| geneid | 154214 |
|---|---|
| ensemblid | ENSG00000146373.17 |
| hgncid | 21487 |
| symbol | RNF217 |
| name | ring finger protein 217 |
| refseq_nuc | NM_001286398.3 |
| refseq_prot | NP_001273327.1 |
| ensembl_nuc | ENST00000521654.7 |
| ensembl_prot | ENSP00000428698.2 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 124962437 |
| end | 125092633 |
| strand | + |
| ver | v1.2 |
| region | chr6:124962437-125092633 |
| region5000 | chr6:124957437-125097633 |
| regionname0 | RNF217_chr6_124962437_125092633 |
| regionname5000 | RNF217_chr6_124957437_125097633 |
| 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 | 0/0 | 542 | 215 | 67 | 43 | 75 | 5 | 25 | 56 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0002 | 1/1 | 542 | 33 | 6 | 7 | 12 | 1 | 5 | 10 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0003 | 0/0 | 542 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0004 | 0/0 | 542 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0005 | 0/0 | 542 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0006 | 0/0 | 542 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0007 | 0/0 | 542 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0008 | 0/0 | 542 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0009 | 0/0 | 542 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0010 | 0/0 | 542 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0011 | 0/0 | 542 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| 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 | 0/0 | 1629 | 198 | 52 | 41 | 75 | 5 | 25 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| c0002 | 1/1 | 1629 | 30 | 5 | 7 | 10 | 1 | 5 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| c0003 | 0/0 | 1629 | 14 | 12 | 2 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| c0004 | 0/0 | 1629 | 7 | 6 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| c0005 | 0/0 | 1629 | 3 | 0 | 3 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| c0006 | 0/0 | 1629 | 3 | 1 | 0 | 2 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| c0007 | 0/0 | 1629 | 2 | 2 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| c0008 | 0/0 | 1629 | 2 | 2 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| c0009 | 0/0 | 1629 | 2 | 2 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| c0010 | 0/0 | 1629 | 2 | 2 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| c0011 | 0/0 | 1629 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| c0012 | 0/0 | 1629 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| c0013 | 0/0 | 1629 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| c0014 | 0/0 | 1629 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| c0015 | 0/0 | 1629 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 9805 | 58 | 5 | 21 | 24 | 2 | 6 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0002 | 0/0 | 9805 | 25 | 0 | 9 | 13 | 0 | 3 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0003 | 0/0 | 9801 | 13 | 7 | 2 | 0 | 0 | 4 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0004 | 0/0 | 9802 | 11 | 2 | 0 | 6 | 0 | 3 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0005 | 0/0 | 9805 | 11 | 0 | 3 | 8 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0006 | 0/0 | 9805 | 9 | 9 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0007 | 1/0 | 9805 | 9 | 0 | 0 | 5 | 0 | 3 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0008 | 0/0 | 9804 | 8 | 7 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0009 | 0/1 | 9805 | 8 | 0 | 3 | 1 | 1 | 2 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0010 | 0/0 | 9804 | 7 | 7 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0011 | 0/0 | 9801 | 6 | 5 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0012 | 0/0 | 9802 | 5 | 0 | 2 | 0 | 1 | 2 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0013 | 0/0 | 9805 | 5 | 2 | 1 | 2 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0014 | 0/0 | 9805 | 4 | 0 | 0 | 4 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0015 | 0/0 | 9802 | 4 | 0 | 0 | 4 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0016 | 0/0 | 9804 | 3 | 0 | 0 | 0 | 0 | 3 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0017 | 0/0 | 9802 | 3 | 3 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0018 | 0/0 | 9804 | 3 | 0 | 0 | 3 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0019 | 0/0 | 9805 | 3 | 0 | 0 | 3 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0020 | 0/0 | 9806 | 3 | 0 | 3 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0021 | 0/0 | 9804 | 3 | 3 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0022 | 0/0 | 9802 | 3 | 3 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0023 | 0/0 | 9803 | 2 | 2 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0024 | 0/0 | 9804 | 2 | 2 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0025 | 0/0 | 9806 | 2 | 0 | 1 | 0 | 1 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0026 | 0/0 | 9805 | 2 | 2 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0027 | 0/0 | 9803 | 2 | 1 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0028 | 0/0 | 9801 | 2 | 2 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0029 | 0/0 | 9805 | 2 | 0 | 0 | 2 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0030 | 0/0 | 9805 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0031 | 0/0 | 9805 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0032 | 0/0 | 9805 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0033 | 0/0 | 9805 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0034 | 0/0 | 9805 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0035 | 0/0 | 9805 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0036 | 0/0 | 9805 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0037 | 0/0 | 9803 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0038 | 0/0 | 9805 | 1 | 0 | 0 | 0 | 1 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0039 | 0/0 | 9806 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0040 | 0/0 | 9806 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0041 | 0/0 | 9801 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0042 | 0/0 | 9802 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0043 | 0/0 | 9801 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0044 | 0/0 | 9802 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0045 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0046 | 0/0 | 9802 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0047 | 0/0 | 9801 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0048 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0049 | 0/0 | 9806 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0050 | 0/0 | 9802 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0051 | 0/0 | 9803 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0052 | 0/0 | 9805 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0053 | 0/0 | 9805 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0054 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0055 | 0/0 | 9805 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0056 | 0/0 | 9805 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0057 | 0/0 | 9805 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0058 | 0/0 | 9805 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0059 | 0/0 | 9805 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0060 | 0/0 | 9805 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0061 | 0/0 | 9805 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0062 | 0/0 | 9806 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0063 | 0/0 | 9782 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0064 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0065 | 0/0 | 9805 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0066 | 0/0 | 9805 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0067 | 0/0 | 9805 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0068 | 0/0 | 9803 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0069 | 0/0 | 9803 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0070 | 0/0 | 9805 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0071 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0072 | 0/0 | 9805 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0073 | 0/0 | 9802 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0074 | 0/0 | 9802 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0075 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0076 | 0/0 | 9805 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0077 | 0/0 | 9805 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0078 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| t0079 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0014 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0031 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| 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 | 0/0 | 1629 | 198 | 52 | 41 | 75 | 5 | 25 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0003 | 0/0 | 1629 | 14 | 12 | 2 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0008 | 0/0 | 1629 | 2 | 2 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0012 | 0/0 | 1629 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0002c0002 | 1/1 | 1629 | 30 | 5 | 7 | 10 | 1 | 5 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0002c0006 | 0/0 | 1629 | 3 | 1 | 0 | 2 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0003c0004 | 0/0 | 1629 | 7 | 6 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0004c0005 | 0/0 | 1629 | 3 | 0 | 3 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0005c0007 | 0/0 | 1629 | 2 | 2 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0006c0009 | 0/0 | 1629 | 2 | 2 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0007c0010 | 0/0 | 1629 | 2 | 2 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0008c0015 | 0/0 | 1629 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0009c0014 | 0/0 | 1629 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0010c0013 | 0/0 | 1629 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0011c0011 | 0/0 | 1629 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 11433 | 55 | 3 | 21 | 23 | 2 | 6 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0002 | 0/0 | 11433 | 25 | 0 | 9 | 13 | 0 | 3 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0003 | 0/0 | 11429 | 11 | 5 | 2 | 0 | 0 | 4 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0004 | 0/0 | 11430 | 11 | 2 | 0 | 6 | 0 | 3 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0005 | 0/0 | 11433 | 11 | 0 | 3 | 8 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0006 | 0/0 | 11433 | 8 | 8 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0008 | 0/0 | 11432 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0010 | 0/0 | 11432 | 5 | 5 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0012 | 0/0 | 11430 | 5 | 0 | 2 | 0 | 1 | 2 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0014 | 0/0 | 11433 | 4 | 0 | 0 | 4 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0015 | 0/0 | 11430 | 4 | 0 | 0 | 4 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0016 | 0/0 | 11432 | 3 | 0 | 0 | 0 | 0 | 3 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0017 | 0/0 | 11430 | 3 | 3 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0018 | 0/0 | 11432 | 3 | 0 | 0 | 3 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0019 | 0/0 | 11433 | 3 | 0 | 0 | 3 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0021 | 0/0 | 11432 | 2 | 2 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0022 | 0/0 | 11430 | 3 | 3 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0023 | 0/0 | 11431 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0024 | 0/0 | 11432 | 2 | 2 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0025 | 0/0 | 11434 | 2 | 0 | 1 | 0 | 1 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0026 | 0/0 | 11433 | 2 | 2 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0032 | 0/0 | 11433 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0033 | 0/0 | 11433 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0034 | 0/0 | 11433 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0035 | 0/0 | 11433 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0036 | 0/0 | 11433 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0037 | 0/0 | 11431 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0038 | 0/0 | 11433 | 1 | 0 | 0 | 0 | 1 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0039 | 0/0 | 11434 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0040 | 0/0 | 11434 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0041 | 0/0 | 11429 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0042 | 0/0 | 11430 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0043 | 0/0 | 11429 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0045 | 0/0 | 11432 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0046 | 0/0 | 11430 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0047 | 0/0 | 11429 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0048 | 0/0 | 11432 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0049 | 0/0 | 11434 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0050 | 0/0 | 11430 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0051 | 0/0 | 11431 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0052 | 0/0 | 11433 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0054 | 0/0 | 11432 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0055 | 0/0 | 11433 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0056 | 0/0 | 11433 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0057 | 0/0 | 11433 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0058 | 0/0 | 11433 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0059 | 0/0 | 11433 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0060 | 0/0 | 11433 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0061 | 0/0 | 11433 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0062 | 0/0 | 11434 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0063 | 0/0 | 11410 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0066 | 0/0 | 11433 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0067 | 0/0 | 11433 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0068 | 0/0 | 11431 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0001t0069 | 0/0 | 11431 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0003t0008 | 0/0 | 11432 | 7 | 6 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0003t0010 | 0/0 | 11432 | 2 | 2 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0003t0013 | 0/0 | 11433 | 2 | 2 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0003t0023 | 0/0 | 11431 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0003t0064 | 0/0 | 11432 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0003t0065 | 0/0 | 11433 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0008t0003 | 0/0 | 11429 | 2 | 2 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0001c0012t0031 | 0/0 | 11433 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0002c0002t0007 | 1/0 | 11433 | 9 | 0 | 0 | 5 | 0 | 3 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0002c0002t0009 | 0/1 | 11433 | 8 | 0 | 3 | 1 | 1 | 2 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0002c0002t0013 | 0/0 | 11433 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0002c0002t0027 | 0/0 | 11431 | 2 | 1 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0002c0002t0029 | 0/0 | 11433 | 2 | 0 | 0 | 2 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0002c0002t0070 | 0/0 | 11433 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0002c0002t0071 | 0/0 | 11432 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0002c0002t0072 | 0/0 | 11433 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0002c0002t0073 | 0/0 | 11430 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0002c0002t0074 | 0/0 | 11430 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0002c0002t0075 | 0/0 | 11432 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0002c0002t0076 | 0/0 | 11433 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0002c0002t0077 | 0/0 | 11433 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0002c0006t0013 | 0/0 | 11433 | 2 | 0 | 0 | 2 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0002c0006t0078 | 0/0 | 11432 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0003c0004t0011 | 0/0 | 11429 | 6 | 5 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0003c0004t0044 | 0/0 | 11430 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0004c0005t0020 | 0/0 | 11434 | 3 | 0 | 3 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0005c0007t0006 | 0/0 | 11433 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0005c0007t0021 | 0/0 | 11432 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0006c0009t0001 | 0/0 | 11433 | 2 | 2 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0007c0010t0028 | 0/0 | 11429 | 2 | 2 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0008c0015t0053 | 0/0 | 11433 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0009c0014t0001 | 0/0 | 11433 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0010c0013t0030 | 0/0 | 11433 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| a0011c0011t0079 | 0/0 | 11432 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | copy fasta | chr6 | 124957437 | 125097633 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0003g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0004g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0004g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0004g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0005g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0005g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0005g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0005g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0005g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0005g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0005g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0005g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0005g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0005g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0005g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0006g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0006g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0006g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0006g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0006g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0006g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0006g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0006g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0008g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0010g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0010g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0010g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0010g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0010g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0012g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0012g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0012g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0012g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0012g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0014g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0014g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0014g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0014g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0015g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0015g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0015g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0015g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0016g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0016g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0016g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0017g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0017g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0017g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0018g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0018g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0018g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0019g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0019g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0019g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0021g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0021g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0022g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0022g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0022g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0023g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0024g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0024g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0025g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0025g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0026g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0026g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0032g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0033g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0034g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0035g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0036g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0037g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0038g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0039g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0040g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0041g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0042g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0043g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0045g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0046g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0047g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0048g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0049g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0050g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0051g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0052g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0054g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0055g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0056g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0057g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0058g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0059g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0060g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0061g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0062g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0063g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0066g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0067g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0068g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0069g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0003t0008g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0003t0008g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0003t0008g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0003t0008g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0003t0008g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0003t0008g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0003t0008g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0003t0010g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0003t0010g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0003t0013g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0003t0013g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0003t0023g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0003t0064g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0003t0065g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0008t0003g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0012t0031g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0007g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0007g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0007g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0007g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0007g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0007g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0007g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0007g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0007g0031 