | ||||||
| chr5:179967490
|
A | T | 1 | a0001c0001t0001g0280 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.946-480T>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179967490 | ||||||
| chr5:179967583
|
T | C | 1 | a0001c0001t0001g0267 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.946-573A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179967583 | ||||||
| chr5:179967666
|
C | T | 1 | a0001c0001t0001g0293 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.946-656G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179967666 | ||||||
| chr5:179967695
|
G | C | 1 | a0001c0001t0001g0240 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.946-685C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179967695 | ||||||
| chr5:179967810
|
G | T | 13 | a0001c0001t0001g0202a0001c0001t0001g0212a0001c0001t0001g0215others(10): Show | 13 | HG01243.hp2 HG01891.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.946-800C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179967810 | ||||||
| chr5:179967948
|
A | G | 1 | a0001c0003t0001g0182 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.946-938T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179967948 | ||||||
| chr5:179967952
|
T | C | 1 | a0001c0004t0001g0135 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.946-942A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179967952 | ||||||
| chr5:179968039
|
T | C | 1 | a0001c0001t0001g0325 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.946-1029A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179968039 | ||||||
| chr5:179968071
|
A | G | 2 | a0001c0001t0001g0252a0001c0002t0001g0106 | 2 | HG02132.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.946-1061T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179968071 | ||||||
| chr5:179968122
|
C | T | 1 | a0001c0002t0001g0008 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.946-1112G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179968122 | ||||||
| chr5:179968156
|
A | G | 11 | a0001c0001t0001g0328a0001c0002t0001g0036a0001c0002t0001g0094others(8): Show | 12 | HG01256.hp1 HG01361.hp2 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.946-1146T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179968156 | ||||||
| chr5:179968173
|
T | C | 3 | a0001c0001t0001g0251a0001c0001t0001g0266a0001c0001t0001g0271 | 3 | NA18955.hp2 NA19005.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.946-1163A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179968173 | ||||||
| chr5:179968175
|
C | G | 4 | a0001c0002t0001g0043a0001c0003t0001g0144a0001c0003t0001g0145others(1): Show | 4 | HG01261.hp2 HG01496.hp2 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.946-1165G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179968175 | ||||||
| chr5:179968187
|
C | T | 6 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0237others(3): Show | 6 | HG02145.hp1 HG03041.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.946-1177G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179968187 | ||||||
| chr5:179968293
|
A | AAAAC | 20 | a0001c0001t0001g0198a0001c0001t0001g0261a0001c0001t0001g0265others(17): Show | 20 | HG00735.hp2 HG01071.hp2 HG01358.hp1 others(17): Show |
intron_variant | MODIFIER | c.946-1287_946-1284d others(6): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179968293 | ||||||
| chr5:179968293
|
AAAACAAA others(1): Show |
A | 5 | a0001c0001t0001g0314a0001c0003t0001g0002a0001c0003t0001g0169others(2): Show | 6 | HG01069.hp1 HG01071.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.946-1291_946-1284d others(10): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179968293 | ||||||
| chr5:179968322
|
A | G | 1 | a0001c0002t0001g0030 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.946-1312T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179968322 | ||||||
| chr5:179968323
|
A | C | 1 | a0001c0002t0001g0030 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.946-1313T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179968323 | ||||||
| chr5:179968325
|
G | A | 171 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(168): Show | 174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.946-1315C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179968325 | ||||||
| chr5:179968326
|
C | A | 171 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(168): Show | 174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.946-1316G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179968326 | ||||||
| chr5:179968493
|
C | G | 146 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0213others(143): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.946-1483G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179968493 | ||||||
| chr5:179968498
|
T | G | 1 | a0001c0003t0001g0155 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.946-1488A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179968498 | ||||||
| chr5:179968534
|
C | T | 1 | a0001c0003t0001g0155 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.946-1524G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179968534 | ||||||
| chr5:179968667
|
T | TA | 33 | a0001c0001t0001g0202a0001c0001t0001g0206a0001c0001t0001g0215others(30): Show | 33 | HG00408.hp1 HG00544.hp2 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.946-1658dupT | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179968667 | ||||||
| chr5:179968667
|
TA | T | 12 | a0001c0001t0001g0210a0001c0001t0001g0262a0001c0001t0001g0306others(9): Show | 12 | HG00323.hp1 HG00609.hp1 HG00733.hp2 others(9): Show |
intron_variant | MODIFIER | c.946-1658delT | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179968667 | ||||||
| chr5:179968686
|
A | G | 1 | a0001c0002t0001g0006 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.946-1676T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179968686 | ||||||
| chr5:179968687
|
A | G | 5 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(2): Show | 5 | HG02572.hp2 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.946-1677T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179968687 | ||||||
| chr5:179968728
|
T | C | 1 | a0001c0002t0001g0005 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.945+1682A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179968728 | ||||||
| chr5:179968736
|
G | C | 1 | a0001c0001t0001g0229 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.945+1674C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179968736 | ||||||
| chr5:179968739
|
A | G | 2 | a0001c0003t0001g0158a0001c0003t0001g0159 | 2 | HG03041.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.945+1671T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179968739 | ||||||
| chr5:179968789
|
C | T | 3 | a0001c0005t0003g0161a0001c0005t0003g0190a0001c0005t0003g0191 | 3 | HG02572.hp1 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.945+1621G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179968789 | ||||||
| chr5:179968992
|
C | T | 3 | a0001c0003t0001g0003a0001c0003t0001g0171a0001c0003t0001g0184 | 4 | HG01081.hp1 HG01257.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.945+1418G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179968992 | ||||||
| chr5:179968995
|
C | G | 1 | a0001c0002t0001g0043 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.945+1415G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179968995 | ||||||
| chr5:179969187
|
T | C | 1 | a0001c0002t0001g0103 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.945+1223A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179969187 | ||||||
| chr5:179969235
|
G | A | 1 | a0001c0003t0001g0160 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.945+1175C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179969235 | ||||||
| chr5:179969340
|
C | T | 5 | a0001c0001t0002g0242a0001c0002t0002g0128a0001c0003t0002g0153others(2): Show | 5 | HG01884.hp2 HG02717.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.945+1070G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179969340 | ||||||
| chr5:179969502
|
T | C | 62 | a0001c0001t0001g0251a0001c0001t0001g0253a0001c0001t0001g0254others(59): Show | 64 | HG00673.hp1 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.945+908A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179969502 | ||||||
| chr5:179969636
|
G | A | 2 | a0001c0001t0001g0308a0001c0002t0001g0109 | 2 | HG02083.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.945+774C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179969636 | ||||||
| chr5:179969852
|
G | C | 1 | a0001c0001t0001g0274 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.945+558C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179969852 | ||||||
| chr5:179969859
|
C | T | 2 | a0001c0002t0001g0075a0001c0002t0001g0107 | 2 | NA18977.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.945+551G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179969859 | ||||||
| chr5:179969866
|
C | T | 8 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(5): Show | 8 | HG02572.hp2 HG02818.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.945+544G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179969866 | ||||||
| chr5:179969950
|
C | T | 1 | a0001c0001t0002g0242 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.945+460G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179969950 | ||||||
| chr5:179969977
|
G | A | 1 | a0001c0003t0001g0193 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.945+433C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179969977 | ||||||
| chr5:179970087
|
C | T | 1 | a0001c0001t0001g0274 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.945+323G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179970087 | ||||||
| chr5:179970183
|
C | T | 1 | a0001c0002t0001g0106 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.945+227G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179970183 | ||||||
| chr5:179970407
|
T | C | 1 | a0001c0003t0001g0183 | 1 | HG02056.hp1 | splice_region_variant&intron_variant | LOW | c.945+3A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179970407 | ||||||
| chr5:179970595
|
T | C | 3 | a0001c0001t0001g0198a0001c0001t0001g0261a0001c0002t0001g0108 | 3 | HG01071.hp2 HG02683.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.849-89A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179970595 | ||||||
| chr5:179970604
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.849-98G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179970604 | ||||||
| chr5:179970609
|
T | G | 2 | a0001c0001t0001g0198a0001c0001t0001g0261 | 2 | HG01071.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.849-103A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179970609 | ||||||
| chr5:179970697
|
T | A | 13 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(10): Show | 13 | HG01884.hp2 HG02572.hp2 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.849-191A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179970697 | ||||||
| chr5:179970868
|
T | C | 7 | a0001c0001t0001g0236a0001c0001t0001g0243a0001c0001t0001g0244others(4): Show | 7 | HG02055.hp2 HG02896.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.849-362A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179970868 | ||||||
| chr5:179970937
|
A | T | 5 | a0001c0003t0001g0155a0001c0005t0001g0194a0001c0005t0003g0161others(2): Show | 5 | HG02280.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.849-431T>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179970937 | ||||||
| chr5:179971027
|
TA | T | 3 | a0001c0005t0003g0161a0001c0005t0003g0190a0001c0005t0003g0191 | 3 | HG02572.hp1 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.849-522delT | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179971027 | ||||||
| chr5:179971103
|
A | ATTTTCT | 4 | a0001c0002t0001g0043a0001c0003t0001g0144a0001c0003t0001g0145others(1): Show | 4 | HG01261.hp2 HG01496.hp2 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.849-603_849-598dup others(6): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179971103 | ||||||
| chr5:179971318
|
G | C | 146 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0213others(143): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.849-812C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179971318 | ||||||
| chr5:179971365
|
G | T | 1 | a0001c0001t0001g0238 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.849-859C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179971365 | ||||||
| chr5:179971400
|
T | C | 5 | a0001c0003t0001g0155a0001c0005t0001g0194a0001c0005t0003g0161others(2): Show | 5 | HG02280.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.849-894A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179971400 | ||||||
| chr5:179971536
|
A | T | 2 | a0001c0001t0001g0330a0001c0001t0001g0331 | 2 | HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.849-1030T>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179971536 | ||||||
| chr5:179971563
|
G | A | 5 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(2): Show | 5 | HG02572.hp2 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.849-1057C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179971563 | ||||||
| chr5:179972082
|
C | T | 1 | a0001c0001t0001g0297 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.849-1576G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179972082 | ||||||
| chr5:179972118
|
G | A | 1 | a0001c0002t0001g0059 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.849-1612C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179972118 | ||||||
| chr5:179972125
|
C | G | 2 | a0001c0001t0001g0320a0001c0003t0001g0155 | 2 | HG00438.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.849-1619G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179972125 | ||||||
| chr5:179972274
|
T | C | 3 | a0001c0005t0003g0161a0001c0005t0003g0190a0001c0005t0003g0191 | 3 | HG02572.hp1 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.849-1768A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179972274 | ||||||
| chr5:179972307
|
G | A | 5 | a0001c0003t0001g0155a0001c0005t0001g0194a0001c0005t0003g0161others(2): Show | 5 | HG02280.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.849-1801C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179972307 | ||||||
| chr5:179972500
|
A | G | 1 | a0001c0005t0001g0194 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.849-1994T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179972500 | ||||||
| chr5:179972568
|
G | A | 1 | a0001c0002t0001g0121 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.849-2062C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179972568 | ||||||
| chr5:179972647
|
G | A | 3 | a0001c0002t0001g0029a0001c0002t0001g0030a0001c0002t0001g0038 | 3 | NA19054.hp2 NA19057.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.849-2141C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179972647 | ||||||
| chr5:179973026
|
C | T | 1 | a0001c0005t0001g0194 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.849-2520G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179973026 | ||||||
| chr5:179973353
|
T | C | 9 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(6): Show | 9 | HG02572.hp2 HG02630.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.849-2847A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179973353 | ||||||
| chr5:179973422
|
C | A | 1 | a0001c0002t0001g0032 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.849-2916G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179973422 | ||||||
| chr5:179973446
|
T | C | 172 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(169): Show | 175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.849-2940A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179973446 | ||||||
| chr5:179973505
|
G | A | 5 | a0001c0001t0002g0242a0001c0002t0002g0128a0001c0003t0002g0153others(2): Show | 5 | HG01884.hp2 HG02717.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.849-2999C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179973505 | ||||||
| chr5:179973589
|
C | T | 1 | a0001c0002t0001g0034 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.849-3083G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179973589 | ||||||
| chr5:179973625
|
C | T | 1 | a0001c0002t0001g0086 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.849-3119G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179973625 | ||||||
| chr5:179973634
|
G | A | 6 | a0001c0001t0001g0328a0001c0001t0002g0242a0001c0002t0002g0128others(3): Show | 6 | HG01884.hp2 HG02165.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.849-3128C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179973634 | ||||||
| chr5:179973635
|
C | T | 1 | a0001c0002t0001g0092 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.849-3129G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179973635 | ||||||
| chr5:179973650
|
T | C | 7 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(4): Show | 7 | HG02572.hp2 HG02630.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.849-3144A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179973650 | ||||||
| chr5:179973847
|
C | A | 153 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(150): Show | 155 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.849-3341G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179973847 | ||||||
| chr5:179973867
|
G | A | 1 | a0001c0002t0001g0038 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.849-3361C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179973867 | ||||||
| chr5:179973870
|
C | T | 5 | a0001c0001t0001g0314a0001c0003t0001g0002a0001c0003t0001g0169others(2): Show | 6 | HG01069.hp1 HG01071.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.849-3364G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179973870 | ||||||
| chr5:179973970
|
C | T | 1 | a0001c0001t0001g0234 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.849-3464G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179973970 | ||||||
| chr5:179973992
|
C | T | 1 | a0001c0003t0002g0157 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.849-3486G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179973992 | ||||||
| chr5:179974087
|
G | A | 1 | a0001c0002t0001g0115 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.849-3581C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179974087 | ||||||
| chr5:179974090
|
G | A | 1 | a0001c0001t0001g0273 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.849-3584C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179974090 | ||||||
| chr5:179974207
|
C | T | 5 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(2): Show | 5 | HG02055.hp1 HG02109.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.849-3701G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179974207 | ||||||
| chr5:179974244
|
G | A | 5 | a0001c0001t0001g0210a0001c0001t0001g0212a0001c0001t0001g0216others(2): Show | 5 | HG01074.hp1 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.849-3738C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179974244 | ||||||
| chr5:179974287
|
C | T | 10 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0261others(7): Show | 10 | HG01361.hp1 HG01934.hp2 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.849-3781G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179974287 | ||||||
| chr5:179974333
|
G | A | 24 | a0001c0001t0001g0219a0001c0001t0001g0250a0001c0001t0001g0251others(21): Show | 24 | HG00544.hp2 HG00673.hp1 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.849-3827C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179974333 | ||||||
| chr5:179974490
|
C | T | 60 | a0001c0001t0001g0198a0001c0001t0001g0249a0001c0001t0001g0250others(57): Show | 60 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.848+3713G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179974490 | ||||||
| chr5:179974525
|
A | C | 8 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0213others(5): Show | 8 | HG01891.hp2 HG02055.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.848+3678T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179974525 | ||||||
| chr5:179974542
|
G | A | 30 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0204others(27): Show | 30 | HG01243.hp1 HG01884.hp1 HG01978.hp1 others(27): Show |
intron_variant | MODIFIER | c.848+3661C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179974542 | ||||||
| chr5:179974553
|
G | A | 1 | a0001c0011t0001g0143 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.848+3650C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179974553 | ||||||
| chr5:179974608
|
G | A | 2 | a0001c0003t0001g0168a0001c0005t0001g0194 | 2 | HG03704.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.848+3595C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179974608 | ||||||
| chr5:179974618
|
A | C | 1 | a0001c0001t0001g0293 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.848+3585T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179974618 | ||||||
| chr5:179974699
|
G | A | 34 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0204others(31): Show | 34 | HG01243.hp1 HG01884.hp1 HG01978.hp1 others(31): Show |
intron_variant | MODIFIER | c.848+3504C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179974699 | ||||||
| chr5:179974751
|
G | A | 1 | a0001c0002t0001g0006 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.848+3452C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179974751 | ||||||
| chr5:179974805
|
G | A | 1 | a0001c0002t0001g0118 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.848+3398C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179974805 | ||||||
| chr5:179974874
|
G | A | 2 | a0001c0002t0001g0059a0001c0002t0001g0120 | 2 | HG01192.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.848+3329C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179974874 | ||||||
| chr5:179974890
|
G | A | 2 | a0001c0002t0001g0076a0001c0002t0001g0111 | 2 | NA18977.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.848+3313C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179974890 | ||||||
| chr5:179974939
|
C | A | 3 | a0001c0002t0001g0071a0001c0002t0001g0093a0001c0002t0001g0096 | 3 | HG03834.hp1 NA18943.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.848+3264G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179974939 | ||||||
| chr5:179974955
|
G | A | 1 | a0001c0001t0001g0284 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.848+3248C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179974955 | ||||||
| chr5:179975025
|
T | C | 4 | a0001c0001t0001g0330a0001c0001t0001g0331a0001c0001t0001g0332others(1): Show | 4 | HG02258.hp1 HG02809.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.848+3178A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179975025 | ||||||
| chr5:179975034
|
G | A | 1 | a0003c0009t0001g0010 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.848+3169C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179975034 | ||||||
| chr5:179975137
|
A | G | 1 | a0001c0003t0001g0155 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.848+3066T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179975137 | ||||||
| chr5:179975151
|
C | A | 1 | a0001c0001t0001g0328 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.848+3052G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179975151 | ||||||
| chr5:179975190
|
G | T | 1 | a0001c0003t0001g0173 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.848+3013C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179975190 | ||||||
| chr5:179975211
|
A | C | 53 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(50): Show | 53 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.848+2992T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179975211 | ||||||
| chr5:179975274
|
G | A | 3 | a0001c0001t0001g0334a0001c0001t0001g0335a0001c0002t0001g0045 | 3 | HG02622.hp1 HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.848+2929C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179975274 | ||||||
| chr5:179975275
|
T | G | 190 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(187): Show | 190 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.848+2928A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179975275 | ||||||
| chr5:179975523
|
C | T | 2 | a0001c0001t0001g0278a0001c0001t0001g0281 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.848+2680G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179975523 | ||||||
| chr5:179975624
|
G | A | 1 | a0001c0001t0001g0308 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.848+2579C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179975624 | ||||||
| chr5:179975769
|
C | T | 61 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0251others(58): Show | 61 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.848+2434G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179975769 | ||||||
| chr5:179976000
|
C | CAG | 217 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(214): Show | 220 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.848+2201_848+2202d others(4): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179976000 | ||||||
| chr5:179976058
|
A | G | 1 | a0001c0001t0001g0253 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.848+2145T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179976058 | ||||||
| chr5:179976061
|
C | T | 61 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0252others(58): Show | 61 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.848+2142G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179976061 | ||||||
| chr5:179976124
|
G | A | 1 | a0001c0002t0001g0076 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.848+2079C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179976124 | ||||||
| chr5:179976258
|
A | C | 175 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(172): Show | 175 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.848+1945T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179976258 | ||||||
| chr5:179976334
|
C | T | 4 | a0001c0003t0001g0165a0001c0003t0001g0168a0001c0003t0001g0172others(1): Show | 4 | HG01943.hp1 HG02559.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.848+1869G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179976334 | ||||||
| chr5:179976347
|
G | C | 3 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0016 | 3 | HG01516.hp1 NA20129.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.848+1856C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179976347 | ||||||
| chr5:179976606
|
A | G | 62 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0251others(59): Show | 62 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.848+1597T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179976606 | ||||||
| chr5:179976688
|
T | G | 1 | a0001c0002t0001g0110 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.848+1515A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179976688 | ||||||
| chr5:179976691
|
A | AT | 29 | a0001c0002t0001g0006a0001c0002t0001g0047a0001c0002t0001g0048others(26): Show | 32 | HG00099.hp1 HG00280.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.848+1511dupA | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179976691 | ||||||
| chr5:179976691
|
A | G | 1 | a0001c0003t0002g0153 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.848+1512T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179976691 | ||||||
| chr5:179976691
|
AT | A | 23 | a0001c0001t0001g0205a0001c0001t0001g0222a0001c0001t0001g0223others(20): Show | 23 | HG01081.hp2 HG01496.hp2 HG01943.hp2 others(20): Show |
intron_variant | MODIFIER | c.848+1511delA | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179976691 | ||||||
| chr5:179976707
|
T | A | 95 | a0001c0001t0001g0199a0001c0001t0001g0202a0001c0001t0001g0204others(92): Show | 95 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.848+1496A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179976707 | ||||||
| chr5:179976708
|
A | T | 3 | a0001c0001t0001g0293a0001c0001t0001g0296a0001c0001t0001g0333 | 3 | HG00738.hp2 HG02486.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.848+1495T>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179976708 | ||||||
| chr5:179976788
|
C | T | 1 | a0001c0001t0001g0328 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.848+1415G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179976788 | ||||||
| chr5:179977001
|
C | T | 1 | a0001c0001t0001g0316 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.848+1202G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179977001 | ||||||
| chr5:179977008
|
A | C | 172 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(169): Show | 172 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.848+1195T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179977008 | ||||||
| chr5:179977039
|
G | C | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0328 | 3 | HG00280.hp1 HG00639.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.848+1164C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179977039 | ||||||
| chr5:179977051
|
C | T | 1 | a0001c0001t0001g0328 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.848+1152G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179977051 | ||||||
| chr5:179977069
|
C | A | 3 | a0001c0003t0001g0155a0001c0003t0002g0153a0001c0003t0002g0154 | 3 | HG01884.hp2 HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.848+1134G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179977069 | ||||||
| chr5:179977114
|
C | T | 62 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0251others(59): Show | 62 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.848+1089G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179977114 | ||||||
| chr5:179977227
|
C | A | 4 | a0001c0001t0001g0330a0001c0001t0001g0331a0001c0001t0001g0332others(1): Show | 4 | HG02258.hp1 HG02809.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.848+976G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179977227 | ||||||
| chr5:179977330
|
T | C | 4 | a0001c0003t0001g0155a0001c0003t0002g0153a0001c0003t0002g0154others(1): Show | 4 | HG01884.hp2 HG02280.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.848+873A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179977330 | ||||||
| chr5:179977375
|
G | A | 216 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(213): Show | 219 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.848+828C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179977375 | ||||||
| chr5:179977425
|
CAGGAATC others(8): Show |
C | 39 | a0001c0001t0001g0294a0001c0001t0001g0333a0001c0002t0001g0094others(36): Show | 42 | HG00280.hp2 HG00738.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.848+763_848+777del others(15): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179977425 | ||||||
| chr5:179977441
|
A | T | 39 | a0001c0001t0001g0294a0001c0001t0001g0333a0001c0002t0001g0094others(36): Show | 42 | HG00280.hp2 HG00738.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.848+762T>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179977441 | ||||||
| chr5:179977451
|
C | T | 1 | a0001c0002t0001g0014 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.848+752G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179977451 | ||||||
| chr5:179977510
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.848+693C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179977510 | ||||||
| chr5:179977744
|
C | T | 3 | a0001c0003t0001g0156a0001c0003t0001g0158a0001c0003t0001g0159 | 3 | HG03041.hp1 HG03139.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.848+459G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179977744 | ||||||
| chr5:179977973
|
G | A | 12 | a0001c0001t0001g0203a0001c0001t0001g0210a0001c0001t0001g0211others(9): Show | 12 | HG02451.hp2 HG02717.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.848+230C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179977973 | ||||||
| chr5:179978025
|
C | T | 49 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(46): Show | 49 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(46): Show |
intron_variant | MODIFIER | c.848+178G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179978025 | ||||||
| chr5:179978144
|
A | G | 53 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(50): Show | 53 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.848+59T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179978144 | ||||||
| chr5:179978379
|
