| geneid | 285671 |
|---|---|
| ensemblid | ENSG00000164197.12 |
| hgncid | 27752 |
| symbol | RNF180 |
| name | ring finger protein 180 |
| refseq_nuc | NM_001113561.2 |
| refseq_prot | NP_001107033.1 |
| ensembl_nuc | ENST00000389100.9 |
| ensembl_prot | ENSP00000373752.4 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 64165843 |
| end | 64372869 |
| strand | + |
| ver | v1.2 |
| region | chr5:64165843-64372869 |
| region5000 | chr5:64160843-64377869 |
| regionname0 | RNF180_chr5_64165843_64372869 |
| regionname5000 | RNF180_chr5_64160843_64377869 |
| 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 | 592 | 227 | 66 | 51 | 69 | 11 | 28 | 57 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| a0002 | 0/0 | 592 | 19 | 6 | 10 | 0 | 1 | 2 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| a0003 | 0/0 | 592 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| a0004 | 0/0 | 428 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| a0005 | 0/0 | 592 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| a0006 | 0/0 | 592 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| 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 | 1/1 | 1779 | 226 | 66 | 51 | 68 | 11 | 28 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| c0002 | 0/0 | 1779 | 19 | 6 | 10 | 0 | 1 | 2 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| c0003 | 0/0 | 1779 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| c0004 | 0/0 | 1607 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| c0005 | 0/0 | 1779 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| c0006 | 0/0 | 1779 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| c0007 | 0/0 | 1779 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 3167 | 57 | 17 | 17 | 9 | 5 | 9 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| t0002 | 0/0 | 3167 | 45 | 3 | 13 | 22 | 1 | 6 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| t0003 | 1/1 | 3167 | 39 | 9 | 6 | 12 | 3 | 7 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| t0004 | 0/0 | 3167 | 28 | 8 | 7 | 12 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| t0005 | 0/0 | 3167 | 26 | 14 | 0 | 12 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| t0006 | 0/0 | 3167 | 10 | 0 | 8 | 0 | 1 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| t0007 | 0/0 | 3167 | 9 | 1 | 5 | 1 | 0 | 2 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| t0008 | 0/0 | 3167 | 4 | 2 | 2 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| t0009 | 0/0 | 3167 | 4 | 1 | 1 | 0 | 1 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| t0010 | 0/0 | 3167 | 3 | 3 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| t0011 | 0/0 | 3168 | 3 | 3 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| t0012 | 0/0 | 3167 | 3 | 3 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| t0013 | 0/0 | 3167 | 2 | 0 | 1 | 0 | 1 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| t0014 | 0/0 | 3168 | 2 | 2 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| t0015 | 0/0 | 3167 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| t0016 | 0/0 | 3167 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| t0017 | 0/0 | 3167 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| t0018 | 0/0 | 3167 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| t0019 | 0/0 | 3167 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| t0020 | 0/0 | 3167 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| t0021 | 0/0 | 3167 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| t0022 | 0/0 | 3167 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| t0023 | 0/0 | 3167 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| t0024 | 0/0 | 3167 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| t0025 | 0/0 | 3167 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| t0026 | 0/0 | 3167 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| t0027 | 0/0 | 3167 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| t0028 | 0/0 | 3167 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| t0029 | 0/0 | 3167 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| 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 | 2 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0028 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0047 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| 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 | 1/1 | 1779 | 226 | 66 | 51 | 68 | 11 | 28 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| a0001c0003 | 0/0 | 1779 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| a0002c0002 | 0/0 | 1779 | 19 | 6 | 10 | 0 | 1 | 2 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| a0003c0007 | 0/0 | 1779 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| a0004c0004 | 0/0 | 1607 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| a0005c0005 | 0/0 | 1779 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| a0006c0006 | 0/0 | 1779 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4945 | 56 | 16 | 17 | 9 | 5 | 9 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| a0001c0001t0002 | 0/0 | 4945 | 42 | 3 | 12 | 20 | 1 | 6 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| a0001c0001t0003 | 1/1 | 4945 | 39 | 9 | 6 | 12 | 3 | 7 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| a0001c0001t0004 | 0/0 | 4945 | 27 | 7 | 7 | 12 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| a0001c0001t0005 | 0/0 | 4945 | 26 | 14 | 0 | 12 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| a0001c0001t0007 | 0/0 | 4945 | 9 | 1 | 5 | 1 | 0 | 2 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| a0001c0001t0009 | 0/0 | 4945 | 4 | 1 | 1 | 0 | 1 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| a0001c0001t0011 | 0/0 | 4946 | 3 | 3 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| a0001c0001t0012 | 0/0 | 4945 | 3 | 3 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| a0001c0001t0013 | 0/0 | 4945 | 2 | 0 | 1 | 0 | 1 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| a0001c0001t0014 | 0/0 | 4946 | 2 | 2 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| a0001c0001t0015 | 0/0 | 4945 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| a0001c0001t0017 | 0/0 | 4945 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| a0001c0001t0019 | 0/0 | 4945 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| a0001c0001t0020 | 0/0 | 4945 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| a0001c0001t0021 | 0/0 | 4945 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| a0001c0001t0022 | 0/0 | 4945 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| a0001c0001t0023 | 0/0 | 4945 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| a0001c0001t0024 | 0/0 | 4945 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| a0001c0001t0025 | 0/0 | 4945 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| a0001c0001t0026 | 0/0 | 4945 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| a0001c0001t0027 | 0/0 | 4945 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| a0001c0001t0028 | 0/0 | 4945 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| a0001c0001t0029 | 0/0 | 4945 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| a0001c0003t0002 | 0/0 | 4945 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| a0002c0002t0006 | 0/0 | 4945 | 10 | 0 | 8 | 0 | 1 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| a0002c0002t0008 | 0/0 | 4945 | 4 | 2 | 2 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| a0002c0002t0010 | 0/0 | 4945 | 3 | 3 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| a0002c0002t0016 | 0/0 | 4945 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| a0002c0002t0018 | 0/0 | 4945 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| a0003c0007t0002 | 0/0 | 4945 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| a0004c0004t0004 | 0/0 | 4773 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| a0005c0005t0001 | 0/0 | 4945 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| a0006c0006t0002 | 0/0 | 4945 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | copy fasta | chr5 | 64160843 | 64377869 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0002g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0003g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0003g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0003g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0003g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0003g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0003g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0003g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0003g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0003g0028 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0003g0047 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0004g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0004g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0004g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0004g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0004g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0004g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0004g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0004g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0004g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0004g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0004g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0005g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0005g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0005g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0005g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0005g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0005g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0005g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0005g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0005g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0005g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0005g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0005g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0005g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0005g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0005g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0005g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0005g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0005g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0005g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0005g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0005g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0005g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0005g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0005g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0005g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0005g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0007g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0007g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0007g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0007g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0007g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0007g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0007g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0007g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0009g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0009g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0009g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0009g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0011g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0011g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0011g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0012g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0012g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0012g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0013g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0013g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0014g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0014g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0015g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0017g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0019g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0020g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0021g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0022g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0023g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0024g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0025g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0026g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0027g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0028g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0001t0029g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0001c0003t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0002c0002t0006g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0002c0002t0006g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0002c0002t0006g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0002c0002t0006g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0002c0002t0006g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0002c0002t0006g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0002c0002t0006g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0002c0002t0006g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0002c0002t0006g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0002c0002t0006g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0002c0002t0008g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0002c0002t0008g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0002c0002t0008g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0002c0002t0008g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0002c0002t0010g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0002c0002t0010g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0002c0002t0010g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0002c0002t0016g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0002c0002t0018g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0003c0007t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0004c0004t0004g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0005c0005t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| a0006c0006t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0141 | EUR | GBR | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0210 | EUR | GBR | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0081 | EUR | FIN | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG00323 | hp2 | a0001 | c0001 | t0009 | g0036 | EUR | FIN | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | CHS | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG00597 | hp1 | a0001 | c0001 | t0005 | g0237 | EAS | CHS | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | CHS | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0211 | AMR | PUR | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG00642 | hp2 | a0001 | c0001 | t0021 | g0046 | AMR | PUR | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0180 | AMR | PUR | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0174 | AMR | PUR | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG00741 | hp2 | a0002 | c0002 | t0008 | g0062 | AMR | PUR | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01074 | hp2 | a0002 | c0002 | t0006 | g0068 | AMR | PUR | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01081 | hp1 | a0002 | c0002 | t0006 | g0071 | AMR | PUR | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0177 | AMR | PUR | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0124 | AMR | PUR | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01168 | hp2 | a0001 | c0001 | t0020 | g0023 | AMR | PUR | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01175 | hp1 | a0002 | c0002 | t0006 | g0072 | AMR | PUR | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01175 | hp2 | a0001 | c0001 | t0009 | g0042 | AMR | PUR | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0214 | AMR | PUR | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0245 | AMR | PUR | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01255 | hp1 | a0001 | c0001 | t0004 | g0096 | AMR | CLM | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01255 | hp2 | a0001 | c0001 | t0007 | g0001 | AMR | CLM | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0108 | AMR | CLM | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01257 | hp1 | a0002 | c0002 | t0006 | g0074 | AMR | CLM | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01257 | hp2 | a0002 | c0002 | t0008 | g0063 | AMR | CLM | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01258 | hp1 | a0002 | c0002 | t0006 | g0075 | AMR | CLM | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01258 | hp2 | a0001 | c0001 | t0004 | g0109 | AMR | CLM | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0040 | AMR | CLM | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01261 | hp2 | a0001 | c0001 | t0013 | g0008 | AMR | CLM | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01346 | hp1 | a0001 | c0001 | t0007 | g0001 | AMR | CLM | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0045 | AMR | CLM | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0024 | AMR | CLM | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0176 | AMR | CLM | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0095 | AMR | CLM | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0005 | EUR | IBS | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0122 | EUR | IBS | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0135 | EUR | IBS | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01516 | hp2 | a0001 | c0001 | t0013 | g0012 | EUR | IBS | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0006 | EUR | IBS | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0088 | EUR | IBS | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0184 | AFR | ACB | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0190 | AFR | ACB | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0212 | AMR | PEL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0202 | AMR | PEL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01943 | hp2 | a0001 | c0001 | t0007 | g0031 | AMR | PEL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01952 | hp1 | a0001 | c0001 | t0007 | g0033 | AMR | PEL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01952 | hp2 | a0006 | c0006 | t0002 | g0175 | AMR | PEL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0213 | AMR | PEL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01975 | hp2 | a0002 | c0002 | t0006 | g0070 | AMR | PEL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01978 | hp1 | a0002 | c0002 | t0006 | g0065 | AMR | PEL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01978 | hp2 | a0001 | c0001 | t0004 | g0248 | AMR | PEL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01993 | hp1 | a0002 | c0002 | t0006 | g0069 | AMR | PEL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0215 | AMR | PEL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0208 | AMR | PEL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | KHV | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02040 | hp2 | a0001 | c0003 | t0002 | g0246 | EAS | KHV | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0168 | AFR | ACB | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | KHV | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | KHV | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02083 | hp2 | a0001 | c0001 | t0004 | g0104 | EAS | KHV | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0216 | AMR | PEL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02257 | hp1 | a0001 | c0001 | t0009 | g0035 | AFR | ACB | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02257 | hp2 | a0001 | c0001 | t0005 | g0084 | AFR | ACB | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0077 | AFR | ACB | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02273 | hp1 | a0001 | c0001 | t0004 | g0097 | AMR | PEL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02280 | hp1 | a0002 | c0002 | t0008 | g0061 | AFR | ACB | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02280 | hp2 | a0001 | c0001 | t0005 | g0169 | AFR | ACB | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0187 | AFR | GWD | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0170 | AFR | GWD | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0013 | SAS | PJL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0181 | SAS | PJL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0100 | AFR | GWD | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02615 | hp2 | a0001 | c0001 | t0005 | g0167 | AFR | GWD | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02622 | hp2 | a0002 | c0002 | t0010 | g0057 | AFR | GWD | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0025 | AFR | GWD | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0171 | AFR | GWD | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02647 | hp2 | a0004 | c0004 | t0004 | g0093 | AFR | GWD | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0026 | SAS | PJL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02735 | hp1 | a0002 | c0002 | t0016 | g0067 | SAS | PJL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0183 | SAS | PJL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02818 | hp1 | a0001 | c0001 | t0026 | g0247 | AFR | GWD | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0194 | AFR | GWD | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0144 | AFR | GWD | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02886 | hp2 | a0001 | c0001 | t0019 | g0166 | AFR | GWD | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0189 | AFR | GWD | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0092 | AFR | GWD | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02896 | hp2 | a0001 | c0001 | t0028 | g0193 | AFR | GWD | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0086 | AFR | GWD | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0173 | AFR | ESN | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0099 | AFR | ESN | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02970 | hp1 | a0001 | c0001 | t0011 | g0054 | AFR | ESN | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0146 | AFR | GWD | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG03041 | hp2 | a0001 | c0001 | t0025 | g0105 | AFR | GWD | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | MSL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0186 | AFR | MSL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | ESN | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0191 | AFR | ESN | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0201 | AFR | ESN | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG03139 | hp2 | a0001 | c0001 | t0011 | g0053 | AFR | ESN | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG03195 | hp1 | a0005 | c0005 | t0001 | g0140 | AFR | ESN | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0200 | AFR | ESN | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | MSL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0145 | AFR | MSL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG03225 | hp1 | a0002 | c0002 | t0010 | g0076 | AFR | MSL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG03225 | hp2 | a0001 | c0001 | t0012 | g0196 | AFR | MSL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0178 | SAS | PJL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | MSL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG03453 | hp2 | a0002 | c0002 | t0010 | g0058 | AFR | MSL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0010 | SAS | PJL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0179 | SAS | PJL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG03516 | hp1 | a0001 | c0001 | t0027 | g0060 | AFR | ESN | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ESN | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG03540 | hp2 | a0001 | c0001 | t0011 | g0052 | AFR | GWD | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0030 | SAS | PJL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG03710 | hp1 | a0001 | c0001 | t0007 | g0051 | SAS | PJL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0016 | SAS | PJL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | BEB | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0007 | SAS | BEB | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG04115 | hp1 | a0001 | c0001 | t0004 | g0106 | SAS | STU | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG04115 | hp2 | a0001 | c0001 | t0017 | g0019 | SAS | STU | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG04184 | hp1 | a0001 | c0001 | t0022 | g0018 | SAS | BEB | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0038 | SAS | STU | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG04199 | hp2 | a0001 | c0001 | t0009 | g0182 | SAS | STU | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | STU | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0020 | SAS | STU | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG04228 | hp1 | a0002 | c0002 | t0006 | g0066 | SAS | STU | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | STU | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA18522 | hp1 | a0001 | c0001 | t0012 | g0197 | AFR | YRI | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0198 | AFR | YRI | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | CHB | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA18747 | hp2 | a0001 | c0001 | t0004 | g0091 | EAS | CHB | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0185 | AFR | YRI | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0188 | AFR | YRI | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA18942 | hp2 | a0001 | c0001 | t0005 | g0244 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA18943 | hp1 | a0001 | c0001 | t0004 | g0103 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA18943 | hp2 | a0001 | c0001 | t0015 | g0032 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA18946 | hp1 | a0001 | c0001 | t0005 | g0238 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA18947 | hp2 | a0001 | c0001 | t0005 | g0233 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA18950 | hp2 | a0001 | c0001 | t0007 | g0022 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA18954 | hp2 | a0001 | c0001 | t0005 | g0241 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA18956 | hp1 | a0001 | c0001 | t0004 | g0089 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA18960 | hp1 | a0001 | c0001 | t0004 | g0078 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA18964 | hp2 | a0001 | c0001 | t0004 | g0094 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA18966 | hp1 | a0001 | c0001 | t0029 | g0236 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA18968 | hp2 | a0001 | c0001 | t0005 | g0232 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA18971 | hp2 | a0001 | c0001 | t0004 | g0102 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA18977 | hp1 | a0001 | c0001 | t0005 | g0243 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA18989 | hp2 | a0001 | c0001 | t0004 | g0110 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA19004 | hp1 | a0001 | c0001 | t0004 | g0098 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA19011 | hp2 | a0001 | c0001 | t0004 | g0107 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | LWK | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | LWK | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA19056 | hp2 | a0001 | c0001 | t0005 | g0240 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA19060 | hp2 | a0001 | c0001 | t0005 | g0242 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA19063 | hp2 | a0001 | c0001 | t0005 | g0234 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA19068 | hp1 | a0001 | c0001 | t0005 | g0235 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA19076 | hp1 | a0001 | c0001 | t0005 | g0239 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA19076 | hp2 | a0003 | c0007 | t0002 | g0205 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA19088 | hp1 | a0001 | c0001 | t0004 | g0101 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA19240 | hp1 | a0001 | c0001 | t0014 | g0056 | AFR | YRI | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | YRI | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA20129 | hp1 | a0001 | c0001 | t0005 | g0172 | AFR | ASW | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | ASW | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA20752 | hp1 | a0002 | c0002 | t0006 | g0073 | EUR | TSI | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0027 | EUR | TSI | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA20905 | hp1 | a0001 | c0001 | t0007 | g0034 | SAS | GIH | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | GIH | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG01123 | hp2 | a0001 | c0001 | t0007 | g0029 | AMR | CLM | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02109 | hp1 | a0001 | c0001 | t0012 | g0195 | AFR | ACB | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02109 | hp2 | a0002 | c0002 | t0018 | g0059 | AFR | ACB | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02559 | hp1 | a0001 | c0001 | t0024 | g0192 | AFR | ACB | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0199 | AFR | ACB | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0080 | AFR | MSL | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG06807 | hp1 | a0002 | c0002 | t0008 | g0064 | AFR | USA | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| HG06807 | hp2 | a0001 | c0001 | t0007 | g0037 | AFR | USA | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA18955 | hp2 | a0001 | c0001 | t0004 | g0090 | EAS | JPT | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA20300 | hp1 | a0001 | c0001 | t0014 | g0055 | AFR | USA | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| NA20300 | hp2 | a0001 | c0001 | t0023 | g0165 | AFR | USA | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0028 | REF | REF | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0047 | REF | REF | RNF180_chr5_64160843_64377869 | RNF180 | chr5 | 64160843 | 64377869 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:64165951
|
C | A | 1 | a0002 | 1 | HG02735.hp1 | splice_region_variant | LOW | c.-3C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/8 | chr5 | 64165951 | ||||||
| chr5:64212109
|
G | T | 1 | a0003 | 1 | NA19076.hp2 | missense_variant | MODERATE | c.180G>T | p.Trp60Cys | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 3/8 | 291/4945 | 180/1779 | 60/592 | chr5 | 64212109 | ||
| chr5:64213964
|
A | G | 1 | a0006 | 1 | HG01952.hp2 | missense_variant | MODERATE | c.638A>G | p.Gln213Arg | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 4/8 | 749/4945 | 638/1779 | 213/592 | chr5 | 64213964 | ||
| chr5:64214071
|
C | T | 1 | a0005 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.745C>T | p.His249Tyr | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 4/8 | 856/4945 | 745/1779 | 249/592 | chr5 | 64214071 | ||
| chr5:64324627
|
TCCCATAA others(723): Show |
T | 1 | a0004 | 1 | HG02647.hp2 | frameshift_variant&splice_acceptor_variant&splice_region_variant&intron_variant | HIGH | c.1228-558_1399del | p.Thr410fs | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/8 | 1228/1779 | 410/592 | chr5 | 64324627 | |||
| chr5:64369621
|
G | A | 1 | a0002 | 19 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(16): Show |
missense_variant | MODERATE | c.1586G>A | p.Arg529His | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 1697/4945 | 1586/1779 | 529/592 | chr5 | 64369621 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:64214199
|
G | C | 1 | a0001c0003 | 1 | HG02040.hp2 | synonymous_variant | LOW | c.873G>C | p.Leu291Leu | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 4/8 | 984/4945 | 873/1779 | 291/592 | chr5 | 64214199 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:64165874
|
G | C | 1 | a0001c0001t0015 | 1 | NA18943.hp2 | 5_prime_UTR_variant | MODIFIER | c.-80G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/8 | 34934 | chr5 | 64165874 | |||||
| chr5:64369836
|
T | C | 1 | a0002c0002t0008 | 4 | HG00741.hp2 HG01257.hp2 HG02280.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*22T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 22 | chr5 | 64369836 | |||||
| chr5:64370030
|
A | G | 1 | a0001c0001t0012 | 3 | HG02109.hp1 HG03225.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*216A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 216 | chr5 | 64370030 | |||||
| chr5:64370034
|
A | G | 12 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(9): Show | 118 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*220A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 220 | chr5 | 64370034 | |||||
| chr5:64370090
|
T | C | 1 | a0001c0001t0017 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*276T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 276 | chr5 | 64370090 | |||||
| chr5:64370119
|
A | C | 1 | a0001c0001t0029 | 1 | NA18966.hp1 | 3_prime_UTR_variant | MODIFIER | c.*305A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 305 | chr5 | 64370119 | |||||
| chr5:64370136
|
C | T | 1 | a0001c0001t0028 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*322C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 322 | chr5 | 64370136 | |||||
| chr5:64370289
|
A | G | 2 | a0001c0001t0011a0001c0001t0014 | 5 | HG02970.hp1 HG03139.hp2 HG03540.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*475A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 475 | chr5 | 64370289 | |||||
| chr5:64370452
|
C | A | 25 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(22): Show | 189 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(186): Show |
3_prime_UTR_variant | MODIFIER | c.*638C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 638 | chr5 | 64370452 | |||||
| chr5:64370453
|
T | G | 25 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(22): Show | 189 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(186): Show |
3_prime_UTR_variant | MODIFIER | c.*639T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 639 | chr5 | 64370453 | |||||
| chr5:64370457
|
T | C | 2 | a0001c0001t0013a0001c0001t0021 | 3 | HG00642.hp2 HG01261.hp2 HG01516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*643T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 643 | chr5 | 64370457 | |||||
| chr5:64370488
|
A | G | 1 | a0001c0001t0022 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*674A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 674 | chr5 | 64370488 | |||||
| chr5:64370643
|
A | C | 1 | a0001c0001t0027 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*829A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 829 | chr5 | 64370643 | |||||
| chr5:64370862
|
G | A | 1 | a0001c0001t0009 | 4 | HG00323.hp2 HG01175.hp2 HG02257.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1048G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 1048 | chr5 | 64370862 | |||||
| chr5:64371361
|
T | C | 5 | a0002c0002t0006a0002c0002t0008a0002c0002t0010others(2): Show | 19 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1547T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 1547 | chr5 | 64371361 | |||||
| chr5:64371369
|
G | C | 1 | a0001c0001t0019 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1555G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 1555 | chr5 | 64371369 | |||||
| chr5:64371471
|
A | T | 3 | a0001c0001t0007a0001c0001t0009a0001c0001t0015 | 14 | HG00323.hp2 HG01123.hp2 HG01175.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1657A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 1657 | chr5 | 64371471 | |||||
| chr5:64371695
|
C | T | 1 | a0001c0001t0011 | 3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1881C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 1881 | chr5 | 64371695 | |||||
| chr5:64371834
|
T | C | 1 | a0001c0001t0020 | 1 | HG01168.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2020T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 2020 | chr5 | 64371834 | |||||
| chr5:64371944
|
T | A | 1 | a0001c0001t0023 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2130T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 2130 | chr5 | 64371944 | |||||
| chr5:64372189
|
T | TA | 2 | a0001c0001t0011a0001c0001t0014 | 5 | HG02970.hp1 HG03139.hp2 HG03540.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2382dupA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 2383 | INFO_REALIGN_3_PRIME | chr5 | 64372189 | ||||
| chr5:64372190
|
A | T | 2 | a0001c0001t0026a0002c0002t0018 | 2 | HG02109.hp2 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2376A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 2376 | chr5 | 64372190 | |||||
| chr5:64372196
|
A | G | 2 | a0002c0002t0006a0002c0002t0016 | 11 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2382A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 2382 | chr5 | 64372196 | |||||
| chr5:64372212
|
A | G | 4 | a0001c0001t0001a0001c0001t0023a0001c0001t0025others(1): Show | 59 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*2398A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 2398 | chr5 | 64372212 | |||||
| chr5:64372466
|
C | T | 1 | a0001c0001t0025 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2652C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 2652 | chr5 | 64372466 | |||||
| chr5:64372543
|
A | C | 1 | a0001c0001t0021 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2729A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 2729 | chr5 | 64372543 | |||||
| chr5:64372556
|
A | G | 7 | a0001c0001t0005a0001c0001t0019a0001c0001t0024others(4): Show | 32 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*2742A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 2742 | chr5 | 64372556 | |||||
| chr5:64372774
|
C | A | 1 | a0001c0001t0024 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2960C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 8/8 | 2960 | chr5 | 64372774 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:64166002
|
T | A | 1 | a0001c0001t0002g0003 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-1+49T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64166002 | ||||||
| chr5:64166149
|
C | G | 199 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(196): Show | 200 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.-1+196C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64166149 | ||||||
| chr5:64166243
|
T | C | 1 | a0001c0001t0011g0052 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-1+290T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64166243 | ||||||
| chr5:64166283
|
A | T | 1 | a0001c0001t0004g0248 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-1+330A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64166283 | ||||||
| chr5:64166738
|
C | T | 1 | a0001c0001t0007g0051 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-1+785C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64166738 | ||||||
| chr5:64166800
|
T | C | 5 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054others(2): Show | 5 | HG02970.hp1 HG03139.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1+847T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64166800 | ||||||
| chr5:64166851
|
G | A | 3 | a0002c0002t0010g0057a0002c0002t0010g0058a0002c0002t0018g0059 | 3 | HG02109.hp2 HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-1+898G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64166851 | ||||||
| chr5:64166915
|
A | G | 1 | a0001c0001t0026g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-1+962A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64166915 | ||||||
| chr5:64167316
|
G | A | 20 | a0001c0001t0027g0060a0002c0002t0006g0065a0002c0002t0006g0066others(17): Show | 20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.-1+1363G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64167316 | ||||||
| chr5:64167544
|
G | C | 1 | a0001c0001t0004g0248 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-1+1591G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64167544 | ||||||
| chr5:64167623
|
T | A | 1 | a0001c0001t0027g0060 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-1+1670T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64167623 | ||||||
| chr5:64167694
|
A | G | 16 | a0001c0001t0027g0060a0002c0002t0006g0065a0002c0002t0006g0066others(13): Show | 16 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.-1+1741A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64167694 | ||||||
| chr5:64167745
|
G | T | 1 | a0001c0003t0002g0246 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-1+1792G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64167745 | ||||||
| chr5:64168030
|
G | T | 1 | a0001c0001t0004g0245 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-1+2077G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64168030 | ||||||
| chr5:64168055
|
G | T | 1 | a0001c0001t0026g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-1+2102G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64168055 | ||||||
| chr5:64168120
|
A | G | 13 | a0001c0001t0005g0232a0001c0001t0005g0233a0001c0001t0005g0234others(10): Show | 13 | HG00597.hp1 NA18942.hp2 NA18946.hp1 others(10): Show |
intron_variant | MODIFIER | c.-1+2167A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64168120 | ||||||
| chr5:64168412
|
G | A | 1 | a0001c0001t0003g0077 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-1+2459G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64168412 | ||||||
| chr5:64168466
|
G | C | 1 | a0001c0001t0004g0078 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-1+2513G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64168466 | ||||||
| chr5:64168695
|
A | G | 3 | a0002c0002t0008g0062a0002c0002t0008g0063a0002c0002t0008g0064 | 3 | HG00741.hp2 HG01257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-1+2742A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64168695 | ||||||
| chr5:64168726
|
C | T | 1 | a0001c0001t0005g0244 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-1+2773C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64168726 | ||||||
| chr5:64168799
|
T | G | 1 | a0001c0001t0001g0079 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-1+2846T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64168799 | ||||||
| chr5:64169022
|
T | C | 1 | a0001c0001t0026g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-1+3069T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64169022 | ||||||
| chr5:64169859
|
G | C | 1 | a0001c0001t0002g0080 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-1+3906G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64169859 | ||||||
| chr5:64169887
|
G | A | 3 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0006 | 3 | HG00741.hp1 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-1+3934G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64169887 | ||||||
| chr5:64170063
|
C | T | 3 | a0002c0002t0010g0057a0002c0002t0010g0058a0002c0002t0018g0059 | 3 | HG02109.hp2 HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-1+4110C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64170063 | ||||||
| chr5:64170078
|
G | C | 1 | a0001c0001t0003g0007 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-1+4125G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64170078 | ||||||
| chr5:64170092
|
G | A | 3 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054 | 3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-1+4139G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64170092 | ||||||
| chr5:64170240
|
G | T | 1 | a0001c0001t0027g0060 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-1+4287G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64170240 | ||||||
| chr5:64170429
|
G | A | 111 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(108): Show | 112 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.-1+4476G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64170429 | ||||||
| chr5:64170965
|
T | C | 20 | a0001c0001t0027g0060a0002c0002t0006g0065a0002c0002t0006g0066others(17): Show | 20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.-1+5012T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64170965 | ||||||
| chr5:64171079
|
A | C | 1 | a0001c0001t0023g0165 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-1+5126A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64171079 | ||||||
| chr5:64171195
|
G | T | 3 | a0002c0002t0010g0057a0002c0002t0010g0058a0002c0002t0018g0059 | 3 | HG02109.hp2 HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-1+5242G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64171195 | ||||||
| chr5:64171386
|
A | G | 4 | a0002c0002t0010g0057a0002c0002t0010g0058a0002c0002t0010g0076others(1): Show | 4 | HG02109.hp2 HG02622.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1+5433A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64171386 | ||||||
| chr5:64171411
|
C | T | 10 | a0001c0001t0002g0222a0001c0001t0002g0223a0001c0001t0002g0224others(7): Show | 10 | HG02040.hp1 NA18950.hp1 NA18955.hp1 others(7): Show |
intron_variant | MODIFIER | c.-1+5458C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64171411 | ||||||
| chr5:64171593
|
T | G | 3 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083 | 3 | HG00323.hp1 HG01106.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.-1+5640T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64171593 | ||||||
| chr5:64171712
|
A | G | 2 | a0002c0002t0006g0074a0002c0002t0006g0075 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-1+5759A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64171712 | ||||||
| chr5:64171827
|
G | C | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-1+5874G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64171827 | ||||||
| chr5:64171836
|
C | T | 21 | a0001c0001t0002g0202a0001c0001t0002g0203a0001c0001t0002g0204others(18): Show | 21 | HG00099.hp2 HG00597.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.-1+5883C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64171836 | ||||||
| chr5:64171849
|
C | G | 2 | a0001c0001t0003g0200a0001c0001t0003g0201 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-1+5896C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64171849 | ||||||
| chr5:64171990
|
C | T | 2 | a0001c0001t0014g0055a0001c0001t0014g0056 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-1+6037C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64171990 | ||||||
| chr5:64172058
|
C | T | 12 | a0001c0001t0003g0048a0001c0001t0003g0049a0001c0001t0003g0050others(9): Show | 12 | HG00408.hp1 HG02074.hp1 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.-1+6105C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64172058 | ||||||
| chr5:64172192
|
G | A | 1 | a0001c0001t0026g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-1+6239G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64172192 | ||||||
| chr5:64172300
|
T | C | 92 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(89): Show | 93 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.-1+6347T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64172300 | ||||||
| chr5:64172398
|
G | T | 1 | a0001c0001t0014g0056 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-1+6445G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64172398 | ||||||
| chr5:64172419
|
G | T | 1 | a0001c0001t0002g0231 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-1+6466G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64172419 | ||||||
| chr5:64172458
|
G | A | 20 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(17): Show | 20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.-1+6505G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64172458 | ||||||
| chr5:64172553
|
T | A | 247 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(244): Show | 249 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.-1+6600T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64172553 | ||||||
| chr5:64172780
|
G | A | 1 | a0001c0001t0001g0085 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-1+6827G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64172780 | ||||||
| chr5:64172858
|
A | G | 1 | a0001c0001t0019g0166 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-1+6905A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64172858 | ||||||
| chr5:64172943
|
A | G | 20 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(17): Show | 20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.-1+6990A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64172943 | ||||||
| chr5:64173383
|
G | T | 2 | a0001c0001t0003g0045a0001c0001t0021g0046 | 2 | HG00642.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.-1+7430G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64173383 | ||||||
| chr5:64173578
|
C | T | 2 | a0001c0001t0014g0055a0001c0001t0014g0056 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-1+7625C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64173578 | ||||||
| chr5:64173595
|
A | G | 1 | a0001c0001t0028g0193 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-1+7642A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64173595 | ||||||
| chr5:64173697
|
C | G | 11 | a0002c0002t0006g0065a0002c0002t0006g0066a0002c0002t0006g0068others(8): Show | 11 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.-1+7744C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64173697 | ||||||
| chr5:64173703
|
T | C | 2 | a0001c0001t0019g0166a0001c0001t0026g0247 | 2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-1+7750T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64173703 | ||||||
| chr5:64173712
|
A | G | 147 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(144): Show | 148 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.-1+7759A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64173712 | ||||||
| chr5:64173717
|
C | CT | 25 | a0001c0001t0003g0044a0001c0001t0003g0198a0001c0001t0003g0199others(22): Show | 25 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.-1+7780dupT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64173717 | |||||
| chr5:64173717
|
CT | C | 32 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0002g0222others(29): Show | 33 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(30): Show |
intron_variant | MODIFIER | c.-1+7780delT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64173717 | |||||
| chr5:64173802
|
G | A | 4 | a0002c0002t0008g0061a0002c0002t0008g0062a0002c0002t0008g0063others(1): Show | 4 | HG00741.hp2 HG01257.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1+7849G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64173802 | ||||||
| chr5:64174107
|
C | T | 2 | a0001c0001t0014g0055a0001c0001t0014g0056 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-1+8154C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64174107 | ||||||
| chr5:64174555
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-1+8602A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64174555 | ||||||
| chr5:64174589
|
A | G | 26 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(23): Show | 26 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.-1+8636A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64174589 | ||||||
