Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 285498 |
|---|---|
| ensemblid | ENSG00000178222.14 |
| hgncid | 27729 |
| symbol | RNF212 |
| name | ring finger protein 212 |
| refseq_nuc | NM_001131034.4 |
| refseq_prot | NP_001124506.1 |
| ensembl_nuc | ENST00000433731.7 |
| ensembl_prot | ENSP00000389709.2 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 1071478 |
| end | 1113564 |
| strand | - |
| ver | v1.2 |
| region | chr4:1071478-1113564 |
| region5000 | chr4:1066478-1118564 |
| regionname0 | RNF212_chr4_1071478_1113564 |
| regionname5000 | RNF212_chr4_1066478_1118564 |
| 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 | 297 | 389 | 82 | 76 | 180 | 7 | 42 | 139 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| a0002 | 0/0 | 297 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| a0003 | 0/0 | 297 | 4 | 0 | 0 | 4 | 0 | 0 | 3 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| a0004 | 0/0 | 297 | 3 | 1 | 1 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| a0005 | 0/0 | 297 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| a0006 | 0/0 | 297 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| a0007 | 0/0 | 297 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| a0008 | 0/0 | 297 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| 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 | 0/1 | 894 | 219 | 33 | 42 | 111 | 5 | 27 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| c0002 | 1/0 | 894 | 169 | 48 | 34 | 69 | 2 | 15 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| c0003 | 0/0 | 894 | 5 | 5 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| c0004 | 0/0 | 894 | 4 | 0 | 0 | 4 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| c0005 | 0/0 | 894 | 3 | 1 | 1 | 0 | 1 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| c0006 | 0/0 | 894 | 2 | 0 | 0 | 0 | 0 | 2 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| c0007 | 0/0 | 894 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| c0008 | 0/0 | 894 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| c0009 | 0/0 | 894 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| c0010 | 0/0 | 894 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| 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 | 0/1 | 1496 | 240 | 57 | 42 | 110 | 5 | 25 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| t0002 | 1/0 | 1497 | 113 | 4 | 27 | 68 | 3 | 10 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| t0003 | 0/0 | 1496 | 24 | 12 | 7 | 0 | 0 | 5 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| t0004 | 0/0 | 1497 | 7 | 7 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| t0005 | 0/0 | 1496 | 4 | 0 | 0 | 0 | 0 | 4 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| t0006 | 0/0 | 1496 | 4 | 3 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| t0007 | 0/0 | 1524 | 3 | 3 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| t0008 | 0/0 | 1496 | 2 | 0 | 0 | 2 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| t0009 | 0/0 | 1487 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| t0010 | 0/0 | 1496 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| t0011 | 0/0 | 1497 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| t0012 | 0/0 | 1497 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| t0013 | 0/0 | 1496 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| t0014 | 0/0 | 1496 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| t0015 | 0/0 | 1496 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| t0016 | 0/0 | 1496 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| t0017 | 0/0 | 1497 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| 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 | 4 | 0 | 3 | 0 | 1 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0002 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0011 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0027 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0031 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0099 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| 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 | 0/1 | 894 | 219 | 33 | 42 | 111 | 5 | 27 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| a0001c0002 | 1/0 | 894 | 169 | 48 | 34 | 69 | 2 | 15 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| a0001c0009 | 0/0 | 894 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| a0002c0003 | 0/0 | 894 | 5 | 5 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| a0003c0004 | 0/0 | 894 | 4 | 0 | 0 | 4 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| a0004c0005 | 0/0 | 894 | 3 | 1 | 1 | 0 | 1 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| a0005c0006 | 0/0 | 894 | 2 | 0 | 0 | 0 | 0 | 2 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| a0006c0007 | 0/0 | 894 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| a0007c0008 | 0/0 | 894 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| a0008c0010 | 0/0 | 894 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2389 | 206 | 30 | 41 | 106 | 5 | 23 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| a0001c0001t0005 | 0/0 | 2389 | 4 | 0 | 0 | 0 | 0 | 4 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| a0001c0001t0006 | 0/0 | 2389 | 3 | 2 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| a0001c0001t0008 | 0/0 | 2389 | 2 | 0 | 0 | 2 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| a0001c0001t0009 | 0/0 | 2380 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| a0001c0001t0010 | 0/0 | 2389 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| a0001c0001t0014 | 0/0 | 2389 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| a0001c0001t0015 | 0/0 | 2389 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| a0001c0002t0001 | 0/0 | 2389 | 22 | 21 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| a0001c0002t0002 | 1/0 | 2390 | 109 | 3 | 25 | 68 | 2 | 10 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| a0001c0002t0003 | 0/0 | 2389 | 23 | 11 | 7 | 0 | 0 | 5 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| a0001c0002t0004 | 0/0 | 2390 | 7 | 7 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| a0001c0002t0006 | 0/0 | 2389 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| a0001c0002t0007 | 0/0 | 2417 | 3 | 3 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| a0001c0002t0012 | 0/0 | 2390 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| a0001c0002t0013 | 0/0 | 2389 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| a0001c0002t0016 | 0/0 | 2389 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| a0001c0002t0017 | 0/0 | 2390 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| a0001c0009t0003 | 0/0 | 2389 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| a0002c0003t0001 | 0/0 | 2389 | 5 | 5 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| a0003c0004t0001 | 0/0 | 2389 | 4 | 0 | 0 | 4 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| a0004c0005t0002 | 0/0 | 2390 | 3 | 1 | 1 | 0 | 1 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| a0005c0006t0001 | 0/0 | 2389 | 2 | 0 | 0 | 0 | 0 | 2 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| a0006c0007t0002 | 0/0 | 2390 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| a0007c0008t0011 | 0/0 | 2390 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| a0008c0010t0001 | 0/0 | 2389 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | copy fasta | chr4 | 1066478 | 1118564 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0031 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0005g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0005g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0005g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0005g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0006g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0006g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0006g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0008g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0008g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0009g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0010g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0014g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0001t0015g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0002 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0027 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0099 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0002g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0003g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0003g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0003g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0003g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0003g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0003g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0003g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0003g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0003g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0003g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0003g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0003g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0003g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0003g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0003g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0003g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0003g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0003g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0003g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0003g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0003g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0003g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0004g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0004g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0006g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0007g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0007g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0007g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0012g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0013g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0016g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0002t0017g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0001c0009t0003g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0002c0003t0001g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0002c0003t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0002c0003t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0003c0004t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0003c0004t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0003c0004t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0003c0004t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0004c0005t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0004c0005t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0004c0005t0002g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0005c0006t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0005c0006t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0006c0007t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0007c0008t0011g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| a0008c0010t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0002 | g0274 | EUR | GBR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00099 | hp2 | a0004 | c0005 | t0002 | g0254 | EUR | GBR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0128 | EUR | GBR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0194 | EUR | FIN | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0199 | EUR | FIN | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00408 | hp1 | a0001 | c0002 | t0002 | g0166 | EAS | CHS | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00423 | hp1 | a0001 | c0002 | t0002 | g0225 | EAS | CHS | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00423 | hp2 | a0001 | c0002 | t0002 | g0239 | EAS | CHS | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00438 | hp1 | a0001 | c0002 | t0002 | g0255 | EAS | CHS | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | CHS | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00597 | hp1 | a0003 | c0004 | t0001 | g0224 | EAS | CHS | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00597 | hp2 | a0001 | c0002 | t0002 | g0241 | EAS | CHS | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | CHS | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0320 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00642 | hp2 | a0001 | c0002 | t0003 | g0354 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00673 | hp2 | a0001 | c0002 | t0002 | g0266 | EAS | CHS | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00735 | hp1 | a0001 | c0002 | t0003 | g0351 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0260 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0026 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01074 | hp2 | a0001 | c0002 | t0003 | g0348 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01109 | hp1 | a0001 | c0002 | t0002 | g0058 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01167 | hp1 | a0001 | c0001 | t0006 | g0358 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01167 | hp2 | a0001 | c0002 | t0002 | g0215 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01168 | hp1 | a0001 | c0002 | t0002 | g0261 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01169 | hp2 | a0001 | c0002 | t0002 | g0214 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0298 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0325 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0304 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01243 | hp2 | a0001 | c0002 | t0003 | g0334 | AMR | PUR | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0308 | AMR | CLM | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0329 | AMR | CLM | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01256 | hp1 | a0001 | c0002 | t0002 | g0027 | AMR | CLM | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01261 | hp2 | a0004 | c0005 | t0002 | g0330 | AMR | CLM | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01346 | hp1 | a0001 | c0002 | t0002 | g0231 | AMR | CLM | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01358 | hp2 | a0001 | c0002 | t0003 | g0355 | AMR | CLM | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01361 | hp2 | a0001 | c0002 | t0002 | g0315 | AMR | CLM | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01433 | hp1 | a0001 | c0002 | t0016 | g0345 | AMR | CLM | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01433 | hp2 | a0001 | c0002 | t0003 | g0347 | AMR | CLM | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01496 | hp2 | a0001 | c0002 | t0002 | g0240 | AMR | CLM | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0037 | AFR | ACB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01891 | hp1 | a0007 | c0008 | t0011 | g0040 | AFR | ACB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01928 | hp1 | a0001 | c0002 | t0002 | g0242 | AMR | PEL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01934 | hp1 | a0001 | c0002 | t0003 | g0352 | AMR | PEL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01934 | hp2 | a0001 | c0002 | t0002 | g0025 | AMR | PEL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01952 | hp1 | a0001 | c0002 | t0002 | g0230 | AMR | PEL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01975 | hp2 | a0006 | c0007 | t0002 | g0233 | AMR | PEL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01978 | hp1 | a0001 | c0002 | t0002 | g0236 | AMR | PEL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01978 | hp2 | a0001 | c0002 | t0002 | g0057 | AMR | PEL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01981 | hp1 | a0001 | c0002 | t0002 | g0025 | AMR | PEL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02004 | hp1 | a0001 | c0002 | t0002 | g0235 | AMR | PEL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PEL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02027 | hp1 | a0001 | c0002 | t0002 | g0168 | EAS | KHV | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | KHV | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02071 | hp1 | a0001 | c0001 | t0008 | g0052 | EAS | KHV | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02071 | hp2 | a0001 | c0002 | t0002 | g0277 | EAS | KHV | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | KHV | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | KHV | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02135 | hp2 | a0001 | c0002 | t0002 | g0317 | EAS | KHV | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02155 | hp1 | a0001 | c0002 | t0002 | g0262 | EAS | CDX | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CDX | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02165 | hp1 | a0001 | c0002 | t0002 | g0318 | EAS | CDX | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | CDX | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0059 | AFR | ACB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02258 | hp1 | a0001 | c0002 | t0007 | g0362 | AFR | ACB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02273 | hp1 | a0001 | c0002 | t0002 | g0312 | AMR | PEL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0016 | AFR | ACB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02293 | hp2 | a0001 | c0002 | t0002 | g0026 | AMR | PEL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02300 | hp1 | a0001 | c0002 | t0002 | g0243 | AMR | PEL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02300 | hp2 | a0001 | c0002 | t0002 | g0249 | AMR | PEL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0097 | AFR | ACB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02451 | hp2 | a0001 | c0002 | t0003 | g0337 | AFR | ACB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02523 | hp1 | a0001 | c0002 | t0002 | g0270 | EAS | KHV | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | KHV | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02572 | hp1 | a0002 | c0003 | t0001 | g0006 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02602 | hp2 | a0001 | c0002 | t0002 | g0328 | SAS | PJL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0327 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02622 | hp1 | a0001 | c0002 | t0002 | g0155 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02622 | hp2 | a0001 | c0002 | t0003 | g0336 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02630 | hp1 | a0001 | c0002 | t0012 | g0103 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02630 | hp2 | a0001 | c0002 | t0003 | g0342 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0015 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02647 | hp2 | a0002 | c0003 | t0001 | g0332 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02683 | hp1 | a0005 | c0006 | t0001 | g0139 | SAS | PJL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0234 | SAS | PJL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02698 | hp2 | a0005 | c0006 | t0001 | g0133 | SAS | PJL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02717 | hp1 | a0001 | c0002 | t0004 | g0009 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02717 | hp2 | a0001 | c0002 | t0013 | g0102 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0305 | SAS | PJL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02809 | hp1 | a0001 | c0001 | t0006 | g0359 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02886 | hp1 | a0001 | c0002 | t0003 | g0339 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02895 | hp1 | a0002 | c0003 | t0001 | g0333 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02896 | hp2 | a0001 | c0002 | t0002 | g0244 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02922 | hp1 | a0001 | c0001 | t0010 | g0191 | AFR | ESN | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02922 | hp2 | a0001 | c0002 | t0004 | g0008 | AFR | ESN | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02965 | hp1 | a0001 | c0009 | t0003 | g0335 | AFR | ESN | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02965 | hp2 | a0001 | c0002 | t0003 | g0338 | AFR | ESN | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02970 | hp1 | a0001 | c0002 | t0003 | g0349 | AFR | ESN | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0156 | AFR | ESN | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02976 | hp1 | a0001 | c0002 | t0004 | g0048 | AFR | ESN | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02976 | hp2 | a0001 | c0002 | t0003 | g0341 | AFR | ESN | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0209 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0021 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0303 | AFR | MSL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0042 | AFR | MSL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03139 | hp1 | a0001 | c0002 | t0004 | g0009 | AFR | ESN | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03139 | hp2 | a0001 | c0002 | t0004 | g0008 | AFR | ESN | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0101 | AFR | ESN | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03195 | hp2 | a0001 | c0002 | t0007 | g0363 | AFR | ESN | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03209 | hp1 | a0001 | c0002 | t0007 | g0364 | AFR | MSL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0034 | AFR | MSL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0100 | AFR | MSL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0041 | AFR | MSL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0021 | AFR | MSL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03490 | hp1 | a0001 | c0002 | t0002 | g0030 | SAS | PJL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03491 | hp1 | a0001 | c0001 | t0005 | g0046 | SAS | PJL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03492 | hp1 | a0001 | c0001 | t0005 | g0045 | SAS | PJL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03492 | hp2 | a0001 | c0002 | t0002 | g0030 | SAS | PJL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03516 | hp2 | a0001 | c0002 | t0006 | g0360 | AFR | ESN | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03540 | hp2 | a0001 | c0002 | t0003 | g0343 | AFR | GWD | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0035 | AFR | MSL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0015 | AFR | MSL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03669 | hp1 | a0001 | c0002 | t0003 | g0350 | SAS | PJL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03669 | hp2 | a0001 | c0002 | t0002 | g0273 | SAS | PJL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0319 | SAS | STU | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03688 | hp2 | a0001 | c0002 | t0003 | g0033 | SAS | STU | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03704 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03710 | hp2 | a0001 | c0001 | t0005 | g0047 | SAS | PJL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | BEB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | BEB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03834 | hp1 | a0001 | c0002 | t0003 | g0353 | SAS | BEB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | BEB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03927 | hp1 | a0001 | c0002 | t0003 | g0356 | SAS | BEB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | BEB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | STU | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0301 | SAS | STU | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0284 | SAS | BEB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | BEB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG04199 | hp1 | a0001 | c0002 | t0003 | g0033 | SAS | STU | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG04199 | hp2 | a0001 | c0002 | t0002 | g0036 | SAS | STU | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0306 | SAS | STU | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG04204 | hp2 | a0001 | c0001 | t0005 | g0043 | SAS | STU | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG04228 | hp1 | a0001 | c0002 | t0002 | g0278 | SAS | STU | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0280 | SAS | STU | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18522 | hp1 | a0008 | c0010 | t0001 | g0092 | AFR | YRI | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | YRI | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | CHB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18747 | hp2 | a0001 | c0002 | t0002 | g0257 | EAS | CHB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | YRI | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | YRI | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18939 | hp1 | a0001 | c0002 | t0002 | g0228 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18940 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18941 | hp1 | a0001 | c0002 | t0002 | g0028 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18942 | hp2 | a0001 | c0002 | t0002 | g0252 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18943 | hp1 | a0001 | c0002 | t0002 | g0167 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18944 | hp1 | a0003 | c0004 | t0001 | g0146 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18944 | hp2 | a0001 | c0002 | t0002 | g0282 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18945 | hp1 | a0001 | c0002 | t0002 | g0229 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18948 | hp1 | a0001 | c0002 | t0002 | g0269 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18950 | hp1 | a0001 | c0002 | t0002 | g0272 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18956 | hp2 | a0001 | c0002 | t0002 | g0323 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18957 | hp1 | a0001 | c0002 | t0002 | g0107 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0263 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18960 | hp2 | a0001 | c0002 | t0002 | g0251 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18961 | hp1 | a0001 | c0002 | t0002 | g0256 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0150 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18966 | hp1 | a0001 | c0002 | t0002 | g0313 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18966 | hp2 | a0001 | c0001 | t0015 | g0204 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18967 | hp2 | a0001 | c0002 | t0002 | g0253 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18969 | hp1 | a0001 | c0002 | t0002 | g0027 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18970 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18973 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18975 | hp2 | a0001 | c0002 | t0002 | g0295 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18978 | hp1 | a0001 | c0002 | t0002 | g0300 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0226 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18981 | hp2 | a0001 | c0002 | t0002 | g0165 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18982 | hp2 | a0001 | c0002 | t0002 | g0268 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18983 | hp1 | a0001 | c0002 | t0002 | g0267 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18988 | hp1 | a0001 | c0002 | t0002 | g0028 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18990 | hp2 | a0001 | c0001 | t0014 | g0088 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18992 | hp1 | a0001 | c0001 | t0009 | g0365 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18992 | hp2 | a0001 | c0002 | t0002 | g0271 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18994 | hp1 | a0001 | c0001 | t0008 | g0053 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18997 | hp2 | a0001 | c0002 | t0002 | g0321 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18998 | hp1 | a0001 | c0002 | t0002 | g0311 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19004 | hp1 | a0001 | c0002 | t0002 | g0264 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19004 | hp2 | a0001 | c0002 | t0002 | g0237 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19005 | hp1 | a0003 | c0004 | t0001 | g0145 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19005 | hp2 | a0001 | c0002 | t0002 | g0169 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19007 | hp2 | a0001 | c0002 | t0002 | g0246 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19009 | hp2 | a0001 | c0002 | t0017 | g0361 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19010 | hp1 | a0001 | c0002 | t0002 | g0314 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19010 | hp2 | a0001 | c0002 | t0002 | g0309 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19011 | hp1 | a0001 | c0002 | t0002 | g0060 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19011 | hp2 | a0001 | c0002 | t0002 | g0310 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19012 | hp2 | a0001 | c0002 | t0002 | g0029 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19030 | hp1 | a0001 | c0002 | t0004 | g0038 | AFR | LWK | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0307 | AFR | LWK | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | LWK | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0297 | AFR | LWK | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19056 | hp2 | a0001 | c0002 | t0002 | g0153 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19058 | hp1 | a0001 | c0002 | t0002 | g0285 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19058 | hp2 | a0001 | c0002 | t0002 | g0276 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19060 | hp1 | a0001 | c0002 | t0002 | g0259 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19063 | hp2 | a0001 | c0002 | t0002 | g0250 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19065 | hp1 | a0001 | c0002 | t0002 | g0227 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19065 | hp2 | a0003 | c0004 | t0001 | g0147 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19066 | hp2 | a0001 | c0002 | t0002 | g0170 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19067 | hp1 | a0001 | c0002 | t0002 | g0029 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19072 | hp2 | a0001 | c0002 | t0002 | g0324 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19074 | hp2 | a0001 | c0002 | t0002 | g0258 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19079 | hp1 | a0001 | c0002 | t0002 | g0296 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19084 | hp1 | a0001 | c0002 | t0002 | g0283 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19085 | hp1 | a0001 | c0002 | t0002 | g0238 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19086 | hp1 | a0001 | c0002 | t0002 | g0316 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19087 | hp1 | a0001 | c0002 | t0002 | g0275 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19240 | hp1 | a0002 | c0003 | t0001 | g0006 | AFR | YRI | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA19240 | hp2 | a0001 | c0002 | t0003 | g0340 | AFR | YRI | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA20129 | hp1 | a0001 | c0002 | t0003 | g0346 | AFR | ASW | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ASW | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0127 | EUR | TSI | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA20752 | hp2 | a0001 | c0002 | t0002 | g0245 | EUR | TSI | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01123 | hp1 | a0001 | c0002 | t0002 | g0232 | AMR | CLM | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG01123 | hp2 | a0001 | c0002 | t0002 | g0248 | AMR | CLM | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0098 | AFR | ACB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0357 | AFR | ACB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02486 | hp1 | a0004 | c0005 | t0002 | g0247 | AFR | ACB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02486 | hp2 | a0002 | c0003 | t0001 | g0006 | AFR | ACB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0016 | AFR | ACB | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | MSL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | MSL | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG06807 | hp1 | a0001 | c0002 | t0002 | g0299 | AFR | USA | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| HG06807 | hp2 | a0001 | c0002 | t0004 | g0039 | AFR | USA | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA18955 | hp2 | a0001 | c0002 | t0002 | g0265 | EAS | JPT | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | USA | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| NA20300 | hp2 | a0001 | c0002 | t0003 | g0344 | AFR | USA | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0031 | REF | REF | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0002 | g0099 | REF | REF | RNF212_chr4_1066478_1118564 | RNF212 | chr4 | 1066478 | 1118564 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:1072981