T | C | 1 | a0001c0002t0001g0095 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.766-94A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 4/8 | chr5 | 179978379 | ||||||
| chr5:179978399
|
C | G | 171 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(168): Show | 171 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.766-114G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 4/8 | chr5 | 179978399 | ||||||
| chr5:179978538
|
C | T | 3 | a0001c0001t0001g0266a0001c0002t0001g0104a0001c0002t0004g0084 | 3 | HG02074.hp2 NA18953.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.766-253G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 4/8 | chr5 | 179978538 | ||||||
| chr5:179979233
|
G | T | 1 | a0001c0001t0001g0328 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.765+896C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 4/8 | chr5 | 179979233 | ||||||
| chr5:179979244
|
C | T | 6 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.765+885G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 4/8 | chr5 | 179979244 | ||||||
| chr5:179979341
|
G | A | 1 | a0001c0004t0004g0142 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.765+788C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 4/8 | chr5 | 179979341 | ||||||
| chr5:179979368
|
T | C | 1 | a0001c0005t0003g0161 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.765+761A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 4/8 | chr5 | 179979368 | ||||||
| chr5:179979809
|
T | C | 1 | a0001c0005t0003g0190 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.765+320A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 4/8 | chr5 | 179979809 | ||||||
| chr5:179980229
|
C | T | 253 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(250): Show | 256 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.694-29G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179980229 | ||||||
| chr5:179980378
|
T | G | 1 | a0001c0001t0001g0334 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.694-178A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179980378 | ||||||
| chr5:179980416
|
A | C | 1 | a0001c0001t0001g0249 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.694-216T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179980416 | ||||||
| chr5:179980428
|
G | C | 1 | a0001c0003t0001g0150 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.694-228C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179980428 | ||||||
| chr5:179980708
|
C | T | 1 | a0001c0002t0001g0091 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.694-508G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179980708 | ||||||
| chr5:179980885
|
T | C | 34 | a0001c0001t0001g0333a0001c0002t0001g0094a0001c0003t0001g0001others(31): Show | 37 | HG00280.hp2 HG00738.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.694-685A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179980885 | ||||||
| chr5:179980965
|
G | C | 2 | a0001c0001t0001g0332a0001c0001t0001g0336 | 2 | HG02258.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.694-765C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179980965 | ||||||
| chr5:179980987
|
T | C | 172 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(169): Show | 172 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.694-787A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179980987 | ||||||
| chr5:179981024
|
G | C | 3 | a0001c0003t0001g0156a0001c0003t0001g0158a0001c0003t0001g0159 | 3 | HG03041.hp1 HG03139.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.694-824C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179981024 | ||||||
| chr5:179981095
|
G | A | 1 | a0001c0001t0001g0310 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.694-895C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179981095 | ||||||
| chr5:179981107
|
T | C | 2 | a0001c0004t0001g0132a0001c0004t0001g0134 | 2 | NA18974.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.694-907A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179981107 | ||||||
| chr5:179981174
|
G | GT | 71 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(68): Show | 71 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.694-975dupA | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179981174 | ||||||
| chr5:179981279
|
C | T | 5 | a0001c0001t0001g0330a0001c0001t0001g0331a0001c0001t0001g0332others(2): Show | 5 | HG02258.hp1 HG02809.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.694-1079G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179981279 | ||||||
| chr5:179981357
|
C | T | 1 | a0001c0001t0001g0328 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.694-1157G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179981357 | ||||||
| chr5:179981358
|
G | T | 172 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(169): Show | 172 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.694-1158C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179981358 | ||||||
| chr5:179981366
|
C | T | 8 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(5): Show | 8 | HG02572.hp2 HG02809.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.694-1166G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179981366 | ||||||
| chr5:179981535
|
C | T | 2 | a0001c0001t0001g0334a0001c0001t0001g0335 | 2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.694-1335G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179981535 | ||||||
| chr5:179981536
|
T | G | 172 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(169): Show | 172 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.694-1336A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179981536 | ||||||
| chr5:179981559
|
C | G | 1 | a0001c0003t0001g0175 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.694-1359G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179981559 | ||||||
| chr5:179981631
|
C | T | 1 | a0001c0001t0001g0216 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.694-1431G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179981631 | ||||||
| chr5:179981728
|
C | T | 1 | a0001c0002t0002g0128 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.694-1528G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179981728 | ||||||
| chr5:179981895
|
T | C | 5 | a0001c0001t0001g0209a0001c0003t0001g0155a0001c0003t0002g0153others(2): Show | 5 | HG01884.hp2 HG02280.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.694-1695A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179981895 | ||||||
| chr5:179982108
|
C | T | 219 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(216): Show | 222 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.694-1908G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179982108 | ||||||
| chr5:179982369
|
T | G | 1 | a0001c0001t0001g0285 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.694-2169A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179982369 | ||||||
| chr5:179982405
|
G | C | 3 | a0001c0002t0001g0051a0001c0002t0001g0052a0001c0002t0001g0053 | 3 | HG01069.hp2 HG01168.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.694-2205C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179982405 | ||||||
| chr5:179982434
|
T | C | 2 | a0001c0001t0001g0292a0001c0001t0001g0298 | 2 | HG01109.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.694-2234A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179982434 | ||||||
| chr5:179982566
|
G | GTGTTT | 114 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(111): Show | 114 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.694-2371_694-2367d others(7): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179982566 | ||||||
| chr5:179982566
|
GTGTTT | G | 59 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(56): Show | 59 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.694-2371_694-2367d others(7): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179982566 | ||||||
| chr5:179982613
|
C | T | 109 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(106): Show | 109 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.694-2413G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179982613 | ||||||
| chr5:179982772
|
C | T | 1 | a0001c0002t0001g0114 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.694-2572G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179982772 | ||||||
| chr5:179983029
|
T | C | 1 | a0001c0001t0001g0261 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.694-2829A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179983029 | ||||||
| chr5:179983333
|
CT | C | 110 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(107): Show | 110 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.694-3134delA | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179983333 | ||||||
| chr5:179983546
|
T | C | 1 | a0001c0002t0001g0108 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.694-3346A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179983546 | ||||||
| chr5:179983628
|
G | C | 1 | a0001c0002t0001g0039 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.694-3428C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179983628 | ||||||
| chr5:179983833
|
C | G | 5 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0213others(2): Show | 5 | HG01891.hp2 HG02145.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.694-3633G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179983833 | ||||||
| chr5:179984243
|
C | A | 5 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288others(2): Show | 5 | HG00733.hp1 HG01106.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.694-4043G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179984243 | ||||||
| chr5:179984254
|
T | C | 1 | a0001c0001t0001g0303 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.694-4054A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179984254 | ||||||
| chr5:179984289
|
G | A | 101 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(98): Show | 101 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.694-4089C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179984289 | ||||||
| chr5:179984476
|
C | T | 1 | a0001c0001t0001g0328 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.694-4276G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179984476 | ||||||
| chr5:179984477
|
G | A | 8 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0264others(5): Show | 8 | HG00323.hp1 HG01109.hp2 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.694-4277C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179984477 | ||||||
| chr5:179984482
|
A | G | 5 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288others(2): Show | 5 | HG00733.hp1 HG01106.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.694-4282T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179984482 | ||||||
| chr5:179984660
|
G | T | 210 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(207): Show | 213 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.694-4460C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179984660 | ||||||
| chr5:179985122
|
C | T | 1 | a0001c0002t0001g0065 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.694-4922G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179985122 | ||||||
| chr5:179985153
|
C | CT | 181 | a0001c0001t0001g0198a0001c0001t0001g0202a0001c0001t0001g0203others(178): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.694-4954dupA | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179985153 | ||||||
| chr5:179985153
|
C | CTT | 131 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0209others(128): Show | 131 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.694-4955_694-4954d others(4): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179985153 | ||||||
| chr5:179985153
|
C | CTTT | 16 | a0001c0001t0001g0200a0001c0001t0001g0222a0001c0001t0001g0223others(13): Show | 16 | HG00673.hp1 HG02056.hp2 HG02083.hp1 others(13): Show |
intron_variant | MODIFIER | c.694-4956_694-4954d others(5): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179985153 | ||||||
| chr5:179985337
|
T | G | 4 | a0001c0003t0001g0155a0001c0003t0002g0153a0001c0003t0002g0154others(1): Show | 4 | HG01884.hp2 HG02280.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.694-5137A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179985337 | ||||||
| chr5:179985370
|
T | A | 1 | a0001c0001t0001g0234 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.694-5170A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179985370 | ||||||
| chr5:179985418
|
C | T | 1 | a0001c0002t0001g0089 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.694-5218G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179985418 | ||||||
| chr5:179985482
|
G | A | 215 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(212): Show | 218 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.694-5282C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179985482 | ||||||
| chr5:179985653
|
T | A | 2 | a0001c0003t0001g0192a0001c0005t0003g0191 | 2 | HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.694-5453A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179985653 | ||||||
| chr5:179985707
|
T | G | 215 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(212): Show | 218 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.694-5507A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179985707 | ||||||
| chr5:179985870
|
C | T | 36 | a0001c0001t0001g0330a0001c0001t0001g0331a0001c0001t0001g0333others(33): Show | 39 | HG00280.hp2 HG00738.hp2 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.694-5670G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179985870 | ||||||
| chr5:179986168
|
G | A | 101 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(98): Show | 101 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.694-5968C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179986168 | ||||||
| chr5:179986190
|
T | A | 1 | a0001c0003t0001g0155 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.694-5990A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179986190 | ||||||
| chr5:179986465
|
T | C | 6 | a0001c0003t0001g0177a0001c0003t0001g0178a0001c0003t0001g0179others(3): Show | 6 | HG00558.hp2 HG02056.hp1 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.694-6265A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179986465 | ||||||
| chr5:179986643
|
G | A | 1 | a0001c0001t0001g0230 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.694-6443C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179986643 | ||||||
| chr5:179986779
|
A | C | 1 | a0001c0001t0001g0264 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.694-6579T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179986779 | ||||||
| chr5:179986893
|
GTATTT | G | 4 | a0001c0003t0001g0155a0001c0003t0002g0153a0001c0003t0002g0154others(1): Show | 4 | HG01884.hp2 HG02280.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.694-6698_694-6694d others(7): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179986893 | ||||||
| chr5:179987050
|
A | C | 57 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0252others(54): Show | 57 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.694-6850T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179987050 | ||||||
| chr5:179987053
|
T | A | 1 | a0001c0002t0001g0130 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.694-6853A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179987053 | ||||||
| chr5:179987054
|
C | A | 2 | a0001c0004t0001g0133a0001c0004t0001g0137 | 2 | NA19068.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.694-6854G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179987054 | ||||||
| chr5:179987249
|
C | A | 1 | a0001c0003t0002g0157 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.694-7049G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179987249 | ||||||
| chr5:179987621
|
G | A | 2 | a0001c0002t0001g0008a0001c0002t0001g0009 | 2 | HG02165.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.694-7421C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179987621 | ||||||
| chr5:179987645
|
T | C | 53 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(50): Show | 53 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.694-7445A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179987645 | ||||||
| chr5:179987695
|
C | T | 1 | a0001c0001t0001g0264 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.694-7495G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179987695 | ||||||
| chr5:179987911
|
T | C | 6 | a0001c0001t0001g0334a0001c0001t0001g0335a0001c0003t0001g0155others(3): Show | 6 | HG01884.hp2 HG02280.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.694-7711A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179987911 | ||||||
| chr5:179987945
|
G | A | 2 | a0001c0002t0001g0015a0001c0002t0001g0016 | 2 | HG01516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.694-7745C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179987945 | ||||||
| chr5:179988171
|
G | A | 1 | a0001c0002t0001g0063 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.694-7971C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179988171 | ||||||
| chr5:179988201
|
T | A | 1 | a0001c0002t0001g0005 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.694-8001A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179988201 | ||||||
| chr5:179988259
|
G | T | 4 | a0001c0001t0001g0330a0001c0001t0001g0331a0001c0001t0001g0332others(1): Show | 4 | HG02258.hp1 HG02809.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.694-8059C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179988259 | ||||||
| chr5:179988289
|
C | G | 2 | a0001c0002t0001g0085a0001c0002t0001g0103 | 2 | NA18995.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.694-8089G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179988289 | ||||||
| chr5:179988451
|
T | A | 2 | a0001c0001t0001g0295a0001c0001t0001g0297 | 2 | HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.694-8251A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179988451 | ||||||
| chr5:179988561
|
C | A | 3 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0016 | 3 | HG01516.hp1 NA20129.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.694-8361G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179988561 | ||||||
| chr5:179988579
|
G | T | 1 | a0001c0002t0001g0046 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.694-8379C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179988579 | ||||||
| chr5:179988609
|
CATTT | C | 53 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(50): Show | 53 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.694-8413_694-8410d others(6): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179988609 | ||||||
| chr5:179988654
|
A | C | 56 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(53): Show | 56 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(53): Show |
intron_variant | MODIFIER | c.694-8454T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179988654 | ||||||
| chr5:179988891
|
C | T | 1 | a0001c0005t0003g0190 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.694-8691G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179988891 | ||||||
| chr5:179988985
|
G | A | 57 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0252others(54): Show | 57 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.694-8785C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179988985 | ||||||
| chr5:179989059
|
C | T | 172 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(169): Show | 172 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.694-8859G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179989059 | ||||||
| chr5:179989104
|
G | T | 1 | a0001c0003t0002g0154 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.694-8904C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179989104 | ||||||
| chr5:179989210
|
C | T | 53 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(50): Show | 53 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.694-9010G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179989210 | ||||||
| chr5:179989221
|
T | C | 11 | a0001c0004t0001g0131a0001c0004t0001g0132a0001c0004t0001g0133others(8): Show | 11 | HG02293.hp2 HG03834.hp2 NA18951.hp1 others(8): Show |
intron_variant | MODIFIER | c.694-9021A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179989221 | ||||||
| chr5:179989335
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.694-9135C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179989335 | ||||||
| chr5:179989507
|
C | T | 7 | a0001c0001t0001g0236a0001c0001t0001g0243a0001c0001t0001g0244others(4): Show | 7 | HG02055.hp2 HG02257.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.694-9307G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179989507 | ||||||
| chr5:179989699
|
C | T | 210 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(207): Show | 213 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.694-9499G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179989699 | ||||||
| chr5:179989868
|
G | A | 2 | a0001c0001t0001g0328a0001c0002t0001g0094 | 2 | HG02165.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.694-9668C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179989868 | ||||||
| chr5:179989930
|
T | A | 2 | a0001c0001t0001g0211a0001c0001t0001g0218 | 2 | HG03098.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.694-9730A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179989930 | ||||||
| chr5:179990034
|
G | A | 172 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(169): Show | 172 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.694-9834C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179990034 | ||||||
| chr5:179990078
|
C | T | 172 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(169): Show | 172 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.694-9878G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179990078 | ||||||
| chr5:179990170
|
C | A | 63 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0251others(60): Show | 63 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.694-9970G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179990170 | ||||||
| chr5:179990185
|
A | G | 210 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(207): Show | 213 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.694-9985T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179990185 | ||||||
| chr5:179990204
|
A | G | 3 | a0001c0002t0001g0082a0001c0002t0001g0083a0001c0002t0001g0091 | 3 | HG02683.hp2 HG03017.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.694-10004T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179990204 | ||||||
| chr5:179990205
|
A | G | 1 | a0001c0001t0002g0242 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.694-10005T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179990205 | ||||||
| chr5:179990271
|
T | C | 3 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256 | 3 | HG03209.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.694-10071A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179990271 | ||||||
| chr5:179990335
|
C | T | 53 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(50): Show | 53 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.694-10135G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179990335 | ||||||
| chr5:179990449
|
C | T | 56 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(53): Show | 56 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(53): Show |
intron_variant | MODIFIER | c.694-10249G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179990449 | ||||||
| chr5:179990564
|
G | A | 1 | a0001c0001t0001g0310 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.694-10364C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179990564 | ||||||
| chr5:179990645
|
A | G | 253 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(250): Show | 256 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.694-10445T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179990645 | ||||||
| chr5:179990666
|
C | T | 1 | a0001c0002t0001g0130 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.694-10466G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179990666 | ||||||
| chr5:179990797
|
C | T | 53 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(50): Show | 53 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.694-10597G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179990797 | ||||||
| chr5:179991116
|
T | A | 53 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(50): Show | 53 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.694-10916A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179991116 | ||||||
| chr5:179991116
|
T | G | 1 | a0001c0002t0001g0111 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.694-10916A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179991116 | ||||||
| chr5:179991134
|
T | G | 53 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(50): Show | 53 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.694-10934A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179991134 | ||||||
| chr5:179991172
|
T | C | 38 | a0001c0001t0001g0333a0001c0002t0001g0094a0001c0003t0001g0001others(35): Show | 41 | HG00280.hp2 HG00738.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.694-10972A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179991172 | ||||||
| chr5:179991271
|
C | A | 6 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.694-11071G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179991271 | ||||||
| chr5:179991534
|
G | T | 16 | a0001c0001t0001g0198a0001c0002t0001g0041a0001c0002t0001g0076others(13): Show | 16 | HG00735.hp2 HG01071.hp2 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.694-11334C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179991534 | ||||||
| chr5:179991635
|
C | T | 3 | a0001c0002t0001g0026a0001c0002t0001g0129a0004c0010t0001g0027 | 3 | HG01243.hp2 HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.694-11435G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179991635 | ||||||
| chr5:179991800
|
C | T | 49 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(46): Show | 49 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(46): Show |
intron_variant | MODIFIER | c.694-11600G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179991800 | ||||||
| chr5:179991964
|
G | A | 12 | a0001c0001t0001g0203a0001c0001t0001g0210a0001c0001t0001g0211others(9): Show | 12 | HG02451.hp2 HG02717.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.694-11764C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179991964 | ||||||
| chr5:179991998
|
A | T | 2 | a0001c0002t0001g0015a0001c0002t0001g0016 | 2 | HG01516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.694-11798T>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179991998 | ||||||
| chr5:179992028
|
G | A | 1 | a0001c0001t0001g0260 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.694-11828C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179992028 | ||||||
| chr5:179992070
|
T | C | 1 | a0001c0003t0001g0155 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.694-11870A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179992070 | ||||||
| chr5:179992158
|
T | C | 1 | a0001c0002t0001g0095 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.694-11958A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179992158 | ||||||
| chr5:179992220
|
T | C | 172 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(169): Show | 172 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.694-12020A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179992220 | ||||||
| chr5:179992303
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.694-12103C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179992303 | ||||||
| chr5:179992332
|
G | A | 63 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0251others(60): Show | 63 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.694-12132C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179992332 | ||||||
| chr5:179992544
|
G | A | 1 | a0001c0002t0001g0059 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.694-12344C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179992544 | ||||||
| chr5:179992594
|
T | G | 12 | a0001c0001t0001g0203a0001c0001t0001g0210a0001c0001t0001g0211others(9): Show | 12 | HG02451.hp2 HG02717.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.694-12394A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179992594 | ||||||
| chr5:179992623
|
C | T | 49 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(46): Show | 49 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(46): Show |
intron_variant | MODIFIER | c.694-12423G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179992623 | ||||||
| chr5:179992769
|
C | T | 1 | a0001c0002t0001g0044 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.694-12569G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179992769 | ||||||
| chr5:179992779
|
G | C | 6 | a0001c0001t0001g0334a0001c0001t0001g0335a0001c0003t0001g0155others(3): Show | 6 | HG01884.hp2 HG02280.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.694-12579C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179992779 | ||||||
| chr5:179992914
|
C | G | 1 | a0001c0001t0001g0314 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.694-12714G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179992914 | ||||||
| chr5:179993013
|
T | C | 53 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(50): Show | 53 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.694-12813A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179993013 | ||||||
| chr5:179993071
|
T | C | 1 | a0001c0002t0001g0130 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.694-12871A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179993071 | ||||||
| chr5:179993113
|
C | A | 53 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(50): Show | 53 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.694-12913G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179993113 | ||||||
| chr5:179993187
|
G | A | 3 | a0001c0002t0001g0098a0001c0002t0001g0099a0001c0002t0001g0100 | 3 | NA18979.hp1 NA19079.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.694-12987C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179993187 | ||||||
| chr5:179993213
|
G | A | 1 | a0001c0006t0001g0195 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.694-13013C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179993213 | ||||||
| chr5:179993568
|
GTTGT | G | 32 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(29): Show | 32 | HG00438.hp2 HG00544.hp1 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.694-13372_694-1336 others(8): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179993568 | ||||||
| chr5:179993614
|
T | A | 56 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(53): Show | 56 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(53): Show |
intron_variant | MODIFIER | c.694-13414A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179993614 | ||||||
| chr5:179993991
|
C | T | 63 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0251others(60): Show | 63 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.694-13791G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179993991 | ||||||
| chr5:179994162
|
C | T | 3 | a0001c0002t0001g0042a0001c0002t0001g0064a0001c0002t0001g0097 | 3 | HG01106.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.694-13962G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179994162 | ||||||
| chr5:179994191
|
C | A | 49 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(46): Show | 49 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(46): Show |
intron_variant | MODIFIER | c.694-13991G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179994191 | ||||||
| chr5:179994482
|
G | C | 7 | a0001c0001t0001g0202a0001c0001t0001g0235a0001c0001t0001g0237others(4): Show | 7 | HG02280.hp1 HG02630.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.694-14282C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179994482 | ||||||
| chr5:179994634
|
T | C | 49 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(46): Show | 49 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(46): Show |
intron_variant | MODIFIER | c.694-14434A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179994634 | ||||||
| chr5:179994654
|
T | C | 1 | a0001c0002t0001g0083 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.694-14454A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179994654 | ||||||
| chr5:179994883
|