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0009g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0009g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0009g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0009g0014 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0009g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0009g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0009g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0009g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0013g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0027g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0027g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0029g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0029g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0070g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0071g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0072g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0073g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0074g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0075g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0076g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0077g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0006t0013g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0006t0013g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0006t0078g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0003c0004t0011g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0003c0004t0011g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0003c0004t0011g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0003c0004t0011g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0003c0004t0011g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0003c0004t0011g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0003c0004t0044g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0004c0005t0020g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0004c0005t0020g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0004c0005t0020g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0005c0007t0006g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0005c0007t0021g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0006c0009t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0006c0009t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0007c0010t0028g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0007c0010t0028g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0008c0015t0053g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0009c0014t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0010c0013t0030g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0011c0011t0079g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0038 | g0204 | EUR | GBR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0137 | EUR | GBR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG00140 | hp1 | a0001 | c0001 | t0012 | g0126 | EUR | GBR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG00140 | hp2 | a0001 | c0001 | t0025 | g0142 | EUR | GBR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0231 | EUR | FIN | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG00323 | hp2 | a0002 | c0002 | t0009 | g0035 | EUR | FIN | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG00408 | hp2 | a0001 | c0001 | t0005 | g0092 | EAS | CHS | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG00423 | hp1 | a0002 | c0002 | t0007 | g0008 | EAS | CHS | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG00423 | hp2 | a0001 | c0001 | t0032 | g0079 | EAS | CHS | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG00609 | hp1 | a0001 | c0001 | t0014 | g0238 | EAS | CHS | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG00639 | hp1 | a0001 | c0003 | t0065 | g0167 | AMR | PUR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0234 | AMR | PUR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0085 | AMR | PUR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0067 | AMR | PUR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | PUR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0198 | AMR | PUR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG00738 | hp2 | a0002 | c0002 | t0027 | g0019 | AMR | PUR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG00741 | hp1 | a0003 | c0004 | t0011 | g0157 | AMR | PUR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG00741 | hp2 | a0004 | c0005 | t0020 | g0088 | AMR | PUR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01069 | hp1 | a0002 | c0002 | t0072 | g0006 | AMR | PUR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01069 | hp2 | a0001 | c0001 | t0025 | g0165 | AMR | PUR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0205 | AMR | PUR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0211 | AMR | PUR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01106 | hp1 | a0002 | c0002 | t0013 | g0011 | AMR | PUR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01106 | hp2 | a0001 | c0001 | t0037 | g0139 | AMR | PUR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0141 | AMR | PUR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01169 | hp2 | a0004 | c0005 | t0020 | g0090 | AMR | PUR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01192 | hp2 | a0001 | c0001 | t0012 | g0065 | AMR | PUR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01243 | hp1 | a0001 | c0003 | t0008 | g0188 | AMR | PUR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0164 | AMR | CLM | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01257 | hp1 | a0002 | c0002 | t0009 | g0013 | AMR | CLM | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01257 | hp2 | a0004 | c0005 | t0020 | g0089 | AMR | CLM | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01258 | hp2 | a0002 | c0002 | t0009 | g0012 | AMR | CLM | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01346 | hp1 | a0002 | c0002 | t0009 | g0025 | AMR | CLM | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | CLM | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01433 | hp1 | a0001 | c0001 | t0005 | g0081 | AMR | CLM | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01433 | hp2 | a0001 | c0001 | t0056 | g0112 | AMR | CLM | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01884 | hp1 | a0005 | c0007 | t0006 | g0094 | AFR | ACB | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01884 | hp2 | a0001 | c0001 | t0017 | g0154 | AFR | ACB | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01891 | hp2 | a0001 | c0001 | t0010 | g0163 | AFR | ACB | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01928 | hp2 | a0001 | c0001 | t0005 | g0214 | AMR | PEL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01934 | hp1 | a0002 | c0002 | t0077 | g0034 | AMR | PEL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01952 | hp2 | a0001 | c0001 | t0055 | g0073 | AMR | PEL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01981 | hp1 | a0001 | c0001 | t0012 | g0220 | AMR | PEL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0086 | AMR | PEL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01993 | hp1 | a0001 | c0001 | t0005 | g0110 | AMR | PEL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PEL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0230 | AMR | PEL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02055 | hp1 | a0007 | c0010 | t0028 | g0032 | AFR | ACB | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02055 | hp2 | a0001 | c0001 | t0008 | g0182 | AFR | ACB | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02056 | hp1 | a0001 | c0001 | t0019 | g0076 | EAS | KHV | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | KHV | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02071 | hp2 | a0002 | c0002 | t0076 | g0020 | EAS | KHV | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | KHV | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0117 | EAS | KHV | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02083 | hp1 | a0001 | c0001 | t0047 | g0226 | EAS | KHV | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02083 | hp2 | a0009 | c0014 | t0001 | g0127 | EAS | KHV | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | KHV | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | CDX | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02155 | hp2 | a0001 | c0001 | t0060 | g0233 | EAS | CDX | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02257 | hp1 | a0006 | c0009 | t0001 | g0194 | AFR | ACB | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02257 | hp2 | a0001 | c0001 | t0040 | g0261 | AFR | ACB | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02258 | hp1 | a0001 | c0001 | t0049 | g0262 | AFR | ACB | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02258 | hp2 | a0001 | c0001 | t0017 | g0254 | AFR | ACB | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02280 | hp1 | a0001 | c0003 | t0008 | g0187 | AFR | ACB | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02280 | hp2 | a0001 | c0001 | t0006 | g0174 | AFR | ACB | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0178 | AFR | ACB | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02451 | hp2 | a0001 | c0003 | t0023 | g0143 | AFR | ACB | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02523 | hp2 | a0001 | c0001 | t0018 | g0219 | EAS | KHV | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0169 | AFR | GWD | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02572 | hp2 | a0001 | c0001 | t0006 | g0264 | AFR | GWD | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0087 | SAS | PJL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02602 | hp2 | a0001 | c0001 | t0016 | g0222 | SAS | PJL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0172 | AFR | GWD | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02615 | hp2 | a0002 | c0006 | t0078 | g0007 | AFR | GWD | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02622 | hp1 | a0001 | c0001 | t0010 | g0145 | AFR | GWD | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0183 | AFR | GWD | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02630 | hp1 | a0003 | c0004 | t0011 | g0149 | AFR | GWD | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02630 | hp2 | a0001 | c0001 | t0006 | g0177 | AFR | GWD | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02647 | hp1 | a0003 | c0004 | t0011 | g0150 | AFR | GWD | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02647 | hp2 | a0001 | c0001 | t0022 | g0042 | AFR | GWD | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0203 | SAS | PJL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02683 | hp2 | a0001 | c0001 | t0066 | g0166 | SAS | PJL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02698 | hp1 | a0001 | c0001 | t0036 | g0232 | SAS | PJL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02735 | hp1 | a0001 | c0001 | t0012 | g0062 | SAS | PJL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02809 | hp1 | a0005 | c0007 | t0021 | g0095 | AFR | GWD | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02809 | hp2 | a0001 | c0001 | t0051 | g0173 | AFR | GWD | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02818 | hp1 | a0001 | c0001 | t0010 | g0148 | AFR | GWD | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02818 | hp2 | a0003 | c0004 | t0011 | g0190 | AFR | GWD | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0176 | AFR | GWD | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02886 | hp2 | a0001 | c0001 | t0022 | g0132 | AFR | GWD | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02895 | hp1 | a0001 | c0001 | t0026 | g0160 | AFR | GWD | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02895 | hp2 | a0001 | c0003 | t0064 | g0189 | AFR | GWD | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02896 | hp1 | a0001 | c0001 | t0059 | g0171 | AFR | GWD | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02896 | hp2 | a0001 | c0008 | t0003 | g0001 | AFR | GWD | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02897 | hp1 | a0001 | c0008 | t0003 | g0001 | AFR | GWD | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02897 | hp2 | a0001 | c0001 | t0021 | g0159 | AFR | GWD | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02922 | hp1 | a0008 | c0015 | t0053 | g0248 | AFR | ESN | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02922 | hp2 | a0001 | c0003 | t0010 | g0266 | AFR | ESN | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02965 | hp1 | a0001 | c0001 | t0050 | g0041 | AFR | ESN | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02965 | hp2 | a0001 | c0001 | t0041 | g0099 | AFR | ESN | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02970 | hp1 | a0001 | c0001 | t0033 | g0134 | AFR | ESN | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02970 | hp2 | a0010 | c0013 | t0030 | g0192 | AFR | ESN | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02976 | hp1 | a0003 | c0004 | t0044 | g0100 | AFR | ESN | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02976 | hp2 | a0001 | c0001 | t0024 | g0170 | AFR | ESN | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03041 | hp1 | a0001 | c0003 | t0010 | g0259 | AFR | GWD | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03041 | hp2 | a0001 | c0001 | t0048 | g0162 | AFR | GWD | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03098 | hp1 | a0001 | c0003 | t0008 | g0151 | AFR | MSL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03098 | hp2 | a0001 | c0001 | t0023 | g0250 | AFR | MSL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03130 | hp1 | a0001 | c0001 | t0046 | g0196 | AFR | ESN | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03130 | hp2 | a0001 | c0003 | t0013 | g0185 | AFR | ESN | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03139 | hp1 | a0003 | c0004 | t0011 | g0258 | AFR | ESN | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03139 | hp2 | a0001 | c0001 | t0006 | g0191 | AFR | ESN | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03209 | hp1 | a0001 | c0001 | t0010 | g0195 | AFR | MSL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03209 | hp2 | a0002 | c0002 | t0071 | g0038 | AFR | MSL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03225 | hp1 | a0011 | c0011 | t0079 | g0036 | AFR | MSL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03225 | hp2 | a0002 | c0002 | t0073 | g0030 | AFR | MSL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03239 | hp1 | a0001 | c0001 | t0012 | g0201 | SAS | PJL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03239 | hp2 | a0001 | c0001 | t0035 | g0140 | SAS | PJL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03453 | hp1 | a0001 | c0001 | t0017 | g0101 | AFR | MSL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03453 | hp2 | a0001 | c0001 | t0034 | g0146 | AFR | MSL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03486 | hp1 | a0001 | c0001 | t0026 | g0168 | AFR | MSL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03486 | hp2 | a0001 | c0001 | t0010 | g0153 | AFR | MSL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03491 | hp1 | a0002 | c0002 | t0007 | g0027 | SAS | PJL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03492 | hp1 | a0001 | c0001 | t0067 | g0199 | SAS | PJL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03540 | hp1 | a0001 | c0001 | t0022 | g0180 | AFR | GWD | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03540 | hp2 | a0003 | c0004 | t0011 | g0260 | AFR | GWD | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03579 | hp1 | a0001 | c0012 | t0031 | g0256 | AFR | MSL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03579 | hp2 | a0001 | c0003 | t0008 | g0193 | AFR | MSL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03669 | hp1 | a0002 | c0002 | t0007 | g0026 | SAS | PJL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0240 | SAS | PJL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0242 | SAS | STU | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | STU | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03704 | hp1 | a0001 | c0001 | t0016 | g0083 | SAS | PJL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03704 | hp2 | a0001 | c0001 | t0016 | g0144 | SAS | PJL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0244 | SAS | BEB | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03834 | hp2 | a0001 | c0001 | t0004 | g0227 | SAS | BEB | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0221 | SAS | STU | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG04115 | hp2 | a0002 | c0002 | t0009 | g0028 | SAS | STU | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG04184 | hp1 | a0002 | c0002 | t0009 | g0024 | SAS | BEB | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | BEB | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0243 | SAS | STU | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG04204 | hp2 | a0002 | c0002 | t0007 | g0015 | SAS | STU | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0115 | SAS | STU | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | STU | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18522 | hp1 | a0001 | c0001 | t0021 | g0133 | AFR | YRI | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18522 | hp2 | a0001 | c0001 | t0039 | g0179 | AFR | YRI | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | CHB | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18747 | hp2 | a0001 | c0001 | t0052 | g0049 | EAS | CHB | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18906 | hp1 | a0001 | c0001 | t0006 | g0003 | AFR | YRI | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18906 | hp2 | a0006 | c0009 | t0001 | g0265 | AFR | YRI | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18942 | hp2 | a0001 | c0001 | t0015 | g0252 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18943 | hp1 | a0001 | c0001 | t0069 | g0118 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18943 | hp2 | a0001 | c0001 | t0018 | g0224 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18946 | hp1 | a0001 | c0001 | t0015 | g0225 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18946 | hp2 | a0001 | c0001 | t0005 | g0082 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0075 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18949 | hp2 | a0001 | c0001 | t0005 | g0114 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18956 | hp1 | a0002 | c0002 | t0009 | g0009 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18959 | hp1 | a0001 | c0001 | t0004 | g0071 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18959 | hp2 | a0002 | c0002 | t0007 | g0016 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18962 | hp2 | a0001 | c0001 | t0005 | g0130 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0096 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18970 | hp2 | a0001 | c0001 | t0063 | g0091 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18971 | hp1 | a0001 | c0001 | t0019 | g0119 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18971 | hp2 | a0002 | c0002 | t0007 | g0022 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18975 | hp1 | a0001 | c0001 | t0005 | g0218 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18983 | hp1 | a0001 | c0001 | t0061 | g0253 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18983 | hp2 | a0001 | c0001 | t0015 | g0207 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18988 | hp1 | a0001 | c0001 | t0005 | g0061 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18988 | hp2 | a0002 | c0002 | t0074 | g0037 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18989 | hp2 | a0001 | c0001 | t0014 | g0097 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18994 | hp1 | a0001 | c0001 | t0058 | g0054 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18994 | hp2 | a0001 | c0001 | t0018 | g0223 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18999 | hp1 | a0001 | c0001 | t0015 | g0045 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18999 | hp2 | a0002 | c0002 | t0007 | g0023 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19002 | hp1 | a0002 | c0006 | t0013 | g0017 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19002 | hp2 | a0001 | c0001 | t0019 | g0239 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19010 | hp1 | a0001 | c0001 | t0014 | g0060 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19010 | hp2 | a0001 | c0001 | t0057 | g0246 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19011 | hp2 | a0001 | c0001 | t0062 | g0197 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19030 | hp1 | a0001 | c0001 | t0024 | g0184 | AFR | LWK | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0155 | AFR | LWK | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19043 | hp1 | a0001 | c0003 | t0008 | g0257 | AFR | LWK | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19043 | hp2 | a0002 | c0002 | t0075 | g0040 | AFR | LWK | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19056 | hp1 | a0001 | c0001 | t0005 | g0208 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19056 | hp2 | a0002 | c0002 | t0029 | g0033 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19065 | hp1 | a0002 | c0002 | t0029 | g0005 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19066 | hp1 | a0002 | c0002 | t0007 | g0021 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19068 | hp2 | a0001 | c0001 | t0014 | g0103 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19070 | hp1 | a0002 | c0006 | t0013 | g0010 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19076 | hp1 | a0001 | c0001 | t0042 | g0053 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19083 | hp1 | a0001 | c0001 | t0004 | g0046 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19084 | hp1 | a0001 | c0001 | t0005 | g0202 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19085 | hp1 | a0001 | c0001 | t0004 | g0123 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA20129 | hp1 | a0007 | c0010 | t0028 | g0029 | AFR | ASW | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | ASW | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02109 | hp1 | a0001 | c0001 | t0054 | g0181 | AFR | ACB | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0147 | AFR | ACB | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02486 | hp1 | a0001 | c0001 | t0043 | g0004 | AFR | ACB | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02559 | hp1 | a0001 | c0003 | t0013 | g0186 | AFR | ACB | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0255 | AFR | ACB | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03471 | hp1 | a0001 | c0001 | t0006 | g0251 | AFR | MSL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03471 | hp2 | a0001 | c0003 | t0008 | g0175 | AFR | MSL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG06807 | hp1 | a0001 | c0003 | t0008 | g0131 | AFR | USA | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG06807 | hp2 | a0002 | c0002 | t0070 | g0039 | AFR | USA | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA20300 | hp1 | a0001 | c0001 | t0045 | g0161 | AFR | USA | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA20300 | hp2 | a0001 | c0001 | t0068 | g0245 | AFR | USA | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA21309 | hp1 | a0001 | c0001 | t0006 | g0156 | AFR | LWK | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA21309 | hp2 | a0002 | c0002 | t0027 | g0018 | AFR | LWK | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0009 | g0014 | REF | REF | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| homoSapiens_grch38 | hp1 | a0002 | c0002 | t0007 | g0031 | REF | REF | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:124962663