| chr5:64174909
|
T | C | 1 | a0001c0001t0013g0008 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-1+8956T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64174909 | ||||||
| chr5:64174929
|
C | A | 247 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(244): Show | 249 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.-1+8976C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64174929 | ||||||
| chr5:64174959
|
C | CT | 92 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0001g0083others(89): Show | 93 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(90): Show |
intron_variant | MODIFIER | c.-1+9032dupT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64174959 | |||||
| chr5:64174959
|
C | CTT | 7 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(4): Show | 7 | HG01109.hp2 HG01928.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.-1+9031_-1+9032dup others(2): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64174959 | |||||
| chr5:64174959
|
C | CTTTTT | 20 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0170others(17): Show | 20 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.-1+9028_-1+9032dup others(5): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64174959 | |||||
| chr5:64174959
|
CT | C | 8 | a0001c0001t0002g0202a0001c0001t0002g0203a0001c0001t0002g0204others(5): Show | 8 | HG00597.hp2 HG01943.hp1 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.-1+9032delT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64174959 | |||||
| chr5:64174959
|
CTTTTTTT others(4): Show |
C | 20 | a0001c0001t0027g0060a0002c0002t0006g0065a0002c0002t0006g0066others(17): Show | 20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.-1+9022_-1+9032del others(11): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64174959 | |||||
| chr5:64174959
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0003g0009 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-1+9019_-1+9032del others(14): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64174959 | |||||
| chr5:64175012
|
G | T | 1 | a0001c0001t0002g0231 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-1+9059G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64175012 | ||||||
| chr5:64175037
|
G | A | 2 | a0001c0001t0002g0184a0001c0001t0002g0187 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.-1+9084G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64175037 | ||||||
| chr5:64175060
|
C | T | 1 | a0001c0001t0002g0183 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-1+9107C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64175060 | ||||||
| chr5:64175088
|
C | T | 2 | a0002c0002t0006g0074a0002c0002t0006g0075 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-1+9135C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64175088 | ||||||
| chr5:64175213
|
C | T | 2 | a0001c0001t0003g0198a0001c0001t0003g0199 | 2 | HG02559.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-1+9260C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64175213 | ||||||
| chr5:64175263
|
C | T | 1 | a0001c0001t0003g0050 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-1+9310C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64175263 | ||||||
| chr5:64175264
|
G | A | 27 | a0001c0001t0004g0002a0001c0001t0004g0078a0001c0001t0004g0086others(24): Show | 28 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.-1+9311G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64175264 | ||||||
| chr5:64175302
|
T | C | 1 | a0001c0001t0013g0012 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-1+9349T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64175302 | ||||||
| chr5:64175517
|
A | C | 5 | a0001c0001t0005g0188a0001c0001t0005g0190a0001c0001t0005g0191others(2): Show | 5 | HG01891.hp2 HG02559.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1+9564A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64175517 | ||||||
| chr5:64175785
|
G | A | 1 | a0001c0001t0026g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-1+9832G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64175785 | ||||||
| chr5:64175805
|
A | G | 1 | a0001c0001t0001g0158 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-1+9852A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64175805 | ||||||
| chr5:64175861
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-1+9908G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64175861 | ||||||
| chr5:64175875
|
G | A | 2 | a0001c0001t0005g0185a0001c0001t0005g0186 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-1+9922G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64175875 | ||||||
| chr5:64175997
|
T | G | 140 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(137): Show | 141 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.-1+10044T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64175997 | ||||||
| chr5:64176208
|
G | A | 27 | a0001c0001t0004g0002a0001c0001t0004g0078a0001c0001t0004g0086others(24): Show | 28 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.-1+10255G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64176208 | ||||||
| chr5:64176276
|
A | G | 2 | a0001c0001t0005g0185a0001c0001t0005g0186 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-1+10323A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64176276 | ||||||
| chr5:64176599
|
A | G | 2 | a0001c0001t0005g0185a0001c0001t0005g0186 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-1+10646A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64176599 | ||||||
| chr5:64176665
|
T | G | 1 | a0001c0001t0002g0208 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-1+10712T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64176665 | ||||||
| chr5:64176785
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-1+10832C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64176785 | ||||||
| chr5:64176946
|
C | T | 1 | a0001c0001t0019g0166 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-1+10993C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64176946 | ||||||
| chr5:64176957
|
T | C | 20 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(17): Show | 20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.-1+11004T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64176957 | ||||||
| chr5:64177049
|
G | T | 2 | a0001c0001t0005g0185a0001c0001t0005g0186 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-1+11096G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64177049 | ||||||
| chr5:64177237
|
A | G | 1 | a0001c0001t0024g0192 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-1+11284A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64177237 | ||||||
| chr5:64177241
|
A | T | 140 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(137): Show | 141 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.-1+11288A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64177241 | ||||||
| chr5:64177247
|
G | A | 20 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(17): Show | 20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.-1+11294G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64177247 | ||||||
| chr5:64177466
|
A | G | 2 | a0001c0001t0004g0108a0001c0001t0004g0109 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-1+11513A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64177466 | ||||||
| chr5:64177485
|
T | C | 4 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(1): Show | 4 | HG02055.hp2 HG02622.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1+11532T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64177485 | ||||||
| chr5:64177526
|
C | CAT | 19 | a0001c0001t0002g0026a0001c0001t0002g0178a0001c0001t0002g0215others(16): Show | 19 | HG00741.hp1 HG01168.hp2 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.-1+11612_-1+11613d others(4): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64177526 | |||||
| chr5:64177526
|
C | CATAT | 28 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0183others(25): Show | 28 | HG00639.hp1 HG01109.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.-1+11610_-1+11613d others(6): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64177526 | |||||
| chr5:64177526
|
C | CATATAT | 8 | a0001c0001t0002g0211a0001c0001t0002g0220a0001c0001t0002g0224others(5): Show | 8 | HG00642.hp1 HG00642.hp2 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.-1+11608_-1+11613d others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64177526 | |||||
| chr5:64177526
|
C | CATATATA others(1): Show |
4 | a0001c0001t0002g0187a0001c0001t0003g0014a0001c0001t0003g0015others(1): Show | 4 | HG00408.hp1 HG02572.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1+11606_-1+11613d others(10): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64177526 | |||||
| chr5:64177526
|
C | CATATATA others(3): Show |
3 | a0001c0001t0002g0209a0001c0001t0002g0210a0001c0001t0002g0223 | 3 | HG00099.hp2 NA18954.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.-1+11604_-1+11613d others(12): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64177526 | |||||
| chr5:64177526
|
C | CATATATA others(5): Show |
3 | a0001c0001t0002g0174a0001c0001t0002g0230a0001c0001t0003g0013 | 3 | HG00738.hp2 HG02602.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.-1+11602_-1+11613d others(14): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64177526 | |||||
| chr5:64177526
|
C | CATATATA others(7): Show |
4 | a0001c0001t0002g0202a0001c0001t0002g0203a0001c0001t0002g0228others(1): Show | 4 | HG00597.hp2 HG01943.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1+11600_-1+11613d others(16): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64177526 | |||||
| chr5:64177526
|
CAT | C | 5 | a0001c0001t0002g0080a0001c0001t0002g0207a0001c0001t0002g0218others(2): Show | 5 | HG03471.hp2 HG03927.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1+11612_-1+11613d others(4): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64177526 | |||||
| chr5:64177526
|
CATATATA others(1): Show |
C | 7 | a0001c0001t0005g0172a0001c0001t0005g0189a0001c0001t0005g0232others(4): Show | 7 | HG00597.hp1 HG01175.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1+11606_-1+11613d others(10): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64177526 | |||||
| chr5:64177526
|
CATATATA others(3): Show |
C | 19 | a0001c0001t0002g0038a0001c0001t0005g0167a0001c0001t0005g0168others(16): Show | 20 | HG00323.hp2 HG01255.hp2 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.-1+11604_-1+11613d others(12): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64177526 | |||||
| chr5:64177526
|
CATATATA others(5): Show |
C | 5 | a0001c0001t0005g0234a0001c0001t0005g0240a0001c0001t0005g0241others(2): Show | 5 | NA18954.hp2 NA18977.hp1 NA19056.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1+11602_-1+11613d others(14): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64177526 | |||||
| chr5:64177526
|
CATATATA others(7): Show |
C | 6 | a0001c0001t0002g0219a0001c0001t0005g0173a0001c0001t0011g0052others(3): Show | 6 | HG02280.hp1 HG02922.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1+11600_-1+11613d others(16): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64177526 | |||||
| chr5:64177526
|
CATATATA others(9): Show |
C | 2 | a0001c0001t0014g0055a0001c0001t0014g0056 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-1+11598_-1+11613d others(18): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64177526 | |||||
| chr5:64177526
|
CATATATA others(11): Show |
C | 5 | a0001c0001t0003g0043a0002c0002t0010g0057a0002c0002t0010g0058others(2): Show | 5 | HG02109.hp2 HG02622.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1+11596_-1+11613d others(20): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64177526 | |||||
| chr5:64177526
|
CATATATA others(13): Show |
C | 16 | a0001c0001t0004g0248a0001c0001t0027g0060a0002c0002t0006g0065others(13): Show | 16 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.-1+11594_-1+11613d others(22): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64177526 | |||||
| chr5:64177526
|
CATATATA others(15): Show |
C | 91 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(88): Show | 92 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.-1+11592_-1+11613d others(24): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64177526 | |||||
| chr5:64177526
|
CATATATA others(17): Show |
C | 3 | a0001c0001t0003g0039a0001c0001t0005g0185a0001c0001t0005g0186 | 3 | HG03098.hp2 NA18906.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.-1+11590_-1+11613d others(26): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64177526 | |||||
| chr5:64177561
|
A | G | 1 | a0001c0001t0005g0172 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-1+11608A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64177561 | ||||||
| chr5:64177563
|
A | G | 1 | a0001c0001t0028g0193 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-1+11610A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64177563 | ||||||
| chr5:64177565
|
A | G | 6 | a0001c0001t0005g0188a0001c0001t0005g0189a0001c0001t0005g0190others(3): Show | 6 | HG01891.hp2 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1+11612A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64177565 | ||||||
| chr5:64177932
|
G | A | 2 | a0001c0001t0005g0235a0001c0001t0029g0236 | 2 | NA18966.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.-1+11979G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64177932 | ||||||
| chr5:64178014
|
A | G | 20 | a0001c0001t0027g0060a0002c0002t0006g0065a0002c0002t0006g0066others(17): Show | 20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.-1+12061A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64178014 | ||||||
| chr5:64178184
|
C | T | 1 | a0001c0001t0001g0114 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-1+12231C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64178184 | ||||||
| chr5:64178202
|
CA | C | 197 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(194): Show | 199 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.-1+12269delA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64178202 | |||||
| chr5:64178218
|
A | G | 1 | a0001c0001t0028g0193 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-1+12265A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64178218 | ||||||
| chr5:64178307
|
C | T | 12 | a0001c0001t0027g0060a0002c0002t0006g0065a0002c0002t0006g0066others(9): Show | 12 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.-1+12354C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64178307 | ||||||
| chr5:64178326
|
T | A | 1 | a0001c0001t0001g0111 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-1+12373T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64178326 | ||||||
| chr5:64178363
|
G | A | 1 | a0001c0001t0001g0085 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-1+12410G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64178363 | ||||||
| chr5:64178422
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-1+12469G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64178422 | ||||||
| chr5:64178532
|
T | G | 16 | a0001c0001t0027g0060a0002c0002t0006g0065a0002c0002t0006g0066others(13): Show | 16 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.-1+12579T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64178532 | ||||||
| chr5:64178556
|
G | A | 5 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054others(2): Show | 5 | HG02970.hp1 HG03139.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1+12603G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64178556 | ||||||
| chr5:64178632
|
G | A | 1 | a0001c0001t0007g0022 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-1+12679G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64178632 | ||||||
| chr5:64178939
|
G | A | 1 | a0006c0006t0002g0175 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-1+12986G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64178939 | ||||||
| chr5:64179019
|
C | G | 1 | a0001c0001t0002g0204 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-1+13066C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64179019 | ||||||
| chr5:64179156
|
A | G | 1 | a0001c0001t0002g0207 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-1+13203A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64179156 | ||||||
| chr5:64179238
|
C | T | 20 | a0001c0001t0027g0060a0002c0002t0006g0065a0002c0002t0006g0066others(17): Show | 20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.-1+13285C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64179238 | ||||||
| chr5:64179280
|
A | G | 5 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(2): Show | 5 | HG01433.hp2 HG01928.hp1 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1+13327A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64179280 | ||||||
| chr5:64179322
|
T | C | 2 | a0001c0001t0003g0040a0001c0001t0013g0012 | 2 | HG01261.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.-1+13369T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64179322 | ||||||
| chr5:64179431
|
TTTGCTAC others(7): Show |
T | 61 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(58): Show | 61 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.-1+13480_-1+13493d others(16): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64179431 | |||||
| chr5:64180143
|
G | T | 1 | a0001c0001t0024g0192 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-1+14190G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64180143 | ||||||
| chr5:64180785
|
G | A | 1 | a0001c0001t0019g0166 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-1+14832G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64180785 | ||||||
| chr5:64180983
|
C | T | 2 | a0001c0001t0005g0185a0001c0001t0005g0186 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-1+15030C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64180983 | ||||||
| chr5:64181054
|
G | A | 1 | a0001c0001t0022g0018 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-1+15101G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64181054 | ||||||
| chr5:64181222
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-1+15269T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64181222 | ||||||
| chr5:64181391
|
A | G | 1 | a0001c0001t0001g0152 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-1+15438A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64181391 | ||||||
| chr5:64181686
|
T | C | 5 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1+15733T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64181686 | ||||||
| chr5:64181720
|
G | A | 111 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(108): Show | 112 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.-1+15767G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64181720 | ||||||
| chr5:64181802
|
A | G | 1 | a0001c0001t0003g0017 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-1+15849A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64181802 | ||||||
| chr5:64181986
|
C | CT | 19 | a0001c0001t0002g0038a0001c0001t0002g0203a0001c0001t0002g0204others(16): Show | 19 | HG00323.hp2 HG00597.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.-1+16056dupT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64181986 | |||||
| chr5:64181986
|
CT | C | 55 | a0001c0001t0001g0153a0001c0001t0003g0005a0001c0001t0004g0002others(52): Show | 56 | HG01074.hp2 HG01081.hp1 HG01123.hp2 others(53): Show |
intron_variant | MODIFIER | c.-1+16056delT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64181986 | |||||
| chr5:64181986
|
CTT | C | 80 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(77): Show | 80 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.-1+16055_-1+16056d others(4): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64181986 | |||||
| chr5:64181986
|
CTTT | C | 8 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0005g0188others(5): Show | 8 | HG00738.hp1 HG01515.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.-1+16054_-1+16056d others(5): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64181986 | |||||
| chr5:64182076
|
C | T | 3 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054 | 3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-1+16123C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64182076 | ||||||
| chr5:64182147
|
C | T | 27 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(24): Show | 27 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(24): Show |
intron_variant | MODIFIER | c.-1+16194C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64182147 | ||||||
| chr5:64182156
|
A | G | 1 | a0001c0001t0004g0106 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-1+16203A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64182156 | ||||||
| chr5:64182184
|
A | G | 1 | a0002c0002t0006g0073 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-1+16231A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64182184 | ||||||
| chr5:64182240
|
T | C | 214 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(211): Show | 215 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.-1+16287T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64182240 | ||||||
| chr5:64182351
|
A | T | 2 | a0001c0001t0005g0232a0001c0001t0005g0233 | 2 | NA18947.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.-1+16398A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64182351 | ||||||
| chr5:64182728
|
G | C | 2 | a0001c0001t0004g0089a0001c0001t0004g0090 | 2 | NA18955.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.-1+16775G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64182728 | ||||||
| chr5:64182911
|
C | T | 2 | a0001c0001t0005g0232a0001c0001t0005g0233 | 2 | NA18947.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.-1+16958C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64182911 | ||||||
| chr5:64182928
|
A | T | 1 | a0001c0001t0002g0178 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-1+16975A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64182928 | ||||||
| chr5:64183441
|
C | CT | 60 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(57): Show | 60 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.1-17341dupT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64183441 | |||||
| chr5:64183441
|
C | CTT | 23 | a0001c0001t0001g0088a0001c0001t0001g0116a0001c0001t0001g0117others(20): Show | 23 | HG01074.hp2 HG01257.hp1 HG01258.hp1 others(20): Show |
intron_variant | MODIFIER | c.1-17342_1-17341dup others(2): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64183441 | |||||
| chr5:64183441
|
C | CTTT | 12 | a0001c0001t0001g0119a0001c0001t0001g0162a0001c0001t0027g0060others(9): Show | 12 | HG01081.hp1 HG01175.hp1 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1-17343_1-17341dup others(3): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64183441 | |||||
| chr5:64183441
|
CT | C | 5 | a0001c0001t0002g0209a0001c0001t0002g0215a0001c0001t0003g0198others(2): Show | 5 | HG01993.hp2 HG02257.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1-17341delT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64183441 | |||||
| chr5:64184056
|
T | G | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1-16752T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64184056 | ||||||
| chr5:64184085
|
G | T | 1 | a0001c0001t0009g0042 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1-16723G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64184085 | ||||||
| chr5:64184108
|
T | G | 1 | a0001c0001t0005g0189 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1-16700T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64184108 | ||||||
| chr5:64184210
|
C | A | 1 | a0001c0001t0004g0248 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1-16598C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64184210 | ||||||
| chr5:64184362
|
GTACTT | G | 4 | a0001c0001t0001g0120a0001c0001t0001g0147a0001c0001t0001g0148others(1): Show | 4 | HG02258.hp2 HG02647.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1-16443_1-16439del others(5): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64184362 | |||||
| chr5:64184404
|
A | T | 1 | a0001c0001t0004g0090 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1-16404A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64184404 | ||||||
| chr5:64184672
|
G | C | 53 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(50): Show | 53 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.1-16136G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64184672 | ||||||
| chr5:64184749
|
G | A | 2 | a0001c0001t0014g0055a0001c0001t0014g0056 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1-16059G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64184749 | ||||||
| chr5:64184799
|
A | T | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1-16009A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64184799 | ||||||
| chr5:64185177
|
T | G | 1 | a0001c0001t0001g0085 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1-15631T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64185177 | ||||||
| chr5:64185207
|
A | G | 2 | a0001c0001t0014g0055a0001c0001t0014g0056 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1-15601A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64185207 | ||||||
| chr5:64186000
|
G | A | 2 | a0001c0001t0002g0184a0001c0001t0002g0187 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1-14808G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64186000 | ||||||
| chr5:64186061
|
T | C | 1 | a0001c0001t0012g0197 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1-14747T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64186061 | ||||||
| chr5:64186136
|
A | G | 1 | a0001c0001t0001g0087 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1-14672A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64186136 | ||||||
| chr5:64186288
|
C | T | 144 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(141): Show | 145 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.1-14520C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64186288 | ||||||
| chr5:64186376
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1-14432G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64186376 | ||||||
| chr5:64186765
|
A | G | 2 | a0001c0001t0003g0005a0001c0001t0003g0006 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1-14043A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64186765 | ||||||
| chr5:64187436
|
G | T | 10 | a0001c0001t0002g0038a0001c0001t0003g0016a0001c0001t0007g0001others(7): Show | 11 | HG00323.hp2 HG01175.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.1-13372G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64187436 | ||||||
| chr5:64187528
|
G | C | 1 | a0001c0001t0004g0078 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1-13280G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64187528 | ||||||
| chr5:64187567
|
A | T | 20 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(17): Show | 20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1-13241A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64187567 | ||||||
| chr5:64187621
|
T | C | 8 | a0001c0001t0005g0188a0001c0001t0005g0189a0001c0001t0005g0190others(5): Show | 8 | HG01891.hp2 HG02559.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1-13187T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64187621 | ||||||
| chr5:64187839
|
T | G | 1 | a0001c0001t0024g0192 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1-12969T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64187839 | ||||||
| chr5:64188029
|
C | T | 1 | a0001c0001t0004g0146 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1-12779C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64188029 | ||||||
| chr5:64188134
|
A | G | 2 | a0001c0001t0002g0183a0001c0001t0003g0179 | 2 | HG02735.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1-12674A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64188134 | ||||||
| chr5:64188253
|
A | G | 1 | a0001c0001t0005g0172 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1-12555A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64188253 | ||||||
| chr5:64188838
|
T | A | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1-11970T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64188838 | ||||||
| chr5:64189081
|
A | G | 3 | a0001c0001t0005g0240a0001c0001t0005g0241a0001c0001t0005g0242 | 3 | NA18954.hp2 NA19056.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1-11727A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64189081 | ||||||
| chr5:64189268
|
A | G | 1 | a0001c0001t0002g0211 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1-11540A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64189268 | ||||||
| chr5:64189288
|
T | C | 1 | a0002c0002t0008g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1-11520T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64189288 | ||||||
| chr5:64189354
|
C | T | 3 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054 | 3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1-11454C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64189354 | ||||||
| chr5:64189529
|
G | A | 2 | a0001c0001t0005g0237a0001c0001t0005g0244 | 2 | HG00597.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.1-11279G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64189529 | ||||||
| chr5:64190051
|
C | G | 1 | a0001c0001t0004g0104 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1-10757C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64190051 | ||||||
| chr5:64190076
|
T | C | 11 | a0002c0002t0006g0065a0002c0002t0006g0066a0002c0002t0006g0068others(8): Show | 11 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.1-10732T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64190076 | ||||||
| chr5:64190350
|
A | G | 2 | a0001c0001t0005g0232a0001c0001t0005g0233 | 2 | NA18947.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.1-10458A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64190350 | ||||||
| chr5:64190433
|
C | T | 4 | a0002c0002t0008g0061a0002c0002t0008g0062a0002c0002t0008g0063others(1): Show | 4 | HG00741.hp2 HG01257.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1-10375C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64190433 | ||||||
| chr5:64190576
|
T | C | 1 | a0001c0001t0004g0106 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1-10232T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64190576 | ||||||
| chr5:64190713
|
G | T | 2 | a0001c0001t0005g0185a0001c0001t0005g0186 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1-10095G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64190713 | ||||||
| chr5:64190776
|
G | A | 2 | a0001c0001t0002g0184a0001c0001t0002g0187 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1-10032G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64190776 | ||||||
| chr5:64190784
|
G | A | 2 | a0001c0001t0003g0015a0001c0001t0003g0039 | 2 | NA18946.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1-10024G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64190784 | ||||||
| chr5:64190811
|
G | A | 1 | a0001c0001t0004g0091 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1-9997G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64190811 | ||||||
| chr5:64190821
|
A | G | 1 | a0001c0001t0002g0184 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1-9987A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64190821 | ||||||
| chr5:64190994
|
C | T | 144 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(141): Show | 145 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.1-9814C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64190994 | ||||||
| chr5:64190995
|
G | A | 1 | a0001c0001t0002g0176 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1-9813G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64190995 | ||||||
| chr5:64191091
|
G | T | 20 | a0001c0001t0027g0060a0002c0002t0006g0065a0002c0002t0006g0066others(17): Show | 20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1-9717G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64191091 | ||||||
| chr5:64191405
|
C | G | 1 | a0001c0001t0001g0156 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1-9403C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64191405 | ||||||
| chr5:64191418
|
C | T | 1 | a0001c0001t0007g0031 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1-9390C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64191418 | ||||||
| chr5:64191693
|
T | G | 4 | a0002c0002t0006g0065a0002c0002t0006g0069a0002c0002t0006g0070others(1): Show | 4 | HG01081.hp1 HG01975.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1-9115T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64191693 | ||||||
| chr5:64191953
|
G | A | 1 | a0001c0001t0003g0017 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1-8855G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64191953 | ||||||
| chr5:64192155
|
G | T | 3 | a0002c0002t0008g0062a0002c0002t0008g0063a0002c0002t0008g0064 | 3 | HG00741.hp2 HG01257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1-8653G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64192155 | ||||||
| chr5:64192179
|
G | A | 2 | a0001c0001t0014g0055a0001c0001t0014g0056 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1-8629G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64192179 | ||||||
| chr5:64192187
|
A | G | 90 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(87): Show | 91 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1-8621A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64192187 | ||||||
| chr5:64192205
|
C | T | 1 | a0001c0001t0005g0190 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1-8603C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64192205 | ||||||
| chr5:64192245
|
C | T | 4 | a0002c0002t0008g0061a0002c0002t0008g0062a0002c0002t0008g0063others(1): Show | 4 | HG00741.hp2 HG01257.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1-8563C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64192245 | ||||||
| chr5:64192285
|
G | C | 28 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(25): Show | 28 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.1-8523G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64192285 | ||||||
| chr5:64192286
|
G | A | 1 | a0001c0001t0026g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1-8522G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64192286 | ||||||
| chr5:64192335
|
G | A | 1 | a0001c0001t0005g0188 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1-8473G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64192335 | ||||||
| chr5:64192399
|
C | T | 1 | a0001c0001t0003g0027 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1-8409C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64192399 | ||||||
| chr5:64192449
|
G | A | 2 | a0001c0001t0002g0184a0001c0001t0002g0187 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1-8359G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64192449 | ||||||
| chr5:64192541
|
G | A | 90 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(87): Show | 91 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1-8267G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64192541 | ||||||
| chr5:64192542
|
C | T | 3 | a0001c0001t0002g0026a0001c0001t0003g0030a0001c0001t0007g0029 | 3 | HG01123.hp2 HG02698.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1-8266C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64192542 | ||||||
| chr5:64192575
|
G | A | 1 | a0001c0001t0003g0039 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1-8233G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64192575 | ||||||
| chr5:64192628
|
C | T | 5 | a0001c0001t0001g0158a0001c0001t0003g0144a0001c0001t0003g0145others(2): Show | 5 | HG02886.hp1 HG03098.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1-8180C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64192628 | ||||||
| chr5:64192791
|
A | G | 2 | a0001c0001t0004g0102a0001c0001t0004g0103 | 2 | NA18943.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.1-8017A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64192791 | ||||||
| chr5:64192900
|
C | CATGTATA others(49): Show |
1 | a0001c0001t0011g0053 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1-7869_1-7868insTA others(54): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192900 | |||||
| chr5:64192900
|
C | CATGTATA others(47): Show |
1 | a0001c0001t0011g0054 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1-7869_1-7868insTA others(52): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192900 | |||||
| chr5:64192900
|
C | CATGTATA others(45): Show |
1 | a0001c0001t0011g0052 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1-7869_1-7868insTA others(50): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192900 | |||||
| chr5:64192903
|
G | GTA | 14 | a0001c0001t0002g0183a0001c0001t0002g0220a0001c0001t0003g0007others(11): Show | 14 | HG00408.hp1 HG00639.hp1 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.1-7870_1-7869dupTA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | |||||
| chr5:64192903
|
G | GTATA | 31 | a0001c0001t0002g0080a0001c0001t0002g0181a0001c0001t0002g0203others(28): Show | 32 | HG00099.hp2 HG00597.hp2 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.1-7872_1-7869dupTA others(2): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | |||||
| chr5:64192903
|
G | GTATATA | 12 | a0001c0001t0002g0038a0001c0001t0002g0211a0001c0001t0002g0213others(9): Show | 12 | HG00323.hp2 HG00642.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.1-7874_1-7869dupTA others(4): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | |||||
| chr5:64192903
|
G | GTATATAT others(1): Show |
7 | a0001c0001t0002g0202a0001c0001t0002g0230a0001c0001t0003g0040others(4): Show | 7 | HG01261.hp1 HG01943.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1-7876_1-7869dupTA others(6): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | |||||
| chr5:64192903
|
G | GTATATAT others(3): Show |
6 | a0001c0001t0002g0226a0001c0001t0002g0229a0001c0001t0003g0124others(3): Show | 6 | HG00597.hp1 HG01168.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.1-7878_1-7869dupTA others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | |||||
| chr5:64192903
|
G | GTATATAT others(5): Show |
11 | a0001c0001t0002g0003a0001c0001t0002g0177a0001c0001t0002g0227others(8): Show | 11 | HG00741.hp1 HG01109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1-7880_1-7869dupTA others(10): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | |||||
| chr5:64192903
|
G | GTATATAT others(7): Show |
1 | a0001c0001t0029g0236 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1-7882_1-7869dupTA others(12): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | |||||
| chr5:64192903
|
G | GTATATAT others(9): Show |
8 | a0001c0001t0002g0223a0001c0001t0005g0171a0001c0001t0005g0232others(5): Show | 8 | HG02630.hp2 HG02818.hp1 NA18522.hp1 others(5): Show |
intron_variant | MODIFIER | c.1-7884_1-7869dupTA others(14): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | |||||
| chr5:64192903
|
G | GTATATAT others(11): Show |
9 | a0001c0001t0002g0026a0001c0001t0002g0174a0001c0001t0002g0209others(6): Show | 9 | HG00738.hp2 HG01516.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1-7886_1-7869dupTA others(16): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | |||||
| chr5:64192903
|
G | GTATATAT others(13): Show |
3 | a0001c0001t0005g0173a0001c0001t0007g0029a0001c0001t0014g0056 | 3 | HG01123.hp2 HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1-7888_1-7869dupTA others(18): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | |||||
| chr5:64192903
|
G | GTATATAT others(15): Show |
3 | a0001c0001t0002g0176a0001c0001t0003g0199a0001c0001t0012g0195 | 3 | HG01496.hp1 HG02109.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1-7890_1-7869dupTA others(20): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | |||||
| chr5:64192903
|
G | GTATATAT others(17): Show |
5 | a0001c0001t0002g0178a0001c0001t0002g0206a0001c0001t0003g0194others(2): Show | 5 | HG02818.hp2 HG03139.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1-7892_1-7869dupTA others(22): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | |||||
| chr5:64192903
|
G | GTATATAT others(19): Show |
2 | a0001c0001t0005g0235a0001c0001t0014g0055 | 2 | NA19068.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1-7894_1-7869dupTA others(24): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | |||||
| chr5:64192903
|
G | GTATATAT others(21): Show |
2 | a0001c0001t0003g0077a0001c0001t0012g0196 | 2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1-7896_1-7869dupTA others(26): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | |||||
| chr5:64192903
|
G | GTATATAT others(23): Show |
2 | a0001c0001t0003g0005a0001c0001t0003g0006 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1-7898_1-7869dupTA others(28): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | |||||
| chr5:64192903
|
G | GTATGTAT others(21): Show |
1 | a0001c0001t0021g0046 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1-7902_1-7901insGT others(26): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | |||||
| chr5:64192903
|
G | GTGTATAT others(9): Show |
1 | a0001c0001t0002g0187 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1-7904_1-7903insGT others(14): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | |||||
| chr5:64192903
|
G | GTGTATAT others(11): Show |
1 | a0001c0001t0002g0184 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1-7904_1-7903insGT others(16): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | |||||
| chr5:64192903
|
G | GTGTATAT others(17): Show |
2 | a0001c0001t0005g0185a0001c0001t0005g0186 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1-7904_1-7903insGT others(22): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | |||||
| chr5:64192903
|
G | GTGTGTAT others(5): Show |
1 | a0002c0002t0008g0063 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1-7904_1-7903insGT others(10): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | |||||
| chr5:64192903
|
G | GTGTGTAT others(11): Show |
2 | a0002c0002t0008g0062a0002c0002t0008g0064 | 2 | HG00741.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1-7904_1-7903insGT others(16): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | |||||
| chr5:64192903
|
G | GTGTGTGT others(25): Show |
1 | a0002c0002t0008g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1-7904_1-7903insGT others(30): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | |||||
| chr5:64192903
|
GTATATA | G | 12 | a0001c0001t0001g0113a0001c0001t0001g0125a0001c0001t0001g0126others(9): Show | 12 | HG01074.hp1 HG01074.hp2 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.1-7874_1-7869delTA others(4): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | |||||
| chr5:64192903
|
GTATATAT others(1): Show |
G | 13 | a0001c0001t0001g0079a0001c0001t0001g0111a0001c0001t0001g0153others(10): Show | 13 | HG00639.hp2 HG01081.hp1 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1-7876_1-7869delTA others(6): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | |||||
| chr5:64192903
|
GTATATAT others(3): Show |
G | 8 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0142others(5): Show | 8 | HG00738.hp1 HG01515.hp2 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.1-7878_1-7869delTA others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | |||||
| chr5:64192903
|
GTATATAT others(5): Show |
G | 46 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(43): Show | 46 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.1-7880_1-7869delTA others(10): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | |||||
| chr5:64192903
|
GTATATAT others(7): Show |
G | 25 | a0001c0001t0004g0002a0001c0001t0004g0078a0001c0001t0004g0086others(22): Show | 26 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.1-7882_1-7869delTA others(12): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192903 | |||||
| chr5:64192911
|
A | G | 6 | a0002c0002t0006g0068a0002c0002t0006g0072a0002c0002t0010g0057others(3): Show | 6 | HG01074.hp2 HG01175.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1-7897A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64192911 | ||||||
| chr5:64192913
|
A | G | 16 | a0001c0001t0027g0060a0002c0002t0006g0065a0002c0002t0006g0066others(13): Show | 16 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.1-7895A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64192913 | ||||||
| chr5:64192915
|
A | G | 10 | a0001c0001t0027g0060a0002c0002t0006g0065a0002c0002t0006g0066others(7): Show | 10 | HG01081.hp1 HG01257.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1-7893A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64192915 | ||||||
| chr5:64192928
|
TATATATA others(5): Show |
T | 1 | a0001c0001t0005g0172 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1-7878_1-7867delTA others(10): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64192928 | |||||
| chr5:64192939
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0003g0045 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1-7869_1-7868insTA others(19): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64192939 | ||||||
| chr5:64192940
|
A | T | 19 | a0001c0001t0003g0040a0001c0001t0005g0167a0001c0001t0005g0168others(16): Show | 19 | HG00597.hp1 HG01261.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1-7868A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64192940 | ||||||
| chr5:64192941
|
A | T | 1 | a0001c0001t0013g0008 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1-7867A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64192941 | ||||||
| chr5:64193049
|
C | A | 1 | a0001c0001t0005g0190 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1-7759C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64193049 | ||||||
| chr5:64193058
|
A | T | 1 | a0001c0001t0005g0189 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1-7750A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64193058 | ||||||
| chr5:64193446
|
G | A | 144 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(141): Show | 145 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.1-7362G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64193446 | ||||||
| chr5:64193460
|
C | T | 2 | a0001c0001t0014g0055a0001c0001t0014g0056 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1-7348C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64193460 | ||||||
| chr5:64193518
|
C | G | 20 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(17): Show | 20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1-7290C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64193518 | ||||||
| chr5:64193565
|
C | G | 1 | a0001c0001t0001g0158 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1-7243C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64193565 | ||||||
| chr5:64193574
|
A | T | 1 | a0002c0002t0010g0076 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1-7234A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64193574 | ||||||
| chr5:64193773
|
G | A | 1 | a0002c0002t0010g0076 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1-7035G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64193773 | ||||||
| chr5:64193900
|
A | G | 1 | a0001c0001t0005g0189 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1-6908A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64193900 | ||||||
| chr5:64194036
|
G | A | 2 | a0001c0001t0005g0185a0001c0001t0005g0186 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1-6772G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64194036 | ||||||
| chr5:64194111
|
G | A | 1 | a0001c0001t0019g0166 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1-6697G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64194111 | ||||||
| chr5:64194341
|
T | G | 3 | a0001c0001t0012g0195a0001c0001t0012g0196a0001c0001t0012g0197 | 3 | HG02109.hp1 HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1-6467T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64194341 | ||||||
| chr5:64194354
|
A | G | 1 | a0001c0001t0005g0189 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1-6454A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64194354 | ||||||
| chr5:64194396
|
A | G | 1 | a0001c0001t0005g0190 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1-6412A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64194396 | ||||||
| chr5:64194407
|
T | A | 1 | a0001c0001t0003g0014 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1-6401T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64194407 | ||||||
| chr5:64194433
|
T | C | 2 | a0001c0001t0001g0129a0001c0001t0001g0142 | 2 | HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1-6375T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64194433 | ||||||
| chr5:64194603
|
T | G | 1 | a0002c0002t0010g0076 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1-6205T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64194603 | ||||||
| chr5:64194728
|
T | C | 2 | a0001c0001t0003g0010a0001c0001t0007g0051 | 2 | HG03491.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1-6080T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64194728 | ||||||
| chr5:64194912
|
G | T | 199 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(196): Show | 200 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.1-5896G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64194912 | ||||||
| chr5:64195231
|
C | T | 2 | a0001c0001t0005g0185a0001c0001t0005g0186 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1-5577C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64195231 | ||||||
| chr5:64195273
|
T | C | 139 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(136): Show | 140 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.1-5535T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64195273 | ||||||
| chr5:64195275
|
A | G | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1-5533A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64195275 | ||||||
| chr5:64195396
|
C | T | 1 | a0001c0001t0004g0104 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1-5412C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64195396 | ||||||
| chr5:64195439
|
T | A | 2 | a0001c0001t0014g0055a0001c0001t0014g0056 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1-5369T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64195439 | ||||||
| chr5:64195516
|
A | C | 20 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(17): Show | 20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1-5292A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64195516 | ||||||
| chr5:64195603
|
A | G | 20 | a0001c0001t0027g0060a0002c0002t0006g0065a0002c0002t0006g0066others(17): Show | 20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1-5205A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64195603 | ||||||
| chr5:64195899
|
T | C | 1 | a0002c0002t0008g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1-4909T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64195899 | ||||||
| chr5:64195903
|
A | G | 3 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054 | 3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1-4905A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64195903 | ||||||
| chr5:64196084
|
A | C | 8 | a0001c0001t0005g0188a0001c0001t0005g0189a0001c0001t0005g0190others(5): Show | 8 | HG01891.hp2 HG02559.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1-4724A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64196084 | ||||||
| chr5:64196103
|