A | G | 210 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(207): Show | 213 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.694-14683T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179994883 | ||||||
| chr5:179994985
|
G | T | 1 | a0001c0001t0001g0328 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.694-14785C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179994985 | ||||||
| chr5:179995047
|
G | C | 172 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(169): Show | 172 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.694-14847C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179995047 | ||||||
| chr5:179995195
|
G | A | 2 | a0001c0001t0001g0334a0001c0001t0001g0335 | 2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.694-14995C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179995195 | ||||||
| chr5:179995201
|
C | CCT | 38 | a0001c0001t0001g0333a0001c0002t0001g0094a0001c0003t0001g0001others(35): Show | 41 | HG00280.hp2 HG00738.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.694-15003_694-1500 others(6): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179995201 | ||||||
| chr5:179995419
|
G | T | 3 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0319 | 3 | NA18979.hp2 NA19070.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.694-15219C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179995419 | ||||||
| chr5:179995420
|
G | C | 3 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0319 | 3 | NA18979.hp2 NA19070.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.694-15220C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179995420 | ||||||
| chr5:179995460
|
A | G | 2 | a0001c0001t0001g0334a0001c0001t0001g0335 | 2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.694-15260T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179995460 | ||||||
| chr5:179995573
|
T | C | 1 | a0001c0001t0001g0334 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.694-15373A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179995573 | ||||||
| chr5:179995646
|
C | T | 4 | a0001c0001t0001g0205a0001c0001t0001g0207a0001c0001t0001g0209others(1): Show | 4 | HG02055.hp1 HG02109.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.694-15446G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179995646 | ||||||
| chr5:179995809
|
A | T | 1 | a0001c0001t0001g0283 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.694-15609T>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179995809 | ||||||
| chr5:179995835
|
G | A | 38 | a0001c0001t0001g0333a0001c0002t0001g0094a0001c0003t0001g0001others(35): Show | 41 | HG00280.hp2 HG00738.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.694-15635C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179995835 | ||||||
| chr5:179995970
|
A | C | 1 | a0001c0002t0001g0115 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.694-15770T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179995970 | ||||||
| chr5:179996379
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.694-16179C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179996379 | ||||||
| chr5:179996519
|
C | T | 172 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(169): Show | 172 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.694-16319G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179996519 | ||||||
| chr5:179996536
|
T | C | 1 | a0001c0001t0001g0261 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.694-16336A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179996536 | ||||||
| chr5:179996663
|
C | T | 1 | a0001c0001t0001g0259 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.693+16398G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179996663 | ||||||
| chr5:179996860
|
G | A | 55 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(52): Show | 55 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(52): Show |
intron_variant | MODIFIER | c.693+16201C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179996860 | ||||||
| chr5:179996947
|
C | G | 3 | a0001c0002t0001g0051a0001c0002t0001g0052a0001c0002t0001g0053 | 3 | HG01069.hp2 HG01168.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.693+16114G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179996947 | ||||||
| chr5:179997001
|
G | A | 34 | a0001c0001t0001g0333a0001c0002t0001g0094a0001c0003t0001g0001others(31): Show | 37 | HG00280.hp2 HG00738.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.693+16060C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179997001 | ||||||
| chr5:179997044
|
G | A | 1 | a0001c0002t0001g0112 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.693+16017C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179997044 | ||||||
| chr5:179997069
|
T | C | 4 | a0001c0001t0001g0270a0001c0001t0001g0275a0001c0001t0001g0291others(1): Show | 4 | NA18998.hp1 NA19007.hp1 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.693+15992A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179997069 | ||||||
| chr5:179997196
|
C | T | 3 | a0001c0003t0001g0155a0001c0003t0002g0153a0001c0003t0002g0154 | 3 | HG01884.hp2 HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.693+15865G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179997196 | ||||||
| chr5:179997244
|
T | C | 14 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259others(11): Show | 14 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.693+15817A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179997244 | ||||||
| chr5:179997424
|
A | C | 334 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(331): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.693+15637T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179997424 | ||||||
| chr5:179997605
|
G | A | 1 | a0001c0002t0001g0072 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.693+15456C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179997605 | ||||||
| chr5:179997765
|
C | T | 34 | a0001c0001t0001g0333a0001c0002t0001g0094a0001c0003t0001g0001others(31): Show | 37 | HG00280.hp2 HG00738.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.693+15296G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179997765 | ||||||
| chr5:179997821
|
T | G | 8 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(5): Show | 8 | HG02572.hp2 HG02809.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.693+15240A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179997821 | ||||||
| chr5:179998109
|
G | A | 1 | a0001c0003t0001g0193 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.693+14952C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998109 | ||||||
| chr5:179998119
|
G | A | 1 | a0001c0002t0001g0060 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.693+14942C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998119 | ||||||
| chr5:179998128
|
T | C | 4 | a0001c0003t0001g0155a0001c0003t0002g0153a0001c0003t0002g0154others(1): Show | 4 | HG01884.hp2 HG02280.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.693+14933A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998128 | ||||||
| chr5:179998132
|
C | A | 30 | a0001c0001t0001g0333a0001c0002t0001g0094a0001c0003t0001g0001others(27): Show | 33 | HG00280.hp2 HG00738.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.693+14929G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998132 | ||||||
| chr5:179998496
|
C | T | 2 | a0001c0002t0001g0075a0001c0002t0001g0107 | 2 | NA18977.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.693+14565G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998496 | ||||||
| chr5:179998697
|
T | C | 1 | a0001c0001t0001g0297 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.693+14364A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998697 | ||||||
| chr5:179998750
|
G | A | 4 | a0001c0001t0001g0330a0001c0001t0001g0331a0001c0001t0001g0332others(1): Show | 4 | HG02258.hp1 HG02809.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.693+14311C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998750 | ||||||
| chr5:179998773
|
G | A | 2 | a0001c0001t0001g0334a0001c0001t0001g0335 | 2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.693+14288C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998773 | ||||||
| chr5:179998780
|
C | T | 1 | a0001c0001t0001g0332 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.693+14281G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998780 | ||||||
| chr5:179998854
|
ATT | A | 5 | a0001c0001t0001g0203a0001c0002t0001g0020a0001c0002t0001g0022others(2): Show | 5 | HG01934.hp1 NA18959.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.693+14205_693+1420 others(6): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998854 | ||||||
| chr5:179998855
|
T | TATATATA others(10): Show |
1 | a0001c0001t0001g0287 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.693+14205_693+1420 others(21): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998855 | ||||||
| chr5:179998857
|
T | A | 42 | a0001c0001t0001g0250a0001c0001t0001g0254a0001c0001t0001g0255others(39): Show | 42 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(39): Show |
intron_variant | MODIFIER | c.693+14204A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998857 | ||||||
| chr5:179998857
|
T | TATATATA others(24): Show |
1 | a0001c0002t0001g0023 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.693+14203_693+1420 others(35): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998857 | ||||||
| chr5:179998857
|
T | TTA | 10 | a0001c0001t0001g0213a0001c0001t0001g0321a0001c0002t0001g0024others(7): Show | 10 | HG00544.hp1 HG02132.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.693+14203_693+1420 others(6): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998857 | ||||||
| chr5:179998857
|
T | TTATA | 3 | a0001c0001t0001g0331a0001c0001t0001g0334a0001c0002t0001g0054 | 3 | HG02257.hp1 HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.693+14203_693+1420 others(8): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998857 | ||||||
| chr5:179998857
|
T | TTATATAT others(1): Show |
4 | a0001c0001t0001g0299a0001c0001t0001g0300a0001c0001t0001g0330others(1): Show | 4 | HG02056.hp1 HG02074.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.693+14203_693+1420 others(12): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998857 | ||||||
| chr5:179998857
|
T | TTATATAT others(7): Show |
2 | a0001c0001t0001g0314a0001c0001t0001g0335 | 2 | HG01358.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.693+14203_693+1420 others(18): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998857 | ||||||
| chr5:179998857
|
T | TTATATAT others(9): Show |
2 | a0001c0001t0001g0302a0001c0005t0001g0194 | 2 | HG00673.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.693+14203_693+1420 others(20): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998857 | ||||||
| chr5:179998857
|
T | TTATATAT others(11): Show |
2 | a0001c0001t0001g0324a0001c0003t0001g0155 | 2 | HG01169.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.693+14203_693+1420 others(22): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998857 | ||||||
| chr5:179998857
|
T | TTATATAT others(15): Show |
4 | a0001c0001t0001g0308a0001c0001t0001g0329a0001c0002t0001g0046others(1): Show | 4 | HG00558.hp2 HG00735.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.693+14203_693+1420 others(26): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998857 | ||||||
| chr5:179998857
|
T | TTATATAT others(17): Show |
3 | a0001c0001t0001g0322a0001c0003t0001g0162a0001c0003t0001g0178 | 3 | HG00642.hp1 NA18612.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.693+14203_693+1420 others(28): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998857 | ||||||
| chr5:179998857
|
T | TTATATAT others(19): Show |
1 | a0001c0003t0002g0154 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.693+14203_693+1420 others(30): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998857 | ||||||
| chr5:179998857
|
T | TTATATAT others(21): Show |
5 | a0001c0001t0001g0306a0001c0001t0001g0323a0001c0002t0001g0123others(2): Show | 5 | HG01261.hp1 HG02486.hp2 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.693+14203_693+1420 others(32): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998857 | ||||||
| chr5:179998857
|
T | TTATATAT others(23): Show |
2 | a0001c0001t0001g0303a0001c0001t0001g0307 | 2 | HG00140.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.693+14203_693+1420 others(34): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998857 | ||||||
| chr5:179998857
|
T | TTATATAT others(25): Show |
2 | a0001c0003t0001g0152a0001c0003t0001g0179 | 2 | HG00408.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.693+14203_693+1420 others(36): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998857 | ||||||
| chr5:179998857
|
T | TTATATAT others(27): Show |
4 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0003t0001g0144others(1): Show | 4 | HG01261.hp2 NA18943.hp1 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.693+14203_693+1420 others(38): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998857 | ||||||
| chr5:179998857
|
T | TTATATAT others(29): Show |
6 | a0001c0001t0001g0304a0001c0001t0001g0309a0001c0001t0001g0312others(3): Show | 6 | HG01123.hp2 HG03492.hp2 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.693+14203_693+1420 others(40): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998857 | ||||||
| chr5:179998857
|
T | TTATATAT others(31): Show |
5 | a0001c0001t0001g0305a0001c0001t0001g0325a0001c0003t0001g0145others(2): Show | 5 | HG00733.hp2 HG01175.hp1 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.693+14203_693+1420 others(42): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998857 | ||||||
| chr5:179998857
|
T | TTATATAT others(33): Show |
1 | a0001c0003t0001g0164 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.693+14203_693+1420 others(44): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998857 | ||||||
| chr5:179998857
|
T | TTATATAT others(41): Show |
1 | a0001c0003t0001g0146 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.693+14203_693+1420 others(52): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998857 | ||||||
| chr5:179998857
|
T | TTATATAT others(47): Show |
1 | a0001c0001t0001g0313 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.693+14203_693+1420 others(58): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998857 | ||||||
| chr5:179998857
|
TTTTATA | T | 3 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0319 | 3 | NA18979.hp2 NA19070.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.693+14198_693+1420 others(10): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998857 | ||||||
| chr5:179998857
|
TTTTATAT others(3): Show |
T | 7 | a0001c0001t0001g0199a0001c0001t0001g0301a0001c0001t0001g0320others(4): Show | 7 | HG00438.hp2 HG02135.hp1 HG03654.hp2 others(4): Show |
intron_variant | MODIFIER | c.693+14194_693+1420 others(14): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998857 | ||||||
| chr5:179998859
|
T | A | 156 | a0001c0001t0001g0213a0001c0001t0001g0249a0001c0001t0001g0250others(153): Show | 159 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.693+14202A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998859 | ||||||
| chr5:179998859
|
T | TTA | 12 | a0001c0001t0001g0200a0001c0001t0001g0214a0001c0001t0001g0215others(9): Show | 12 | HG00323.hp2 HG00639.hp2 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.693+14200_693+1420 others(6): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998859 | ||||||
| chr5:179998859
|
T | TTATATA | 3 | a0001c0001t0001g0201a0001c0001t0001g0226a0001c0001t0001g0336 | 3 | HG01123.hp1 HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.693+14196_693+1420 others(10): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998859 | ||||||
| chr5:179998859
|
T | TTATATAT others(27): Show |
1 | a0001c0001t0002g0242 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.693+14201_693+1420 others(38): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998859 | ||||||
| chr5:179998859
|
TTA | T | 107 | a0001c0001t0001g0198a0001c0001t0001g0204a0001c0001t0001g0205others(104): Show | 107 | HG00438.hp1 HG00673.hp2 HG00735.hp2 others(104): Show |
intron_variant | MODIFIER | c.693+14200_693+1420 others(6): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998859 | ||||||
| chr5:179998869
|
ATATATAT others(12): Show |
A | 1 | a0001c0001t0001g0253 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.693+14173_693+1419 others(23): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998869 | ||||||
| chr5:179998885
|
G | A | 59 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0251others(56): Show | 59 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.693+14176C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998885 | ||||||
| chr5:179998886
|
T | TA | 3 | a0001c0001t0001g0278a0001c0001t0001g0281a0001c0001t0001g0287 | 3 | HG02109.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.693+14174_693+1417 others(5): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998886 | ||||||
| chr5:179998886
|
T | TATATATA others(4): Show |
4 | a0001c0001t0001g0254a0001c0001t0001g0273a0001c0001t0001g0280others(1): Show | 4 | HG00609.hp2 HG01981.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.693+14174_693+1417 others(15): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998886 | ||||||
| chr5:179998886
|
T | TATATATA others(6): Show |
5 | a0001c0001t0001g0258a0001c0001t0001g0264a0001c0001t0001g0267others(2): Show | 5 | HG00280.hp1 HG02559.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.693+14174_693+1417 others(17): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998886 | ||||||
| chr5:179998886
|
T | TATATATA others(8): Show |
5 | a0001c0001t0001g0262a0001c0001t0001g0279a0001c0001t0001g0296others(2): Show | 5 | HG00323.hp1 HG01433.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.693+14174_693+1417 others(19): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998886 | ||||||
| chr5:179998886
|
T | TATATATA others(10): Show |
4 | a0001c0001t0001g0257a0001c0001t0001g0259a0001c0001t0001g0260others(1): Show | 4 | HG00639.hp1 HG01081.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.693+14174_693+1417 others(21): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998886 | ||||||
| chr5:179998886
|
T | TATATATA others(12): Show |
5 | a0001c0001t0001g0250a0001c0001t0001g0263a0001c0001t0001g0271others(2): Show | 5 | HG00544.hp2 HG00733.hp1 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.693+14174_693+1417 others(23): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998886 | ||||||
| chr5:179998886
|
T | TATATATA others(14): Show |
8 | a0001c0001t0001g0252a0001c0001t0001g0255a0001c0001t0001g0256others(5): Show | 8 | HG01106.hp1 HG02132.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.693+14174_693+1417 others(25): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998886 | ||||||
| chr5:179998886
|
T | TATATATA others(16): Show |
5 | a0001c0001t0001g0261a0001c0001t0001g0272a0001c0001t0001g0277others(2): Show | 5 | NA18951.hp1 NA18989.hp1 NA19077.hp1 others(2): Show |
intron_variant | MODIFIER | c.693+14174_693+1417 others(27): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998886 | ||||||
| chr5:179998886
|
T | TATATATA others(18): Show |
2 | a0001c0001t0001g0274a0001c0001t0001g0276 | 2 | HG00408.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.693+14174_693+1417 others(29): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998886 | ||||||
| chr5:179998886
|
T | TATATATA others(20): Show |
2 | a0001c0001t0001g0265a0001c0001t0001g0270 | 2 | HG02155.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.693+14174_693+1417 others(31): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998886 | ||||||
| chr5:179998886
|
T | TATATATA others(22): Show |
7 | a0001c0001t0001g0266a0001c0001t0001g0275a0001c0004t0001g0132others(4): Show | 7 | HG02293.hp2 NA18962.hp1 NA18974.hp2 others(4): Show |
intron_variant | MODIFIER | c.693+14174_693+1417 others(33): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998886 | ||||||
| chr5:179998886
|
T | TATATATA others(24): Show |
5 | a0001c0001t0001g0251a0001c0001t0001g0288a0001c0001t0001g0297others(2): Show | 5 | HG01358.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.693+14174_693+1417 others(35): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998886 | ||||||
| chr5:179998886
|
T | TATATATA others(26): Show |
1 | a0001c0001t0001g0268 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.693+14174_693+1417 others(37): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998886 | ||||||
| chr5:179998886
|
T | TATATATA others(28): Show |
1 | a0001c0001t0001g0249 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.693+14174_693+1417 others(39): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998886 | ||||||
| chr5:179998886
|
T | TATATATA others(30): Show |
1 | a0001c0004t0001g0131 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.693+14174_693+1417 others(41): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998886 | ||||||
| chr5:179998888
|
T | A | 58 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0251others(55): Show | 58 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.693+14173A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998888 | ||||||
| chr5:179998888
|
T | C | 1 | a0001c0001t0001g0257 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.693+14173A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998888 | ||||||
| chr5:179998894
|
A | G | 5 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0213others(2): Show | 5 | HG01891.hp2 HG02145.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.693+14167T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998894 | ||||||
| chr5:179998930
|
C | T | 2 | a0001c0002t0001g0113a0001c0002t0001g0116 | 2 | HG00735.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.693+14131G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998930 | ||||||
| chr5:179998971
|
A | G | 1 | a0001c0004t0001g0132 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.693+14090T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998971 | ||||||
| chr5:179998979
|
A | T | 1 | a0001c0001t0001g0310 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.693+14082T>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998979 | ||||||
| chr5:179999107
|
C | CTGCCTTG others(5): Show |
63 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0251others(60): Show | 63 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.693+13942_693+1395 others(16): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179999107 | ||||||
| chr5:179999182
|
G | A | 1 | a0001c0002t0001g0059 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.693+13879C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179999182 | ||||||
| chr5:179999460
|
G | A | 1 | a0001c0001t0001g0309 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.693+13601C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179999460 | ||||||
| chr5:179999464
|
G | C | 1 | a0001c0002t0001g0115 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.693+13597C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179999464 | ||||||
| chr5:179999493
|
G | A | 1 | a0001c0001t0001g0333 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.693+13568C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179999493 | ||||||
| chr5:179999619
|
AG | A | 3 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256 | 3 | HG03209.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.693+13441delC | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179999619 | ||||||
| chr5:179999649
|
G | A | 7 | a0001c0001t0001g0236a0001c0001t0001g0243a0001c0001t0001g0244others(4): Show | 7 | HG02055.hp2 HG02257.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.693+13412C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179999649 | ||||||
| chr5:179999662
|
A | G | 1 | a0001c0003t0001g0183 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.693+13399T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179999662 | ||||||
| chr5:179999670
|
T | C | 1 | a0001c0002t0001g0065 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.693+13391A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179999670 | ||||||
| chr5:179999698
|
G | C | 116 | a0001c0001t0001g0199a0001c0001t0001g0249a0001c0001t0001g0250others(113): Show | 116 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.693+13363C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179999698 | ||||||
| chr5:179999800
|
A | G | 5 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288others(2): Show | 5 | HG00733.hp1 HG01106.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.693+13261T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179999800 | ||||||
| chr5:179999998
|
C | T | 2 | a0001c0001t0001g0257a0001c0001t0001g0258 | 2 | HG00280.hp1 HG00639.hp1 |
intron_variant | MODIFIER | c.693+13063G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179999998 | ||||||
| chr5:180000060
|
G | C | 4 | a0001c0001t0001g0299a0001c0001t0001g0300a0001c0001t0001g0321others(1): Show | 4 | HG00544.hp1 HG02074.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.693+13001C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180000060 | ||||||
| chr5:180000089
|
A | G | 63 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0251others(60): Show | 63 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.693+12972T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180000089 | ||||||
| chr5:180000246
|
T | A | 40 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(37): Show | 40 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.693+12815A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180000246 | ||||||
| chr5:180000268
|
C | T | 1 | a0001c0001t0001g0297 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.693+12793G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180000268 | ||||||
| chr5:180000400
|
A | G | 166 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(163): Show | 166 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.693+12661T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180000400 | ||||||
| chr5:180000551
|
A | T | 1 | a0001c0001t0001g0269 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.693+12510T>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180000551 | ||||||
| chr5:180000584
|
CTTAT | C | 5 | a0001c0004t0001g0133a0001c0004t0001g0134a0001c0004t0001g0135others(2): Show | 5 | HG02293.hp2 NA18962.hp1 NA19055.hp1 others(2): Show |
intron_variant | MODIFIER | c.693+12473_693+1247 others(8): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180000584 | ||||||
| chr5:180000592
|
T | C | 1 | a0001c0004t0001g0132 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.693+12469A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180000592 | ||||||
| chr5:180000627
|
C | A | 1 | a0001c0001t0001g0297 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.693+12434G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180000627 | ||||||
| chr5:180000658
|
A | G | 11 | a0001c0002t0001g0005a0001c0002t0001g0067a0001c0002t0001g0071others(8): Show | 11 | HG00673.hp2 HG01993.hp1 HG01993.hp2 others(8): Show |
intron_variant | MODIFIER | c.693+12403T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180000658 | ||||||
| chr5:180000807
|
G | A | 1 | a0001c0002t0001g0011 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.693+12254C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180000807 | ||||||
| chr5:180000836
|
C | T | 49 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(46): Show | 49 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(46): Show |
intron_variant | MODIFIER | c.693+12225G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180000836 | ||||||
| chr5:180000873
|
A | G | 53 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(50): Show | 53 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.693+12188T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180000873 | ||||||
| chr5:180001177
|
T | C | 6 | a0001c0001t0001g0334a0001c0001t0001g0335a0001c0003t0001g0155others(3): Show | 6 | HG01884.hp2 HG02280.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.693+11884A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180001177 | ||||||
| chr5:180001285
|
G | T | 1 | a0001c0001t0001g0296 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.693+11776C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180001285 | ||||||
| chr5:180001401
|
G | C | 1 | a0001c0001t0001g0203 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.693+11660C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180001401 | ||||||
| chr5:180001441
|
G | T | 1 | a0001c0001t0001g0309 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.693+11620C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180001441 | ||||||
| chr5:180001735
|
T | C | 172 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(169): Show | 172 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.693+11326A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180001735 | ||||||
| chr5:180001867
|
G | A | 6 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.693+11194C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180001867 | ||||||
| chr5:180001887
|
G | A | 63 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0251others(60): Show | 63 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.693+11174C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180001887 | ||||||
| chr5:180002159
|
C | T | 3 | a0001c0002t0001g0026a0001c0002t0001g0129a0004c0010t0001g0027 | 3 | HG01243.hp2 HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.693+10902G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180002159 | ||||||
| chr5:180002358
|
C | T | 1 | a0001c0003t0002g0157 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.693+10703G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180002358 | ||||||
| chr5:180002469
|
G | A | 2 | a0001c0003t0001g0187a0001c0003t0001g0189 | 2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.693+10592C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180002469 | ||||||
| chr5:180002592
|
G | C | 1 | a0001c0002t0001g0049 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.693+10469C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180002592 | ||||||
| chr5:180002673
|
C | T | 2 | a0001c0002t0001g0118a0001c0002t0001g0119 | 2 | HG00099.hp2 HG00642.hp2 |
intron_variant | MODIFIER | c.693+10388G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180002673 | ||||||
| chr5:180003005
|
A | G | 2 | a0001c0001t0001g0244a0001c0001t0001g0247 | 2 | HG02055.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.693+10056T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180003005 | ||||||
| chr5:180003046
|
T | C | 4 | a0001c0001t0001g0310a0001c0001t0001g0315a0001c0001t0001g0316others(1): Show | 4 | NA18963.hp1 NA18979.hp2 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.693+10015A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180003046 | ||||||
| chr5:180003261
|
G | A | 17 | a0001c0002t0001g0006a0001c0002t0001g0018a0001c0002t0001g0019others(14): Show | 17 | HG00099.hp1 HG00738.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.693+9800C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180003261 | ||||||
| chr5:180003266
|
T | C | 172 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(169): Show | 172 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.693+9795A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180003266 | ||||||
| chr5:180003267
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.693+9794C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180003267 | ||||||
| chr5:180003282
|
G | A | 1 | a0001c0001t0001g0303 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.693+9779C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180003282 | ||||||
| chr5:180003530
|
C | T | 53 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(50): Show | 53 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.693+9531G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180003530 | ||||||
| chr5:180003536
|
T | C | 1 | a0001c0001t0001g0302 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.693+9525A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180003536 | ||||||
| chr5:180003607
|
C | G | 1 | a0001c0003t0001g0149 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.693+9454G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180003607 | ||||||
| chr5:180003688
|
A | AT | 57 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0252others(54): Show | 57 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.693+9372dupA | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180003688 | ||||||