|
C | A | 1 | a0011 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.119C>A | p.Ala40Glu | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/6 | 227/11433 | 119/1629 | 40/542 | chr6 | 124962663 | ||
| chr6:124963010
|
T | C | 1 | a0005 | 2 | HG01884.hp1 HG02809.hp1 |
missense_variant | MODERATE | c.466T>C | p.Ser156Pro | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/6 | 574/11433 | 466/1629 | 156/542 | chr6 | 124963010 | ||
| chr6:124963149
|
C | G | 1 | a0008 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.605C>G | p.Ser202Cys | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/6 | 713/11433 | 605/1629 | 202/542 | chr6 | 124963149 | ||
| chr6:124963311
|
T | C | 8 | a0001a0003a0004others(5): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
missense_variant | MODERATE | c.767T>C | p.Val256Ala | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/6 | 875/11433 | 767/1629 | 256/542 | chr6 | 124963311 | ||
| chr6:125057966
|
G | A | 3 | a0003a0007a0008 | 10 | HG00741.hp1 HG02055.hp1 HG02630.hp1 others(7): Show |
missense_variant | MODERATE | c.1141G>A | p.Val381Ile | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/6 | 1249/11433 | 1141/1629 | 381/542 | chr6 | 125057966 | ||
| chr6:125058056
|
A | G | 1 | a0004 | 3 | HG00741.hp2 HG01169.hp2 HG01257.hp2 |
missense_variant | MODERATE | c.1231A>G | p.Ser411Gly | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/6 | 1339/11433 | 1231/1629 | 411/542 | chr6 | 125058056 | ||
| chr6:125076745
|
G | A | 1 | a0006 | 2 | HG02257.hp1 NA18906.hp2 |
missense_variant | MODERATE | c.1370G>A | p.Arg457His | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/6 | 1478/11433 | 1370/1629 | 457/542 | chr6 | 125076745 | ||
| chr6:125081449
|
C | A | 1 | a0010 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.1497C>A | p.Phe499Leu | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 5/6 | 1605/11433 | 1497/1629 | 499/542 | chr6 | 125081449 | ||
| chr6:125082926
|
A | G | 1 | a0009 | 1 | HG02083.hp2 | missense_variant | MODERATE | c.1618A>G | p.Met540Val | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 1726/11433 | 1618/1629 | 540/542 | chr6 | 125082926 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:125057980
|
G | A | 4 | a0001c0003a0001c0008a0001c0012others(1): Show | 20 | HG00639.hp1 HG01243.hp1 HG02280.hp1 others(17): Show |
synonymous_variant | LOW | c.1155G>A | p.Lys385Lys | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/6 | 1263/11433 | 1155/1629 | 385/542 | chr6 | 125057980 | ||
| chr6:125076686
|
C | T | 1 | a0001c0008 | 2 | HG02896.hp2 HG02897.hp1 |
synonymous_variant | LOW | c.1311C>T | p.Asp437Asp | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/6 | 1419/11433 | 1311/1629 | 437/542 | chr6 | 125076686 | ||
| chr6:125081497
|
G | A | 1 | a0001c0012 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.1545G>A | p.Ala515Ala | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 5/6 | 1653/11433 | 1545/1629 | 515/542 | chr6 | 125081497 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:124962484
|
G | C | 71 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(68): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
5_prime_UTR_variant | MODIFIER | c.-61G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/6 | 61 | chr6 | 124962484 | |||||
| chr6:125083165
|
A | G | 2 | a0001c0001t0015a0001c0001t0069 | 5 | NA18942.hp2 NA18943.hp1 NA18946.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*228A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 228 | chr6 | 125083165 | |||||
| chr6:125083257
|
G | A | 2 | a0002c0002t0070a0010c0013t0030 | 2 | HG02970.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*320G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 320 | chr6 | 125083257 | |||||
| chr6:125083275
|
T | G | 1 | a0001c0012t0031 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*338T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 338 | chr6 | 125083275 | |||||
| chr6:125083505
|
T | C | 1 | a0001c0001t0032 | 1 | HG00423.hp2 | 3_prime_UTR_variant | MODIFIER | c.*568T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 568 | chr6 | 125083505 | |||||
| chr6:125083672
|
G | A | 1 | a0001c0001t0033 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*735G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 735 | chr6 | 125083672 | |||||
| chr6:125083918
|
A | G | 2 | a0002c0002t0070a0010c0013t0030 | 2 | HG02970.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*981A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 981 | chr6 | 125083918 | |||||
| chr6:125084060
|
C | A | 12 | a0001c0001t0002a0001c0001t0016a0001c0001t0033others(9): Show | 46 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*1123C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 1123 | chr6 | 125084060 | |||||
| chr6:125084085
|
A | G | 1 | a0001c0001t0022 | 3 | HG02647.hp2 HG02886.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1148A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 1148 | chr6 | 125084085 | |||||
| chr6:125084100
|
C | G | 1 | a0002c0002t0070 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1163C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 1163 | chr6 | 125084100 | |||||
| chr6:125084325
|
A | G | 7 | a0001c0001t0008a0001c0001t0021a0001c0001t0026others(4): Show | 15 | HG01243.hp1 HG02055.hp2 HG02280.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1388A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 1388 | chr6 | 125084325 | |||||
| chr6:125084850
|
T | C | 1 | a0001c0001t0041 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1913T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 1913 | chr6 | 125084850 | |||||
| chr6:125085101
|
G | A | 7 | a0001c0001t0008a0001c0001t0021a0001c0001t0026others(4): Show | 15 | HG01243.hp1 HG02055.hp2 HG02280.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2164G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 2164 | chr6 | 125085101 | |||||
| chr6:125085288
|
A | G | 1 | a0001c0001t0068 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2351A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 2351 | chr6 | 125085288 | |||||
| chr6:125085364
|
A | G | 1 | a0001c0001t0067 | 1 | HG03492.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2427A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 2427 | chr6 | 125085364 | |||||
| chr6:125085453
|
T | C | 1 | a0001c0001t0042 | 1 | NA19076.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2516T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 2516 | chr6 | 125085453 | |||||
| chr6:125085845
|
T | C | 3 | a0001c0001t0023a0001c0001t0068a0001c0003t0023 | 3 | HG02451.hp2 HG03098.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2908T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 2908 | chr6 | 125085845 | |||||
| chr6:125085861
|
ACT | A | 1 | a0001c0001t0022 | 3 | HG02647.hp2 HG02886.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2927_*2928delCT | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 2927 | INFO_REALIGN_3_PRIME | chr6 | 125085861 | ||||
| chr6:125085938
|
A | G | 4 | a0001c0001t0021a0001c0001t0026a0005c0007t0021others(1): Show | 6 | HG02809.hp1 HG02895.hp1 HG02897.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3001A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 3001 | chr6 | 125085938 | |||||
| chr6:125086091
|
C | T | 3 | a0001c0001t0008a0001c0003t0008a0002c0006t0078 | 9 | HG01243.hp1 HG02055.hp2 HG02280.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3154C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 3154 | chr6 | 125086091 | |||||
| chr6:125086097
|
G | A | 9 | a0001c0001t0023a0001c0001t0043a0001c0001t0045others(6): Show | 15 | HG00741.hp1 HG02055.hp1 HG02451.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3160G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 3160 | chr6 | 125086097 | |||||
| chr6:125086319
|
A | G | 20 | a0001c0001t0002a0001c0001t0016a0001c0001t0025others(17): Show | 59 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*3382A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 3382 | chr6 | 125086319 | |||||
| chr6:125086334
|
TGAG | T | 5 | a0001c0001t0003a0001c0001t0041a0001c0001t0046others(2): Show | 16 | HG00642.hp1 HG00735.hp2 HG02083.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*3401_*3403delGAG | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 3401 | INFO_REALIGN_3_PRIME | chr6 | 125086334 | ||||
| chr6:125086368
|
G | A | 3 | a0001c0001t0023a0001c0001t0068a0001c0003t0023 | 3 | HG02451.hp2 HG03098.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3431G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 3431 | chr6 | 125086368 | |||||
| chr6:125086399
|
CTT | C | 4 | a0001c0001t0043a0003c0004t0011a0003c0004t0044others(1): Show | 10 | HG00741.hp1 HG02055.hp1 HG02486.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3463_*3464delTT | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 3463 | chr6 | 125086399 | |||||
| chr6:125086510
|
T | C | 1 | a0002c0002t0072 | 1 | HG01069.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3573T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 3573 | chr6 | 125086510 | |||||
| chr6:125086521
|
A | C | 1 | a0001c0003t0064 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3584A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 3584 | chr6 | 125086521 | |||||
| chr6:125086671
|
G | A | 1 | a0001c0001t0012 | 5 | HG00140.hp1 HG01192.hp2 HG01981.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3734G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 3734 | chr6 | 125086671 | |||||
| chr6:125086779
|
C | A | 4 | a0001c0001t0006a0001c0001t0048a0001c0001t0049others(1): Show | 11 | HG01884.hp1 HG02109.hp2 HG02258.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3842C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 3842 | chr6 | 125086779 | |||||
| chr6:125086960
|
A | C | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4023A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4023 | chr6 | 125086960 | |||||
| chr6:125086961
|
C | G | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4024C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4024 | chr6 | 125086961 | |||||
| chr6:125086962
|
C | A | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4025C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4025 | chr6 | 125086962 | |||||
| chr6:125086963
|
A | T | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4026A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4026 | chr6 | 125086963 | |||||
| chr6:125086964
|
C | T | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4027C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4027 | chr6 | 125086964 | |||||
| chr6:125086966
|
G | A | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4029G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4029 | chr6 | 125086966 | |||||
| chr6:125086971
|
C | T | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4034C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4034 | chr6 | 125086971 | |||||
| chr6:125086974
|
T | C | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4037T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4037 | chr6 | 125086974 | |||||
| chr6:125086975
|
T | A | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4038T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4038 | chr6 | 125086975 | |||||
| chr6:125086977
|
C | A | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4040C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4040 | chr6 | 125086977 | |||||
| chr6:125086979
|
G | A | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4042G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4042 | chr6 | 125086979 | |||||
| chr6:125086982
|
C | A | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4045C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4045 | chr6 | 125086982 | |||||
| chr6:125086985
|
G | A | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4048G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4048 | chr6 | 125086985 | |||||
| chr6:125086987
|
T | C | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4050T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4050 | chr6 | 125086987 | |||||
| chr6:125086989
|
C | T | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4052C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4052 | chr6 | 125086989 | |||||
| chr6:125086990
|
C | A | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4053C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4053 | chr6 | 125086990 | |||||
| chr6:125086992
|
C | A | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4055C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4055 | chr6 | 125086992 | |||||
| chr6:125086994
|
C | A | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4057C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4057 | chr6 | 125086994 | |||||
| chr6:125086995
|
T | A | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4058T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4058 | chr6 | 125086995 | |||||
| chr6:125086998
|
A | T | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4061A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4061 | chr6 | 125086998 | |||||
| chr6:125087000
|
C | A | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4063C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4063 | chr6 | 125087000 | |||||
| chr6:125087001
|
C | T | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4064C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4064 | chr6 | 125087001 | |||||
| chr6:125087002
|
T | G | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4065T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4065 | chr6 | 125087002 | |||||
| chr6:125087003
|
C | T | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4066C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4066 | chr6 | 125087003 | |||||
| chr6:125087012
|
C | G | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4075C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4075 | chr6 | 125087012 | |||||
| chr6:125087013
|
C | A | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4076C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4076 | chr6 | 125087013 | |||||
| chr6:125087016
|
A | T | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4079A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4079 | chr6 | 125087016 | |||||
| chr6:125087017
|
C | G | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4080C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4080 | chr6 | 125087017 | |||||
| chr6:125087020
|
C | G | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4083C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4083 | chr6 | 125087020 | |||||
| chr6:125087024
|
T | A | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4087T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4087 | chr6 | 125087024 | |||||
| chr6:125087025
|
A | T | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4088A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4088 | chr6 | 125087025 | |||||
| chr6:125087028
|
C | A | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4091C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4091 | chr6 | 125087028 | |||||
| chr6:125087032
|
C | A | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4095C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4095 | chr6 | 125087032 | |||||
| chr6:125087035
|
T | C | 1 | a0001c0001t0022 | 3 | HG02647.hp2 HG02886.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4098T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4098 | chr6 | 125087035 | |||||
| chr6:125087040
|
C | T | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4103C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4103 | chr6 | 125087040 | |||||
| chr6:125087045
|
CTGAAGGA others(16): Show |
C | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4109_*4131delTGAA others(19): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4109 | chr6 | 125087045 | |||||
| chr6:125087070
|
G | A | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4133G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4133 | chr6 | 125087070 | |||||
| chr6:125087071
|
G | T | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4134G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4134 | chr6 | 125087071 | |||||
| chr6:125087075
|
C | A | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4138C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4138 | chr6 | 125087075 | |||||
| chr6:125087075
|
C | G | 5 | a0001c0001t0003a0001c0001t0041a0001c0001t0046others(2): Show | 16 | HG00642.hp1 HG00735.hp2 HG02083.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*4138C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4138 | chr6 | 125087075 | |||||
| chr6:125087079
|
A | T | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4142A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4142 | chr6 | 125087079 | |||||
| chr6:125087082
|
C | G | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4145C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4145 | chr6 | 125087082 | |||||
| chr6:125087084
|
C | T | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4147C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4147 | chr6 | 125087084 | |||||
| chr6:125087085
|
A | C | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4148A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4148 | chr6 | 125087085 | |||||
| chr6:125087098
|
G | A | 1 | a0002c0002t0070 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4161G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4161 | chr6 | 125087098 | |||||
| chr6:125087117
|
C | G | 5 | a0001c0001t0003a0001c0001t0041a0001c0001t0046others(2): Show | 16 | HG00642.hp1 HG00735.hp2 HG02083.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*4180C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4180 | chr6 | 125087117 | |||||
| chr6:125087292
|
G | T | 6 | a0001c0001t0043a0001c0001t0045a0002c0002t0071others(3): Show | 12 | HG00741.hp1 HG02055.hp1 HG02486.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*4355G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4355 | chr6 | 125087292 | |||||
| chr6:125087304
|
AC | A | 1 | a0001c0001t0016 | 3 | HG02602.hp2 HG03704.hp1 HG03704.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4368delC | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4368 | chr6 | 125087304 | |||||
| chr6:125087306
|
G | A | 4 | a0001c0001t0017a0001c0001t0050a0001c0001t0051others(1): Show | 6 | HG01884.hp2 HG02258.hp2 HG02809.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4369G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4369 | chr6 | 125087306 | |||||
| chr6:125087347
|
T | G | 1 | a0001c0001t0052 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4410T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4410 | chr6 | 125087347 | |||||
| chr6:125087421
|
G | A | 66 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(63): Show | 164 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(161): Show |
3_prime_UTR_variant | MODIFIER | c.*4484G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4484 | chr6 | 125087421 | |||||
| chr6:125087572
|
A | G | 9 | a0001c0001t0023a0001c0001t0043a0001c0001t0045others(6): Show | 15 | HG00741.hp1 HG02055.hp1 HG02451.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*4635A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4635 | chr6 | 125087572 | |||||
| chr6:125087885
|
C | G | 34 | a0001c0001t0003a0001c0001t0006a0001c0001t0008others(31): Show | 73 | HG00642.hp1 HG00735.hp2 HG00741.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*4948C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4948 | chr6 | 125087885 | |||||
| chr6:125087899
|
T | G | 3 | a0001c0001t0022a0002c0002t0070a0010c0013t0030 | 5 | HG02647.hp2 HG02886.hp2 HG02970.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4962T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4962 | chr6 | 125087899 | |||||
| chr6:125087925
|
C | G | 1 | a0001c0001t0047 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4988C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4988 | chr6 | 125087925 | |||||
| chr6:125087987
|
CT | C | 9 | a0001c0001t0023a0001c0001t0043a0001c0001t0045others(6): Show | 15 | HG00741.hp1 HG02055.hp1 HG02451.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*5051delT | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 5051 | chr6 | 125087987 | |||||
| chr6:125088014
|
C | CT | 6 | a0001c0001t0025a0001c0001t0039a0001c0001t0040others(3): Show | 9 | HG00140.hp2 HG00741.hp2 HG01069.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5099dupT | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 5100 | INFO_REALIGN_3_PRIME | chr6 | 125088014 | ||||