T | C | 20 | a0001c0001t0027g0060a0002c0002t0006g0065a0002c0002t0006g0066others(17): Show | 20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1-4705T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64196103 | ||||||
| chr5:64196123
|
T | C | 1 | a0001c0001t0004g0248 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1-4685T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64196123 | ||||||
| chr5:64196190
|
G | GT | 15 | a0001c0001t0005g0172a0001c0001t0005g0173a0001c0001t0005g0232others(12): Show | 15 | HG00597.hp1 HG02922.hp1 NA18942.hp2 others(12): Show |
intron_variant | MODIFIER | c.1-4605dupT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64196190 | |||||
| chr5:64196190
|
GT | G | 108 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(105): Show | 109 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.1-4605delT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64196190 | |||||
| chr5:64196203
|
T | C | 2 | a0001c0001t0003g0200a0001c0001t0003g0201 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1-4605T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64196203 | ||||||
| chr5:64196203
|
T | TC | 5 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1-4602dupC | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64196203 | |||||
| chr5:64196295
|
T | C | 2 | a0001c0001t0001g0129a0001c0001t0001g0142 | 2 | HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1-4513T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64196295 | ||||||
| chr5:64196733
|
C | G | 2 | a0001c0001t0002g0026a0001c0001t0003g0030 | 2 | HG02698.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1-4075C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64196733 | ||||||
| chr5:64197186
|
A | C | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1-3622A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64197186 | ||||||
| chr5:64197285
|
A | G | 8 | a0001c0001t0005g0188a0001c0001t0005g0189a0001c0001t0005g0190others(5): Show | 8 | HG01891.hp2 HG02559.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1-3523A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64197285 | ||||||
| chr5:64197376
|
G | A | 54 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(51): Show | 54 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.1-3432G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64197376 | ||||||
| chr5:64197381
|
C | T | 2 | a0002c0002t0008g0062a0002c0002t0008g0064 | 2 | HG00741.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1-3427C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64197381 | ||||||
| chr5:64197753
|
C | T | 4 | a0001c0001t0001g0120a0001c0001t0001g0147a0001c0001t0001g0148others(1): Show | 4 | HG02258.hp2 HG02647.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1-3055C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64197753 | ||||||
| chr5:64197843
|
A | T | 1 | a0001c0001t0003g0077 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1-2965A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64197843 | ||||||
| chr5:64197893
|
A | G | 3 | a0002c0002t0010g0057a0002c0002t0010g0058a0002c0002t0018g0059 | 3 | HG02109.hp2 HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1-2915A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64197893 | ||||||
| chr5:64197932
|
G | A | 1 | a0001c0001t0020g0023 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1-2876G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64197932 | ||||||
| chr5:64197944
|
A | G | 4 | a0001c0001t0003g0198a0001c0001t0003g0199a0001c0001t0003g0200others(1): Show | 4 | HG02559.hp2 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1-2864A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64197944 | ||||||
| chr5:64198150
|
A | G | 33 | a0001c0001t0001g0079a0001c0001t0001g0085a0001c0001t0001g0087others(30): Show | 33 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.1-2658A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64198150 | ||||||
| chr5:64198159
|
T | C | 1 | a0001c0001t0003g0041 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1-2649T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64198159 | ||||||
| chr5:64198456
|
G | A | 1 | a0001c0001t0003g0025 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1-2352G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64198456 | ||||||
| chr5:64198818
|
A | AT | 27 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(24): Show | 27 | HG00597.hp1 HG00741.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.1-1976dupT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 64198818 | |||||
| chr5:64198818
|
A | T | 3 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054 | 3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1-1990A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64198818 | ||||||
| chr5:64198849
|
C | T | 62 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(59): Show | 62 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.1-1959C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64198849 | ||||||
| chr5:64198884
|
C | T | 28 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(25): Show | 28 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.1-1924C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64198884 | ||||||
| chr5:64198897
|
C | T | 20 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(17): Show | 20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1-1911C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64198897 | ||||||
| chr5:64198955
|
A | G | 2 | a0001c0001t0003g0198a0001c0001t0003g0199 | 2 | HG02559.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1-1853A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64198955 | ||||||
| chr5:64199043
|
C | G | 30 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(27): Show | 30 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1-1765C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64199043 | ||||||
| chr5:64199059
|
C | T | 3 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054 | 3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1-1749C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64199059 | ||||||
| chr5:64199097
|
C | T | 3 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0023g0165 | 3 | HG01081.hp2 HG01346.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1-1711C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64199097 | ||||||
| chr5:64200208
|
A | G | 1 | a0001c0001t0005g0186 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1-600A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64200208 | ||||||
| chr5:64200319
|
G | A | 89 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(86): Show | 90 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1-489G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64200319 | ||||||
| chr5:64200332
|
A | G | 3 | a0002c0002t0010g0057a0002c0002t0010g0058a0002c0002t0018g0059 | 3 | HG02109.hp2 HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1-476A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64200332 | ||||||
| chr5:64200371
|
C | G | 2 | a0001c0001t0014g0055a0001c0001t0014g0056 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1-437C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64200371 | ||||||
| chr5:64200623
|
G | A | 1 | a0001c0001t0002g0181 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1-185G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64200623 | ||||||
| chr5:64200717
|
G | A | 7 | a0001c0001t0001g0113a0001c0001t0001g0125a0001c0001t0001g0126others(4): Show | 7 | HG01074.hp1 HG01081.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.1-91G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 1/7 | chr5 | 64200717 | ||||||
| chr5:64200981
|
A | G | 20 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(17): Show | 20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.135+39A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64200981 | ||||||
| chr5:64200998
|
A | G | 22 | a0001c0001t0002g0208a0001c0001t0002g0212a0001c0001t0002g0213others(19): Show | 22 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.135+56A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64200998 | ||||||
| chr5:64201030
|
CTTA | C | 30 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(27): Show | 30 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.135+92_135+94delTT others(1): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 64201030 | |||||
| chr5:64201040
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.135+98A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64201040 | ||||||
| chr5:64201251
|
A | G | 1 | a0001c0001t0002g0178 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.135+309A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64201251 | ||||||
| chr5:64201319
|
A | G | 4 | a0001c0001t0003g0198a0001c0001t0003g0199a0001c0001t0003g0200others(1): Show | 4 | HG02559.hp2 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+377A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64201319 | ||||||
| chr5:64201324
|
T | C | 1 | a0003c0007t0002g0205 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.135+382T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64201324 | ||||||
| chr5:64201353
|
A | G | 144 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(141): Show | 145 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.135+411A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64201353 | ||||||
| chr5:64201435
|
A | C | 1 | a0001c0001t0003g0006 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.135+493A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64201435 | ||||||
| chr5:64201961
|
G | A | 2 | a0001c0001t0003g0010a0001c0001t0007g0051 | 2 | HG03491.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.135+1019G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64201961 | ||||||
| chr5:64201994
|
T | A | 1 | a0001c0001t0002g0209 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.135+1052T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64201994 | ||||||
| chr5:64202009
|
T | A | 144 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(141): Show | 145 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.135+1067T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64202009 | ||||||
| chr5:64202384
|
A | G | 30 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(27): Show | 30 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.135+1442A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64202384 | ||||||
| chr5:64202694
|
C | T | 247 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(244): Show | 249 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.135+1752C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64202694 | ||||||
| chr5:64203205
|
G | A | 1 | a0001c0001t0013g0012 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.135+2263G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64203205 | ||||||
| chr5:64203410
|
C | A | 20 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(17): Show | 20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.135+2468C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64203410 | ||||||
| chr5:64204134
|
T | C | 1 | a0001c0001t0028g0193 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.135+3192T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64204134 | ||||||
| chr5:64204396
|
T | C | 1 | a0001c0001t0002g0219 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.135+3454T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64204396 | ||||||
| chr5:64204730
|
T | C | 1 | a0001c0001t0002g0177 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.135+3788T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64204730 | ||||||
| chr5:64204919
|
G | T | 3 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054 | 3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.135+3977G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64204919 | ||||||
| chr5:64205055
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.135+4113C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64205055 | ||||||
| chr5:64205139
|
C | T | 1 | a0001c0001t0002g0206 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.135+4197C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64205139 | ||||||
| chr5:64205344
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.135+4402A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64205344 | ||||||
| chr5:64205349
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.135+4407G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64205349 | ||||||
| chr5:64205706
|
T | C | 139 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(136): Show | 140 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.135+4764T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64205706 | ||||||
| chr5:64205896
|
A | T | 1 | a0001c0001t0003g0024 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.135+4954A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64205896 | ||||||
| chr5:64206191
|
C | T | 3 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083 | 3 | HG00323.hp1 HG01106.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.135+5249C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64206191 | ||||||
| chr5:64206569
|
C | T | 2 | a0001c0001t0005g0185a0001c0001t0005g0186 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.136-5496C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64206569 | ||||||
| chr5:64207022
|
G | A | 1 | a0001c0001t0026g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.136-5043G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64207022 | ||||||
| chr5:64207081
|
T | C | 89 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(86): Show | 90 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.136-4984T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64207081 | ||||||
| chr5:64207422
|
T | C | 144 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(141): Show | 145 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.136-4643T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64207422 | ||||||
| chr5:64207440
|
T | G | 1 | a0001c0001t0003g0016 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.136-4625T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64207440 | ||||||
| chr5:64207465
|
A | C | 1 | a0001c0001t0001g0113 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.136-4600A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64207465 | ||||||
| chr5:64207502
|
G | A | 1 | a0001c0001t0028g0193 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.136-4563G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64207502 | ||||||
| chr5:64207678
|
T | A | 2 | a0001c0001t0005g0185a0001c0001t0005g0186 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.136-4387T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64207678 | ||||||
| chr5:64207950
|
A | G | 3 | a0002c0002t0008g0062a0002c0002t0008g0063a0002c0002t0008g0064 | 3 | HG00741.hp2 HG01257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.136-4115A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64207950 | ||||||
| chr5:64208155
|
TTAAAA | T | 2 | a0001c0001t0002g0003a0001c0001t0002g0026 | 2 | HG02698.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.136-3906_136-3902d others(7): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 64208155 | |||||
| chr5:64208403
|
A | G | 4 | a0002c0002t0008g0061a0002c0002t0008g0062a0002c0002t0008g0063others(1): Show | 4 | HG00741.hp2 HG01257.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-3662A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64208403 | ||||||
| chr5:64208553
|
TCTTTA | T | 20 | a0001c0001t0027g0060a0002c0002t0006g0065a0002c0002t0006g0066others(17): Show | 20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.136-3508_136-3504d others(7): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 64208553 | |||||
| chr5:64208710
|
C | T | 1 | a0002c0002t0006g0073 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.136-3355C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64208710 | ||||||
| chr5:64208759
|
A | G | 1 | a0001c0001t0002g0174 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.136-3306A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64208759 | ||||||
| chr5:64208796
|
T | G | 28 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(25): Show | 28 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.136-3269T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64208796 | ||||||
| chr5:64208836
|
AT | A | 10 | a0001c0001t0001g0111a0001c0001t0001g0116a0001c0001t0001g0117others(7): Show | 10 | HG02055.hp2 HG02622.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.136-3228delT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64208836 | ||||||
| chr5:64208995
|
A | T | 1 | a0001c0001t0002g0183 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.136-3070A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64208995 | ||||||
| chr5:64209031
|
G | A | 6 | a0001c0001t0001g0114a0001c0001t0001g0122a0001c0001t0001g0123others(3): Show | 6 | HG00738.hp1 HG01256.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.136-3034G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64209031 | ||||||
| chr5:64209093
|
C | T | 12 | a0001c0001t0027g0060a0002c0002t0006g0065a0002c0002t0006g0066others(9): Show | 12 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.136-2972C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64209093 | ||||||
| chr5:64209536
|
GT | G | 45 | a0001c0001t0002g0003a0001c0001t0002g0080a0001c0001t0002g0174others(42): Show | 45 | HG00099.hp2 HG00597.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.136-2526delT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 64209536 | |||||
| chr5:64209603
|
A | G | 2 | a0001c0001t0012g0195a0001c0001t0012g0196 | 2 | HG02109.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.136-2462A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64209603 | ||||||
| chr5:64209745
|
T | C | 3 | a0002c0002t0010g0057a0002c0002t0010g0058a0002c0002t0018g0059 | 3 | HG02109.hp2 HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.136-2320T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64209745 | ||||||
| chr5:64209768
|
G | A | 16 | a0001c0001t0027g0060a0002c0002t0006g0065a0002c0002t0006g0066others(13): Show | 16 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.136-2297G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64209768 | ||||||
| chr5:64209772
|
T | G | 1 | a0002c0002t0016g0067 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.136-2293T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64209772 | ||||||
| chr5:64209809
|
G | A | 3 | a0001c0001t0001g0112a0001c0001t0001g0132a0001c0001t0001g0133 | 3 | HG03491.hp1 HG03492.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.136-2256G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64209809 | ||||||
| chr5:64210001
|
G | A | 3 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054 | 3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.136-2064G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64210001 | ||||||
| chr5:64210131
|
G | A | 20 | a0001c0001t0027g0060a0002c0002t0006g0065a0002c0002t0006g0066others(17): Show | 20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.136-1934G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64210131 | ||||||
| chr5:64210187
|
G | A | 2 | a0001c0001t0014g0055a0001c0001t0014g0056 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.136-1878G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64210187 | ||||||
| chr5:64210320
|
C | A | 1 | a0001c0001t0005g0173 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.136-1745C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64210320 | ||||||
| chr5:64210553
|
C | T | 27 | a0001c0001t0004g0002a0001c0001t0004g0078a0001c0001t0004g0086others(24): Show | 28 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.136-1512C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64210553 | ||||||
| chr5:64210801
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.136-1264A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64210801 | ||||||
| chr5:64210913
|
A | G | 1 | a0001c0001t0003g0145 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.136-1152A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64210913 | ||||||
| chr5:64211053
|
C | T | 1 | a0002c0002t0008g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.136-1012C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64211053 | ||||||
| chr5:64211171
|
T | C | 1 | a0002c0002t0008g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.136-894T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64211171 | ||||||
| chr5:64211180
|
G | A | 1 | a0001c0001t0005g0189 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.136-885G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64211180 | ||||||
| chr5:64211832
|
A | G | 1 | a0001c0001t0003g0050 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.136-233A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64211832 | ||||||
| chr5:64211866
|
C | G | 1 | a0001c0001t0002g0227 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.136-199C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64211866 | ||||||
| chr5:64211880
|
G | T | 1 | a0001c0001t0005g0170 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.136-185G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64211880 | ||||||
| chr5:64211889
|
A | T | 5 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054others(2): Show | 5 | HG02970.hp1 HG03139.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-176A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64211889 | ||||||
| chr5:64211994
|
A | G | 9 | a0001c0001t0003g0077a0001c0001t0003g0194a0001c0001t0003g0198others(6): Show | 9 | HG02109.hp1 HG02258.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.136-71A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64211994 | ||||||
| chr5:64212044
|
T | A | 28 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(25): Show | 28 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.136-21T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64212044 | ||||||
| chr5:64212053
|
T | G | 1 | a0001c0001t0013g0008 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.136-12T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 2/7 | chr5 | 64212053 | ||||||
| chr5:64212344
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.231+184G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 3/7 | chr5 | 64212344 | ||||||
| chr5:64212353
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.231+193C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 3/7 | chr5 | 64212353 | ||||||
| chr5:64212371
|
CAT | C | 3 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054 | 3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.231+213_231+214del others(2): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 64212371 | |||||
| chr5:64212377
|
A | G | 1 | a0001c0001t0017g0019 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.231+217A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 3/7 | chr5 | 64212377 | ||||||
| chr5:64212418
|
T | C | 5 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054others(2): Show | 5 | HG02970.hp1 HG03139.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.231+258T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 3/7 | chr5 | 64212418 | ||||||
| chr5:64212797
|
T | C | 20 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(17): Show | 20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.231+637T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 3/7 | chr5 | 64212797 | ||||||
| chr5:64213089
|
A | G | 1 | a0001c0001t0003g0016 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.232-469A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 3/7 | chr5 | 64213089 | ||||||
| chr5:64213132
|
G | A | 2 | a0001c0001t0005g0185a0001c0001t0005g0186 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.232-426G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 3/7 | chr5 | 64213132 | ||||||
| chr5:64213258
|
G | A | 1 | a0002c0002t0006g0072 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.232-300G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 3/7 | chr5 | 64213258 | ||||||
| chr5:64213323
|
T | G | 2 | a0001c0001t0005g0185a0001c0001t0005g0186 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.232-235T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 3/7 | chr5 | 64213323 | ||||||
| chr5:64213353
|
A | G | 1 | a0001c0001t0001g0111 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.232-205A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 3/7 | chr5 | 64213353 | ||||||
| chr5:64213522
|
G | A | 15 | a0001c0001t0027g0060a0002c0002t0006g0065a0002c0002t0006g0066others(12): Show | 15 | HG01081.hp1 HG01175.hp1 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.232-36G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 3/7 | chr5 | 64213522 | ||||||
| chr5:64214947
|
CATTT | C | 20 | a0001c0001t0027g0060a0002c0002t0006g0065a0002c0002t0006g0066others(17): Show | 20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1191+433_1191+436d others(6): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 64214947 | |||||
| chr5:64215280
|
T | C | 1 | a0001c0001t0002g0184 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1191+763T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 4/7 | chr5 | 64215280 | ||||||
| chr5:64215297
|
A | G | 2 | a0001c0001t0005g0185a0001c0001t0005g0186 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1191+780A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 4/7 | chr5 | 64215297 | ||||||
| chr5:64215758
|
A | C | 1 | a0001c0001t0003g0020 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1191+1241A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 4/7 | chr5 | 64215758 | ||||||
| chr5:64215989
|
G | GT | 17 | a0001c0001t0002g0183a0001c0001t0003g0179a0001c0001t0003g0198others(14): Show | 17 | HG00597.hp1 HG02735.hp2 HG03492.hp2 others(14): Show |
intron_variant | MODIFIER | c.1192-1362dupT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 64215989 | |||||
| chr5:64215989
|
G | GTT | 7 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(4): Show | 7 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1192-1363_1192-136 others(6): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 64215989 | |||||
| chr5:64215989
|
GT | G | 28 | a0001c0001t0004g0002a0001c0001t0004g0078a0001c0001t0004g0086others(25): Show | 29 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.1192-1362delT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 64215989 | |||||
| chr5:64216002
|
A | G | 1 | a0001c0001t0001g0081 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1192-1359A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 4/7 | chr5 | 64216002 | ||||||
| chr5:64216044
|
G | A | 7 | a0001c0001t0001g0113a0001c0001t0001g0125a0001c0001t0001g0126others(4): Show | 7 | HG01074.hp1 HG01081.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.1192-1317G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 4/7 | chr5 | 64216044 | ||||||
| chr5:64216076
|
C | G | 2 | a0001c0001t0005g0185a0001c0001t0005g0186 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1192-1285C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 4/7 | chr5 | 64216076 | ||||||
| chr5:64216609
|
A | G | 144 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(141): Show | 145 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.1192-752A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 4/7 | chr5 | 64216609 | ||||||
| chr5:64216712
|
C | A | 1 | a0001c0001t0001g0121 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1192-649C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 4/7 | chr5 | 64216712 | ||||||
| chr5:64216735
|
G | A | 4 | a0002c0002t0008g0061a0002c0002t0008g0062a0002c0002t0008g0063others(1): Show | 4 | HG00741.hp2 HG01257.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1192-626G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 4/7 | chr5 | 64216735 | ||||||
| chr5:64216903
|
G | A | 4 | a0002c0002t0008g0061a0002c0002t0008g0062a0002c0002t0008g0063others(1): Show | 4 | HG00741.hp2 HG01257.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1192-458G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 4/7 | chr5 | 64216903 | ||||||
| chr5:64217040
|
A | G | 1 | a0001c0001t0001g0158 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1192-321A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 4/7 | chr5 | 64217040 | ||||||
| chr5:64217042
|
T | A | 89 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(86): Show | 90 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1192-319T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 4/7 | chr5 | 64217042 | ||||||
| chr5:64217272
|
A | G | 144 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(141): Show | 145 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.1192-89A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 4/7 | chr5 | 64217272 | ||||||
| chr5:64217417
|
A | G | 1 | a0001c0001t0005g0172 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1227+21A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64217417 | ||||||
| chr5:64217442
|
A | C | 1 | a0001c0001t0005g0189 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1227+46A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64217442 | ||||||
| chr5:64217768
|
A | G | 1 | a0001c0001t0002g0226 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1227+372A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64217768 | ||||||
| chr5:64217923
|
C | T | 8 | a0001c0001t0005g0188a0001c0001t0005g0189a0001c0001t0005g0190others(5): Show | 8 | HG01891.hp2 HG02559.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1227+527C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64217923 | ||||||
| chr5:64217942
|
A | C | 61 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(58): Show | 61 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.1227+546A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64217942 | ||||||
| chr5:64217958
|
T | G | 1 | a0001c0001t0001g0085 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1227+562T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64217958 | ||||||
| chr5:64218044
|
T | C | 2 | a0001c0001t0005g0185a0001c0001t0005g0186 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1227+648T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64218044 | ||||||
| chr5:64218100
|
T | G | 1 | a0001c0001t0001g0152 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1227+704T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64218100 | ||||||
| chr5:64218129
|
C | T | 124 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(121): Show | 125 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.1227+733C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64218129 | ||||||
| chr5:64218203
|
G | A | 44 | a0001c0001t0002g0003a0001c0001t0002g0080a0001c0001t0002g0174others(41): Show | 44 | HG00099.hp2 HG00597.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.1227+807G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64218203 | ||||||
| chr5:64218229
|
C | T | 119 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(116): Show | 120 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.1227+833C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64218229 | ||||||
| chr5:64218325
|
A | G | 27 | a0001c0001t0004g0002a0001c0001t0004g0078a0001c0001t0004g0086others(24): Show | 28 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.1227+929A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64218325 | ||||||
| chr5:64218498
|
A | AC | 6 | a0001c0001t0001g0085a0001c0001t0001g0152a0001c0001t0002g0208others(3): Show | 6 | HG00733.hp1 HG01361.hp2 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.1227+1106dupC | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64218498 | |||||
| chr5:64218558
|
T | C | 4 | a0002c0002t0006g0065a0002c0002t0006g0069a0002c0002t0006g0070others(1): Show | 4 | HG01081.hp1 HG01975.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1227+1162T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64218558 | ||||||
| chr5:64218689
|
C | T | 1 | a0001c0001t0005g0190 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1227+1293C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64218689 | ||||||
| chr5:64218921
|
A | T | 1 | a0001c0001t0002g0206 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1227+1525A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64218921 | ||||||
| chr5:64218924
|
C | T | 1 | a0001c0001t0001g0149 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1227+1528C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64218924 | ||||||
| chr5:64219187
|
G | C | 2 | a0001c0001t0014g0055a0001c0001t0014g0056 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1227+1791G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64219187 | ||||||
| chr5:64219201
|
G | A | 28 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(25): Show | 28 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.1227+1805G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64219201 | ||||||
| chr5:64219223
|
GT | G | 146 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(143): Show | 147 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.1227+1830delT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64219223 | |||||
| chr5:64219368
|
A | AT | 89 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(86): Show | 90 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1227+1978dupT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64219368 | |||||
| chr5:64219531
|
A | G | 1 | a0001c0001t0003g0194 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1227+2135A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64219531 | ||||||
| chr5:64219575
|
C | T | 20 | a0001c0001t0027g0060a0002c0002t0006g0065a0002c0002t0006g0066others(17): Show | 20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1227+2179C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64219575 | ||||||
| chr5:64219643
|
A | T | 1 | a0001c0001t0001g0079 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1227+2247A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64219643 | ||||||
| chr5:64219680
|
AT | A | 119 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(116): Show | 120 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.1227+2296delT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64219680 | |||||
| chr5:64219768
|
C | A | 3 | a0002c0002t0008g0062a0002c0002t0008g0063a0002c0002t0008g0064 | 3 | HG00741.hp2 HG01257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1227+2372C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64219768 | ||||||
| chr5:64219811
|
G | A | 1 | a0001c0001t0002g0209 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1227+2415G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64219811 | ||||||
| chr5:64220092
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1227+2696C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64220092 | ||||||
| chr5:64220181
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1227+2785A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64220181 | ||||||
| chr5:64220257
|
T | C | 20 | a0001c0001t0027g0060a0002c0002t0006g0065a0002c0002t0006g0066others(17): Show | 20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1227+2861T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64220257 | ||||||
| chr5:64220286
|
AATTT | A | 5 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1227+2895_1227+289 others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64220286 | |||||
| chr5:64220420
|
G | A | 20 | a0001c0001t0027g0060a0002c0002t0006g0065a0002c0002t0006g0066others(17): Show | 20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1227+3024G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64220420 | ||||||
| chr5:64220622
|
A | T | 1 | a0001c0001t0003g0198 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1227+3226A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64220622 | ||||||
| chr5:64220737
|
C | G | 30 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(27): Show | 30 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1227+3341C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64220737 | ||||||
| chr5:64220863
|
A | T | 89 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(86): Show | 90 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1227+3467A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64220863 | ||||||
| chr5:64220869
|
A | G | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1227+3473A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64220869 | ||||||
| chr5:64220934
|
A | T | 8 | a0001c0001t0002g0204a0001c0001t0002g0208a0001c0001t0002g0212others(5): Show | 8 | HG01243.hp1 HG01928.hp2 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.1227+3538A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64220934 | ||||||
| chr5:64222211
|
G | C | 1 | a0002c0002t0010g0076 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1227+4815G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64222211 | ||||||
| chr5:64222250
|
G | A | 1 | a0001c0001t0005g0169 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1227+4854G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64222250 | ||||||
| chr5:64222289
|
G | GT | 20 | a0001c0001t0027g0060a0002c0002t0006g0065a0002c0002t0006g0066others(17): Show | 20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1227+4902dupT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64222289 | |||||
| chr5:64222326
|
G | A | 2 | a0001c0001t0003g0198a0001c0001t0003g0199 | 2 | HG02559.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1227+4930G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64222326 | ||||||
| chr5:64222350
|
A | G | 1 | a0001c0001t0003g0041 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1227+4954A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64222350 | ||||||
| chr5:64222395
|
T | A | 27 | a0001c0001t0004g0002a0001c0001t0004g0078a0001c0001t0004g0086others(24): Show | 28 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.1227+4999T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64222395 | ||||||
| chr5:64222438
|
G | T | 1 | a0001c0001t0001g0121 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1227+5042G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64222438 | ||||||
| chr5:64222441
|
A | G | 144 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(141): Show | 145 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.1227+5045A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64222441 | ||||||
| chr5:64222492
|
G | A | 2 | a0001c0001t0019g0166a0001c0001t0026g0247 | 2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1227+5096G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64222492 | ||||||
| chr5:64222526
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1227+5130C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64222526 | ||||||
| chr5:64222548
|
A | T | 1 | a0001c0001t0001g0152 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1227+5152A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64222548 | ||||||
| chr5:64222810
|
A | G | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1227+5414A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64222810 | ||||||
| chr5:64222941
|
CAG | C | 20 | a0001c0001t0027g0060a0002c0002t0006g0065a0002c0002t0006g0066others(17): Show | 20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1227+5548_1227+554 others(6): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64222941 | |||||
| chr5:64223363
|
T | G | 89 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(86): Show | 90 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1227+5967T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64223363 | ||||||
| chr5:64223556
|
C | CAGAG | 144 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(141): Show | 145 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.1227+6160_1227+616 others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64223556 | ||||||
| chr5:64223643
|
C | T | 20 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(17): Show | 20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1227+6247C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64223643 | ||||||
| chr5:64223644
|
A | G | 2 | a0001c0001t0005g0185a0001c0001t0005g0186 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1227+6248A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64223644 | ||||||
| chr5:64223684
|
C | CT | 5 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1227+6297dupT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64223684 | |||||
| chr5:64223801
|
CAAGTATT others(3): Show |
C | 1 | a0001c0001t0005g0239 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1227+6406_1227+641 others(14): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64223801 | ||||||
| chr5:64223835
|
A | G | 144 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(141): Show | 145 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.1227+6439A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64223835 | ||||||
| chr5:64223837
|
C | T | 1 | a0001c0001t0002g0209 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1227+6441C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64223837 | ||||||
| chr5:64223861
|
G | A | 20 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(17): Show | 20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1227+6465G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64223861 | ||||||
| chr5:64223977
|
G | A | 2 | a0001c0001t0005g0185a0001c0001t0005g0186 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1227+6581G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64223977 | ||||||
| chr5:64223990
|
G | A | 1 | a0001c0001t0003g0045 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1227+6594G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64223990 | ||||||
| chr5:64224062
|
G | GGT | 75 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0111others(72): Show | 75 | HG00099.hp2 HG00408.hp2 HG01123.hp2 others(72): Show |
intron_variant | MODIFIER | c.1227+6707_1227+670 others(6): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64224062 | |||||
| chr5:64224062
|
G | GGTGT | 28 | a0001c0001t0001g0079a0001c0001t0001g0113a0001c0001t0001g0115others(25): Show | 29 | HG00099.hp1 HG00639.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1227+6705_1227+670 others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64224062 | |||||
| chr5:64224062
|
G | GGTGTGT | 3 | a0001c0001t0001g0133a0001c0001t0001g0160a0001c0001t0004g0091 | 3 | HG01109.hp2 HG03927.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.1227+6703_1227+670 others(10): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64224062 | |||||
| chr5:64224062
|
GGT | G | 42 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0085others(39): Show | 42 | HG00323.hp1 HG00597.hp1 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.1227+6707_1227+670 others(6): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64224062 | |||||
| chr5:64224062
|
GGTGT | G | 4 | a0001c0001t0003g0027a0001c0001t0003g0179a0001c0001t0009g0035others(1): Show | 4 | HG02257.hp1 HG03492.hp2 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.1227+6705_1227+670 others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64224062 | |||||
| chr5:64224062
|
GGTGTGT | G | 4 | a0001c0001t0002g0229a0002c0002t0008g0062a0002c0002t0008g0063others(1): Show | 4 | HG00741.hp2 HG01257.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1227+6703_1227+670 others(10): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64224062 | |||||
| chr5:64224062
|
GGTGTGTG others(5): Show |
G | 2 | a0001c0001t0002g0208a0003c0007t0002g0205 | 2 | HG02004.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.1227+6697_1227+670 others(16): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64224062 | |||||
| chr5:64224065
|
G | A | 1 | a0001c0001t0002g0003 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1227+6669G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64224065 | ||||||
| chr5:64224270
|
G | A | 1 | a0001c0001t0007g0051 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1227+6874G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64224270 | ||||||
| chr5:64224478
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1227+7082C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64224478 | ||||||
| chr5:64224678
|
A | G | 1 | a0001c0001t0002g0218 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1227+7282A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64224678 | ||||||
| chr5:64224722
|
T | C | 1 | a0001c0001t0002g0229 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1227+7326T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64224722 | ||||||
| chr5:64224886
|
GCTTGCTC others(16): Show |
G | 1 | a0001c0001t0002g0207 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1227+7491_1227+751 others(27): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64224886 | ||||||
| chr5:64225078
|
T | A | 61 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(58): Show | 61 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.1227+7682T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64225078 | ||||||
| chr5:64225121
|
C | T | 2 | a0001c0001t0014g0055a0001c0001t0014g0056 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1227+7725C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64225121 | ||||||
| chr5:64225164
|
A | T | 1 | a0001c0001t0002g0183 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1227+7768A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64225164 | ||||||
| chr5:64225252
|
A | G | 144 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(141): Show | 145 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.1227+7856A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64225252 | ||||||
| chr5:64225345
|
A | AGTGAGGA others(147): Show |
1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1227+7972_1227+797 others(158): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64225345 | |||||
| chr5:64225369
|
G | A | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1227+7973G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64225369 | ||||||
| chr5:64225369
|
G | GCCCTGTC others(147): Show |
86 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(83): Show | 87 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.1227+8126_1227+812 others(158): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64225369 | |||||
| chr5:64225369
|
G | GCCCTGTC others(147): Show |
1 | a0001c0001t0001g0079 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1227+8044_1227+804 others(158): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64225369 | |||||
| chr5:64225428
|
A | G | 4 | a0002c0002t0008g0061a0002c0002t0008g0062a0002c0002t0008g0063others(1): Show | 4 | HG00741.hp2 HG01257.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1227+8032A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64225428 | ||||||
| chr5:64225430
|
C | CGCCTCTG others(147): Show |
1 | a0001c0001t0001g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1227+8126_1227+812 others(158): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64225430 | |||||
| chr5:64225441
|
A | G | 1 | a0001c0001t0002g0206 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1227+8045A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64225441 | ||||||
| chr5:64225445
|
G | A | 1 | a0001c0001t0003g0024 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1227+8049G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64225445 | ||||||
| chr5:64225452
|
G | A | 20 | a0001c0001t0027g0060a0002c0002t0006g0065a0002c0002t0006g0066others(17): Show | 20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1227+8056G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64225452 | ||||||
| chr5:64225489
|
CCGTCTGG others(32): Show |
C | 1 | a0001c0001t0002g0174 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1227+8122_1227+816 others(43): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64225489 | |||||
| chr5:64225491
|
G | A | 1 | a0001c0001t0003g0025 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1227+8095G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64225491 | ||||||
| chr5:64225567
|
G | A | 3 | a0001c0001t0002g0003a0001c0001t0002g0177a0001c0001t0009g0182 | 3 | HG01109.hp1 HG02698.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1227+8171G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64225567 | ||||||
| chr5:64225640
|
C | T | 29 | a0001c0001t0003g0200a0001c0001t0003g0201a0001c0001t0004g0002others(26): Show | 30 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.1227+8244C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64225640 | ||||||
| chr5:64225672
|
T | TGCCCCGT others(30): Show |
2 | a0001c0001t0001g0122a0001c0001t0001g0123 | 2 | HG00738.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.1227+8314_1227+835 others(41): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64225672 | |||||
| chr5:64225696
|
G | A | 20 | a0001c0001t0027g0060a0002c0002t0006g0065a0002c0002t0006g0066others(17): Show | 20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1227+8300G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64225696 | ||||||
| chr5:64225774
|
C | T | 2 | a0001c0001t0005g0185a0001c0001t0005g0186 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1227+8378C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64225774 | ||||||
| chr5:64225775
|
T | A | 2 | a0001c0001t0005g0185a0001c0001t0005g0186 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1227+8379T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64225775 | ||||||
| chr5:64225825
|
G | A | 8 | a0001c0001t0005g0188a0001c0001t0005g0189a0001c0001t0005g0190others(5): Show | 8 | HG01891.hp2 HG02559.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1227+8429G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64225825 | ||||||
| chr5:64225829
|
C | T | 1 | a0002c0002t0006g0073 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1227+8433C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64225829 | ||||||
| chr5:64225844
|
G | A | 1 | a0001c0001t0003g0020 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1227+8448G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64225844 | ||||||
| chr5:64225884
|
T | G | 30 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(27): Show | 30 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1227+8488T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64225884 | ||||||
| chr5:64225895
|
G | A | 4 | a0002c0002t0010g0057a0002c0002t0010g0058a0002c0002t0010g0076others(1): Show | 4 | HG02109.hp2 HG02622.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1227+8499G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64225895 | ||||||
| chr5:64225935
|
G | A | 1 | a0001c0001t0004g0107 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1227+8539G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64225935 | ||||||
| chr5:64225948
|
T | TGCCCCGT others(67): Show |
1 | a0001c0001t0003g0015 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1227+8585_1227+865 others(78): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64225948 | |||||
| chr5:64225972
|
G | A | 1 | a0001c0001t0003g0021 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1227+8576G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64225972 | ||||||
| chr5:64225981
|
C | T | 1 | a0001c0001t0003g0009 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1227+8585C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64225981 | ||||||
| chr5:64226055
|