|
C | T | 1 | a0003 | 4 | HG00597.hp1 NA18944.hp1 NA19005.hp1 others(1): Show |
missense_variant | MODERATE | c.787G>A | p.Val263Ile | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 10/10 | 887/2390 | 787/894 | 263/297 | chr4 | 1072981 | ||
| chr4:1073170
|
A | C | 1 | a0007 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.598T>G | p.Cys200Gly | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 10/10 | 698/2390 | 598/894 | 200/297 | chr4 | 1073170 | ||
| chr4:1081428
|
G | C | 1 | a0005 | 2 | HG02683.hp1 HG02698.hp2 |
missense_variant | MODERATE | c.455C>G | p.Ala152Gly | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 7/10 | 555/2390 | 455/894 | 152/297 | chr4 | 1081428 | ||
| chr4:1081584
|
A | G | 1 | a0008 | 1 | NA18522.hp1 | missense_variant | MODERATE | c.398T>C | p.Ile133Thr | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 6/10 | 498/2390 | 398/894 | 133/297 | chr4 | 1081584 | ||
| chr4:1081619
|
A | C | 1 | a0006 | 1 | HG01975.hp2 | missense_variant&splice_region_variant | MODERATE | c.363T>G | p.Ser121Arg | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 6/10 | 463/2390 | 363/894 | 121/297 | chr4 | 1081619 | ||
| chr4:1096836
|
C | T | 1 | a0004 | 3 | HG00099.hp2 HG01261.hp2 HG02486.hp1 |
missense_variant | MODERATE | c.175G>A | p.Asp59Asn | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/10 | 275/2390 | 175/894 | 59/297 | chr4 | 1096836 | ||
| chr4:1113457
|
T | C | 1 | a0002 | 5 | HG02486.hp2 HG02572.hp1 HG02647.hp2 others(2): Show |
missense_variant | MODERATE | c.8A>G | p.Asn3Ser | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/10 | 108/2390 | 8/894 | 3/297 | chr4 | 1113457 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:1072925
|
A | G | 1 | a0001c0009 | 1 | HG02965.hp1 | synonymous_variant | LOW | c.843T>C | p.Ala281Ala | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 10/10 | 943/2390 | 843/894 | 281/297 | chr4 | 1072925 | ||
| chr4:1096837
|
G | A | 4 | a0001c0001a0003c0004a0005c0006others(1): Show | 226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
splice_region_variant&synonymous_variant | LOW | c.174C>T | p.Thr58Thr | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/10 | 274/2390 | 174/894 | 58/297 | chr4 | 1096837 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:1071587
|
T | G | 1 | a0001c0001t0005 | 4 | HG03491.hp1 HG03492.hp1 HG03710.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1287A>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 10/10 | 1287 | chr4 | 1071587 | |||||
| chr4:1071698
|
T | C | 3 | a0001c0002t0004a0001c0002t0012a0007c0008t0011 | 9 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1176A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 10/10 | 1176 | chr4 | 1071698 | |||||
| chr4:1071922
|
T | C | 1 | a0001c0002t0013 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*952A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 10/10 | 952 | chr4 | 1071922 | |||||
| chr4:1071976
|
T | C | 1 | a0001c0001t0014 | 1 | NA18990.hp2 | 3_prime_UTR_variant | MODIFIER | c.*898A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 10/10 | 898 | chr4 | 1071976 | |||||
| chr4:1071994
|
T | C | 1 | a0001c0002t0012 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*880A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 10/10 | 880 | chr4 | 1071994 | |||||
| chr4:1072055
|
A | C | 1 | a0001c0001t0008 | 2 | HG02071.hp1 NA18994.hp1 |
3_prime_UTR_variant | MODIFIER | c.*819T>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 10/10 | 819 | chr4 | 1072055 | |||||
| chr4:1072125
|
C | T | 3 | a0001c0002t0004a0001c0002t0012a0007c0008t0011 | 9 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*749G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 10/10 | 749 | chr4 | 1072125 | |||||
| chr4:1072154
|
G | A | 1 | a0001c0001t0015 | 1 | NA18966.hp2 | 3_prime_UTR_variant | MODIFIER | c.*720C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 10/10 | 720 | chr4 | 1072154 | |||||
| chr4:1072214
|
C | T | 1 | a0007c0008t0011 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*660G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 10/10 | 660 | chr4 | 1072214 | |||||
| chr4:1072284
|
AT | A | 19 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(16): Show | 283 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
3_prime_UTR_variant | MODIFIER | c.*589delA | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 10/10 | 589 | chr4 | 1072284 | |||||
| chr4:1072493
|
G | T | 1 | a0001c0001t0010 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*381C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 10/10 | 381 | chr4 | 1072493 | |||||
| chr4:1072602
|
A | G | 1 | a0001c0002t0016 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*272T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 10/10 | 272 | chr4 | 1072602 | |||||
| chr4:1113490
|
G | A | 4 | a0001c0002t0003a0001c0002t0007a0001c0002t0016others(1): Show | 28 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(25): Show |
5_prime_UTR_variant | MODIFIER | c.-26C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/10 | 26 | chr4 | 1113490 | |||||
| chr4:1113528
|
G | A | 2 | a0001c0001t0006a0001c0002t0006 | 4 | HG01167.hp1 HG02109.hp2 HG02809.hp1 others(1): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-64C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/10 | chr4 | 1113528 | ||||||
| chr4:1113534
|
C | A | 1 | a0001c0002t0017 | 1 | NA19009.hp2 | 5_prime_UTR_variant | MODIFIER | c.-70G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/10 | 70 | chr4 | 1113534 | |||||
| chr4:1113549
|
A | C | 1 | a0001c0001t0009 | 1 | NA18992.hp1 | 5_prime_UTR_variant | MODIFIER | c.-85T>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/10 | 85 | chr4 | 1113549 | |||||
| chr4:1113550
|
G | A | 1 | a0001c0001t0009 | 1 | NA18992.hp1 | 5_prime_UTR_variant | MODIFIER | c.-86C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/10 | 86 | chr4 | 1113550 | |||||
| chr4:1113552
|
C | G | 1 | a0001c0001t0009 | 1 | NA18992.hp1 | 5_prime_UTR_variant | MODIFIER | c.-88G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/10 | 88 | chr4 | 1113552 | |||||
| chr4:1113553
|
G | GGGCAGCT others(21): Show |
1 | a0001c0002t0007 | 3 | HG02258.hp1 HG03195.hp2 HG03209.hp1 |
5_prime_UTR_variant | MODIFIER | c.-90_-89insGTCGACTT others(20): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/10 | 90 | chr4 | 1113553 | |||||
| chr4:1113555
|
GCAGCTCT others(8): Show |
G | 1 | a0001c0001t0009 | 1 | NA18992.hp1 | 5_prime_UTR_variant | MODIFIER | c.-106_-92delGCAGGCG others(8): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/10 | 92 | chr4 | 1113555 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:1073244
|
G | A | 45 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(42): Show | 49 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.575-51C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 9/9 | chr4 | 1073244 | ||||||
| chr4:1073387
|
T | G | 1 | a0001c0001t0001g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.575-194A>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 9/9 | chr4 | 1073387 | ||||||
| chr4:1073451
|
T | A | 14 | a0001c0002t0002g0107a0001c0002t0002g0165a0001c0002t0002g0225others(11): Show | 14 | HG00423.hp1 HG00673.hp2 HG02155.hp1 others(11): Show |
intron_variant | MODIFIER | c.574+148A>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 9/9 | chr4 | 1073451 | ||||||
| chr4:1073461
|
T | C | 190 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(187): Show | 214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.574+138A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 9/9 | chr4 | 1073461 | ||||||
| chr4:1073479
|
G | T | 261 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(258): Show | 293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.574+120C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 9/9 | chr4 | 1073479 | ||||||
| chr4:1073569
|
C | T | 1 | a0001c0001t0001g0136 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.574+30G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 9/9 | chr4 | 1073569 | ||||||
| chr4:1073742
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.511-80T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1073742 | ||||||
| chr4:1073834
|
C | G | 4 | a0001c0002t0001g0035a0001c0002t0001g0100a0001c0002t0001g0101others(1): Show | 4 | HG03195.hp1 HG03225.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.511-172G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1073834 | ||||||
| chr4:1073850
|
T | G | 254 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(251): Show | 285 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.511-188A>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1073850 | ||||||
| chr4:1073863
|
TATTACCT others(1): Show |
T | 7 | a0001c0002t0004g0008a0001c0002t0004g0009a0001c0002t0004g0038others(4): Show | 9 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.511-209_511-202del others(8): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1073863 | ||||||
| chr4:1073980
|
G | A | 1 | a0001c0002t0002g0227 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.511-318C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1073980 | ||||||
| chr4:1074119
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.511-457A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1074119 | ||||||
| chr4:1074246
|
CCT | C | 3 | a0001c0002t0002g0282a0001c0002t0002g0283a0001c0002t0002g0318 | 3 | HG02165.hp1 NA18944.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.511-586_511-585del others(2): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1074246 | ||||||
| chr4:1074338
|
C | T | 1 | a0001c0002t0002g0168 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.511-676G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1074338 | ||||||
| chr4:1074390
|
C | T | 1 | a0001c0002t0002g0309 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.511-728G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1074390 | ||||||
| chr4:1074447
|
C | T | 1 | a0007c0008t0011g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.511-785G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1074447 | ||||||
| chr4:1074488
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.511-826G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1074488 | ||||||
| chr4:1074639
|
G | A | 1 | a0007c0008t0011g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.511-977C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1074639 | ||||||
| chr4:1074660
|
C | T | 27 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0114others(24): Show | 30 | HG00597.hp1 HG00621.hp2 HG02523.hp2 others(27): Show |
intron_variant | MODIFIER | c.511-998G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1074660 | ||||||
| chr4:1074777
|
CAGG | C | 3 | a0001c0001t0006g0357a0001c0001t0006g0358a0001c0001t0006g0359 | 3 | HG01167.hp1 HG02109.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.511-1118_511-1116d others(5): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1074777 | ||||||
| chr4:1074916
|
T | TC | 260 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(257): Show | 292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.511-1255dupG | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1074916 | ||||||
| chr4:1074937
|
A | C | 2 | a0001c0001t0005g0045a0001c0001t0005g0046 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.511-1275T>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1074937 | ||||||
| chr4:1074989
|
C | T | 2 | a0001c0002t0004g0009a0001c0002t0004g0048 | 3 | HG02717.hp1 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.511-1327G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1074989 | ||||||
| chr4:1074990
|
A | G | 260 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(257): Show | 292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.511-1328T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1074990 | ||||||
| chr4:1075031
|
G | A | 253 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(250): Show | 283 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.511-1369C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1075031 | ||||||
| chr4:1075190
|
G | T | 1 | a0001c0002t0002g0317 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.511-1528C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1075190 | ||||||
| chr4:1075293
|
G | A | 1 | a0001c0002t0002g0155 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.511-1631C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1075293 | ||||||
| chr4:1075306
|
G | C | 1 | a0001c0001t0001g0010 | 2 | HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.511-1644C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1075306 | ||||||
| chr4:1075345
|
A | G | 1 | a0001c0001t0010g0191 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.511-1683T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1075345 | ||||||
| chr4:1075397
|
C | T | 1 | a0001c0002t0002g0057 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.511-1735G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1075397 | ||||||
| chr4:1075497
|
G | C | 1 | a0001c0002t0002g0150 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.511-1835C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1075497 | ||||||
| chr4:1075507
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.511-1845C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1075507 | ||||||
| chr4:1075527
|
G | C | 2 | a0001c0001t0001g0055a0001c0001t0001g0056 | 2 | HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.511-1865C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1075527 | ||||||
| chr4:1075762
|
A | G | 6 | a0001c0001t0001g0012a0001c0001t0001g0065a0001c0001t0001g0066others(3): Show | 7 | HG01243.hp1 HG02257.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.511-2100T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1075762 | ||||||
| chr4:1076063
|
A | G | 260 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(257): Show | 292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.511-2401T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1076063 | ||||||
| chr4:1076078
|
A | G | 260 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(257): Show | 292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.511-2416T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1076078 | ||||||
| chr4:1076099
|
C | T | 1 | a0007c0008t0011g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.511-2437G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1076099 | ||||||
| chr4:1076185
|
C | T | 253 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(250): Show | 283 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.511-2523G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1076185 | ||||||
| chr4:1076220
|
T | A | 1 | a0007c0008t0011g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.511-2558A>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1076220 | ||||||
| chr4:1076352
|
G | T | 253 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(250): Show | 283 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.511-2690C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1076352 | ||||||
| chr4:1076451
|
C | A | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(1): Show | 4 | HG02818.hp2 HG03471.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.511-2789G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1076451 | ||||||
| chr4:1076547
|
C | T | 1 | a0001c0001t0001g0142 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.511-2885G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1076547 | ||||||
| chr4:1076576
|
C | A | 1 | a0001c0002t0002g0150 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.511-2914G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1076576 | ||||||
| chr4:1076675
|
A | C | 3 | a0001c0002t0004g0008a0001c0002t0004g0038a0001c0002t0004g0039 | 4 | HG02922.hp2 HG03139.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.510+2968T>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1076675 | ||||||
| chr4:1076703
|
G | A | 7 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0001g0105others(4): Show | 7 | HG02040.hp1 HG03491.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.510+2940C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1076703 | ||||||
| chr4:1076781
|
A | G | 1 | a0001c0002t0002g0107 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.510+2862T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1076781 | ||||||
| chr4:1076841
|
A | G | 7 | a0001c0002t0004g0008a0001c0002t0004g0009a0001c0002t0004g0038others(4): Show | 9 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.510+2802T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1076841 | ||||||
| chr4:1076998
|
G | A | 1 | a0001c0001t0001g0062 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.510+2645C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1076998 | ||||||
| chr4:1077038
|
A | T | 1 | a0001c0001t0010g0191 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.510+2605T>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1077038 | ||||||
| chr4:1077064
|
C | T | 246 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(243): Show | 276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.510+2579G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1077064 | ||||||
| chr4:1077142
|
T | C | 1 | a0001c0001t0001g0177 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.510+2501A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1077142 | ||||||
| chr4:1077176
|
C | T | 2 | a0001c0002t0004g0009a0001c0002t0004g0048 | 3 | HG02717.hp1 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.510+2467G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1077176 | ||||||
| chr4:1077177
|
G | A | 41 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(38): Show | 45 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(42): Show |
intron_variant | MODIFIER | c.510+2466C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1077177 | ||||||
| chr4:1077279
|
T | C | 254 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(251): Show | 285 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.510+2364A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1077279 | ||||||
| chr4:1077280
|
G | A | 2 | a0001c0001t0001g0064a0001c0001t0001g0071 | 2 | NA18948.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.510+2363C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1077280 | ||||||
| chr4:1077289
|
T | C | 1 | a0001c0002t0002g0232 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.510+2354A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1077289 | ||||||
| chr4:1077537
|
G | A | 1 | a0001c0002t0002g0298 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.510+2106C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1077537 | ||||||
| chr4:1077657
|
C | G | 1 | a0001c0002t0004g0009 | 2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.510+1986G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1077657 | ||||||
| chr4:1077661
|
C | T | 3 | a0001c0002t0002g0256a0001c0002t0002g0275a0001c0002t0017g0361 | 3 | NA18961.hp1 NA19009.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.510+1982G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1077661 | ||||||
| chr4:1077720
|
G | T | 1 | a0001c0002t0002g0264 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.510+1923C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1077720 | ||||||
| chr4:1077797
|
C | A | 3 | a0001c0001t0001g0075a0001c0001t0001g0184a0001c0001t0001g0185 | 3 | HG00609.hp2 HG02083.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.510+1846G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1077797 | ||||||
| chr4:1077888
|
C | T | 1 | a0001c0002t0003g0351 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.510+1755G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1077888 | ||||||
| chr4:1077901
|
C | T | 1 | a0001c0001t0001g0069 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.510+1742G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1077901 | ||||||
| chr4:1077902
|
G | A | 1 | a0001c0002t0004g0048 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.510+1741C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1077902 | ||||||
| chr4:1077948
|
T | A | 2 | a0001c0002t0002g0274a0001c0002t0002g0328 | 2 | HG00099.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.510+1695A>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1077948 | ||||||
| chr4:1078002
|
C | T | 1 | a0001c0002t0012g0103 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.510+1641G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078002 | ||||||
| chr4:1078057
|
C | A | 7 | a0001c0002t0004g0008a0001c0002t0004g0009a0001c0002t0004g0038others(4): Show | 9 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.510+1586G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078057 | ||||||
| chr4:1078119
|
A | G | 102 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 116 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.510+1524T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078119 | ||||||
| chr4:1078237
|
G | A | 1 | a0001c0002t0002g0312 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.510+1406C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078237 | ||||||
| chr4:1078247
|
C | A | 1 | a0001c0001t0001g0143 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.510+1396G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078247 | ||||||
| chr4:1078403
|
G | A | 2 | a0001c0001t0001g0154a0001c0001t0010g0191 | 2 | HG02922.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.510+1240C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078403 | ||||||
| chr4:1078432
|
C | T | 190 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(187): Show | 214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.510+1211G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078432 | ||||||
| chr4:1078485
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.510+1158C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078485 | ||||||
| chr4:1078543
|
C | T | 1 | a0001c0001t0001g0206 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.510+1100G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078543 | ||||||
| chr4:1078561
|
A | G | 9 | a0001c0002t0001g0034a0001c0002t0001g0041a0001c0002t0001g0042others(6): Show | 11 | HG02486.hp2 HG02572.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.510+1082T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078561 | ||||||
| chr4:1078697
|
C | T | 190 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(187): Show | 214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.510+946G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078697 | ||||||
| chr4:1078729
|
C | T | 7 | a0001c0001t0001g0032a0001c0001t0001g0171a0001c0001t0001g0172others(4): Show | 8 | NA18977.hp2 NA18986.hp2 NA18988.hp2 others(5): Show |
intron_variant | MODIFIER | c.510+914G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078729 | ||||||
| chr4:1078749
|
G | T | 1 | a0001c0002t0012g0103 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.510+894C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078749 | ||||||
| chr4:1078801
|
T | C | 2 | a0001c0001t0001g0073a0001c0001t0001g0074 | 2 | NA18941.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.510+842A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078801 | ||||||
| chr4:1078835
|
GGGACCAA others(4): Show |
G | 1 | a0001c0002t0002g0313 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.510+797_510+807del others(11): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078835 | ||||||
| chr4:1078836
|
G | A | 1 | a0001c0002t0012g0103 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.510+807C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078836 | ||||||
| chr4:1078852
|
A | G | 1 | a0001c0002t0001g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.510+791T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078852 | ||||||
| chr4:1078884
|
C | T | 1 | a0001c0002t0002g0309 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.510+759G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078884 | ||||||
| chr4:1078923
|
G | GGGACCAA others(4): Show |
7 | a0001c0002t0001g0059a0001c0002t0001g0097a0001c0002t0001g0307others(4): Show | 7 | HG01255.hp1 HG01433.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.510+709_510+719dup others(11): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078923 | ||||||
| chr4:1078925
|
G | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0049a0001c0001t0001g0050 | 4 | HG02559.hp1 HG02809.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.510+718C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078925 | ||||||
| chr4:1078937
|
G | A | 42 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(39): Show | 47 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.510+706C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078937 | ||||||
| chr4:1078938
|
T | C | 42 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(39): Show | 47 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.510+705A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078938 | ||||||
| chr4:1078948
|