| chr5:180003689
|
T | A | 1 | a0001c0001t0001g0328 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.693+9372A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180003689 | ||||||
| chr5:180003727
|
G | T | 117 | a0001c0001t0001g0199a0001c0001t0001g0249a0001c0001t0001g0250others(114): Show | 117 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.693+9334C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180003727 | ||||||
| chr5:180003960
|
C | A | 34 | a0001c0001t0001g0333a0001c0002t0001g0094a0001c0003t0001g0001others(31): Show | 37 | HG00280.hp2 HG00738.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.693+9101G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180003960 | ||||||
| chr5:180004140
|
T | G | 2 | a0001c0002t0001g0011a0001c0002t0001g0013 | 2 | HG01517.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.693+8921A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180004140 | ||||||
| chr5:180004193
|
T | C | 2 | a0001c0001t0001g0334a0001c0001t0001g0335 | 2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.693+8868A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180004193 | ||||||
| chr5:180004306
|
T | C | 63 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0251others(60): Show | 63 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.693+8755A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180004306 | ||||||
| chr5:180004558
|
C | A | 3 | a0001c0002t0001g0026a0001c0002t0001g0129a0004c0010t0001g0027 | 3 | HG01243.hp2 HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.693+8503G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180004558 | ||||||
| chr5:180004684
|
T | C | 49 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(46): Show | 49 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(46): Show |
intron_variant | MODIFIER | c.693+8377A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180004684 | ||||||
| chr5:180004703
|
G | C | 7 | a0001c0001t0001g0202a0001c0001t0001g0235a0001c0001t0001g0237others(4): Show | 7 | HG02280.hp1 HG02630.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.693+8358C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180004703 | ||||||
| chr5:180004933
|
T | C | 1 | a0001c0001t0001g0336 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.693+8128A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180004933 | ||||||
| chr5:180004934
|
T | G | 2 | a0001c0001t0001g0334a0001c0001t0001g0335 | 2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.693+8127A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180004934 | ||||||
| chr5:180004990
|
G | T | 2 | a0001c0002t0001g0067a0001c0002t0001g0074 | 2 | HG01993.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.693+8071C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180004990 | ||||||
| chr5:180005085
|
C | T | 1 | a0001c0002t0001g0012 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.693+7976G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180005085 | ||||||
| chr5:180005096
|
G | A | 53 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(50): Show | 53 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.693+7965C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180005096 | ||||||
| chr5:180005104
|
A | G | 3 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215 | 3 | HG01891.hp2 HG02886.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.693+7957T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180005104 | ||||||
| chr5:180005135
|
A | AC | 3 | a0001c0003t0001g0151a0001c0003t0001g0163a0001c0003t0001g0164 | 3 | HG00733.hp2 HG01074.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.693+7925dupG | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180005135 | ||||||
| chr5:180005148
|
C | T | 1 | a0001c0002t0002g0128 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.693+7913G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180005148 | ||||||
| chr5:180005164
|
G | A | 3 | a0001c0001t0001g0293a0001c0001t0001g0294a0001c0001t0001g0296 | 3 | HG02486.hp1 HG02647.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.693+7897C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180005164 | ||||||
| chr5:180005433
|
A | AAAC | 62 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0251others(59): Show | 62 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.693+7625_693+7627d others(5): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180005433 | ||||||
| chr5:180005447
|
A | C | 1 | a0001c0003t0002g0157 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.693+7614T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180005447 | ||||||
| chr5:180005577
|
C | T | 2 | a0001c0002t0001g0015a0001c0002t0001g0016 | 2 | HG01516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.693+7484G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180005577 | ||||||
| chr5:180005701
|
A | G | 1 | a0001c0001t0001g0252 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.693+7360T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180005701 | ||||||
| chr5:180005894
|
T | C | 1 | a0001c0002t0001g0041 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.693+7167A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180005894 | ||||||
| chr5:180005913
|
A | C | 1 | a0001c0001t0001g0250 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.693+7148T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180005913 | ||||||
| chr5:180006023
|
T | C | 1 | a0001c0001t0001g0262 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.693+7038A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180006023 | ||||||
| chr5:180006295
|
GA | G | 53 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(50): Show | 53 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.693+6765delT | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180006295 | ||||||
| chr5:180006524
|
T | C | 1 | a0001c0003t0001g0174 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.693+6537A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180006524 | ||||||
| chr5:180007232
|
C | T | 10 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0262others(7): Show | 10 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(7): Show |
intron_variant | MODIFIER | c.693+5829G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180007232 | ||||||
| chr5:180007347
|
G | C | 1 | a0001c0003t0001g0172 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.693+5714C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180007347 | ||||||
| chr5:180007613
|
G | A | 1 | a0001c0002t0001g0044 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.693+5448C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180007613 | ||||||
| chr5:180007725
|
T | C | 48 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(45): Show | 48 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(45): Show |
intron_variant | MODIFIER | c.693+5336A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180007725 | ||||||
| chr5:180007877
|
C | T | 1 | a0001c0001t0001g0330 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.693+5184G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180007877 | ||||||
| chr5:180007988
|
G | GT | 171 | a0001c0001t0001g0198a0001c0001t0001g0272a0001c0001t0001g0278others(168): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.693+5072dupA | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180007988 | ||||||
| chr5:180007988
|
G | GTT | 58 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0251others(55): Show | 58 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.693+5071_693+5072d others(4): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180007988 | ||||||
| chr5:180007988
|
GT | G | 9 | a0001c0001t0001g0236a0001c0001t0001g0243a0001c0001t0001g0244others(6): Show | 9 | HG00558.hp2 HG02055.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.693+5072delA | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180007988 | ||||||
| chr5:180008011
|
C | T | 1 | a0001c0001t0001g0285 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.693+5050G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180008011 | ||||||
| chr5:180008118
|
T | C | 283 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0201others(280): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.693+4943A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180008118 | ||||||
| chr5:180008185
|
G | A | 1 | a0001c0001t0001g0328 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.693+4876C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180008185 | ||||||
| chr5:180008230
|
A | G | 3 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215 | 3 | HG01891.hp2 HG02886.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.693+4831T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180008230 | ||||||
| chr5:180008348
|
G | A | 63 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0251others(60): Show | 63 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.693+4713C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180008348 | ||||||
| chr5:180008576
|
G | C | 1 | a0001c0003t0001g0183 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.693+4485C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180008576 | ||||||
| chr5:180008621
|
A | C | 63 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0251others(60): Show | 63 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.693+4440T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180008621 | ||||||
| chr5:180008705
|
T | C | 49 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(46): Show | 49 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(46): Show |
intron_variant | MODIFIER | c.693+4356A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180008705 | ||||||
| chr5:180008746
|
C | T | 1 | a0001c0002t0001g0045 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.693+4315G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180008746 | ||||||
| chr5:180008750
|
G | A | 1 | a0001c0003t0001g0181 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.693+4311C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180008750 | ||||||
| chr5:180008898
|
A | G | 1 | a0001c0002t0001g0101 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.693+4163T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180008898 | ||||||
| chr5:180008980
|
A | G | 3 | a0001c0003t0001g0156a0001c0003t0001g0158a0001c0003t0001g0159 | 3 | HG03041.hp1 HG03139.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.693+4081T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180008980 | ||||||
| chr5:180009030
|
T | C | 1 | a0001c0001t0001g0308 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.693+4031A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180009030 | ||||||
| chr5:180009278
|
T | C | 63 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0251others(60): Show | 63 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.693+3783A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180009278 | ||||||
| chr5:180009337
|
T | C | 1 | a0001c0001t0001g0224 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.693+3724A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180009337 | ||||||
| chr5:180009466
|
T | C | 57 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0252others(54): Show | 57 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.693+3595A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180009466 | ||||||
| chr5:180009499
|
A | G | 63 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0251others(60): Show | 63 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.693+3562T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180009499 | ||||||
| chr5:180009547
|
C | T | 1 | a0001c0003t0001g0188 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.693+3514G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180009547 | ||||||
| chr5:180009554
|
C | T | 1 | a0001c0002t0001g0109 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.693+3507G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180009554 | ||||||
| chr5:180009670
|
C | T | 3 | a0001c0001t0001g0293a0001c0001t0001g0294a0001c0001t0001g0296 | 3 | HG02486.hp1 HG02647.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.693+3391G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180009670 | ||||||
| chr5:180009696
|
T | G | 283 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0201others(280): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.693+3365A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180009696 | ||||||
| chr5:180009734
|
A | C | 283 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0201others(280): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.693+3327T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180009734 | ||||||
| chr5:180009960
|
T | C | 1 | a0001c0001t0001g0249 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.693+3101A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180009960 | ||||||
| chr5:180010027
|
C | G | 1 | a0001c0002t0001g0028 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.693+3034G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180010027 | ||||||
| chr5:180010043
|
C | G | 2 | a0001c0001t0001g0283a0001c0001t0001g0284 | 2 | HG02647.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.693+3018G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180010043 | ||||||
| chr5:180010059
|
A | G | 2 | a0001c0001t0001g0308a0001c0003t0001g0152 | 2 | HG00408.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.693+3002T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180010059 | ||||||
| chr5:180010181
|
A | G | 1 | a0001c0001t0001g0328 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.693+2880T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180010181 | ||||||
| chr5:180010244
|
C | CA | 42 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(39): Show | 42 | HG01106.hp1 HG01123.hp1 HG01192.hp1 others(39): Show |
intron_variant | MODIFIER | c.693+2816dupT | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180010244 | ||||||
| chr5:180010244
|
C | CAA | 11 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0209others(8): Show | 11 | HG02055.hp1 HG02145.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.693+2815_693+2816d others(4): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180010244 | ||||||
| chr5:180010244
|
CA | C | 174 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0249others(171): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.693+2816delT | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180010244 | ||||||
| chr5:180010425
|
T | A | 1 | a0001c0001t0001g0303 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.693+2636A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180010425 | ||||||
| chr5:180010519
|
C | T | 49 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(46): Show | 49 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(46): Show |
intron_variant | MODIFIER | c.693+2542G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180010519 | ||||||
| chr5:180010653
|
C | T | 2 | a0001c0001t0001g0244a0001c0001t0001g0247 | 2 | HG02055.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.693+2408G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180010653 | ||||||
| chr5:180010730
|
TA | T | 8 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(5): Show | 8 | HG02572.hp2 HG02809.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.693+2330delT | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180010730 | ||||||
| chr5:180010800
|
T | C | 220 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0201others(217): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.693+2261A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180010800 | ||||||
| chr5:180010915
|
G | A | 1 | a0001c0002t0002g0128 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.693+2146C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180010915 | ||||||
| chr5:180010934
|
T | C | 11 | a0001c0002t0001g0007a0001c0002t0001g0029a0001c0002t0001g0030others(8): Show | 11 | HG02040.hp2 NA18947.hp2 NA18962.hp2 others(8): Show |
intron_variant | MODIFIER | c.693+2127A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180010934 | ||||||
| chr5:180010963
|
A | G | 1 | a0001c0001t0001g0328 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.693+2098T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180010963 | ||||||
| chr5:180011023
|
T | C | 1 | a0001c0001t0001g0309 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.693+2038A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180011023 | ||||||
| chr5:180011105
|
C | T | 4 | a0001c0003t0001g0003a0001c0003t0001g0166a0001c0003t0001g0171others(1): Show | 5 | HG00280.hp2 HG01081.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.693+1956G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180011105 | ||||||
| chr5:180011433
|
C | T | 63 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0251others(60): Show | 63 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.693+1628G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180011433 | ||||||
| chr5:180011626
|
T | G | 283 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0201others(280): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.693+1435A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180011626 | ||||||
| chr5:180011766
|
T | TA | 63 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0251others(60): Show | 63 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.693+1294dupT | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180011766 | ||||||
| chr5:180011891
|
T | C | 49 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(46): Show | 49 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(46): Show |
intron_variant | MODIFIER | c.693+1170A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180011891 | ||||||
| chr5:180011920
|
T | A | 283 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0201others(280): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.693+1141A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180011920 | ||||||
| chr5:180011926
|
A | G | 1 | a0001c0001t0001g0328 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.693+1135T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180011926 | ||||||
| chr5:180011997
|
G | A | 5 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256others(2): Show | 5 | HG02896.hp2 HG02897.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.693+1064C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180011997 | ||||||
| chr5:180012014
|
CCACAGTC others(27): Show |
C | 1 | a0001c0002t0001g0101 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.693+1013_693+1046d others(36): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180012014 | ||||||
| chr5:180012129
|
G | A | 1 | a0001c0002t0001g0108 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.693+932C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180012129 | ||||||
| chr5:180012345
|
A | G | 283 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0201others(280): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.693+716T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180012345 | ||||||
| chr5:180012516
|
C | T | 283 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0201others(280): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.693+545G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180012516 | ||||||
| chr5:180013002
|
G | A | 7 | a0001c0001t0001g0202a0001c0001t0001g0235a0001c0001t0001g0237others(4): Show | 7 | HG02280.hp1 HG02630.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.693+59C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180013002 | ||||||
| chr5:180013358
|
T | C | 48 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(45): Show | 48 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(45): Show |
intron_variant | MODIFIER | c.443-47A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180013358 | ||||||
| chr5:180013576
|
A | C | 9 | a0001c0001t0001g0308a0001c0001t0001g0309a0001c0001t0001g0329others(6): Show | 9 | HG00408.hp2 HG00735.hp1 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.443-265T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180013576 | ||||||
| chr5:180013631
|
A | G | 1 | a0001c0001t0001g0230 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.443-320T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180013631 | ||||||
| chr5:180013838
|
C | A | 1 | a0001c0001t0002g0242 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.443-527G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180013838 | ||||||
| chr5:180013908
|
T | C | 12 | a0001c0001t0001g0203a0001c0001t0001g0210a0001c0001t0001g0211others(9): Show | 12 | HG02451.hp2 HG02717.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.443-597A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180013908 | ||||||
| chr5:180014151
|
G | A | 1 | a0001c0002t0001g0017 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.443-840C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180014151 | ||||||
| chr5:180014173
|
A | G | 2 | a0001c0002t0001g0020a0001c0002t0001g0022 | 2 | NA18974.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.443-862T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180014173 | ||||||
| chr5:180014199
|
T | C | 3 | a0001c0001t0001g0199a0001c0001t0001g0337a0001c0004t0004g0142 | 3 | NA18953.hp2 NA19074.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.443-888A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180014199 | ||||||
| chr5:180014246
|
T | C | 6 | a0001c0001t0001g0329a0001c0002t0001g0046a0001c0002t0001g0123others(3): Show | 6 | HG00735.hp1 HG01261.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.443-935A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180014246 | ||||||
| chr5:180014301
|
C | T | 1 | a0001c0001t0001g0263 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.443-990G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180014301 | ||||||
| chr5:180014331
|
T | A | 220 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0201others(217): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.443-1020A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180014331 | ||||||
| chr5:180014342
|
G | A | 1 | a0001c0001t0001g0328 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.443-1031C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180014342 | ||||||
| chr5:180014648
|
C | G | 62 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0252others(59): Show | 62 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.443-1337G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180014648 | ||||||
| chr5:180014782
|
C | T | 1 | a0001c0002t0001g0061 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.443-1471G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180014782 | ||||||
| chr5:180014842
|
T | C | 283 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0201others(280): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.443-1531A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180014842 | ||||||
| chr5:180014952
|
C | A | 12 | a0001c0002t0001g0006a0001c0002t0001g0047a0001c0002t0001g0048others(9): Show | 12 | HG00099.hp1 HG00738.hp1 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.443-1641G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180014952 | ||||||
| chr5:180015013
|
G | T | 1 | a0001c0002t0001g0008 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.443-1702C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015013 | ||||||
| chr5:180015049
|
C | T | 1 | a0001c0001t0001g0303 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.443-1738G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015049 | ||||||
| chr5:180015437
|
CAAGCTGG others(5): Show |
C | 1 | a0001c0001t0001g0265 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.443-2138_443-2127d others(14): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015437 | ||||||
| chr5:180015445
|
A | AAAAGGAG others(5): Show |
39 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0203others(36): Show | 39 | HG00639.hp2 HG01123.hp1 HG01891.hp2 others(36): Show |
intron_variant | MODIFIER | c.443-2146_443-2135d others(14): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015445 | ||||||
| chr5:180015445
|
AAAAGGAG others(5): Show |
A | 6 | a0001c0001t0001g0334a0001c0001t0001g0335a0001c0003t0001g0155others(3): Show | 6 | HG01884.hp2 HG02280.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.443-2146_443-2135d others(14): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015445 | ||||||
| chr5:180015451
|
A | AGTAGGGA others(17): Show |
1 | a0001c0001t0001g0202 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.443-2141_443-2140i others(26): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015451 | ||||||
| chr5:180015479
|
GGGAAAGG others(4): Show |
G | 1 | a0001c0001t0001g0199 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.443-2179_443-2169d others(13): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015479 | ||||||
| chr5:180015490
|
AGGAAAGG others(5): Show |
A | 3 | a0001c0002t0001g0082a0001c0002t0001g0083a0001c0002t0001g0091 | 3 | HG02683.hp2 HG03017.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.443-2191_443-2180d others(14): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015490 | ||||||
| chr5:180015513
|
A | AG | 8 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(5): Show | 8 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.443-2203dupC | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015513 | ||||||
| chr5:180015524
|
AG | A | 220 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0201others(217): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.443-2214delC | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015524 | ||||||
| chr5:180015536
|
A | AG | 5 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0213others(2): Show | 5 | HG01891.hp2 HG02145.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.443-2226dupC | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015536 | ||||||
| chr5:180015547
|
AG | A | 5 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0213others(2): Show | 5 | HG01891.hp2 HG02145.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.443-2237delC | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015547 | ||||||
| chr5:180015551
|
G | A | 278 | a0001c0001t0001g0198a0001c0001t0001g0202a0001c0001t0001g0203others(275): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.443-2240C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015551 | ||||||
| chr5:180015562
|
G | A | 2 | a0001c0002t0001g0059a0001c0002t0001g0120 | 2 | HG01192.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.443-2251C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015562 | ||||||
| chr5:180015562
|
G | GA | 5 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0213others(2): Show | 5 | HG01891.hp2 HG02145.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.443-2252dupT | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015562 | ||||||
| chr5:180015562
|
GAAGGAGT others(5): Show |
G | 8 | a0001c0001t0001g0309a0001c0002t0001g0046a0001c0002t0001g0123others(5): Show | 8 | HG00408.hp2 HG00735.hp1 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.443-2263_443-2252d others(14): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015562 | ||||||
| chr5:180015562
|
GAAGGAGT others(17): Show |
G | 2 | a0001c0001t0001g0303a0001c0001t0001g0308 | 2 | HG00140.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.443-2275_443-2252d others(26): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015562 | ||||||
| chr5:180015571
|
G | GGGAAAGG others(108): Show |
2 | a0001c0002t0001g0059a0001c0002t0001g0120 | 2 | HG01192.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.443-2261_443-2260i others(117): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015571 | ||||||
| chr5:180015583
|
G | GGGAAAGG others(40): Show |
12 | a0001c0001t0001g0203a0001c0001t0001g0210a0001c0001t0001g0211others(9): Show | 12 | HG02451.hp2 HG02717.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.443-2319_443-2273d others(49): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015583 | ||||||
| chr5:180015595
|
G | GGGAAAGG others(4): Show |
1 | a0001c0003t0001g0149 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.443-2295_443-2285d others(13): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015595 | ||||||
| chr5:180015595
|
G | GGGAAAGG others(26): Show |
1 | a0001c0002t0001g0063 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.443-2285_443-2284i others(35): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015595 | ||||||
| chr5:180015607
|
G | GGGAAAGG others(27): Show |
1 | a0001c0002t0001g0061 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.443-2297_443-2296i others(36): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015607 | ||||||
| chr5:180015607
|
G | GGGAAAGG others(39): Show |
124 | a0001c0001t0001g0198a0001c0001t0001g0236a0001c0001t0001g0243others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.443-2297_443-2296i others(48): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015607 | ||||||
| chr5:180015607
|
G | GGGAAAGG others(16): Show |
1 | a0001c0001t0001g0328 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.443-2319_443-2297d others(25): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015607 | ||||||
| chr5:180015607
|
G | GGGAAAGG others(51): Show |
29 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(26): Show | 29 | HG00639.hp2 HG01123.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.443-2297_443-2296i others(60): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015607 | ||||||
| chr5:180015619
|
G | GGAAAGGA others(26): Show |
1 | a0001c0003t0001g0176 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.443-2309_443-2308i others(35): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015619 | ||||||
| chr5:180015619
|
G | GGAAAGGA others(27): Show |
39 | a0001c0001t0001g0333a0001c0002t0001g0049a0001c0002t0001g0094others(36): Show | 42 | HG00280.hp2 HG00738.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.443-2309_443-2308i others(36): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015619 | ||||||
| chr5:180015619
|
G | GGAAAGGA others(74): Show |
1 | a0001c0002t0002g0128 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.443-2309_443-2308i others(83): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015619 | ||||||
| chr5:180015619
|
G | GGGAAAGG others(4): Show |
1 | a0001c0003t0001g0149 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.443-2319_443-2309d others(13): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015619 | ||||||
| chr5:180015619
|
G | GGGAAAGG others(39): Show |
7 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(4): Show | 7 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.443-2309_443-2308i others(48): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015619 | ||||||
| chr5:180015631
|
G | GGAAAGGA others(15): Show |
1 | a0001c0001t0001g0297 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.443-2321_443-2320i others(24): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015631 | ||||||
| chr5:180015631
|
G | GGAAAGGA others(27): Show |
61 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0252others(58): Show | 61 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.443-2321_443-2320i others(36): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015631 | ||||||
| chr5:180015643
|
G | GGGAAAGG others(62): Show |
1 | a0001c0002t0001g0114 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.443-2333_443-2332i others(71): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015643 | ||||||
| chr5:180015643
|
GGGAAAGG others(4): Show |
G | 1 | a0001c0001t0001g0311 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.443-2343_443-2333d others(13): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015643 | ||||||
| chr5:180015654
|
A | AG | 63 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0252others(60): Show | 63 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.443-2344dupC | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015654 | ||||||
| chr5:180015654
|
A | AGGAAAGG others(17): Show |
1 | a0001c0001t0001g0251 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.443-2344_443-2343i others(26): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015654 | ||||||
| chr5:180015741
|
G | A | 1 | a0001c0003t0001g0185 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.443-2430C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015741 | ||||||