T | C | 2 | a0001c0001t0002g0222a0001c0003t0002g0246 | 2 | HG02040.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1227+8659T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64226055 | ||||||
| chr5:64226065
|
A | G | 1 | a0001c0001t0007g0022 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1227+8669A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64226065 | ||||||
| chr5:64226074
|
G | A | 89 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(86): Show | 90 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1227+8678G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64226074 | ||||||
| chr5:64226203
|
A | G | 1 | a0001c0001t0019g0166 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1227+8807A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64226203 | ||||||
| chr5:64226460
|
G | T | 2 | a0001c0001t0014g0055a0001c0001t0014g0056 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1227+9064G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64226460 | ||||||
| chr5:64226471
|
G | C | 1 | a0001c0001t0001g0127 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1227+9075G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64226471 | ||||||
| chr5:64226540
|
C | A | 53 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(50): Show | 53 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.1227+9144C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64226540 | ||||||
| chr5:64226626
|
C | G | 1 | a0001c0001t0003g0041 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1227+9230C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64226626 | ||||||
| chr5:64226665
|
TA | T | 5 | a0001c0001t0001g0162a0001c0001t0002g0222a0001c0001t0003g0015others(2): Show | 5 | HG01168.hp1 HG02040.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1227+9282delA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64226665 | |||||
| chr5:64226678
|
A | G | 20 | a0001c0001t0027g0060a0002c0002t0006g0065a0002c0002t0006g0066others(17): Show | 20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1227+9282A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64226678 | ||||||
| chr5:64226746
|
G | A | 3 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054 | 3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1227+9350G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64226746 | ||||||
| chr5:64226768
|
C | T | 12 | a0001c0001t0027g0060a0002c0002t0006g0065a0002c0002t0006g0066others(9): Show | 12 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.1227+9372C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64226768 | ||||||
| chr5:64226892
|
G | A | 1 | a0001c0001t0003g0015 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1227+9496G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64226892 | ||||||
| chr5:64226901
|
C | T | 8 | a0001c0001t0005g0188a0001c0001t0005g0189a0001c0001t0005g0190others(5): Show | 8 | HG01891.hp2 HG02559.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1227+9505C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64226901 | ||||||
| chr5:64227089
|
C | T | 3 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054 | 3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1227+9693C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64227089 | ||||||
| chr5:64227130
|
G | A | 8 | a0001c0001t0004g0002a0001c0001t0004g0086a0001c0001t0004g0092others(5): Show | 9 | HG01243.hp2 HG02615.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1227+9734G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64227130 | ||||||
| chr5:64227207
|
G | A | 1 | a0001c0001t0001g0114 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1227+9811G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64227207 | ||||||
| chr5:64227368
|
C | T | 1 | a0002c0002t0008g0063 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1227+9972C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64227368 | ||||||
| chr5:64227459
|
G | A | 1 | a0001c0001t0024g0192 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1227+10063G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64227459 | ||||||
| chr5:64227539
|
C | T | 2 | a0001c0001t0001g0129a0001c0001t0001g0142 | 2 | HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1227+10143C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64227539 | ||||||
| chr5:64227587
|
A | G | 89 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(86): Show | 90 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1227+10191A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64227587 | ||||||
| chr5:64227611
|
C | T | 3 | a0001c0001t0005g0235a0001c0001t0005g0239a0001c0001t0029g0236 | 3 | NA18966.hp1 NA19068.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.1227+10215C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64227611 | ||||||
| chr5:64227708
|
T | C | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1227+10312T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64227708 | ||||||
| chr5:64227732
|
T | G | 4 | a0001c0001t0001g0120a0001c0001t0001g0147a0001c0001t0001g0148others(1): Show | 4 | HG02258.hp2 HG02647.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1227+10336T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64227732 | ||||||
| chr5:64227856
|
C | T | 20 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(17): Show | 20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1227+10460C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64227856 | ||||||
| chr5:64228283
|
G | A | 3 | a0001c0001t0001g0158a0001c0001t0003g0144a0001c0001t0003g0145 | 3 | HG02886.hp1 HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1227+10887G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64228283 | ||||||
| chr5:64228871
|
A | G | 1 | a0001c0001t0026g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1227+11475A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64228871 | ||||||
| chr5:64228915
|
C | CT | 15 | a0001c0001t0001g0112a0001c0001t0001g0132a0001c0001t0001g0142others(12): Show | 15 | HG00597.hp2 HG00738.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.1227+11543dupT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64228915 | |||||
| chr5:64228915
|
CT | C | 40 | a0001c0001t0001g0113a0001c0001t0001g0125a0001c0001t0001g0126others(37): Show | 40 | HG00597.hp1 HG01074.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.1227+11543delT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64228915 | |||||
| chr5:64228915
|
CTT | C | 30 | a0001c0001t0004g0002a0001c0001t0004g0086a0001c0001t0004g0092others(27): Show | 31 | HG01243.hp2 HG01891.hp2 HG02280.hp2 others(28): Show |
intron_variant | MODIFIER | c.1227+11542_1227+11 others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64228915 | |||||
| chr5:64228915
|
CTTT | C | 16 | a0001c0001t0019g0166a0001c0001t0027g0060a0002c0002t0006g0065others(13): Show | 16 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.1227+11541_1227+11 others(9): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64228915 | |||||
| chr5:64229216
|
C | T | 1 | a0001c0001t0019g0166 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1227+11820C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64229216 | ||||||
| chr5:64229244
|
A | T | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1227+11848A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64229244 | ||||||
| chr5:64229345
|
A | T | 1 | a0001c0001t0003g0010 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1227+11949A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64229345 | ||||||
| chr5:64229878
|
G | T | 9 | a0001c0001t0001g0085a0001c0001t0001g0087a0001c0001t0001g0134others(6): Show | 9 | HG00408.hp2 HG02074.hp2 NA18942.hp1 others(6): Show |
intron_variant | MODIFIER | c.1227+12482G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64229878 | ||||||
| chr5:64229968
|
G | A | 1 | a0001c0001t0002g0211 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1227+12572G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64229968 | ||||||
| chr5:64230051
|
ATTTTTCT others(2): Show |
A | 27 | a0001c0001t0004g0002a0001c0001t0004g0078a0001c0001t0004g0086others(24): Show | 28 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.1227+12660_1227+12 others(15): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64230051 | |||||
| chr5:64230298
|
A | C | 1 | a0001c0001t0002g0231 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1227+12902A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64230298 | ||||||
| chr5:64230347
|
G | T | 1 | a0001c0001t0001g0153 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1227+12951G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64230347 | ||||||
| chr5:64230348
|
G | GACATAAC others(39): Show |
1 | a0001c0001t0001g0153 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1227+12952_1227+12 others(52): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64230348 | ||||||
| chr5:64230415
|
A | G | 3 | a0001c0001t0003g0011a0001c0001t0003g0021a0001c0001t0003g0044 | 3 | NA18964.hp1 NA18983.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1227+13019A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64230415 | ||||||
| chr5:64230680
|
GGCCTCTT others(4): Show |
G | 1 | a0001c0001t0001g0158 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1227+13286_1227+13 others(17): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64230680 | |||||
| chr5:64230734
|
G | A | 3 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054 | 3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1227+13338G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64230734 | ||||||
| chr5:64230965
|
G | T | 2 | a0001c0001t0005g0185a0001c0001t0005g0186 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1227+13569G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64230965 | ||||||
| chr5:64231016
|
C | G | 10 | a0001c0001t0001g0111a0001c0001t0001g0116a0001c0001t0001g0117others(7): Show | 10 | HG02055.hp2 HG02622.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.1227+13620C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64231016 | ||||||
| chr5:64231138
|
A | T | 1 | a0001c0001t0002g0204 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1227+13742A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64231138 | ||||||
| chr5:64231219
|
A | C | 1 | a0001c0001t0007g0033 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1227+13823A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64231219 | ||||||
| chr5:64231298
|
G | A | 2 | a0002c0002t0006g0074a0002c0002t0006g0075 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1227+13902G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64231298 | ||||||
| chr5:64232001
|
T | G | 237 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(234): Show | 239 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.1227+14605T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64232001 | ||||||
| chr5:64232031
|
T | G | 1 | a0001c0001t0003g0021 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1227+14635T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64232031 | ||||||
| chr5:64232748
|
A | G | 3 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054 | 3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1227+15352A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64232748 | ||||||
| chr5:64232829
|
A | T | 1 | a0001c0001t0002g0227 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1227+15433A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64232829 | ||||||
| chr5:64232912
|
A | T | 3 | a0001c0001t0002g0026a0001c0001t0003g0030a0001c0001t0007g0029 | 3 | HG01123.hp2 HG02698.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1227+15516A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64232912 | ||||||
| chr5:64233216
|
G | T | 2 | a0001c0001t0005g0185a0001c0001t0005g0186 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1227+15820G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64233216 | ||||||
| chr5:64233447
|
C | T | 90 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(87): Show | 91 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1227+16051C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64233447 | ||||||
| chr5:64233535
|
T | G | 2 | a0001c0001t0005g0185a0001c0001t0005g0186 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1227+16139T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64233535 | ||||||
| chr5:64233615
|
A | G | 6 | a0001c0001t0001g0114a0001c0001t0001g0122a0001c0001t0001g0123others(3): Show | 6 | HG00738.hp1 HG01256.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.1227+16219A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64233615 | ||||||
| chr5:64233618
|
A | C | 1 | a0001c0001t0001g0120 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1227+16222A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64233618 | ||||||
| chr5:64233634
|
T | C | 1 | a0001c0001t0003g0124 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1227+16238T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64233634 | ||||||
| chr5:64233947
|
A | G | 5 | a0001c0001t0005g0188a0001c0001t0005g0190a0001c0001t0005g0191others(2): Show | 5 | HG01891.hp2 HG02559.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1227+16551A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64233947 | ||||||
| chr5:64234021
|
T | C | 2 | a0001c0001t0005g0185a0001c0001t0005g0186 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1227+16625T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64234021 | ||||||
| chr5:64234123
|
C | T | 7 | a0001c0001t0001g0113a0001c0001t0001g0125a0001c0001t0001g0126others(4): Show | 7 | HG01074.hp1 HG01081.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.1227+16727C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64234123 | ||||||
| chr5:64234269
|
T | C | 1 | a0001c0001t0003g0014 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1227+16873T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64234269 | ||||||
| chr5:64234427
|
G | A | 3 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083 | 3 | HG00323.hp1 HG01106.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1227+17031G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64234427 | ||||||
| chr5:64234467
|
AAAATAAA others(3): Show |
A | 1 | a0002c0002t0006g0073 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1227+17079_1227+17 others(16): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64234467 | |||||
| chr5:64234524
|
C | G | 2 | a0001c0001t0003g0200a0001c0001t0003g0201 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1227+17128C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64234524 | ||||||
| chr5:64234575
|
GTTCTTTT others(8): Show |
G | 2 | a0001c0001t0014g0055a0001c0001t0014g0056 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1227+17182_1227+17 others(21): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64234575 | |||||
| chr5:64234578
|
C | CT | 28 | a0001c0001t0002g0003a0001c0001t0002g0026a0001c0001t0002g0038others(25): Show | 28 | HG00642.hp1 HG00733.hp2 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.1227+17221dupT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64234578 | |||||
| chr5:64234578
|
C | CTT | 8 | a0001c0001t0002g0177a0001c0001t0002g0226a0001c0001t0002g0230others(5): Show | 8 | HG00741.hp1 HG01109.hp1 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.1227+17220_1227+17 others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64234578 | |||||
| chr5:64234578
|
C | CTTT | 12 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0048others(9): Show | 12 | HG00408.hp1 HG00639.hp1 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.1227+17219_1227+17 others(9): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64234578 | |||||
| chr5:64234578
|
C | CTTTT | 10 | a0001c0001t0002g0183a0001c0001t0003g0011a0001c0001t0003g0044others(7): Show | 10 | HG01074.hp2 HG01081.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1227+17218_1227+17 others(10): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64234578 | |||||
| chr5:64234578
|
C | CTTTTTTT others(3): Show |
1 | a0002c0002t0010g0076 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1227+17212_1227+17 others(16): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64234578 | |||||
| chr5:64234578
|
C | CTTTTTTT others(4): Show |
2 | a0002c0002t0010g0058a0002c0002t0018g0059 | 2 | HG02109.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1227+17211_1227+17 others(17): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64234578 | |||||
| chr5:64234578
|
C | CTTTTTTT others(5): Show |
1 | a0002c0002t0006g0072 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1227+17210_1227+17 others(18): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64234578 | |||||
| chr5:64234578
|
CT | C | 10 | a0001c0001t0002g0206a0001c0001t0002g0210a0001c0001t0002g0212others(7): Show | 10 | HG00099.hp2 HG00741.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1227+17221delT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64234578 | |||||
| chr5:64234578
|
CTT | C | 14 | a0001c0001t0002g0187a0001c0001t0002g0202a0001c0001t0002g0203others(11): Show | 14 | HG00597.hp2 HG01243.hp1 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.1227+17220_1227+17 others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64234578 | |||||
| chr5:64234578
|
CTTTTTTT others(3): Show |
C | 3 | a0001c0001t0005g0234a0001c0001t0005g0239a0001c0001t0005g0244 | 3 | NA18942.hp2 NA19063.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.1227+17212_1227+17 others(16): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64234578 | |||||
| chr5:64234578
|
CTTTTTTT others(4): Show |
C | 16 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(13): Show | 16 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.1227+17211_1227+17 others(17): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64234578 | |||||
| chr5:64234578
|
CTTTTTTT others(5): Show |
C | 11 | a0001c0001t0002g0227a0001c0001t0005g0172a0001c0001t0005g0185others(8): Show | 11 | HG01891.hp2 HG02559.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.1227+17210_1227+17 others(18): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64234578 | |||||
| chr5:64234578
|
CTTTTTTT others(6): Show |
C | 3 | a0001c0001t0003g0028a0001c0001t0003g0077a0001c0001t0028g0193 | 3 | HG02258.hp1 HG02896.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1227+17209_1227+17 others(19): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64234578 | |||||
| chr5:64234578
|
CTTTTTTT others(8): Show |
C | 2 | a0001c0001t0001g0160a0001c0001t0004g0107 | 2 | HG01109.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.1227+17207_1227+17 others(21): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64234578 | |||||
| chr5:64234578
|
CTTTTTTT others(9): Show |
C | 83 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(80): Show | 84 | HG00323.hp1 HG00408.hp2 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.1227+17206_1227+17 others(22): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64234578 | |||||
| chr5:64234578
|
CTTTTTTT others(10): Show |
C | 6 | a0001c0001t0001g0088a0001c0001t0001g0126a0001c0001t0001g0138others(3): Show | 6 | HG00099.hp1 HG01517.hp2 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.1227+17205_1227+17 others(23): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64234578 | |||||
| chr5:64234578
|
CTTTTTTT others(16): Show |
C | 1 | a0001c0001t0002g0204 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1227+17199_1227+17 others(29): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64234578 | |||||
| chr5:64234599
|
T | G | 2 | a0001c0001t0014g0055a0001c0001t0014g0056 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1227+17203T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64234599 | ||||||
| chr5:64234603
|
T | G | 2 | a0001c0001t0014g0055a0001c0001t0014g0056 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1227+17207T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64234603 | ||||||
| chr5:64234745
|
G | A | 11 | a0001c0001t0002g0026a0001c0001t0003g0004a0001c0001t0003g0005others(8): Show | 11 | HG00642.hp2 HG00741.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.1227+17349G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64234745 | ||||||
| chr5:64234760
|
T | G | 1 | a0001c0001t0007g0022 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1227+17364T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64234760 | ||||||
| chr5:64234800
|
C | T | 2 | a0001c0001t0002g0184a0001c0001t0002g0187 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1227+17404C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64234800 | ||||||
| chr5:64234859
|
G | A | 125 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(122): Show | 126 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.1227+17463G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64234859 | ||||||
| chr5:64234948
|
T | C | 1 | a0001c0001t0001g0127 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1227+17552T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64234948 | ||||||
| chr5:64235316
|
T | C | 1 | a0001c0001t0002g0177 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1227+17920T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64235316 | ||||||
| chr5:64235532
|
T | A | 28 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(25): Show | 28 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.1227+18136T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64235532 | ||||||
| chr5:64235594
|
A | G | 1 | a0001c0001t0007g0022 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1227+18198A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64235594 | ||||||
| chr5:64235605
|
C | T | 2 | a0001c0001t0001g0151a0001c0001t0001g0162 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1227+18209C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64235605 | ||||||
| chr5:64236004
|
G | A | 1 | a0001c0001t0004g0091 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1227+18608G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64236004 | ||||||
| chr5:64236372
|
C | A | 1 | a0001c0001t0004g0245 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1227+18976C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64236372 | ||||||
| chr5:64236435
|
C | G | 1 | a0001c0001t0005g0190 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1227+19039C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64236435 | ||||||
| chr5:64236716
|
C | T | 8 | a0001c0001t0005g0188a0001c0001t0005g0189a0001c0001t0005g0190others(5): Show | 8 | HG01891.hp2 HG02559.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1227+19320C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64236716 | ||||||
| chr5:64236744
|
A | G | 2 | a0001c0001t0005g0188a0001c0001t0024g0192 | 2 | HG02559.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1227+19348A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64236744 | ||||||
| chr5:64236792
|
A | C | 1 | a0001c0001t0002g0206 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1227+19396A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64236792 | ||||||
| chr5:64236902
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1227+19506C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64236902 | ||||||
| chr5:64236958
|
A | G | 1 | a0001c0001t0026g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1227+19562A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64236958 | ||||||
| chr5:64237265
|
G | A | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1227+19869G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64237265 | ||||||
| chr5:64237569
|
G | C | 1 | a0001c0001t0005g0170 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1227+20173G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64237569 | ||||||
| chr5:64237639
|
T | G | 4 | a0001c0001t0004g0078a0001c0001t0004g0094a0001c0001t0004g0101others(1): Show | 4 | NA18960.hp1 NA18964.hp2 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.1227+20243T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64237639 | ||||||
| chr5:64237851
|
C | A | 1 | a0001c0001t0026g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1227+20455C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64237851 | ||||||
| chr5:64237901
|
C | T | 12 | a0001c0001t0027g0060a0002c0002t0006g0065a0002c0002t0006g0066others(9): Show | 12 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.1227+20505C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64237901 | ||||||
| chr5:64238210
|
T | A | 190 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(187): Show | 191 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.1227+20814T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64238210 | ||||||
| chr5:64238357
|
G | T | 1 | a0001c0001t0027g0060 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1227+20961G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64238357 | ||||||
| chr5:64238370
|
G | A | 1 | a0001c0001t0002g0177 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1227+20974G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64238370 | ||||||
| chr5:64238734
|
C | A | 1 | a0001c0001t0001g0119 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1227+21338C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64238734 | ||||||
| chr5:64238794
|
G | A | 2 | a0001c0001t0013g0008a0001c0001t0020g0023 | 2 | HG01168.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1227+21398G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64238794 | ||||||
| chr5:64238797
|
G | A | 1 | a0001c0001t0017g0019 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1227+21401G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64238797 | ||||||
| chr5:64238838
|
A | G | 1 | a0001c0001t0007g0051 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1227+21442A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64238838 | ||||||
| chr5:64238953
|
C | T | 144 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(141): Show | 145 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.1227+21557C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64238953 | ||||||
| chr5:64239018
|
A | G | 3 | a0002c0002t0008g0062a0002c0002t0008g0063a0002c0002t0008g0064 | 3 | HG00741.hp2 HG01257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1227+21622A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64239018 | ||||||
| chr5:64239137
|
T | A | 1 | a0001c0001t0002g0038 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1227+21741T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64239137 | ||||||
| chr5:64239447
|
T | C | 44 | a0001c0001t0002g0003a0001c0001t0002g0080a0001c0001t0002g0174others(41): Show | 44 | HG00099.hp2 HG00597.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.1227+22051T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64239447 | ||||||
| chr5:64239515
|
G | A | 5 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097others(2): Show | 5 | HG01255.hp1 HG01256.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1227+22119G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64239515 | ||||||
| chr5:64239532
|
A | G | 4 | a0002c0002t0010g0057a0002c0002t0010g0058a0002c0002t0010g0076others(1): Show | 4 | HG02109.hp2 HG02622.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1227+22136A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64239532 | ||||||
| chr5:64239806
|
C | T | 3 | a0001c0001t0012g0195a0001c0001t0012g0196a0001c0001t0012g0197 | 3 | HG02109.hp1 HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1227+22410C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64239806 | ||||||
| chr5:64239874
|
A | G | 89 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(86): Show | 90 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1227+22478A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64239874 | ||||||
| chr5:64240036
|
T | G | 1 | a0001c0001t0002g0210 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1227+22640T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64240036 | ||||||
| chr5:64240109
|
T | C | 1 | a0002c0002t0008g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1227+22713T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64240109 | ||||||
| chr5:64240419
|
A | T | 5 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1227+23023A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64240419 | ||||||
| chr5:64240466
|
A | C | 2 | a0001c0001t0002g0184a0001c0001t0002g0187 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1227+23070A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64240466 | ||||||
| chr5:64240660
|
C | T | 1 | a0001c0001t0003g0124 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1227+23264C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64240660 | ||||||
| chr5:64240764
|
A | G | 3 | a0002c0002t0008g0062a0002c0002t0008g0063a0002c0002t0008g0064 | 3 | HG00741.hp2 HG01257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1227+23368A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64240764 | ||||||
| chr5:64240810
|
T | C | 2 | a0001c0001t0014g0055a0001c0001t0014g0056 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1227+23414T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64240810 | ||||||
| chr5:64240927
|
A | C | 7 | a0001c0001t0001g0113a0001c0001t0001g0125a0001c0001t0001g0126others(4): Show | 7 | HG01074.hp1 HG01081.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.1227+23531A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64240927 | ||||||
| chr5:64240965
|
T | C | 246 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(243): Show | 248 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.1227+23569T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64240965 | ||||||
| chr5:64241046
|
T | C | 1 | a0001c0001t0005g0188 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1227+23650T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64241046 | ||||||
| chr5:64241100
|
C | T | 1 | a0001c0001t0028g0193 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1227+23704C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64241100 | ||||||
| chr5:64241487
|
G | A | 2 | a0001c0001t0001g0087a0001c0001t0001g0161 | 2 | NA18984.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1227+24091G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64241487 | ||||||
| chr5:64241608
|
T | C | 30 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(27): Show | 30 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1227+24212T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64241608 | ||||||
| chr5:64241611
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1227+24215C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64241611 | ||||||
| chr5:64241846
|
G | T | 6 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(3): Show | 6 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1227+24450G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64241846 | ||||||
| chr5:64241855
|
G | A | 3 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054 | 3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1227+24459G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64241855 | ||||||
| chr5:64242016
|
T | G | 5 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054others(2): Show | 5 | HG02970.hp1 HG03139.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1227+24620T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64242016 | ||||||
| chr5:64242106
|
C | T | 1 | a0001c0001t0003g0020 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1227+24710C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64242106 | ||||||
| chr5:64242325
|
G | A | 1 | a0001c0001t0002g0214 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1227+24929G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64242325 | ||||||
| chr5:64242434
|
A | G | 2 | a0001c0001t0002g0184a0001c0001t0002g0187 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1227+25038A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64242434 | ||||||
| chr5:64243251
|
C | T | 1 | a0001c0001t0024g0192 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1227+25855C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64243251 | ||||||
| chr5:64243306
|
C | T | 1 | a0001c0001t0003g0194 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1227+25910C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64243306 | ||||||
| chr5:64243435
|
G | A | 1 | a0001c0001t0003g0145 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1227+26039G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64243435 | ||||||
| chr5:64243626
|
A | T | 1 | a0001c0001t0002g0183 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1227+26230A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64243626 | ||||||
| chr5:64244062
|
G | A | 1 | a0001c0001t0002g0207 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1227+26666G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64244062 | ||||||
| chr5:64244067
|
C | T | 5 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1227+26671C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64244067 | ||||||
| chr5:64244322
|
C | T | 2 | a0001c0001t0014g0055a0001c0001t0014g0056 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1227+26926C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64244322 | ||||||
| chr5:64244361
|
T | A | 1 | a0001c0001t0007g0034 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1227+26965T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64244361 | ||||||
| chr5:64244397
|
AC | A | 20 | a0001c0001t0027g0060a0002c0002t0006g0065a0002c0002t0006g0066others(17): Show | 20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1227+27003delC | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64244397 | |||||
| chr5:64244410
|
G | GA | 62 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(59): Show | 62 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.1227+27022dupA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64244410 | |||||
| chr5:64244719
|
A | G | 2 | a0001c0001t0005g0185a0001c0001t0005g0186 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1227+27323A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64244719 | ||||||
| chr5:64244821
|
G | T | 1 | a0001c0001t0003g0007 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1227+27425G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64244821 | ||||||
| chr5:64244858
|
A | G | 19 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(16): Show | 19 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.1227+27462A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64244858 | ||||||
| chr5:64244906
|
C | T | 11 | a0001c0001t0003g0077a0001c0001t0003g0144a0001c0001t0003g0145others(8): Show | 11 | HG02109.hp1 HG02258.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1227+27510C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64244906 | ||||||
| chr5:64244907
|
A | T | 11 | a0001c0001t0003g0077a0001c0001t0003g0144a0001c0001t0003g0145others(8): Show | 11 | HG02109.hp1 HG02258.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1227+27511A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64244907 | ||||||
| chr5:64244908
|
A | T | 11 | a0001c0001t0003g0077a0001c0001t0003g0144a0001c0001t0003g0145others(8): Show | 11 | HG02109.hp1 HG02258.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1227+27512A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64244908 | ||||||
| chr5:64244910
|
CCAGAAGA others(3): Show |
C | 11 | a0001c0001t0003g0077a0001c0001t0003g0144a0001c0001t0003g0145others(8): Show | 11 | HG02109.hp1 HG02258.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1227+27515_1227+27 others(16): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64244910 | ||||||
| chr5:64244921
|
T | A | 11 | a0001c0001t0003g0077a0001c0001t0003g0144a0001c0001t0003g0145others(8): Show | 11 | HG02109.hp1 HG02258.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1227+27525T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64244921 | ||||||
| chr5:64245071
|
C | T | 87 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(84): Show | 88 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1227+27675C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64245071 | ||||||
| chr5:64245407
|
C | A | 1 | a0001c0001t0001g0083 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1227+28011C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64245407 | ||||||
| chr5:64245601
|
A | C | 5 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097others(2): Show | 5 | HG01255.hp1 HG01256.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1227+28205A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64245601 | ||||||
| chr5:64245625
|
T | C | 13 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(10): Show | 13 | HG00323.hp1 HG01106.hp2 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.1227+28229T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64245625 | ||||||
| chr5:64245659
|
A | G | 1 | a0001c0001t0015g0032 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1227+28263A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64245659 | ||||||
| chr5:64245798
|
G | A | 246 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(243): Show | 248 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.1227+28402G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64245798 | ||||||
| chr5:64245799
|
A | G | 1 | a0001c0001t0001g0154 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1227+28403A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64245799 | ||||||
| chr5:64246292
|
C | T | 21 | a0001c0001t0002g0202a0001c0001t0002g0203a0001c0001t0002g0204others(18): Show | 21 | HG00099.hp2 HG00597.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.1227+28896C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64246292 | ||||||
| chr5:64246487
|
A | G | 1 | a0001c0001t0002g0209 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1227+29091A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64246487 | ||||||
| chr5:64246653
|
T | C | 210 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(207): Show | 211 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.1227+29257T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64246653 | ||||||
| chr5:64246738
|
G | A | 1 | a0001c0001t0004g0106 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1227+29342G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64246738 | ||||||
| chr5:64246741
|
T | A | 1 | a0001c0001t0004g0106 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1227+29345T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64246741 | ||||||
| chr5:64246837
|
G | T | 1 | a0001c0001t0002g0219 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1227+29441G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64246837 | ||||||
| chr5:64247101
|
T | A | 2 | a0001c0001t0005g0185a0001c0001t0005g0186 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1227+29705T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64247101 | ||||||
| chr5:64247239
|
T | C | 146 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(143): Show | 147 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.1227+29843T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64247239 | ||||||
| chr5:64247375
|
G | A | 1 | a0001c0001t0019g0166 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1227+29979G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64247375 | ||||||
| chr5:64247418
|
C | T | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1227+30022C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64247418 | ||||||
| chr5:64247705
|
A | C | 30 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(27): Show | 30 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1227+30309A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64247705 | ||||||
| chr5:64247710
|
A | G | 5 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054others(2): Show | 5 | HG02970.hp1 HG03139.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1227+30314A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64247710 | ||||||
| chr5:64247813
|
C | T | 12 | a0001c0001t0027g0060a0002c0002t0006g0065a0002c0002t0006g0066others(9): Show | 12 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.1227+30417C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64247813 | ||||||
| chr5:64247830
|
G | T | 1 | a0001c0001t0026g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1227+30434G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64247830 | ||||||
| chr5:64247897
|
G | A | 3 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0023g0165 | 3 | HG01081.hp2 HG01346.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1227+30501G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64247897 | ||||||
| chr5:64247946
|
A | G | 2 | a0001c0001t0014g0055a0001c0001t0014g0056 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1227+30550A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64247946 | ||||||
| chr5:64247954
|
A | T | 6 | a0001c0001t0002g0208a0001c0001t0002g0212a0001c0001t0002g0213others(3): Show | 6 | HG01243.hp1 HG01928.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1227+30558A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64247954 | ||||||
| chr5:64248056
|
C | T | 3 | a0001c0001t0003g0048a0001c0001t0003g0049a0001c0001t0003g0050 | 3 | HG00408.hp1 HG02074.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.1227+30660C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64248056 | ||||||
| chr5:64248061
|
A | G | 2 | a0001c0001t0014g0055a0001c0001t0014g0056 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1227+30665A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64248061 | ||||||
| chr5:64248201
|
A | G | 1 | a0001c0001t0005g0191 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1227+30805A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64248201 | ||||||
| chr5:64248260
|
G | A | 144 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(141): Show | 145 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.1227+30864G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64248260 | ||||||
| chr5:64248353
|
A | G | 89 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(86): Show | 90 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1227+30957A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64248353 | ||||||
| chr5:64248445
|
C | T | 2 | a0001c0001t0005g0185a0001c0001t0005g0186 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1227+31049C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64248445 | ||||||
| chr5:64248582
|
C | T | 1 | a0001c0001t0003g0194 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1227+31186C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64248582 | ||||||
| chr5:64248861
|
C | G | 1 | a0001c0001t0002g0080 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1227+31465C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64248861 | ||||||
| chr5:64248968
|
G | C | 30 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(27): Show | 30 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1227+31572G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64248968 | ||||||
| chr5:64249184
|
G | A | 2 | a0001c0001t0002g0206a0001c0001t0003g0009 | 2 | HG00639.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.1227+31788G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64249184 | ||||||
| chr5:64249187
|
G | T | 1 | a0001c0001t0005g0172 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1227+31791G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64249187 | ||||||
| chr5:64249252
|
T | TA | 4 | a0002c0002t0008g0061a0002c0002t0008g0062a0002c0002t0008g0063others(1): Show | 4 | HG00741.hp2 HG01257.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1227+31863dupA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64249252 | |||||
| chr5:64249276
|
T | C | 1 | a0001c0001t0002g0225 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1227+31880T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64249276 | ||||||
| chr5:64249375
|
C | T | 1 | a0001c0001t0002g0217 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1227+31979C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64249375 | ||||||
| chr5:64249437
|
C | T | 1 | a0002c0002t0016g0067 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1227+32041C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64249437 | ||||||
| chr5:64249492
|
G | A | 3 | a0001c0001t0003g0048a0001c0001t0003g0049a0001c0001t0003g0050 | 3 | HG00408.hp1 HG02074.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.1227+32096G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64249492 | ||||||
| chr5:64249543
|
T | TAAGAAAT others(311): Show |
1 | a0001c0001t0005g0185 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1227+32158_1227+32 others(324): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64249543 | |||||
| chr5:64249543
|
T | TAAGAAAT others(312): Show |
1 | a0001c0001t0005g0186 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1227+32158_1227+32 others(325): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64249543 | |||||
| chr5:64249655
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1227+32259A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64249655 | ||||||
| chr5:64249698
|
T | A | 3 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054 | 3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1227+32302T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64249698 | ||||||
| chr5:64250034
|
G | A | 20 | a0001c0001t0027g0060a0002c0002t0006g0065a0002c0002t0006g0066others(17): Show | 20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1227+32638G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64250034 | ||||||
| chr5:64250111
|
A | C | 1 | a0001c0001t0004g0107 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1227+32715A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64250111 | ||||||
| chr5:64250255
|
T | C | 1 | a0002c0002t0008g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1227+32859T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64250255 | ||||||
| chr5:64250265
|
A | T | 1 | a0001c0001t0001g0157 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1227+32869A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64250265 | ||||||
| chr5:64250485
|
G | T | 60 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(57): Show | 60 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.1227+33089G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64250485 | ||||||
| chr5:64250538
|
G | T | 20 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(17): Show | 20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1227+33142G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64250538 | ||||||
| chr5:64250670
|
A | C | 6 | a0001c0001t0005g0188a0001c0001t0005g0189a0001c0001t0005g0190others(3): Show | 6 | HG01891.hp2 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1227+33274A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64250670 | ||||||
| chr5:64250780
|
A | T | 6 | a0001c0001t0005g0188a0001c0001t0005g0189a0001c0001t0005g0190others(3): Show | 6 | HG01891.hp2 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1227+33384A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64250780 | ||||||
| chr5:64250820
|
A | G | 7 | a0001c0001t0001g0113a0001c0001t0001g0125a0001c0001t0001g0126others(4): Show | 7 | HG01074.hp1 HG01081.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.1227+33424A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64250820 | ||||||
| chr5:64250957
|
C | A | 2 | a0001c0001t0003g0010a0001c0001t0007g0051 | 2 | HG03491.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1227+33561C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64250957 | ||||||
| chr5:64251044
|
G | A | 144 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(141): Show | 145 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.1227+33648G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64251044 | ||||||
| chr5:64251056
|
A | G | 1 | a0002c0002t0006g0072 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1227+33660A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64251056 | ||||||
| chr5:64251386
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1227+33990C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64251386 | ||||||
| chr5:64251522
|
G | A | 1 | a0001c0001t0002g0214 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1227+34126G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64251522 | ||||||
| chr5:64251596
|
T | A | 2 | a0001c0001t0002g0184a0001c0001t0002g0187 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1227+34200T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64251596 | ||||||
| chr5:64251634
|
C | T | 1 | a0001c0001t0019g0166 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1227+34238C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64251634 | ||||||
| chr5:64251638
|
A | T | 1 | a0002c0002t0016g0067 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1227+34242A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64251638 | ||||||
| chr5:64251663
|
C | T | 2 | a0001c0001t0003g0198a0001c0001t0003g0199 | 2 | HG02559.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1227+34267C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64251663 | ||||||
| chr5:64251684
|
G | A | 119 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(116): Show | 120 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.1227+34288G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64251684 | ||||||
| chr5:64251733
|
C | G | 6 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0198others(3): Show | 6 | HG02559.hp2 HG02886.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1227+34337C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64251733 | ||||||
| chr5:64251746
|
T | A | 3 | a0002c0002t0008g0062a0002c0002t0008g0063a0002c0002t0008g0064 | 3 | HG00741.hp2 HG01257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1227+34350T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64251746 | ||||||
| chr5:64251973
|
A | G | 89 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(86): Show | 90 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1227+34577A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64251973 | ||||||
| chr5:64251978
|
T | C | 8 | a0001c0001t0004g0002a0001c0001t0004g0086a0001c0001t0004g0092others(5): Show | 9 | HG01243.hp2 HG02615.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1227+34582T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64251978 | ||||||
| chr5:64252029
|
A | G | 1 | a0001c0001t0007g0022 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1227+34633A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64252029 | ||||||
| chr5:64252511
|
A | G | 1 | a0001c0001t0020g0023 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1227+35115A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64252511 | ||||||
| chr5:64252554
|
T | C | 44 | a0001c0001t0002g0003a0001c0001t0002g0080a0001c0001t0002g0174others(41): Show | 44 | HG00099.hp2 HG00597.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.1227+35158T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64252554 | ||||||
| chr5:64252562
|
C | T | 20 | a0001c0001t0027g0060a0002c0002t0006g0065a0002c0002t0006g0066others(17): Show | 20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1227+35166C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64252562 | ||||||
| chr5:64252839
|
G | A | 1 | a0002c0002t0008g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1227+35443G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64252839 | ||||||
| chr5:64252982
|