A | G | 42 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(39): Show | 47 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.510+695T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078948 | ||||||
| chr4:1078949
|
C | T | 42 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(39): Show | 47 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.510+694G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078949 | ||||||
| chr4:1078956
|
A | G | 212 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(209): Show | 238 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.510+687T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078956 | ||||||
| chr4:1078966
|
T | C | 38 | a0001c0002t0001g0016a0001c0002t0001g0021a0001c0002t0001g0035others(35): Show | 40 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.510+677A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078966 | ||||||
| chr4:1078977
|
C | T | 36 | a0001c0002t0001g0016a0001c0002t0001g0021a0001c0002t0001g0035others(33): Show | 38 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.510+666G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078977 | ||||||
| chr4:1078981
|
G | A | 36 | a0001c0002t0001g0016a0001c0002t0001g0021a0001c0002t0001g0035others(33): Show | 38 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.510+662C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078981 | ||||||
| chr4:1078982
|
T | C | 36 | a0001c0002t0001g0016a0001c0002t0001g0021a0001c0002t0001g0035others(33): Show | 38 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.510+661A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078982 | ||||||
| chr4:1078992
|
A | G | 36 | a0001c0002t0001g0016a0001c0002t0001g0021a0001c0002t0001g0035others(33): Show | 38 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.510+651T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078992 | ||||||
| chr4:1078993
|
C | T | 37 | a0001c0001t0001g0054a0001c0002t0001g0016a0001c0002t0001g0021others(34): Show | 39 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.510+650G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078993 | ||||||
| chr4:1078999
|
T | C | 36 | a0001c0002t0001g0016a0001c0002t0001g0021a0001c0002t0001g0035others(33): Show | 38 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.510+644A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078999 | ||||||
| chr4:1078999
|
T | G | 4 | a0001c0001t0005g0043a0001c0001t0005g0045a0001c0001t0005g0046others(1): Show | 4 | HG03491.hp1 HG03492.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.510+644A>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078999 | ||||||
| chr4:1078999
|
TAGGACCA others(4): Show |
T | 13 | a0001c0002t0001g0015a0001c0002t0001g0059a0001c0002t0001g0097others(10): Show | 16 | HG01255.hp1 HG01433.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.510+633_510+643del others(11): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1078999 | ||||||
| chr4:1079000
|
A | G | 205 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(202): Show | 231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.510+643T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1079000 | ||||||
| chr4:1079010
|
C | T | 36 | a0001c0002t0001g0016a0001c0002t0001g0021a0001c0002t0001g0035others(33): Show | 38 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.510+633G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1079010 | ||||||
| chr4:1079023
|
G | A | 10 | a0001c0002t0001g0034a0001c0002t0001g0037a0001c0002t0001g0041others(7): Show | 12 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.510+620C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1079023 | ||||||
| chr4:1079028
|
AACATGGG others(39): Show |
A | 5 | a0001c0001t0001g0044a0001c0001t0001g0105a0001c0001t0005g0043others(2): Show | 5 | HG02040.hp1 HG03491.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.510+569_510+614del others(46): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1079028 | ||||||
| chr4:1079030
|
CATGGGAC others(6): Show |
C | 2 | a0001c0001t0001g0061a0001c0001t0005g0045 | 2 | HG03492.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.510+600_510+612del others(13): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1079030 | ||||||
| chr4:1079032
|
T | C | 1 | a0001c0002t0001g0059 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.510+611A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1079032 | ||||||
| chr4:1079066
|
G | GGGACCAA others(26): Show |
1 | a0007c0008t0011g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.510+544_510+576dup others(33): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1079066 | ||||||
| chr4:1079066
|
GGGACCAA others(26): Show |
G | 3 | a0001c0001t0001g0061a0001c0001t0005g0045a0001c0002t0006g0360 | 3 | HG03492.hp1 HG03516.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.510+544_510+576del others(33): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1079066 | ||||||
| chr4:1079070
|
CCAACACA others(4): Show |
C | 2 | a0001c0001t0001g0110a0001c0001t0001g0222 | 2 | NA18970.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.510+562_510+572del others(11): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1079070 | ||||||
| chr4:1079079
|
G | A | 5 | a0001c0001t0001g0044a0001c0001t0001g0105a0001c0001t0005g0043others(2): Show | 5 | HG02040.hp1 HG03491.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.510+564C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1079079 | ||||||
| chr4:1079098
|
T | C | 1 | a0001c0002t0002g0321 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.510+545A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1079098 | ||||||
| chr4:1079099
|
A | G | 5 | a0001c0001t0001g0044a0001c0001t0001g0105a0001c0001t0005g0043others(2): Show | 5 | HG02040.hp1 HG03491.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.510+544T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1079099 | ||||||
| chr4:1079133
|
G | C | 3 | a0001c0001t0001g0022a0001c0001t0001g0173a0001c0001t0001g0174 | 4 | HG02155.hp2 NA18984.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.510+510C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1079133 | ||||||
| chr4:1079208
|
T | C | 212 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(209): Show | 238 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.510+435A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1079208 | ||||||
| chr4:1079211
|
A | G | 212 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(209): Show | 238 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.510+432T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1079211 | ||||||
| chr4:1079219
|
C | T | 100 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(97): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.510+424G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1079219 | ||||||
| chr4:1079251
|
A | C | 7 | a0001c0001t0001g0032a0001c0001t0001g0171a0001c0001t0001g0172others(4): Show | 8 | NA18977.hp2 NA18986.hp2 NA18988.hp2 others(5): Show |
intron_variant | MODIFIER | c.510+392T>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1079251 | ||||||
| chr4:1079331
|
G | A | 1 | a0007c0008t0011g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.510+312C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1079331 | ||||||
| chr4:1079369
|
T | G | 1 | a0001c0002t0002g0150 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.510+274A>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1079369 | ||||||
| chr4:1079496
|
T | A | 1 | a0001c0002t0001g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.510+147A>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1079496 | ||||||
| chr4:1079498
|
A | C | 1 | a0001c0002t0001g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.510+145T>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1079498 | ||||||
| chr4:1079514
|
C | T | 7 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0001g0105others(4): Show | 7 | HG02040.hp1 HG03491.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.510+129G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1079514 | ||||||
| chr4:1079523
|
G | A | 1 | a0007c0008t0011g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.510+120C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1079523 | ||||||
| chr4:1079602
|
G | A | 1 | a0001c0002t0002g0269 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.510+41C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 8/9 | chr4 | 1079602 | ||||||
| chr4:1079743
|
C | T | 1 | a0001c0001t0001g0140 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.465-55G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 7/9 | chr4 | 1079743 | ||||||
| chr4:1079749
|
T | C | 2 | a0001c0001t0001g0154a0001c0001t0010g0191 | 2 | HG02922.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.465-61A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 7/9 | chr4 | 1079749 | ||||||
| chr4:1079972
|
C | T | 212 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(209): Show | 238 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.465-284G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 7/9 | chr4 | 1079972 | ||||||
| chr4:1080047
|
G | A | 1 | a0001c0002t0001g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.465-359C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 7/9 | chr4 | 1080047 | ||||||
| chr4:1080058
|
G | A | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(1): Show | 4 | HG02818.hp2 HG03471.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.465-370C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 7/9 | chr4 | 1080058 | ||||||
| chr4:1080131
|
C | G | 1 | a0001c0002t0001g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.465-443G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 7/9 | chr4 | 1080131 | ||||||
| chr4:1080134
|
G | T | 1 | a0001c0002t0001g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.465-446C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 7/9 | chr4 | 1080134 | ||||||
| chr4:1080135
|
T | C | 1 | a0001c0002t0001g0297 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.465-447A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 7/9 | chr4 | 1080135 | ||||||
| chr4:1080221
|
C | T | 212 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(209): Show | 238 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.465-533G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 7/9 | chr4 | 1080221 | ||||||
| chr4:1080444
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.465-756G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 7/9 | chr4 | 1080444 | ||||||
| chr4:1080445
|
G | A | 1 | a0001c0001t0001g0216 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.465-757C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 7/9 | chr4 | 1080445 | ||||||
| chr4:1080578
|
C | T | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | HG01243.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.464+841G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 7/9 | chr4 | 1080578 | ||||||
| chr4:1080611
|
C | T | 2 | a0001c0001t0001g0001a0001c0001t0001g0109 | 5 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(2): Show |
intron_variant | MODIFIER | c.464+808G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 7/9 | chr4 | 1080611 | ||||||
| chr4:1080624
|
T | C | 260 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(257): Show | 292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.464+795A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 7/9 | chr4 | 1080624 | ||||||
| chr4:1080648
|
G | A | 48 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(45): Show | 54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.464+771C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 7/9 | chr4 | 1080648 | ||||||
| chr4:1080686
|
CT | C | 14 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(11): Show | 16 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.464+732delA | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 7/9 | chr4 | 1080686 | ||||||
| chr4:1080733
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.464+686C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 7/9 | chr4 | 1080733 | ||||||
| chr4:1080777
|
G | A | 4 | a0001c0002t0001g0015a0001c0002t0001g0097a0001c0002t0001g0307others(1): Show | 5 | HG01255.hp1 HG02451.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.464+642C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 7/9 | chr4 | 1080777 | ||||||
| chr4:1080902
|
C | A | 2 | a0001c0002t0002g0274a0001c0002t0002g0328 | 2 | HG00099.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.464+517G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 7/9 | chr4 | 1080902 | ||||||
| chr4:1080950
|
G | A | 3 | a0001c0002t0001g0021a0001c0002t0001g0156a0001c0002t0003g0339 | 4 | HG02886.hp1 HG02970.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.464+469C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 7/9 | chr4 | 1080950 | ||||||
| chr4:1081069
|
C | A | 3 | a0001c0001t0001g0096a0001c0001t0001g0183a0001c0001t0001g0301 | 3 | HG02258.hp2 HG03710.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.464+350G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 7/9 | chr4 | 1081069 | ||||||
| chr4:1081193
|
C | T | 7 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0001g0105others(4): Show | 7 | HG02040.hp1 HG03491.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.464+226G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 7/9 | chr4 | 1081193 | ||||||
| chr4:1081221
|
C | T | 1 | a0001c0002t0002g0155 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.464+198G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 7/9 | chr4 | 1081221 | ||||||
| chr4:1081312
|
T | A | 12 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0063others(9): Show | 15 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(12): Show |
intron_variant | MODIFIER | c.464+107A>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 7/9 | chr4 | 1081312 | ||||||
| chr4:1081374
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.464+45C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 7/9 | chr4 | 1081374 | ||||||
| chr4:1081483
|
C | T | 78 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0012others(75): Show | 88 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.416-16G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 6/9 | chr4 | 1081483 | ||||||
| chr4:1081552
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.415+15G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 6/9 | chr4 | 1081552 | ||||||
| chr4:1081627
|
G | A | 1 | a0001c0001t0001g0219 | 1 | NA19087.hp2 | splice_region_variant&intron_variant | LOW | c.363-8C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1081627 | ||||||
| chr4:1081893
|
T | C | 7 | a0001c0002t0004g0008a0001c0002t0004g0009a0001c0002t0004g0038others(4): Show | 9 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.363-274A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1081893 | ||||||
| chr4:1081896
|
G | A | 7 | a0001c0002t0004g0008a0001c0002t0004g0009a0001c0002t0004g0038others(4): Show | 9 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.363-277C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1081896 | ||||||
| chr4:1081907
|
G | T | 1 | a0001c0002t0012g0103 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.363-288C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1081907 | ||||||
| chr4:1081942
|
C | T | 1 | a0001c0002t0001g0101 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.363-323G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1081942 | ||||||
| chr4:1081983
|
C | T | 187 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(184): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.363-364G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1081983 | ||||||
| chr4:1081997
|
T | A | 4 | a0001c0002t0003g0033a0001c0002t0003g0351a0001c0002t0003g0354others(1): Show | 5 | HG00642.hp2 HG00735.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.363-378A>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1081997 | ||||||
| chr4:1082029
|
T | C | 1 | a0001c0001t0001g0077 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.363-410A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1082029 | ||||||
| chr4:1082090
|
C | G | 3 | a0001c0002t0004g0008a0001c0002t0004g0038a0001c0002t0004g0039 | 4 | HG02922.hp2 HG03139.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.363-471G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1082090 | ||||||
| chr4:1082145
|
A | G | 1 | a0001c0001t0001g0202 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.363-526T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1082145 | ||||||
| chr4:1082152
|
A | G | 260 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(257): Show | 292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.363-533T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1082152 | ||||||
| chr4:1082392
|
T | C | 1 | a0001c0001t0001g0173 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.363-773A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1082392 | ||||||
| chr4:1082536
|
T | C | 1 | a0001c0002t0002g0155 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.363-917A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1082536 | ||||||
| chr4:1082564
|
G | A | 1 | a0001c0001t0001g0190 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.363-945C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1082564 | ||||||
| chr4:1082629
|
G | C | 1 | a0001c0002t0001g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.363-1010C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1082629 | ||||||
| chr4:1082667
|
T | C | 1 | a0007c0008t0011g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.363-1048A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1082667 | ||||||
| chr4:1082672
|
G | C | 8 | a0001c0001t0001g0096a0001c0002t0004g0008a0001c0002t0004g0009others(5): Show | 10 | HG01891.hp1 HG02258.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.363-1053C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1082672 | ||||||
| chr4:1082709
|
C | G | 8 | a0001c0001t0001g0157a0001c0001t0001g0160a0001c0001t0001g0161others(5): Show | 8 | HG01192.hp1 HG01255.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.363-1090G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1082709 | ||||||
| chr4:1082721
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.363-1102G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1082721 | ||||||
| chr4:1082809
|
G | A | 1 | a0007c0008t0011g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.363-1190C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1082809 | ||||||
| chr4:1082891
|
T | C | 1 | a0001c0001t0001g0123 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.363-1272A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1082891 | ||||||
| chr4:1082905
|
A | C | 7 | a0001c0002t0004g0008a0001c0002t0004g0009a0001c0002t0004g0038others(4): Show | 9 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.363-1286T>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1082905 | ||||||
| chr4:1083001
|
C | T | 7 | a0001c0002t0004g0008a0001c0002t0004g0009a0001c0002t0004g0038others(4): Show | 9 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.363-1382G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083001 | ||||||
| chr4:1083097
|
C | G | 41 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(38): Show | 45 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(42): Show |
intron_variant | MODIFIER | c.363-1478G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083097 | ||||||
| chr4:1083157
|
C | T | 1 | a0001c0002t0002g0248 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.363-1538G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083157 | ||||||
| chr4:1083219
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.363-1600C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083219 | ||||||
| chr4:1083353
|
T | G | 1 | a0001c0001t0001g0056 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.363-1734A>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083353 | ||||||
| chr4:1083494
|
T | C | 7 | a0001c0002t0004g0008a0001c0002t0004g0009a0001c0002t0004g0038others(4): Show | 9 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.363-1875A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083494 | ||||||
| chr4:1083504
|
G | A | 7 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0001g0105others(4): Show | 7 | HG02040.hp1 HG03491.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.363-1885C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083504 | ||||||
| chr4:1083511
|
G | T | 6 | a0001c0002t0004g0008a0001c0002t0004g0009a0001c0002t0004g0038others(3): Show | 8 | HG01891.hp1 HG02717.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.363-1892C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083511 | ||||||
| chr4:1083562
|
C | T | 1 | a0001c0002t0001g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.363-1943G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083562 | ||||||
| chr4:1083592
|
C | T | 6 | a0001c0001t0001g0157a0001c0001t0001g0160a0001c0001t0001g0161others(3): Show | 6 | HG01884.hp1 HG01891.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.363-1973G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083592 | ||||||
| chr4:1083629
|
C | T | 4 | a0001c0002t0001g0034a0002c0003t0001g0006a0002c0003t0001g0332others(1): Show | 6 | HG02486.hp2 HG02572.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.363-2010G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083629 | ||||||
| chr4:1083639
|
A | AAAAC | 10 | a0001c0001t0001g0055a0001c0001t0001g0081a0001c0001t0001g0288others(7): Show | 10 | HG00673.hp2 HG01952.hp1 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.363-2024_363-2021d others(6): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083639 | ||||||
| chr4:1083639
|
A | AAAACAAA others(1): Show |
3 | a0001c0001t0001g0051a0001c0001t0001g0091a0001c0001t0001g0151 | 3 | HG01175.hp2 HG03654.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.363-2028_363-2021d others(10): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083639 | ||||||
| chr4:1083639
|
AAAAC | A | 141 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(138): Show | 159 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.363-2024_363-2021d others(6): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083639 | ||||||
| chr4:1083639
|
AAAACAAA others(1): Show |
A | 12 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0112others(9): Show | 15 | HG00408.hp2 HG00621.hp1 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.363-2028_363-2021d others(10): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083639 | ||||||
| chr4:1083639
|
AAAACAAA others(5): Show |
A | 1 | a0001c0001t0001g0171 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.363-2032_363-2021d others(14): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083639 | ||||||
| chr4:1083639
|
AAAACAAA others(9): Show |
A | 1 | a0001c0002t0012g0103 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.363-2036_363-2021d others(18): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083639 | ||||||
| chr4:1083646
|
AC | A | 7 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0001g0105others(4): Show | 7 | HG02040.hp1 HG03491.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.363-2028delG | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083646 | ||||||
| chr4:1083672
|
A | T | 1 | a0001c0001t0001g0192 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.363-2053T>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083672 | ||||||
| chr4:1083688
|
A | G | 1 | a0001c0002t0001g0042 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.363-2069T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083688 | ||||||
| chr4:1083754
|
C | T | 260 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(257): Show | 292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.363-2135G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083754 | ||||||
| chr4:1083787
|
G | A | 191 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(188): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.362+2109C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083787 | ||||||
| chr4:1083868
|
C | T | 2 | a0001c0002t0002g0245a0001c0002t0002g0248 | 2 | HG01123.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.362+2028G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083868 | ||||||
| chr4:1083945
|
A | AT | 99 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(96): Show | 113 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.362+1950dupA | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083945 | ||||||
| chr4:1083945
|
A | ATT | 14 | a0001c0001t0001g0108a0001c0001t0001g0134a0001c0001t0001g0141others(11): Show | 16 | HG00438.hp2 HG01981.hp2 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.362+1949_362+1950d others(4): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083945 | ||||||
| chr4:1083945
|
A | ATTT | 76 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0012others(73): Show | 86 | HG00609.hp1 HG00609.hp2 HG00673.hp1 others(83): Show |
intron_variant | MODIFIER | c.362+1948_362+1950d others(5): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083945 | ||||||
| chr4:1083945
|
A | ATTTT | 14 | a0001c0001t0001g0054a0001c0001t0001g0073a0001c0001t0001g0077others(11): Show | 14 | HG00558.hp1 HG00558.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.362+1947_362+1950d others(6): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083945 | ||||||
| chr4:1083945
|
A | T | 2 | a0001c0001t0001g0162a0001c0002t0002g0155 | 2 | HG01891.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.362+1951T>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083945 | ||||||
| chr4:1083945
|
AT | A | 17 | a0001c0001t0001g0044a0001c0001t0005g0046a0001c0002t0001g0015others(14): Show | 19 | HG00099.hp1 HG01255.hp1 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.362+1950delA | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083945 | ||||||
| chr4:1083945
|
ATT | A | 30 | a0001c0002t0001g0021a0001c0002t0001g0059a0001c0002t0001g0156others(27): Show | 32 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.362+1949_362+1950d others(4): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083945 | ||||||
| chr4:1083970
|
C | T | 1 | a0001c0002t0003g0344 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.362+1926G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083970 | ||||||
| chr4:1083971
|
G | A | 2 | a0001c0002t0012g0103a0007c0008t0011g0040 | 2 | HG01891.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.362+1925C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1083971 | ||||||
| chr4:1084020
|
C | T | 1 | a0001c0002t0003g0340 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.362+1876G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1084020 | ||||||
| chr4:1084092
|
G | A | 45 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(42): Show | 49 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.362+1804C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1084092 | ||||||
| chr4:1084096
|
G | C | 1 | a0001c0002t0002g0155 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.362+1800C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1084096 | ||||||
| chr4:1084163
|
T | C | 1 | a0001c0002t0012g0103 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.362+1733A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1084163 | ||||||
| chr4:1084205
|
C | T | 6 | a0001c0001t0001g0012a0001c0001t0001g0065a0001c0001t0001g0066others(3): Show | 7 | HG01243.hp1 HG02257.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.362+1691G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1084205 | ||||||
| chr4:1084336
|
G | A | 100 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(97): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.362+1560C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1084336 | ||||||
| chr4:1084363
|
A | G | 1 | a0007c0008t0011g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.362+1533T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1084363 | ||||||
| chr4:1084384
|
G | A | 73 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0013others(70): Show | 82 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.362+1512C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1084384 | ||||||
| chr4:1084399
|
G | A | 260 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(257): Show | 292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.362+1497C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1084399 | ||||||
| chr4:1084451
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.362+1445G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1084451 | ||||||
| chr4:1084596
|
G | T | 7 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0001g0105others(4): Show | 7 | HG02040.hp1 HG03491.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.362+1300C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1084596 | ||||||
| chr4:1084601
|
G | A | 1 | a0001c0001t0010g0191 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.362+1295C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1084601 | ||||||