| chr6:125088014
|
CT | C | 33 | a0001c0001t0003a0001c0001t0004a0001c0001t0008others(30): Show | 86 | HG00140.hp1 HG00642.hp1 HG00735.hp2 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*5099delT | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 5099 | INFO_REALIGN_3_PRIME | chr6 | 125088014 | ||||
| chr6:125088038
|
A | G | 11 | a0001c0001t0002a0001c0001t0016a0001c0001t0025others(8): Show | 48 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*5101A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 5101 | chr6 | 125088038 | |||||
| chr6:125088053
|
C | T | 1 | a0001c0001t0054 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5116C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 5116 | chr6 | 125088053 | |||||
| chr6:125088070
|
G | T | 4 | a0001c0001t0043a0003c0004t0011a0003c0004t0044others(1): Show | 10 | HG00741.hp1 HG02055.hp1 HG02486.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*5133G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 5133 | chr6 | 125088070 | |||||
| chr6:125088301
|
G | C | 1 | a0001c0001t0055 | 1 | HG01952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5364G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 5364 | chr6 | 125088301 | |||||
| chr6:125088358
|
C | T | 2 | a0001c0001t0019a0002c0002t0076 | 4 | HG02056.hp1 HG02071.hp2 NA18971.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5421C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 5421 | chr6 | 125088358 | |||||
| chr6:125088504
|
C | T | 2 | a0001c0001t0015a0001c0001t0069 | 5 | NA18942.hp2 NA18943.hp1 NA18946.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5567C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 5567 | chr6 | 125088504 | |||||
| chr6:125088611
|
A | G | 1 | a0001c0001t0038 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5674A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 5674 | chr6 | 125088611 | |||||
| chr6:125088818
|
T | G | 1 | a0001c0001t0035 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5881T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 5881 | chr6 | 125088818 | |||||
| chr6:125088914
|
A | G | 1 | a0004c0005t0020 | 3 | HG00741.hp2 HG01169.hp2 HG01257.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5977A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 5977 | chr6 | 125088914 | |||||
| chr6:125089513
|
T | C | 1 | a0001c0001t0056 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6576T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 6576 | chr6 | 125089513 | |||||
| chr6:125089531
|
A | G | 1 | a0001c0001t0061 | 1 | NA18983.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6594A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 6594 | chr6 | 125089531 | |||||
| chr6:125089609
|
C | T | 5 | a0001c0001t0003a0001c0001t0041a0001c0001t0046others(2): Show | 16 | HG00642.hp1 HG00735.hp2 HG02083.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*6672C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 6672 | chr6 | 125089609 | |||||
| chr6:125089661
|
A | G | 4 | a0001c0001t0021a0001c0001t0026a0005c0007t0021others(1): Show | 6 | HG02809.hp1 HG02895.hp1 HG02897.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6724A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 6724 | chr6 | 125089661 | |||||
| chr6:125089698
|
G | T | 1 | a0001c0012t0031 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6761G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 6761 | chr6 | 125089698 | |||||
| chr6:125089888
|
C | A | 1 | a0001c0012t0031 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6951C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 6951 | chr6 | 125089888 | |||||
| chr6:125090334
|
T | C | 1 | a0001c0001t0039 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7397T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 7397 | chr6 | 125090334 | |||||
| chr6:125090375
|
A | C | 1 | a0001c0001t0060 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7438A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 7438 | chr6 | 125090375 | |||||
| chr6:125090484
|
T | C | 1 | a0001c0001t0057 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7547T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 7547 | chr6 | 125090484 | |||||
| chr6:125090503
|
C | T | 66 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(63): Show | 164 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(161): Show |
3_prime_UTR_variant | MODIFIER | c.*7566C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 7566 | chr6 | 125090503 | |||||
| chr6:125090613
|
T | C | 1 | a0010c0013t0030 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7676T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 7676 | chr6 | 125090613 | |||||
| chr6:125090630
|
T | C | 1 | a0001c0001t0043 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7693T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 7693 | chr6 | 125090630 | |||||
| chr6:125090702
|
G | A | 1 | a0001c0001t0050 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7765G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 7765 | chr6 | 125090702 | |||||
| chr6:125090764
|
A | G | 2 | a0001c0001t0014a0002c0002t0029 | 6 | HG00609.hp1 NA18989.hp2 NA19010.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*7827A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 7827 | chr6 | 125090764 | |||||
| chr6:125090773
|
G | T | 66 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(63): Show | 164 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(161): Show |
3_prime_UTR_variant | MODIFIER | c.*7836G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 7836 | chr6 | 125090773 | |||||
| chr6:125090873
|
A | T | 12 | a0001c0001t0002a0001c0001t0016a0001c0001t0033others(9): Show | 46 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*7936A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 7936 | chr6 | 125090873 | |||||
| chr6:125090900
|
A | G | 4 | a0001c0001t0006a0001c0001t0048a0001c0001t0049others(1): Show | 11 | HG01884.hp1 HG02109.hp2 HG02258.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*7963A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 7963 | chr6 | 125090900 | |||||
| chr6:125091071
|
A | G | 1 | a0001c0001t0059 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8134A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 8134 | chr6 | 125091071 | |||||
| chr6:125091073
|
A | G | 5 | a0001c0001t0003a0001c0001t0041a0001c0001t0046others(2): Show | 16 | HG00642.hp1 HG00735.hp2 HG02083.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*8136A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 8136 | chr6 | 125091073 | |||||
| chr6:125091085
|
A | C | 5 | a0001c0001t0003a0001c0001t0041a0001c0001t0046others(2): Show | 16 | HG00642.hp1 HG00735.hp2 HG02083.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*8148A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 8148 | chr6 | 125091085 | |||||
| chr6:125091204
|
G | A | 6 | a0001c0001t0043a0001c0001t0045a0002c0002t0071others(3): Show | 12 | HG00741.hp1 HG02055.hp1 HG02486.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*8267G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 8267 | chr6 | 125091204 | |||||
| chr6:125091564
|
A | G | 2 | a0001c0001t0005a0001c0001t0032 | 12 | HG00408.hp2 HG00423.hp2 HG01433.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*8627A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 8627 | chr6 | 125091564 | |||||
| chr6:125091645
|
TCA | T | 12 | a0001c0001t0004a0001c0001t0012a0001c0001t0015others(9): Show | 32 | HG00140.hp1 HG00738.hp2 HG01106.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*8709_*8710delCA | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 8709 | chr6 | 125091645 | |||||
| chr6:125091721
|
C | T | 1 | a0001c0001t0058 | 1 | NA18994.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8784C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 8784 | chr6 | 125091721 | |||||
| chr6:125092107
|
A | G | 12 | a0001c0001t0006a0001c0001t0023a0001c0001t0043others(9): Show | 25 | HG00741.hp1 HG01884.hp1 HG02055.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*9170A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 9170 | chr6 | 125092107 | |||||
| chr6:125092517
|
G | T | 4 | a0001c0001t0043a0002c0002t0071a0003c0004t0011others(1): Show | 10 | HG00741.hp1 HG02055.hp1 HG02486.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*9580G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 9580 | chr6 | 125092517 | |||||
| chr6:125092577
|
C | T | 1 | a0001c0001t0036 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9640C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 9640 | chr6 | 125092577 | |||||
| chr6:125092591
|
A | G | 1 | a0002c0002t0077 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9654A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 9654 | chr6 | 125092591 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:124963785
|
G | A | 2 | a0001c0001t0006g0003a0001c0001t0043g0004 | 2 | HG02486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.882+359G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124963785 | ||||||
| chr6:124963829
|
A | G | 8 | a0001c0001t0001g0263a0001c0001t0006g0264a0001c0001t0040g0261others(5): Show | 8 | HG01192.hp1 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.882+403A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124963829 | ||||||
| chr6:124963893
|
A | C | 1 | a0003c0004t0011g0258 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.882+467A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124963893 | ||||||
| chr6:124963977
|
C | T | 230 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(227): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.882+551C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124963977 | ||||||
| chr6:124964314
|
T | C | 2 | a0001c0001t0006g0003a0001c0001t0043g0004 | 2 | HG02486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.882+888T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124964314 | ||||||
| chr6:124964441
|
T | TA | 58 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(55): Show | 58 | HG00408.hp2 HG00423.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.882+1016dupA | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 124964441 | |||||
| chr6:124964475
|
C | T | 4 | a0001c0001t0003g0255a0001c0001t0017g0254a0001c0003t0008g0257others(1): Show | 4 | HG02258.hp2 HG02559.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+1049C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124964475 | ||||||
| chr6:124964612
|
A | G | 1 | a0001c0001t0061g0253 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.882+1186A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124964612 | ||||||
| chr6:124964658
|
G | T | 1 | a0001c0001t0015g0252 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.882+1232G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124964658 | ||||||
| chr6:124964738
|
A | T | 1 | a0002c0002t0075g0040 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.882+1312A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124964738 | ||||||
| chr6:124964841
|
C | T | 2 | a0001c0001t0002g0098a0001c0001t0014g0097 | 2 | NA18952.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.882+1415C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124964841 | ||||||
| chr6:124965105
|
A | G | 2 | a0001c0001t0006g0251a0001c0001t0023g0250 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.882+1679A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124965105 | ||||||
| chr6:124965114
|
A | C | 1 | a0001c0001t0004g0096 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.882+1688A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124965114 | ||||||
| chr6:124965249
|
A | G | 1 | a0001c0001t0002g0249 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.882+1823A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124965249 | ||||||
| chr6:124965447
|
C | T | 1 | a0008c0015t0053g0248 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.882+2021C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124965447 | ||||||
| chr6:124965866
|
A | G | 1 | a0001c0001t0001g0247 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.882+2440A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124965866 | ||||||
| chr6:124965933
|
C | T | 1 | a0001c0003t0008g0257 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.882+2507C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124965933 | ||||||
| chr6:124965937
|
G | A | 3 | a0001c0001t0017g0101a0001c0001t0041g0099a0003c0004t0044g0100 | 3 | HG02965.hp2 HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.882+2511G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124965937 | ||||||
| chr6:124965963
|
A | G | 2 | a0005c0007t0006g0094a0005c0007t0021g0095 | 2 | HG01884.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.882+2537A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124965963 | ||||||
| chr6:124966194
|
G | T | 54 | a0001c0001t0001g0200a0001c0001t0001g0209a0001c0001t0001g0210others(51): Show | 55 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.882+2768G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124966194 | ||||||
| chr6:124966249
|
T | A | 3 | a0001c0001t0017g0101a0001c0001t0041g0099a0003c0004t0044g0100 | 3 | HG02965.hp2 HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.882+2823T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124966249 | ||||||
| chr6:124966313
|
A | C | 1 | a0001c0001t0057g0246 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.882+2887A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124966313 | ||||||
| chr6:124966314
|
T | A | 1 | a0001c0001t0057g0246 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.882+2888T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124966314 | ||||||
| chr6:124966357
|
A | G | 1 | a0001c0001t0062g0197 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.882+2931A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124966357 | ||||||
| chr6:124966415
|
G | A | 81 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(78): Show | 81 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.882+2989G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124966415 | ||||||
| chr6:124966629
|
A | G | 2 | a0005c0007t0006g0094a0005c0007t0021g0095 | 2 | HG01884.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.882+3203A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124966629 | ||||||
| chr6:124966750
|
A | G | 1 | a0001c0001t0001g0093 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.882+3324A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124966750 | ||||||
| chr6:124966876
|
A | G | 1 | a0001c0003t0065g0167 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.882+3450A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124966876 | ||||||
| chr6:124967020
|
C | T | 2 | a0005c0007t0006g0094a0005c0007t0021g0095 | 2 | HG01884.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.882+3594C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124967020 | ||||||
| chr6:124967116
|
A | G | 1 | a0001c0001t0068g0245 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.882+3690A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124967116 | ||||||
| chr6:124967362
|
C | T | 3 | a0001c0001t0002g0164a0001c0001t0025g0165a0001c0001t0066g0166 | 3 | HG01069.hp2 HG01255.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.882+3936C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124967362 | ||||||
| chr6:124967802
|
G | T | 1 | a0002c0002t0070g0039 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.882+4376G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124967802 | ||||||
| chr6:124967843
|
A | G | 12 | a0001c0001t0006g0191a0001c0001t0010g0195a0001c0001t0046g0196others(9): Show | 13 | HG01243.hp1 HG02257.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.882+4417A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124967843 | ||||||
| chr6:124967858
|
A | G | 54 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(51): Show | 54 | HG00408.hp2 HG00423.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.882+4432A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124967858 | ||||||
| chr6:124967903
|
T | C | 2 | a0005c0007t0006g0094a0005c0007t0021g0095 | 2 | HG01884.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.882+4477T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124967903 | ||||||
| chr6:124967996
|
T | C | 2 | a0005c0007t0006g0094a0005c0007t0021g0095 | 2 | HG01884.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.882+4570T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124967996 | ||||||
| chr6:124968032
|
G | A | 1 | a0002c0002t0029g0005 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.882+4606G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124968032 | ||||||
| chr6:124968073
|
T | C | 143 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(140): Show | 145 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.882+4647T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124968073 | ||||||
| chr6:124968463
|
C | T | 2 | a0005c0007t0006g0094a0005c0007t0021g0095 | 2 | HG01884.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.882+5037C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124968463 | ||||||
| chr6:124968733
|
G | A | 35 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(32): Show | 35 | HG00140.hp1 HG00609.hp2 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.882+5307G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124968733 | ||||||
| chr6:124968738
|
T | G | 2 | a0005c0007t0006g0094a0005c0007t0021g0095 | 2 | HG01884.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.882+5312T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124968738 | ||||||
| chr6:124969016
|
A | G | 1 | a0001c0001t0005g0130 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.882+5590A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124969016 | ||||||
| chr6:124969049
|
T | A | 1 | a0001c0001t0001g0043 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.882+5623T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124969049 | ||||||
| chr6:124969363
|
A | G | 2 | a0005c0007t0006g0094a0005c0007t0021g0095 | 2 | HG01884.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.882+5937A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124969363 | ||||||
| chr6:124969382
|
T | C | 1 | a0001c0001t0001g0093 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.882+5956T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124969382 | ||||||
| chr6:124969506
|
C | T | 1 | a0001c0001t0004g0183 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.882+6080C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124969506 | ||||||
| chr6:124969572
|
G | A | 227 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(224): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.882+6146G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124969572 | ||||||
| chr6:124969612
|
G | A | 4 | a0001c0001t0001g0044a0001c0001t0001g0047a0001c0001t0004g0046others(1): Show | 4 | HG02523.hp1 NA18999.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+6186G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124969612 | ||||||
| chr6:124969660
|
T | C | 3 | a0005c0007t0006g0094a0005c0007t0021g0095a0008c0015t0053g0248 | 3 | HG01884.hp1 HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.882+6234T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124969660 | ||||||
| chr6:124969663
|
A | T | 4 | a0001c0001t0008g0182a0001c0001t0022g0180a0001c0001t0039g0179others(1): Show | 4 | HG02055.hp2 HG02109.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+6237A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124969663 | ||||||
| chr6:124969766
|
T | C | 1 | a0001c0001t0026g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.882+6340T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124969766 | ||||||
| chr6:124969871
|
GGGGTTGT others(22): Show |
G | 1 | a0001c0001t0026g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.882+6449_882+6477d others(31): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 124969871 | |||||
| chr6:124969990
|
A | G | 3 | a0005c0007t0006g0094a0005c0007t0021g0095a0008c0015t0053g0248 | 3 | HG01884.hp1 HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.882+6564A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124969990 | ||||||
| chr6:124970339
|
C | T | 1 | a0001c0001t0048g0162 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.882+6913C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124970339 | ||||||
| chr6:124970398
|
A | G | 2 | a0005c0007t0006g0094a0005c0007t0021g0095 | 2 | HG01884.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.882+6972A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124970398 | ||||||
| chr6:124970404
|
G | A | 1 | a0001c0003t0008g0131 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.882+6978G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124970404 | ||||||
| chr6:124970551
|
C | T | 1 | a0002c0002t0070g0039 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.882+7125C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124970551 | ||||||
| chr6:124970741
|
A | G | 1 | a0001c0001t0045g0161 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.882+7315A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124970741 | ||||||
| chr6:124970766
|
C | T | 1 | a0002c0002t0071g0038 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.882+7340C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124970766 | ||||||
| chr6:124970779
|
A | C | 2 | a0001c0001t0021g0159a0001c0001t0026g0160 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.882+7353A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124970779 | ||||||
| chr6:124970867
|
G | T | 1 | a0001c0001t0002g0129 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.882+7441G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124970867 | ||||||
| chr6:124971327
|
G | A | 1 | a0002c0002t0072g0006 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.882+7901G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124971327 | ||||||
| chr6:124971558
|
C | A | 3 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0052g0049 | 3 | HG02132.hp2 NA18747.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.882+8132C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124971558 | ||||||
| chr6:124971563
|
C | A | 1 | a0008c0015t0053g0248 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.882+8137C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124971563 | ||||||
| chr6:124971663
|
C | T | 2 | a0001c0001t0001g0244a0001c0001t0004g0243 | 2 | HG03834.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.882+8237C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124971663 | ||||||
| chr6:124971714
|
G | T | 2 | a0001c0001t0005g0092a0001c0001t0063g0091 | 2 | HG00408.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.882+8288G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124971714 | ||||||