G | A | 1 | a0001c0001t0003g0041 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1227+35586G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64252982 | ||||||
| chr5:64253244
|
A | G | 1 | a0001c0001t0022g0018 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1227+35848A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64253244 | ||||||
| chr5:64253264
|
A | G | 1 | a0001c0001t0026g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1227+35868A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64253264 | ||||||
| chr5:64253370
|
GT | G | 28 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(25): Show | 28 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.1227+35975delT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64253370 | ||||||
| chr5:64253502
|
C | A | 1 | a0001c0001t0002g0003 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1227+36106C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64253502 | ||||||
| chr5:64253593
|
T | A | 1 | a0001c0001t0003g0044 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1227+36197T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64253593 | ||||||
| chr5:64253951
|
A | G | 44 | a0001c0001t0002g0003a0001c0001t0002g0080a0001c0001t0002g0174others(41): Show | 44 | HG00099.hp2 HG00597.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.1227+36555A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64253951 | ||||||
| chr5:64253982
|
A | G | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1227+36586A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64253982 | ||||||
| chr5:64254187
|
T | C | 9 | a0001c0001t0002g0038a0001c0001t0007g0001a0001c0001t0007g0031others(6): Show | 10 | HG00323.hp2 HG01175.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.1227+36791T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64254187 | ||||||
| chr5:64254202
|
G | A | 1 | a0001c0001t0003g0009 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1227+36806G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64254202 | ||||||
| chr5:64254360
|
T | C | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1227+36964T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64254360 | ||||||
| chr5:64254686
|
T | C | 1 | a0001c0001t0003g0145 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1227+37290T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64254686 | ||||||
| chr5:64254766
|
G | A | 1 | a0001c0001t0004g0104 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1227+37370G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64254766 | ||||||
| chr5:64255059
|
A | AT | 44 | a0001c0001t0002g0003a0001c0001t0002g0080a0001c0001t0002g0174others(41): Show | 44 | HG00099.hp2 HG00597.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.1227+37669dupT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64255059 | |||||
| chr5:64255106
|
A | T | 2 | a0001c0001t0014g0055a0001c0001t0014g0056 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1227+37710A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64255106 | ||||||
| chr5:64255187
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1227+37791C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64255187 | ||||||
| chr5:64255267
|
A | T | 2 | a0001c0001t0002g0228a0001c0001t0002g0231 | 2 | NA18955.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.1227+37871A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64255267 | ||||||
| chr5:64255350
|
C | T | 2 | a0001c0001t0003g0200a0001c0001t0003g0201 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1227+37954C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64255350 | ||||||
| chr5:64255427
|
C | T | 2 | a0001c0001t0014g0055a0001c0001t0014g0056 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1227+38031C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64255427 | ||||||
| chr5:64255547
|
G | A | 28 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(25): Show | 28 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.1227+38151G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64255547 | ||||||
| chr5:64255549
|
A | G | 8 | a0001c0001t0001g0111a0001c0001t0001g0116a0001c0001t0001g0117others(5): Show | 8 | HG02055.hp2 HG02622.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1227+38153A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64255549 | ||||||
| chr5:64255644
|
G | A | 3 | a0002c0002t0008g0062a0002c0002t0008g0063a0002c0002t0008g0064 | 3 | HG00741.hp2 HG01257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1227+38248G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64255644 | ||||||
| chr5:64255767
|
A | C | 5 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054others(2): Show | 5 | HG02970.hp1 HG03139.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1227+38371A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64255767 | ||||||
| chr5:64255827
|
G | C | 1 | a0001c0001t0019g0166 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1227+38431G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64255827 | ||||||
| chr5:64255835
|
A | G | 1 | a0001c0001t0001g0120 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1227+38439A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64255835 | ||||||
| chr5:64255885
|
T | C | 1 | a0001c0001t0005g0172 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1227+38489T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64255885 | ||||||
| chr5:64255886
|
G | A | 1 | a0001c0001t0005g0172 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1227+38490G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64255886 | ||||||
| chr5:64255953
|
A | C | 16 | a0001c0001t0027g0060a0002c0002t0006g0065a0002c0002t0006g0066others(13): Show | 16 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.1227+38557A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64255953 | ||||||
| chr5:64256003
|
G | A | 2 | a0001c0001t0014g0055a0001c0001t0014g0056 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1227+38607G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64256003 | ||||||
| chr5:64256019
|
T | C | 2 | a0001c0001t0002g0184a0001c0001t0002g0187 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1227+38623T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64256019 | ||||||
| chr5:64256026
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1227+38630C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64256026 | ||||||
| chr5:64256035
|
G | T | 1 | a0002c0002t0010g0057 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1227+38639G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64256035 | ||||||
| chr5:64256186
|
C | A | 6 | a0001c0001t0005g0188a0001c0001t0005g0189a0001c0001t0005g0190others(3): Show | 6 | HG01891.hp2 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1227+38790C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64256186 | ||||||
| chr5:64256228
|
G | T | 4 | a0002c0002t0008g0061a0002c0002t0008g0062a0002c0002t0008g0063others(1): Show | 4 | HG00741.hp2 HG01257.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1227+38832G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64256228 | ||||||
| chr5:64256238
|
C | T | 3 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054 | 3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1227+38842C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64256238 | ||||||
| chr5:64256276
|
G | A | 87 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(84): Show | 88 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1227+38880G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64256276 | ||||||
| chr5:64256318
|
G | T | 2 | a0001c0001t0002g0203a0001c0001t0002g0207 | 2 | HG00597.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.1227+38922G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64256318 | ||||||
| chr5:64256367
|
G | T | 2 | a0001c0001t0001g0151a0001c0001t0001g0162 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1227+38971G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64256367 | ||||||
| chr5:64256384
|
G | A | 3 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054 | 3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1227+38988G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64256384 | ||||||
| chr5:64256586
|
G | T | 1 | a0001c0001t0003g0025 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1227+39190G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64256586 | ||||||
| chr5:64256595
|
T | G | 3 | a0002c0002t0008g0062a0002c0002t0008g0063a0002c0002t0008g0064 | 3 | HG00741.hp2 HG01257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1227+39199T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64256595 | ||||||
| chr5:64256768
|
A | G | 2 | a0001c0001t0005g0185a0001c0001t0005g0186 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1227+39372A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64256768 | ||||||
| chr5:64256964
|
A | G | 1 | a0001c0001t0002g0177 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1227+39568A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64256964 | ||||||
| chr5:64257065
|
T | C | 89 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(86): Show | 90 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1227+39669T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64257065 | ||||||
| chr5:64257127
|
A | C | 3 | a0001c0001t0001g0158a0001c0001t0003g0144a0001c0001t0003g0145 | 3 | HG02886.hp1 HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1227+39731A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64257127 | ||||||
| chr5:64257147
|
A | G | 3 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054 | 3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1227+39751A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64257147 | ||||||
| chr5:64257166
|
C | A | 1 | a0001c0001t0005g0185 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1227+39770C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64257166 | ||||||
| chr5:64257169
|
A | C | 7 | a0001c0001t0001g0112a0001c0001t0001g0132a0001c0001t0001g0133others(4): Show | 7 | HG00741.hp2 HG01257.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1227+39773A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64257169 | ||||||
| chr5:64257238
|
C | T | 2 | a0001c0001t0005g0185a0001c0001t0005g0186 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1227+39842C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64257238 | ||||||
| chr5:64257269
|
T | C | 2 | a0001c0001t0014g0055a0001c0001t0014g0056 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1227+39873T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64257269 | ||||||
| chr5:64257410
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1227+40014G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64257410 | ||||||
| chr5:64257414
|
G | A | 1 | a0001c0001t0003g0199 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1227+40018G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64257414 | ||||||
| chr5:64257517
|
G | A | 2 | a0001c0001t0014g0055a0001c0001t0014g0056 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1227+40121G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64257517 | ||||||
| chr5:64257563
|
A | G | 2 | a0001c0001t0014g0055a0001c0001t0014g0056 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1227+40167A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64257563 | ||||||
| chr5:64257740
|
C | T | 1 | a0001c0001t0002g0211 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1227+40344C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64257740 | ||||||
| chr5:64257819
|
T | A | 1 | a0001c0001t0003g0179 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1227+40423T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64257819 | ||||||
| chr5:64257915
|
C | T | 1 | a0001c0001t0015g0032 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1227+40519C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64257915 | ||||||
| chr5:64258017
|
A | G | 61 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(58): Show | 61 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.1227+40621A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64258017 | ||||||
| chr5:64258269
|
T | C | 89 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(86): Show | 90 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1227+40873T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64258269 | ||||||
| chr5:64258389
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1227+40993T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64258389 | ||||||
| chr5:64258566
|
C | T | 1 | a0004c0004t0004g0093 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1227+41170C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64258566 | ||||||
| chr5:64258833
|
G | A | 3 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054 | 3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1227+41437G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64258833 | ||||||
| chr5:64258985
|
C | A | 1 | a0001c0001t0001g0087 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1227+41589C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64258985 | ||||||
| chr5:64259030
|
ATTGT | A | 2 | a0001c0001t0005g0185a0001c0001t0005g0186 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1227+41657_1227+41 others(10): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64259030 | |||||
| chr5:64259157
|
T | G | 3 | a0002c0002t0010g0057a0002c0002t0010g0058a0002c0002t0018g0059 | 3 | HG02109.hp2 HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1227+41761T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64259157 | ||||||
| chr5:64259480
|
T | C | 1 | a0001c0001t0003g0039 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1227+42084T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64259480 | ||||||
| chr5:64259514
|
C | G | 1 | a0001c0001t0003g0198 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1227+42118C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64259514 | ||||||
| chr5:64259621
|
A | G | 1 | a0001c0001t0004g0146 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1227+42225A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64259621 | ||||||
| chr5:64259704
|
C | T | 5 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054others(2): Show | 5 | HG02970.hp1 HG03139.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1227+42308C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64259704 | ||||||
| chr5:64259824
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1227+42428G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64259824 | ||||||
| chr5:64259845
|
C | T | 1 | a0001c0001t0003g0043 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1227+42449C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64259845 | ||||||
| chr5:64259933
|
C | A | 4 | a0002c0002t0006g0065a0002c0002t0006g0069a0002c0002t0006g0070others(1): Show | 4 | HG01081.hp1 HG01975.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1227+42537C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64259933 | ||||||
| chr5:64259943
|
A | T | 1 | a0001c0001t0003g0145 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1227+42547A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64259943 | ||||||
| chr5:64259979
|
T | G | 2 | a0001c0001t0014g0055a0001c0001t0014g0056 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1227+42583T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64259979 | ||||||
| chr5:64260144
|
A | G | 1 | a0004c0004t0004g0093 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1227+42748A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64260144 | ||||||
| chr5:64260167
|
G | A | 1 | a0001c0001t0005g0188 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1227+42771G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64260167 | ||||||
| chr5:64260207
|
T | TC | 32 | a0001c0001t0002g0204a0001c0001t0005g0167a0001c0001t0005g0168others(29): Show | 32 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.1227+42816dupC | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64260207 | |||||
| chr5:64260443
|
T | C | 1 | a0001c0001t0019g0166 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1227+43047T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64260443 | ||||||
| chr5:64260500
|
A | G | 1 | a0001c0001t0004g0248 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1227+43104A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64260500 | ||||||
| chr5:64260583
|
C | T | 1 | a0001c0001t0002g0080 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1227+43187C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64260583 | ||||||
| chr5:64260752
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1227+43356A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64260752 | ||||||
| chr5:64260866
|
A | G | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1227+43470A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64260866 | ||||||
| chr5:64260880
|
T | C | 1 | a0001c0001t0026g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1227+43484T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64260880 | ||||||
| chr5:64260910
|
A | C | 2 | a0001c0001t0014g0055a0001c0001t0014g0056 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1227+43514A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64260910 | ||||||
| chr5:64260940
|
C | CT | 13 | a0001c0001t0002g0184a0001c0001t0002g0187a0001c0001t0003g0015others(10): Show | 13 | HG01123.hp2 HG01891.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1227+43558dupT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64260940 | |||||
| chr5:64260940
|
CT | C | 26 | a0001c0001t0003g0017a0001c0001t0004g0002a0001c0001t0004g0078others(23): Show | 27 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.1227+43558delT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64260940 | |||||
| chr5:64260941
|
T | C | 1 | a0001c0001t0002g0224 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1227+43545T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64260941 | ||||||
| chr5:64261151
|
A | T | 2 | a0001c0001t0005g0185a0001c0001t0005g0186 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1227+43755A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64261151 | ||||||
| chr5:64261426
|
G | A | 2 | a0001c0001t0014g0055a0001c0001t0014g0056 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1227+44030G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64261426 | ||||||
| chr5:64261911
|
G | A | 61 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(58): Show | 61 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.1227+44515G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64261911 | ||||||
| chr5:64262417
|
G | A | 2 | a0001c0001t0002g0220a0001c0001t0002g0221 | 2 | NA18966.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.1227+45021G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64262417 | ||||||
| chr5:64262524
|
G | A | 1 | a0001c0001t0015g0032 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1227+45128G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64262524 | ||||||
| chr5:64262574
|
G | GA | 21 | a0001c0001t0002g0204a0001c0001t0005g0167a0001c0001t0005g0168others(18): Show | 21 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.1227+45184dupA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64262574 | |||||
| chr5:64262605
|
C | T | 2 | a0001c0001t0002g0222a0001c0003t0002g0246 | 2 | HG02040.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1227+45209C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64262605 | ||||||
| chr5:64263093
|
T | G | 1 | a0001c0001t0002g0180 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1227+45697T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64263093 | ||||||
| chr5:64263101
|
G | A | 2 | a0001c0001t0003g0045a0001c0001t0021g0046 | 2 | HG00642.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.1227+45705G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64263101 | ||||||
| chr5:64263404
|
G | T | 245 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(242): Show | 247 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.1227+46008G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64263404 | ||||||
| chr5:64263810
|
G | C | 1 | a0001c0001t0005g0189 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1227+46414G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64263810 | ||||||
| chr5:64263861
|
T | A | 1 | a0001c0001t0003g0198 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1227+46465T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64263861 | ||||||
| chr5:64263939
|
C | G | 1 | a0001c0001t0002g0220 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1227+46543C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64263939 | ||||||
| chr5:64264463
|
G | T | 1 | a0001c0001t0024g0192 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1227+47067G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64264463 | ||||||
| chr5:64264469
|
G | A | 1 | a0001c0001t0002g0209 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1227+47073G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64264469 | ||||||
| chr5:64264537
|
A | G | 27 | a0001c0001t0004g0002a0001c0001t0004g0078a0001c0001t0004g0086others(24): Show | 28 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.1227+47141A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64264537 | ||||||
| chr5:64264837
|
A | G | 1 | a0001c0001t0001g0153 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1227+47441A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64264837 | ||||||
| chr5:64264985
|
T | A | 1 | a0001c0001t0028g0193 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1227+47589T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64264985 | ||||||
| chr5:64265284
|
G | A | 1 | a0001c0001t0005g0172 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1227+47888G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64265284 | ||||||
| chr5:64265308
|
A | G | 20 | a0001c0001t0027g0060a0002c0002t0006g0065a0002c0002t0006g0066others(17): Show | 20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1227+47912A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64265308 | ||||||
| chr5:64265367
|
G | A | 88 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(85): Show | 89 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.1227+47971G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64265367 | ||||||
| chr5:64265782
|
G | A | 88 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(85): Show | 89 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.1227+48386G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64265782 | ||||||
| chr5:64266048
|
T | G | 2 | a0001c0001t0005g0185a0001c0001t0005g0186 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1227+48652T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64266048 | ||||||
| chr5:64266105
|
T | C | 1 | a0001c0001t0004g0090 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1227+48709T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64266105 | ||||||
| chr5:64266108
|
A | T | 1 | a0001c0001t0012g0197 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1227+48712A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64266108 | ||||||
| chr5:64266147
|
A | C | 1 | a0001c0001t0002g0176 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1227+48751A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64266147 | ||||||
| chr5:64266204
|
C | T | 1 | a0001c0001t0025g0105 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1227+48808C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64266204 | ||||||
| chr5:64266402
|
TTATAA | T | 58 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(55): Show | 58 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.1227+49011_1227+49 others(11): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64266402 | |||||
| chr5:64266465
|
T | A | 20 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(17): Show | 20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1227+49069T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64266465 | ||||||
| chr5:64266610
|
G | A | 1 | a0001c0001t0003g0021 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1227+49214G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64266610 | ||||||
| chr5:64266645
|
A | T | 1 | a0001c0001t0001g0115 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1227+49249A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64266645 | ||||||
| chr5:64266870
|
A | G | 1 | a0001c0001t0028g0193 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1227+49474A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64266870 | ||||||
| chr5:64267391
|
G | C | 2 | a0001c0001t0003g0011a0001c0001t0003g0044 | 2 | NA18964.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1227+49995G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64267391 | ||||||
| chr5:64267409
|
A | C | 1 | a0001c0001t0001g0079 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1227+50013A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64267409 | ||||||
| chr5:64267486
|
A | G | 1 | a0001c0001t0004g0146 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1227+50090A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64267486 | ||||||
| chr5:64267560
|
A | G | 20 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(17): Show | 20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1227+50164A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64267560 | ||||||
| chr5:64267904
|
C | A | 1 | a0001c0001t0023g0165 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1227+50508C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64267904 | ||||||
| chr5:64267926
|
T | C | 1 | a0001c0001t0003g0198 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1227+50530T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64267926 | ||||||
| chr5:64268210
|
G | T | 20 | a0001c0001t0027g0060a0002c0002t0006g0065a0002c0002t0006g0066others(17): Show | 20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1227+50814G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64268210 | ||||||
| chr5:64268454
|
A | G | 20 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(17): Show | 20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1227+51058A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64268454 | ||||||
| chr5:64268463
|
G | C | 2 | a0001c0001t0005g0185a0001c0001t0005g0186 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1227+51067G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64268463 | ||||||
| chr5:64268578
|
C | G | 3 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054 | 3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1227+51182C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64268578 | ||||||
| chr5:64268712
|
C | G | 22 | a0001c0001t0002g0003a0001c0001t0002g0174a0001c0001t0002g0176others(19): Show | 22 | HG00733.hp2 HG00738.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1227+51316C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64268712 | ||||||
| chr5:64268827
|
T | C | 27 | a0001c0001t0004g0002a0001c0001t0004g0078a0001c0001t0004g0086others(24): Show | 28 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.1227+51431T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64268827 | ||||||
| chr5:64268943
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1227+51547C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64268943 | ||||||
| chr5:64268968
|
CTAA | C | 27 | a0001c0001t0004g0002a0001c0001t0004g0078a0001c0001t0004g0086others(24): Show | 28 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.1227+51574_1227+51 others(9): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64268968 | |||||
| chr5:64269120
|
G | T | 5 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054others(2): Show | 5 | HG02970.hp1 HG03139.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1227+51724G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64269120 | ||||||
| chr5:64269265
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1227+51869C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64269265 | ||||||
| chr5:64269568
|
T | C | 16 | a0001c0001t0027g0060a0002c0002t0006g0065a0002c0002t0006g0066others(13): Show | 16 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.1227+52172T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64269568 | ||||||
| chr5:64269592
|
C | T | 2 | a0001c0001t0005g0185a0001c0001t0005g0186 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1227+52196C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64269592 | ||||||
| chr5:64269701
|
A | G | 4 | a0001c0001t0001g0120a0001c0001t0001g0147a0001c0001t0001g0148others(1): Show | 4 | HG02258.hp2 HG02647.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1227+52305A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64269701 | ||||||
| chr5:64269743
|
T | C | 89 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(86): Show | 90 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1227+52347T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64269743 | ||||||
| chr5:64269766
|
A | G | 1 | a0001c0001t0005g0172 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1227+52370A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64269766 | ||||||
| chr5:64269785
|
G | T | 10 | a0001c0001t0002g0038a0001c0001t0003g0016a0001c0001t0007g0001others(7): Show | 11 | HG00323.hp2 HG01175.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.1227+52389G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64269785 | ||||||
| chr5:64269846
|
G | A | 1 | a0001c0001t0027g0060 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1227+52450G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64269846 | ||||||
| chr5:64269982
|
A | C | 28 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(25): Show | 28 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.1227+52586A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64269982 | ||||||
| chr5:64270026
|
A | AAC | 22 | a0001c0001t0002g0206a0001c0001t0002g0229a0001c0001t0004g0090others(19): Show | 22 | HG00741.hp2 HG01257.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.1227+52652_1227+52 others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64270026 | |||||
| chr5:64270026
|
A | AACAC | 23 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(20): Show | 23 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.1227+52650_1227+52 others(10): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64270026 | |||||
| chr5:64270026
|
AAC | A | 58 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(55): Show | 58 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.1227+52652_1227+52 others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64270026 | |||||
| chr5:64270048
|
C | CAA | 12 | a0001c0001t0027g0060a0002c0002t0006g0065a0002c0002t0006g0066others(9): Show | 12 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.1227+52655_1227+52 others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64270048 | |||||
| chr5:64270055
|
C | T | 8 | a0001c0001t0005g0188a0001c0001t0005g0189a0001c0001t0005g0190others(5): Show | 8 | HG01891.hp2 HG02559.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1227+52659C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64270055 | ||||||
| chr5:64270212
|
T | TA | 30 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(27): Show | 30 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1227+52818dupA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64270212 | |||||
| chr5:64270303
|
T | C | 142 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(139): Show | 143 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1227+52907T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64270303 | ||||||
| chr5:64270367
|
A | G | 9 | a0001c0001t0004g0002a0001c0001t0004g0086a0001c0001t0004g0092others(6): Show | 10 | HG01243.hp2 HG01978.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1227+52971A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64270367 | ||||||
| chr5:64270368
|
T | C | 1 | a0001c0001t0001g0160 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1227+52972T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64270368 | ||||||
| chr5:64270443
|
T | C | 8 | a0001c0001t0005g0188a0001c0001t0005g0189a0001c0001t0005g0190others(5): Show | 8 | HG01891.hp2 HG02559.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1227+53047T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64270443 | ||||||
| chr5:64270795
|
A | T | 2 | a0001c0001t0004g0078a0001c0001t0004g0101 | 2 | NA18960.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1227+53399A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64270795 | ||||||
| chr5:64270957
|
C | T | 2 | a0001c0001t0014g0055a0001c0001t0014g0056 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1227+53561C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64270957 | ||||||
| chr5:64271267
|
A | C | 62 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(59): Show | 62 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.1227+53871A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64271267 | ||||||
| chr5:64271390
|
G | A | 1 | a0002c0002t0016g0067 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1228-53796G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64271390 | ||||||
| chr5:64271598
|
C | T | 87 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(84): Show | 88 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1228-53588C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64271598 | ||||||
| chr5:64271726
|
C | T | 1 | a0001c0001t0002g0176 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1228-53460C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64271726 | ||||||
| chr5:64271769
|
G | GAAAC | 101 | a0001c0001t0002g0003a0001c0001t0002g0080a0001c0001t0002g0174others(98): Show | 101 | HG00099.hp2 HG00597.hp1 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.1228-53414_1228-53 others(10): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64271769 | |||||
| chr5:64271865
|
C | T | 60 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(57): Show | 60 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.1228-53321C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64271865 | ||||||
| chr5:64272647
|
C | G | 62 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(59): Show | 62 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.1228-52539C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64272647 | ||||||
| chr5:64273037
|
T | C | 1 | a0001c0001t0005g0237 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1228-52149T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64273037 | ||||||
| chr5:64273213
|
C | T | 20 | a0001c0001t0027g0060a0002c0002t0006g0065a0002c0002t0006g0066others(17): Show | 20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1228-51973C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64273213 | ||||||
| chr5:64273572
|
T | C | 27 | a0001c0001t0004g0002a0001c0001t0004g0078a0001c0001t0004g0086others(24): Show | 28 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.1228-51614T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64273572 | ||||||
| chr5:64273810
|
A | G | 1 | a0001c0001t0004g0146 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1228-51376A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64273810 | ||||||
| chr5:64274163
|
G | A | 10 | a0001c0001t0002g0026a0001c0001t0003g0004a0001c0001t0003g0005others(7): Show | 10 | HG00642.hp2 HG00741.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.1228-51023G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64274163 | ||||||
| chr5:64274410
|
A | G | 20 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(17): Show | 20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1228-50776A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64274410 | ||||||
| chr5:64274479
|
A | G | 1 | a0001c0001t0003g0025 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1228-50707A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64274479 | ||||||
| chr5:64274522
|
T | C | 11 | a0001c0001t0002g0203a0001c0001t0002g0204a0001c0001t0002g0207others(8): Show | 11 | HG00597.hp2 HG01243.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.1228-50664T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64274522 | ||||||
| chr5:64274731
|
TG | T | 3 | a0002c0002t0008g0062a0002c0002t0008g0063a0002c0002t0008g0064 | 3 | HG00741.hp2 HG01257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1228-50454delG | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64274731 | ||||||
| chr5:64274756
|
C | T | 1 | a0001c0001t0019g0166 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1228-50430C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64274756 | ||||||
| chr5:64274953
|
T | C | 13 | a0001c0001t0005g0232a0001c0001t0005g0233a0001c0001t0005g0234others(10): Show | 13 | HG00597.hp1 NA18942.hp2 NA18946.hp1 others(10): Show |
intron_variant | MODIFIER | c.1228-50233T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64274953 | ||||||
| chr5:64275029
|
A | G | 53 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(50): Show | 53 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.1228-50157A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64275029 | ||||||
| chr5:64275122
|
A | T | 61 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(58): Show | 61 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.1228-50064A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64275122 | ||||||
| chr5:64275210
|
G | T | 1 | a0001c0001t0002g0219 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1228-49976G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64275210 | ||||||
| chr5:64275312
|
AGAATTCT others(15): Show |
A | 1 | a0001c0001t0007g0033 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1228-49873_1228-49 others(28): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64275312 | ||||||
| chr5:64275314
|
AATTCTCT others(7): Show |
A | 1 | a0001c0001t0005g0172 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1228-49852_1228-49 others(20): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64275314 | |||||
| chr5:64275643
|
C | T | 87 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(84): Show | 88 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1228-49543C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64275643 | ||||||
| chr5:64275697
|
A | T | 1 | a0001c0001t0002g0217 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1228-49489A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64275697 | ||||||
| chr5:64275908
|
T | C | 2 | a0001c0001t0005g0235a0001c0001t0029g0236 | 2 | NA18966.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1228-49278T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64275908 | ||||||
| chr5:64275964
|
C | T | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1228-49222C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64275964 | ||||||
| chr5:64276165
|
T | C | 18 | a0001c0001t0004g0078a0001c0001t0004g0089a0001c0001t0004g0090others(15): Show | 18 | HG01255.hp1 HG01256.hp1 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.1228-49021T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64276165 | ||||||
| chr5:64276167
|
G | A | 2 | a0001c0001t0014g0055a0001c0001t0014g0056 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1228-49019G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64276167 | ||||||
| chr5:64276318
|
T | TGG | 5 | a0001c0001t0005g0188a0001c0001t0005g0189a0001c0001t0005g0240others(2): Show | 5 | HG02895.hp1 NA18906.hp2 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.1228-48867_1228-48 others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64276318 | |||||
| chr5:64276319
|
G | GGGGT | 4 | a0001c0001t0005g0234a0001c0001t0005g0243a0001c0001t0024g0192others(1): Show | 4 | HG02559.hp1 HG02896.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.1228-48866_1228-48 others(10): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64276319 | |||||
| chr5:64276319
|
G | GGT | 31 | a0001c0001t0001g0113a0001c0001t0001g0141a0001c0001t0001g0164others(28): Show | 31 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.1228-48828_1228-48 others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64276319 | |||||
| chr5:64276319
|
G | GGTGT | 46 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(43): Show | 47 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.1228-48830_1228-48 others(10): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64276319 | |||||
| chr5:64276319
|
G | GGTGTGT | 25 | a0001c0001t0001g0085a0001c0001t0001g0115a0001c0001t0001g0116others(22): Show | 25 | HG00408.hp2 HG01433.hp2 HG01928.hp1 others(22): Show |
intron_variant | MODIFIER | c.1228-48832_1228-48 others(12): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64276319 | |||||
| chr5:64276319
|
G | GGTGTGTG others(1): Show |
11 | a0001c0001t0001g0079a0001c0001t0001g0087a0001c0001t0001g0114others(8): Show | 11 | HG00639.hp2 HG00738.hp1 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.1228-48834_1228-48 others(14): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64276319 | |||||
| chr5:64276319
|
G | GGTGTGTG others(3): Show |
7 | a0001c0001t0001g0120a0001c0001t0001g0131a0001c0001t0001g0142others(4): Show | 7 | HG02257.hp2 HG02258.hp2 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.1228-48836_1228-48 others(16): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64276319 | |||||
| chr5:64276319
|
G | GGTGTGTG others(5): Show |
5 | a0001c0001t0001g0088a0001c0001t0001g0129a0001c0001t0001g0135others(2): Show | 5 | HG00733.hp1 HG01516.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1228-48838_1228-48 others(18): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64276319 | |||||
| chr5:64276319
|
G | GGTGTGTG others(7): Show |
2 | a0001c0001t0001g0117a0001c0001t0001g0130 | 2 | HG01256.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.1228-48840_1228-48 others(20): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64276319 | |||||
| chr5:64276319
|
GGT | G | 31 | a0001c0001t0002g0026a0001c0001t0003g0004a0001c0001t0003g0005others(28): Show | 32 | HG00642.hp2 HG00741.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.1228-48828_1228-48 others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64276319 | |||||
| chr5:64276319
|
GGTGT | G | 20 | a0001c0001t0003g0050a0001c0001t0004g0097a0001c0001t0004g0108others(17): Show | 20 | HG01256.hp1 HG01258.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1228-48830_1228-48 others(10): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64276319 | |||||
| chr5:64276319
|
GGTGTGT | G | 3 | a0001c0001t0005g0233a0001c0001t0019g0166a0002c0002t0006g0072 | 3 | HG01175.hp1 HG02886.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.1228-48832_1228-48 others(12): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64276319 | |||||
| chr5:64276319
|
GGTGTGTG others(7): Show |
G | 7 | a0001c0001t0002g0208a0001c0001t0002g0212a0001c0001t0002g0213others(4): Show | 7 | HG01243.hp1 HG01928.hp2 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.1228-48840_1228-48 others(20): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64276319 | |||||
| chr5:64276321
|
T | G | 8 | a0001c0001t0005g0232a0001c0001t0005g0235a0001c0001t0005g0237others(5): Show | 8 | HG00597.hp1 HG02818.hp1 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.1228-48865T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64276321 | ||||||
| chr5:64276323
|
T | G | 1 | a0001c0001t0005g0173 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1228-48863T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64276323 | ||||||
| chr5:64276325
|
T | G | 6 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(3): Show | 6 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1228-48861T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64276325 | ||||||
| chr5:64276327
|
T | G | 2 | a0001c0001t0005g0233a0001c0001t0019g0166 | 2 | HG02886.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.1228-48859T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64276327 | ||||||
| chr5:64276374
|
G | GGT | 4 | a0001c0001t0001g0156a0001c0001t0005g0084a0001c0001t0014g0055others(1): Show | 4 | HG02257.hp2 HG02273.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1228-48795_1228-48 others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64276374 | |||||
| chr5:64276374
|
G | GGTGT | 111 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(108): Show | 112 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.1228-48797_1228-48 others(10): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64276374 | |||||
| chr5:64276374
|
G | GGTGTGT | 23 | a0001c0001t0001g0129a0001c0001t0001g0142a0001c0001t0005g0167others(20): Show | 23 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.1228-48799_1228-48 others(12): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64276374 | |||||
| chr5:64276374
|
G | GGTGTGTG others(1): Show |
3 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054 | 3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1228-48801_1228-48 others(14): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64276374 | |||||
| chr5:64276393
|
T | G | 1 | a0001c0001t0005g0173 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1228-48793T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64276393 | ||||||
| chr5:64276448
|
G | A | 8 | a0001c0001t0004g0002a0001c0001t0004g0086a0001c0001t0004g0092others(5): Show | 9 | HG01243.hp2 HG02615.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1228-48738G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64276448 | ||||||
| chr5:64276520
|
C | T | 1 | a0001c0001t0005g0235 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1228-48666C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64276520 | ||||||
| chr5:64276686
|
A | T | 59 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(56): Show | 59 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.1228-48500A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64276686 | ||||||
| chr5:64276704
|
A | G | 12 | a0001c0001t0027g0060a0002c0002t0006g0065a0002c0002t0006g0066others(9): Show | 12 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.1228-48482A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64276704 | ||||||
| chr5:64276850
|
G | A | 142 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(139): Show | 143 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1228-48336G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64276850 | ||||||
| chr5:64277018
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1228-48168C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64277018 | ||||||
| chr5:64277020
|
C | CTG | 6 | a0001c0001t0005g0188a0001c0001t0005g0189a0001c0001t0005g0190others(3): Show | 6 | HG01891.hp2 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1228-48164_1228-48 others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64277020 | |||||
| chr5:64277046
|
T | G | 1 | a0001c0001t0003g0009 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1228-48140T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64277046 | ||||||
| chr5:64277170
|
G | A | 3 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054 | 3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1228-48016G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64277170 | ||||||
| chr5:64277190
|
A | AG | 6 | a0001c0001t0001g0113a0001c0001t0001g0126a0001c0001t0001g0127others(3): Show | 6 | HG01074.hp1 HG01081.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.1228-47992dupG | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64277190 | |||||
| chr5:64277190
|
A | G | 21 | a0001c0001t0001g0134a0001c0001t0002g0207a0001c0001t0027g0060others(18): Show | 21 | HG00408.hp2 HG00741.hp2 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.1228-47996A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64277190 | ||||||
| chr5:64277194
|
G | A | 2 | a0001c0001t0001g0134a0001c0001t0001g0143 | 2 | HG00408.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.1228-47992G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64277194 | ||||||
| chr5:64277194
|
G | GA | 74 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(71): Show | 75 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.1228-47979dupA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64277194 | |||||
| chr5:64277195
|
A | G | 23 | a0001c0001t0003g0045a0001c0001t0005g0167a0001c0001t0005g0168others(20): Show | 23 | HG00597.hp1 HG00642.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.1228-47991A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64277195 | ||||||
| chr5:64277196
|
A | G | 6 | a0001c0001t0005g0234a0001c0001t0005g0238a0001c0001t0005g0240others(3): Show | 6 | NA18946.hp1 NA18954.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.1228-47990A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64277196 | ||||||
| chr5:64277540
|
T | G | 4 | a0001c0001t0001g0120a0001c0001t0001g0147a0001c0001t0001g0148others(1): Show | 4 | HG02258.hp2 HG02647.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1228-47646T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64277540 | ||||||
| chr5:64277749
|
A | G | 1 | a0001c0001t0003g0014 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1228-47437A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64277749 | ||||||
| chr5:64277757
|
C | T | 1 | a0005c0005t0001g0140 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1228-47429C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64277757 | ||||||
| chr5:64278419
|
A | G | 1 | a0005c0005t0001g0140 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1228-46767A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64278419 | ||||||
| chr5:64278601
|
A | G | 142 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(139): Show | 143 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1228-46585A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64278601 | ||||||
| chr5:64278657
|
G | T | 1 | a0001c0001t0026g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1228-46529G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64278657 | ||||||
| chr5:64278845
|
C | T | 2 | a0001c0001t0005g0185a0001c0001t0005g0186 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1228-46341C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64278845 | ||||||
| chr5:64278909
|
T | C | 1 | a0001c0001t0003g0027 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1228-46277T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64278909 | ||||||
| chr5:64279299
|
T | A | 1 | a0001c0001t0002g0218 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1228-45887T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64279299 | ||||||
| chr5:64279338
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1228-45848A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64279338 | ||||||
| chr5:64279457
|
T | C | 87 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(84): Show | 88 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1228-45729T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64279457 | ||||||
| chr5:64279984
|
G | A | 30 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(27): Show | 30 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1228-45202G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64279984 | ||||||
| chr5:64280248
|
C | A | 1 | a0002c0002t0006g0071 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1228-44938C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64280248 | ||||||
| chr5:64280484
|
A | G | 87 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(84): Show | 88 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1228-44702A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64280484 | ||||||