| chr4:1084613
|
C | G | 2 | a0001c0001t0001g0132a0001c0001t0001g0327 | 2 | HG02615.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.362+1283G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1084613 | ||||||
| chr4:1084726
|
C | CA | 30 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0001g0105others(27): Show | 30 | HG00673.hp2 HG01261.hp2 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.362+1169dupT | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1084726 | ||||||
| chr4:1084726
|
CA | C | 60 | a0001c0001t0001g0050a0001c0001t0001g0082a0001c0001t0001g0124others(57): Show | 64 | HG00609.hp1 HG00642.hp2 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.362+1169delT | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1084726 | ||||||
| chr4:1084726
|
CAA | C | 173 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(170): Show | 197 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.362+1168_362+1169d others(4): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1084726 | ||||||
| chr4:1084726
|
CAAA | C | 13 | a0001c0001t0001g0071a0001c0001t0001g0083a0001c0001t0001g0106others(10): Show | 15 | HG01168.hp2 HG01169.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.362+1167_362+1169d others(5): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1084726 | ||||||
| chr4:1084738
|
A | T | 1 | a0007c0008t0011g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.362+1158T>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1084738 | ||||||
| chr4:1084808
|
C | T | 79 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0012others(76): Show | 89 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.362+1088G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1084808 | ||||||
| chr4:1084951
|
T | C | 1 | a0001c0002t0012g0103 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.362+945A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1084951 | ||||||
| chr4:1084960
|
C | A | 2 | a0001c0002t0001g0209a0001c0002t0001g0303 | 2 | HG03041.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.362+936G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1084960 | ||||||
| chr4:1084979
|
C | T | 1 | a0001c0002t0002g0036 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.362+917G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1084979 | ||||||
| chr4:1085139
|
G | A | 1 | a0001c0002t0012g0103 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.362+757C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1085139 | ||||||
| chr4:1085167
|
G | A | 1 | a0001c0002t0004g0009 | 2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.362+729C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1085167 | ||||||
| chr4:1085250
|
C | A | 1 | a0001c0002t0012g0103 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.362+646G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1085250 | ||||||
| chr4:1085295
|
T | C | 1 | a0007c0008t0011g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.362+601A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1085295 | ||||||
| chr4:1085488
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.362+408A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1085488 | ||||||
| chr4:1085773
|
T | C | 7 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0001g0105others(4): Show | 7 | HG02040.hp1 HG03491.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.362+123A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1085773 | ||||||
| chr4:1085835
|
G | A | 1 | a0001c0002t0002g0269 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.362+61C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 5/9 | chr4 | 1085835 | ||||||
| chr4:1086105
|
G | A | 2 | a0001c0001t0001g0127a0001c0002t0002g0155 | 2 | HG02622.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.304-151C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1086105 | ||||||
| chr4:1086295
|
C | G | 261 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(258): Show | 293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.304-341G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1086295 | ||||||
| chr4:1086370
|
G | C | 1 | a0001c0002t0001g0297 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.304-416C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1086370 | ||||||
| chr4:1086603
|
G | C | 260 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(257): Show | 292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.304-649C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1086603 | ||||||
| chr4:1086617
|
A | G | 1 | a0001c0002t0002g0271 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.304-663T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1086617 | ||||||
| chr4:1086631
|
T | A | 1 | a0001c0002t0002g0271 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.304-677A>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1086631 | ||||||
| chr4:1086651
|
T | A | 48 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(45): Show | 54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.304-697A>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1086651 | ||||||
| chr4:1086678
|
G | C | 1 | a0001c0002t0002g0298 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.304-724C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1086678 | ||||||
| chr4:1086680
|
TGGGGTGG others(13): Show |
T | 1 | a0001c0002t0012g0103 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.304-746_304-727del others(20): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1086680 | ||||||
| chr4:1086685
|
T | G | 1 | a0001c0002t0002g0271 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.304-731A>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1086685 | ||||||
| chr4:1086686
|
G | T | 1 | a0001c0002t0002g0271 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.304-732C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1086686 | ||||||
| chr4:1086727
|
G | C | 3 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179 | 3 | NA18955.hp1 NA18993.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.304-773C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1086727 | ||||||
| chr4:1086745
|
G | A | 3 | a0001c0002t0001g0041a0001c0002t0001g0042a0001c0002t0006g0360 | 3 | HG03098.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.304-791C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1086745 | ||||||
| chr4:1086773
|
G | A | 3 | a0001c0002t0004g0008a0001c0002t0004g0038a0001c0002t0004g0039 | 4 | HG02922.hp2 HG03139.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.304-819C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1086773 | ||||||
| chr4:1086866
|
A | G | 1 | a0001c0002t0001g0059 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.304-912T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1086866 | ||||||
| chr4:1087048
|
C | CGGTGGCA others(13): Show |
1 | a0001c0001t0001g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.304-1095_304-1094i others(22): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087048 | ||||||
| chr4:1087059
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.304-1105A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087059 | ||||||
| chr4:1087062
|
C | G | 1 | a0001c0001t0001g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.304-1108G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087062 | ||||||
| chr4:1087063
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.304-1109T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087063 | ||||||
| chr4:1087072
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.304-1118C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087072 | ||||||
| chr4:1087073
|
C | G | 1 | a0001c0001t0001g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.304-1119G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087073 | ||||||
| chr4:1087082
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.304-1128T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087082 | ||||||
| chr4:1087090
|
T | A | 1 | a0001c0001t0001g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.304-1136A>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087090 | ||||||
| chr4:1087106
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.304-1152T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087106 | ||||||
| chr4:1087109
|
T | A | 1 | a0001c0001t0001g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.304-1155A>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087109 | ||||||
| chr4:1087109
|
T | TGAGAGGA others(31): Show |
4 | a0001c0002t0003g0033a0001c0002t0003g0351a0001c0002t0003g0354others(1): Show | 5 | HG00642.hp2 HG00735.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.304-1156_304-1155i others(40): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087109 | ||||||
| chr4:1087118
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.304-1164C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087118 | ||||||
| chr4:1087118
|
G | GGGGTGGG others(31): Show |
1 | a0001c0002t0001g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.304-1165_304-1164i others(40): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087118 | ||||||
| chr4:1087123
|
G | GGGGGAGA others(31): Show |
1 | a0001c0001t0001g0127 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.304-1170_304-1169i others(40): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087123 | ||||||
| chr4:1087123
|
G | GGGGGAGA others(31): Show |
200 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(197): Show | 226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.304-1170_304-1169i others(40): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087123 | ||||||
| chr4:1087123
|
G | GGGGGAGA others(31): Show |
46 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0001g0105others(43): Show | 50 | HG01074.hp2 HG01255.hp1 HG01433.hp1 others(47): Show |
intron_variant | MODIFIER | c.304-1170_304-1169i others(40): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087123 | ||||||
| chr4:1087123
|
G | GGGGGAGA others(29): Show |
1 | a0001c0001t0001g0071 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.304-1170_304-1169i others(38): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087123 | ||||||
| chr4:1087123
|
G | GGGGGAGA others(31): Show |
2 | a0001c0002t0003g0334a0001c0002t0003g0337 | 2 | HG01243.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.304-1170_304-1169i others(40): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087123 | ||||||
| chr4:1087123
|
G | GGGGGGAG others(32): Show |
1 | a0001c0001t0001g0106 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.304-1170_304-1169i others(41): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087123 | ||||||
| chr4:1087123
|
G | T | 5 | a0001c0001t0001g0096a0001c0002t0003g0033a0001c0002t0003g0351others(2): Show | 6 | HG00642.hp2 HG00735.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.304-1169C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087123 | ||||||
| chr4:1087123
|
GGGGGAGA others(108): Show |
G | 3 | a0001c0002t0004g0008a0001c0002t0004g0038a0001c0002t0004g0039 | 4 | HG02922.hp2 HG03139.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.304-1284_304-1170d others(2): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087123 | ||||||
| chr4:1087142
|
G | T | 1 | a0001c0002t0001g0098 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.304-1188C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087142 | ||||||
| chr4:1087160
|
G | C | 1 | a0001c0001t0001g0185 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.304-1206C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087160 | ||||||
| chr4:1087163
|
GGA | G | 212 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(209): Show | 238 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.304-1211_304-1210d others(4): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087163 | ||||||
| chr4:1087205
|
TGAGAGGA others(12): Show |
T | 2 | a0001c0002t0007g0362a0001c0002t0007g0364 | 2 | HG02258.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.304-1270_304-1252d others(21): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087205 | ||||||
| chr4:1087206
|
G | C | 3 | a0001c0002t0001g0041a0001c0002t0001g0042a0001c0002t0006g0360 | 3 | HG03098.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.304-1252C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087206 | ||||||
| chr4:1087213
|
TGGGGTAG others(12): Show |
T | 255 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(252): Show | 286 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.304-1278_304-1260d others(21): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087213 | ||||||
| chr4:1087257
|
A | G | 260 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(257): Show | 292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.304-1303T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087257 | ||||||
| chr4:1087281
|
T | A | 3 | a0001c0002t0001g0016a0001c0002t0001g0098a0001c0002t0013g0102 | 4 | HG02109.hp1 HG02280.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.304-1327A>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087281 | ||||||
| chr4:1087503
|
TGGGGGGT others(14): Show |
T | 1 | a0001c0002t0004g0048 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.304-1570_304-1550d others(23): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087503 | ||||||
| chr4:1087523
|
T | TG | 17 | a0001c0001t0001g0077a0001c0001t0001g0142a0001c0001t0001g0177others(14): Show | 17 | HG01175.hp1 HG01361.hp2 HG01978.hp1 others(14): Show |
intron_variant | MODIFIER | c.304-1570dupC | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087523 | ||||||
| chr4:1087593
|
T | C | 1 | a0007c0008t0011g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.304-1639A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087593 | ||||||
| chr4:1087631
|
G | A | 19 | a0001c0002t0002g0025a0001c0002t0002g0026a0001c0002t0002g0027others(16): Show | 22 | HG00408.hp1 HG01074.hp1 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.304-1677C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087631 | ||||||
| chr4:1087695
|
T | C | 8 | a0001c0001t0001g0157a0001c0001t0001g0160a0001c0001t0001g0161others(5): Show | 8 | HG01192.hp1 HG01255.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.304-1741A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087695 | ||||||
| chr4:1087791
|
G | A | 2 | a0005c0006t0001g0133a0005c0006t0001g0139 | 2 | HG02683.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.304-1837C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087791 | ||||||
| chr4:1087818
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.304-1864G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087818 | ||||||
| chr4:1087834
|
C | A | 1 | a0001c0001t0001g0076 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.304-1880G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087834 | ||||||
| chr4:1087949
|
C | T | 1 | a0001c0002t0012g0103 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.304-1995G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087949 | ||||||
| chr4:1087967
|
C | T | 18 | a0001c0002t0003g0033a0001c0002t0003g0338a0001c0002t0003g0340others(15): Show | 19 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.304-2013G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087967 | ||||||
| chr4:1087993
|
A | T | 1 | a0001c0002t0002g0271 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.304-2039T>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1087993 | ||||||
| chr4:1088096
|
TG | T | 3 | a0001c0001t0005g0045a0001c0001t0005g0046a0001c0002t0002g0271 | 3 | HG03491.hp1 HG03492.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.304-2143delC | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1088096 | ||||||
| chr4:1088109
|
A | G | 1 | a0001c0001t0001g0054 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.304-2155T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1088109 | ||||||
| chr4:1088121
|
A | G | 7 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0001g0105others(4): Show | 7 | HG02040.hp1 HG03491.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.304-2167T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1088121 | ||||||
| chr4:1088273
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.304-2319G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1088273 | ||||||
| chr4:1088398
|
C | T | 46 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(43): Show | 52 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(49): Show |
intron_variant | MODIFIER | c.303+2384G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1088398 | ||||||
| chr4:1088584
|
T | C | 3 | a0001c0001t0001g0051a0001c0001t0001g0091a0001c0001t0001g0151 | 3 | HG01175.hp2 HG03654.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.303+2198A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1088584 | ||||||
| chr4:1088792
|
C | G | 1 | a0001c0002t0001g0059 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.303+1990G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1088792 | ||||||
| chr4:1088813
|
T | C | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(1): Show | 4 | HG02818.hp2 HG03471.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.303+1969A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1088813 | ||||||
| chr4:1088825
|
A | T | 48 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(45): Show | 54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.303+1957T>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1088825 | ||||||
| chr4:1088919
|
G | C | 261 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(258): Show | 293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.303+1863C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1088919 | ||||||
| chr4:1089041
|
T | C | 261 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(258): Show | 293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.303+1741A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1089041 | ||||||
| chr4:1089087
|
C | A | 48 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(45): Show | 54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.303+1695G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1089087 | ||||||
| chr4:1089099
|
C | T | 213 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(210): Show | 239 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.303+1683G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1089099 | ||||||
| chr4:1089201
|
G | A | 1 | a0001c0001t0001g0190 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.303+1581C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1089201 | ||||||
| chr4:1089211
|
G | A | 190 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(187): Show | 214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.303+1571C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1089211 | ||||||
| chr4:1089213
|
T | C | 1 | a0001c0002t0002g0273 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.303+1569A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1089213 | ||||||
| chr4:1089241
|
C | G | 1 | a0001c0002t0002g0276 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.303+1541G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1089241 | ||||||
| chr4:1089282
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.303+1500A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1089282 | ||||||
| chr4:1089324
|
C | T | 261 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(258): Show | 293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.303+1458G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1089324 | ||||||
| chr4:1089443
|
A | C | 3 | a0001c0001t0006g0357a0001c0001t0006g0358a0001c0001t0006g0359 | 3 | HG01167.hp1 HG02109.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.303+1339T>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1089443 | ||||||
| chr4:1089483
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.303+1299A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1089483 | ||||||
| chr4:1089519
|
G | A | 73 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0013others(70): Show | 82 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.303+1263C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1089519 | ||||||
| chr4:1089558
|
T | C | 29 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(26): Show | 32 | HG00609.hp1 HG01109.hp2 HG02015.hp2 others(29): Show |
intron_variant | MODIFIER | c.303+1224A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1089558 | ||||||
| chr4:1089596
|
G | C | 1 | a0001c0002t0006g0360 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.303+1186C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1089596 | ||||||
| chr4:1089604
|
CA | C | 5 | a0001c0001t0001g0013a0001c0001t0001g0064a0001c0001t0001g0070others(2): Show | 6 | NA18948.hp2 NA18956.hp1 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.303+1177delT | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1089604 | ||||||
| chr4:1089636
|
C | T | 7 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0001g0105others(4): Show | 7 | HG02040.hp1 HG03491.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.303+1146G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1089636 | ||||||
| chr4:1089671
|
T | C | 10 | a0001c0002t0001g0034a0001c0002t0001g0037a0001c0002t0001g0041others(7): Show | 12 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.303+1111A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1089671 | ||||||
| chr4:1089689
|
C | T | 6 | a0001c0002t0003g0338a0001c0002t0003g0340a0001c0002t0003g0341others(3): Show | 6 | HG02630.hp2 HG02965.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.303+1093G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1089689 | ||||||
| chr4:1089706
|
A | AT | 41 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(38): Show | 45 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(42): Show |
intron_variant | MODIFIER | c.303+1075dupA | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1089706 | ||||||
| chr4:1089797
|
C | T | 48 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(45): Show | 54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.303+985G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1089797 | ||||||
| chr4:1089886
|
G | A | 1 | a0001c0002t0002g0252 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.303+896C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1089886 | ||||||
| chr4:1089968
|
G | A | 14 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(11): Show | 16 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.303+814C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1089968 | ||||||
| chr4:1090079
|
G | A | 1 | a0001c0002t0002g0270 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.303+703C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1090079 | ||||||
| chr4:1090110
|
G | A | 6 | a0001c0002t0001g0034a0001c0002t0001g0209a0001c0002t0001g0303others(3): Show | 8 | HG02486.hp2 HG02572.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.303+672C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1090110 | ||||||
| chr4:1090273
|
C | T | 79 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0012others(76): Show | 89 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.303+509G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1090273 | ||||||
| chr4:1090349
|
T | C | 261 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(258): Show | 293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.303+433A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1090349 | ||||||
| chr4:1090350
|
G | A | 1 | a0001c0002t0004g0009 | 2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.303+432C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1090350 | ||||||
| chr4:1090358
|
G | A | 3 | a0004c0005t0002g0247a0004c0005t0002g0254a0004c0005t0002g0330 | 3 | HG00099.hp2 HG01261.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.303+424C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1090358 | ||||||
| chr4:1090513
|
C | G | 2 | a0001c0002t0002g0295a0001c0002t0002g0296 | 2 | NA18975.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.303+269G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1090513 | ||||||
| chr4:1090515
|
A | G | 48 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(45): Show | 54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.303+267T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1090515 | ||||||
| chr4:1090543
|
G | A | 48 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(45): Show | 54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.303+239C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1090543 | ||||||
| chr4:1090547
|
G | C | 8 | a0001c0001t0001g0157a0001c0001t0001g0160a0001c0001t0001g0161others(5): Show | 8 | HG01192.hp1 HG01255.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.303+235C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1090547 | ||||||
| chr4:1090674
|
T | C | 3 | a0001c0002t0004g0008a0001c0002t0004g0038a0001c0002t0004g0039 | 4 | HG02922.hp2 HG03139.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.303+108A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 4/9 | chr4 | 1090674 | ||||||
| chr4:1090894
|
A | G | 1 | a0001c0001t0001g0223 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.247-56T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1090894 | ||||||
| chr4:1090935
|
G | C | 297 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(294): Show | 332 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.247-97C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1090935 | ||||||
| chr4:1090951
|
T | A | 3 | a0001c0001t0006g0357a0001c0001t0006g0358a0001c0001t0006g0359 | 3 | HG01167.hp1 HG02109.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.247-113A>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1090951 | ||||||
| chr4:1090977
|
C | T | 48 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(45): Show | 54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.247-139G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1090977 | ||||||
| chr4:1091059
|
G | A | 48 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(45): Show | 54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.247-221C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1091059 | ||||||
| chr4:1091096
|
T | C | 48 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(45): Show | 54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.247-258A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1091096 | ||||||
| chr4:1091132
|
T | C | 48 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(45): Show | 54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.247-294A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1091132 | ||||||
| chr4:1091183
|
G | C | 47 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(44): Show | 53 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(50): Show |
intron_variant | MODIFIER | c.247-345C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1091183 | ||||||
| chr4:1091228
|
C | T | 2 | a0001c0002t0002g0057a0001c0002t0002g0058 | 2 | HG01109.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.247-390G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1091228 | ||||||
| chr4:1091377
|
C | T | 48 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(45): Show | 54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.247-539G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1091377 | ||||||
| chr4:1091431
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.247-593G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1091431 | ||||||
| chr4:1091582
|
G | A | 7 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0001g0105others(4): Show | 7 | HG02040.hp1 HG03491.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.247-744C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1091582 | ||||||
| chr4:1091953
|
C | A | 7 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0001g0105others(4): Show | 7 | HG02040.hp1 HG03491.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.247-1115G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1091953 | ||||||
| chr4:1092010
|
C | T | 3 | a0001c0002t0004g0008a0001c0002t0004g0038a0001c0002t0004g0039 | 4 | HG02922.hp2 HG03139.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.247-1172G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092010 | ||||||
| chr4:1092038
|
A | G | 261 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(258): Show | 293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.247-1200T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092038 | ||||||
| chr4:1092103
|
C | A | 1 | a0001c0001t0001g0118 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.247-1265G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092103 | ||||||
| chr4:1092146
|
T | C | 48 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(45): Show | 54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.247-1308A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092146 | ||||||
| chr4:1092158
|
A | G | 1 | a0001c0002t0002g0256 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.247-1320T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092158 | ||||||