| chr6:124971766
|
A | T | 3 | a0004c0005t0020g0088a0004c0005t0020g0089a0004c0005t0020g0090 | 3 | HG00741.hp2 HG01169.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.882+8340A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124971766 | ||||||
| chr6:124971930
|
C | A | 1 | a0002c0006t0078g0007 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.882+8504C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124971930 | ||||||
| chr6:124972012
|
C | T | 56 | a0001c0001t0001g0102a0001c0001t0001g0128a0001c0001t0001g0200others(53): Show | 57 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.882+8586C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124972012 | ||||||
| chr6:124972312
|
C | T | 2 | a0005c0007t0006g0094a0005c0007t0021g0095 | 2 | HG01884.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.882+8886C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124972312 | ||||||
| chr6:124972515
|
G | A | 1 | a0002c0006t0078g0007 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.882+9089G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124972515 | ||||||
| chr6:124972588
|
C | T | 1 | a0001c0001t0002g0087 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.882+9162C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124972588 | ||||||
| chr6:124972589
|
C | T | 1 | a0009c0014t0001g0127 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.882+9163C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124972589 | ||||||
| chr6:124972705
|
C | T | 2 | a0001c0001t0002g0098a0001c0001t0014g0097 | 2 | NA18952.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.882+9279C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124972705 | ||||||
| chr6:124972922
|
A | G | 2 | a0005c0007t0006g0094a0005c0007t0021g0095 | 2 | HG01884.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.882+9496A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124972922 | ||||||
| chr6:124973094
|
G | T | 1 | a0001c0001t0026g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.882+9668G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124973094 | ||||||
| chr6:124973129
|
G | A | 4 | a0002c0002t0075g0040a0005c0007t0006g0094a0005c0007t0021g0095others(1): Show | 4 | HG01884.hp1 HG02809.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+9703G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124973129 | ||||||
| chr6:124973234
|
A | G | 2 | a0002c0002t0075g0040a0008c0015t0053g0248 | 2 | HG02922.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.882+9808A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124973234 | ||||||
| chr6:124973487
|
A | C | 1 | a0002c0002t0074g0037 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.882+10061A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124973487 | ||||||
| chr6:124973539
|
C | T | 1 | a0001c0001t0004g0242 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.882+10113C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124973539 | ||||||
| chr6:124973563
|
TTATAA | T | 4 | a0002c0002t0075g0040a0005c0007t0006g0094a0005c0007t0021g0095others(1): Show | 4 | HG01884.hp1 HG02809.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+10141_882+1014 others(9): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 124973563 | |||||
| chr6:124973665
|
A | G | 1 | a0002c0002t0075g0040 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.882+10239A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124973665 | ||||||
| chr6:124973669
|
A | G | 1 | a0001c0001t0002g0086 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.882+10243A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124973669 | ||||||
| chr6:124973901
|
C | T | 1 | a0001c0001t0046g0196 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.882+10475C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124973901 | ||||||
| chr6:124973962
|
C | T | 1 | a0002c0002t0071g0038 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.882+10536C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124973962 | ||||||
| chr6:124973985
|
T | G | 1 | a0001c0001t0062g0197 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.882+10559T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124973985 | ||||||
| chr6:124974091
|
G | A | 2 | a0001c0001t0002g0164a0001c0001t0025g0165 | 2 | HG01069.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.882+10665G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124974091 | ||||||
| chr6:124974312
|
A | T | 1 | a0002c0002t0071g0038 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.882+10886A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124974312 | ||||||
| chr6:124974388
|
T | G | 1 | a0001c0001t0003g0198 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.882+10962T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124974388 | ||||||
| chr6:124974626
|
G | A | 1 | a0002c0002t0075g0040 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.882+11200G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124974626 | ||||||
| chr6:124974754
|
A | C | 1 | a0001c0001t0003g0178 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.882+11328A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124974754 | ||||||
| chr6:124974880
|
T | C | 2 | a0001c0001t0003g0255a0001c0001t0017g0254 | 2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.882+11454T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124974880 | ||||||
| chr6:124974894
|
G | A | 1 | a0001c0001t0039g0179 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.882+11468G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124974894 | ||||||
| chr6:124975012
|
C | T | 1 | a0001c0001t0026g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.882+11586C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124975012 | ||||||
| chr6:124975107
|
A | G | 2 | a0001c0001t0006g0003a0001c0001t0043g0004 | 2 | HG02486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.882+11681A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124975107 | ||||||
| chr6:124975892
|
T | C | 1 | a0001c0001t0001g0051 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.882+12466T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124975892 | ||||||
| chr6:124975953
|
TC | T | 12 | a0001c0001t0006g0191a0001c0001t0010g0195a0001c0001t0046g0196others(9): Show | 13 | HG01243.hp1 HG02257.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.882+12528delC | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124975953 | ||||||
| chr6:124976036
|
T | C | 1 | a0008c0015t0053g0248 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.882+12610T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124976036 | ||||||
| chr6:124976190
|
C | G | 1 | a0001c0001t0010g0163 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.882+12764C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124976190 | ||||||
| chr6:124976231
|
G | A | 1 | a0001c0001t0010g0163 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.882+12805G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124976231 | ||||||
| chr6:124976250
|
A | C | 1 | a0002c0006t0078g0007 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.882+12824A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124976250 | ||||||
| chr6:124976250
|
ACTCC | A | 5 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(2): Show | 5 | HG00423.hp1 HG01243.hp2 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+12846_882+1284 others(8): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 124976250 | |||||
| chr6:124976275
|
C | T | 61 | a0001c0001t0001g0102a0001c0001t0001g0125a0001c0001t0001g0128others(58): Show | 62 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.882+12849C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124976275 | ||||||
| chr6:124976276
|
G | T | 1 | a0001c0001t0026g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.882+12850G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124976276 | ||||||
| chr6:124976290
|
C | G | 61 | a0001c0001t0001g0102a0001c0001t0001g0125a0001c0001t0001g0128others(58): Show | 62 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.882+12864C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124976290 | ||||||
| chr6:124976302
|
C | CCTTCCTT others(3): Show |
216 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(213): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.882+12878_882+1287 others(14): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 124976302 | |||||
| chr6:124976373
|
A | G | 1 | a0008c0015t0053g0248 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.882+12947A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124976373 | ||||||
| chr6:124976534
|
C | T | 1 | a0001c0001t0043g0004 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.882+13108C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124976534 | ||||||
| chr6:124976609
|
C | G | 1 | a0001c0001t0010g0195 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.882+13183C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124976609 | ||||||
| chr6:124976624
|
C | T | 2 | a0001c0001t0068g0245a0002c0002t0075g0040 | 2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.882+13198C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124976624 | ||||||
| chr6:124976695
|
G | A | 8 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(5): Show | 8 | HG00609.hp2 HG01358.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.882+13269G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124976695 | ||||||
| chr6:124976750
|
C | A | 3 | a0001c0001t0017g0101a0001c0001t0041g0099a0003c0004t0044g0100 | 3 | HG02965.hp2 HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.882+13324C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124976750 | ||||||
| chr6:124976890
|
C | A | 216 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(213): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.882+13464C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124976890 | ||||||
| chr6:124977194
|
C | A | 215 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(212): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.882+13768C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124977194 | ||||||
| chr6:124977225
|
T | C | 1 | a0002c0002t0070g0039 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.882+13799T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124977225 | ||||||
| chr6:124977445
|
TAATG | T | 58 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(55): Show | 58 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.882+14022_882+1402 others(8): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 124977445 | |||||
| chr6:124977611
|
C | T | 2 | a0001c0003t0013g0185a0001c0003t0013g0186 | 2 | HG02559.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.882+14185C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124977611 | ||||||
| chr6:124977813
|
C | A | 3 | a0001c0001t0017g0101a0001c0001t0041g0099a0003c0004t0044g0100 | 3 | HG02965.hp2 HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.882+14387C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124977813 | ||||||
| chr6:124977848
|
T | C | 3 | a0001c0001t0001g0244a0001c0001t0004g0243a0001c0001t0067g0199 | 3 | HG03492.hp1 HG03834.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.882+14422T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124977848 | ||||||
| chr6:124977900
|
A | G | 1 | a0001c0001t0001g0241 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.882+14474A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124977900 | ||||||
| chr6:124978083
|
A | T | 1 | a0001c0001t0026g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.882+14657A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124978083 | ||||||
| chr6:124978100
|
C | T | 1 | a0002c0002t0075g0040 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.882+14674C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124978100 | ||||||
| chr6:124978227
|
T | A | 37 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(34): Show | 37 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.882+14801T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124978227 | ||||||
| chr6:124978229
|
C | T | 17 | a0001c0001t0003g0169a0001c0001t0003g0172a0001c0001t0003g0176others(14): Show | 17 | HG02055.hp2 HG02109.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.882+14803C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124978229 | ||||||
| chr6:124978313
|
G | C | 60 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(57): Show | 60 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.882+14887G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124978313 | ||||||
| chr6:124978314
|
C | A | 8 | a0001c0001t0001g0052a0001c0001t0001g0057a0001c0001t0002g0055others(5): Show | 8 | HG01261.hp1 HG02132.hp1 NA18942.hp1 others(5): Show |
intron_variant | MODIFIER | c.882+14888C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124978314 | ||||||
| chr6:124978367
|
G | A | 1 | a0001c0001t0017g0154 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.882+14941G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124978367 | ||||||
| chr6:124978408
|
C | T | 1 | a0002c0002t0075g0040 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.882+14982C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124978408 | ||||||
| chr6:124978512
|
C | G | 1 | a0001c0001t0010g0153 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.882+15086C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124978512 | ||||||
| chr6:124978618
|
A | G | 5 | a0001c0001t0001g0120a0001c0001t0002g0121a0001c0001t0002g0122others(2): Show | 5 | NA18964.hp2 NA18968.hp2 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.882+15192A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124978618 | ||||||
| chr6:124978749
|
C | G | 1 | a0001c0001t0001g0084 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.882+15323C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124978749 | ||||||
| chr6:124978882
|
G | C | 1 | a0008c0015t0053g0248 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.882+15456G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124978882 | ||||||
| chr6:124978967
|
G | A | 3 | a0001c0001t0021g0133a0001c0001t0022g0132a0001c0001t0033g0134 | 3 | HG02886.hp2 HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.882+15541G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124978967 | ||||||
| chr6:124979111
|
G | A | 2 | a0001c0001t0006g0003a0001c0001t0043g0004 | 2 | HG02486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.882+15685G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124979111 | ||||||
| chr6:124979133
|
T | C | 62 | a0001c0001t0001g0102a0001c0001t0001g0125a0001c0001t0001g0128others(59): Show | 63 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.882+15707T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124979133 | ||||||
| chr6:124979177
|
C | T | 2 | a0001c0001t0006g0003a0001c0001t0043g0004 | 2 | HG02486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.882+15751C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124979177 | ||||||
| chr6:124979705
|
A | T | 2 | a0001c0003t0010g0266a0006c0009t0001g0265 | 2 | HG02922.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.882+16279A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124979705 | ||||||
| chr6:124979740
|
C | G | 1 | a0001c0001t0006g0177 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.882+16314C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124979740 | ||||||
| chr6:124979928
|
C | T | 3 | a0001c0001t0021g0133a0001c0001t0022g0132a0001c0001t0033g0134 | 3 | HG02886.hp2 HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.882+16502C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124979928 | ||||||
| chr6:124979981
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.882+16555G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124979981 | ||||||
| chr6:124980029
|
G | C | 58 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(55): Show | 58 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.882+16603G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124980029 | ||||||
| chr6:124980074
|
T | C | 2 | a0005c0007t0006g0094a0005c0007t0021g0095 | 2 | HG01884.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.882+16648T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124980074 | ||||||
| chr6:124980516
|
G | T | 2 | a0001c0001t0001g0263a0001c0001t0006g0264 | 2 | HG01192.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.882+17090G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124980516 | ||||||
| chr6:124980575
|
C | T | 1 | a0003c0004t0011g0258 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.882+17149C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124980575 | ||||||
| chr6:124980655
|
A | C | 1 | a0001c0001t0010g0153 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.882+17229A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124980655 | ||||||
| chr6:124980694
|
TTAGAG | T | 38 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(35): Show | 38 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.882+17275_882+1727 others(9): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 124980694 | |||||
| chr6:124980751
|
G | A | 1 | a0011c0011t0079g0036 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.882+17325G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124980751 | ||||||
| chr6:124980986
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.882+17560C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124980986 | ||||||
| chr6:124981091
|
T | A | 3 | a0001c0001t0001g0102a0001c0001t0001g0200a0001c0001t0012g0201 | 3 | HG01928.hp1 HG03239.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.882+17665T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124981091 | ||||||
| chr6:124981135
|
A | C | 12 | a0001c0001t0006g0191a0001c0001t0010g0195a0001c0001t0046g0196others(9): Show | 13 | HG01243.hp1 HG02257.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.882+17709A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124981135 | ||||||
| chr6:124981207
|
T | C | 12 | a0001c0001t0006g0191a0001c0001t0010g0195a0001c0001t0046g0196others(9): Show | 13 | HG01243.hp1 HG02257.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.882+17781T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124981207 | ||||||
| chr6:124981462
|
G | A | 13 | a0001c0001t0006g0003a0001c0001t0006g0191a0001c0001t0010g0195others(10): Show | 14 | HG01243.hp1 HG02280.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.882+18036G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124981462 | ||||||
| chr6:124981468
|
G | A | 1 | a0001c0003t0008g0187 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.882+18042G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124981468 | ||||||
| chr6:124981536
|
G | A | 1 | a0001c0001t0001g0043 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.882+18110G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124981536 | ||||||
| chr6:124981586
|
A | C | 1 | a0002c0002t0075g0040 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.882+18160A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124981586 | ||||||
| chr6:124981689
|
T | C | 77 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(74): Show | 77 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.882+18263T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124981689 | ||||||
| chr6:124981726
|
G | A | 1 | a0002c0002t0075g0040 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.882+18300G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124981726 | ||||||
| chr6:124981884
|
C | T | 1 | a0002c0002t0075g0040 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.882+18458C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124981884 | ||||||
| chr6:124981888
|
C | T | 1 | a0001c0001t0012g0201 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.882+18462C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124981888 | ||||||
| chr6:124981889
|
G | A | 61 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(58): Show | 61 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.882+18463G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124981889 | ||||||
| chr6:124981953
|
G | A | 1 | a0002c0002t0075g0040 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.882+18527G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124981953 | ||||||
| chr6:124981957
|
G | A | 1 | a0001c0001t0005g0202 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.882+18531G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124981957 | ||||||
| chr6:124981977
|
G | A | 1 | a0001c0001t0022g0180 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.882+18551G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124981977 | ||||||
| chr6:124982013
|
C | T | 7 | a0001c0001t0006g0147a0001c0001t0010g0145a0001c0001t0010g0148others(4): Show | 7 | HG02109.hp2 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.882+18587C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124982013 | ||||||
| chr6:124982026
|
C | CA | 69 | a0001c0001t0001g0102a0001c0001t0001g0125a0001c0001t0001g0128others(66): Show | 70 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.882+18621dupA | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 124982026 | |||||
| chr6:124982026
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0016g0144 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.882+18610_882+1862 others(16): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 124982026 | |||||
| chr6:124982075
|
T | C | 1 | a0001c0001t0006g0177 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.882+18649T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124982075 | ||||||
| chr6:124982187
|
C | G | 1 | a0002c0002t0075g0040 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.882+18761C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124982187 | ||||||
| chr6:124982307
|
C | A | 56 | a0001c0001t0001g0125a0001c0001t0001g0128a0001c0001t0001g0200others(53): Show | 57 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.882+18881C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124982307 | ||||||
| chr6:124982337
|
A | G | 232 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(229): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.882+18911A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124982337 | ||||||
| chr6:124982436
|
T | G | 1 | a0002c0002t0075g0040 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.882+19010T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124982436 | ||||||
| chr6:124982456
|
T | C | 2 | a0005c0007t0006g0094a0005c0007t0021g0095 | 2 | HG01884.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.882+19030T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124982456 | ||||||
| chr6:124982599
|
A | T | 1 | a0001c0001t0017g0154 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.882+19173A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124982599 | ||||||