| chr5:64280573
|
A | C | 1 | a0001c0001t0007g0033 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1228-44613A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64280573 | ||||||
| chr5:64280622
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1228-44564G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64280622 | ||||||
| chr5:64280911
|
T | C | 1 | a0001c0001t0005g0186 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1228-44275T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64280911 | ||||||
| chr5:64281349
|
T | C | 1 | a0001c0001t0015g0032 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1228-43837T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64281349 | ||||||
| chr5:64281422
|
A | T | 3 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083 | 3 | HG00323.hp1 HG01106.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1228-43764A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64281422 | ||||||
| chr5:64281453
|
C | T | 1 | a0001c0001t0005g0190 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1228-43733C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64281453 | ||||||
| chr5:64281677
|
C | T | 142 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(139): Show | 143 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1228-43509C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64281677 | ||||||
| chr5:64281705
|
C | A | 2 | a0001c0001t0003g0048a0001c0001t0003g0049 | 2 | HG00408.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.1228-43481C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64281705 | ||||||
| chr5:64281718
|
G | A | 2 | a0001c0001t0002g0220a0001c0001t0002g0221 | 2 | NA18966.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.1228-43468G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64281718 | ||||||
| chr5:64281743
|
G | A | 2 | a0001c0001t0014g0055a0001c0001t0014g0056 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1228-43443G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64281743 | ||||||
| chr5:64281776
|
C | G | 117 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(114): Show | 118 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.1228-43410C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64281776 | ||||||
| chr5:64281932
|
C | T | 6 | a0001c0001t0005g0188a0001c0001t0005g0189a0001c0001t0005g0190others(3): Show | 6 | HG01891.hp2 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1228-43254C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64281932 | ||||||
| chr5:64282123
|
G | T | 3 | a0001c0001t0002g0226a0001c0001t0002g0229a0001c0001t0002g0230 | 3 | NA18989.hp1 NA18994.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.1228-43063G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64282123 | ||||||
| chr5:64282132
|
C | T | 87 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(84): Show | 88 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1228-43054C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64282132 | ||||||
| chr5:64282238
|
T | C | 1 | a0001c0001t0025g0105 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1228-42948T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64282238 | ||||||
| chr5:64282305
|
A | G | 1 | a0001c0001t0015g0032 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1228-42881A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64282305 | ||||||
| chr5:64282358
|
G | A | 2 | a0001c0001t0005g0185a0001c0001t0005g0186 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1228-42828G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64282358 | ||||||
| chr5:64282894
|
C | T | 1 | a0001c0001t0002g0225 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1228-42292C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64282894 | ||||||
| chr5:64283002
|
A | C | 1 | a0001c0001t0002g0180 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1228-42184A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64283002 | ||||||
| chr5:64283111
|
G | A | 1 | a0001c0001t0005g0185 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1228-42075G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64283111 | ||||||
| chr5:64283209
|
G | A | 1 | a0001c0001t0004g0110 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1228-41977G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64283209 | ||||||
| chr5:64283589
|
T | C | 142 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(139): Show | 143 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1228-41597T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64283589 | ||||||
| chr5:64283667
|
A | G | 20 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(17): Show | 20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1228-41519A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64283667 | ||||||
| chr5:64283942
|
C | A | 3 | a0002c0002t0008g0062a0002c0002t0008g0063a0002c0002t0008g0064 | 3 | HG00741.hp2 HG01257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1228-41244C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64283942 | ||||||
| chr5:64284020
|
C | G | 1 | a0001c0001t0003g0013 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1228-41166C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64284020 | ||||||
| chr5:64284236
|
A | T | 3 | a0002c0002t0008g0062a0002c0002t0008g0063a0002c0002t0008g0064 | 3 | HG00741.hp2 HG01257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1228-40950A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64284236 | ||||||
| chr5:64284246
|
C | CT | 247 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(244): Show | 249 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.1228-40938dupT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64284246 | |||||
| chr5:64284486
|
C | T | 4 | a0002c0002t0008g0061a0002c0002t0008g0062a0002c0002t0008g0063others(1): Show | 4 | HG00741.hp2 HG01257.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1228-40700C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64284486 | ||||||
| chr5:64284537
|
G | A | 1 | a0001c0001t0002g0223 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1228-40649G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64284537 | ||||||
| chr5:64284835
|
A | C | 1 | a0001c0001t0005g0189 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1228-40351A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64284835 | ||||||
| chr5:64284848
|
A | G | 8 | a0001c0001t0005g0188a0001c0001t0005g0189a0001c0001t0005g0190others(5): Show | 8 | HG01891.hp2 HG02559.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1228-40338A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64284848 | ||||||
| chr5:64284866
|
G | A | 27 | a0001c0001t0004g0002a0001c0001t0004g0078a0001c0001t0004g0086others(24): Show | 28 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.1228-40320G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64284866 | ||||||
| chr5:64285006
|
G | A | 4 | a0001c0001t0004g0098a0001c0001t0004g0102a0001c0001t0004g0103others(1): Show | 4 | HG01993.hp1 NA18943.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.1228-40180G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64285006 | ||||||
| chr5:64285117
|
C | T | 2 | a0001c0001t0003g0198a0001c0001t0003g0199 | 2 | HG02559.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1228-40069C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64285117 | ||||||
| chr5:64285456
|
TTTGGCTG others(36): Show |
T | 1 | a0001c0001t0001g0141 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1228-39726_1228-39 others(49): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64285456 | |||||
| chr5:64285590
|
T | C | 5 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054others(2): Show | 5 | HG02970.hp1 HG03139.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1228-39596T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64285590 | ||||||
| chr5:64285654
|
G | T | 1 | a0001c0001t0001g0081 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1228-39532G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64285654 | ||||||
| chr5:64285659
|
C | T | 1 | a0001c0001t0017g0019 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1228-39527C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64285659 | ||||||
| chr5:64285799
|
G | A | 3 | a0001c0001t0001g0112a0001c0001t0001g0132a0001c0001t0001g0133 | 3 | HG03491.hp1 HG03492.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1228-39387G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64285799 | ||||||
| chr5:64285890
|
G | A | 1 | a0001c0001t0022g0018 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1228-39296G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64285890 | ||||||
| chr5:64286149
|
A | G | 1 | a0002c0002t0006g0071 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1228-39037A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64286149 | ||||||
| chr5:64286430
|
C | G | 1 | a0001c0001t0003g0039 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1228-38756C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64286430 | ||||||
| chr5:64286474
|
C | T | 1 | a0001c0001t0002g0206 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1228-38712C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64286474 | ||||||
| chr5:64286587
|
A | T | 1 | a0001c0003t0002g0246 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1228-38599A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64286587 | ||||||
| chr5:64286743
|
A | G | 5 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097others(2): Show | 5 | HG01255.hp1 HG01256.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1228-38443A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64286743 | ||||||
| chr5:64287049
|
C | G | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1228-38137C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64287049 | ||||||
| chr5:64287092
|
G | A | 1 | a0001c0001t0002g0204 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1228-38094G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64287092 | ||||||
| chr5:64287216
|
C | T | 18 | a0001c0001t0004g0078a0001c0001t0004g0089a0001c0001t0004g0090others(15): Show | 18 | HG01255.hp1 HG01256.hp1 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.1228-37970C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64287216 | ||||||
| chr5:64287255
|
G | A | 1 | a0001c0001t0002g0178 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1228-37931G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64287255 | ||||||
| chr5:64287744
|
T | A | 1 | a0001c0001t0002g0218 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1228-37442T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64287744 | ||||||
| chr5:64287853
|
C | T | 1 | a0001c0001t0026g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1228-37333C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64287853 | ||||||
| chr5:64288349
|
G | T | 1 | a0002c0002t0008g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1228-36837G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64288349 | ||||||
| chr5:64288441
|
C | T | 1 | a0002c0002t0008g0064 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1228-36745C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64288441 | ||||||
| chr5:64288486
|
C | T | 1 | a0001c0001t0026g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1228-36700C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64288486 | ||||||
| chr5:64288554
|
G | A | 3 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054 | 3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1228-36632G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64288554 | ||||||
| chr5:64288597
|
G | A | 1 | a0001c0001t0005g0189 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1228-36589G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64288597 | ||||||
| chr5:64288811
|
A | T | 1 | a0001c0001t0004g0104 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1228-36375A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64288811 | ||||||
| chr5:64288915
|
T | C | 3 | a0002c0002t0008g0062a0002c0002t0008g0063a0002c0002t0008g0064 | 3 | HG00741.hp2 HG01257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1228-36271T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64288915 | ||||||
| chr5:64289190
|
C | T | 1 | a0001c0001t0012g0196 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1228-35996C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64289190 | ||||||
| chr5:64289297
|
A | G | 16 | a0001c0001t0027g0060a0002c0002t0006g0065a0002c0002t0006g0066others(13): Show | 16 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.1228-35889A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64289297 | ||||||
| chr5:64289644
|
T | C | 1 | a0001c0001t0005g0173 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1228-35542T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64289644 | ||||||
| chr5:64289870
|
T | C | 51 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(48): Show | 51 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.1228-35316T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64289870 | ||||||
| chr5:64289910
|
T | C | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1228-35276T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64289910 | ||||||
| chr5:64290005
|
T | G | 2 | a0001c0001t0003g0048a0001c0001t0003g0049 | 2 | HG00408.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.1228-35181T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64290005 | ||||||
| chr5:64290026
|
A | G | 2 | a0001c0001t0005g0185a0001c0001t0005g0186 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1228-35160A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64290026 | ||||||
| chr5:64290182
|
A | G | 142 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(139): Show | 143 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1228-35004A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64290182 | ||||||
| chr5:64290462
|
T | C | 1 | a0001c0001t0012g0197 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1228-34724T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64290462 | ||||||
| chr5:64290700
|
T | G | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1228-34486T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64290700 | ||||||
| chr5:64290869
|
T | C | 2 | a0001c0001t0002g0026a0001c0001t0003g0030 | 2 | HG02698.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1228-34317T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64290869 | ||||||
| chr5:64291184
|
T | C | 58 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(55): Show | 58 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.1228-34002T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64291184 | ||||||
| chr5:64291416
|
C | CT | 42 | a0001c0001t0002g0038a0001c0001t0002g0174a0001c0001t0002g0203others(39): Show | 42 | HG00597.hp1 HG00597.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.1228-33744dupT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64291416 | |||||
| chr5:64291416
|
C | CTT | 6 | a0001c0001t0001g0118a0001c0001t0005g0186a0001c0001t0005g0189others(3): Show | 6 | HG02622.hp1 HG02895.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1228-33745_1228-33 others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64291416 | |||||
| chr5:64291416
|
CT | C | 29 | a0001c0001t0001g0141a0001c0001t0001g0163a0001c0001t0002g0183others(26): Show | 30 | HG00099.hp1 HG01243.hp2 HG01255.hp1 others(27): Show |
intron_variant | MODIFIER | c.1228-33744delT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64291416 | |||||
| chr5:64291416
|
CTT | C | 50 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(47): Show | 50 | HG00323.hp1 HG00408.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.1228-33745_1228-33 others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64291416 | |||||
| chr5:64291416
|
CTTT | C | 7 | a0001c0001t0001g0085a0001c0001t0001g0112a0001c0001t0001g0122others(4): Show | 7 | HG01109.hp2 HG01515.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.1228-33746_1228-33 others(9): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64291416 | |||||
| chr5:64291520
|
G | C | 2 | a0001c0001t0002g0184a0001c0001t0002g0187 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1228-33666G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64291520 | ||||||
| chr5:64291532
|
C | T | 1 | a0001c0001t0019g0166 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1228-33654C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64291532 | ||||||
| chr5:64291565
|
C | T | 1 | a0001c0001t0002g0184 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1228-33621C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64291565 | ||||||
| chr5:64291591
|
A | AT | 85 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(82): Show | 86 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.1228-33586dupT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64291591 | |||||
| chr5:64291717
|
G | A | 1 | a0002c0002t0008g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1228-33469G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64291717 | ||||||
| chr5:64291723
|
G | A | 1 | a0001c0001t0001g0138 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1228-33463G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64291723 | ||||||
| chr5:64291939
|
G | A | 1 | a0001c0001t0003g0050 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1228-33247G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64291939 | ||||||
| chr5:64291971
|
A | G | 1 | a0001c0001t0002g0178 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1228-33215A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64291971 | ||||||
| chr5:64292186
|
G | A | 1 | a0001c0001t0011g0052 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1228-33000G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64292186 | ||||||
| chr5:64292247
|
C | G | 1 | a0005c0005t0001g0140 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1228-32939C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64292247 | ||||||
| chr5:64292384
|
G | C | 1 | a0001c0001t0001g0127 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1228-32802G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64292384 | ||||||
| chr5:64292648
|
G | C | 3 | a0002c0002t0010g0057a0002c0002t0010g0058a0002c0002t0018g0059 | 3 | HG02109.hp2 HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1228-32538G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64292648 | ||||||
| chr5:64292788
|
A | G | 1 | a0001c0001t0004g0091 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1228-32398A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64292788 | ||||||
| chr5:64293010
|
C | T | 1 | a0001c0001t0002g0174 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1228-32176C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64293010 | ||||||
| chr5:64293071
|
C | G | 1 | a0002c0002t0008g0063 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1228-32115C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64293071 | ||||||
| chr5:64293171
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1228-32015G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64293171 | ||||||
| chr5:64293232
|
G | T | 2 | a0001c0001t0001g0087a0001c0001t0001g0161 | 2 | NA18984.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1228-31954G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64293232 | ||||||
| chr5:64293394
|
G | A | 1 | a0001c0001t0005g0186 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1228-31792G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64293394 | ||||||
| chr5:64293397
|
C | T | 20 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(17): Show | 20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1228-31789C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64293397 | ||||||
| chr5:64293668
|
G | A | 11 | a0001c0001t0001g0088a0001c0001t0001g0135a0001c0001t0001g0137others(8): Show | 11 | HG00099.hp1 HG00733.hp1 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.1228-31518G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64293668 | ||||||
| chr5:64293787
|
G | A | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1228-31399G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64293787 | ||||||
| chr5:64293788
|
C | T | 2 | a0001c0001t0019g0166a0001c0001t0026g0247 | 2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1228-31398C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64293788 | ||||||
| chr5:64294012
|
G | A | 2 | a0001c0001t0005g0235a0001c0001t0029g0236 | 2 | NA18966.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1228-31174G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64294012 | ||||||
| chr5:64294086
|
C | A | 1 | a0001c0001t0019g0166 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1228-31100C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64294086 | ||||||
| chr5:64294122
|
G | T | 2 | a0001c0001t0014g0055a0001c0001t0014g0056 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1228-31064G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64294122 | ||||||
| chr5:64294203
|
G | T | 1 | a0001c0001t0003g0009 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1228-30983G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64294203 | ||||||
| chr5:64294241
|
G | A | 1 | a0001c0001t0003g0144 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1228-30945G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64294241 | ||||||
| chr5:64294324
|
A | G | 1 | a0001c0001t0002g0209 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1228-30862A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64294324 | ||||||
| chr5:64294749
|
A | G | 2 | a0001c0001t0002g0026a0001c0001t0003g0030 | 2 | HG02698.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1228-30437A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64294749 | ||||||
| chr5:64294807
|
A | G | 6 | a0001c0001t0005g0188a0001c0001t0005g0189a0001c0001t0005g0190others(3): Show | 6 | HG01891.hp2 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1228-30379A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64294807 | ||||||
| chr5:64295295
|
G | A | 1 | a0001c0001t0002g0224 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1228-29891G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64295295 | ||||||
| chr5:64295440
|
G | A | 1 | a0001c0001t0003g0043 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1228-29746G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64295440 | ||||||
| chr5:64295510
|
G | A | 1 | a0001c0001t0002g0003 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1228-29676G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64295510 | ||||||
| chr5:64295572
|
T | C | 16 | a0001c0001t0027g0060a0002c0002t0006g0065a0002c0002t0006g0066others(13): Show | 16 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.1228-29614T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64295572 | ||||||
| chr5:64295776
|
T | C | 1 | a0001c0001t0028g0193 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1228-29410T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64295776 | ||||||
| chr5:64295809
|
C | A | 1 | a0001c0001t0003g0043 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1228-29377C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64295809 | ||||||
| chr5:64295851
|
G | T | 5 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054others(2): Show | 5 | HG02970.hp1 HG03139.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1228-29335G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64295851 | ||||||
| chr5:64296084
|
T | G | 1 | a0001c0001t0002g0038 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1228-29102T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64296084 | ||||||
| chr5:64296296
|
G | A | 1 | a0001c0001t0003g0024 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1228-28890G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64296296 | ||||||
| chr5:64296534
|
A | T | 1 | a0001c0001t0024g0192 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1228-28652A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64296534 | ||||||
| chr5:64296545
|
A | G | 27 | a0001c0001t0004g0002a0001c0001t0004g0078a0001c0001t0004g0086others(24): Show | 28 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.1228-28641A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64296545 | ||||||
| chr5:64296657
|
C | CA | 59 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(56): Show | 59 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.1228-28517dupA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64296657 | |||||
| chr5:64296657
|
CA | C | 23 | a0001c0001t0002g0207a0001c0001t0011g0053a0001c0001t0011g0054others(20): Show | 23 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.1228-28517delA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64296657 | |||||
| chr5:64296740
|
G | A | 3 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054 | 3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1228-28446G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64296740 | ||||||
| chr5:64296786
|
T | G | 142 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(139): Show | 143 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1228-28400T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64296786 | ||||||
| chr5:64296877
|
G | C | 1 | a0001c0001t0007g0022 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1228-28309G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64296877 | ||||||
| chr5:64297080
|
G | T | 20 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(17): Show | 20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1228-28106G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64297080 | ||||||
| chr5:64297293
|
G | T | 1 | a0001c0001t0001g0131 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1228-27893G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64297293 | ||||||
| chr5:64297445
|
TAGA | T | 3 | a0002c0002t0008g0062a0002c0002t0008g0063a0002c0002t0008g0064 | 3 | HG00741.hp2 HG01257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1228-27735_1228-27 others(9): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64297445 | |||||
| chr5:64297455
|
G | A | 1 | a0001c0001t0002g0222 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1228-27731G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64297455 | ||||||
| chr5:64297473
|
T | C | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1228-27713T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64297473 | ||||||
| chr5:64297614
|
G | A | 1 | a0001c0001t0002g0218 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1228-27572G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64297614 | ||||||
| chr5:64297684
|
A | G | 1 | a0001c0001t0003g0179 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1228-27502A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64297684 | ||||||
| chr5:64297976
|
G | A | 12 | a0001c0001t0027g0060a0002c0002t0006g0065a0002c0002t0006g0066others(9): Show | 12 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.1228-27210G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64297976 | ||||||
| chr5:64298136
|
A | C | 1 | a0001c0001t0002g0174 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1228-27050A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64298136 | ||||||
| chr5:64298172
|
G | A | 1 | a0001c0001t0003g0025 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1228-27014G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64298172 | ||||||
| chr5:64298330
|
G | C | 1 | a0001c0001t0003g0179 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1228-26856G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64298330 | ||||||
| chr5:64298481
|
T | C | 2 | a0001c0001t0003g0011a0001c0001t0003g0044 | 2 | NA18964.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1228-26705T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64298481 | ||||||
| chr5:64298520
|
C | T | 1 | a0001c0001t0005g0186 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1228-26666C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64298520 | ||||||
| chr5:64298595
|
G | A | 2 | a0001c0001t0012g0195a0001c0001t0012g0196 | 2 | HG02109.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1228-26591G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64298595 | ||||||
| chr5:64298746
|
G | C | 1 | a0001c0001t0021g0046 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1228-26440G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64298746 | ||||||
| chr5:64299843
|
A | C | 5 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054others(2): Show | 5 | HG02970.hp1 HG03139.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1228-25343A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64299843 | ||||||
| chr5:64299869
|
T | G | 3 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054 | 3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1228-25317T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64299869 | ||||||
| chr5:64300209
|
T | C | 1 | a0001c0001t0002g0213 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1228-24977T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64300209 | ||||||
| chr5:64300323
|
A | G | 1 | a0001c0001t0005g0169 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1228-24863A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64300323 | ||||||
| chr5:64300436
|
G | A | 1 | a0001c0001t0002g0187 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1228-24750G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64300436 | ||||||
| chr5:64300491
|
C | T | 6 | a0001c0001t0003g0011a0001c0001t0003g0021a0001c0001t0003g0044others(3): Show | 6 | HG00408.hp1 HG02074.hp1 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.1228-24695C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64300491 | ||||||
| chr5:64300520
|
A | T | 1 | a0001c0001t0005g0189 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1228-24666A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64300520 | ||||||
| chr5:64301091
|
TA | T | 121 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(118): Show | 122 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.1228-24093delA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64301091 | |||||
| chr5:64301254
|
G | C | 1 | a0001c0001t0003g0020 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1228-23932G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64301254 | ||||||
| chr5:64301300
|
A | T | 28 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(25): Show | 28 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.1228-23886A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64301300 | ||||||
| chr5:64301701
|
A | ATGTGTGT others(5): Show |
2 | a0001c0001t0005g0167a0001c0001t0005g0168 | 2 | HG02055.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1228-23473_1228-23 others(18): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64301701 | |||||
| chr5:64301701
|
A | ATGTGTGT others(7): Show |
18 | a0001c0001t0005g0169a0001c0001t0005g0170a0001c0001t0005g0171others(15): Show | 18 | HG00597.hp1 HG02280.hp2 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.1228-23475_1228-23 others(20): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64301701 | |||||
| chr5:64301701
|
A | ATGTGTGT others(9): Show |
1 | a0001c0001t0019g0166 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1228-23477_1228-23 others(22): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64301701 | |||||
| chr5:64301701
|
A | ATGTGTGT others(11): Show |
4 | a0001c0001t0005g0189a0001c0001t0005g0190a0001c0001t0014g0055others(1): Show | 4 | HG01891.hp2 HG02895.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1228-23479_1228-23 others(24): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64301701 | |||||
| chr5:64301701
|
A | ATGTGTGT others(13): Show |
2 | a0001c0001t0005g0185a0001c0001t0005g0186 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1228-23481_1228-23 others(26): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64301701 | |||||
| chr5:64301701
|
A | ATGTGTGT others(15): Show |
2 | a0001c0001t0005g0191a0001c0001t0026g0247 | 2 | HG02818.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1228-23483_1228-23 others(28): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64301701 | |||||
| chr5:64301701
|
A | ATGTGTGT others(19): Show |
6 | a0001c0001t0005g0188a0001c0001t0011g0052a0001c0001t0011g0053others(3): Show | 6 | HG02559.hp1 HG02896.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1228-23462_1228-23 others(32): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64301701 | |||||
| chr5:64301701
|
ATGTG | A | 20 | a0001c0001t0027g0060a0002c0002t0006g0065a0002c0002t0006g0066others(17): Show | 20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1228-23465_1228-23 others(10): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64301701 | |||||
| chr5:64301763
|
G | A | 1 | a0001c0001t0004g0146 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1228-23423G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64301763 | ||||||
| chr5:64301904
|
C | T | 1 | a0001c0001t0003g0007 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1228-23282C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64301904 | ||||||
| chr5:64302228
|
A | G | 16 | a0001c0001t0027g0060a0002c0002t0006g0065a0002c0002t0006g0066others(13): Show | 16 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.1228-22958A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64302228 | ||||||
| chr5:64302250
|
A | G | 142 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(139): Show | 143 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1228-22936A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64302250 | ||||||
| chr5:64302298
|
A | G | 27 | a0001c0001t0004g0002a0001c0001t0004g0078a0001c0001t0004g0086others(24): Show | 28 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.1228-22888A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64302298 | ||||||
| chr5:64302340
|
T | A | 2 | a0001c0001t0001g0088a0001c0001t0001g0135 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1228-22846T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64302340 | ||||||
| chr5:64302349
|
G | A | 3 | a0002c0002t0008g0062a0002c0002t0008g0063a0002c0002t0008g0064 | 3 | HG00741.hp2 HG01257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1228-22837G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64302349 | ||||||
| chr5:64302512
|
A | T | 1 | a0001c0001t0003g0040 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1228-22674A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64302512 | ||||||
| chr5:64303154
|
A | C | 3 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054 | 3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1228-22032A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64303154 | ||||||
| chr5:64303550
|
A | G | 1 | a0001c0001t0001g0117 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1228-21636A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64303550 | ||||||
| chr5:64303682
|
T | C | 2 | a0001c0001t0005g0185a0001c0001t0005g0186 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1228-21504T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64303682 | ||||||
| chr5:64304160
|
CAG | C | 58 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(55): Show | 58 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.1228-21025_1228-21 others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64304160 | ||||||
| chr5:64304184
|
G | C | 3 | a0001c0001t0002g0226a0001c0001t0002g0229a0001c0001t0002g0230 | 3 | NA18989.hp1 NA18994.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.1228-21002G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64304184 | ||||||
| chr5:64304191
|
G | A | 141 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(138): Show | 142 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.1228-20995G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64304191 | ||||||
| chr5:64304348
|
G | A | 1 | a0001c0001t0007g0033 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1228-20838G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64304348 | ||||||
| chr5:64304406
|
A | T | 141 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(138): Show | 142 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.1228-20780A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64304406 | ||||||
| chr5:64304836
|
G | A | 5 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054others(2): Show | 5 | HG02970.hp1 HG03139.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1228-20350G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64304836 | ||||||
| chr5:64305026
|
C | T | 143 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(140): Show | 144 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.1228-20160C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64305026 | ||||||
| chr5:64305084
|
G | A | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1228-20102G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64305084 | ||||||
| chr5:64305298
|
C | T | 1 | a0001c0001t0002g0213 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1228-19888C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64305298 | ||||||
| chr5:64305397
|
C | G | 52 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(49): Show | 52 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.1228-19789C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64305397 | ||||||
| chr5:64305430
|
G | C | 2 | a0002c0002t0006g0074a0002c0002t0006g0075 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1228-19756G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64305430 | ||||||
| chr5:64305478
|
AT | A | 6 | a0001c0001t0001g0155a0001c0001t0003g0011a0001c0001t0003g0044others(3): Show | 6 | HG01433.hp2 HG02970.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1228-19697delT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64305478 | |||||
| chr5:64305600
|
AAC | A | 20 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(17): Show | 20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1228-19584_1228-19 others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64305600 | |||||
| chr5:64305698
|
A | G | 1 | a0001c0001t0001g0119 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1228-19488A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64305698 | ||||||
| chr5:64306179
|
C | G | 1 | a0001c0001t0002g0181 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1228-19007C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64306179 | ||||||
| chr5:64306209
|
T | C | 2 | a0001c0001t0014g0055a0001c0001t0014g0056 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1228-18977T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64306209 | ||||||
| chr5:64306264
|
A | G | 1 | a0001c0001t0021g0046 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1228-18922A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64306264 | ||||||
| chr5:64306601
|
T | G | 1 | a0001c0001t0007g0051 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1228-18585T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64306601 | ||||||
| chr5:64306631
|
A | C | 2 | a0001c0001t0005g0185a0001c0001t0005g0186 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1228-18555A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64306631 | ||||||
| chr5:64306773
|
A | G | 1 | a0001c0001t0001g0159 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1228-18413A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64306773 | ||||||
| chr5:64306806
|
A | G | 1 | a0001c0001t0001g0122 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1228-18380A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64306806 | ||||||
| chr5:64306830
|
G | C | 1 | a0001c0001t0002g0218 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1228-18356G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64306830 | ||||||
| chr5:64306977
|
TAATAA | T | 2 | a0001c0001t0005g0185a0001c0001t0005g0186 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1228-18201_1228-18 others(11): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64306977 | |||||
| chr5:64307006
|
TA | T | 16 | a0001c0001t0027g0060a0002c0002t0006g0065a0002c0002t0006g0066others(13): Show | 16 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.1228-18171delA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64307006 | |||||
| chr5:64307111
|
GCTTT | G | 86 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(83): Show | 87 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.1228-18072_1228-18 others(10): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64307111 | |||||
| chr5:64307391
|
G | A | 2 | a0001c0001t0001g0129a0001c0001t0001g0142 | 2 | HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1228-17795G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64307391 | ||||||
| chr5:64307420
|
G | A | 30 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(27): Show | 30 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1228-17766G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64307420 | ||||||
| chr5:64307696
|
T | C | 117 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(114): Show | 118 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.1228-17490T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64307696 | ||||||
| chr5:64307713
|
T | C | 27 | a0001c0001t0004g0002a0001c0001t0004g0078a0001c0001t0004g0086others(24): Show | 28 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.1228-17473T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64307713 | ||||||
| chr5:64307778
|
G | A | 1 | a0001c0001t0003g0028 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1228-17408G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64307778 | ||||||
| chr5:64307933
|
G | A | 3 | a0002c0002t0010g0057a0002c0002t0010g0058a0002c0002t0018g0059 | 3 | HG02109.hp2 HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1228-17253G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64307933 | ||||||
| chr5:64307983
|
C | T | 121 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(118): Show | 122 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.1228-17203C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64307983 | ||||||
| chr5:64308063
|
A | G | 117 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(114): Show | 118 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.1228-17123A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64308063 | ||||||
| chr5:64308237
|
C | T | 1 | a0001c0001t0025g0105 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1228-16949C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64308237 | ||||||
| chr5:64308302
|
A | C | 8 | a0001c0001t0005g0188a0001c0001t0005g0189a0001c0001t0005g0190others(5): Show | 8 | HG01891.hp2 HG02559.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1228-16884A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64308302 | ||||||
| chr5:64308399
|
C | T | 4 | a0001c0001t0001g0120a0001c0001t0001g0147a0001c0001t0001g0148others(1): Show | 4 | HG02258.hp2 HG02647.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1228-16787C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64308399 | ||||||
| chr5:64308431
|
G | A | 87 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(84): Show | 88 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1228-16755G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64308431 | ||||||
| chr5:64308793
|
A | T | 20 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(17): Show | 20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1228-16393A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64308793 | ||||||
| chr5:64309142
|
G | T | 1 | a0001c0001t0026g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1228-16044G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64309142 | ||||||
| chr5:64309589
|
G | C | 6 | a0001c0001t0001g0113a0001c0001t0001g0126a0001c0001t0001g0127others(3): Show | 6 | HG01074.hp1 HG01081.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.1228-15597G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64309589 | ||||||
| chr5:64309764
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1228-15422T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64309764 | ||||||
| chr5:64309925
|
C | T | 2 | a0001c0001t0003g0200a0001c0001t0003g0201 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1228-15261C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64309925 | ||||||
| chr5:64310279
|
T | C | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1228-14907T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64310279 | ||||||
| chr5:64310516
|
C | CA | 5 | a0001c0001t0001g0088a0001c0001t0001g0135a0002c0002t0008g0061others(2): Show | 5 | HG01516.hp1 HG01517.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1228-14656dupA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64310516 | |||||
| chr5:64310518
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1228-14668A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64310518 | ||||||
| chr5:64310623
|
C | T | 141 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(138): Show | 142 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.1228-14563C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64310623 | ||||||
| chr5:64310665
|
T | C | 1 | a0001c0001t0001g0133 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1228-14521T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64310665 | ||||||
| chr5:64311071
|
G | T | 1 | a0001c0001t0019g0166 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1228-14115G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64311071 | ||||||
| chr5:64311196
|
G | C | 1 | a0001c0001t0001g0133 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1228-13990G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64311196 | ||||||
| chr5:64311217
|
T | C | 1 | a0001c0001t0001g0154 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1228-13969T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64311217 | ||||||
| chr5:64311417
|
G | A | 1 | a0001c0001t0007g0051 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1228-13769G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64311417 | ||||||
| chr5:64311444
|
G | A | 3 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054 | 3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1228-13742G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64311444 | ||||||
| chr5:64311498
|
T | G | 3 | a0001c0001t0004g0097a0001c0001t0004g0108a0001c0001t0004g0109 | 3 | HG01256.hp1 HG01258.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.1228-13688T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64311498 | ||||||
| chr5:64311705
|
A | G | 1 | a0002c0002t0008g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1228-13481A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64311705 | ||||||
| chr5:64311774
|
A | C | 1 | a0001c0001t0013g0012 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1228-13412A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64311774 | ||||||
| chr5:64311861
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1228-13325A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64311861 | ||||||
| chr5:64312026
|
C | G | 59 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(56): Show | 59 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.1228-13160C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64312026 | ||||||
| chr5:64312255
|
A | G | 6 | a0001c0001t0005g0185a0001c0001t0005g0186a0002c0002t0008g0061others(3): Show | 6 | HG00741.hp2 HG01257.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1228-12931A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64312255 | ||||||
| chr5:64312538
|
TCAGA | T | 8 | a0001c0001t0005g0188a0001c0001t0005g0189a0001c0001t0005g0190others(5): Show | 8 | HG01891.hp2 HG02559.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1228-12645_1228-12 others(10): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64312538 | |||||
| chr5:64312709
|
C | A | 3 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054 | 3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1228-12477C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64312709 | ||||||
| chr5:64313029
|
A | C | 1 | a0001c0001t0019g0166 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1228-12157A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64313029 | ||||||
| chr5:64313102
|
A | C | 1 | a0001c0001t0002g0225 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1228-12084A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64313102 | ||||||
| chr5:64313205
|
T | C | 1 | a0001c0001t0003g0025 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1228-11981T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64313205 | ||||||
| chr5:64313466
|
G | A | 1 | a0001c0001t0004g0146 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1228-11720G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64313466 | ||||||
| chr5:64313604
|
C | T | 1 | a0001c0001t0003g0021 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1228-11582C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64313604 | ||||||
| chr5:64313984
|
T | C | 1 | a0001c0001t0005g0172 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1228-11202T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64313984 | ||||||
| chr5:64314079
|
T | C | 1 | a0002c0002t0008g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1228-11107T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64314079 | ||||||
| chr5:64314152
|
G | T | 1 | a0002c0002t0006g0071 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1228-11034G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64314152 | ||||||
| chr5:64314288
|
AT | A | 114 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(111): Show | 115 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.1228-10889delT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64314288 | |||||
| chr5:64314332
|
G | C | 9 | a0001c0001t0002g0026a0001c0001t0003g0004a0001c0001t0003g0005others(6): Show | 9 | HG00642.hp2 HG00741.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.1228-10854G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64314332 | ||||||
| chr5:64314628
|
C | T | 1 | a0001c0001t0002g0215 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1228-10558C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64314628 | ||||||
| chr5:64314793
|
A | G | 1 | a0001c0001t0001g0128 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1228-10393A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64314793 | ||||||
| chr5:64314799
|
A | G | 11 | a0001c0001t0002g0203a0001c0001t0002g0204a0001c0001t0002g0207others(8): Show | 11 | HG00597.hp2 HG01243.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.1228-10387A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64314799 | ||||||
| chr5:64315290
|
G | A | 1 | a0001c0001t0002g0227 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1228-9896G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64315290 | ||||||
| chr5:64315482
|
C | T | 2 | a0001c0001t0014g0055a0001c0001t0014g0056 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1228-9704C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64315482 | ||||||
| chr5:64315533
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1228-9653T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64315533 | ||||||
| chr5:64315546
|
A | G | 5 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054others(2): Show | 5 | HG02970.hp1 HG03139.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1228-9640A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64315546 | ||||||