| chr4:1092164
|
G | A | 1 | a0001c0002t0002g0155 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.247-1326C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092164 | ||||||
| chr4:1092238
|
C | T | 2 | a0001c0002t0002g0029a0001c0002t0002g0316 | 3 | NA19012.hp2 NA19067.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.247-1400G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092238 | ||||||
| chr4:1092340
|
G | C | 1 | a0001c0002t0002g0259 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.247-1502C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092340 | ||||||
| chr4:1092452
|
G | C | 2 | a0001c0002t0002g0274a0001c0002t0002g0328 | 2 | HG00099.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.247-1614C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092452 | ||||||
| chr4:1092453
|
A | T | 2 | a0001c0002t0002g0274a0001c0002t0002g0328 | 2 | HG00099.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.247-1615T>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092453 | ||||||
| chr4:1092459
|
T | G | 189 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(186): Show | 213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.247-1621A>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092459 | ||||||
| chr4:1092499
|
C | T | 49 | a0001c0001t0001g0135a0001c0001t0001g0195a0001c0002t0001g0015others(46): Show | 55 | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.247-1661G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092499 | ||||||
| chr4:1092517
|
G | GA | 48 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(45): Show | 54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.247-1680_247-1679i others(3): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092517 | ||||||
| chr4:1092631
|
A | T | 1 | a0001c0001t0001g0141 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.247-1793T>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092631 | ||||||
| chr4:1092715
|
C | T | 48 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(45): Show | 54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.247-1877G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092715 | ||||||
| chr4:1092725
|
G | C | 7 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0001g0105others(4): Show | 7 | HG02040.hp1 HG03491.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.247-1887C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092725 | ||||||
| chr4:1092756
|
C | G | 2 | a0001c0002t0004g0008a0001c0002t0004g0039 | 3 | HG02922.hp2 HG03139.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.247-1918G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092756 | ||||||
| chr4:1092756
|
C | T | 2 | a0001c0001t0001g0105a0007c0008t0011g0040 | 2 | HG01891.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.247-1918G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092756 | ||||||
| chr4:1092778
|
C | T | 2 | a0001c0001t0001g0157a0001c0001t0001g0163 | 2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.247-1940G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092778 | ||||||
| chr4:1092779
|
G | A | 1 | a0001c0002t0002g0284 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.247-1941C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092779 | ||||||
| chr4:1092801
|
G | A | 48 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(45): Show | 54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.247-1963C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092801 | ||||||
| chr4:1092802
|
C | A | 48 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(45): Show | 54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.247-1964G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092802 | ||||||
| chr4:1092880
|
G | A | 46 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(43): Show | 52 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(49): Show |
intron_variant | MODIFIER | c.247-2042C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092880 | ||||||
| chr4:1092914
|
G | A | 48 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(45): Show | 54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.247-2076C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092914 | ||||||
| chr4:1092926
|
G | C | 48 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(45): Show | 54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.247-2088C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092926 | ||||||
| chr4:1092975
|
A | C | 261 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(258): Show | 293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.247-2137T>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092975 | ||||||
| chr4:1092976
|
A | G | 261 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(258): Show | 293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.247-2138T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092976 | ||||||
| chr4:1092989
|
CCAGGGTC others(43): Show |
C | 203 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(200): Show | 227 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.247-2201_247-2152d others(52): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1092989 | ||||||
| chr4:1093041
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.247-2203C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1093041 | ||||||
| chr4:1093075
|
G | A | 1 | a0001c0002t0002g0036 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.247-2237C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1093075 | ||||||
| chr4:1093083
|
T | C | 203 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(200): Show | 227 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.247-2245A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1093083 | ||||||
| chr4:1093278
|
G | A | 48 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(45): Show | 54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.247-2440C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1093278 | ||||||
| chr4:1093380
|
A | AAT | 251 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(248): Show | 281 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.247-2544_247-2543d others(4): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1093380 | ||||||
| chr4:1093383
|
G | T | 251 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(248): Show | 281 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.247-2545C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1093383 | ||||||
| chr4:1093451
|
G | A | 4 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0001g0189others(1): Show | 4 | HG02015.hp2 HG02027.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.247-2613C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1093451 | ||||||
| chr4:1093477
|
T | C | 261 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(258): Show | 293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.247-2639A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1093477 | ||||||
| chr4:1093525
|
T | C | 6 | a0001c0001t0001g0013a0001c0001t0001g0064a0001c0001t0001g0070others(3): Show | 7 | NA18948.hp2 NA18956.hp1 NA18962.hp2 others(4): Show |
intron_variant | MODIFIER | c.247-2687A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1093525 | ||||||
| chr4:1093539
|
G | GCTGCCCA others(14): Show |
257 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(254): Show | 288 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.247-2702_247-2701i others(23): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1093539 | ||||||
| chr4:1093539
|
G | GCTGCCCT others(14): Show |
3 | a0001c0002t0001g0015a0001c0002t0001g0307a0001c0002t0001g0308 | 4 | HG01255.hp1 HG02647.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.247-2702_247-2701i others(23): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1093539 | ||||||
| chr4:1093541
|
C | T | 260 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(257): Show | 292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.247-2703G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1093541 | ||||||
| chr4:1093550
|
C | T | 260 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(257): Show | 292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.247-2712G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1093550 | ||||||
| chr4:1093574
|
C | T | 48 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(45): Show | 54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.247-2736G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1093574 | ||||||
| chr4:1093581
|
C | G | 10 | a0001c0002t0001g0034a0001c0002t0001g0037a0001c0002t0001g0041others(7): Show | 12 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.247-2743G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1093581 | ||||||
| chr4:1093605
|
G | T | 48 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(45): Show | 54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.247-2767C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1093605 | ||||||
| chr4:1093613
|
G | A | 6 | a0001c0001t0001g0031a0001c0001t0001g0279a0001c0001t0001g0280others(3): Show | 7 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.247-2775C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1093613 | ||||||
| chr4:1093699
|
G | A | 10 | a0001c0001t0001g0011a0001c0001t0001g0152a0001c0001t0001g0158others(7): Show | 11 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.247-2861C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1093699 | ||||||
| chr4:1093726
|
T | C | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(1): Show | 4 | HG02818.hp2 HG03471.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.247-2888A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1093726 | ||||||
| chr4:1093743
|
T | C | 48 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(45): Show | 54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.247-2905A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1093743 | ||||||
| chr4:1093829
|
C | A | 48 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(45): Show | 54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.246+2936G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1093829 | ||||||
| chr4:1093878
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.246+2887G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1093878 | ||||||
| chr4:1093938
|
G | A | 1 | a0001c0002t0012g0103 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.246+2827C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1093938 | ||||||
| chr4:1093984
|
G | A | 3 | a0001c0001t0006g0357a0001c0001t0006g0358a0001c0001t0006g0359 | 3 | HG01167.hp1 HG02109.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.246+2781C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1093984 | ||||||
| chr4:1094050
|
G | GCTTGCTG others(12): Show |
48 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(45): Show | 54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.246+2714_246+2715i others(21): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1094050 | ||||||
| chr4:1094113
|
A | G | 100 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(97): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.246+2652T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1094113 | ||||||
| chr4:1094141
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.246+2624G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1094141 | ||||||
| chr4:1094212
|
G | A | 2 | a0001c0002t0003g0334a0001c0002t0003g0337 | 2 | HG01243.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.246+2553C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1094212 | ||||||
| chr4:1094232
|
C | T | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(1): Show | 4 | HG02818.hp2 HG03471.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+2533G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1094232 | ||||||
| chr4:1094405
|
G | A | 3 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179 | 3 | NA18955.hp1 NA18993.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.246+2360C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1094405 | ||||||
| chr4:1094484
|
C | T | 48 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(45): Show | 54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.246+2281G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1094484 | ||||||
| chr4:1094530
|
A | G | 1 | a0001c0001t0001g0281 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.246+2235T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1094530 | ||||||
| chr4:1094630
|
G | C | 2 | a0001c0002t0004g0009a0001c0002t0004g0048 | 3 | HG02717.hp1 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.246+2135C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1094630 | ||||||
| chr4:1094631
|
G | A | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(1): Show | 4 | HG02818.hp2 HG03471.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+2134C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1094631 | ||||||
| chr4:1094686
|
G | C | 45 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(42): Show | 50 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.246+2079C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1094686 | ||||||
| chr4:1094817
|
G | A | 1 | a0001c0001t0001g0121 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.246+1948C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1094817 | ||||||
| chr4:1094888
|
A | T | 1 | a0006c0007t0002g0233 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.246+1877T>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1094888 | ||||||
| chr4:1094903
|
C | G | 1 | a0001c0002t0002g0250 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.246+1862G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1094903 | ||||||
| chr4:1095001
|
T | C | 3 | a0001c0001t0001g0020a0001c0001t0001g0148a0001c0001t0001g0306 | 4 | HG03017.hp2 HG03831.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+1764A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095001 | ||||||
| chr4:1095055
|
G | C | 14 | a0001c0002t0002g0028a0001c0002t0002g0060a0001c0002t0002g0246others(11): Show | 15 | HG00099.hp2 HG01261.hp2 HG02165.hp1 others(12): Show |
intron_variant | MODIFIER | c.246+1710C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095055 | ||||||
| chr4:1095083
|
C | T | 21 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0022others(18): Show | 25 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.246+1682G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095083 | ||||||
| chr4:1095084
|
GGAACCAA others(465): Show |
G | 1 | a0001c0002t0002g0272 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.246+1209_246+1680d others(2): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095084 | ||||||
| chr4:1095123
|
T | C | 1 | a0001c0001t0001g0141 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.246+1642A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095123 | ||||||
| chr4:1095127
|
G | A | 48 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(45): Show | 54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.246+1638C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095127 | ||||||
| chr4:1095155
|
G | A | 48 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(45): Show | 54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.246+1610C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095155 | ||||||
| chr4:1095155
|
GCCCCCCA others(111): Show |
G | 82 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0012others(79): Show | 92 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.246+1492_246+1609d others(2): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095155 | ||||||
| chr4:1095184
|
G | C | 1 | a0001c0002t0002g0060 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.246+1581C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095184 | ||||||
| chr4:1095185
|
C | T | 48 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(45): Show | 54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.246+1580G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095185 | ||||||
| chr4:1095202
|
AGAACCAA others(1291): Show |
A | 48 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(45): Show | 54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.246+265_246+1562de others(1): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095202 | ||||||
| chr4:1095216
|
T | C | 5 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0177others(2): Show | 5 | NA18941.hp2 NA18989.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.246+1549A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095216 | ||||||
| chr4:1095217
|
C | T | 5 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0177others(2): Show | 5 | NA18941.hp2 NA18989.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.246+1548G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095217 | ||||||
| chr4:1095230
|
TGGTCTCG others(996): Show |
T | 1 | a0001c0001t0001g0113 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.246+532_246+1534de others(1): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095230 | ||||||
| chr4:1095237
|
G | A | 5 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0177others(2): Show | 5 | NA18941.hp2 NA18989.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.246+1528C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095237 | ||||||
| chr4:1095239
|
G | C | 5 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0177others(2): Show | 5 | NA18941.hp2 NA18989.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.246+1526C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095239 | ||||||
| chr4:1095260
|
C | T | 7 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0001g0105others(4): Show | 7 | HG02040.hp1 HG03491.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.246+1505G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095260 | ||||||
| chr4:1095277
|
CCCACAGC others(110): Show |
C | 1 | a0001c0001t0001g0177 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.246+1371_246+1487d others(2): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095277 | ||||||
| chr4:1095289
|
T | C | 4 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0188others(1): Show | 4 | NA18941.hp2 NA18990.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+1476A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095289 | ||||||
| chr4:1095320
|
A | G | 4 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0188others(1): Show | 4 | NA18941.hp2 NA18990.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+1445T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095320 | ||||||
| chr4:1095335
|
T | C | 4 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0188others(1): Show | 4 | NA18941.hp2 NA18990.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+1430A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095335 | ||||||
| chr4:1095348
|
T | C | 4 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0188others(1): Show | 4 | NA18941.hp2 NA18990.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+1417A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095348 | ||||||
| chr4:1095355
|
A | G | 1 | a0001c0002t0002g0226 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.246+1410T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095355 | ||||||
| chr4:1095357
|
C | G | 5 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0188others(2): Show | 5 | NA18941.hp2 NA18979.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.246+1408G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095357 | ||||||
| chr4:1095362
|
C | T | 4 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0188others(1): Show | 4 | NA18941.hp2 NA18990.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+1403G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095362 | ||||||
| chr4:1095379
|
A | G | 184 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(181): Show | 208 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.246+1386T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095379 | ||||||
| chr4:1095392
|
A | C | 189 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(186): Show | 213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.246+1373T>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095392 | ||||||
| chr4:1095394
|
T | C | 184 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(181): Show | 208 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.246+1371A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095394 | ||||||
| chr4:1095407
|
T | C | 185 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(182): Show | 209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.246+1358A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095407 | ||||||
| chr4:1095407
|
TGGTCTCG others(52): Show |
T | 1 | a0001c0001t0001g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.246+1299_246+1357d others(61): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095407 | ||||||
| chr4:1095414
|
G | A | 1 | a0001c0002t0002g0226 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.246+1351C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095414 | ||||||
| chr4:1095416
|
G | C | 1 | a0001c0002t0002g0226 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.246+1349C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095416 | ||||||
| chr4:1095421
|
C | T | 4 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0188others(1): Show | 4 | NA18941.hp2 NA18990.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+1344G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095421 | ||||||
| chr4:1095438
|
A | G | 185 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(182): Show | 209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.246+1327T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095438 | ||||||
| chr4:1095451
|
A | C | 188 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(185): Show | 212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.246+1314T>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095451 | ||||||
| chr4:1095453
|
T | C | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(180): Show | 206 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.246+1312A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095453 | ||||||
| chr4:1095453
|
T | G | 2 | a0001c0001t0001g0024a0001c0001t0001g0287 | 3 | HG02074.hp1 NA18945.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.246+1312A>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095453 | ||||||
| chr4:1095466
|
C | T | 5 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0188others(2): Show | 5 | NA18941.hp2 NA18979.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.246+1299G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095466 | ||||||
| chr4:1095473
|
G | A | 189 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(186): Show | 213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.246+1292C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095473 | ||||||
| chr4:1095475
|
G | C | 4 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0188others(1): Show | 4 | NA18941.hp2 NA18990.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+1290C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095475 | ||||||
| chr4:1095480
|
C | T | 193 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(190): Show | 217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.246+1285G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095480 | ||||||
| chr4:1095510
|
A | C | 5 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0188others(2): Show | 5 | NA18941.hp2 NA18979.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.246+1255T>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095510 | ||||||
| chr4:1095512
|
T | C | 4 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0188others(1): Show | 4 | NA18941.hp2 NA18990.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+1253A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095512 | ||||||
| chr4:1095532
|
G | A | 1 | a0001c0002t0002g0226 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.246+1233C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095532 | ||||||
| chr4:1095534
|
G | C | 1 | a0001c0002t0002g0226 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.246+1231C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095534 | ||||||
| chr4:1095539
|
T | C | 5 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0188others(2): Show | 5 | NA18941.hp2 NA18979.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.246+1226A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095539 | ||||||
| chr4:1095569
|
C | A | 5 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0188others(2): Show | 5 | NA18941.hp2 NA18979.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.246+1196G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095569 | ||||||
| chr4:1095571
|
T | C | 1 | a0001c0002t0002g0272 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.246+1194A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095571 | ||||||
| chr4:1095591
|
A | G | 5 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0188others(2): Show | 5 | NA18941.hp2 NA18979.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.246+1174T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095591 | ||||||
| chr4:1095593
|
C | G | 5 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0188others(2): Show | 5 | NA18941.hp2 NA18979.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.246+1172G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095593 | ||||||
| chr4:1095598
|
C | T | 4 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0188others(1): Show | 4 | NA18941.hp2 NA18990.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+1167G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095598 | ||||||
| chr4:1095628
|
C | A | 1 | a0001c0002t0002g0226 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.246+1137G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095628 | ||||||
| chr4:1095630
|
C | T | 5 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0188others(2): Show | 5 | NA18941.hp2 NA18979.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.246+1135G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095630 | ||||||
| chr4:1095643
|
T | C | 1 | a0001c0002t0002g0226 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.246+1122A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095643 | ||||||
| chr4:1095650
|
G | A | 4 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0188others(1): Show | 4 | NA18941.hp2 NA18990.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+1115C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095650 | ||||||
| chr4:1095650
|
G | C | 4 | a0001c0001t0001g0130a0001c0001t0001g0291a0001c0001t0001g0292others(1): Show | 4 | HG00438.hp2 HG02080.hp1 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+1115C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095650 | ||||||
| chr4:1095652
|
G | C | 4 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0188others(1): Show | 4 | NA18941.hp2 NA18990.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+1113C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095652 | ||||||
| chr4:1095674
|
A | G | 6 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0094others(3): Show | 6 | HG01975.hp1 HG02280.hp1 NA18941.hp2 others(3): Show |
intron_variant | MODIFIER | c.246+1091T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095674 | ||||||
| chr4:1095687
|
C | A | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(205): Show | 234 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.246+1078G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095687 | ||||||
| chr4:1095689
|
T | C | 4 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0188others(1): Show | 4 | NA18941.hp2 NA18990.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+1076A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095689 | ||||||
| chr4:1095716
|
C | T | 197 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(194): Show | 221 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.246+1049G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095716 | ||||||
| chr4:1095741
|
G | C | 4 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0188others(1): Show | 4 | NA18941.hp2 NA18990.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+1024C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095741 | ||||||
| chr4:1095748
|
T | C | 4 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0188others(1): Show | 4 | NA18941.hp2 NA18990.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+1017A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095748 | ||||||
| chr4:1095774
|
G | A | 1 | a0001c0002t0002g0309 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.246+991C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095774 | ||||||
| chr4:1095792
|
G | A | 5 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0188others(2): Show | 5 | NA18941.hp2 NA18979.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.246+973C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095792 | ||||||