| chr6:124982607
|
C | T | 1 | a0001c0001t0004g0242 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.882+19181C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124982607 | ||||||
| chr6:124982608
|
G | A | 1 | a0001c0001t0005g0061 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.882+19182G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124982608 | ||||||
| chr6:124982844
|
C | T | 1 | a0001c0001t0056g0112 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.882+19418C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124982844 | ||||||
| chr6:124983062
|
A | G | 2 | a0001c0001t0021g0159a0001c0001t0026g0160 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.882+19636A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124983062 | ||||||
| chr6:124983148
|
G | T | 1 | a0002c0006t0078g0007 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.882+19722G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124983148 | ||||||
| chr6:124983160
|
T | C | 3 | a0001c0001t0017g0101a0001c0001t0041g0099a0003c0004t0044g0100 | 3 | HG02965.hp2 HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.882+19734T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124983160 | ||||||
| chr6:124983600
|
G | A | 1 | a0002c0002t0075g0040 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.882+20174G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124983600 | ||||||
| chr6:124983785
|
T | C | 63 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(60): Show | 63 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.882+20359T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124983785 | ||||||
| chr6:124984123
|
C | A | 1 | a0001c0001t0003g0085 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.882+20697C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124984123 | ||||||
| chr6:124984181
|
G | C | 1 | a0001c0001t0012g0062 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.882+20755G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124984181 | ||||||
| chr6:124984423
|
C | T | 1 | a0001c0001t0016g0144 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.882+20997C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124984423 | ||||||
| chr6:124984501
|
A | G | 1 | a0001c0001t0001g0047 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.882+21075A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124984501 | ||||||
| chr6:124984541
|
CA | C | 89 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(86): Show | 89 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.882+21135delA | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 124984541 | |||||
| chr6:124984546
|
A | AAAT | 62 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(59): Show | 62 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.882+21122_882+2112 others(7): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 124984546 | |||||
| chr6:124984554
|
A | G | 62 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(59): Show | 62 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.882+21128A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124984554 | ||||||
| chr6:124984558
|
A | G | 64 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(61): Show | 64 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.882+21132A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124984558 | ||||||
| chr6:124984705
|
A | C | 72 | a0001c0001t0001g0102a0001c0001t0001g0125a0001c0001t0001g0128others(69): Show | 74 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.882+21279A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124984705 | ||||||
| chr6:124984865
|
A | G | 1 | a0001c0003t0008g0175 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.882+21439A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124984865 | ||||||
| chr6:124985301
|
A | G | 1 | a0001c0001t0067g0199 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.882+21875A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124985301 | ||||||
| chr6:124985316
|
G | A | 1 | a0008c0015t0053g0248 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.882+21890G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124985316 | ||||||
| chr6:124985668
|
A | G | 57 | a0001c0001t0001g0102a0001c0001t0001g0125a0001c0001t0001g0128others(54): Show | 58 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.882+22242A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124985668 | ||||||
| chr6:124985738
|
A | G | 62 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(59): Show | 62 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.882+22312A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124985738 | ||||||
| chr6:124985889
|
T | G | 1 | a0001c0001t0002g0203 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.882+22463T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124985889 | ||||||
| chr6:124985940
|
A | G | 1 | a0001c0001t0036g0232 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.882+22514A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124985940 | ||||||
| chr6:124986000
|
T | C | 2 | a0001c0001t0001g0120a0001c0001t0002g0121 | 2 | NA18964.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.882+22574T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124986000 | ||||||
| chr6:124986136
|
T | C | 1 | a0001c0001t0001g0063 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.882+22710T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124986136 | ||||||
| chr6:124986288
|
G | A | 3 | a0001c0001t0017g0101a0001c0001t0041g0099a0003c0004t0044g0100 | 3 | HG02965.hp2 HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.882+22862G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124986288 | ||||||
| chr6:124986840
|
A | G | 2 | a0001c0001t0006g0174a0001c0001t0051g0173 | 2 | HG02280.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.882+23414A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124986840 | ||||||
| chr6:124986940
|
G | A | 62 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(59): Show | 62 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.882+23514G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124986940 | ||||||
| chr6:124987019
|
A | G | 2 | a0001c0001t0003g0255a0001c0001t0017g0254 | 2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.882+23593A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124987019 | ||||||
| chr6:124987042
|
T | C | 1 | a0001c0001t0001g0064 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.882+23616T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124987042 | ||||||
| chr6:124987066
|
C | A | 58 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(55): Show | 58 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.882+23640C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124987066 | ||||||
| chr6:124987241
|
G | A | 39 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(36): Show | 39 | HG00423.hp1 HG00609.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.882+23815G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124987241 | ||||||
| chr6:124987339
|
C | T | 2 | a0001c0001t0008g0182a0001c0001t0022g0180 | 2 | HG02055.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.882+23913C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124987339 | ||||||
| chr6:124987367
|
A | G | 1 | a0001c0001t0016g0083 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.882+23941A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124987367 | ||||||
| chr6:124987370
|
A | G | 1 | a0006c0009t0001g0194 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.882+23944A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124987370 | ||||||
| chr6:124987414
|
C | T | 2 | a0005c0007t0006g0094a0005c0007t0021g0095 | 2 | HG01884.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.882+23988C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124987414 | ||||||
| chr6:124987612
|
C | T | 1 | a0002c0002t0070g0039 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.882+24186C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124987612 | ||||||
| chr6:124987668
|
G | T | 1 | a0008c0015t0053g0248 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.882+24242G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124987668 | ||||||
| chr6:124987731
|
C | A | 2 | a0001c0001t0004g0243a0001c0001t0067g0199 | 2 | HG03492.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.882+24305C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124987731 | ||||||
| chr6:124987733
|
G | A | 2 | a0001c0001t0006g0003a0001c0001t0043g0004 | 2 | HG02486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.882+24307G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124987733 | ||||||
| chr6:124987750
|
A | G | 1 | a0001c0001t0049g0262 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.882+24324A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124987750 | ||||||
| chr6:124987835
|
T | A | 1 | a0001c0001t0038g0204 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.882+24409T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124987835 | ||||||
| chr6:124987915
|
A | G | 62 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(59): Show | 62 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.882+24489A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124987915 | ||||||
| chr6:124987974
|
A | G | 1 | a0001c0001t0026g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.882+24548A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124987974 | ||||||
| chr6:124988150
|
C | T | 9 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(6): Show | 9 | HG00323.hp1 HG00609.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.882+24724C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124988150 | ||||||
| chr6:124988794
|
A | T | 2 | a0001c0001t0001g0231a0001c0001t0003g0198 | 2 | HG00323.hp1 HG00735.hp2 |
intron_variant | MODIFIER | c.882+25368A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124988794 | ||||||
| chr6:124988868
|
G | A | 58 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(55): Show | 58 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.882+25442G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124988868 | ||||||
| chr6:124988871
|
T | C | 58 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(55): Show | 58 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.882+25445T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124988871 | ||||||
| chr6:124988879
|
T | A | 1 | a0001c0001t0001g0051 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.882+25453T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124988879 | ||||||
| chr6:124988959
|
A | T | 1 | a0001c0001t0002g0230 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.882+25533A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124988959 | ||||||
| chr6:124989019
|
AT | A | 5 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(2): Show | 5 | HG00423.hp1 HG01243.hp2 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+25600delT | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 124989019 | |||||
| chr6:124989057
|
A | ATTACCTT others(20): Show |
62 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(59): Show | 62 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.882+25633_882+2563 others(31): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 124989057 | |||||
| chr6:124989214
|
C | T | 62 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(59): Show | 62 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.882+25788C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124989214 | ||||||
| chr6:124989269
|
C | T | 11 | a0001c0001t0001g0263a0001c0001t0006g0264a0001c0001t0010g0153others(8): Show | 11 | HG01192.hp1 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.882+25843C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124989269 | ||||||
| chr6:124989281
|
A | T | 1 | a0001c0001t0001g0057 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.882+25855A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124989281 | ||||||
| chr6:124989306
|
C | T | 2 | a0001c0001t0001g0200a0001c0001t0012g0201 | 2 | HG01928.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.882+25880C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124989306 | ||||||
| chr6:124989389
|
G | T | 58 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(55): Show | 58 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.882+25963G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124989389 | ||||||
| chr6:124989391
|
A | G | 1 | a0001c0001t0001g0241 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.882+25965A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124989391 | ||||||
| chr6:124989572
|
C | G | 1 | a0002c0002t0075g0040 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.882+26146C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124989572 | ||||||
| chr6:124989617
|
C | T | 1 | a0001c0001t0005g0092 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.882+26191C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124989617 | ||||||
| chr6:124989637
|
A | ATTTGAG | 262 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(259): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.882+26216_882+2621 others(10): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 124989637 | |||||
| chr6:124989815
|
T | C | 1 | a0001c0001t0003g0178 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.882+26389T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124989815 | ||||||
| chr6:124989867
|
G | GA | 13 | a0001c0001t0001g0051a0001c0001t0001g0058a0001c0001t0001g0068others(10): Show | 13 | HG00642.hp2 HG00735.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.882+26451dupA | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 124989867 | |||||
| chr6:124989883
|
A | T | 11 | a0001c0001t0006g0191a0001c0001t0010g0195a0001c0001t0046g0196others(8): Show | 12 | HG01243.hp1 HG02280.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.882+26457A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124989883 | ||||||
| chr6:124990326
|
T | C | 56 | a0001c0001t0001g0102a0001c0001t0001g0125a0001c0001t0001g0128others(53): Show | 57 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.882+26900T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124990326 | ||||||
| chr6:124990332
|
A | G | 6 | a0002c0002t0007g0026a0002c0002t0007g0027a0002c0002t0009g0024others(3): Show | 6 | HG00323.hp2 HG01346.hp1 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.882+26906A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124990332 | ||||||
| chr6:124990352
|
C | T | 1 | a0002c0006t0078g0007 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.882+26926C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124990352 | ||||||
| chr6:124990633
|
A | C | 61 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(58): Show | 61 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.882+27207A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124990633 | ||||||
| chr6:124990863
|
G | A | 1 | a0001c0001t0001g0064 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.882+27437G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124990863 | ||||||
| chr6:124991006
|
G | T | 9 | a0001c0001t0006g0003a0001c0001t0006g0191a0001c0001t0010g0195others(6): Show | 10 | HG02486.hp1 HG02818.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.882+27580G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124991006 | ||||||
| chr6:124991248
|
G | C | 6 | a0001c0001t0001g0158a0001c0001t0004g0155a0001c0001t0006g0156others(3): Show | 6 | HG00741.hp1 HG01891.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.882+27822G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124991248 | ||||||
| chr6:124991423
|
C | T | 1 | a0001c0001t0002g0229 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.882+27997C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124991423 | ||||||
| chr6:124991504
|
T | C | 60 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(57): Show | 60 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.882+28078T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124991504 | ||||||
| chr6:124991556
|
C | T | 1 | a0001c0001t0026g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.882+28130C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124991556 | ||||||
| chr6:124991664
|
T | C | 2 | a0002c0002t0029g0005a0002c0006t0013g0010 | 2 | NA19065.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.882+28238T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124991664 | ||||||
| chr6:124992116
|
A | G | 1 | a0001c0001t0010g0195 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.882+28690A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124992116 | ||||||
| chr6:124992137
|
A | G | 1 | a0001c0001t0026g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.882+28711A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124992137 | ||||||
| chr6:124992144
|
C | G | 6 | a0001c0001t0040g0261a0001c0001t0049g0262a0001c0003t0010g0266others(3): Show | 6 | HG02257.hp2 HG02258.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.882+28718C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124992144 | ||||||
| chr6:124992177
|
CT | C | 60 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(57): Show | 60 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.882+28752delT | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124992177 | ||||||
| chr6:124992405
|
C | A | 1 | a0001c0001t0004g0096 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.882+28979C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124992405 | ||||||
| chr6:124992407
|
A | G | 1 | a0002c0002t0075g0040 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.882+28981A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124992407 | ||||||
| chr6:124992417
|
A | G | 3 | a0001c0001t0017g0101a0001c0001t0041g0099a0003c0004t0044g0100 | 3 | HG02965.hp2 HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.882+28991A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124992417 | ||||||
| chr6:124992420
|
A | G | 9 | a0001c0001t0006g0191a0001c0001t0010g0195a0001c0001t0046g0196others(6): Show | 10 | HG01884.hp1 HG02809.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.882+28994A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124992420 | ||||||
| chr6:124992529
|
C | T | 60 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(57): Show | 60 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.882+29103C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124992529 | ||||||
| chr6:124992566
|
T | G | 60 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(57): Show | 60 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.882+29140T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124992566 | ||||||
| chr6:124992645
|
G | A | 1 | a0001c0001t0002g0237 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.882+29219G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124992645 | ||||||
| chr6:124992735
|
C | T | 5 | a0001c0001t0008g0182a0001c0001t0022g0180a0001c0001t0039g0179others(2): Show | 5 | HG02055.hp2 HG02109.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.882+29309C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124992735 | ||||||
| chr6:124992894
|
C | T | 1 | a0001c0001t0002g0056 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.882+29468C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124992894 | ||||||
| chr6:124992903
|
T | A | 86 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(83): Show | 86 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.882+29477T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124992903 | ||||||
| chr6:124993009
|
C | A | 1 | a0001c0001t0004g0155 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.882+29583C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124993009 | ||||||
| chr6:124993088
|
G | A | 1 | a0001c0001t0010g0195 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.882+29662G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124993088 | ||||||
| chr6:124993404
|
T | G | 84 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(81): Show | 84 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.882+29978T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124993404 | ||||||
| chr6:124993564
|
A | G | 1 | a0011c0011t0079g0036 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.882+30138A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124993564 | ||||||
| chr6:124993576
|
A | C | 1 | a0001c0001t0039g0179 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.882+30150A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124993576 | ||||||
| chr6:124993704
|
G | A | 10 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(7): Show | 10 | HG00099.hp2 HG00639.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.882+30278G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124993704 | ||||||
| chr6:124994277
|
G | A | 60 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(57): Show | 60 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.882+30851G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124994277 | ||||||
| chr6:124994368
|
C | T | 215 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(212): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.882+30942C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124994368 | ||||||
| chr6:124994376
|
G | A | 60 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(57): Show | 60 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.882+30950G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124994376 | ||||||
| chr6:124994719
|
A | G | 1 | a0002c0006t0078g0007 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.882+31293A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124994719 | ||||||
| chr6:124994725
|
A | C | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG01243.hp2 HG01934.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.882+31299A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124994725 | ||||||
| chr6:124994850
|
G | C | 1 | a0001c0001t0001g0069 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.882+31424G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124994850 | ||||||
| chr6:124994922
|
G | T | 1 | a0008c0015t0053g0248 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.882+31496G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124994922 | ||||||
| chr6:124995129
|
C | T | 1 | a0002c0006t0078g0007 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.882+31703C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124995129 | ||||||
| chr6:124995215
|
T | C | 9 | a0001c0001t0006g0191a0001c0001t0010g0195a0001c0001t0046g0196others(6): Show | 10 | HG01884.hp1 HG02809.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.882+31789T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124995215 | ||||||
| chr6:124995261
|
A | G | 3 | a0001c0001t0017g0101a0001c0001t0041g0099a0003c0004t0044g0100 | 3 | HG02965.hp2 HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.882+31835A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124995261 | ||||||