| chr5:64315628
|
C | CAGCTATT others(1): Show |
30 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(27): Show | 30 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1228-9555_1228-954 others(12): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64315628 | |||||
| chr5:64315664
|
G | A | 144 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(141): Show | 145 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.1228-9522G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64315664 | ||||||
| chr5:64315691
|
G | A | 20 | a0001c0001t0027g0060a0002c0002t0006g0065a0002c0002t0006g0066others(17): Show | 20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1228-9495G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64315691 | ||||||
| chr5:64315734
|
C | CA | 18 | a0001c0001t0001g0082a0001c0001t0001g0120a0001c0001t0001g0150others(15): Show | 18 | HG01361.hp1 HG02109.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.1228-9432dupA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64315734 | |||||
| chr5:64315734
|
CA | C | 21 | a0001c0001t0001g0119a0001c0001t0001g0154a0001c0001t0001g0155others(18): Show | 21 | HG00408.hp1 HG01433.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.1228-9432delA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64315734 | |||||
| chr5:64315807
|
A | C | 87 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(84): Show | 88 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1228-9379A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64315807 | ||||||
| chr5:64316015
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1228-9171C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64316015 | ||||||
| chr5:64316043
|
G | A | 1 | a0001c0001t0003g0077 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1228-9143G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64316043 | ||||||
| chr5:64316494
|
C | A | 1 | a0001c0001t0005g0186 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1228-8692C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64316494 | ||||||
| chr5:64316759
|
G | A | 1 | a0001c0001t0003g0179 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1228-8427G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64316759 | ||||||
| chr5:64317100
|
A | G | 87 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(84): Show | 88 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1228-8086A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64317100 | ||||||
| chr5:64317147
|
T | C | 30 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(27): Show | 30 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1228-8039T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64317147 | ||||||
| chr5:64317149
|
C | T | 30 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(27): Show | 30 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1228-8037C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64317149 | ||||||
| chr5:64317246
|
G | T | 1 | a0002c0002t0018g0059 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1228-7940G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64317246 | ||||||
| chr5:64317330
|
A | C | 4 | a0002c0002t0008g0061a0002c0002t0008g0062a0002c0002t0008g0063others(1): Show | 4 | HG00741.hp2 HG01257.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1228-7856A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64317330 | ||||||
| chr5:64317491
|
G | A | 3 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054 | 3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1228-7695G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64317491 | ||||||
| chr5:64317561
|
C | T | 117 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(114): Show | 118 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.1228-7625C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64317561 | ||||||
| chr5:64317563
|
C | CATACATA others(3): Show |
86 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(83): Show | 87 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.1228-7617_1228-760 others(14): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64317563 | |||||
| chr5:64317563
|
C | CATACATA others(13): Show |
1 | a0001c0001t0004g0078 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1228-7608_1228-760 others(24): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64317563 | |||||
| chr5:64317594
|
T | TTA | 25 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(22): Show | 25 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.1228-7589_1228-758 others(6): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64317594 | |||||
| chr5:64317599
|
C | T | 117 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(114): Show | 118 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.1228-7587C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64317599 | ||||||
| chr5:64317600
|
A | G | 3 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083 | 3 | HG00323.hp1 HG01106.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1228-7586A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64317600 | ||||||
| chr5:64317617
|
C | T | 4 | a0001c0001t0002g0181a0001c0001t0002g0184a0001c0001t0002g0187others(1): Show | 4 | HG01891.hp1 HG02572.hp1 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.1228-7569C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64317617 | ||||||
| chr5:64317619
|
T | C | 8 | a0001c0001t0001g0134a0001c0001t0005g0235a0001c0001t0005g0239others(5): Show | 8 | HG00408.hp2 HG00741.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.1228-7567T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64317619 | ||||||
| chr5:64317621
|
TATACAC | T | 4 | a0001c0001t0002g0181a0001c0001t0002g0184a0001c0001t0002g0187others(1): Show | 4 | HG01891.hp1 HG02572.hp1 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.1228-7563_1228-755 others(10): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64317621 | |||||
| chr5:64317623
|
T | TAC | 12 | a0001c0001t0001g0160a0001c0001t0003g0010a0001c0001t0003g0013others(9): Show | 12 | HG00642.hp2 HG01109.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1228-7537_1228-753 others(6): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64317623 | |||||
| chr5:64317623
|
T | TACAC | 17 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(14): Show | 17 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.1228-7539_1228-753 others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64317623 | |||||
| chr5:64317623
|
TAC | T | 77 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(74): Show | 78 | HG00323.hp1 HG00639.hp2 HG00741.hp2 others(75): Show |
intron_variant | MODIFIER | c.1228-7537_1228-753 others(6): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64317623 | |||||
| chr5:64317623
|
TACAC | T | 61 | a0001c0001t0001g0115a0001c0001t0002g0003a0001c0001t0002g0038others(58): Show | 61 | HG00099.hp2 HG00597.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.1228-7539_1228-753 others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64317623 | |||||
| chr5:64317625
|
C | T | 4 | a0001c0001t0001g0134a0001c0001t0005g0235a0001c0001t0005g0239others(1): Show | 4 | HG00408.hp2 NA18966.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.1228-7561C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64317625 | ||||||
| chr5:64317627
|
C | T | 4 | a0002c0002t0006g0072a0002c0002t0008g0062a0002c0002t0008g0063others(1): Show | 4 | HG00741.hp2 HG01175.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.1228-7559C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64317627 | ||||||
| chr5:64317629
|
C | T | 4 | a0002c0002t0006g0065a0002c0002t0006g0069a0002c0002t0006g0070others(1): Show | 4 | HG01081.hp1 HG01975.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1228-7557C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64317629 | ||||||
| chr5:64317758
|
T | A | 1 | a0001c0001t0001g0158 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1228-7428T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64317758 | ||||||
| chr5:64317775
|
G | T | 33 | a0001c0001t0001g0085a0001c0001t0001g0087a0001c0001t0001g0088others(30): Show | 33 | HG00099.hp1 HG00408.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.1228-7411G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64317775 | ||||||
| chr5:64317796
|
T | A | 1 | a0001c0001t0001g0123 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1228-7390T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64317796 | ||||||
| chr5:64317805
|
GA | G | 117 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(114): Show | 118 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.1228-7376delA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64317805 | |||||
| chr5:64317812
|
G | A | 142 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(139): Show | 143 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1228-7374G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64317812 | ||||||
| chr5:64317893
|
G | A | 142 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(139): Show | 143 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1228-7293G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64317893 | ||||||
| chr5:64318238
|
A | G | 1 | a0001c0001t0002g0038 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1228-6948A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64318238 | ||||||
| chr5:64318246
|
T | C | 1 | a0001c0001t0001g0127 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1228-6940T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64318246 | ||||||
| chr5:64318269
|
C | T | 1 | a0001c0001t0002g0210 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1228-6917C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64318269 | ||||||
| chr5:64318403
|
A | G | 1 | a0001c0001t0002g0209 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1228-6783A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64318403 | ||||||
| chr5:64318482
|
A | G | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG02258.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1228-6704A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64318482 | ||||||
| chr5:64318700
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1228-6486A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64318700 | ||||||
| chr5:64319102
|
G | A | 1 | a0002c0002t0006g0072 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1228-6084G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64319102 | ||||||
| chr5:64319174
|
T | TA | 30 | a0001c0001t0003g0050a0001c0001t0004g0002a0001c0001t0004g0078others(27): Show | 31 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(28): Show |
intron_variant | MODIFIER | c.1228-5995dupA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64319174 | |||||
| chr5:64319174
|
TA | T | 30 | a0001c0001t0001g0130a0001c0001t0002g0026a0001c0001t0002g0206others(27): Show | 30 | HG00642.hp2 HG00741.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.1228-5995delA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64319174 | |||||
| chr5:64319482
|
G | A | 1 | a0001c0001t0007g0037 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1228-5704G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64319482 | ||||||
| chr5:64320090
|
C | G | 4 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0198others(1): Show | 4 | HG02559.hp2 HG02886.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1228-5096C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64320090 | ||||||
| chr5:64320234
|
C | T | 2 | a0001c0001t0001g0129a0001c0001t0001g0142 | 2 | HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1228-4952C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64320234 | ||||||
| chr5:64320250
|
A | T | 142 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(139): Show | 143 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1228-4936A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64320250 | ||||||
| chr5:64320419
|
A | G | 1 | a0001c0001t0019g0166 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1228-4767A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64320419 | ||||||
| chr5:64320732
|
G | A | 1 | a0001c0001t0003g0194 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1228-4454G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64320732 | ||||||
| chr5:64320897
|
G | C | 87 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(84): Show | 88 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1228-4289G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64320897 | ||||||
| chr5:64321027
|
G | A | 1 | a0001c0001t0005g0188 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1228-4159G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64321027 | ||||||
| chr5:64321037
|
CA | C | 87 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(84): Show | 88 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1228-4138delA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64321037 | |||||
| chr5:64321193
|
A | G | 28 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(25): Show | 28 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.1228-3993A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64321193 | ||||||
| chr5:64321245
|
A | G | 27 | a0001c0001t0004g0002a0001c0001t0004g0078a0001c0001t0004g0086others(24): Show | 28 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.1228-3941A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64321245 | ||||||
| chr5:64321359
|
A | G | 20 | a0001c0001t0027g0060a0002c0002t0006g0065a0002c0002t0006g0066others(17): Show | 20 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1228-3827A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64321359 | ||||||
| chr5:64321375
|
A | G | 1 | a0001c0001t0002g0226 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1228-3811A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64321375 | ||||||
| chr5:64321597
|
G | A | 27 | a0001c0001t0004g0002a0001c0001t0004g0078a0001c0001t0004g0086others(24): Show | 28 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.1228-3589G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64321597 | ||||||
| chr5:64321628
|
T | C | 2 | a0001c0001t0014g0055a0001c0001t0014g0056 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1228-3558T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64321628 | ||||||
| chr5:64321674
|
C | T | 4 | a0002c0002t0010g0057a0002c0002t0010g0058a0002c0002t0010g0076others(1): Show | 4 | HG02109.hp2 HG02622.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1228-3512C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64321674 | ||||||
| chr5:64321721
|
A | G | 1 | a0001c0001t0001g0114 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1228-3465A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64321721 | ||||||
| chr5:64321738
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1228-3448G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64321738 | ||||||
| chr5:64321879
|
C | T | 1 | a0001c0001t0005g0173 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1228-3307C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64321879 | ||||||
| chr5:64322602
|
C | CGT | 23 | a0001c0001t0003g0007a0001c0001t0003g0013a0001c0001t0004g0078others(20): Show | 23 | HG00642.hp2 HG01255.hp1 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.1228-2549_1228-254 others(6): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64322602 | |||||
| chr5:64322602
|
C | CGTGT | 13 | a0001c0001t0002g0038a0001c0001t0002g0177a0001c0001t0002g0180others(10): Show | 13 | HG00733.hp2 HG01109.hp1 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.1228-2551_1228-254 others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64322602 | |||||
| chr5:64322602
|
C | CGTGTGT | 19 | a0001c0001t0002g0202a0001c0001t0002g0203a0001c0001t0002g0207others(16): Show | 19 | HG00597.hp2 HG00741.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.1228-2553_1228-254 others(10): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64322602 | |||||
| chr5:64322602
|
C | CGTGTGTG others(1): Show |
24 | a0001c0001t0002g0003a0001c0001t0002g0080a0001c0001t0002g0176others(21): Show | 25 | HG00099.hp2 HG01074.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.1228-2555_1228-254 others(12): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64322602 | |||||
| chr5:64322602
|
C | CGTGTGTG others(3): Show |
11 | a0001c0001t0002g0174a0001c0001t0002g0206a0001c0001t0002g0215others(8): Show | 11 | HG00738.hp2 HG01243.hp2 HG01993.hp2 others(8): Show |
intron_variant | MODIFIER | c.1228-2557_1228-254 others(14): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64322602 | |||||
| chr5:64322602
|
C | CGTGTGTG others(5): Show |
11 | a0001c0001t0002g0183a0001c0001t0002g0208a0001c0001t0002g0214others(8): Show | 11 | HG01243.hp1 HG02004.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1228-2559_1228-254 others(16): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64322602 | |||||
| chr5:64322602
|
C | CGTGTGTG others(7): Show |
5 | a0001c0001t0002g0211a0001c0001t0002g0212a0001c0001t0002g0217others(2): Show | 5 | HG00642.hp1 HG01928.hp2 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.1228-2561_1228-254 others(18): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64322602 | |||||
| chr5:64322602
|
CGT | C | 6 | a0001c0001t0002g0184a0001c0001t0002g0187a0001c0001t0003g0027others(3): Show | 6 | HG01891.hp1 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1228-2549_1228-254 others(6): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64322602 | |||||
| chr5:64322602
|
CGTGTGT | C | 9 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(6): Show | 9 | HG02055.hp2 HG02622.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.1228-2553_1228-254 others(10): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64322602 | |||||
| chr5:64322602
|
CGTGTGTG others(1): Show |
C | 49 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(46): Show | 49 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.1228-2555_1228-254 others(12): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64322602 | |||||
| chr5:64322602
|
CGTGTGTG others(3): Show |
C | 3 | a0001c0001t0005g0185a0001c0001t0005g0186a0001c0001t0019g0166 | 3 | HG02886.hp2 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1228-2557_1228-254 others(14): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64322602 | |||||
| chr5:64322602
|
CGTGTGTG others(5): Show |
C | 27 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(24): Show | 27 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.1228-2559_1228-254 others(16): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64322602 | |||||
| chr5:64322656
|
A | G | 87 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(84): Show | 88 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1228-2530A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64322656 | ||||||
| chr5:64322672
|
G | A | 1 | a0002c0002t0008g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1228-2514G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64322672 | ||||||
| chr5:64323286
|
A | T | 2 | a0001c0001t0014g0055a0001c0001t0014g0056 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1228-1900A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64323286 | ||||||
| chr5:64323396
|
T | C | 1 | a0001c0001t0019g0166 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1228-1790T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64323396 | ||||||
| chr5:64323539
|
A | AAATAAT | 4 | a0001c0001t0001g0120a0001c0001t0001g0147a0001c0001t0001g0148others(1): Show | 4 | HG02258.hp2 HG02647.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1228-1633_1228-162 others(10): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 64323539 | |||||
| chr5:64323583
|
T | C | 1 | a0001c0001t0027g0060 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1228-1603T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64323583 | ||||||
| chr5:64323640
|
C | T | 1 | a0002c0002t0010g0076 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1228-1546C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64323640 | ||||||
| chr5:64323948
|
G | T | 1 | a0001c0001t0019g0166 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1228-1238G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64323948 | ||||||
| chr5:64324137
|
A | G | 1 | a0001c0001t0002g0080 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1228-1049A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64324137 | ||||||
| chr5:64324426
|
G | A | 4 | a0001c0001t0002g0176a0001c0001t0002g0180a0001c0001t0020g0023others(1): Show | 4 | HG00733.hp2 HG01168.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.1228-760G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64324426 | ||||||
| chr5:64324489
|
G | A | 2 | a0001c0001t0005g0185a0001c0001t0005g0186 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1228-697G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64324489 | ||||||
| chr5:64324508
|
G | A | 2 | a0001c0001t0005g0185a0001c0001t0005g0186 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1228-678G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64324508 | ||||||
| chr5:64324563
|
T | G | 1 | a0001c0001t0005g0172 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1228-623T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64324563 | ||||||
| chr5:64324742
|
G | A | 1 | a0002c0002t0016g0067 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1228-444G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64324742 | ||||||
| chr5:64324815
|
A | G | 1 | a0001c0001t0003g0013 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1228-371A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64324815 | ||||||
| chr5:64324832
|
A | G | 1 | a0001c0001t0003g0077 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1228-354A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 5/7 | chr5 | 64324832 | ||||||
| chr5:64325419
|
T | G | 1 | a0002c0002t0008g0061 | 1 | HG02280.hp1 | splice_region_variant&intron_variant | LOW | c.1453+8T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64325419 | ||||||
| chr5:64325568
|
T | G | 1 | a0001c0001t0003g0028 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1453+157T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64325568 | ||||||
| chr5:64325673
|
G | C | 6 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(3): Show | 6 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1453+262G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64325673 | ||||||
| chr5:64325713
|
T | C | 30 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(27): Show | 30 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1453+302T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64325713 | ||||||
| chr5:64325790
|
C | A | 1 | a0001c0001t0005g0239 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1453+379C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64325790 | ||||||
| chr5:64325791
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1453+380C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64325791 | ||||||
| chr5:64326049
|
A | G | 30 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(27): Show | 30 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1453+638A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64326049 | ||||||
| chr5:64326091
|
A | G | 87 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(84): Show | 88 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1453+680A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64326091 | ||||||
| chr5:64326164
|
G | A | 117 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(114): Show | 118 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.1453+753G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64326164 | ||||||
| chr5:64326190
|
G | A | 3 | a0001c0001t0003g0048a0001c0001t0003g0049a0001c0001t0003g0050 | 3 | HG00408.hp1 HG02074.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.1453+779G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64326190 | ||||||
| chr5:64326206
|
T | G | 246 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(243): Show | 248 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.1453+795T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64326206 | ||||||
| chr5:64326246
|
C | G | 1 | a0001c0001t0004g0099 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1453+835C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64326246 | ||||||
| chr5:64326283
|
T | C | 1 | a0001c0001t0005g0188 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1453+872T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64326283 | ||||||
| chr5:64326354
|
T | C | 142 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(139): Show | 143 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1453+943T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64326354 | ||||||
| chr5:64326360
|
A | G | 1 | a0001c0001t0001g0160 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1453+949A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64326360 | ||||||
| chr5:64326593
|
A | C | 142 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(139): Show | 143 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1453+1182A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64326593 | ||||||
| chr5:64326674
|
G | T | 7 | a0001c0001t0004g0002a0001c0001t0004g0099a0001c0001t0004g0100others(4): Show | 8 | HG01243.hp2 HG01978.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1453+1263G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64326674 | ||||||
| chr5:64326784
|
T | C | 1 | a0001c0001t0003g0077 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1453+1373T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64326784 | ||||||
| chr5:64326913
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1453+1502G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64326913 | ||||||
| chr5:64327084
|
G | A | 6 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0198others(3): Show | 6 | HG02559.hp2 HG02886.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1453+1673G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64327084 | ||||||
| chr5:64327448
|
T | C | 1 | a0001c0001t0002g0080 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1453+2037T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64327448 | ||||||
| chr5:64327547
|
G | A | 1 | a0001c0001t0004g0089 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1453+2136G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64327547 | ||||||
| chr5:64327794
|
T | C | 27 | a0001c0001t0004g0002a0001c0001t0004g0078a0001c0001t0004g0086others(24): Show | 28 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.1453+2383T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64327794 | ||||||
| chr5:64327882
|
T | C | 2 | a0001c0001t0014g0055a0001c0001t0014g0056 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1454-2399T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64327882 | ||||||
| chr5:64328171
|
C | T | 2 | a0001c0001t0002g0184a0001c0001t0002g0187 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1454-2110C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64328171 | ||||||
| chr5:64328206
|
TG | T | 8 | a0001c0001t0005g0188a0001c0001t0005g0189a0001c0001t0005g0190others(5): Show | 8 | HG01891.hp2 HG02559.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1454-2068delG | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr5 | 64328206 | |||||
| chr5:64328599
|
G | A | 21 | a0001c0001t0002g0003a0001c0001t0002g0038a0001c0001t0002g0174others(18): Show | 21 | HG00733.hp2 HG00738.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.1454-1682G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64328599 | ||||||
| chr5:64328752
|
A | G | 87 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(84): Show | 88 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1454-1529A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64328752 | ||||||
| chr5:64329018
|
A | G | 1 | a0001c0001t0004g0245 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1454-1263A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64329018 | ||||||
| chr5:64329274
|
T | C | 1 | a0001c0001t0004g0091 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1454-1007T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64329274 | ||||||
| chr5:64329292
|
C | T | 142 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(139): Show | 143 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1454-989C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64329292 | ||||||
| chr5:64329372
|
A | G | 1 | a0001c0001t0012g0197 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1454-909A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64329372 | ||||||
| chr5:64329383
|
G | A | 2 | a0002c0002t0006g0074a0002c0002t0006g0075 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1454-898G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64329383 | ||||||
| chr5:64329457
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1454-824C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64329457 | ||||||
| chr5:64329457
|
CT | C | 7 | a0001c0001t0004g0091a0001c0001t0007g0029a0001c0001t0007g0051others(4): Show | 7 | HG01123.hp2 HG02280.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1454-809delT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr5 | 64329457 | |||||
| chr5:64329472
|
T | C | 1 | a0001c0001t0003g0010 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1454-809T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64329472 | ||||||
| chr5:64329479
|
A | G | 1 | a0001c0001t0003g0015 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1454-802A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64329479 | ||||||
| chr5:64329526
|
C | A | 2 | a0001c0001t0005g0185a0001c0001t0005g0186 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1454-755C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64329526 | ||||||
| chr5:64329657
|
C | T | 1 | a0002c0002t0008g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1454-624C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64329657 | ||||||
| chr5:64329787
|
C | T | 5 | a0001c0001t0005g0188a0001c0001t0005g0190a0001c0001t0005g0191others(2): Show | 5 | HG01891.hp2 HG02559.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1454-494C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64329787 | ||||||
| chr5:64329949
|
G | C | 59 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(56): Show | 59 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.1454-332G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64329949 | ||||||
| chr5:64330190
|
A | G | 3 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054 | 3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1454-91A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 6/7 | chr5 | 64330190 | ||||||
| chr5:64330466
|
A | G | 1 | a0001c0001t0002g0038 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1579+60A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64330466 | ||||||
| chr5:64330663
|
T | C | 1 | a0001c0001t0004g0078 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1579+257T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64330663 | ||||||
| chr5:64331187
|
G | A | 87 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(84): Show | 88 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1579+781G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64331187 | ||||||
| chr5:64331291
|
G | T | 1 | a0001c0001t0019g0166 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1579+885G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64331291 | ||||||
| chr5:64331344
|
G | A | 1 | a0002c0002t0008g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1579+938G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64331344 | ||||||
| chr5:64331400
|
A | G | 1 | a0001c0001t0003g0043 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1579+994A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64331400 | ||||||
| chr5:64331406
|
A | T | 27 | a0001c0001t0004g0002a0001c0001t0004g0078a0001c0001t0004g0086others(24): Show | 28 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.1579+1000A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64331406 | ||||||
| chr5:64331550
|
G | A | 2 | a0001c0001t0004g0248a0001c0001t0005g0189 | 2 | HG01978.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1579+1144G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64331550 | ||||||
| chr5:64331591
|
T | G | 1 | a0001c0001t0001g0116 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1579+1185T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64331591 | ||||||
| chr5:64331753
|
G | A | 1 | a0001c0001t0003g0027 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1579+1347G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64331753 | ||||||
| chr5:64331796
|
G | A | 5 | a0001c0001t0001g0113a0001c0001t0001g0125a0001c0001t0001g0128others(2): Show | 5 | HG01074.hp1 HG01081.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.1579+1390G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64331796 | ||||||
| chr5:64331852
|
C | T | 2 | a0001c0001t0007g0029a0001c0001t0007g0051 | 2 | HG01123.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1579+1446C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64331852 | ||||||
| chr5:64332005
|
G | A | 1 | a0001c0001t0001g0154 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1579+1599G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64332005 | ||||||
| chr5:64332532
|
T | C | 142 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(139): Show | 143 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1579+2126T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64332532 | ||||||
| chr5:64332750
|
G | A | 20 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(17): Show | 20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1579+2344G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64332750 | ||||||
| chr5:64332850
|
A | G | 1 | a0001c0001t0001g0122 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1579+2444A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64332850 | ||||||
| chr5:64332859
|
A | G | 1 | a0001c0001t0005g0191 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1579+2453A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64332859 | ||||||
| chr5:64333364
|
G | A | 2 | a0001c0001t0002g0184a0001c0001t0002g0187 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1579+2958G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64333364 | ||||||
| chr5:64333912
|
G | A | 105 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(102): Show | 106 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.1579+3506G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64333912 | ||||||
| chr5:64334274
|
C | T | 2 | a0001c0001t0005g0185a0001c0001t0005g0186 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1579+3868C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64334274 | ||||||
| chr5:64334547
|
GTTC | G | 23 | a0001c0001t0002g0204a0001c0001t0004g0086a0001c0001t0004g0092others(20): Show | 23 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.1579+4147_1579+414 others(7): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64334547 | |||||
| chr5:64334672
|
A | G | 18 | a0001c0001t0004g0086a0001c0001t0004g0092a0001c0001t0027g0060others(15): Show | 18 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.1579+4266A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64334672 | ||||||
| chr5:64334713
|
C | T | 1 | a0001c0001t0002g0210 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1579+4307C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64334713 | ||||||
| chr5:64334746
|
T | C | 4 | a0001c0001t0003g0007a0001c0001t0003g0009a0001c0001t0003g0024others(1): Show | 4 | HG00639.hp1 HG01433.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.1579+4340T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64334746 | ||||||
| chr5:64334853
|
C | G | 58 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(55): Show | 58 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.1579+4447C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64334853 | ||||||
| chr5:64334921
|
G | A | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1579+4515G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64334921 | ||||||
| chr5:64334924
|
T | C | 2 | a0001c0001t0003g0198a0001c0001t0003g0199 | 2 | HG02559.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1579+4518T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64334924 | ||||||
| chr5:64335013
|
T | C | 2 | a0001c0001t0014g0055a0001c0001t0014g0056 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1579+4607T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64335013 | ||||||
| chr5:64335127
|
T | G | 115 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(112): Show | 116 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1579+4721T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64335127 | ||||||
| chr5:64335177
|
T | A | 4 | a0001c0001t0007g0001a0001c0001t0007g0031a0001c0001t0007g0033others(1): Show | 5 | HG01255.hp2 HG01346.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.1579+4771T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64335177 | ||||||
| chr5:64335256
|
A | G | 1 | a0001c0001t0002g0210 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1579+4850A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64335256 | ||||||
| chr5:64335501
|
G | T | 1 | a0001c0001t0004g0091 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1579+5095G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64335501 | ||||||
| chr5:64335508
|
TG | T | 22 | a0001c0001t0004g0086a0001c0001t0004g0092a0001c0001t0027g0060others(19): Show | 22 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.1579+5104delG | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64335508 | |||||
| chr5:64335844
|
A | G | 25 | a0001c0001t0004g0002a0001c0001t0004g0078a0001c0001t0004g0089others(22): Show | 26 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.1579+5438A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64335844 | ||||||
| chr5:64335936
|
T | C | 1 | a0001c0001t0028g0193 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1579+5530T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64335936 | ||||||
| chr5:64335970
|
G | A | 1 | a0001c0001t0003g0039 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1579+5564G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64335970 | ||||||
| chr5:64335999
|
G | A | 1 | a0001c0001t0007g0031 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1579+5593G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64335999 | ||||||
| chr5:64336042
|
G | C | 1 | a0001c0001t0004g0091 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1579+5636G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64336042 | ||||||
| chr5:64336345
|
T | C | 1 | a0001c0001t0021g0046 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1579+5939T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64336345 | ||||||
| chr5:64336377
|
A | G | 3 | a0001c0001t0003g0010a0001c0001t0003g0013a0001c0001t0003g0016 | 3 | HG02602.hp1 HG03491.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1579+5971A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64336377 | ||||||
| chr5:64336384
|
G | A | 1 | a0001c0001t0005g0170 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1579+5978G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64336384 | ||||||
| chr5:64336390
|
CTATT | C | 33 | a0001c0001t0001g0085a0001c0001t0001g0087a0001c0001t0001g0088others(30): Show | 33 | HG00099.hp1 HG00408.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.1579+5985_1579+598 others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64336390 | ||||||
| chr5:64336451
|
C | G | 1 | a0001c0001t0026g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1579+6045C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64336451 | ||||||
| chr5:64336453
|
A | G | 1 | a0002c0002t0016g0067 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1579+6047A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64336453 | ||||||
| chr5:64336758
|
C | A | 2 | a0001c0001t0005g0185a0001c0001t0005g0186 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1579+6352C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64336758 | ||||||
| chr5:64336997
|
TG | T | 82 | a0001c0001t0001g0079a0001c0001t0001g0085a0001c0001t0001g0087others(79): Show | 82 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.1579+6592delG | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64336997 | ||||||
| chr5:64336998
|
G | T | 49 | a0001c0001t0004g0002a0001c0001t0004g0086a0001c0001t0004g0092others(46): Show | 50 | HG00597.hp1 HG01074.hp2 HG01081.hp1 others(47): Show |
intron_variant | MODIFIER | c.1579+6592G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64336998 | ||||||
| chr5:64337001
|
G | GTT | 3 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083 | 3 | HG00323.hp1 HG01106.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1579+6596_1579+659 others(6): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64337001 | |||||
| chr5:64337009
|
T | G | 12 | a0001c0001t0001g0111a0001c0001t0001g0116a0001c0001t0001g0117others(9): Show | 12 | HG01891.hp2 HG02055.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1579+6603T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64337009 | ||||||
| chr5:64337009
|
T | TG | 3 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083 | 3 | HG00323.hp1 HG01106.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1579+6603_1579+660 others(5): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64337009 | ||||||
| chr5:64337092
|
G | T | 4 | a0001c0001t0009g0035a0001c0001t0009g0036a0001c0001t0009g0042others(1): Show | 4 | HG00323.hp2 HG01175.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1579+6686G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64337092 | ||||||
| chr5:64337130
|
C | T | 28 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(25): Show | 28 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.1579+6724C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64337130 | ||||||
| chr5:64337176
|
G | T | 2 | a0001c0001t0014g0055a0001c0001t0014g0056 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1579+6770G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64337176 | ||||||
| chr5:64337420
|
A | G | 6 | a0001c0001t0005g0188a0001c0001t0005g0189a0001c0001t0005g0190others(3): Show | 6 | HG01891.hp2 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1579+7014A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64337420 | ||||||
| chr5:64337583
|
G | A | 2 | a0001c0001t0003g0200a0001c0001t0003g0201 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1579+7177G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64337583 | ||||||
| chr5:64337753
|
G | A | 5 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1579+7347G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64337753 | ||||||
| chr5:64338114
|
T | C | 85 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(82): Show | 86 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.1579+7708T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64338114 | ||||||
| chr5:64338272
|
A | G | 2 | a0001c0001t0014g0055a0001c0001t0014g0056 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1579+7866A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64338272 | ||||||
| chr5:64338402
|
A | T | 1 | a0001c0001t0002g0181 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1579+7996A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64338402 | ||||||
| chr5:64338451
|
G | A | 1 | a0001c0001t0026g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1579+8045G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64338451 | ||||||
| chr5:64338452
|
G | T | 18 | a0001c0001t0004g0078a0001c0001t0004g0089a0001c0001t0004g0090others(15): Show | 18 | HG01255.hp1 HG01256.hp1 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.1579+8046G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64338452 | ||||||
| chr5:64338493
|
G | T | 1 | a0001c0001t0002g0206 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1579+8087G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64338493 | ||||||
| chr5:64338504
|
G | A | 3 | a0001c0001t0002g0180a0001c0001t0020g0023a0006c0006t0002g0175 | 3 | HG00733.hp2 HG01168.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.1579+8098G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64338504 | ||||||
| chr5:64338506
|
G | A | 2 | a0001c0001t0002g0184a0001c0001t0002g0187 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1579+8100G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64338506 | ||||||
| chr5:64338591
|
C | T | 1 | a0001c0001t0026g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1579+8185C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64338591 | ||||||
| chr5:64338634
|
C | CA | 23 | a0001c0001t0003g0025a0001c0001t0005g0167a0001c0001t0005g0168others(20): Show | 23 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.1579+8244dupA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64338634 | |||||
| chr5:64338634
|
CA | C | 11 | a0001c0001t0001g0136a0001c0001t0002g0204a0001c0001t0004g0086others(8): Show | 11 | HG01516.hp2 HG02109.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1579+8244delA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64338634 | |||||
| chr5:64338797
|
T | A | 22 | a0001c0001t0002g0080a0001c0001t0002g0202a0001c0001t0002g0203others(19): Show | 22 | HG00099.hp2 HG00597.hp2 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.1579+8391T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64338797 | ||||||
| chr5:64338831
|
C | T | 1 | a0001c0001t0025g0105 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1579+8425C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64338831 | ||||||
| chr5:64338909
|
C | T | 1 | a0001c0001t0002g0176 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1579+8503C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64338909 | ||||||
| chr5:64339089
|
G | A | 1 | a0001c0001t0003g0007 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1579+8683G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64339089 | ||||||
| chr5:64339139
|
G | A | 1 | a0001c0001t0004g0245 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1579+8733G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64339139 | ||||||
| chr5:64339407
|
AT | A | 28 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(25): Show | 28 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.1579+9007delT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64339407 | |||||
| chr5:64339694
|
T | G | 1 | a0001c0001t0004g0002 | 2 | HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1579+9288T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64339694 | ||||||
| chr5:64339797
|
A | G | 2 | a0001c0001t0002g0184a0001c0001t0002g0187 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1579+9391A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64339797 | ||||||
| chr5:64339988
|
T | C | 1 | a0001c0001t0005g0189 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1579+9582T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64339988 | ||||||
| chr5:64340054
|
A | G | 3 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0143 | 3 | HG01256.hp2 HG02148.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1579+9648A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64340054 | ||||||
| chr5:64340500
|
T | C | 1 | a0003c0007t0002g0205 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1579+10094T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64340500 | ||||||
| chr5:64340753
|
G | T | 1 | a0001c0001t0005g0172 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1579+10347G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64340753 | ||||||
| chr5:64341379
|
G | A | 2 | a0001c0001t0003g0200a0001c0001t0003g0201 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1579+10973G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64341379 | ||||||
| chr5:64341481
|
G | A | 2 | a0001c0001t0005g0185a0001c0001t0005g0186 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1579+11075G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64341481 | ||||||
| chr5:64341526
|
G | A | 12 | a0001c0001t0027g0060a0002c0002t0006g0065a0002c0002t0006g0066others(9): Show | 12 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.1579+11120G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64341526 | ||||||
| chr5:64341538
|
C | T | 5 | a0001c0001t0005g0188a0001c0001t0005g0190a0001c0001t0005g0191others(2): Show | 5 | HG01891.hp2 HG02559.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1579+11132C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64341538 | ||||||
| chr5:64341621
|
G | A | 2 | a0001c0001t0005g0185a0001c0001t0005g0186 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1579+11215G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64341621 | ||||||
| chr5:64342078
|
C | T | 2 | a0001c0001t0005g0185a0001c0001t0005g0186 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1579+11672C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64342078 | ||||||
| chr5:64342213
|
C | T | 1 | a0001c0001t0002g0228 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1579+11807C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64342213 | ||||||
| chr5:64342348
|
T | C | 1 | a0001c0001t0001g0126 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1579+11942T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64342348 | ||||||
| chr5:64342431
|
G | T | 3 | a0002c0002t0010g0057a0002c0002t0010g0058a0002c0002t0018g0059 | 3 | HG02109.hp2 HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1579+12025G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64342431 | ||||||
| chr5:64342505
|
G | C | 5 | a0001c0001t0007g0037a0001c0001t0009g0035a0001c0001t0009g0036others(2): Show | 5 | HG00323.hp2 HG01175.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1579+12099G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64342505 | ||||||
| chr5:64342823
|
T | C | 1 | a0001c0001t0005g0189 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1579+12417T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64342823 | ||||||
| chr5:64343462
|
AATTTTCC others(485): Show |
A | 1 | a0001c0001t0002g0217 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1579+13218_1579+13 others(6): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64343462 | |||||
| chr5:64343533
|
GA | G | 5 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1579+13130delA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64343533 | |||||
| chr5:64343772
|
A | G | 5 | a0001c0001t0007g0037a0001c0001t0009g0035a0001c0001t0009g0036others(2): Show | 5 | HG00323.hp2 HG01175.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1579+13366A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64343772 | ||||||
| chr5:64343870
|
A | T | 5 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054others(2): Show | 5 | HG02970.hp1 HG03139.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1579+13464A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64343870 | ||||||
| chr5:64343956
|
T | C | 1 | a0001c0001t0019g0166 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1579+13550T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64343956 | ||||||
| chr5:64344144
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1579+13738C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64344144 | ||||||
| chr5:64344183
|