| chr4:1095807
|
C | T | 4 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0188others(1): Show | 4 | NA18941.hp2 NA18990.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+958G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095807 | ||||||
| chr4:1095829
|
GATAGCGC others(52): Show |
G | 4 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0188others(1): Show | 4 | NA18941.hp2 NA18990.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+877_246+935del others(59): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095829 | ||||||
| chr4:1095859
|
C | G | 1 | a0001c0002t0002g0226 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.246+906G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095859 | ||||||
| chr4:1095866
|
C | T | 1 | a0001c0002t0002g0226 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.246+899G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095866 | ||||||
| chr4:1095886
|
A | G | 2 | a0001c0002t0002g0036a0001c0002t0002g0226 | 2 | HG04199.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.246+879T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095886 | ||||||
| chr4:1095888
|
C | G | 1 | a0001c0002t0002g0226 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.246+877G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095888 | ||||||
| chr4:1095893
|
C | T | 4 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0188others(1): Show | 4 | NA18941.hp2 NA18990.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+872G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095893 | ||||||
| chr4:1095923
|
C | A | 4 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0188others(1): Show | 4 | NA18941.hp2 NA18990.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+842G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095923 | ||||||
| chr4:1095923
|
CCTCCCAC others(52): Show |
C | 1 | a0001c0001t0001g0080 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.246+783_246+841del others(59): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095923 | ||||||
| chr4:1095925
|
T | TCCCACAG others(111): Show |
1 | a0001c0002t0002g0226 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.246+839_246+840ins others(118): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095925 | ||||||
| chr4:1095945
|
G | A | 1 | a0001c0002t0002g0226 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.246+820C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095945 | ||||||
| chr4:1095947
|
G | C | 1 | a0001c0002t0002g0226 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.246+818C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095947 | ||||||
| chr4:1095952
|
C | T | 194 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(191): Show | 220 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.246+813G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095952 | ||||||
| chr4:1095969
|
A | G | 4 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0188others(1): Show | 4 | NA18941.hp2 NA18990.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+796T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095969 | ||||||
| chr4:1095982
|
A | C | 5 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0188others(2): Show | 5 | NA18941.hp2 NA18979.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.246+783T>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095982 | ||||||
| chr4:1095984
|
T | C | 4 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0188others(1): Show | 4 | NA18941.hp2 NA18990.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+781A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095984 | ||||||
| chr4:1095984
|
T | TCCCACAG others(52): Show |
12 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0110others(9): Show | 15 | HG00408.hp2 HG00621.hp2 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.246+722_246+780dup others(59): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095984 | ||||||
| chr4:1095984
|
T | TCCCACAG others(170): Show |
2 | a0001c0001t0001g0206a0001c0001t0001g0208 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.246+780_246+781ins others(177): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095984 | ||||||
| chr4:1095984
|
T | TCCCACAG others(229): Show |
2 | a0001c0001t0001g0205a0001c0001t0001g0207 | 2 | HG02818.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.246+780_246+781ins others(236): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1095984 | ||||||
| chr4:1096002
|
T | C | 7 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0001g0105others(4): Show | 7 | HG02040.hp1 HG03491.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.246+763A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096002 | ||||||
| chr4:1096011
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.246+754G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096011 | ||||||
| chr4:1096028
|
G | A | 1 | a0001c0002t0002g0226 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.246+737C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096028 | ||||||
| chr4:1096041
|
C | A | 1 | a0001c0002t0002g0226 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.246+724G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096041 | ||||||
| chr4:1096041
|
C | CCCCCCAC others(52): Show |
1 | a0001c0001t0001g0142 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.246+723_246+724ins others(59): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096041 | ||||||
| chr4:1096043
|
C | T | 1 | a0001c0002t0002g0226 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.246+722G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096043 | ||||||
| chr4:1096056
|
T | C | 10 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0174others(7): Show | 10 | HG00099.hp1 HG01123.hp2 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.246+709A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096056 | ||||||
| chr4:1096056
|
TGGTCTCG others(52): Show |
T | 1 | a0001c0001t0001g0119 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.246+650_246+708del others(59): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096056 | ||||||
| chr4:1096086
|
C | T | 6 | a0001c0001t0001g0022a0001c0001t0001g0069a0001c0001t0001g0083others(3): Show | 7 | HG00558.hp1 HG02155.hp2 NA18983.hp2 others(4): Show |
intron_variant | MODIFIER | c.246+679G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096086 | ||||||
| chr4:1096115
|
C | T | 207 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(204): Show | 231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.246+650G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096115 | ||||||
| chr4:1096116
|
G | T | 1 | a0001c0001t0001g0121 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.246+649C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096116 | ||||||
| chr4:1096128
|
G | A | 1 | a0001c0001t0001g0074 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.246+637C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096128 | ||||||
| chr4:1096154
|
G | C | 1 | a0001c0001t0001g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.246+611C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096154 | ||||||
| chr4:1096154
|
G | GCACACCC others(229): Show |
1 | a0001c0002t0002g0150 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.246+610_246+611ins others(236): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096154 | ||||||
| chr4:1096154
|
GCACACCC others(170): Show |
G | 10 | a0001c0002t0001g0034a0001c0002t0001g0037a0001c0002t0001g0041others(7): Show | 12 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.246+434_246+610del | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096154 | ||||||
| chr4:1096174
|
C | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(151): Show | 172 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.246+591G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096174 | ||||||
| chr4:1096213
|
GCACACCC others(111): Show |
G | 1 | a0001c0002t0002g0155 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.246+434_246+551del | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096213 | ||||||
| chr4:1096233
|
C | T | 77 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(74): Show | 91 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.246+532G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096233 | ||||||
| chr4:1096241
|
G | A | 1 | a0001c0002t0002g0272 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.246+524C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096241 | ||||||
| chr4:1096263
|
C | T | 4 | a0001c0002t0002g0214a0001c0002t0002g0215a0001c0002t0002g0304others(1): Show | 4 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+502G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096263 | ||||||
| chr4:1096272
|
GCACACCC others(52): Show |
G | 7 | a0001c0001t0001g0096a0001c0001t0005g0043a0001c0001t0005g0047others(4): Show | 7 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.246+434_246+492del others(59): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096272 | ||||||
| chr4:1096278
|
C | T | 5 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0001g0105others(2): Show | 5 | HG02040.hp1 HG03491.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.246+487G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096278 | ||||||
| chr4:1096289
|
C | T | 1 | a0001c0001t0006g0359 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.246+476G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096289 | ||||||
| chr4:1096292
|
C | T | 1 | a0001c0001t0001g0118 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.246+473G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096292 | ||||||
| chr4:1096298
|
C | T | 1 | a0001c0001t0001g0012 | 2 | HG02257.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.246+467G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096298 | ||||||
| chr4:1096307
|
G | A | 1 | a0001c0002t0002g0260 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.246+458C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096307 | ||||||
| chr4:1096321
|
A | G | 3 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162 | 3 | HG01891.hp2 HG02572.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.246+444T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096321 | ||||||
| chr4:1096331
|
C | G | 188 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(185): Show | 212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.246+434G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096331 | ||||||
| chr4:1096331
|
CCACACCC others(52): Show |
C | 88 | a0001c0001t0001g0024a0001c0001t0001g0050a0001c0001t0001g0119others(85): Show | 97 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.246+375_246+433del others(59): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096331 | ||||||
| chr4:1096351
|
C | T | 10 | a0001c0002t0001g0034a0001c0002t0001g0037a0001c0002t0001g0041others(7): Show | 12 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.246+414G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096351 | ||||||
| chr4:1096384
|
A | T | 1 | a0001c0001t0001g0132 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.246+381T>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096384 | ||||||
| chr4:1096390
|
G | C | 189 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(186): Show | 213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.246+375C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096390 | ||||||
| chr4:1096390
|
G | GCACACCC others(52): Show |
3 | a0001c0001t0001g0116a0001c0001t0001g0205a0001c0001t0001g0207 | 3 | HG02818.hp2 HG03471.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.246+374_246+375ins others(59): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096390 | ||||||
| chr4:1096390
|
G | GCACACCC others(111): Show |
2 | a0001c0001t0001g0206a0001c0001t0001g0208 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.246+374_246+375ins others(118): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096390 | ||||||
| chr4:1096410
|
C | T | 10 | a0001c0002t0001g0034a0001c0002t0001g0037a0001c0002t0001g0041others(7): Show | 12 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.246+355G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096410 | ||||||
| chr4:1096440
|
C | CGGAACCA others(52): Show |
1 | a0001c0001t0001g0118 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.246+324_246+325ins others(59): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096440 | ||||||
| chr4:1096449
|
G | C | 3 | a0001c0001t0001g0186a0001c0001t0005g0043a0001c0001t0005g0047 | 3 | HG02015.hp2 HG03710.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.246+316C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096449 | ||||||
| chr4:1096469
|
C | T | 10 | a0001c0002t0001g0034a0001c0002t0001g0037a0001c0002t0001g0041others(7): Show | 12 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.246+296G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096469 | ||||||
| chr4:1096475
|
C | G | 1 | a0001c0001t0001g0148 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.246+290G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096475 | ||||||
| chr4:1096476
|
GGGATAGC others(52): Show |
G | 12 | a0001c0001t0001g0096a0001c0001t0001g0180a0001c0002t0002g0057others(9): Show | 12 | HG01109.hp1 HG01123.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.246+230_246+288del others(59): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096476 | ||||||
| chr4:1096500
|
G | A | 11 | a0001c0002t0001g0034a0001c0002t0001g0037a0001c0002t0001g0041others(8): Show | 13 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.246+265C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096500 | ||||||
| chr4:1096513
|
C | A | 48 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(45): Show | 54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.246+252G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096513 | ||||||
| chr4:1096515
|
C | T | 48 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(45): Show | 54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.246+250G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096515 | ||||||
| chr4:1096535
|
A | G | 79 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0061others(76): Show | 86 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(83): Show |
intron_variant | MODIFIER | c.246+230T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096535 | ||||||
| chr4:1096559
|
A | G | 35 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0096others(32): Show | 38 | HG00280.hp2 HG00597.hp1 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.246+206T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096559 | ||||||
| chr4:1096618
|
A | G | 5 | a0001c0001t0001g0096a0001c0001t0001g0120a0001c0001t0001g0121others(2): Show | 5 | HG02258.hp2 NA19056.hp1 NA19057.hp1 others(2): Show |
intron_variant | MODIFIER | c.246+147T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096618 | ||||||
| chr4:1096633
|
C | T | 48 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(45): Show | 54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.246+132G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096633 | ||||||
| chr4:1096635
|
T | C | 48 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(45): Show | 54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.246+130A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096635 | ||||||
| chr4:1096697
|
T | C | 48 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(45): Show | 54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.246+68A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096697 | ||||||
| chr4:1096714
|
G | A | 47 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(44): Show | 53 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(50): Show |
intron_variant | MODIFIER | c.246+51C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 3/9 | chr4 | 1096714 | ||||||
| chr4:1096974
|
A | C | 45 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(42): Show | 50 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.172-135T>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1096974 | ||||||
| chr4:1096974
|
A | T | 3 | a0001c0002t0004g0008a0001c0002t0004g0038a0001c0002t0004g0039 | 4 | HG02922.hp2 HG03139.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.172-135T>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1096974 | ||||||
| chr4:1096997
|
C | T | 1 | a0007c0008t0011g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.172-158G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1096997 | ||||||
| chr4:1096998
|
G | A | 46 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(43): Show | 52 | HG00642.hp2 HG00735.hp1 HG01243.hp2 others(49): Show |
intron_variant | MODIFIER | c.172-159C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1096998 | ||||||
| chr4:1097037
|
G | A | 1 | a0001c0002t0002g0278 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.172-198C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097037 | ||||||
| chr4:1097163
|
C | T | 1 | a0001c0002t0002g0228 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.172-324G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097163 | ||||||
| chr4:1097274
|
A | G | 250 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(247): Show | 280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.172-435T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097274 | ||||||
| chr4:1097319
|
C | T | 48 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(45): Show | 54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.172-480G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097319 | ||||||
| chr4:1097327
|
G | A | 1 | a0001c0002t0001g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.172-488C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097327 | ||||||
| chr4:1097375
|
C | T | 52 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(49): Show | 58 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(55): Show |
intron_variant | MODIFIER | c.172-536G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097375 | ||||||
| chr4:1097473
|
C | T | 8 | a0001c0001t0001g0157a0001c0001t0001g0160a0001c0001t0001g0161others(5): Show | 8 | HG01192.hp1 HG01255.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.172-634G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097473 | ||||||
| chr4:1097474
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.172-635C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097474 | ||||||
| chr4:1097663
|
T | A | 7 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0001g0105others(4): Show | 7 | HG02040.hp1 HG03491.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.172-824A>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097663 | ||||||
| chr4:1097676
|
C | A | 1 | a0001c0001t0001g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-837G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097676 | ||||||
| chr4:1097677
|
C | G | 1 | a0001c0001t0001g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-838G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097677 | ||||||
| chr4:1097678
|
T | C | 1 | a0001c0002t0002g0155 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.172-839A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097678 | ||||||
| chr4:1097678
|
T | G | 1 | a0001c0001t0001g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-839A>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097678 | ||||||
| chr4:1097680
|
T | A | 1 | a0001c0001t0001g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-841A>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097680 | ||||||
| chr4:1097683
|
C | G | 1 | a0001c0001t0001g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-844G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097683 | ||||||
| chr4:1097685
|
T | A | 1 | a0001c0001t0001g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-846A>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097685 | ||||||
| chr4:1097689
|
C | G | 1 | a0001c0001t0001g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-850G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097689 | ||||||
| chr4:1097690
|
T | G | 1 | a0001c0001t0001g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-851A>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097690 | ||||||
| chr4:1097695
|
T | TGTGAAGG others(12): Show |
1 | a0001c0001t0001g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-857_172-856ins others(19): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097695 | ||||||
| chr4:1097698
|
C | T | 1 | a0001c0001t0001g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-859G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097698 | ||||||
| chr4:1097699
|
C | G | 1 | a0001c0001t0001g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-860G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097699 | ||||||
| chr4:1097702
|
G | C | 48 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(45): Show | 54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.172-863C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097702 | ||||||
| chr4:1097708
|
A | G | 1 | a0001c0001t0001g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-869T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097708 | ||||||
| chr4:1097713
|
A | G | 48 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(45): Show | 54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.172-874T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097713 | ||||||
| chr4:1097716
|
A | G | 1 | a0001c0001t0001g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-877T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097716 | ||||||
| chr4:1097717
|
G | T | 1 | a0001c0001t0001g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-878C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097717 | ||||||
| chr4:1097718
|
C | A | 1 | a0001c0001t0001g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-879G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097718 | ||||||
| chr4:1097721
|
A | C | 1 | a0001c0001t0001g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-882T>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097721 | ||||||
| chr4:1097726
|
A | T | 1 | a0001c0001t0001g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-887T>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097726 | ||||||
| chr4:1097727
|
C | G | 1 | a0001c0001t0001g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-888G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097727 | ||||||
| chr4:1097728
|
T | C | 1 | a0001c0001t0001g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-889A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097728 | ||||||
| chr4:1097729
|
A | T | 1 | a0001c0001t0001g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-890T>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097729 | ||||||
| chr4:1097731
|
G | T | 1 | a0001c0001t0001g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-892C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097731 | ||||||
| chr4:1097733
|
G | T | 1 | a0001c0001t0001g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-894C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097733 | ||||||
| chr4:1097734
|
A | T | 1 | a0001c0001t0001g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-895T>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097734 | ||||||
| chr4:1097736
|
A | T | 1 | a0001c0001t0001g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-897T>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097736 | ||||||
| chr4:1097737
|
G | T | 1 | a0001c0001t0001g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-898C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097737 | ||||||
| chr4:1097740
|
G | T | 1 | a0001c0001t0001g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-901C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097740 | ||||||
| chr4:1097741
|
T | G | 1 | a0001c0001t0001g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-902A>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097741 | ||||||
| chr4:1097744
|
T | C | 1 | a0001c0001t0001g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-905A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097744 | ||||||
| chr4:1097749
|
A | C | 1 | a0001c0001t0001g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-910T>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097749 | ||||||
| chr4:1097750
|
T | C | 1 | a0007c0008t0011g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.172-911A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097750 | ||||||
| chr4:1097759
|
C | A | 1 | a0001c0001t0001g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-920G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097759 | ||||||
| chr4:1097766
|
T | G | 1 | a0001c0001t0001g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-927A>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097766 | ||||||
| chr4:1097767
|
A | T | 1 | a0001c0001t0001g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-928T>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097767 | ||||||
| chr4:1097768
|
G | A | 1 | a0001c0001t0001g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-929C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097768 | ||||||
| chr4:1097772
|
C | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0210 | 3 | HG01081.hp2 HG01257.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.172-933G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097772 | ||||||
| chr4:1097773
|
G | T | 1 | a0001c0001t0001g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-934C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097773 | ||||||
| chr4:1097775
|
T | G | 1 | a0001c0001t0001g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-936A>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097775 | ||||||
| chr4:1097776
|
T | A | 1 | a0001c0001t0001g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-937A>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097776 | ||||||
| chr4:1097778
|
A | C | 1 | a0001c0001t0001g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-939T>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097778 | ||||||
| chr4:1097779
|
G | T | 1 | a0001c0001t0001g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-940C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097779 | ||||||
| chr4:1097782
|
G | C | 1 | a0001c0001t0001g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-943C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097782 | ||||||
| chr4:1097784
|
C | G | 1 | a0001c0001t0001g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-945G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097784 | ||||||
| chr4:1097801
|
A | C | 1 | a0001c0001t0001g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-962T>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097801 | ||||||
| chr4:1097803
|
G | T | 1 | a0001c0001t0001g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-964C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097803 | ||||||
| chr4:1097812
|
C | G | 1 | a0001c0001t0001g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-973G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097812 | ||||||
| chr4:1097815
|
AGCACTTT others(19): Show |
A | 1 | a0001c0001t0001g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-1002_172-977de others(27): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097815 | ||||||
| chr4:1097842
|
A | T | 1 | a0001c0001t0001g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-1003T>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097842 | ||||||
| chr4:1097845
|
G | T | 1 | a0001c0001t0001g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-1006C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097845 | ||||||
| chr4:1097847
|
T | C | 1 | a0001c0001t0001g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-1008A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097847 | ||||||
| chr4:1097852
|
G | C | 1 | a0001c0001t0001g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-1013C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097852 | ||||||
| chr4:1097855
|
A | C | 1 | a0001c0001t0001g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-1016T>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097855 | ||||||
| chr4:1097856
|
G | T | 1 | a0001c0001t0001g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-1017C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097856 | ||||||
| chr4:1097872
|
C | T | 1 | a0001c0001t0001g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-1033G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097872 | ||||||
| chr4:1097873
|
T | G | 1 | a0001c0001t0001g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-1034A>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097873 | ||||||
| chr4:1097878
|
A | T | 1 | a0001c0001t0001g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.172-1039T>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1097878 | ||||||
| chr4:1098009
|
G | T | 26 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(23): Show | 29 | HG00609.hp1 HG01109.hp2 HG02015.hp2 others(26): Show |