| chr5:180015746
|
A | AGGAAAGG others(5): Show |
280 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0201others(277): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.443-2447_443-2436d others(14): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015746 | ||||||
| chr5:180015776
|
G | GGAGTAGG others(5): Show |
1 | a0001c0001t0001g0237 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.443-2466_443-2465i others(14): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015776 | ||||||
| chr5:180015840
|
G | C | 1 | a0001c0007t0001g0004 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.443-2529C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015840 | ||||||
| chr5:180015987
|
T | G | 1 | a0001c0001t0001g0303 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.443-2676A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015987 | ||||||
| chr5:180016133
|
C | T | 220 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0201others(217): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.443-2822G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180016133 | ||||||
| chr5:180016156
|
A | AAGGACTG others(1385): Show |
1 | a0001c0001t0001g0262 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.443-2846_443-2845i others(1394): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180016156 | ||||||
| chr5:180016190
|
G | T | 53 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(50): Show | 53 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.443-2879C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180016190 | ||||||
| chr5:180016342
|
T | TAAGGAGG others(6): Show |
1 | a0001c0001t0001g0330 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.443-3032_443-3031i others(15): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180016342 | ||||||
| chr5:180016342
|
T | TCAGGAGG others(6): Show |
278 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(275): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.443-3032_443-3031i others(15): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180016342 | ||||||
| chr5:180016379
|
C | T | 3 | a0001c0002t0001g0026a0001c0002t0001g0129a0004c0010t0001g0027 | 3 | HG01243.hp2 HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.443-3068G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180016379 | ||||||
| chr5:180016423
|
C | T | 53 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(50): Show | 53 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.443-3112G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180016423 | ||||||
| chr5:180016563
|
G | A | 48 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(45): Show | 48 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(45): Show |
intron_variant | MODIFIER | c.443-3252C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180016563 | ||||||
| chr5:180016603
|
T | C | 1 | a0001c0001t0001g0328 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.443-3292A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180016603 | ||||||
| chr5:180016630
|
T | G | 1 | a0001c0002t0001g0112 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.443-3319A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180016630 | ||||||
| chr5:180016664
|
T | C | 8 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(5): Show | 8 | HG02572.hp2 HG02809.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.443-3353A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180016664 | ||||||
| chr5:180016888
|
G | A | 1 | a0001c0001t0001g0236 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.443-3577C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180016888 | ||||||
| chr5:180016929
|
A | G | 1 | a0001c0001t0001g0328 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.443-3618T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180016929 | ||||||
| chr5:180016956
|
C | G | 1 | a0001c0002t0001g0105 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.443-3645G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180016956 | ||||||
| chr5:180017079
|
T | C | 1 | a0001c0001t0001g0328 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.443-3768A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180017079 | ||||||
| chr5:180017267
|
C | T | 273 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(270): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.443-3956G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180017267 | ||||||
| chr5:180017271
|
T | A | 1 | a0001c0002t0001g0123 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.443-3960A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180017271 | ||||||
| chr5:180017395
|
T | C | 219 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0201others(216): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.443-4084A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180017395 | ||||||
| chr5:180017413
|
C | T | 1 | a0001c0002t0001g0097 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.443-4102G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180017413 | ||||||
| chr5:180017783
|
C | G | 1 | a0001c0001t0001g0335 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.443-4472G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180017783 | ||||||
| chr5:180018029
|
T | C | 8 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(5): Show | 8 | HG02572.hp2 HG02809.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.443-4718A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180018029 | ||||||
| chr5:180018248
|
C | T | 279 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(276): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.443-4937G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180018248 | ||||||
| chr5:180018294
|
C | T | 1 | a0001c0001t0001g0267 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.443-4983G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180018294 | ||||||
| chr5:180018294
|
CA | C | 266 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(263): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.443-4984delT | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180018294 | ||||||
| chr5:180018617
|
C | T | 1 | a0001c0002t0001g0006 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.443-5306G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180018617 | ||||||
| chr5:180018711
|
C | T | 1 | a0001c0001t0001g0294 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.443-5400G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180018711 | ||||||
| chr5:180018751
|
T | C | 4 | a0001c0003t0001g0155a0001c0003t0002g0153a0001c0003t0002g0154others(1): Show | 4 | HG01884.hp2 HG02280.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.443-5440A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180018751 | ||||||
| chr5:180018797
|
T | C | 335 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(332): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.443-5486A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180018797 | ||||||
| chr5:180018907
|
C | A | 1 | a0001c0002t0001g0098 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.443-5596G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180018907 | ||||||
| chr5:180018908
|
A | G | 1 | a0001c0002t0001g0098 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.443-5597T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180018908 | ||||||
| chr5:180018909
|
G | A | 1 | a0001c0002t0001g0098 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.443-5598C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180018909 | ||||||
| chr5:180019052
|
G | A | 1 | a0001c0003t0001g0150 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.443-5741C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180019052 | ||||||
| chr5:180019189
|
CCTGA | C | 220 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0201others(217): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.443-5882_443-5879d others(6): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180019189 | ||||||
| chr5:180019251
|
G | T | 83 | a0001c0002t0001g0005a0001c0002t0001g0007a0001c0002t0001g0008others(80): Show | 83 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.443-5940C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180019251 | ||||||
| chr5:180019277
|
G | A | 7 | a0001c0001t0001g0236a0001c0001t0001g0243a0001c0001t0001g0244others(4): Show | 7 | HG02055.hp2 HG02257.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.443-5966C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180019277 | ||||||
| chr5:180019363
|
G | A | 6 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0213others(3): Show | 6 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.443-6052C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180019363 | ||||||
| chr5:180019371
|
G | A | 220 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0201others(217): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.443-6060C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180019371 | ||||||
| chr5:180019383
|
C | CA | 49 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(46): Show | 49 | HG00639.hp2 HG01123.hp1 HG01361.hp1 others(46): Show |
intron_variant | MODIFIER | c.443-6073dupT | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180019383 | ||||||
| chr5:180019383
|
CA | C | 9 | a0001c0001t0001g0249a0001c0001t0001g0330a0001c0001t0001g0331others(6): Show | 9 | HG02004.hp2 HG02083.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.443-6073delT | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180019383 | ||||||
| chr5:180019468
|
A | G | 1 | a0001c0001t0001g0330 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.443-6157T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180019468 | ||||||
| chr5:180019500
|
G | A | 49 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(46): Show | 49 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(46): Show |
intron_variant | MODIFIER | c.443-6189C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180019500 | ||||||
| chr5:180019857
|
C | G | 1 | a0001c0001t0001g0249 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.443-6546G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180019857 | ||||||
| chr5:180020200
|
C | A | 273 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(270): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.443-6889G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180020200 | ||||||
| chr5:180020221
|
C | T | 4 | a0001c0003t0001g0165a0001c0003t0001g0168a0001c0003t0001g0172others(1): Show | 4 | HG01943.hp1 HG02559.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.443-6910G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180020221 | ||||||
| chr5:180020255
|
G | A | 3 | a0001c0002t0001g0113a0001c0002t0001g0114a0001c0002t0001g0116 | 3 | HG00735.hp2 HG01361.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.443-6944C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180020255 | ||||||
| chr5:180020307
|
G | C | 1 | a0001c0002t0001g0098 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.443-6996C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180020307 | ||||||
| chr5:180020310
|
A | G | 1 | a0001c0002t0001g0098 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.443-6999T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180020310 | ||||||
| chr5:180020335
|
A | C | 2 | a0001c0001t0001g0278a0001c0001t0001g0281 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.443-7024T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180020335 | ||||||
| chr5:180020456
|
C | T | 1 | a0001c0001t0001g0333 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.443-7145G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180020456 | ||||||
| chr5:180020528
|
C | T | 6 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.443-7217G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180020528 | ||||||
| chr5:180020569
|
G | T | 1 | a0003c0009t0001g0010 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.443-7258C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180020569 | ||||||
| chr5:180020659
|
C | T | 1 | a0001c0002t0001g0044 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.443-7348G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180020659 | ||||||
| chr5:180020661
|
A | T | 53 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(50): Show | 53 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.443-7350T>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180020661 | ||||||
| chr5:180020755
|
A | C | 220 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0201others(217): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.443-7444T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180020755 | ||||||
| chr5:180020888
|
C | T | 1 | a0001c0003t0002g0153 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.443-7577G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180020888 | ||||||
| chr5:180020965
|
T | C | 1 | a0001c0002t0001g0032 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.443-7654A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180020965 | ||||||
| chr5:180021042
|
C | CGCAATCT others(9): Show |
273 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(270): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.443-7732_443-7731i others(18): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180021042 | ||||||
| chr5:180021057
|
G | C | 275 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(272): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.443-7746C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180021057 | ||||||
| chr5:180021103
|
T | C | 1 | a0001c0002t0001g0054 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.443-7792A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180021103 | ||||||
| chr5:180021329
|
T | C | 1 | a0001c0001t0001g0296 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.443-8018A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180021329 | ||||||
| chr5:180021737
|
C | A | 1 | a0001c0002t0001g0130 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.443-8426G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180021737 | ||||||
| chr5:180021742
|
G | A | 1 | a0001c0002t0001g0007 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.443-8431C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180021742 | ||||||
| chr5:180021833
|
T | A | 1 | a0001c0001t0001g0328 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.443-8522A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180021833 | ||||||
| chr5:180021857
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.443-8546G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180021857 | ||||||
| chr5:180021891
|
G | T | 6 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(3): Show | 6 | HG02572.hp2 HG02922.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.443-8580C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180021891 | ||||||
| chr5:180022010
|
C | G | 4 | a0001c0003t0001g0155a0001c0003t0002g0153a0001c0003t0002g0154others(1): Show | 4 | HG01884.hp2 HG02280.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.443-8699G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180022010 | ||||||
| chr5:180022105
|
T | A | 1 | a0001c0002t0001g0085 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.443-8794A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180022105 | ||||||
| chr5:180022121
|
C | A | 14 | a0001c0001t0001g0199a0001c0001t0001g0301a0001c0001t0001g0310others(11): Show | 14 | HG00438.hp2 HG02135.hp1 HG03654.hp2 others(11): Show |
intron_variant | MODIFIER | c.443-8810G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180022121 | ||||||
| chr5:180022370
|
C | T | 3 | a0001c0001t0001g0299a0001c0001t0001g0300a0001c0001t0001g0321 | 3 | HG00544.hp1 HG02074.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.443-9059G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180022370 | ||||||
| chr5:180022480
|
C | T | 1 | a0001c0001t0001g0203 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.443-9169G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180022480 | ||||||
| chr5:180022534
|
A | G | 1 | a0001c0002t0001g0099 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.443-9223T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180022534 | ||||||
| chr5:180022902
|
G | A | 7 | a0001c0002t0001g0094a0001c0003t0001g0001a0001c0003t0001g0173others(4): Show | 8 | HG01256.hp1 HG01928.hp1 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.443-9591C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180022902 | ||||||
| chr5:180023080
|
G | A | 120 | a0001c0001t0001g0198a0001c0002t0001g0005a0001c0002t0001g0006others(117): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.443-9769C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180023080 | ||||||
| chr5:180023252
|
G | A | 1 | a0003c0009t0001g0010 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.443-9941C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180023252 | ||||||
| chr5:180023267
|
G | A | 1 | a0001c0001t0001g0328 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.443-9956C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180023267 | ||||||
| chr5:180023540
|
A | C | 1 | a0001c0002t0001g0098 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.443-10229T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180023540 | ||||||
| chr5:180023544
|
C | A | 1 | a0001c0002t0001g0098 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.443-10233G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180023544 | ||||||
| chr5:180023544
|
C | T | 1 | a0001c0001t0001g0328 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.443-10233G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180023544 | ||||||
| chr5:180023545
|
A | C | 1 | a0001c0002t0001g0098 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.443-10234T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180023545 | ||||||
| chr5:180023814
|
T | C | 1 | a0001c0001t0001g0274 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.443-10503A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180023814 | ||||||
| chr5:180023851
|
G | A | 273 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(270): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.443-10540C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180023851 | ||||||
| chr5:180023882
|
A | C | 1 | a0001c0001t0001g0204 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.443-10571T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180023882 | ||||||
| chr5:180024222
|
G | A | 2 | a0001c0001t0001g0334a0001c0001t0001g0335 | 2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.443-10911C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180024222 | ||||||
| chr5:180024532
|
C | T | 6 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.443-11221G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180024532 | ||||||
| chr5:180024632
|
A | G | 3 | a0001c0003t0001g0174a0001c0003t0001g0175a0001c0003t0001g0182 | 3 | HG01256.hp1 HG01928.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.443-11321T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180024632 | ||||||
| chr5:180024750
|
T | C | 1 | a0001c0001t0001g0303 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.443-11439A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180024750 | ||||||
| chr5:180024772
|
G | A | 1 | a0001c0002t0001g0089 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.443-11461C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180024772 | ||||||
| chr5:180024899
|
T | C | 5 | a0001c0002t0001g0018a0001c0002t0001g0019a0001c0002t0001g0020others(2): Show | 5 | NA18948.hp2 NA18970.hp1 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.443-11588A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180024899 | ||||||
| chr5:180024983
|
C | G | 1 | a0001c0001t0001g0263 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.443-11672G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180024983 | ||||||
| chr5:180025256
|
C | T | 2 | a0001c0001t0001g0200a0001c0001t0001g0201 | 2 | HG02145.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.443-11945G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180025256 | ||||||
| chr5:180025260
|
G | A | 1 | a0001c0002t0001g0069 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.443-11949C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180025260 | ||||||
| chr5:180025523
|
C | T | 12 | a0001c0001t0001g0203a0001c0001t0001g0210a0001c0001t0001g0211others(9): Show | 12 | HG02451.hp2 HG02717.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.443-12212G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180025523 | ||||||
| chr5:180025549
|
T | C | 67 | a0001c0001t0001g0199a0001c0001t0001g0301a0001c0001t0001g0302others(64): Show | 70 | HG00280.hp2 HG00438.hp2 HG00673.hp1 others(67): Show |
intron_variant | MODIFIER | c.443-12238A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180025549 | ||||||
| chr5:180026077
|
A | C | 24 | a0001c0001t0001g0299a0001c0001t0001g0300a0001c0001t0001g0303others(21): Show | 24 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(21): Show |
intron_variant | MODIFIER | c.443-12766T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180026077 | ||||||
| chr5:180026117
|
CA | C | 48 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(45): Show | 48 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(45): Show |
intron_variant | MODIFIER | c.443-12807delT | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180026117 | ||||||
| chr5:180026271
|
A | T | 1 | a0001c0003t0001g0193 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.443-12960T>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180026271 | ||||||
| chr5:180026403
|
G | A | 49 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(46): Show | 49 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(46): Show |
intron_variant | MODIFIER | c.443-13092C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180026403 | ||||||
| chr5:180026680
|
T | C | 54 | a0001c0001t0001g0199a0001c0001t0001g0212a0001c0001t0001g0299others(51): Show | 54 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.443-13369A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180026680 | ||||||
| chr5:180026733
|
C | G | 1 | a0001c0002t0001g0060 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.443-13422G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180026733 | ||||||
| chr5:180026736
|
T | C | 1 | a0001c0003t0001g0160 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.443-13425A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180026736 | ||||||
| chr5:180026793
|
C | A | 1 | a0001c0004t0005g0140 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.443-13482G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180026793 | ||||||
| chr5:180027428
|
G | A | 249 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(246): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.442+13025C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180027428 | ||||||
| chr5:180027508
|
T | C | 67 | a0001c0001t0001g0199a0001c0001t0001g0301a0001c0001t0001g0302others(64): Show | 70 | HG00280.hp2 HG00438.hp2 HG00673.hp1 others(67): Show |
intron_variant | MODIFIER | c.442+12945A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180027508 | ||||||
| chr5:180027656
|
C | T | 24 | a0001c0001t0001g0299a0001c0001t0001g0300a0001c0001t0001g0303others(21): Show | 24 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(21): Show |
intron_variant | MODIFIER | c.442+12797G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180027656 | ||||||
| chr5:180027670
|
G | A | 1 | a0001c0002t0001g0129 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.442+12783C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180027670 | ||||||
| chr5:180027856
|
C | T | 4 | a0001c0003t0001g0156a0001c0003t0001g0158a0001c0003t0001g0159others(1): Show | 4 | HG02451.hp1 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.442+12597G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180027856 | ||||||
| chr5:180028067
|
G | A | 1 | a0001c0002t0001g0072 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.442+12386C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180028067 | ||||||
| chr5:180028414
|
C | T | 1 | a0001c0002t0001g0129 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.442+12039G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180028414 | ||||||
| chr5:180028562
|
AGAAC | A | 220 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0201others(217): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.442+11887_442+1189 others(8): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180028562 | ||||||
| chr5:180028601
|
C | T | 2 | a0001c0001t0001g0332a0001c0001t0001g0336 | 2 | HG02258.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.442+11852G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180028601 | ||||||
| chr5:180028752
|
A | G | 1 | a0001c0005t0001g0194 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.442+11701T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180028752 | ||||||
| chr5:180028773
|
G | A | 3 | a0001c0002t0001g0098a0001c0002t0001g0099a0001c0002t0001g0100 | 3 | NA18979.hp1 NA19079.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.442+11680C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180028773 | ||||||
| chr5:180028852
|
A | G | 220 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0201others(217): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.442+11601T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180028852 | ||||||
| chr5:180028967
|
A | G | 1 | a0001c0007t0001g0004 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.442+11486T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180028967 | ||||||
| chr5:180029155
|
A | G | 273 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(270): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.442+11298T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180029155 | ||||||
| chr5:180029289
|
C | T | 4 | a0001c0001t0001g0330a0001c0001t0001g0331a0001c0001t0001g0332others(1): Show | 4 | HG02258.hp1 HG02809.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.442+11164G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180029289 | ||||||
| chr5:180029483
|
A | G | 1 | a0001c0002t0001g0130 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.442+10970T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180029483 | ||||||
| chr5:180029531
|
A | G | 1 | a0001c0001t0001g0328 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.442+10922T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180029531 | ||||||
| chr5:180029852
|
C | CT | 141 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(138): Show | 144 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.442+10600dupA | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180029852 | ||||||
| chr5:180029852
|
C | CTT | 129 | a0001c0001t0001g0198a0001c0001t0001g0228a0001c0001t0001g0236others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.442+10599_442+1060 others(6): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180029852 | ||||||
| chr5:180030040
|
G | GA | 248 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(245): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.442+10412_442+1041 others(5): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180030040 | ||||||
| chr5:180030108
|
G | C | 4 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0266others(1): Show | 4 | HG02132.hp2 NA18955.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.442+10345C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180030108 | ||||||
| chr5:180030177
|
T | C | 6 | a0001c0001t0001g0334a0001c0001t0001g0335a0001c0003t0001g0155others(3): Show | 6 | HG01884.hp2 HG02280.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.442+10276A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180030177 | ||||||
| chr5:180030223
|
G | T | 1 | a0001c0002t0001g0026 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.442+10230C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180030223 | ||||||
| chr5:180030505
|
C | T | 1 | a0001c0003t0001g0168 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.442+9948G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180030505 | ||||||
| chr5:180030643
|
G | T | 6 | a0001c0002t0001g0018a0001c0002t0001g0019a0001c0002t0001g0020others(3): Show | 6 | HG03710.hp1 NA18948.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.442+9810C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180030643 | ||||||
| chr5:180030818
|
C | A | 1 | a0001c0003t0002g0157 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.442+9635G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180030818 | ||||||
| chr5:180030898
|
C | T | 205 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(202): Show | 205 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.442+9555G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180030898 | ||||||
| chr5:180031009
|
T | C | 24 | a0001c0001t0001g0299a0001c0001t0001g0300a0001c0001t0001g0303others(21): Show | 24 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(21): Show |
intron_variant | MODIFIER | c.442+9444A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180031009 | ||||||
| chr5:180031026
|
A | G | 5 | a0001c0002t0001g0018a0001c0002t0001g0019a0001c0002t0001g0020others(2): Show | 5 | NA18948.hp2 NA18970.hp1 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.442+9427T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180031026 | ||||||
| chr5:180031072
|
C | G | 1 | a0001c0001t0001g0297 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.442+9381G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180031072 | ||||||
| chr5:180031147
|
C | T | 1 | a0001c0002t0001g0101 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.442+9306G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180031147 | ||||||
| chr5:180031170
|
T | C | 1 | a0001c0003t0002g0154 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.442+9283A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180031170 | ||||||
| chr5:180031395
|
G | T | 1 | a0001c0001t0001g0207 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.442+9058C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180031395 | ||||||
| chr5:180031527
|
C | T | 164 | a0001c0001t0001g0198a0001c0001t0001g0330a0001c0001t0001g0331others(161): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.442+8926G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180031527 | ||||||
| chr5:180031579
|
T | C | 4 | a0001c0002t0001g0043a0001c0002t0001g0117a0001c0002t0001g0118others(1): Show | 4 | HG00099.hp2 HG00642.hp2 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.442+8874A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180031579 | ||||||
| chr5:180031665
|
C | T | 164 | a0001c0001t0001g0198a0001c0001t0001g0330a0001c0001t0001g0331others(161): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.442+8788G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180031665 | ||||||
| chr5:180031761
|
G | C | 56 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(53): Show | 56 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(53): Show |
intron_variant | MODIFIER | c.442+8692C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180031761 | ||||||
| chr5:180031847
|
G | A | 164 | a0001c0001t0001g0198a0001c0001t0001g0330a0001c0001t0001g0331others(161): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.442+8606C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180031847 | ||||||
| chr5:180031913
|
T | C | 1 | a0001c0002t0002g0128 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.442+8540A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180031913 | ||||||
| chr5:180031940
|
T | A | 56 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(53): Show | 56 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(53): Show |
intron_variant | MODIFIER | c.442+8513A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180031940 | ||||||
| chr5:180032027
|
T | C | 1 | a0001c0002t0001g0130 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.442+8426A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180032027 | ||||||
| chr5:180032204
|
G | C | 2 | a0001c0002t0001g0008a0001c0002t0001g0009 | 2 | HG02165.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.442+8249C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180032204 | ||||||
| chr5:180032287
|