C | A | 85 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(82): Show | 86 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.1579+13777C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64344183 | ||||||
| chr5:64344235
|
G | A | 12 | a0001c0001t0027g0060a0002c0002t0006g0065a0002c0002t0006g0066others(9): Show | 12 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.1579+13829G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64344235 | ||||||
| chr5:64344362
|
C | T | 198 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(195): Show | 199 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.1579+13956C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64344362 | ||||||
| chr5:64344368
|
A | C | 1 | a0001c0001t0001g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1579+13962A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64344368 | ||||||
| chr5:64344374
|
C | T | 3 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054 | 3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1579+13968C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64344374 | ||||||
| chr5:64344435
|
G | A | 245 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(242): Show | 247 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.1579+14029G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64344435 | ||||||
| chr5:64344444
|
G | A | 2 | a0001c0001t0014g0055a0001c0001t0014g0056 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1579+14038G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64344444 | ||||||
| chr5:64344530
|
A | AAAAG | 142 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(139): Show | 143 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1579+14127_1579+14 others(10): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64344530 | |||||
| chr5:64344822
|
G | A | 142 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(139): Show | 143 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1579+14416G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64344822 | ||||||
| chr5:64344944
|
C | A | 1 | a0001c0001t0005g0169 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1579+14538C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64344944 | ||||||
| chr5:64345320
|
A | G | 1 | a0001c0001t0004g0100 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1579+14914A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64345320 | ||||||
| chr5:64345568
|
T | G | 30 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(27): Show | 30 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1579+15162T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64345568 | ||||||
| chr5:64345651
|
C | T | 1 | a0001c0001t0003g0014 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1579+15245C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64345651 | ||||||
| chr5:64345698
|
A | G | 2 | a0001c0001t0014g0055a0001c0001t0014g0056 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1579+15292A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64345698 | ||||||
| chr5:64345724
|
G | T | 1 | a0002c0002t0016g0067 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1579+15318G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64345724 | ||||||
| chr5:64345779
|
C | G | 11 | a0001c0001t0002g0203a0001c0001t0002g0204a0001c0001t0002g0207others(8): Show | 11 | HG00597.hp2 HG01243.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.1579+15373C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64345779 | ||||||
| chr5:64345848
|
C | CA | 4 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0198others(1): Show | 4 | HG02559.hp2 HG02886.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1579+15449dupA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64345848 | |||||
| chr5:64345978
|
C | A | 2 | a0001c0001t0002g0222a0001c0003t0002g0246 | 2 | HG02040.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1579+15572C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64345978 | ||||||
| chr5:64345987
|
A | ATCT | 141 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(138): Show | 142 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.1579+15582_1579+15 others(9): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64345987 | |||||
| chr5:64346097
|
T | G | 1 | a0001c0001t0002g0181 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1579+15691T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64346097 | ||||||
| chr5:64346106
|
G | A | 87 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(84): Show | 88 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1579+15700G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64346106 | ||||||
| chr5:64346135
|
G | A | 1 | a0001c0001t0005g0172 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1579+15729G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64346135 | ||||||
| chr5:64346198
|
CATCTT | C | 6 | a0001c0001t0005g0188a0001c0001t0005g0189a0001c0001t0005g0190others(3): Show | 6 | HG01891.hp2 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1579+15798_1579+15 others(11): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64346198 | |||||
| chr5:64346219
|
A | G | 1 | a0001c0001t0004g0248 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1579+15813A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64346219 | ||||||
| chr5:64346296
|
G | GT | 37 | a0001c0001t0001g0085a0001c0001t0001g0087a0001c0001t0001g0088others(34): Show | 37 | HG00099.hp1 HG00408.hp2 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.1579+15899dupT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64346296 | |||||
| chr5:64346359
|
C | CT | 54 | a0001c0001t0001g0117a0001c0001t0001g0154a0001c0001t0001g0155others(51): Show | 54 | HG00733.hp2 HG00738.hp2 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.1579+15980dupT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64346359 | |||||
| chr5:64346359
|
C | CTT | 5 | a0001c0001t0002g0177a0002c0002t0006g0065a0002c0002t0006g0069others(2): Show | 5 | HG00741.hp2 HG01109.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.1579+15979_1579+15 others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64346359 | |||||
| chr5:64346359
|
CT | C | 29 | a0001c0001t0001g0081a0001c0001t0001g0115a0001c0001t0001g0130others(26): Show | 29 | HG00323.hp1 HG01256.hp1 HG01256.hp2 others(26): Show |
intron_variant | MODIFIER | c.1579+15980delT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64346359 | |||||
| chr5:64346359
|
CTT | C | 9 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0198others(6): Show | 9 | HG02109.hp1 HG02559.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1579+15979_1579+15 others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64346359 | |||||
| chr5:64346961
|
T | C | 3 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054 | 3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1579+16555T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64346961 | ||||||
| chr5:64347012
|
C | T | 1 | a0001c0001t0005g0172 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1579+16606C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64347012 | ||||||
| chr5:64347340
|
G | A | 28 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(25): Show | 28 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.1579+16934G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64347340 | ||||||
| chr5:64347374
|
G | A | 1 | a0001c0001t0025g0105 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1579+16968G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64347374 | ||||||
| chr5:64347406
|
A | G | 1 | a0001c0001t0005g0172 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1579+17000A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64347406 | ||||||
| chr5:64347428
|
G | A | 1 | a0001c0001t0004g0097 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1579+17022G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64347428 | ||||||
| chr5:64347435
|
C | G | 1 | a0001c0001t0024g0192 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1579+17029C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64347435 | ||||||
| chr5:64347462
|
G | T | 1 | a0001c0001t0001g0083 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1579+17056G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64347462 | ||||||
| chr5:64347544
|
T | A | 3 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054 | 3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1579+17138T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64347544 | ||||||
| chr5:64347554
|
G | A | 28 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(25): Show | 28 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.1579+17148G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64347554 | ||||||
| chr5:64347830
|
C | G | 20 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(17): Show | 20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1579+17424C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64347830 | ||||||
| chr5:64347880
|
G | T | 1 | a0001c0001t0003g0045 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1579+17474G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64347880 | ||||||
| chr5:64348223
|
G | A | 1 | a0001c0001t0002g0176 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1579+17817G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64348223 | ||||||
| chr5:64348490
|
A | G | 2 | a0001c0001t0014g0055a0001c0001t0014g0056 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1579+18084A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64348490 | ||||||
| chr5:64348495
|
A | AT | 5 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097others(2): Show | 5 | HG01255.hp1 HG01256.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1579+18094dupT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64348495 | |||||
| chr5:64348710
|
C | A | 1 | a0001c0001t0002g0187 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1579+18304C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64348710 | ||||||
| chr5:64348753
|
C | A | 3 | a0002c0002t0008g0062a0002c0002t0008g0063a0002c0002t0008g0064 | 3 | HG00741.hp2 HG01257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1579+18347C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64348753 | ||||||
| chr5:64349096
|
T | G | 12 | a0001c0001t0027g0060a0002c0002t0006g0065a0002c0002t0006g0066others(9): Show | 12 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.1579+18690T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64349096 | ||||||
| chr5:64349283
|
C | T | 1 | a0001c0001t0005g0237 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1579+18877C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64349283 | ||||||
| chr5:64349410
|
C | CT | 86 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0085others(83): Show | 87 | HG00099.hp1 HG00408.hp2 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.1579+19016dupT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64349410 | |||||
| chr5:64349410
|
C | CTT | 16 | a0001c0001t0001g0118a0001c0001t0001g0125a0001c0001t0001g0128others(13): Show | 16 | HG01081.hp2 HG01106.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1579+19015_1579+19 others(8): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64349410 | |||||
| chr5:64349673
|
T | G | 31 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(28): Show | 31 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.1579+19267T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64349673 | ||||||
| chr5:64349702
|
C | T | 1 | a0002c0002t0006g0068 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1579+19296C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64349702 | ||||||
| chr5:64349795
|
C | G | 1 | a0001c0001t0003g0015 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1579+19389C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64349795 | ||||||
| chr5:64349929
|
T | G | 1 | a0001c0001t0004g0104 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1579+19523T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64349929 | ||||||
| chr5:64349935
|
T | A | 2 | a0001c0001t0001g0126a0001c0001t0001g0137 | 2 | HG01123.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1579+19529T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64349935 | ||||||
| chr5:64350187
|
T | C | 15 | a0002c0002t0006g0065a0002c0002t0006g0066a0002c0002t0006g0068others(12): Show | 15 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.1580-19428T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64350187 | ||||||
| chr5:64350322
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1580-19293C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64350322 | ||||||
| chr5:64350352
|
G | A | 27 | a0001c0001t0004g0002a0001c0001t0004g0078a0001c0001t0004g0086others(24): Show | 28 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.1580-19263G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64350352 | ||||||
| chr5:64350435
|
C | G | 3 | a0001c0001t0001g0129a0001c0001t0001g0142a0001c0001t0005g0084 | 3 | HG02257.hp2 HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1580-19180C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64350435 | ||||||
| chr5:64350436
|
G | T | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1580-19179G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64350436 | ||||||
| chr5:64350456
|
T | C | 142 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(139): Show | 143 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1580-19159T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64350456 | ||||||
| chr5:64350465
|
A | G | 1 | a0001c0001t0025g0105 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1580-19150A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64350465 | ||||||
| chr5:64350513
|
A | T | 6 | a0001c0001t0001g0114a0001c0001t0001g0122a0001c0001t0001g0123others(3): Show | 6 | HG00738.hp1 HG01256.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.1580-19102A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64350513 | ||||||
| chr5:64350761
|
G | C | 29 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(26): Show | 29 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.1580-18854G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64350761 | ||||||
| chr5:64350766
|
A | G | 4 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0198others(1): Show | 4 | HG02559.hp2 HG02886.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1580-18849A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64350766 | ||||||
| chr5:64350821
|
A | G | 1 | a0001c0001t0002g0209 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1580-18794A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64350821 | ||||||
| chr5:64350906
|
C | T | 87 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(84): Show | 88 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1580-18709C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64350906 | ||||||
| chr5:64350964
|
A | G | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1580-18651A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64350964 | ||||||
| chr5:64351081
|
T | A | 1 | a0001c0001t0005g0188 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1580-18534T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64351081 | ||||||
| chr5:64351189
|
C | T | 2 | a0001c0001t0002g0184a0001c0001t0002g0187 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1580-18426C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64351189 | ||||||
| chr5:64351354
|
G | A | 1 | a0001c0001t0003g0194 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1580-18261G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64351354 | ||||||
| chr5:64351548
|
A | G | 2 | a0001c0001t0001g0126a0001c0001t0001g0137 | 2 | HG01123.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1580-18067A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64351548 | ||||||
| chr5:64351571
|
A | G | 2 | a0001c0001t0014g0055a0001c0001t0014g0056 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1580-18044A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64351571 | ||||||
| chr5:64351614
|
T | G | 2 | a0001c0001t0001g0126a0001c0001t0001g0137 | 2 | HG01123.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1580-18001T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64351614 | ||||||
| chr5:64351620
|
T | C | 3 | a0001c0001t0002g0180a0001c0001t0020g0023a0006c0006t0002g0175 | 3 | HG00733.hp2 HG01168.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.1580-17995T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64351620 | ||||||
| chr5:64351659
|
T | A | 2 | a0001c0001t0001g0126a0001c0001t0001g0137 | 2 | HG01123.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1580-17956T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64351659 | ||||||
| chr5:64351665
|
A | G | 2 | a0001c0001t0001g0126a0001c0001t0001g0137 | 2 | HG01123.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1580-17950A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64351665 | ||||||
| chr5:64351677
|
T | A | 2 | a0001c0001t0001g0126a0001c0001t0001g0137 | 2 | HG01123.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1580-17938T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64351677 | ||||||
| chr5:64351716
|
T | G | 2 | a0001c0001t0001g0126a0001c0001t0001g0137 | 2 | HG01123.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1580-17899T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64351716 | ||||||
| chr5:64351718
|
G | A | 2 | a0001c0001t0001g0126a0001c0001t0001g0137 | 2 | HG01123.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1580-17897G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64351718 | ||||||
| chr5:64351722
|
G | A | 2 | a0001c0001t0001g0126a0001c0001t0001g0137 | 2 | HG01123.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1580-17893G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64351722 | ||||||
| chr5:64351724
|
T | C | 2 | a0001c0001t0001g0126a0001c0001t0001g0137 | 2 | HG01123.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1580-17891T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64351724 | ||||||
| chr5:64351725
|
G | A | 2 | a0001c0001t0001g0126a0001c0001t0001g0137 | 2 | HG01123.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1580-17890G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64351725 | ||||||
| chr5:64351747
|
A | G | 2 | a0001c0001t0001g0126a0001c0001t0001g0137 | 2 | HG01123.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1580-17868A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64351747 | ||||||
| chr5:64351768
|
T | C | 2 | a0001c0001t0001g0126a0001c0001t0001g0137 | 2 | HG01123.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1580-17847T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64351768 | ||||||
| chr5:64351799
|
A | G | 2 | a0001c0001t0001g0126a0001c0001t0001g0137 | 2 | HG01123.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1580-17816A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64351799 | ||||||
| chr5:64351924
|
G | A | 1 | a0001c0001t0005g0188 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1580-17691G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64351924 | ||||||
| chr5:64351940
|
C | T | 19 | a0002c0002t0006g0065a0002c0002t0006g0066a0002c0002t0006g0068others(16): Show | 19 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.1580-17675C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64351940 | ||||||
| chr5:64351954
|
T | G | 1 | a0001c0001t0025g0105 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1580-17661T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64351954 | ||||||
| chr5:64352217
|
T | G | 1 | a0001c0001t0002g0206 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1580-17398T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64352217 | ||||||
| chr5:64352218
|
A | G | 2 | a0001c0001t0001g0122a0001c0001t0001g0123 | 2 | HG00738.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.1580-17397A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64352218 | ||||||
| chr5:64352495
|
G | A | 118 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(115): Show | 119 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.1580-17120G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64352495 | ||||||
| chr5:64352705
|
T | C | 1 | a0001c0001t0002g0202 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1580-16910T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64352705 | ||||||
| chr5:64352952
|
G | C | 1 | a0001c0001t0028g0193 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1580-16663G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64352952 | ||||||
| chr5:64353251
|
T | G | 2 | a0001c0001t0014g0055a0001c0001t0014g0056 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1580-16364T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64353251 | ||||||
| chr5:64353518
|
G | A | 198 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(195): Show | 199 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.1580-16097G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64353518 | ||||||
| chr5:64353632
|
G | A | 1 | a0001c0001t0005g0189 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1580-15983G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64353632 | ||||||
| chr5:64353682
|
T | C | 1 | a0001c0001t0005g0172 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1580-15933T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64353682 | ||||||
| chr5:64353740
|
T | C | 5 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(2): Show | 5 | HG01433.hp2 HG01928.hp1 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.1580-15875T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64353740 | ||||||
| chr5:64353754
|
T | C | 1 | a0001c0001t0002g0218 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1580-15861T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64353754 | ||||||
| chr5:64353784
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1580-15831G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64353784 | ||||||
| chr5:64353943
|
G | T | 1 | a0001c0001t0003g0028 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1580-15672G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64353943 | ||||||
| chr5:64353997
|
T | G | 1 | a0001c0001t0002g0176 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1580-15618T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64353997 | ||||||
| chr5:64354115
|
C | A | 6 | a0001c0001t0005g0188a0001c0001t0005g0189a0001c0001t0005g0190others(3): Show | 6 | HG01891.hp2 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1580-15500C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64354115 | ||||||
| chr5:64354218
|
A | G | 1 | a0001c0001t0019g0166 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1580-15397A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64354218 | ||||||
| chr5:64354283
|
C | A | 187 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(184): Show | 188 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.1580-15332C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64354283 | ||||||
| chr5:64354434
|
G | A | 1 | a0001c0001t0003g0077 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1580-15181G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64354434 | ||||||
| chr5:64354443
|
T | C | 1 | a0001c0001t0004g0110 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1580-15172T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64354443 | ||||||
| chr5:64354543
|
T | C | 1 | a0001c0001t0003g0020 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1580-15072T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64354543 | ||||||
| chr5:64354606
|
C | A | 1 | a0001c0001t0005g0189 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1580-15009C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64354606 | ||||||
| chr5:64354744
|
C | T | 27 | a0001c0001t0004g0002a0001c0001t0004g0078a0001c0001t0004g0086others(24): Show | 28 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.1580-14871C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64354744 | ||||||
| chr5:64354783
|
TA | T | 20 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(17): Show | 20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1580-14824delA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64354783 | |||||
| chr5:64354794
|
T | G | 246 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(243): Show | 248 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.1580-14821T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64354794 | ||||||
| chr5:64354858
|
G | A | 1 | a0002c0002t0008g0063 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1580-14757G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64354858 | ||||||
| chr5:64354960
|
A | C | 1 | a0001c0001t0002g0177 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1580-14655A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64354960 | ||||||
| chr5:64355056
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1580-14559G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64355056 | ||||||
| chr5:64355609
|
A | G | 1 | a0002c0002t0008g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1580-14006A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64355609 | ||||||
| chr5:64355931
|
G | C | 1 | a0001c0001t0004g0098 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1580-13684G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64355931 | ||||||
| chr5:64356043
|
G | C | 2 | a0001c0001t0002g0184a0001c0001t0002g0187 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1580-13572G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64356043 | ||||||
| chr5:64356255
|
A | G | 2 | a0001c0001t0005g0185a0001c0001t0005g0186 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1580-13360A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64356255 | ||||||
| chr5:64356259
|
C | CA | 11 | a0001c0001t0002g0203a0001c0001t0002g0204a0001c0001t0002g0207others(8): Show | 11 | HG00597.hp2 HG01243.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.1580-13345dupA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64356259 | |||||
| chr5:64357400
|
C | T | 1 | a0001c0001t0003g0194 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1580-12215C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64357400 | ||||||
| chr5:64357711
|
G | A | 87 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(84): Show | 88 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1580-11904G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64357711 | ||||||
| chr5:64357788
|
G | A | 1 | a0001c0001t0013g0012 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1580-11827G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64357788 | ||||||
| chr5:64357800
|
G | A | 1 | a0001c0001t0001g0085 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1580-11815G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64357800 | ||||||
| chr5:64358230
|
G | A | 1 | a0001c0001t0002g0219 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1580-11385G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64358230 | ||||||
| chr5:64358361
|
C | T | 3 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054 | 3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1580-11254C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64358361 | ||||||
| chr5:64358431
|
G | C | 2 | a0001c0001t0005g0185a0001c0001t0005g0186 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1580-11184G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64358431 | ||||||
| chr5:64358558
|
G | A | 1 | a0001c0001t0003g0007 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1580-11057G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64358558 | ||||||
| chr5:64358644
|
A | AT | 7 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054others(4): Show | 7 | HG00741.hp2 HG01257.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1580-10962dupT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64358644 | |||||
| chr5:64358644
|
AT | A | 21 | a0001c0001t0002g0215a0001c0001t0005g0167a0001c0001t0005g0168others(18): Show | 21 | HG00597.hp1 HG01993.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.1580-10962delT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64358644 | |||||
| chr5:64358688
|
T | A | 2 | a0001c0001t0026g0247a0001c0001t0027g0060 | 2 | HG02818.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1580-10927T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64358688 | ||||||
| chr5:64358765
|
A | G | 2 | a0001c0001t0004g0089a0001c0001t0004g0090 | 2 | NA18955.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.1580-10850A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64358765 | ||||||
| chr5:64358790
|
C | G | 5 | a0001c0001t0002g0225a0001c0001t0002g0226a0001c0001t0002g0227others(2): Show | 5 | NA18950.hp1 NA18984.hp2 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.1580-10825C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64358790 | ||||||
| chr5:64358853
|
C | T | 30 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(27): Show | 30 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1580-10762C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64358853 | ||||||
| chr5:64358980
|
C | A | 5 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054others(2): Show | 5 | HG02970.hp1 HG03139.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1580-10635C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64358980 | ||||||
| chr5:64359231
|
A | C | 29 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(26): Show | 29 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.1580-10384A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64359231 | ||||||
| chr5:64359238
|
T | G | 29 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(26): Show | 29 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.1580-10377T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64359238 | ||||||
| chr5:64359244
|
C | T | 1 | a0002c0002t0008g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1580-10371C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64359244 | ||||||
| chr5:64359287
|
C | A | 1 | a0001c0001t0005g0188 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1580-10328C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64359287 | ||||||
| chr5:64359319
|
T | C | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1580-10296T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64359319 | ||||||
| chr5:64359461
|
C | T | 1 | a0001c0001t0002g0225 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1580-10154C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64359461 | ||||||
| chr5:64359830
|
A | G | 1 | a0001c0001t0015g0032 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1580-9785A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64359830 | ||||||
| chr5:64359882
|
T | C | 1 | a0001c0001t0003g0024 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1580-9733T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64359882 | ||||||
| chr5:64360018
|
G | A | 20 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(17): Show | 20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1580-9597G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64360018 | ||||||
| chr5:64360058
|
T | C | 19 | a0002c0002t0006g0065a0002c0002t0006g0066a0002c0002t0006g0068others(16): Show | 19 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.1580-9557T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64360058 | ||||||
| chr5:64360115
|
C | G | 1 | a0001c0001t0002g0206 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1580-9500C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64360115 | ||||||
| chr5:64360226
|
A | G | 3 | a0001c0001t0003g0010a0001c0001t0003g0013a0001c0001t0003g0016 | 3 | HG02602.hp1 HG03491.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1580-9389A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64360226 | ||||||
| chr5:64360264
|
G | A | 5 | a0001c0001t0004g0089a0002c0002t0008g0061a0002c0002t0008g0062others(2): Show | 5 | HG00741.hp2 HG01257.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1580-9351G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64360264 | ||||||
| chr5:64360290
|
A | G | 9 | a0001c0001t0002g0026a0001c0001t0003g0004a0001c0001t0003g0005others(6): Show | 9 | HG00642.hp2 HG00741.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.1580-9325A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64360290 | ||||||
| chr5:64360319
|
G | A | 1 | a0001c0001t0004g0248 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1580-9296G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64360319 | ||||||
| chr5:64360447
|
T | C | 246 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(243): Show | 248 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.1580-9168T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64360447 | ||||||
| chr5:64360495
|
C | T | 2 | a0001c0001t0002g0184a0001c0001t0002g0187 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1580-9120C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64360495 | ||||||
| chr5:64360585
|
G | T | 11 | a0001c0001t0002g0203a0001c0001t0002g0204a0001c0001t0002g0207others(8): Show | 11 | HG00597.hp2 HG01243.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.1580-9030G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64360585 | ||||||
| chr5:64360751
|
G | T | 31 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(28): Show | 31 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.1580-8864G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64360751 | ||||||
| chr5:64360882
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1580-8733G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64360882 | ||||||
| chr5:64361018
|
G | A | 144 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(141): Show | 145 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.1580-8597G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64361018 | ||||||
| chr5:64361068
|
G | C | 3 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054 | 3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1580-8547G>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64361068 | ||||||
| chr5:64361165
|
G | A | 1 | a0002c0002t0016g0067 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1580-8450G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64361165 | ||||||
| chr5:64361236
|
A | C | 1 | a0001c0001t0005g0191 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1580-8379A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64361236 | ||||||
| chr5:64361282
|
A | G | 142 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(139): Show | 143 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1580-8333A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64361282 | ||||||
| chr5:64361283
|
GAC | G | 31 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(28): Show | 31 | HG00597.hp1 HG01891.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.1580-8330_1580-832 others(6): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64361283 | |||||
| chr5:64361713
|
A | C | 2 | a0002c0002t0006g0068a0002c0002t0006g0072 | 2 | HG01074.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.1580-7902A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64361713 | ||||||
| chr5:64361914
|
T | C | 2 | a0001c0001t0005g0185a0001c0001t0005g0186 | 2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1580-7701T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64361914 | ||||||
| chr5:64361984
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1580-7631C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64361984 | ||||||
| chr5:64362057
|
ATTAAAC | A | 4 | a0002c0002t0010g0057a0002c0002t0010g0058a0002c0002t0010g0076others(1): Show | 4 | HG02109.hp2 HG02622.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1580-7552_1580-754 others(10): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64362057 | |||||
| chr5:64362262
|
C | T | 2 | a0001c0001t0002g0026a0001c0001t0003g0030 | 2 | HG02698.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1580-7353C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64362262 | ||||||
| chr5:64362510
|
C | G | 1 | a0001c0001t0005g0189 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1580-7105C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64362510 | ||||||
| chr5:64362514
|
G | A | 1 | a0001c0001t0002g0226 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1580-7101G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64362514 | ||||||
| chr5:64362690
|
A | G | 1 | a0001c0001t0002g0228 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1580-6925A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64362690 | ||||||
| chr5:64362775
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1580-6840A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64362775 | ||||||
| chr5:64362873
|
T | C | 4 | a0002c0002t0010g0057a0002c0002t0010g0058a0002c0002t0010g0076others(1): Show | 4 | HG02109.hp2 HG02622.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1580-6742T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64362873 | ||||||
| chr5:64362908
|
T | TCCTTTGC others(300): Show |
14 | a0001c0001t0005g0234a0001c0001t0005g0235a0001c0001t0005g0237others(11): Show | 14 | HG00597.hp1 HG02818.hp1 HG02886.hp2 others(11): Show |
intron_variant | MODIFIER | c.1580-6691_1580-669 others(311): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64362908 | |||||
| chr5:64362908
|
T | TCCTTTGC others(300): Show |
5 | a0001c0001t0005g0188a0001c0001t0005g0190a0001c0001t0005g0191others(2): Show | 5 | HG01891.hp2 HG02559.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1580-6691_1580-669 others(311): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64362908 | |||||
| chr5:64362908
|
T | TCCTTTGC others(300): Show |
2 | a0001c0001t0005g0232a0001c0001t0005g0233 | 2 | NA18947.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.1580-6691_1580-669 others(311): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64362908 | |||||
| chr5:64362908
|
T | TCCTTTGC others(301): Show |
1 | a0001c0001t0005g0189 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1580-6691_1580-669 others(312): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64362908 | |||||
| chr5:64362908
|
T | TCCTTTGC others(314): Show |
1 | a0001c0001t0005g0173 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1580-6691_1580-669 others(325): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64362908 | |||||
| chr5:64362908
|
T | TCCTTTGC others(326): Show |
1 | a0001c0001t0005g0167 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1580-6691_1580-669 others(337): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64362908 | |||||
| chr5:64362908
|
T | TCCTTTGC others(327): Show |
4 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0170others(1): Show | 4 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1580-6691_1580-669 others(338): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64362908 | |||||
| chr5:64362908
|
T | TCCTTTGC others(329): Show |
1 | a0001c0001t0005g0172 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1580-6691_1580-669 others(340): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64362908 | |||||
| chr5:64363111
|
T | C | 1 | a0001c0001t0003g0028 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1580-6504T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64363111 | ||||||
| chr5:64363406
|
T | C | 1 | a0001c0001t0003g0009 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1580-6209T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64363406 | ||||||
| chr5:64363665
|
C | A | 142 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(139): Show | 143 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1580-5950C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64363665 | ||||||
| chr5:64363720
|
A | C | 15 | a0002c0002t0006g0065a0002c0002t0006g0066a0002c0002t0006g0068others(12): Show | 15 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.1580-5895A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64363720 | ||||||
| chr5:64364090
|
C | G | 1 | a0001c0001t0003g0144 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1580-5525C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64364090 | ||||||
| chr5:64364223
|
A | G | 5 | a0001c0001t0004g0086a0001c0001t0004g0092a0001c0001t0004g0099others(2): Show | 5 | HG02615.hp1 HG02647.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1580-5392A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64364223 | ||||||
| chr5:64364426
|
T | G | 2 | a0001c0001t0014g0055a0001c0001t0014g0056 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1580-5189T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64364426 | ||||||
| chr5:64364468
|
A | G | 11 | a0002c0002t0006g0065a0002c0002t0006g0066a0002c0002t0006g0068others(8): Show | 11 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.1580-5147A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64364468 | ||||||
| chr5:64364597
|
G | A | 2 | a0001c0001t0019g0166a0001c0001t0024g0192 | 2 | HG02559.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1580-5018G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64364597 | ||||||
| chr5:64364619
|
A | G | 2 | a0001c0001t0014g0055a0001c0001t0014g0056 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1580-4996A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64364619 | ||||||
| chr5:64364866
|
G | A | 1 | a0001c0001t0004g0095 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1580-4749G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64364866 | ||||||
| chr5:64364917
|
TC | T | 20 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(17): Show | 20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1580-4694delC | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64364917 | |||||
| chr5:64365000
|
C | CA | 31 | a0001c0001t0001g0120a0001c0001t0001g0147a0001c0001t0001g0148others(28): Show | 32 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(29): Show |
intron_variant | MODIFIER | c.1580-4604dupA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64365000 | |||||
| chr5:64365213
|
T | G | 1 | a0002c0002t0008g0061 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1580-4402T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64365213 | ||||||
| chr5:64365325
|
C | A | 1 | a0001c0001t0024g0192 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1580-4290C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64365325 | ||||||
| chr5:64365722
|
G | A | 4 | a0002c0002t0010g0057a0002c0002t0010g0058a0002c0002t0010g0076others(1): Show | 4 | HG02109.hp2 HG02622.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1580-3893G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64365722 | ||||||
| chr5:64365742
|
G | A | 2 | a0001c0001t0026g0247a0001c0001t0027g0060 | 2 | HG02818.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1580-3873G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64365742 | ||||||
| chr5:64365773
|
T | G | 1 | a0001c0001t0022g0018 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1580-3842T>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64365773 | ||||||
| chr5:64365825
|
T | C | 20 | a0001c0001t0005g0167a0001c0001t0005g0168a0001c0001t0005g0169others(17): Show | 20 | HG00597.hp1 HG02055.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1580-3790T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64365825 | ||||||
| chr5:64365867
|
T | C | 11 | a0002c0002t0006g0065a0002c0002t0006g0066a0002c0002t0006g0068others(8): Show | 11 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.1580-3748T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64365867 | ||||||
| chr5:64365999
|
A | AT | 10 | a0001c0001t0005g0084a0001c0001t0005g0188a0001c0001t0005g0189others(7): Show | 10 | HG01891.hp2 HG02257.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1580-3613dupT | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64365999 | |||||
| chr5:64366488
|
C | T | 1 | a0001c0001t0005g0239 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1580-3127C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64366488 | ||||||
| chr5:64366629
|
A | T | 3 | a0002c0002t0008g0062a0002c0002t0008g0063a0002c0002t0008g0064 | 3 | HG00741.hp2 HG01257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1580-2986A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64366629 | ||||||
| chr5:64366643
|
C | A | 1 | a0001c0001t0025g0105 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1580-2972C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64366643 | ||||||
| chr5:64366787
|
G | A | 3 | a0001c0001t0011g0052a0001c0001t0011g0053a0001c0001t0011g0054 | 3 | HG02970.hp1 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1580-2828G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64366787 | ||||||
| chr5:64367054
|
T | A | 1 | a0001c0001t0004g0098 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1580-2561T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64367054 | ||||||
| chr5:64367204
|
G | A | 142 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(139): Show | 143 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1580-2411G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64367204 | ||||||
| chr5:64367262
|
T | C | 15 | a0002c0002t0006g0065a0002c0002t0006g0066a0002c0002t0006g0068others(12): Show | 15 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.1580-2353T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64367262 | ||||||
| chr5:64367266
|
A | G | 4 | a0002c0002t0010g0057a0002c0002t0010g0058a0002c0002t0010g0076others(1): Show | 4 | HG02109.hp2 HG02622.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1580-2349A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64367266 | ||||||
| chr5:64367347
|
A | G | 1 | a0001c0001t0004g0091 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1580-2268A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64367347 | ||||||
| chr5:64367407
|
A | C | 1 | a0001c0001t0004g0099 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1580-2208A>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64367407 | ||||||
| chr5:64367503
|
G | T | 142 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(139): Show | 143 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1580-2112G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64367503 | ||||||
| chr5:64367564
|
TA | T | 5 | a0001c0001t0005g0189a0001c0001t0005g0190a0001c0001t0005g0191others(2): Show | 5 | HG01891.hp2 HG02559.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1580-2048delA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64367564 | |||||
| chr5:64367848
|
T | A | 1 | a0001c0001t0004g0099 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1580-1767T>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64367848 | ||||||
| chr5:64368076
|
G | T | 87 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(84): Show | 88 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1580-1539G>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64368076 | ||||||
| chr5:64368419
|
T | C | 2 | a0001c0001t0014g0055a0001c0001t0014g0056 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1580-1196T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64368419 | ||||||
| chr5:64368424
|
T | C | 1 | a0001c0001t0002g0227 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1580-1191T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64368424 | ||||||
| chr5:64368630
|
C | T | 1 | a0001c0001t0027g0060 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1580-985C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64368630 | ||||||
| chr5:64368655
|
G | A | 1 | a0001c0001t0002g0183 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1580-960G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64368655 | ||||||
| chr5:64368865
|
C | G | 3 | a0001c0001t0012g0195a0001c0001t0012g0196a0001c0001t0012g0197 | 3 | HG02109.hp1 HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1580-750C>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64368865 | ||||||
| chr5:64368887
|
T | C | 3 | a0001c0001t0003g0024a0001c0001t0003g0040a0001c0001t0003g0124 | 3 | HG01168.hp1 HG01261.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1580-728T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64368887 | ||||||
| chr5:64368908
|
C | T | 1 | a0001c0001t0002g0218 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1580-707C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64368908 | ||||||
| chr5:64368984
|
C | A | 2 | a0001c0001t0004g0086a0001c0001t0004g0092 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1580-631C>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64368984 | ||||||
| chr5:64369058
|
C | T | 1 | a0001c0001t0002g0225 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1580-557C>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64369058 | ||||||
| chr5:64369081
|
T | C | 2 | a0001c0001t0026g0247a0001c0001t0027g0060 | 2 | HG02818.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1580-534T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64369081 | ||||||
| chr5:64369097
|
T | C | 1 | a0001c0001t0002g0223 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1580-518T>C | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64369097 | ||||||
| chr5:64369148
|
A | T | 1 | a0001c0001t0002g0223 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1580-467A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64369148 | ||||||
| chr5:64369159
|
G | A | 1 | a0001c0001t0005g0084 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1580-456G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64369159 | ||||||
| chr5:64369176
|
A | T | 11 | a0002c0002t0006g0065a0002c0002t0006g0066a0002c0002t0006g0068others(8): Show | 11 | HG01074.hp2 HG01081.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.1580-439A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64369176 | ||||||
| chr5:64369204
|
G | A | 59 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(56): Show | 59 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.1580-411G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64369204 | ||||||
| chr5:64369361
|
A | T | 2 | a0002c0002t0006g0074a0002c0002t0006g0075 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1580-254A>T | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64369361 | ||||||
| chr5:64369449
|
TTAAAG | T | 4 | a0001c0001t0005g0190a0001c0001t0005g0191a0001c0001t0024g0192others(1): Show | 4 | HG01891.hp2 HG02559.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1580-163_1580-159d others(7): Show |
RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64369449 | |||||
| chr5:64369466
|
TA | T | 139 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(136): Show | 140 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.1580-139delA | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 64369466 | |||||
| chr5:64369476
|
A | G | 3 | a0001c0001t0005g0185a0001c0001t0005g0186a0001c0001t0005g0188 | 3 | HG03098.hp2 NA18906.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1580-139A>G | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64369476 | ||||||
| chr5:64369477
|
G | A | 3 | a0001c0001t0005g0185a0001c0001t0005g0186a0001c0001t0005g0188 | 3 | HG03098.hp2 NA18906.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1580-138G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64369477 | ||||||
| chr5:64369508
|
G | A | 142 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(139): Show | 143 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1580-107G>A | RNF180 | ENSG00000164197.12 | transcript | ENST00000389100.9 | protein_coding | 7/7 | chr5 | 64369508 |