intron_variant | MODIFIER | c.172-1170C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1098009 | ||||||
| chr4:1098041
|
G | C | 48 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(45): Show | 54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.172-1202C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1098041 | ||||||
| chr4:1098137
|
G | A | 48 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(45): Show | 54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.172-1298C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1098137 | ||||||
| chr4:1098165
|
T | C | 1 | a0001c0001t0015g0204 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.172-1326A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1098165 | ||||||
| chr4:1098186
|
T | TAG | 48 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(45): Show | 54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.172-1349_172-1348d others(4): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1098186 | ||||||
| chr4:1098198
|
A | G | 48 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(45): Show | 54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.172-1359T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1098198 | ||||||
| chr4:1098231
|
G | T | 202 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(199): Show | 226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.172-1392C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1098231 | ||||||
| chr4:1098370
|
T | C | 48 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(45): Show | 54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.172-1531A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1098370 | ||||||
| chr4:1098429
|
C | T | 1 | a0001c0001t0001g0281 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.172-1590G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1098429 | ||||||
| chr4:1098542
|
C | T | 3 | a0001c0002t0001g0041a0001c0002t0001g0042a0001c0002t0006g0360 | 3 | HG03098.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.172-1703G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1098542 | ||||||
| chr4:1098576
|
T | C | 48 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(45): Show | 54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.172-1737A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1098576 | ||||||
| chr4:1098610
|
G | A | 1 | a0001c0001t0014g0088 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.172-1771C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1098610 | ||||||
| chr4:1098617
|
A | G | 250 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(247): Show | 280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.172-1778T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1098617 | ||||||
| chr4:1098690
|
C | T | 48 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(45): Show | 54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.172-1851G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1098690 | ||||||
| chr4:1098720
|
T | C | 48 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(45): Show | 54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.172-1881A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1098720 | ||||||
| chr4:1098731
|
CAG | C | 2 | a0001c0002t0004g0009a0001c0002t0004g0048 | 3 | HG02717.hp1 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.172-1894_172-1893d others(4): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1098731 | ||||||
| chr4:1098760
|
C | T | 3 | a0001c0001t0006g0357a0001c0001t0006g0358a0001c0001t0006g0359 | 3 | HG01167.hp1 HG02109.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.172-1921G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1098760 | ||||||
| chr4:1098813
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.172-1974G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1098813 | ||||||
| chr4:1098839
|
C | T | 48 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(45): Show | 54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.172-2000G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1098839 | ||||||
| chr4:1099117
|
C | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0111others(7): Show | 13 | HG00408.hp2 HG02071.hp1 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.172-2278G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1099117 | ||||||
| chr4:1099149
|
G | A | 1 | a0001c0002t0002g0300 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.172-2310C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1099149 | ||||||
| chr4:1099171
|
G | A | 48 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(45): Show | 54 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.172-2332C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1099171 | ||||||
| chr4:1099189
|
G | A | 2 | a0001c0002t0003g0347a0001c0002t0003g0348 | 2 | HG01074.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.172-2350C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1099189 | ||||||
| chr4:1099232
|
T | C | 316 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(313): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.172-2393A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1099232 | ||||||
| chr4:1099312
|
T | G | 316 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(313): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.172-2473A>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1099312 | ||||||
| chr4:1099337
|
T | C | 4 | a0001c0002t0002g0214a0001c0002t0002g0215a0001c0002t0002g0304others(1): Show | 4 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.172-2498A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1099337 | ||||||
| chr4:1099437
|
A | G | 360 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(357): Show | 401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.172-2598T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1099437 | ||||||
| chr4:1099470
|
C | G | 316 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(313): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.172-2631G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1099470 | ||||||
| chr4:1099575
|
G | A | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(1): Show | 4 | HG02818.hp2 HG03471.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.172-2736C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1099575 | ||||||
| chr4:1099616
|
G | A | 1 | a0001c0001t0015g0204 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.172-2777C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1099616 | ||||||
| chr4:1099766
|
T | C | 10 | a0001c0001t0006g0357a0001c0001t0006g0358a0001c0001t0006g0359others(7): Show | 12 | HG01167.hp1 HG01255.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.172-2927A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1099766 | ||||||
| chr4:1099811
|
C | T | 2 | a0001c0001t0001g0020a0001c0001t0001g0306 | 3 | HG03017.hp2 HG03831.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.172-2972G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1099811 | ||||||
| chr4:1099821
|
C | T | 7 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0001g0105others(4): Show | 7 | HG02040.hp1 HG03491.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.172-2982G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1099821 | ||||||
| chr4:1099859
|
C | G | 3 | a0001c0002t0004g0008a0001c0002t0004g0038a0001c0002t0004g0039 | 4 | HG02922.hp2 HG03139.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.172-3020G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1099859 | ||||||
| chr4:1100043
|
T | C | 2 | a0001c0001t0001g0186a0001c0001t0001g0188 | 2 | HG02015.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.172-3204A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1100043 | ||||||
| chr4:1100111
|
T | C | 6 | a0001c0002t0001g0034a0001c0002t0001g0209a0001c0002t0001g0303others(3): Show | 8 | HG02486.hp2 HG02572.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.172-3272A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1100111 | ||||||
| chr4:1100126
|
A | G | 316 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(313): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.172-3287T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1100126 | ||||||
| chr4:1100196
|
TTTCC | T | 3 | a0001c0001t0001g0032a0001c0001t0001g0171a0001c0001t0001g0172 | 4 | NA18977.hp2 NA19067.hp2 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.172-3361_172-3358d others(6): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1100196 | ||||||
| chr4:1100201
|
C | G | 3 | a0001c0001t0001g0032a0001c0001t0001g0171a0001c0001t0001g0172 | 4 | NA18977.hp2 NA19067.hp2 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.172-3362G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1100201 | ||||||
| chr4:1100237
|
C | T | 10 | a0001c0002t0001g0034a0001c0002t0001g0037a0001c0002t0001g0041others(7): Show | 12 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.172-3398G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1100237 | ||||||
| chr4:1100335
|
C | T | 10 | a0001c0002t0001g0034a0001c0002t0001g0037a0001c0002t0001g0041others(7): Show | 12 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.172-3496G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1100335 | ||||||
| chr4:1100363
|
G | A | 104 | a0001c0002t0002g0002a0001c0002t0002g0025a0001c0002t0002g0026others(101): Show | 113 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.172-3524C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1100363 | ||||||
| chr4:1100398
|
AT | A | 25 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0021others(22): Show | 29 | HG00642.hp2 HG00735.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.172-3560delA | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1100398 | ||||||
| chr4:1100398
|
ATTT | A | 8 | a0001c0001t0001g0076a0001c0001t0001g0205a0001c0001t0001g0206others(5): Show | 10 | HG02083.hp2 HG02717.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.172-3562_172-3560d others(5): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1100398 | ||||||
| chr4:1100398
|
ATTTT | A | 13 | a0001c0001t0001g0031a0001c0001t0001g0050a0001c0001t0001g0117others(10): Show | 14 | HG00438.hp2 HG00639.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.172-3563_172-3560d others(6): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1100398 | ||||||
| chr4:1100398
|
ATTTTT | A | 112 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(109): Show | 127 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.172-3564_172-3560d others(7): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1100398 | ||||||
| chr4:1100398
|
ATTTTTT | A | 85 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0012others(82): Show | 95 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.172-3565_172-3560d others(8): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1100398 | ||||||
| chr4:1100398
|
ATTTTTTT | A | 96 | a0001c0001t0001g0056a0001c0001t0001g0096a0001c0001t0001g0187others(93): Show | 105 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.172-3566_172-3560d others(9): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1100398 | ||||||
| chr4:1100403
|
T | A | 1 | a0001c0001t0001g0076 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.172-3564A>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1100403 | ||||||
| chr4:1100404
|
T | A | 4 | a0001c0001t0001g0130a0001c0001t0001g0291a0001c0001t0001g0292others(1): Show | 4 | HG00438.hp2 HG02080.hp1 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.172-3565A>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1100404 | ||||||
| chr4:1100428
|
G | A | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(1): Show | 4 | HG02818.hp2 HG03471.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.172-3589C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1100428 | ||||||
| chr4:1100526
|
G | A | 202 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(199): Show | 226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.172-3687C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1100526 | ||||||
| chr4:1100598
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.172-3759C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1100598 | ||||||
| chr4:1100660
|
C | T | 8 | a0001c0001t0001g0023a0001c0001t0001g0175a0001c0001t0001g0176others(5): Show | 9 | HG01109.hp2 NA18747.hp1 NA18955.hp1 others(6): Show |
intron_variant | MODIFIER | c.172-3821G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1100660 | ||||||
| chr4:1100720
|
A | G | 1 | a0001c0001t0001g0175 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.172-3881T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1100720 | ||||||
| chr4:1100766
|
T | G | 2 | a0001c0001t0001g0198a0001c0001t0001g0293 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.172-3927A>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1100766 | ||||||
| chr4:1100882
|
T | C | 212 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(209): Show | 238 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.172-4043A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1100882 | ||||||
| chr4:1100957
|
C | T | 4 | a0001c0001t0001g0114a0001c0002t0002g0245a0001c0002t0002g0248others(1): Show | 4 | HG01123.hp2 HG01168.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.172-4118G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1100957 | ||||||
| chr4:1100973
|
T | C | 1 | a0001c0002t0012g0103 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.172-4134A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1100973 | ||||||
| chr4:1101049
|
T | A | 1 | a0001c0001t0001g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.172-4210A>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1101049 | ||||||
| chr4:1101178
|
C | T | 8 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0001g0096others(5): Show | 8 | HG02040.hp1 HG02258.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.172-4339G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1101178 | ||||||
| chr4:1101199
|
A | G | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(1): Show | 4 | HG02818.hp2 HG03471.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.172-4360T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1101199 | ||||||
| chr4:1101213
|
G | A | 7 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0001g0105others(4): Show | 7 | HG02040.hp1 HG03491.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.172-4374C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1101213 | ||||||
| chr4:1101291
|
A | G | 104 | a0001c0002t0002g0002a0001c0002t0002g0025a0001c0002t0002g0026others(101): Show | 113 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.172-4452T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1101291 | ||||||
| chr4:1101402
|
A | G | 1 | a0001c0002t0002g0231 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.172-4563T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1101402 | ||||||
| chr4:1101493
|
A | G | 190 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(187): Show | 214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.172-4654T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1101493 | ||||||
| chr4:1101532
|
C | T | 1 | a0001c0001t0001g0110 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.172-4693G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1101532 | ||||||
| chr4:1101587
|
A | C | 8 | a0001c0001t0001g0157a0001c0001t0001g0160a0001c0001t0001g0161others(5): Show | 8 | HG01192.hp1 HG01255.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.172-4748T>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1101587 | ||||||
| chr4:1101621
|
C | T | 6 | a0001c0002t0002g0255a0001c0002t0002g0256a0001c0002t0002g0257others(3): Show | 6 | HG00438.hp1 HG02071.hp2 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.172-4782G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1101621 | ||||||
| chr4:1101622
|
G | A | 190 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(187): Show | 214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.172-4783C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1101622 | ||||||
| chr4:1101634
|
G | A | 18 | a0001c0002t0003g0033a0001c0002t0003g0338a0001c0002t0003g0340others(15): Show | 19 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.172-4795C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1101634 | ||||||
| chr4:1102053
|
T | C | 1 | a0005c0006t0001g0133 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.172-5214A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1102053 | ||||||
| chr4:1102132
|
C | A | 103 | a0001c0002t0002g0002a0001c0002t0002g0025a0001c0002t0002g0026others(100): Show | 112 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.172-5293G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1102132 | ||||||
| chr4:1102352
|
G | T | 3 | a0001c0001t0006g0357a0001c0001t0006g0358a0001c0001t0006g0359 | 3 | HG01167.hp1 HG02109.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.172-5513C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1102352 | ||||||
| chr4:1102448
|
A | G | 10 | a0001c0002t0001g0034a0001c0002t0001g0037a0001c0002t0001g0041others(7): Show | 12 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.172-5609T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1102448 | ||||||
| chr4:1102458
|
G | A | 10 | a0001c0002t0001g0034a0001c0002t0001g0037a0001c0002t0001g0041others(7): Show | 12 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.172-5619C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1102458 | ||||||
| chr4:1102476
|
C | T | 3 | a0001c0002t0001g0041a0001c0002t0001g0042a0001c0002t0006g0360 | 3 | HG03098.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.172-5637G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1102476 | ||||||
| chr4:1102477
|
C | T | 318 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(315): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.172-5638G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1102477 | ||||||
| chr4:1102579
|
A | G | 316 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(313): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.172-5740T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1102579 | ||||||
| chr4:1102583
|
A | C | 316 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(313): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.172-5744T>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1102583 | ||||||
| chr4:1102594
|
CA | C | 304 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(301): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.171+5748delT | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1102594 | ||||||
| chr4:1102604
|
A | C | 3 | a0001c0002t0004g0008a0001c0002t0004g0038a0001c0002t0004g0039 | 4 | HG02922.hp2 HG03139.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.171+5739T>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1102604 | ||||||
| chr4:1102628
|
A | G | 316 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(313): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.171+5715T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1102628 | ||||||
| chr4:1102635
|
G | A | 2 | a0001c0001t0001g0073a0001c0001t0001g0074 | 2 | NA18941.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.171+5708C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1102635 | ||||||
| chr4:1102712
|
C | T | 1 | a0001c0002t0002g0150 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.171+5631G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1102712 | ||||||
| chr4:1102738
|
G | A | 1 | a0001c0002t0012g0103 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.171+5605C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1102738 | ||||||
| chr4:1102777
|
G | A | 1 | a0001c0002t0001g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.171+5566C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1102777 | ||||||
| chr4:1102808
|
C | T | 1 | a0001c0002t0012g0103 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.171+5535G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1102808 | ||||||
| chr4:1102833
|
C | A | 7 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0001g0105others(4): Show | 7 | HG02040.hp1 HG03491.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.171+5510G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1102833 | ||||||
| chr4:1102899
|
T | G | 316 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(313): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.171+5444A>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1102899 | ||||||
| chr4:1102988
|
CA | C | 206 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(203): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.171+5354delT | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1102988 | ||||||
| chr4:1102988
|
CAA | C | 103 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0012others(100): Show | 113 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.171+5353_171+5354d others(4): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1102988 | ||||||
| chr4:1103020
|
A | G | 1 | a0001c0001t0001g0108 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.171+5323T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1103020 | ||||||
| chr4:1103066
|
A | G | 316 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(313): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.171+5277T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1103066 | ||||||
| chr4:1103327
|
T | C | 1 | a0001c0002t0001g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.171+5016A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1103327 | ||||||
| chr4:1103432
|
A | G | 318 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(315): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.171+4911T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1103432 | ||||||
| chr4:1103545
|
A | C | 316 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(313): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.171+4798T>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1103545 | ||||||
| chr4:1103621
|
TAACAA | T | 202 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(199): Show | 226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.171+4717_171+4721d others(7): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1103621 | ||||||
| chr4:1103827
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.171+4516T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1103827 | ||||||
| chr4:1103888
|
G | A | 103 | a0001c0002t0002g0002a0001c0002t0002g0025a0001c0002t0002g0026others(100): Show | 112 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.171+4455C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1103888 | ||||||
| chr4:1104127
|
G | A | 360 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(357): Show | 401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.171+4216C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1104127 | ||||||
| chr4:1104381
|
T | C | 316 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(313): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.171+3962A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1104381 | ||||||
| chr4:1104407
|
G | A | 7 | a0001c0001t0001g0157a0001c0001t0001g0160a0001c0001t0001g0161others(4): Show | 7 | HG01884.hp1 HG01891.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.171+3936C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1104407 | ||||||
| chr4:1104434
|
A | G | 316 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(313): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.171+3909T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1104434 | ||||||
| chr4:1104701
|
C | T | 1 | a0001c0001t0001g0294 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.171+3642G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1104701 | ||||||
| chr4:1104758
|
C | T | 1 | a0001c0002t0002g0260 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.171+3585G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1104758 | ||||||
| chr4:1104759
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.171+3584C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1104759 | ||||||
| chr4:1104765
|
C | T | 10 | a0001c0002t0001g0034a0001c0002t0001g0037a0001c0002t0001g0041others(7): Show | 12 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.171+3578G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1104765 | ||||||
| chr4:1104778
|
A | C | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(1): Show | 4 | HG02818.hp2 HG03471.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.171+3565T>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1104778 | ||||||
| chr4:1104818
|
C | T | 9 | a0001c0002t0001g0034a0001c0002t0001g0037a0001c0002t0001g0041others(6): Show | 11 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.171+3525G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1104818 | ||||||
| chr4:1104879
|
C | T | 8 | a0001c0002t0002g0255a0001c0002t0002g0256a0001c0002t0002g0257others(5): Show | 8 | HG00438.hp1 HG02071.hp2 NA18747.hp2 others(5): Show |
intron_variant | MODIFIER | c.171+3464G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1104879 | ||||||
| chr4:1104909
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.171+3434G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1104909 | ||||||
| chr4:1104934
|
G | T | 2 | a0001c0002t0007g0362a0001c0002t0007g0364 | 2 | HG02258.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.171+3409C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1104934 | ||||||
| chr4:1104935
|
C | A | 1 | a0001c0001t0001g0089 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.171+3408G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1104935 | ||||||
| chr4:1104987
|
T | C | 2 | a0001c0002t0002g0274a0001c0002t0002g0328 | 2 | HG00099.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.171+3356A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1104987 | ||||||
| chr4:1105009
|
G | C | 314 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(311): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.171+3334C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1105009 | ||||||
| chr4:1105085
|
G | C | 1 | a0001c0001t0001g0199 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.171+3258C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1105085 | ||||||
| chr4:1105162
|
C | T | 1 | a0007c0008t0011g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.171+3181G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1105162 | ||||||
| chr4:1105198
|
C | G | 1 | a0001c0001t0001g0115 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.171+3145G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1105198 | ||||||
| chr4:1105300
|
GT | G | 312 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(309): Show | 347 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(344): Show |
intron_variant | MODIFIER | c.171+3042delA | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1105300 | ||||||
| chr4:1105314
|
C | A | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(1): Show | 4 | HG02818.hp2 HG03471.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.171+3029G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1105314 | ||||||
| chr4:1105314
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.171+3029G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1105314 | ||||||
| chr4:1105326
|
C | A | 96 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(93): Show | 110 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.171+3017G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1105326 | ||||||
| chr4:1105407
|
C | T | 319 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(316): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.171+2936G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1105407 | ||||||
| chr4:1105413
|
G | A | 200 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(197): Show | 224 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.171+2930C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1105413 | ||||||
| chr4:1105512
|
AACACAGC others(3): Show |
A | 1 | a0001c0002t0002g0323 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.171+2821_171+2830d others(12): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1105512 | ||||||
| chr4:1105575
|
C | T | 3 | a0001c0001t0001g0022a0001c0001t0001g0173a0001c0001t0001g0174 | 4 | HG02155.hp2 NA18984.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.171+2768G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1105575 | ||||||
| chr4:1105579
|
T | C | 316 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(313): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.171+2764A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1105579 | ||||||
| chr4:1105647
|
C | T | 10 | a0001c0002t0001g0034a0001c0002t0001g0037a0001c0002t0001g0041others(7): Show | 12 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.171+2696G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1105647 | ||||||
| chr4:1105682
|