| chr6:124995410
|
G | A | 1 | a0001c0001t0003g0169 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.882+31984G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124995410 | ||||||
| chr6:124995895
|
C | G | 1 | a0001c0001t0002g0055 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.882+32469C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124995895 | ||||||
| chr6:124995947
|
A | G | 59 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(56): Show | 59 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.882+32521A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124995947 | ||||||
| chr6:124996132
|
G | A | 3 | a0001c0001t0017g0101a0001c0001t0041g0099a0003c0004t0044g0100 | 3 | HG02965.hp2 HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.882+32706G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124996132 | ||||||
| chr6:124997017
|
GCAAGTTT others(5): Show |
G | 11 | a0001c0001t0006g0003a0001c0001t0006g0191a0001c0001t0010g0195others(8): Show | 12 | HG01884.hp1 HG02486.hp1 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.882+33593_882+3360 others(16): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 124997017 | |||||
| chr6:124997026
|
G | T | 60 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(57): Show | 60 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.882+33600G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124997026 | ||||||
| chr6:124997233
|
C | T | 81 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(78): Show | 81 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.882+33807C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124997233 | ||||||
| chr6:124997396
|
G | T | 1 | a0001c0001t0001g0228 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.882+33970G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124997396 | ||||||
| chr6:124997418
|
A | G | 1 | a0008c0015t0053g0248 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.882+33992A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124997418 | ||||||
| chr6:124997461
|
C | CAA | 174 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(171): Show | 175 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.882+34035_882+3403 others(6): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124997461 | ||||||
| chr6:124997547
|
T | G | 57 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(54): Show | 57 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.882+34121T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124997547 | ||||||
| chr6:124997557
|
C | G | 61 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(58): Show | 61 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.882+34131C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124997557 | ||||||
| chr6:124997671
|
C | T | 16 | a0001c0001t0003g0169a0001c0001t0003g0172a0001c0001t0003g0176others(13): Show | 16 | HG02055.hp2 HG02109.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.882+34245C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124997671 | ||||||
| chr6:124997686
|
A | G | 2 | a0001c0001t0003g0172a0001c0001t0059g0171 | 2 | HG02615.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.882+34260A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124997686 | ||||||
| chr6:124997735
|
A | G | 1 | a0002c0002t0071g0038 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.882+34309A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124997735 | ||||||
| chr6:124997818
|
A | G | 2 | a0001c0001t0005g0092a0001c0001t0063g0091 | 2 | HG00408.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.882+34392A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124997818 | ||||||
| chr6:124997858
|
A | G | 1 | a0002c0002t0007g0023 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.882+34432A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124997858 | ||||||
| chr6:124997902
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.882+34476G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124997902 | ||||||
| chr6:124997924
|
C | T | 1 | a0002c0002t0070g0039 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.882+34498C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124997924 | ||||||
| chr6:124997966
|
A | C | 8 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(5): Show | 8 | HG00609.hp2 HG01358.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.882+34540A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124997966 | ||||||
| chr6:124998069
|
C | G | 175 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(172): Show | 176 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.882+34643C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124998069 | ||||||
| chr6:124998263
|
T | A | 1 | a0011c0011t0079g0036 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.882+34837T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124998263 | ||||||
| chr6:124998404
|
G | C | 8 | a0001c0001t0003g0169a0001c0001t0003g0172a0001c0001t0003g0176others(5): Show | 8 | HG02451.hp1 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.882+34978G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124998404 | ||||||
| chr6:124998412
|
A | T | 44 | a0001c0001t0001g0102a0001c0001t0001g0135a0001c0001t0001g0136others(41): Show | 44 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.882+34986A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124998412 | ||||||
| chr6:124998417
|
C | T | 2 | a0001c0001t0001g0051a0001c0001t0001g0068 | 2 | HG01070.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.882+34991C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124998417 | ||||||
| chr6:124998474
|
A | G | 1 | a0001c0001t0026g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.882+35048A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124998474 | ||||||
| chr6:124998545
|
G | A | 229 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(226): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.882+35119G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124998545 | ||||||
| chr6:124998548
|
G | A | 1 | a0001c0001t0026g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.882+35122G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124998548 | ||||||
| chr6:124998753
|
G | A | 2 | a0008c0015t0053g0248a0011c0011t0079g0036 | 2 | HG02922.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.882+35327G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124998753 | ||||||
| chr6:124998797
|
C | G | 62 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(59): Show | 62 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.882+35371C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124998797 | ||||||
| chr6:124998837
|
G | A | 82 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(79): Show | 82 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.882+35411G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124998837 | ||||||
| chr6:124998893
|
T | C | 1 | a0002c0002t0013g0011 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.882+35467T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124998893 | ||||||
| chr6:124998901
|
A | G | 87 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(84): Show | 87 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.882+35475A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124998901 | ||||||
| chr6:124999094
|
C | T | 1 | a0001c0001t0026g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.882+35668C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124999094 | ||||||
| chr6:124999398
|
A | C | 1 | a0011c0011t0079g0036 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.882+35972A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124999398 | ||||||
| chr6:124999939
|
C | T | 1 | a0009c0014t0001g0127 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.882+36513C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124999939 | ||||||
| chr6:125000245
|
A | C | 1 | a0001c0003t0008g0193 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.882+36819A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125000245 | ||||||
| chr6:125000345
|
A | C | 2 | a0001c0001t0015g0225a0001c0001t0047g0226 | 2 | HG02083.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.882+36919A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125000345 | ||||||
| chr6:125000437
|
C | T | 23 | a0001c0001t0003g0169a0001c0001t0003g0172a0001c0001t0003g0176others(20): Show | 23 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.882+37011C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125000437 | ||||||
| chr6:125000484
|
A | G | 4 | a0001c0001t0001g0102a0001c0001t0002g0164a0001c0001t0003g0085others(1): Show | 4 | HG00642.hp1 HG01069.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+37058A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125000484 | ||||||
| chr6:125000599
|
C | T | 1 | a0002c0002t0075g0040 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.882+37173C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125000599 | ||||||
| chr6:125000648
|
A | G | 3 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0052g0049 | 3 | HG02132.hp2 NA18747.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.882+37222A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125000648 | ||||||
| chr6:125000734
|
T | C | 1 | a0001c0001t0017g0154 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.882+37308T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125000734 | ||||||
| chr6:125001201
|
T | C | 33 | a0001c0001t0003g0169a0001c0001t0003g0172a0001c0001t0003g0176others(30): Show | 33 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(30): Show |
intron_variant | MODIFIER | c.882+37775T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125001201 | ||||||
| chr6:125001346
|
T | C | 1 | a0002c0002t0070g0039 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.882+37920T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125001346 | ||||||
| chr6:125001394
|
C | G | 1 | a0008c0015t0053g0248 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.882+37968C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125001394 | ||||||
| chr6:125001456
|
A | T | 32 | a0001c0001t0003g0169a0001c0001t0003g0172a0001c0001t0003g0176others(29): Show | 32 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.882+38030A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125001456 | ||||||
| chr6:125001655
|
C | T | 11 | a0001c0001t0010g0195a0001c0001t0040g0261a0001c0001t0046g0196others(8): Show | 11 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.882+38229C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125001655 | ||||||
| chr6:125001890
|
A | AT | 6 | a0001c0001t0006g0003a0001c0001t0006g0191a0001c0001t0017g0154others(3): Show | 6 | HG01884.hp2 HG02486.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.882+38466dupT | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125001890 | |||||
| chr6:125002018
|
T | C | 3 | a0001c0001t0021g0133a0001c0001t0022g0132a0001c0001t0033g0134 | 3 | HG02886.hp2 HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.882+38592T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125002018 | ||||||
| chr6:125002100
|
G | C | 1 | a0001c0001t0001g0102 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.882+38674G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125002100 | ||||||
| chr6:125002102
|
G | A | 1 | a0001c0001t0001g0043 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.882+38676G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125002102 | ||||||
| chr6:125002445
|
CT | C | 28 | a0001c0001t0003g0169a0001c0001t0003g0172a0001c0001t0003g0176others(25): Show | 28 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.882+39020delT | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125002445 | ||||||
| chr6:125002482
|
G | C | 59 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(56): Show | 60 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.882+39056G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125002482 | ||||||
| chr6:125002599
|
C | T | 10 | a0001c0001t0001g0120a0001c0001t0002g0121a0001c0001t0002g0122others(7): Show | 10 | HG02080.hp2 NA18943.hp1 NA18946.hp2 others(7): Show |
intron_variant | MODIFIER | c.882+39173C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125002599 | ||||||
| chr6:125002606
|
C | T | 1 | a0001c0001t0002g0229 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.882+39180C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125002606 | ||||||
| chr6:125003043
|
G | A | 11 | a0001c0001t0010g0195a0001c0001t0040g0261a0001c0001t0046g0196others(8): Show | 11 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.882+39617G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125003043 | ||||||
| chr6:125003104
|
G | A | 32 | a0001c0001t0003g0169a0001c0001t0003g0172a0001c0001t0003g0176others(29): Show | 32 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.882+39678G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125003104 | ||||||
| chr6:125003129
|
T | C | 1 | a0001c0001t0049g0262 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.882+39703T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125003129 | ||||||
| chr6:125003183
|
G | A | 31 | a0001c0001t0003g0169a0001c0001t0003g0172a0001c0001t0003g0176others(28): Show | 31 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.882+39757G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125003183 | ||||||
| chr6:125003258
|
G | A | 61 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(58): Show | 62 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.882+39832G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125003258 | ||||||
| chr6:125003373
|
T | TG | 11 | a0001c0001t0010g0195a0001c0001t0040g0261a0001c0001t0046g0196others(8): Show | 11 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.882+39948dupG | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125003373 | |||||
| chr6:125003546
|
A | G | 31 | a0001c0001t0003g0169a0001c0001t0003g0172a0001c0001t0003g0176others(28): Show | 31 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.882+40120A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125003546 | ||||||
| chr6:125003615
|
A | G | 231 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(228): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.882+40189A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125003615 | ||||||
| chr6:125003719
|
C | G | 60 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(57): Show | 61 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.882+40293C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125003719 | ||||||
| chr6:125003761
|
A | G | 1 | a0001c0001t0045g0161 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.882+40335A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125003761 | ||||||
| chr6:125004051
|
A | G | 1 | a0001c0001t0067g0199 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.882+40625A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125004051 | ||||||
| chr6:125004064
|
G | GT | 222 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(219): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.882+40645dupT | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125004064 | |||||
| chr6:125004064
|
G | T | 15 | a0001c0001t0003g0169a0001c0001t0003g0172a0001c0001t0003g0176others(12): Show | 15 | HG02055.hp2 HG02109.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.882+40638G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125004064 | ||||||
| chr6:125004064
|
GTT | G | 7 | a0001c0001t0006g0003a0001c0001t0006g0191a0001c0001t0017g0154others(4): Show | 7 | HG01884.hp2 HG02486.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.882+40644_882+4064 others(6): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125004064 | |||||
| chr6:125004113
|
G | A | 1 | a0002c0002t0075g0040 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.882+40687G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125004113 | ||||||
| chr6:125004186
|
A | G | 1 | a0001c0001t0036g0232 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.882+40760A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125004186 | ||||||
| chr6:125004708
|
G | A | 32 | a0001c0001t0003g0169a0001c0001t0003g0172a0001c0001t0003g0176others(29): Show | 32 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.883-40503G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125004708 | ||||||
| chr6:125004955
|
A | C | 261 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(258): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.883-40256A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125004955 | ||||||
| chr6:125005038
|
G | A | 1 | a0001c0001t0023g0250 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.883-40173G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125005038 | ||||||
| chr6:125005270
|
G | A | 33 | a0001c0001t0003g0169a0001c0001t0003g0172a0001c0001t0003g0176others(30): Show | 33 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(30): Show |
intron_variant | MODIFIER | c.883-39941G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125005270 | ||||||
| chr6:125005399
|
A | G | 2 | a0001c0001t0004g0243a0001c0001t0016g0222 | 2 | HG02602.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.883-39812A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125005399 | ||||||
| chr6:125005478
|
A | G | 2 | a0001c0001t0012g0062a0001c0001t0016g0144 | 2 | HG02735.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.883-39733A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125005478 | ||||||
| chr6:125005704
|
A | G | 1 | a0001c0001t0001g0093 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.883-39507A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125005704 | ||||||
| chr6:125005755
|
T | C | 1 | a0001c0003t0008g0193 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.883-39456T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125005755 | ||||||
| chr6:125005869
|
G | A | 2 | a0001c0001t0021g0159a0001c0001t0026g0160 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.883-39342G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125005869 | ||||||
| chr6:125005931
|
T | G | 1 | a0001c0001t0014g0097 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.883-39280T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125005931 | ||||||
| chr6:125006406
|
C | T | 7 | a0001c0001t0006g0003a0001c0001t0006g0191a0001c0001t0017g0154others(4): Show | 7 | HG01884.hp2 HG02486.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.883-38805C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125006406 | ||||||
| chr6:125006570
|
A | G | 1 | a0002c0002t0072g0006 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.883-38641A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125006570 | ||||||
| chr6:125006601
|
C | T | 1 | a0001c0003t0023g0143 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.883-38610C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125006601 | ||||||
| chr6:125006639
|
G | A | 24 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(21): Show | 24 | HG00609.hp2 HG01358.hp1 HG01433.hp2 others(21): Show |
intron_variant | MODIFIER | c.883-38572G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125006639 | ||||||
| chr6:125006852
|
G | C | 1 | a0002c0002t0007g0008 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.883-38359G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125006852 | ||||||
| chr6:125006881
|
A | G | 110 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(107): Show | 110 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.883-38330A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125006881 | ||||||
| chr6:125006898
|
G | A | 33 | a0001c0001t0003g0169a0001c0001t0003g0172a0001c0001t0003g0176others(30): Show | 33 | HG01192.hp2 HG01884.hp1 HG02055.hp2 others(30): Show |
intron_variant | MODIFIER | c.883-38313G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125006898 | ||||||
| chr6:125007059
|
A | T | 77 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(74): Show | 77 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.883-38152A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125007059 | ||||||
| chr6:125007062
|
A | G | 77 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(74): Show | 77 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.883-38149A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125007062 | ||||||
| chr6:125007249
|
A | AT | 111 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(108): Show | 113 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.883-37949dupT | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125007249 | |||||
| chr6:125007249
|
A | ATT | 6 | a0001c0001t0002g0221a0001c0001t0002g0229a0001c0001t0002g0249others(3): Show | 6 | HG03492.hp1 HG04115.hp1 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.883-37950_883-3794 others(6): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125007249 | |||||
| chr6:125007249
|
ATT | A | 33 | a0001c0001t0003g0169a0001c0001t0003g0172a0001c0001t0003g0176others(30): Show | 33 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(30): Show |
intron_variant | MODIFIER | c.883-37950_883-3794 others(6): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125007249 | |||||
| chr6:125007266
|
A | T | 1 | a0001c0001t0005g0081 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.883-37945A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125007266 | ||||||
| chr6:125007322
|
C | T | 1 | a0001c0001t0004g0242 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.883-37889C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125007322 | ||||||
| chr6:125007323
|
G | A | 1 | a0011c0011t0079g0036 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.883-37888G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125007323 | ||||||
| chr6:125007654
|
T | C | 1 | a0001c0001t0036g0232 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.883-37557T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125007654 | ||||||
| chr6:125007704
|
C | T | 33 | a0001c0001t0003g0169a0001c0001t0003g0172a0001c0001t0003g0176others(30): Show | 33 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(30): Show |
intron_variant | MODIFIER | c.883-37507C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125007704 | ||||||
| chr6:125007797
|
A | G | 33 | a0001c0001t0003g0169a0001c0001t0003g0172a0001c0001t0003g0176others(30): Show | 33 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(30): Show |
intron_variant | MODIFIER | c.883-37414A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125007797 | ||||||
| chr6:125007979
|
G | A | 77 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(74): Show | 77 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.883-37232G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125007979 | ||||||
| chr6:125008041
|
G | A | 33 | a0001c0001t0003g0169a0001c0001t0003g0172a0001c0001t0003g0176others(30): Show | 33 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(30): Show |