A | G | 53 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(50): Show | 53 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.442+8166T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180032287 | ||||||
| chr5:180032291
|
T | C | 1 | a0001c0003t0002g0154 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.442+8162A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180032291 | ||||||
| chr5:180032323
|
A | G | 1 | a0001c0001t0001g0308 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.442+8130T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180032323 | ||||||
| chr5:180032735
|
G | A | 1 | a0001c0003t0001g0160 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.442+7718C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180032735 | ||||||
| chr5:180032895
|
T | A | 4 | a0001c0003t0001g0155a0001c0003t0002g0153a0001c0003t0002g0154others(1): Show | 4 | HG01884.hp2 HG02280.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.442+7558A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180032895 | ||||||
| chr5:180032928
|
A | G | 4 | a0001c0003t0001g0156a0001c0003t0001g0158a0001c0003t0001g0159others(1): Show | 4 | HG02451.hp1 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.442+7525T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180032928 | ||||||
| chr5:180032933
|
G | A | 5 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288others(2): Show | 5 | HG00733.hp1 HG01106.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.442+7520C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180032933 | ||||||
| chr5:180032965
|
T | C | 11 | a0001c0004t0001g0131a0001c0004t0001g0132a0001c0004t0001g0133others(8): Show | 11 | HG02293.hp2 HG03834.hp2 NA18951.hp1 others(8): Show |
intron_variant | MODIFIER | c.442+7488A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180032965 | ||||||
| chr5:180033006
|
G | A | 4 | a0001c0003t0001g0156a0001c0003t0001g0158a0001c0003t0001g0159others(1): Show | 4 | HG02451.hp1 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.442+7447C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180033006 | ||||||
| chr5:180033020
|
C | A | 1 | a0001c0001t0001g0292 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.442+7433G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180033020 | ||||||
| chr5:180033026
|
T | C | 1 | a0001c0001t0001g0266 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.442+7427A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180033026 | ||||||
| chr5:180033155
|
ATTTTTTT | A | 5 | a0001c0003t0001g0003a0001c0003t0001g0150a0001c0003t0001g0166others(2): Show | 6 | HG00280.hp2 HG01081.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.442+7291_442+7297d others(9): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180033155 | ||||||
| chr5:180033471
|
C | T | 1 | a0001c0002t0001g0026 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.442+6982G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180033471 | ||||||
| chr5:180033552
|
T | C | 1 | a0001c0001t0001g0217 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.442+6901A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180033552 | ||||||
| chr5:180033563
|
G | A | 3 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0248 | 3 | HG02257.hp2 HG02896.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.442+6890C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180033563 | ||||||
| chr5:180033582
|
C | T | 1 | a0001c0001t0001g0271 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.442+6871G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180033582 | ||||||
| chr5:180033696
|
TA | T | 272 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(269): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.442+6756delT | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180033696 | ||||||
| chr5:180033773
|
CTTGT | C | 126 | a0001c0001t0001g0198a0001c0001t0001g0330a0001c0001t0001g0331others(123): Show | 126 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.442+6676_442+6679d others(6): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180033773 | ||||||
| chr5:180033791
|
T | A | 83 | a0001c0002t0001g0005a0001c0002t0001g0007a0001c0002t0001g0008others(80): Show | 83 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.442+6662A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180033791 | ||||||
| chr5:180033936
|
A | G | 5 | a0001c0001t0001g0330a0001c0001t0001g0331a0001c0001t0001g0332others(2): Show | 5 | HG02258.hp1 HG02809.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.442+6517T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180033936 | ||||||
| chr5:180033968
|
T | A | 53 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(50): Show | 53 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.442+6485A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180033968 | ||||||
| chr5:180034037
|
G | A | 2 | a0001c0001t0001g0334a0001c0001t0001g0335 | 2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.442+6416C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180034037 | ||||||
| chr5:180034093
|
C | CT | 120 | a0001c0001t0001g0198a0001c0002t0001g0005a0001c0002t0001g0006others(117): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.442+6359dupA | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180034093 | ||||||
| chr5:180034093
|
C | T | 8 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(5): Show | 8 | HG02572.hp2 HG02809.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.442+6360G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180034093 | ||||||
| chr5:180034203
|
T | TA | 23 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0203others(20): Show | 23 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.442+6249dupT | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180034203 | ||||||
| chr5:180034258
|
A | G | 1 | a0001c0003t0001g0183 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.442+6195T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180034258 | ||||||
| chr5:180034270
|
T | G | 1 | a0001c0005t0001g0194 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.442+6183A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180034270 | ||||||
| chr5:180034313
|
G | A | 48 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(45): Show | 48 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(45): Show |
intron_variant | MODIFIER | c.442+6140C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180034313 | ||||||
| chr5:180034591
|
G | GTTCAT | 273 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(270): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.442+5857_442+5861d others(7): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180034591 | ||||||
| chr5:180034662
|
C | T | 1 | a0001c0002t0001g0009 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.442+5791G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180034662 | ||||||
| chr5:180034812
|
T | C | 1 | a0001c0001t0001g0262 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.442+5641A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180034812 | ||||||
| chr5:180034835
|
C | T | 10 | a0001c0001t0001g0202a0001c0001t0001g0219a0001c0001t0001g0226others(7): Show | 10 | HG00639.hp2 HG01123.hp1 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.442+5618G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180034835 | ||||||
| chr5:180034836
|
A | G | 1 | a0001c0001t0001g0328 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.442+5617T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180034836 | ||||||
| chr5:180034837
|
T | C | 10 | a0001c0002t0001g0094a0001c0003t0001g0001a0001c0003t0001g0173others(7): Show | 11 | HG01256.hp1 HG01361.hp2 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.442+5616A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180034837 | ||||||
| chr5:180034974
|
G | C | 4 | a0001c0003t0001g0165a0001c0003t0001g0168a0001c0003t0001g0172others(1): Show | 4 | HG01943.hp1 HG02559.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.442+5479C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180034974 | ||||||
| chr5:180035073
|
C | T | 1 | a0001c0001t0001g0250 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.442+5380G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180035073 | ||||||
| chr5:180035233
|
C | T | 3 | a0001c0003t0001g0187a0001c0003t0001g0188a0001c0003t0001g0189 | 3 | HG01243.hp1 HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.442+5220G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180035233 | ||||||
| chr5:180035635
|
T | C | 1 | a0001c0007t0001g0004 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.442+4818A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180035635 | ||||||
| chr5:180035693
|
G | C | 1 | a0001c0001t0001g0328 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.442+4760C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180035693 | ||||||
| chr5:180035801
|
C | T | 33 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(30): Show | 33 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.442+4652G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180035801 | ||||||
| chr5:180036038
|
T | C | 5 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0213others(2): Show | 5 | HG01891.hp2 HG02145.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.442+4415A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180036038 | ||||||
| chr5:180036057
|
A | G | 2 | a0001c0001t0001g0334a0001c0001t0001g0335 | 2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.442+4396T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180036057 | ||||||
| chr5:180036074
|
C | G | 1 | a0001c0001t0001g0310 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.442+4379G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180036074 | ||||||
| chr5:180036153
|
T | A | 1 | a0001c0001t0001g0320 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.442+4300A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180036153 | ||||||
| chr5:180036627
|
T | A | 1 | a0001c0002t0001g0065 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.442+3826A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180036627 | ||||||
| chr5:180036756
|
CA | C | 53 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(50): Show | 53 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.442+3696delT | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180036756 | ||||||
| chr5:180036825
|
G | C | 1 | a0001c0002t0001g0065 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.442+3628C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180036825 | ||||||
| chr5:180036836
|
C | A | 53 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(50): Show | 53 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.442+3617G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180036836 | ||||||
| chr5:180036845
|
TAAGA | T | 273 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(270): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.442+3604_442+3607d others(6): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180036845 | ||||||
| chr5:180036899
|
T | C | 29 | a0001c0001t0001g0199a0001c0001t0001g0301a0001c0001t0001g0302others(26): Show | 29 | HG00438.hp2 HG00673.hp1 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.442+3554A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180036899 | ||||||
| chr5:180037076
|
G | A | 38 | a0001c0001t0001g0333a0001c0002t0001g0094a0001c0003t0001g0001others(35): Show | 41 | HG00280.hp2 HG00738.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.442+3377C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180037076 | ||||||
| chr5:180037255
|
G | A | 1 | a0001c0002t0001g0048 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.442+3198C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180037255 | ||||||
| chr5:180037449
|
C | T | 1 | a0001c0001t0001g0245 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.442+3004G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180037449 | ||||||
| chr5:180037728
|
G | T | 1 | a0001c0002t0001g0106 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.442+2725C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180037728 | ||||||
| chr5:180038247
|
GTC | G | 52 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(49): Show | 52 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.442+2204_442+2205d others(4): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180038247 | ||||||
| chr5:180038380
|
C | T | 1 | a0001c0003t0002g0153 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.442+2073G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180038380 | ||||||
| chr5:180038385
|
AG | A | 10 | a0001c0002t0001g0094a0001c0003t0001g0001a0001c0003t0001g0173others(7): Show | 11 | HG01256.hp1 HG01361.hp2 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.442+2067delC | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180038385 | ||||||
| chr5:180038390
|
GAA | G | 53 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(50): Show | 53 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.442+2061_442+2062d others(4): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180038390 | ||||||
| chr5:180038403
|
C | G | 1 | a0001c0002t0001g0125 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.442+2050G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180038403 | ||||||
| chr5:180038406
|
G | GT | 3 | a0001c0003t0001g0146a0001c0003t0001g0183a0001c0003t0001g0193 | 3 | HG01261.hp1 HG01952.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.442+2046dupA | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180038406 | ||||||
| chr5:180038410
|
TG | T | 162 | a0001c0001t0001g0198a0001c0001t0001g0330a0001c0001t0001g0331others(159): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.442+2042delC | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180038410 | ||||||
| chr5:180038411
|
G | GT | 12 | a0001c0001t0001g0203a0001c0001t0001g0210a0001c0001t0001g0211others(9): Show | 12 | HG02451.hp2 HG02486.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.442+2041dupA | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180038411 | ||||||
| chr5:180038411
|
G | T | 55 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(52): Show | 55 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.442+2042C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180038411 | ||||||
| chr5:180038418
|
T | A | 1 | a0001c0002t0001g0038 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.442+2035A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180038418 | ||||||
| chr5:180038469
|
A | G | 3 | a0001c0002t0001g0026a0001c0002t0001g0129a0004c0010t0001g0027 | 3 | HG01243.hp2 HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.442+1984T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180038469 | ||||||
| chr5:180038470
|
C | T | 273 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(270): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.442+1983G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180038470 | ||||||
| chr5:180038486
|
C | T | 38 | a0001c0001t0001g0333a0001c0002t0001g0094a0001c0003t0001g0001others(35): Show | 41 | HG00280.hp2 HG00738.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.442+1967G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180038486 | ||||||
| chr5:180038607
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.442+1846C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180038607 | ||||||
| chr5:180038629
|
C | T | 1 | a0001c0002t0001g0101 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.442+1824G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180038629 | ||||||
| chr5:180038678
|
G | A | 2 | a0001c0001t0001g0302a0001c0001t0001g0322 | 2 | HG00673.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.442+1775C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180038678 | ||||||
| chr5:180038776
|
T | G | 5 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0213others(2): Show | 5 | HG01891.hp2 HG02145.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.442+1677A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180038776 | ||||||
| chr5:180038922
|
T | G | 1 | a0001c0005t0001g0194 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.442+1531A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180038922 | ||||||
| chr5:180039044
|
T | C | 4 | a0001c0003t0001g0155a0001c0003t0002g0153a0001c0003t0002g0154others(1): Show | 4 | HG01884.hp2 HG02280.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.442+1409A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180039044 | ||||||
| chr5:180039263
|
G | T | 1 | a0004c0010t0001g0027 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.442+1190C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180039263 | ||||||
| chr5:180039428
|
G | C | 1 | a0001c0001t0001g0201 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.442+1025C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180039428 | ||||||
| chr5:180039502
|
T | C | 50 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(47): Show | 50 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.442+951A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180039502 | ||||||
| chr5:180039611
|
C | A | 3 | a0001c0002t0001g0113a0001c0002t0001g0114a0001c0002t0001g0116 | 3 | HG00735.hp2 HG01361.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.442+842G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180039611 | ||||||
| chr5:180039673
|
T | A | 3 | a0001c0003t0001g0155a0001c0003t0002g0153a0001c0003t0002g0154 | 3 | HG01884.hp2 HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.442+780A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180039673 | ||||||
| chr5:180039790
|
A | G | 1 | a0001c0002t0001g0073 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.442+663T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180039790 | ||||||
| chr5:180039936
|
G | C | 2 | a0001c0001t0001g0268a0001c0001t0001g0277 | 2 | NA18950.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.442+517C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180039936 | ||||||
| chr5:180040334
|
G | A | 1 | a0001c0002t0001g0095 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.442+119C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180040334 | ||||||
| chr5:180040721
|
T | C | 5 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0213others(2): Show | 5 | HG01891.hp2 HG02145.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.248-74A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180040721 | ||||||
| chr5:180040971
|
C | T | 2 | a0001c0001t0001g0334a0001c0001t0001g0335 | 2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.248-324G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180040971 | ||||||
| chr5:180041039
|
C | T | 6 | a0001c0001t0001g0334a0001c0001t0001g0335a0001c0003t0001g0155others(3): Show | 6 | HG01884.hp2 HG02280.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.248-392G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180041039 | ||||||
| chr5:180041234
|
T | C | 2 | a0001c0001t0001g0295a0001c0001t0001g0297 | 2 | HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.248-587A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180041234 | ||||||
| chr5:180041316
|
G | A | 1 | a0001c0002t0001g0120 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.248-669C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180041316 | ||||||
| chr5:180041403
|
G | A | 1 | a0001c0001t0001g0328 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.248-756C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180041403 | ||||||
| chr5:180041529
|
TAAG | T | 48 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(45): Show | 48 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(45): Show |
intron_variant | MODIFIER | c.248-885_248-883del others(3): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180041529 | ||||||
| chr5:180041544
|
G | A | 1 | a0001c0002t0001g0020 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.248-897C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180041544 | ||||||
| chr5:180041607
|
CAGAAGGG others(3): Show |
C | 1 | a0001c0003t0001g0145 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.248-970_248-961del others(10): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180041607 | ||||||
| chr5:180041653
|
C | T | 1 | a0001c0005t0001g0194 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.248-1006G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180041653 | ||||||
| chr5:180041672
|
C | T | 5 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288others(2): Show | 5 | HG00733.hp1 HG01106.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.248-1025G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180041672 | ||||||
| chr5:180041851
|
T | C | 1 | a0001c0001t0001g0328 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.248-1204A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180041851 | ||||||
| chr5:180041855
|
T | C | 2 | a0001c0001t0001g0200a0001c0001t0001g0201 | 2 | HG02145.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.248-1208A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180041855 | ||||||
| chr5:180042094
|
C | T | 1 | a0001c0002t0001g0063 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.248-1447G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180042094 | ||||||
| chr5:180042500
|
T | C | 5 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0213others(2): Show | 5 | HG01891.hp2 HG02145.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.248-1853A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180042500 | ||||||
| chr5:180042532
|
T | C | 50 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(47): Show | 50 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.248-1885A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180042532 | ||||||
| chr5:180042600
|
G | C | 3 | a0001c0001t0001g0219a0001c0001t0001g0226a0001c0001t0001g0227 | 3 | HG00639.hp2 HG01123.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.248-1953C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180042600 | ||||||
| chr5:180042612
|
T | A | 2 | a0001c0002t0001g0024a0001c0002t0001g0025 | 2 | NA18983.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.248-1965A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180042612 | ||||||
| chr5:180042646
|
C | T | 2 | a0001c0001t0001g0334a0001c0001t0001g0335 | 2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.248-1999G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180042646 | ||||||
| chr5:180043141
|
A | T | 1 | a0001c0003t0001g0168 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.248-2494T>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180043141 | ||||||
| chr5:180043642
|
A | G | 273 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(270): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.248-2995T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180043642 | ||||||
| chr5:180043682
|
A | G | 1 | a0001c0001t0001g0237 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.248-3035T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180043682 | ||||||
| chr5:180043773
|
G | C | 273 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(270): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.248-3126C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180043773 | ||||||
| chr5:180043914
|
T | A | 1 | a0001c0001t0001g0241 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.248-3267A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180043914 | ||||||
| chr5:180043930
|
A | G | 173 | a0001c0001t0001g0198a0001c0001t0001g0330a0001c0001t0001g0331others(170): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.248-3283T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180043930 | ||||||
| chr5:180043967
|
G | A | 1 | a0001c0001t0001g0269 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.248-3320C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180043967 | ||||||
| chr5:180044040
|
G | A | 167 | a0001c0001t0001g0198a0001c0001t0001g0330a0001c0001t0001g0331others(164): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.248-3393C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180044040 | ||||||
| chr5:180044145
|
G | A | 167 | a0001c0001t0001g0198a0001c0001t0001g0330a0001c0001t0001g0331others(164): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.248-3498C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180044145 | ||||||
| chr5:180044201
|
C | T | 51 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(48): Show | 51 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.248-3554G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180044201 | ||||||
| chr5:180044272
|
C | A | 1 | a0004c0010t0001g0027 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.248-3625G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180044272 | ||||||
| chr5:180044323
|
A | G | 4 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0266others(1): Show | 4 | HG02132.hp2 NA18955.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.248-3676T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180044323 | ||||||
| chr5:180044337
|
C | T | 1 | a0001c0003t0002g0157 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.248-3690G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180044337 | ||||||
| chr5:180044420
|
G | A | 2 | a0001c0001t0001g0314a0001c0001t0001g0324 | 2 | HG01169.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.248-3773C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180044420 | ||||||
| chr5:180044457
|
G | A | 1 | a0001c0001t0001g0251 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.248-3810C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180044457 | ||||||
| chr5:180044532
|
C | T | 2 | a0001c0001t0001g0334a0001c0001t0001g0335 | 2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.248-3885G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180044532 | ||||||
| chr5:180044556
|
G | A | 50 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(47): Show | 50 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.248-3909C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180044556 | ||||||
| chr5:180044600
|
G | T | 1 | a0001c0002t0001g0091 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.248-3953C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180044600 | ||||||
| chr5:180044810
|
C | T | 48 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(45): Show | 48 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(45): Show |
intron_variant | MODIFIER | c.248-4163G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180044810 | ||||||
| chr5:180044819
|
T | C | 7 | a0001c0001t0001g0236a0001c0001t0001g0243a0001c0001t0001g0244others(4): Show | 7 | HG02055.hp2 HG02257.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.248-4172A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180044819 | ||||||
| chr5:180045009
|
G | C | 2 | a0001c0002t0001g0035a0001c0002t0001g0037 | 2 | NA18989.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.248-4362C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180045009 | ||||||
| chr5:180045011
|
G | A | 1 | a0001c0002t0001g0086 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.248-4364C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180045011 | ||||||
| chr5:180045187
|
A | G | 273 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(270): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.248-4540T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180045187 | ||||||
| chr5:180045314
|
G | A | 1 | a0001c0002t0001g0087 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.248-4667C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180045314 | ||||||
| chr5:180045316
|
G | A | 2 | a0001c0004t0001g0131a0001c0004t0001g0141 | 2 | NA18951.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.248-4669C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180045316 | ||||||
| chr5:180045324
|
A | G | 1 | a0001c0002t0001g0121 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.248-4677T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180045324 | ||||||
| chr5:180045394
|
C | T | 222 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0201others(219): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.248-4747G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180045394 | ||||||
| chr5:180045498
|
G | A | 5 | a0001c0001t0001g0293a0001c0001t0001g0294a0001c0001t0001g0295others(2): Show | 5 | HG02486.hp1 HG02647.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.248-4851C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180045498 | ||||||
| chr5:180045586
|
A | G | 1 | a0001c0002t0001g0030 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.248-4939T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180045586 | ||||||
| chr5:180045728
|
A | G | 273 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(270): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.248-5081T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180045728 | ||||||
| chr5:180045943
|
C | T | 1 | a0001c0002t0001g0093 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.248-5296G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180045943 | ||||||
| chr5:180045985
|
C | T | 50 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(47): Show | 50 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.248-5338G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180045985 | ||||||
| chr5:180045992
|
C | G | 1 | a0001c0002t0001g0066 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.248-5345G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180045992 | ||||||
| chr5:180046044
|
G | A | 50 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(47): Show | 50 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.248-5397C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180046044 | ||||||
| chr5:180046115
|
C | T | 1 | a0001c0001t0002g0242 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.248-5468G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180046115 | ||||||
| chr5:180046129
|
G | A | 222 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0201others(219): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.248-5482C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180046129 | ||||||
| chr5:180046161
|
G | A | 2 | a0001c0002t0001g0011a0001c0002t0001g0013 | 2 | HG01517.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.248-5514C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180046161 | ||||||
| chr5:180046207
|
G | A | 1 | a0001c0002t0001g0096 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.248-5560C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180046207 | ||||||
| chr5:180046218
|
A | T | 173 | a0001c0001t0001g0198a0001c0001t0001g0330a0001c0001t0001g0331others(170): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.248-5571T>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180046218 | ||||||
| chr5:180046328
|
G | A | 51 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(48): Show | 51 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.248-5681C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180046328 | ||||||
| chr5:180046346
|
G | A | 222 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0201others(219): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.248-5699C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180046346 | ||||||
| chr5:180046351
|
C | T | 5 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256others(2): Show | 5 | HG02896.hp2 HG02897.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.248-5704G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180046351 | ||||||
| chr5:180046460
|
G | C | 34 | a0001c0001t0001g0333a0001c0002t0001g0094a0001c0003t0001g0001others(31): Show | 37 | HG00280.hp2 HG00738.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.248-5813C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180046460 | ||||||
| chr5:180046574
|
T | G | 1 | a0001c0003t0002g0167 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.248-5927A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180046574 | ||||||
| chr5:180046604
|
C | T | 1 | a0001c0003t0002g0153 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.248-5957G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180046604 | ||||||
| chr5:180046731
|
T | G | 5 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256others(2): Show | 5 | HG02896.hp2 HG02897.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.248-6084A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180046731 | ||||||
| chr5:180046900
|