C | T | 1 | a0007c0008t0011g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.171+2661G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1105682 | ||||||
| chr4:1105745
|
C | CT | 322 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(319): Show | 358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.171+2597dupA | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1105745 | ||||||
| chr4:1105749
|
C | T | 322 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(319): Show | 358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.171+2594G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1105749 | ||||||
| chr4:1105752
|
C | G | 1 | a0007c0008t0011g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.171+2591G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1105752 | ||||||
| chr4:1105757
|
G | A | 1 | a0001c0002t0003g0353 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.171+2586C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1105757 | ||||||
| chr4:1105818
|
G | A | 1 | a0007c0008t0011g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.171+2525C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1105818 | ||||||
| chr4:1105852
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.171+2491G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1105852 | ||||||
| chr4:1105961
|
C | A | 1 | a0001c0002t0003g0356 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.171+2382G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1105961 | ||||||
| chr4:1106009
|
T | A | 1 | a0001c0002t0002g0298 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.171+2334A>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1106009 | ||||||
| chr4:1106026
|
A | T | 1 | a0001c0001t0001g0306 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.171+2317T>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1106026 | ||||||
| chr4:1106094
|
A | G | 1 | a0001c0002t0002g0253 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.171+2249T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1106094 | ||||||
| chr4:1106121
|
G | C | 1 | a0001c0002t0003g0353 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.171+2222C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1106121 | ||||||
| chr4:1106178
|
A | G | 1 | a0001c0002t0002g0057 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.171+2165T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1106178 | ||||||
| chr4:1106249
|
T | TAC | 25 | a0001c0001t0001g0061a0001c0001t0001g0205a0001c0001t0001g0206others(22): Show | 27 | HG01074.hp1 HG01123.hp1 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.171+2092_171+2093d others(4): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1106249 | ||||||
| chr4:1106249
|
T | TACAC | 22 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0306others(19): Show | 23 | HG00423.hp2 HG00597.hp2 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.171+2090_171+2093d others(6): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1106249 | ||||||
| chr4:1106249
|
T | TACACAC | 7 | a0001c0001t0005g0045a0001c0001t0005g0046a0001c0002t0002g0242others(4): Show | 7 | HG01361.hp2 HG01928.hp1 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.171+2088_171+2093d others(8): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1106249 | ||||||
| chr4:1106249
|
TAC | T | 36 | a0001c0001t0001g0134a0001c0001t0001g0144a0001c0001t0001g0157others(33): Show | 39 | HG00642.hp1 HG00642.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.171+2092_171+2093d others(4): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1106249 | ||||||
| chr4:1106249
|
TACAC | T | 81 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(78): Show | 93 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.171+2090_171+2093d others(6): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1106249 | ||||||
| chr4:1106249
|
TACACAC | T | 11 | a0001c0001t0001g0110a0001c0001t0001g0114a0001c0001t0001g0154others(8): Show | 13 | HG01255.hp1 HG02109.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.171+2088_171+2093d others(8): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1106249 | ||||||
| chr4:1106249
|
TACACACA others(3): Show |
T | 1 | a0001c0002t0012g0103 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.171+2084_171+2093d others(12): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1106249 | ||||||
| chr4:1106249
|
TACACACA others(7): Show |
T | 12 | a0001c0001t0001g0089a0001c0001t0001g0190a0001c0002t0001g0034others(9): Show | 14 | HG01884.hp2 HG02148.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.171+2080_171+2093d others(16): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1106249 | ||||||
| chr4:1106249
|
TACACACA others(9): Show |
T | 77 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0012others(74): Show | 87 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.171+2078_171+2093d others(18): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1106249 | ||||||
| chr4:1106249
|
TACACACA others(11): Show |
T | 7 | a0001c0001t0001g0031a0001c0001t0001g0279a0001c0001t0001g0280others(4): Show | 9 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.171+2076_171+2093d others(20): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1106249 | ||||||
| chr4:1106249
|
TACACACA others(15): Show |
T | 1 | a0001c0001t0001g0113 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.171+2072_171+2093d others(24): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1106249 | ||||||
| chr4:1106249
|
TACACACA others(17): Show |
T | 1 | a0001c0009t0003g0335 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.171+2070_171+2093d others(26): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1106249 | ||||||
| chr4:1106431
|
G | A | 1 | a0005c0006t0001g0139 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.171+1912C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1106431 | ||||||
| chr4:1106564
|
C | T | 10 | a0001c0002t0001g0034a0001c0002t0001g0037a0001c0002t0001g0041others(7): Show | 12 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.171+1779G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1106564 | ||||||
| chr4:1106661
|
C | T | 8 | a0001c0001t0001g0013a0001c0001t0001g0064a0001c0001t0001g0070others(5): Show | 9 | NA18941.hp2 NA18948.hp2 NA18956.hp1 others(6): Show |
intron_variant | MODIFIER | c.171+1682G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1106661 | ||||||
| chr4:1106750
|
G | A | 1 | a0001c0001t0001g0202 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.171+1593C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1106750 | ||||||
| chr4:1106802
|
G | C | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(1): Show | 4 | HG02818.hp2 HG03471.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.171+1541C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1106802 | ||||||
| chr4:1106886
|
A | G | 1 | a0001c0002t0002g0245 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.171+1457T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1106886 | ||||||
| chr4:1106949
|
A | G | 1 | a0001c0002t0002g0310 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.171+1394T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1106949 | ||||||
| chr4:1107021
|
T | C | 1 | a0001c0002t0012g0103 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.171+1322A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1107021 | ||||||
| chr4:1107054
|
C | G | 1 | a0001c0001t0001g0069 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.171+1289G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1107054 | ||||||
| chr4:1107078
|
G | A | 1 | a0001c0002t0013g0102 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.171+1265C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1107078 | ||||||
| chr4:1107082
|
T | G | 1 | a0001c0002t0012g0103 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.171+1261A>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1107082 | ||||||
| chr4:1107088
|
G | C | 1 | a0001c0001t0001g0140 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.171+1255C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1107088 | ||||||
| chr4:1107091
|
G | A | 6 | a0001c0001t0001g0110a0001c0001t0001g0141a0001c0001t0001g0142others(3): Show | 6 | HG02074.hp2 HG02293.hp1 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.171+1252C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1107091 | ||||||
| chr4:1107121
|
A | G | 317 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(314): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.171+1222T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1107121 | ||||||
| chr4:1107180
|
T | C | 114 | a0001c0002t0001g0034a0001c0002t0001g0037a0001c0002t0001g0041others(111): Show | 125 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.171+1163A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1107180 | ||||||
| chr4:1107294
|
G | A | 202 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(199): Show | 226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.171+1049C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1107294 | ||||||
| chr4:1107306
|
C | T | 1 | a0001c0002t0002g0155 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.171+1037G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1107306 | ||||||
| chr4:1107360
|
C | A | 9 | a0001c0002t0003g0033a0001c0002t0003g0350a0001c0002t0003g0351others(6): Show | 10 | HG00642.hp2 HG00735.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.171+983G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1107360 | ||||||
| chr4:1107378
|
A | G | 1 | a0001c0002t0002g0227 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.171+965T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1107378 | ||||||
| chr4:1107428
|
T | C | 316 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(313): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.171+915A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1107428 | ||||||
| chr4:1107458
|
C | CT | 20 | a0001c0001t0001g0012a0001c0001t0001g0062a0001c0001t0001g0064others(17): Show | 21 | HG01167.hp1 HG01175.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.171+884dupA | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1107458 | ||||||
| chr4:1107508
|
T | C | 7 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0001g0105others(4): Show | 7 | HG02040.hp1 HG03491.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.171+835A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1107508 | ||||||
| chr4:1107544
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.171+799C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1107544 | ||||||
| chr4:1107650
|
C | A | 1 | a0001c0001t0001g0320 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.171+693G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1107650 | ||||||
| chr4:1107693
|
G | A | 2 | a0001c0002t0002g0282a0001c0002t0002g0283 | 2 | NA18944.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.171+650C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1107693 | ||||||
| chr4:1107824
|
C | A | 2 | a0001c0001t0001g0149a0001c0002t0002g0058 | 2 | HG01109.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.171+519G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1107824 | ||||||
| chr4:1107824
|
C | G | 319 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(316): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.171+519G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1107824 | ||||||
| chr4:1107862
|
T | C | 7 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0001g0105others(4): Show | 7 | HG02040.hp1 HG03491.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.171+481A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1107862 | ||||||
| chr4:1107877
|
T | C | 1 | a0001c0001t0001g0211 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.171+466A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1107877 | ||||||
| chr4:1107969
|
G | T | 316 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(313): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.171+374C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1107969 | ||||||
| chr4:1108079
|
A | G | 1 | a0001c0001t0001g0111 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.171+264T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1108079 | ||||||
| chr4:1108121
|
G | A | 1 | a0001c0002t0002g0284 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.171+222C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1108121 | ||||||
| chr4:1108212
|
C | G | 2 | a0001c0001t0001g0061a0001c0001t0001g0105 | 2 | NA18984.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.171+131G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1108212 | ||||||
| chr4:1108217
|
A | G | 2 | a0001c0001t0001g0325a0001c0001t0001g0329 | 2 | HG01192.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.171+126T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1108217 | ||||||
| chr4:1108262
|
C | T | 316 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(313): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.171+81G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 2/9 | chr4 | 1108262 | ||||||
| chr4:1108407
|
A | G | 36 | a0001c0002t0002g0025a0001c0002t0002g0026a0001c0002t0002g0027others(33): Show | 39 | HG00408.hp1 HG00423.hp2 HG00597.hp2 others(36): Show |
splice_region_variant&intron_variant | LOW | c.110-3T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1108407 | ||||||
| chr4:1108552
|
A | G | 1 | a0001c0001t0001g0007 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.110-148T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1108552 | ||||||
| chr4:1108577
|
G | C | 10 | a0001c0002t0001g0034a0001c0002t0001g0037a0001c0002t0001g0041others(7): Show | 12 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.110-173C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1108577 | ||||||
| chr4:1108602
|
T | C | 1 | a0007c0008t0011g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.110-198A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1108602 | ||||||
| chr4:1108691
|
A | T | 1 | a0001c0002t0002g0321 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.110-287T>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1108691 | ||||||
| chr4:1108730
|
T | C | 316 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(313): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.110-326A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1108730 | ||||||
| chr4:1108764
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.110-360A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1108764 | ||||||
| chr4:1108787
|
A | C | 316 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(313): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.110-383T>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1108787 | ||||||
| chr4:1108851
|
C | T | 1 | a0001c0001t0001g0172 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.110-447G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1108851 | ||||||
| chr4:1108893
|
G | T | 3 | a0001c0002t0002g0165a0001c0002t0002g0225a0001c0002t0002g0309 | 3 | HG00423.hp1 NA18981.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.110-489C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1108893 | ||||||
| chr4:1108997
|
G | T | 1 | a0001c0002t0002g0321 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.110-593C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1108997 | ||||||
| chr4:1109010
|
C | CT | 184 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(181): Show | 206 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.110-607dupA | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1109010 | ||||||
| chr4:1109010
|
C | CTT | 8 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0106others(5): Show | 8 | HG00738.hp2 HG00741.hp1 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.110-608_110-607dup others(2): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1109010 | ||||||
| chr4:1109010
|
C | CTTT | 108 | a0001c0001t0001g0031a0001c0001t0001g0108a0001c0001t0001g0279others(105): Show | 118 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.110-609_110-607dup others(3): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1109010 | ||||||
| chr4:1109070
|
C | T | 1 | a0001c0002t0012g0103 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.110-666G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1109070 | ||||||
| chr4:1109177
|
T | G | 1 | a0001c0002t0002g0321 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.110-773A>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1109177 | ||||||
| chr4:1109199
|
G | A | 1 | a0001c0002t0002g0284 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.110-795C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1109199 | ||||||
| chr4:1109256
|
C | G | 1 | a0001c0002t0001g0035 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.110-852G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1109256 | ||||||
| chr4:1109260
|
G | A | 1 | a0001c0002t0012g0103 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.110-856C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1109260 | ||||||
| chr4:1109573
|
C | T | 316 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(313): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.110-1169G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1109573 | ||||||
| chr4:1109625
|
T | C | 1 | a0007c0008t0011g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.110-1221A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1109625 | ||||||
| chr4:1109686
|
C | A | 316 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(313): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.110-1282G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1109686 | ||||||
| chr4:1109711
|
A | G | 6 | a0001c0001t0001g0157a0001c0001t0001g0160a0001c0001t0001g0161others(3): Show | 6 | HG01884.hp1 HG01891.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.110-1307T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1109711 | ||||||
| chr4:1109749
|
AC | A | 176 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 198 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.110-1346delG | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1109749 | ||||||
| chr4:1109852
|
C | T | 2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | HG01496.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.110-1448G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1109852 | ||||||
| chr4:1109900
|
C | T | 1 | a0001c0002t0004g0048 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.110-1496G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1109900 | ||||||
| chr4:1109989
|
C | T | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(1): Show | 4 | HG02818.hp2 HG03471.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.110-1585G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1109989 | ||||||
| chr4:1110090
|
T | C | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(1): Show | 4 | HG02818.hp2 HG03471.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.110-1686A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1110090 | ||||||
| chr4:1110159
|
G | A | 5 | a0001c0001t0001g0144a0003c0004t0001g0145a0003c0004t0001g0146others(2): Show | 5 | HG00597.hp1 NA18944.hp1 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.110-1755C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1110159 | ||||||
| chr4:1110215
|
G | A | 316 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(313): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.110-1811C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1110215 | ||||||
| chr4:1110255
|
T | C | 3 | a0001c0002t0002g0295a0001c0002t0002g0296a0001c0002t0002g0323 | 3 | NA18956.hp2 NA18975.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.110-1851A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1110255 | ||||||
| chr4:1110416
|
A | G | 316 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(313): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.110-2012T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1110416 | ||||||
| chr4:1110731
|
C | T | 2 | a0001c0002t0001g0209a0001c0002t0001g0303 | 2 | HG03041.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.110-2327G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1110731 | ||||||
| chr4:1110797
|
C | A | 1 | a0001c0002t0012g0103 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.110-2393G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1110797 | ||||||
| chr4:1110809
|
C | T | 321 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(318): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.110-2405G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1110809 | ||||||
| chr4:1110889
|
G | A | 1 | a0007c0008t0011g0040 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.109+2467C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1110889 | ||||||
| chr4:1111128
|
T | C | 10 | a0001c0002t0001g0034a0001c0002t0001g0037a0001c0002t0001g0041others(7): Show | 12 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.109+2228A>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1111128 | ||||||
| chr4:1111534
|
G | T | 5 | a0001c0001t0001g0044a0001c0001t0005g0043a0001c0001t0005g0045others(2): Show | 5 | HG02040.hp1 HG03491.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.109+1822C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1111534 | ||||||
| chr4:1111604
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.109+1752G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1111604 | ||||||
| chr4:1111676
|
C | G | 318 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(315): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.109+1680G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1111676 | ||||||
| chr4:1111892
|
C | T | 41 | a0001c0002t0001g0021a0001c0002t0001g0034a0001c0002t0001g0037others(38): Show | 46 | HG00642.hp2 HG00735.hp1 HG01243.hp2 others(43): Show |
intron_variant | MODIFIER | c.109+1464G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1111892 | ||||||
| chr4:1111917
|
A | G | 1 | a0001c0001t0001g0213 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.109+1439T>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1111917 | ||||||
| chr4:1111968
|
G | A | 2 | a0001c0002t0002g0057a0001c0002t0002g0058 | 2 | HG01109.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.109+1388C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1111968 | ||||||
| chr4:1111975
|
C | G | 1 | a0001c0002t0002g0155 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.109+1381G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1111975 | ||||||
| chr4:1111985
|
G | C | 6 | a0001c0002t0001g0034a0001c0002t0001g0209a0001c0002t0001g0303others(3): Show | 8 | HG02486.hp2 HG02572.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.109+1371C>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1111985 | ||||||
| chr4:1112032
|
C | A | 1 | a0001c0002t0012g0103 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.109+1324G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1112032 | ||||||
| chr4:1112184
|
G | A | 3 | a0001c0001t0001g0020a0001c0001t0001g0148a0001c0001t0001g0306 | 4 | HG03017.hp2 HG03831.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.109+1172C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1112184 | ||||||
| chr4:1112544
|
C | G | 3 | a0001c0001t0001g0096a0001c0001t0001g0154a0001c0002t0001g0041 | 3 | HG02258.hp2 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.109+812G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1112544 | ||||||
| chr4:1112557
|
G | T | 1 | a0001c0002t0002g0153 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.109+799C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1112557 | ||||||
| chr4:1112680
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.109+676G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1112680 | ||||||
| chr4:1112765
|
C | T | 1 | a0001c0001t0001g0152 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.109+591G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1112765 | ||||||
| chr4:1112816
|
T | TC | 19 | a0001c0001t0001g0050a0001c0001t0001g0091a0001c0001t0001g0096others(16): Show | 19 | HG00597.hp1 HG00621.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.109+539dupG | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1112816 | ||||||
| chr4:1112824
|
A | C | 356 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(353): Show | 396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.109+532T>G | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1112824 | ||||||
| chr4:1112827
|
C | T | 17 | a0001c0001t0001g0011a0001c0001t0001g0051a0001c0001t0001g0054others(14): Show | 19 | HG01109.hp1 HG01175.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.109+529G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1112827 | ||||||
| chr4:1112837
|
C | T | 17 | a0001c0001t0001g0011a0001c0001t0001g0051a0001c0001t0001g0054others(14): Show | 19 | HG01109.hp1 HG01175.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.109+519G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1112837 | ||||||
| chr4:1112903
|
G | A | 5 | a0001c0001t0001g0044a0001c0001t0005g0043a0001c0001t0005g0045others(2): Show | 5 | HG02040.hp1 HG03491.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.109+453C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1112903 | ||||||
| chr4:1112906
|
G | A | 1 | a0001c0002t0012g0103 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.109+450C>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1112906 | ||||||
| chr4:1112936
|
C | T | 1 | a0001c0002t0004g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.109+420G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1112936 | ||||||
| chr4:1112987
|
C | G | 108 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(105): Show | 122 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.109+369G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1112987 | ||||||
| chr4:1113024
|
T | A | 5 | a0001c0001t0001g0044a0001c0001t0005g0043a0001c0001t0005g0045others(2): Show | 5 | HG02040.hp1 HG03491.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.109+332A>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1113024 | ||||||
| chr4:1113063
|
A | AC | 61 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(58): Show | 72 | HG00558.hp1 HG00558.hp2 HG00673.hp1 others(69): Show |
intron_variant | MODIFIER | c.109+292dupG | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1113063 | ||||||
| chr4:1113073
|
G | GC | 138 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0017others(135): Show | 155 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.109+282dupG | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1113073 | ||||||
| chr4:1113073
|
G | GCC | 125 | a0001c0001t0001g0031a0001c0001t0001g0212a0001c0001t0001g0213others(122): Show | 136 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.109+281_109+282dup others(2): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1113073 | ||||||
| chr4:1113073
|
G | GCCC | 25 | a0001c0001t0001g0306a0001c0001t0001g0319a0001c0001t0001g0320others(22): Show | 25 | HG00639.hp1 HG01192.hp1 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.109+280_109+282dup others(3): Show |
RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1113073 | ||||||
| chr4:1113081
|
C | G | 7 | a0001c0001t0001g0044a0001c0001t0005g0043a0001c0001t0005g0045others(4): Show | 7 | HG02040.hp1 HG03098.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.109+275G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1113081 | ||||||
| chr4:1113106
|
C | T | 14 | a0001c0002t0001g0037a0001c0002t0003g0334a0001c0002t0003g0336others(11): Show | 14 | HG01243.hp2 HG01433.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.109+250G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1113106 | ||||||
| chr4:1113119
|
G | GC | 8 | a0001c0001t0001g0032a0001c0001t0001g0326a0001c0001t0001g0327others(5): Show | 9 | HG01255.hp2 HG01261.hp2 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.109+236dupG | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1113119 | ||||||
| chr4:1113149
|
C | A | 1 | a0001c0001t0001g0331 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.109+207G>T | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1113149 | ||||||
| chr4:1113206
|
G | T | 21 | a0001c0002t0001g0037a0001c0002t0003g0334a0001c0002t0003g0336others(18): Show | 22 | HG01074.hp2 HG01243.hp2 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.109+150C>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1113206 | ||||||
| chr4:1113251
|
C | T | 1 | a0001c0002t0002g0036 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.109+105G>A | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1113251 | ||||||
| chr4:1113268
|
C | G | 1 | a0001c0002t0001g0035 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.109+88G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1113268 | ||||||
| chr4:1113288
|
C | G | 2 | a0001c0001t0001g0007a0001c0002t0001g0034 | 3 | HG01069.hp2 HG01071.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.109+68G>C | RNF212 | ENSG00000178222.14 | transcript | ENST00000433731.7 | protein_coding | 1/9 | chr4 | 1113288 |