G | A | 51 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(48): Show | 51 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.248-6253C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180046900 | ||||||
| chr5:180046915
|
A | G | 1 | a0001c0002t0001g0031 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.248-6268T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180046915 | ||||||
| chr5:180047008
|
TTC | T | 173 | a0001c0001t0001g0198a0001c0001t0001g0330a0001c0001t0001g0331others(170): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.248-6363_248-6362d others(4): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180047008 | ||||||
| chr5:180047219
|
T | C | 34 | a0001c0001t0001g0333a0001c0002t0001g0094a0001c0003t0001g0001others(31): Show | 37 | HG00280.hp2 HG00738.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.248-6572A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180047219 | ||||||
| chr5:180047587
|
A | G | 1 | a0001c0001t0002g0242 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.248-6940T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180047587 | ||||||
| chr5:180047637
|
G | A | 51 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(48): Show | 51 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.248-6990C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180047637 | ||||||
| chr5:180047705
|
C | T | 1 | a0001c0002t0001g0130 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.248-7058G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180047705 | ||||||
| chr5:180047768
|
G | A | 1 | a0001c0001t0001g0328 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.248-7121C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180047768 | ||||||
| chr5:180047808
|
C | T | 3 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0016 | 3 | HG01516.hp1 NA20129.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.248-7161G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180047808 | ||||||
| chr5:180047864
|
CCA | C | 3 | a0001c0002t0001g0026a0001c0002t0001g0129a0004c0010t0001g0027 | 3 | HG01243.hp2 HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.248-7219_248-7218d others(4): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180047864 | ||||||
| chr5:180047925
|
C | T | 1 | a0001c0003t0001g0185 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.248-7278G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180047925 | ||||||
| chr5:180047975
|
T | C | 273 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(270): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.248-7328A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180047975 | ||||||
| chr5:180048001
|
C | CT | 250 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(247): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.248-7355dupA | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180048001 | ||||||
| chr5:180048001
|
C | CTT | 17 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(14): Show | 17 | HG02055.hp2 HG02257.hp2 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.248-7356_248-7355d others(4): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180048001 | ||||||
| chr5:180048137
|
G | T | 1 | a0001c0002t0001g0121 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.248-7490C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180048137 | ||||||
| chr5:180048165
|
A | G | 2 | a0001c0001t0001g0304a0001c0001t0001g0305 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.248-7518T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180048165 | ||||||
| chr5:180048239
|
C | T | 222 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0201others(219): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.248-7592G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180048239 | ||||||
| chr5:180048279
|
G | A | 3 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0065 | 3 | HG00099.hp1 HG01109.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.248-7632C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180048279 | ||||||
| chr5:180048336
|
G | A | 1 | a0001c0002t0001g0120 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.248-7689C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180048336 | ||||||
| chr5:180048403
|
A | T | 8 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(5): Show | 8 | HG02572.hp2 HG02809.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.248-7756T>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180048403 | ||||||
| chr5:180048408
|
A | G | 4 | a0001c0003t0001g0156a0001c0003t0001g0158a0001c0003t0001g0159others(1): Show | 4 | HG02451.hp1 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.248-7761T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180048408 | ||||||
| chr5:180048500
|
C | T | 1 | a0001c0002t0001g0121 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.248-7853G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180048500 | ||||||
| chr5:180048501
|
G | A | 1 | a0001c0002t0001g0048 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.248-7854C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180048501 | ||||||
| chr5:180048527
|
C | T | 3 | a0001c0001t0001g0219a0001c0001t0001g0226a0001c0001t0001g0227 | 3 | HG00639.hp2 HG01123.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.248-7880G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180048527 | ||||||
| chr5:180048644
|
G | A | 1 | a0001c0002t0001g0106 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.248-7997C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180048644 | ||||||
| chr5:180048818
|
A | C | 278 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(275): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.248-8171T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180048818 | ||||||
| chr5:180048818
|
A | G | 1 | a0001c0001t0001g0301 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.248-8171T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180048818 | ||||||
| chr5:180049195
|
C | A | 47 | a0001c0002t0001g0007a0001c0002t0001g0012a0001c0002t0001g0023others(44): Show | 47 | HG00438.hp1 HG01074.hp2 HG01255.hp2 others(44): Show |
intron_variant | MODIFIER | c.248-8548G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180049195 | ||||||
| chr5:180049336
|
T | C | 1 | a0001c0002t0001g0049 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.248-8689A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180049336 | ||||||
| chr5:180049388
|
G | C | 4 | a0001c0003t0001g0155a0001c0003t0002g0153a0001c0003t0002g0154others(1): Show | 4 | HG01884.hp2 HG02280.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.248-8741C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180049388 | ||||||
| chr5:180049610
|
T | C | 51 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(48): Show | 51 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.248-8963A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180049610 | ||||||
| chr5:180049645
|
T | C | 1 | a0001c0002t0001g0063 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.248-8998A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180049645 | ||||||
| chr5:180049713
|
G | A | 1 | a0001c0002t0001g0088 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.248-9066C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180049713 | ||||||
| chr5:180049759
|
T | C | 1 | a0001c0002t0001g0093 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.248-9112A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180049759 | ||||||
| chr5:180049913
|
C | G | 1 | a0001c0002t0001g0035 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.248-9266G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180049913 | ||||||
| chr5:180050020
|
A | G | 1 | a0001c0001t0001g0243 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.248-9373T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180050020 | ||||||
| chr5:180050299
|
C | T | 1 | a0001c0001t0001g0320 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.248-9652G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180050299 | ||||||
| chr5:180050523
|
G | A | 3 | a0001c0002t0001g0026a0001c0002t0001g0129a0004c0010t0001g0027 | 3 | HG01243.hp2 HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.248-9876C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180050523 | ||||||
| chr5:180050587
|
T | A | 1 | a0001c0007t0001g0004 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.248-9940A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180050587 | ||||||
| chr5:180050627
|
C | T | 1 | a0001c0003t0002g0154 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.248-9980G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180050627 | ||||||
| chr5:180050707
|
ATCTT | A | 3 | a0001c0001t0001g0330a0001c0001t0001g0331a0001c0001t0001g0332 | 3 | HG02809.hp1 HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.248-10064_248-1006 others(8): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180050707 | ||||||
| chr5:180050787
|
G | T | 4 | a0001c0003t0001g0151a0001c0003t0001g0162a0001c0003t0001g0163others(1): Show | 4 | HG00642.hp1 HG00733.hp2 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.248-10140C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180050787 | ||||||
| chr5:180050847
|
G | A | 129 | a0001c0001t0001g0198a0001c0001t0001g0330a0001c0001t0001g0331others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.248-10200C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180050847 | ||||||
| chr5:180050919
|
T | A | 4 | a0001c0001t0001g0270a0001c0001t0001g0275a0001c0001t0001g0291others(1): Show | 4 | NA18998.hp1 NA19007.hp1 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.248-10272A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180050919 | ||||||
| chr5:180051055
|
G | A | 2 | a0001c0001t0001g0334a0001c0001t0001g0335 | 2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.248-10408C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180051055 | ||||||
| chr5:180051113
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.248-10466G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180051113 | ||||||
| chr5:180051238
|
A | ATATT | 45 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(42): Show | 45 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(42): Show |
intron_variant | MODIFIER | c.248-10595_248-1059 others(8): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180051238 | ||||||
| chr5:180051238
|
A | ATATTTAT others(1): Show |
10 | a0001c0001t0001g0236a0001c0001t0001g0243a0001c0001t0001g0244others(7): Show | 10 | HG02055.hp2 HG02257.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.248-10599_248-1059 others(12): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180051238 | ||||||
| chr5:180051238
|
A | ATATTTAT others(5): Show |
46 | a0001c0001t0001g0199a0001c0001t0001g0302a0001c0001t0001g0320others(43): Show | 47 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.248-10603_248-1059 others(16): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180051238 | ||||||
| chr5:180051238
|
A | ATATTTAT others(9): Show |
134 | a0001c0001t0001g0299a0001c0001t0001g0300a0001c0001t0001g0301others(131): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.248-10607_248-1059 others(20): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180051238 | ||||||
| chr5:180051238
|
A | ATATTTAT others(13): Show |
31 | a0001c0001t0001g0198a0001c0001t0001g0309a0001c0001t0001g0315others(28): Show | 31 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.248-10611_248-1059 others(24): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180051238 | ||||||
| chr5:180051238
|
A | ATATTTAT others(17): Show |
5 | a0001c0001t0001g0308a0001c0002t0001g0050a0001c0002t0001g0107others(2): Show | 5 | HG02683.hp1 HG03710.hp1 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.248-10615_248-1059 others(28): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180051238 | ||||||
| chr5:180051287
|
T | C | 34 | a0001c0001t0001g0333a0001c0002t0001g0094a0001c0003t0001g0001others(31): Show | 37 | HG00280.hp2 HG00738.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.248-10640A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180051287 | ||||||
| chr5:180051319
|
G | A | 1 | a0001c0001t0001g0335 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.248-10672C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180051319 | ||||||
| chr5:180051517
|
G | A | 1 | a0001c0002t0001g0055 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.248-10870C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180051517 | ||||||
| chr5:180051528
|
C | T | 55 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(52): Show | 55 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.248-10881G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180051528 | ||||||
| chr5:180051621
|
T | C | 1 | a0001c0001t0001g0328 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.248-10974A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180051621 | ||||||
| chr5:180051891
|
C | A | 51 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(48): Show | 51 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.248-11244G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180051891 | ||||||
| chr5:180051929
|
T | C | 1 | a0001c0002t0001g0055 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.248-11282A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180051929 | ||||||
| chr5:180052146
|
C | T | 49 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(46): Show | 49 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(46): Show |
intron_variant | MODIFIER | c.248-11499G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180052146 | ||||||
| chr5:180052300
|
T | C | 7 | a0001c0001t0001g0209a0001c0001t0001g0334a0001c0001t0001g0335others(4): Show | 7 | HG01884.hp2 HG02280.hp2 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.248-11653A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180052300 | ||||||
| chr5:180052589
|
C | T | 6 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.248-11942G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180052589 | ||||||
| chr5:180052621
|
G | T | 173 | a0001c0001t0001g0198a0001c0001t0001g0330a0001c0001t0001g0331others(170): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.248-11974C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180052621 | ||||||
| chr5:180053027
|
G | A | 185 | a0001c0001t0001g0198a0001c0001t0001g0276a0001c0001t0001g0330others(182): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.248-12380C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180053027 | ||||||
| chr5:180053137
|
A | C | 2 | a0001c0003t0001g0144a0001c0003t0001g0145 | 2 | HG01261.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.248-12490T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180053137 | ||||||
| chr5:180053172
|
G | A | 45 | a0001c0001t0001g0333a0001c0002t0001g0094a0001c0003t0001g0001others(42): Show | 48 | HG00280.hp2 HG00558.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.248-12525C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180053172 | ||||||
| chr5:180053418
|
G | A | 1 | a0001c0001t0001g0215 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.248-12771C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180053418 | ||||||
| chr5:180053578
|
T | G | 1 | a0001c0001t0001g0249 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.248-12931A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180053578 | ||||||
| chr5:180053772
|
C | T | 1 | a0001c0001t0001g0272 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.248-13125G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180053772 | ||||||
| chr5:180053824
|
TC | T | 39 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(36): Show | 39 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.248-13178delG | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180053824 | ||||||
| chr5:180053825
|
CT | C | 178 | a0001c0001t0001g0198a0001c0001t0001g0271a0001c0001t0001g0328others(175): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.248-13179delA | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180053825 | ||||||
| chr5:180053826
|
T | A | 39 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(36): Show | 39 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.248-13179A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180053826 | ||||||
| chr5:180053968
|
T | C | 3 | a0001c0003t0001g0155a0001c0003t0002g0153a0001c0003t0002g0154 | 3 | HG01884.hp2 HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.248-13321A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180053968 | ||||||
| chr5:180054042
|
C | T | 1 | a0001c0002t0001g0056 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.248-13395G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180054042 | ||||||
| chr5:180054250
|
C | T | 1 | a0001c0001t0001g0234 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.248-13603G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180054250 | ||||||
| chr5:180054302
|
G | A | 184 | a0001c0001t0001g0198a0001c0001t0001g0330a0001c0001t0001g0331others(181): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.248-13655C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180054302 | ||||||
| chr5:180054711
|
C | T | 1 | a0001c0002t0001g0067 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.248-14064G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180054711 | ||||||
| chr5:180054789
|
C | T | 273 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(270): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.248-14142G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180054789 | ||||||
| chr5:180055026
|
A | G | 5 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0213others(2): Show | 5 | HG01891.hp2 HG02145.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.248-14379T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055026 | ||||||
| chr5:180055114
|
G | A | 1 | a0001c0002t0001g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.248-14467C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055114 | ||||||
| chr5:180055126
|
T | C | 1 | a0001c0002t0001g0091 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.248-14479A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055126 | ||||||
| chr5:180055248
|
C | CA | 9 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0001t0001g0272others(6): Show | 9 | HG00408.hp1 HG00609.hp2 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.248-14602dupT | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055248 | ||||||
| chr5:180055248
|
C | CAA | 8 | a0001c0001t0001g0250a0001c0001t0001g0276a0001c0001t0001g0279others(5): Show | 8 | HG00544.hp2 HG01928.hp2 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.248-14603_248-1460 others(6): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055248 | ||||||
| chr5:180055248
|
C | CAAAAAAA others(3): Show |
1 | a0001c0004t0005g0140 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.248-14611_248-1460 others(14): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055248 | ||||||
| chr5:180055248
|
C | CAAAAAAA others(18): Show |
1 | a0001c0001t0001g0284 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.248-14626_248-1460 others(29): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055248 | ||||||
| chr5:180055248
|
CAAAAAAA others(6): Show |
C | 2 | a0001c0001t0001g0278a0001c0001t0001g0281 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.248-14614_248-1460 others(17): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055248 | ||||||
| chr5:180055248
|
CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0001g0292 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.248-14616_248-1460 others(19): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055248 | ||||||
| chr5:180055259
|
AAAAAAAA others(15): Show |
A | 3 | a0001c0003t0001g0155a0001c0003t0002g0154a0001c0005t0001g0194 | 3 | HG01884.hp2 HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.248-14634_248-1461 others(26): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055259 | ||||||
| chr5:180055260
|
AAAAAAAA others(14): Show |
A | 44 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0335others(41): Show | 46 | HG00280.hp2 HG00558.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.248-14634_248-1461 others(25): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055260 | ||||||
| chr5:180055261
|
AAAAAAAA others(13): Show |
A | 122 | a0001c0001t0001g0198a0001c0001t0001g0330a0001c0001t0001g0331others(119): Show | 123 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.248-14634_248-1461 others(24): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055261 | ||||||
| chr5:180055262
|
AAAAAAAA others(12): Show |
A | 15 | a0001c0001t0001g0328a0001c0002t0001g0015a0001c0002t0001g0016others(12): Show | 15 | HG00140.hp2 HG00673.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.248-14634_248-1461 others(23): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055262 | ||||||
| chr5:180055263
|
AAAAAAAA others(11): Show |
A | 1 | a0001c0002t0001g0014 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.248-14634_248-1461 others(22): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055263 | ||||||
| chr5:180055267
|
AAAAAAAA others(7): Show |
A | 2 | a0001c0001t0001g0229a0001c0001t0002g0242 | 2 | HG02818.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.248-14634_248-1462 others(18): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055267 | ||||||
| chr5:180055268
|
AAAAAAAA others(6): Show |
A | 32 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0210others(29): Show | 32 | HG00140.hp1 HG00544.hp1 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.248-14634_248-1462 others(17): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055268 | ||||||
| chr5:180055269
|
AAAAAAAA others(5): Show |
A | 40 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(37): Show | 40 | HG00408.hp2 HG00438.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.248-14634_248-1462 others(16): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055269 | ||||||
| chr5:180055270
|
AAAAAAAA others(4): Show |
A | 11 | a0001c0001t0001g0207a0001c0001t0001g0227a0001c0001t0001g0228others(8): Show | 11 | HG00639.hp2 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.248-14634_248-1462 others(15): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055270 | ||||||
| chr5:180055271
|
AAAAAAAA others(3): Show |
A | 5 | a0001c0001t0001g0243a0001c0001t0001g0246a0001c0001t0001g0248others(2): Show | 5 | HG02257.hp2 HG02970.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.248-14634_248-1462 others(14): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055271 | ||||||
| chr5:180055281
|
C | A | 3 | a0001c0001t0001g0284a0001c0004t0001g0139a0001c0004t0005g0140 | 3 | HG02647.hp2 NA19080.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.248-14634G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055281 | ||||||
| chr5:180055290
|
A | C | 39 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(36): Show | 39 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.248-14643T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055290 | ||||||
| chr5:180055440
|
T | TCTG | 9 | a0001c0003t0001g0155a0001c0003t0001g0177a0001c0003t0001g0178others(6): Show | 9 | HG00558.hp2 HG01884.hp2 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.248-14794_248-1479 others(7): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055440 | ||||||
| chr5:180055440
|
T | TCTGTG | 45 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(42): Show | 45 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.248-14794_248-1479 others(9): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055440 | ||||||
| chr5:180055440
|
T | TCTGTGTG | 204 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0201others(201): Show | 207 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.248-14794_248-1479 others(11): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055440 | ||||||
| chr5:180055440
|
T | TCTGTGTG others(2): Show |
10 | a0001c0002t0001g0006a0001c0002t0001g0050a0001c0002t0001g0051others(7): Show | 10 | HG01069.hp2 HG01168.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.248-14794_248-1479 others(13): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055440 | ||||||
| chr5:180055440
|
T | TCTGTGTG others(4): Show |
4 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0049others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.248-14794_248-1479 others(15): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055440 | ||||||
| chr5:180055451
|
T | C | 4 | a0001c0002t0001g0007a0001c0002t0001g0031a0001c0002t0001g0033others(1): Show | 4 | NA18947.hp2 NA18959.hp2 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.248-14804A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055451 | ||||||
| chr5:180055453
|
C | T | 51 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(48): Show | 51 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.248-14806G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055453 | ||||||
| chr5:180055455
|
T | C | 46 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(43): Show | 46 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.248-14808A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055455 | ||||||
| chr5:180055457
|
T | C | 5 | a0001c0003t0001g0177a0001c0003t0001g0178a0001c0003t0001g0179others(2): Show | 5 | HG00558.hp2 HG02056.hp1 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.248-14810A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055457 | ||||||
| chr5:180055469
|
T | C | 7 | a0001c0001t0001g0236a0001c0001t0001g0243a0001c0001t0001g0244others(4): Show | 7 | HG02055.hp2 HG02257.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.248-14822A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055469 | ||||||
| chr5:180055472
|
G | A | 184 | a0001c0001t0001g0198a0001c0001t0001g0330a0001c0001t0001g0331others(181): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.248-14825C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055472 | ||||||
| chr5:180055476
|
G | A | 1 | a0001c0002t0001g0055 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.248-14829C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055476 | ||||||
| chr5:180055478
|
G | A | 3 | a0001c0003t0001g0192a0001c0005t0003g0190a0001c0005t0003g0191 | 3 | HG02572.hp1 HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.248-14831C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055478 | ||||||
| chr5:180055603
|
A | G | 2 | a0001c0002t0001g0059a0001c0002t0001g0120 | 2 | HG01192.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.248-14956T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055603 | ||||||
| chr5:180055715
|
T | A | 1 | a0001c0002t0001g0093 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.248-15068A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055715 | ||||||
| chr5:180055811
|
G | A | 1 | a0001c0004t0001g0141 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.248-15164C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055811 | ||||||
| chr5:180055812
|
C | T | 14 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259others(11): Show | 14 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.248-15165G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055812 | ||||||
| chr5:180055813
|
G | A | 1 | a0001c0001t0001g0328 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.248-15166C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055813 | ||||||
| chr5:180055821
|
T | C | 273 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(270): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.248-15174A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055821 | ||||||
| chr5:180056045
|
C | T | 1 | a0001c0001t0001g0329 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.248-15398G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180056045 | ||||||
| chr5:180056059
|
G | A | 4 | a0001c0003t0001g0151a0001c0003t0001g0162a0001c0003t0001g0163others(1): Show | 4 | HG00642.hp1 HG00733.hp2 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.247+15397C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180056059 | ||||||
| chr5:180056071
|
G | A | 1 | a0001c0002t0001g0121 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.247+15385C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180056071 | ||||||
| chr5:180056253
|
GA | G | 176 | a0001c0001t0001g0198a0001c0001t0001g0330a0001c0001t0001g0331others(173): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.247+15202delT | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180056253 | ||||||
| chr5:180056254
|
A | G | 1 | a0001c0001t0001g0235 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.247+15202T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180056254 | ||||||
| chr5:180056360
|
T | G | 49 | a0001c0001t0001g0333a0001c0002t0001g0094a0001c0003t0001g0001others(46): Show | 52 | HG00280.hp2 HG00558.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.247+15096A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180056360 | ||||||
| chr5:180056405
|
C | G | 10 | a0001c0001t0001g0202a0001c0001t0001g0219a0001c0001t0001g0226others(7): Show | 10 | HG00639.hp2 HG01123.hp1 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.247+15051G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180056405 | ||||||
| chr5:180056584
|
G | T | 1 | a0001c0002t0001g0106 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.247+14872C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180056584 | ||||||
| chr5:180056622
|
G | A | 1 | a0001c0002t0001g0032 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.247+14834C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180056622 | ||||||
| chr5:180056686
|
T | A | 40 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(37): Show | 40 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.247+14770A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180056686 | ||||||
| chr5:180056799
|
G | A | 1 | a0001c0001t0001g0328 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.247+14657C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180056799 | ||||||
| chr5:180057074
|
A | G | 2 | a0001c0001t0001g0326a0001c0001t0001g0327 | 2 | HG02135.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.247+14382T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180057074 | ||||||
| chr5:180057218
|
G | A | 1 | a0001c0002t0002g0128 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.247+14238C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180057218 | ||||||
| chr5:180057265
|
C | G | 292 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(289): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.247+14191G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180057265 | ||||||
| chr5:180057307
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.247+14149C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180057307 | ||||||
| chr5:180057310
|
A | T | 1 | a0001c0003t0001g0149 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.247+14146T>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180057310 | ||||||
| chr5:180057314
|
C | T | 53 | a0001c0001t0001g0299a0001c0001t0001g0300a0001c0001t0001g0302others(50): Show | 53 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(50): Show |
intron_variant | MODIFIER | c.247+14142G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180057314 | ||||||
| chr5:180057320
|
G | A | 2 | a0001c0002t0001g0043a0001c0002t0001g0117 | 2 | HG01943.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.247+14136C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180057320 | ||||||
| chr5:180057323
|
A | T | 2 | a0001c0002t0001g0043a0001c0002t0001g0117 | 2 | HG01943.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.247+14133T>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180057323 | ||||||
| chr5:180057344
|
T | G | 1 | a0001c0001t0001g0251 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.247+14112A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180057344 | ||||||
| chr5:180057518
|
A | C | 39 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(36): Show | 39 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.247+13938T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180057518 | ||||||
| chr5:180057519
|
G | C | 39 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(36): Show | 39 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.247+13937C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180057519 | ||||||
| chr5:180057547
|
C | CA | 9 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(6): Show | 9 | HG02572.hp2 HG02809.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.247+13908dupT | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180057547 | ||||||
| chr5:180057626
|
T | C | 1 | a0001c0002t0001g0095 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.247+13830A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180057626 | ||||||
| chr5:180057649
|
T | C | 1 | a0001c0001t0001g0234 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.247+13807A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180057649 | ||||||
| chr5:180057838
|
C | A | 224 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0299others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.247+13618G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180057838 | ||||||
| chr5:180057886
|
G | A | 1 | a0001c0001t0001g0321 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.247+13570C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180057886 | ||||||
| chr5:180057896
|
T | A | 224 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0299others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.247+13560A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180057896 | ||||||
| chr5:180058000
|
T | C | 233 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0201others(230): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.247+13456A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180058000 | ||||||
| chr5:180058014
|
A | G | 1 | a0001c0001t0001g0328 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.247+13442T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180058014 | ||||||
| chr5:180058038
|
T | C | 274 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(271): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.247+13418A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180058038 | ||||||
| chr5:180058070
|
A | G | 1 | a0001c0002t0001g0130 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.247+13386T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180058070 | ||||||
| chr5:180058311
|
A | G | 2 | a0001c0002t0001g0125a0002c0008t0001g0124 | 2 | NA18971.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.247+13145T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180058311 | ||||||
| chr5:180058315
|
G | A | 274 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(271): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.247+13141C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180058315 | ||||||
| chr5:180058515
|
C | G | 39 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(36): Show | 39 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.247+12941G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180058515 | ||||||
| chr5:180058528
|
A | G | 2 | a0001c0002t0001g0057a0001c0002t0001g0058 | 2 | HG00609.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.247+12928T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180058528 | ||||||
| chr5:180058595
|
G | A | 1 | a0001c0001t0001g0336 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.247+12861C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180058595 | ||||||
| chr5:180058624
|
C | T | 1 | a0001c0001t0001g0302 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.247+12832G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180058624 | ||||||
| chr5:180058703
|
A | C | 2 | a0001c0001t0001g0220a0001c0001t0001g0221 | 2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.247+12753T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180058703 | ||||||
| chr5:180058957
|
G | C | 1 | a0001c0003t0001g0160 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.247+12499C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180058957 | ||||||
| chr5:180059021
|
C | T | 41 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(38): Show | 41 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.247+12435G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180059021 | ||||||
| chr5:180059068
|
G | T | 1 | a0001c0002t0001g0020 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.247+12388C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180059068 | ||||||
| chr5:180059093
|
C | G | 1 | a0001c0003t0001g0165 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.247+12363G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180059093 | ||||||
| chr5:180059157
|
G | C | 1 | a0001c0002t0001g0014 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.247+12299C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180059157 | ||||||
| chr5:180059400
|
T | C | 16 | a0001c0001t0001g0203a0001c0001t0001g0210a0001c0001t0001g0211others(13): Show | 16 | HG01243.hp2 HG02451.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.247+12056A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180059400 | ||||||
| chr5:180059525
|
G | A | 29 | a0001c0001t0001g0302a0001c0001t0001g0303a0001c0001t0001g0304others(26): Show | 29 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(26): Show |
intron_variant | MODIFIER | c.247+11931C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180059525 | ||||||
| chr5:180059730
|
A | G | 1 | a0001c0003t0001g0185 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.247+11726T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180059730 | ||||||
| chr5:180060030
|
C | T | 1 | a0001c0001t0001g0332 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.247+11426G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180060030 | ||||||
| chr5:180060137
|
G | C | 2 | a0001c0001t0001g0278a0001c0001t0001g0281 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.247+11319C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180060137 | ||||||
| chr5:180060258
|
A | T | 133 | a0001c0001t0001g0198a0001c0001t0001g0329a0001c0001t0001g0330others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.247+11198T>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180060258 | ||||||
| chr5:180060288
|
A | C | 1 | a0001c0002t0001g0130 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.247+11168T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180060288 | ||||||
| chr5:180060323
|
T | A | 1 | a0001c0003t0001g0182 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.247+11133A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180060323 | ||||||
| chr5:180060430
|
G | A | 34 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(31): Show | 34 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.247+11026C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180060430 | ||||||
| chr5:180060531
|
C | T | 3 | a0001c0001t0001g0219a0001c0001t0001g0226a0001c0001t0001g0227 | 3 | HG00639.hp2 HG01123.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.247+10925G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180060531 | ||||||
| chr5:180060563
|
G | A | 1 | a0001c0005t0003g0161 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.247+10893C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180060563 | ||||||
| chr5:180060648
|
C | A | 48 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(45): Show | 48 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(45): Show |
intron_variant | MODIFIER | c.247+10808G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180060648 | ||||||
| chr5:180060691
|
C | T | 8 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(5): Show | 8 | HG02572.hp2 HG02809.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.247+10765G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180060691 | ||||||
| chr5:180060721
|
T | C | 1 | a0001c0002t0001g0056 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.247+10735A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180060721 | ||||||
| chr5:180060803
|
C | T | 1 | a0001c0002t0001g0056 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.247+10653G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180060803 | ||||||
| chr5:180060851
|
C | T | 1 | a0001c0001t0001g0203 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.247+10605G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180060851 | ||||||
| chr5:180060880
|
T | C | 4 | a0001c0002t0001g0125a0001c0002t0001g0126a0001c0002t0001g0127others(1): Show | 4 | NA18942.hp1 NA18961.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.247+10576A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180060880 | ||||||
| chr5:180060925
|
T | C | 1 | a0001c0005t0001g0194 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.247+10531A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180060925 | ||||||
| chr5:180060931
|
A | T | 2 | a0001c0002t0001g0096a0001c0005t0001g0194 | 2 | NA18943.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.247+10525T>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180060931 | ||||||
| chr5:180060935
|
A | G | 273 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(270): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.247+10521T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180060935 | ||||||
| chr5:180060937
|
T | C | 1 | a0001c0005t0001g0194 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.247+10519A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180060937 | ||||||
| chr5:180060973
|
G | A | 1 | a0001c0001t0001g0328 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.247+10483C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180060973 | ||||||
| chr5:180060981
|
A | G | 1 | a0001c0004t0004g0142 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.247+10475T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180060981 | ||||||
| chr5:180060997
|
G | T | 2 | a0001c0001t0001g0334a0001c0001t0001g0335 | 2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.247+10459C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180060997 | ||||||
| chr5:180061068
|
C | CA | 169 | a0001c0001t0001g0198a0001c0001t0001g0202a0001c0001t0001g0220others(166): Show | 172 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.247+10387dupT | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180061068 | ||||||
| chr5:180061068
|
C | CAA | 43 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(40): Show | 43 | HG00642.hp2 HG00673.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.247+10386_247+1038 others(6): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180061068 | ||||||
| chr5:180061068
|
C | CAAA | 15 | a0001c0001t0001g0203a0001c0001t0001g0209a0001c0001t0001g0210others(12): Show | 15 | HG01243.hp2 HG02055.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.247+10385_247+1038 others(7): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180061068 | ||||||
| chr5:180061068
|
C | CAAAA | 9 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0213others(6): Show | 9 | HG01884.hp2 HG01891.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.247+10384_247+1038 others(8): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180061068 | ||||||
| chr5:180061068
|
CA | C | 9 | a0001c0001t0001g0252a0001c0001t0001g0281a0001c0001t0001g0299others(6): Show | 9 | HG00438.hp2 HG00544.hp1 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.247+10387delT | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180061068 | ||||||
| chr5:180061068
|
CAA | C | 26 | a0001c0001t0001g0199a0001c0001t0001g0300a0001c0001t0001g0301others(23): Show | 26 | HG00140.hp1 HG00408.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.247+10386_247+1038 others(6): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180061068 | ||||||
| chr5:180061278
|
C | A | 1 | a0001c0007t0001g0004 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.247+10178G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180061278 | ||||||
| chr5:180061289
|
G | A | 1 | a0001c0002t0001g0041 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.247+10167C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180061289 | ||||||
| chr5:180061372
|
T | A | 16 | a0001c0001t0001g0198a0001c0002t0001g0041a0001c0002t0001g0107others(13): Show | 16 | HG00735.hp2 HG01071.hp2 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.247+10084A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180061372 | ||||||
| chr5:180061400
|
T | A | 1 | a0001c0001t0001g0328 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.247+10056A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180061400 | ||||||
| chr5:180061419
|
G | A | 1 | a0001c0002t0001g0037 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.247+10037C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180061419 | ||||||
| chr5:180061451
|
A | G | 1 | a0001c0002t0001g0046 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.247+10005T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180061451 | ||||||
| chr5:180061570
|
C | T | 23 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0203others(20): Show | 23 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.247+9886G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180061570 | ||||||
| chr5:180061660
|
C | T | 273 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(270): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.247+9796G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180061660 | ||||||
| chr5:180062055
|
CT | C | 11 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231others(8): Show | 12 | HG01256.hp2 HG01257.hp1 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.247+9400delA | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180062055 | ||||||
| chr5:180062199
|
C | T | 132 | a0001c0001t0001g0198a0001c0001t0001g0329a0001c0001t0001g0330others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.247+9257G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180062199 | ||||||
| chr5:180062328
|
G | A | 34 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(31): Show | 34 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.247+9128C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180062328 | ||||||
| chr5:180062353
|
C | T | 1 | a0001c0002t0001g0045 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.247+9103G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180062353 | ||||||
| chr5:180062420
|
A | C | 2 | a0001c0001t0001g0200a0001c0001t0001g0201 | 2 | HG02145.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.247+9036T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180062420 | ||||||
| chr5:180062862
|
A | G | 1 | a0001c0003t0001g0160 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.247+8594T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180062862 | ||||||
| chr5:180063127
|
C | T | 4 | a0001c0003t0001g0151a0001c0003t0001g0162a0001c0003t0001g0163others(1): Show | 4 | HG00642.hp1 HG00733.hp2 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.247+8329G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180063127 | ||||||
| chr5:180063261
|
T | C | 39 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(36): Show | 39 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.247+8195A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180063261 | ||||||
| chr5:180063284
|
G | A | 1 | a0001c0001t0002g0242 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.247+8172C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180063284 | ||||||
| chr5:180063360
|
G | A | 1 | a0001c0002t0001g0034 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.247+8096C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180063360 | ||||||
| chr5:180063447
|
G | C | 38 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(35): Show | 38 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(35): Show |
intron_variant | MODIFIER | c.247+8009C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180063447 | ||||||
| chr5:180063597
|
C | T | 50 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(47): Show | 50 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(47): Show |
intron_variant | MODIFIER | c.247+7859G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180063597 | ||||||
| chr5:180063652
|
T | C | 4 | a0001c0001t0001g0330a0001c0001t0001g0331a0001c0001t0001g0332others(1): Show | 4 | HG02258.hp1 HG02809.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.247+7804A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180063652 | ||||||
| chr5:180063993
|
T | G | 1 | a0001c0003t0002g0154 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.247+7463A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180063993 | ||||||
| chr5:180063995
|
C | T | 2 | a0001c0004t0001g0131a0001c0004t0001g0141 | 2 | NA18951.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.247+7461G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180063995 | ||||||
| chr5:180064461
|
T | C | 1 | a0001c0001t0001g0234 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.247+6995A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180064461 | ||||||
| chr5:180064524
|
C | G | 1 | a0001c0007t0001g0004 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.247+6932G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180064524 | ||||||
| chr5:180064667
|
T | C | 2 | a0001c0002t0001g0118a0001c0002t0001g0119 | 2 | HG00099.hp2 HG00642.hp2 |
intron_variant | MODIFIER | c.247+6789A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180064667 | ||||||
| chr5:180064927
|
TTC | T | 334 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(331): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.247+6527_247+6528d others(4): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180064927 | ||||||
| chr5:180065135
|
T | TA | 36 | a0001c0001t0001g0199a0001c0001t0001g0285a0001c0001t0001g0300others(33): Show | 36 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.247+6320dupT | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180065135 | ||||||
| chr5:180065135
|
TA | T | 45 | a0001c0001t0001g0251a0001c0002t0001g0042a0001c0002t0001g0043others(42): Show | 48 | HG00280.hp2 HG00558.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.247+6320delT | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180065135 | ||||||
| chr5:180065136
|
A | T | 1 | a0001c0002t0001g0041 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.247+6320T>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180065136 | ||||||
| chr5:180065396
|
A | G | 52 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(49): Show | 52 | HG00639.hp2 HG01123.hp1 HG01243.hp2 others(49): Show |
intron_variant | MODIFIER | c.247+6060T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180065396 | ||||||
| chr5:180065455
|
G | T | 1 | a0001c0001t0001g0249 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.247+6001C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180065455 | ||||||
| chr5:180065629
|
G | A | 1 | a0001c0001t0001g0297 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.247+5827C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180065629 | ||||||
| chr5:180065725
|
A | C | 1 | a0001c0005t0003g0161 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.247+5731T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180065725 | ||||||
| chr5:180065739
|
G | A | 1 | a0001c0003t0001g0155 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.247+5717C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180065739 | ||||||
| chr5:180065753
|
CTG | C | 5 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288others(2): Show | 5 | HG00733.hp1 HG01106.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.247+5701_247+5702d others(4): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180065753 | ||||||
| chr5:180065759
|
C | CA | 12 | a0001c0001t0001g0291a0001c0002t0001g0026a0001c0002t0001g0028others(9): Show | 12 | HG01175.hp1 HG01243.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.247+5696dupT | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180065759 | ||||||
| chr5:180065772
|
AC | A | 35 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(32): Show | 35 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.247+5683delG | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180065772 | ||||||
| chr5:180065773
|
C | A | 244 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0201others(241): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.247+5683G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180065773 | ||||||
| chr5:180065811
|
AT | A | 137 | a0001c0001t0001g0198a0001c0001t0001g0329a0001c0001t0001g0330others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.247+5644delA | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180065811 | ||||||
| chr5:180065943
|
A | G | 1 | a0001c0001t0001g0203 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.247+5513T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180065943 | ||||||
| chr5:180066063
|
T | C | 1 | a0001c0002t0001g0017 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.247+5393A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180066063 | ||||||
| chr5:180066225
|
A | G | 1 | a0001c0003t0001g0160 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.247+5231T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180066225 | ||||||
| chr5:180066308
|
C | A | 3 | a0001c0003t0001g0192a0001c0005t0003g0190a0001c0005t0003g0191 | 3 | HG02572.hp1 HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.247+5148G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180066308 | ||||||
| chr5:180066510
|
T | C | 3 | a0001c0003t0001g0187a0001c0003t0001g0188a0001c0003t0001g0189 | 3 | HG01243.hp1 HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.247+4946A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180066510 | ||||||
| chr5:180066621
|
A | T | 2 | a0001c0001t0001g0235a0001c0001t0001g0236 | 2 | HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.247+4835T>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180066621 | ||||||
| chr5:180066693
|
C | T | 32 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(29): Show | 32 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.247+4763G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180066693 | ||||||
| chr5:180066788
|
G | A | 3 | a0001c0003t0001g0192a0001c0005t0003g0190a0001c0005t0003g0191 | 3 | HG02572.hp1 HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.247+4668C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180066788 | ||||||
| chr5:180066794
|
T | C | 1 | a0001c0002t0001g0038 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.247+4662A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180066794 | ||||||
| chr5:180066833
|
T | A | 279 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(276): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.247+4623A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180066833 | ||||||
| chr5:180066840
|
T | C | 1 | a0001c0001t0001g0292 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.247+4616A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180066840 | ||||||
| chr5:180066885
|
T | C | 1 | a0001c0001t0001g0328 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.247+4571A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180066885 | ||||||
| chr5:180067123
|
T | G | 1 | a0001c0002t0001g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.247+4333A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180067123 | ||||||
| chr5:180067325
|
A | T | 1 | a0001c0001t0001g0293 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.247+4131T>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180067325 | ||||||
| chr5:180067341
|
T | C | 1 | a0001c0003t0001g0193 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.247+4115A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180067341 | ||||||
| chr5:180067364
|
C | T | 1 | a0001c0001t0001g0250 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.247+4092G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180067364 | ||||||
| chr5:180067469
|
G | A | 1 | a0001c0002t0001g0123 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.247+3987C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180067469 | ||||||
| chr5:180067563
|
AATC | A | 8 | a0001c0001t0001g0202a0001c0001t0001g0235a0001c0001t0001g0236others(5): Show | 8 | HG02280.hp1 HG02630.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.247+3890_247+3892d others(5): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180067563 | ||||||
| chr5:180067692
|
A | G | 1 | a0001c0001t0001g0328 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.247+3764T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180067692 | ||||||
| chr5:180067853
|
G | A | 4 | a0001c0002t0001g0125a0001c0002t0001g0126a0001c0002t0001g0127others(1): Show | 4 | NA18942.hp1 NA18961.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.247+3603C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180067853 | ||||||
| chr5:180067902
|
A | G | 1 | a0001c0002t0001g0039 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.247+3554T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180067902 | ||||||
| chr5:180067957
|
G | A | 5 | a0001c0001t0001g0293a0001c0001t0001g0294a0001c0001t0001g0295others(2): Show | 5 | HG02486.hp1 HG02647.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.247+3499C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180067957 | ||||||
| chr5:180067958
|
A | G | 11 | a0001c0002t0001g0007a0001c0002t0001g0029a0001c0002t0001g0030others(8): Show | 11 | HG02040.hp2 NA18947.hp2 NA18962.hp2 others(8): Show |
intron_variant | MODIFIER | c.247+3498T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180067958 | ||||||
| chr5:180068190
|
C | G | 1 | a0001c0002t0001g0028 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.247+3266G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180068190 | ||||||
| chr5:180068264
|
C | T | 4 | a0001c0003t0001g0156a0001c0003t0001g0158a0001c0003t0001g0159others(1): Show | 4 | HG02451.hp1 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.247+3192G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180068264 | ||||||
| chr5:180068265
|
G | A | 49 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0203others(46): Show | 49 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(46): Show |
intron_variant | MODIFIER | c.247+3191C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180068265 | ||||||
| chr5:180068311
|
AGT | A | 47 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0204others(44): Show | 47 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(44): Show |
intron_variant | MODIFIER | c.247+3143_247+3144d others(4): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180068311 | ||||||
| chr5:180068532
|
T | C | 48 | a0001c0001t0001g0333a0001c0003t0001g0001a0001c0003t0001g0002others(45): Show | 51 | HG00280.hp2 HG00558.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.247+2924A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180068532 | ||||||
| chr5:180068607
|
T | C | 6 | a0001c0001t0001g0334a0001c0001t0001g0335a0001c0003t0001g0155others(3): Show | 6 | HG01884.hp2 HG02280.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.247+2849A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180068607 | ||||||
| chr5:180068669
|
G | C | 1 | a0001c0002t0002g0128 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.247+2787C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180068669 | ||||||
| chr5:180068677
|
A | G | 1 | a0001c0001t0001g0249 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.247+2779T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180068677 | ||||||
| chr5:180069232
|
T | C | 1 | a0001c0004t0001g0141 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.247+2224A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180069232 | ||||||
| chr5:180069239
|
G | A | 190 | a0001c0001t0001g0198a0001c0001t0001g0329a0001c0001t0001g0330others(187): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.247+2217C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180069239 | ||||||
| chr5:180069272
|
T | A | 1 | a0001c0001t0002g0242 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.247+2184A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180069272 | ||||||
| chr5:180069422
|
C | T | 33 | a0001c0001t0001g0199a0001c0001t0001g0299a0001c0001t0001g0300others(30): Show | 33 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.247+2034G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180069422 | ||||||
| chr5:180069533
|
A | G | 3 | a0001c0002t0001g0026a0001c0002t0001g0129a0004c0010t0001g0027 | 3 | HG01243.hp2 HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.247+1923T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180069533 | ||||||
| chr5:180069579
|
A | G | 1 | a0001c0001t0001g0243 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.247+1877T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180069579 | ||||||
| chr5:180069787
|
C | T | 3 | a0001c0002t0001g0023a0001c0002t0001g0024a0001c0002t0001g0025 | 3 | NA18983.hp2 NA18998.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.247+1669G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180069787 | ||||||
| chr5:180070076
|
C | T | 1 | a0001c0003t0001g0156 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.247+1380G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180070076 | ||||||
| chr5:180070081
|
C | T | 1 | a0001c0002t0001g0014 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.247+1375G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180070081 | ||||||
| chr5:180070110
|
G | A | 1 | a0001c0001t0001g0298 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.247+1346C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180070110 | ||||||
| chr5:180070152
|
G | C | 1 | a0001c0001t0001g0336 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.247+1304C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180070152 | ||||||
| chr5:180070245
|
C | T | 5 | a0001c0002t0001g0018a0001c0002t0001g0019a0001c0002t0001g0020others(2): Show | 5 | NA18948.hp2 NA18970.hp1 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.247+1211G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180070245 | ||||||
| chr5:180070249
|
C | T | 189 | a0001c0001t0001g0198a0001c0001t0001g0330a0001c0001t0001g0331others(186): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.247+1207G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180070249 | ||||||
| chr5:180070300
|
C | T | 4 | a0001c0002t0001g0014a0001c0002t0001g0015a0001c0002t0001g0016others(1): Show | 4 | HG00140.hp2 HG01516.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.247+1156G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180070300 | ||||||
| chr5:180070439
|
C | G | 3 | a0001c0003t0001g0155a0001c0003t0002g0153a0001c0003t0002g0154 | 3 | HG01884.hp2 HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.247+1017G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180070439 | ||||||
| chr5:180070453
|
C | T | 1 | a0001c0002t0001g0006 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.247+1003G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180070453 | ||||||
| chr5:180070476
|
G | A | 6 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0245others(3): Show | 6 | HG02055.hp2 HG02257.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.247+980C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180070476 | ||||||
| chr5:180070641
|
C | T | 49 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(46): Show | 49 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(46): Show |
intron_variant | MODIFIER | c.247+815G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180070641 | ||||||
| chr5:180070748
|
T | C | 224 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0299others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.247+708A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180070748 | ||||||
| chr5:180070870
|
T | C | 1 | a0001c0002t0001g0129 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.247+586A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180070870 | ||||||
| chr5:180070981
|
AC | A | 178 | a0001c0001t0001g0198a0001c0001t0001g0330a0001c0001t0001g0331others(175): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.247+474delG | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180070981 | ||||||
| chr5:180071075
|
G | C | 3 | a0001c0001t0001g0199a0001c0001t0001g0337a0001c0004t0004g0142 | 3 | NA18953.hp2 NA19074.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.247+381C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180071075 | ||||||
| chr5:180071189
|
A | G | 131 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0002t0001g0005others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.247+267T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180071189 | ||||||
| chr5:180071327
|
G | T | 1 | a0001c0002t0001g0005 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.247+129C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180071327 |