intron_variant | MODIFIER | c.883-37170G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125008041 | ||||||
| chr6:125008047
|
T | G | 1 | a0007c0010t0028g0029 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.883-37164T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125008047 | ||||||
| chr6:125008131
|
C | T | 77 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(74): Show | 77 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.883-37080C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125008131 | ||||||
| chr6:125008255
|
C | CA | 32 | a0001c0001t0003g0169a0001c0001t0003g0176a0001c0001t0003g0178others(29): Show | 32 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.883-36943dupA | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125008255 | |||||
| chr6:125008369
|
C | G | 1 | a0001c0003t0008g0193 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.883-36842C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125008369 | ||||||
| chr6:125008467
|
G | A | 240 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(237): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.883-36744G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125008467 | ||||||
| chr6:125008479
|
C | T | 1 | a0001c0003t0008g0257 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.883-36732C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125008479 | ||||||
| chr6:125008738
|
C | CT | 136 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(133): Show | 138 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.883-36455dupT | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125008738 | |||||
| chr6:125008738
|
C | CTT | 9 | a0001c0001t0001g0080a0001c0001t0001g0228a0001c0001t0002g0098others(6): Show | 9 | HG01891.hp2 HG02293.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.883-36456_883-3645 others(6): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125008738 | |||||
| chr6:125008982
|
G | C | 38 | a0001c0001t0001g0102a0001c0001t0001g0135a0001c0001t0001g0136others(35): Show | 38 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.883-36229G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125008982 | ||||||
| chr6:125009285
|
A | G | 1 | a0001c0001t0017g0154 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.883-35926A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125009285 | ||||||
| chr6:125009461
|
T | C | 3 | a0001c0001t0001g0044a0001c0001t0001g0047a0001c0001t0015g0045 | 3 | HG02523.hp1 NA18999.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.883-35750T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125009461 | ||||||
| chr6:125009473
|
GA | G | 77 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(74): Show | 77 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.883-35728delA | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125009473 | |||||
| chr6:125009765
|
G | A | 1 | a0001c0003t0008g0131 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.883-35446G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125009765 | ||||||
| chr6:125009775
|
G | A | 60 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(57): Show | 61 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.883-35436G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125009775 | ||||||
| chr6:125009985
|
CT | C | 178 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(175): Show | 179 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.883-35210delT | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125009985 | |||||
| chr6:125010146
|
A | C | 1 | a0001c0001t0002g0203 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.883-35065A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125010146 | ||||||
| chr6:125010292
|
G | A | 1 | a0001c0003t0023g0143 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.883-34919G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125010292 | ||||||
| chr6:125010383
|
G | A | 1 | a0001c0001t0023g0250 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.883-34828G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125010383 | ||||||
| chr6:125010481
|
G | T | 1 | a0001c0001t0045g0161 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.883-34730G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125010481 | ||||||
| chr6:125010517
|
C | T | 3 | a0001c0001t0001g0116a0001c0001t0004g0096a0001c0001t0005g0114 | 3 | NA18949.hp2 NA18956.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.883-34694C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125010517 | ||||||
| chr6:125010878
|
A | G | 78 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(75): Show | 78 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.883-34333A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125010878 | ||||||
| chr6:125010882
|
C | T | 231 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(228): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.883-34329C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125010882 | ||||||
| chr6:125010937
|
A | G | 1 | a0001c0003t0010g0259 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.883-34274A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125010937 | ||||||
| chr6:125011030
|
C | T | 78 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(75): Show | 78 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.883-34181C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125011030 | ||||||
| chr6:125011379
|
G | T | 5 | a0001c0001t0015g0225a0001c0001t0018g0223a0001c0001t0018g0224others(2): Show | 5 | HG00423.hp2 HG02083.hp1 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-33832G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125011379 | ||||||
| chr6:125011665
|
A | G | 113 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(110): Show | 115 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.883-33546A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125011665 | ||||||
| chr6:125011706
|
A | T | 1 | a0001c0001t0002g0229 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.883-33505A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125011706 | ||||||
| chr6:125011830
|
G | A | 49 | a0001c0001t0001g0084a0001c0001t0001g0125a0001c0001t0001g0128others(46): Show | 50 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.883-33381G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125011830 | ||||||
| chr6:125011857
|
G | A | 1 | a0001c0001t0002g0164 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.883-33354G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125011857 | ||||||
| chr6:125011858
|
G | C | 32 | a0001c0001t0003g0169a0001c0001t0003g0172a0001c0001t0003g0176others(29): Show | 32 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.883-33353G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125011858 | ||||||
| chr6:125011876
|
G | A | 1 | a0008c0015t0053g0248 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.883-33335G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125011876 | ||||||
| chr6:125011961
|
G | C | 1 | a0001c0001t0017g0254 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.883-33250G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125011961 | ||||||
| chr6:125012064
|
G | A | 32 | a0001c0001t0003g0169a0001c0001t0003g0172a0001c0001t0003g0176others(29): Show | 32 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.883-33147G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125012064 | ||||||
| chr6:125012100
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.883-33111C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125012100 | ||||||
| chr6:125012527
|
G | A | 231 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(228): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.883-32684G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125012527 | ||||||
| chr6:125012622
|
A | G | 1 | a0001c0001t0001g0111 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.883-32589A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125012622 | ||||||
| chr6:125012651
|
T | C | 63 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(60): Show | 64 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.883-32560T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125012651 | ||||||
| chr6:125013062
|
G | C | 1 | a0001c0001t0015g0207 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.883-32149G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125013062 | ||||||
| chr6:125013188
|
G | T | 1 | a0001c0001t0001g0236 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.883-32023G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125013188 | ||||||
| chr6:125013345
|
TTGTGTA | T | 24 | a0001c0001t0003g0169a0001c0001t0003g0172a0001c0001t0003g0178others(21): Show | 24 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.883-31860_883-3185 others(10): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125013345 | |||||
| chr6:125013347
|
GTGTA | G | 4 | a0001c0001t0003g0176a0001c0001t0006g0174a0001c0001t0051g0173others(1): Show | 4 | HG02280.hp2 HG02809.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.883-31860_883-3185 others(8): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125013347 | |||||
| chr6:125013351
|
A | ATG | 17 | a0001c0001t0001g0244a0001c0001t0012g0220a0001c0001t0061g0253others(14): Show | 17 | HG00738.hp2 HG01069.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.883-31823_883-3182 others(6): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125013351 | |||||
| chr6:125013351
|
A | ATGTG | 6 | a0001c0001t0017g0154a0001c0001t0026g0168a0001c0001t0043g0004others(3): Show | 6 | HG01884.hp2 HG02071.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.883-31825_883-3182 others(8): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125013351 | |||||
| chr6:125013351
|
A | ATGTGTG | 4 | a0001c0001t0006g0003a0002c0002t0007g0021a0002c0002t0007g0022others(1): Show | 4 | NA18906.hp1 NA18956.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.883-31827_883-3182 others(10): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125013351 | |||||
| chr6:125013351
|
A | ATGTGTGT others(1): Show |
3 | a0001c0001t0006g0191a0003c0004t0011g0190a0010c0013t0030g0192 | 3 | HG02818.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.883-31829_883-3182 others(12): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125013351 | |||||
| chr6:125013351
|
A | G | 3 | a0002c0002t0075g0040a0008c0015t0053g0248a0011c0011t0079g0036 | 3 | HG02922.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.883-31860A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125013351 | ||||||
| chr6:125013351
|
ATG | A | 66 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(63): Show | 67 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.883-31823_883-3182 others(6): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125013351 | |||||
| chr6:125013351
|
ATGTG | A | 116 | a0001c0001t0001g0084a0001c0001t0001g0102a0001c0001t0001g0104others(113): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.883-31825_883-3182 others(8): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125013351 | |||||
| chr6:125013351
|
ATGTGTGT others(7): Show |
A | 1 | a0001c0001t0060g0233 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.883-31835_883-3182 others(18): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125013351 | |||||
| chr6:125013459
|
C | G | 1 | a0001c0001t0004g0227 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.883-31752C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125013459 | ||||||
| chr6:125013550
|
G | GA | 54 | a0001c0001t0001g0051a0001c0001t0001g0068a0001c0001t0001g0084others(51): Show | 55 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.883-31649dupA | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125013550 | |||||
| chr6:125013551
|
A | G | 7 | a0001c0001t0006g0003a0001c0001t0006g0191a0001c0001t0017g0154others(4): Show | 7 | HG01884.hp2 HG02486.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.883-31660A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125013551 | ||||||
| chr6:125013556
|
A | AG | 3 | a0001c0001t0001g0102a0001c0001t0001g0200a0001c0001t0012g0201 | 3 | HG01928.hp1 HG03239.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.883-31655_883-3165 others(5): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125013556 | ||||||
| chr6:125013574
|
G | A | 28 | a0001c0001t0003g0169a0001c0001t0003g0172a0001c0001t0003g0176others(25): Show | 28 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.883-31637G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125013574 | ||||||
| chr6:125013607
|
G | C | 32 | a0001c0001t0003g0169a0001c0001t0003g0172a0001c0001t0003g0176others(29): Show | 32 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.883-31604G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125013607 | ||||||
| chr6:125013942
|
C | T | 3 | a0002c0002t0071g0038a0008c0015t0053g0248a0011c0011t0079g0036 | 3 | HG02922.hp1 HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.883-31269C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125013942 | ||||||
| chr6:125014111
|
C | G | 2 | a0002c0002t0071g0038a0008c0015t0053g0248 | 2 | HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.883-31100C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125014111 | ||||||
| chr6:125014243
|
G | C | 1 | a0011c0011t0079g0036 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.883-30968G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125014243 | ||||||
| chr6:125014266
|
G | A | 32 | a0001c0001t0003g0169a0001c0001t0003g0172a0001c0001t0003g0176others(29): Show | 32 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.883-30945G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125014266 | ||||||
| chr6:125014307
|
A | G | 1 | a0001c0001t0015g0207 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.883-30904A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125014307 | ||||||
| chr6:125014627
|
C | T | 1 | a0001c0001t0005g0114 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.883-30584C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125014627 | ||||||
| chr6:125014772
|
G | A | 1 | a0002c0002t0070g0039 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.883-30439G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125014772 | ||||||
| chr6:125014977
|
G | A | 7 | a0001c0001t0006g0003a0001c0001t0006g0191a0001c0001t0017g0154others(4): Show | 7 | HG01884.hp2 HG02486.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.883-30234G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125014977 | ||||||
| chr6:125015081
|
A | T | 2 | a0001c0003t0013g0185a0001c0003t0013g0186 | 2 | HG02559.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.883-30130A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125015081 | ||||||
| chr6:125015277
|
G | C | 28 | a0001c0001t0003g0169a0001c0001t0003g0172a0001c0001t0003g0176others(25): Show | 28 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.883-29934G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125015277 | ||||||
| chr6:125015340
|
T | G | 1 | a0001c0001t0002g0164 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.883-29871T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125015340 | ||||||
| chr6:125015611
|
C | T | 1 | a0001c0001t0025g0142 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.883-29600C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125015611 | ||||||
| chr6:125015653
|
T | C | 159 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(156): Show | 161 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.883-29558T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125015653 | ||||||
| chr6:125015774
|
A | G | 1 | a0001c0001t0014g0060 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.883-29437A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125015774 | ||||||
| chr6:125015984
|
G | A | 3 | a0002c0002t0071g0038a0008c0015t0053g0248a0011c0011t0079g0036 | 3 | HG02922.hp1 HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.883-29227G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125015984 | ||||||
| chr6:125016021
|
T | A | 1 | a0001c0001t0001g0069 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.883-29190T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125016021 | ||||||
| chr6:125016036
|
T | C | 1 | a0002c0002t0070g0039 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.883-29175T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125016036 | ||||||
| chr6:125016179
|
A | G | 1 | a0002c0002t0075g0040 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.883-29032A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125016179 | ||||||
| chr6:125016303
|
G | A | 2 | a0002c0002t0075g0040a0002c0002t0077g0034 | 2 | HG01934.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.883-28908G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125016303 | ||||||
| chr6:125016745
|
G | T | 1 | a0001c0001t0005g0218 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.883-28466G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125016745 | ||||||
| chr6:125016830
|
T | C | 1 | a0001c0001t0010g0145 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.883-28381T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125016830 | ||||||
| chr6:125016841
|
T | A | 175 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0048others(172): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.883-28370T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125016841 | ||||||
| chr6:125016956
|
A | G | 3 | a0001c0003t0010g0266a0002c0002t0071g0038a0006c0009t0001g0265 | 3 | HG02922.hp2 HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.883-28255A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125016956 | ||||||
| chr6:125017164
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.883-28047C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125017164 | ||||||
| chr6:125017165
|
A | T | 102 | a0001c0001t0001g0064a0001c0001t0001g0084a0001c0001t0001g0102others(99): Show | 103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
intron_variant | MODIFIER | c.883-28046A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125017165 | ||||||
| chr6:125017207
|
C | T | 130 | a0001c0001t0001g0084a0001c0001t0001g0102a0001c0001t0001g0107others(127): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.883-28004C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125017207 | ||||||
| chr6:125017418
|
T | C | 196 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0048others(193): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.883-27793T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125017418 | ||||||
| chr6:125017507
|
G | A | 1 | a0001c0001t0022g0132 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.883-27704G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125017507 | ||||||
| chr6:125017853
|
G | A | 2 | a0001c0001t0017g0101a0001c0001t0041g0099 | 2 | HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.883-27358G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125017853 | ||||||
| chr6:125017957
|
C | T | 1 | a0001c0001t0002g0055 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.883-27254C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125017957 | ||||||
| chr6:125018028
|
G | A | 198 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0048others(195): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.883-27183G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125018028 | ||||||
| chr6:125018123
|
A | T | 1 | a0002c0002t0071g0038 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.883-27088A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125018123 | ||||||
| chr6:125018244
|
T | C | 3 | a0001c0001t0006g0147a0005c0007t0006g0094a0005c0007t0021g0095 | 3 | HG01884.hp1 HG02109.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.883-26967T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125018244 | ||||||
| chr6:125018362
|
C | T | 1 | a0008c0015t0053g0248 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.883-26849C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125018362 | ||||||
| chr6:125018813
|
A | C | 1 | a0001c0001t0001g0228 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.883-26398A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125018813 | ||||||
| chr6:125018907
|
G | C | 1 | a0001c0001t0001g0070 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.883-26304G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125018907 | ||||||
| chr6:125018920
|
G | A | 1 | a0001c0001t0017g0254 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.883-26291G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125018920 | ||||||
| chr6:125019267
|
T | G | 1 | a0001c0001t0004g0071 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.883-25944T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125019267 | ||||||
| chr6:125019269
|
G | T | 1 | a0001c0001t0004g0071 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.883-25942G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125019269 | ||||||
| chr6:125019270
|
T | A | 1 | a0001c0001t0004g0071 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.883-25941T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125019270 | ||||||
| chr6:125019308
|
A | G | 1 | a0001c0001t0004g0243 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.883-25903A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125019308 | ||||||
| chr6:125019445
|
C | T | 198 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0048others(195): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.883-25766C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125019445 | ||||||
| chr6:125019503
|
T | C | 205 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0048others(202): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.883-25708T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125019503 | ||||||
| chr6:125019541
|
T | G | 1 | a0002c0002t0009g0024 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.883-25670T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125019541 | ||||||
| chr6:125019692
|
T | C | 2 | a0001c0001t0017g0101a0001c0001t0041g0099 | 2 | HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.883-25519T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125019692 | ||||||
| chr6:125019830
|
C | CG | 10 | a0001c0001t0001g0111a0001c0001t0001g0215a0001c0001t0001g0235others(7): Show | 10 | HG01358.hp1 HG01433.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.883-25381_883-2538 others(5): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125019830 | ||||||
| chr6:125019831
|
A | AG | 21 | a0001c0001t0001g0158a0001c0001t0001g0209a0001c0001t0001g0217others(18): Show | 21 | HG00408.hp1 HG00408.hp2 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.883-25379dupG | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125019831 | |||||
| chr6:125019831
|
A | AGG | 6 | a0001c0001t0003g0255a0001c0001t0006g0003a0001c0001t0006g0191others(3): Show | 6 | HG02486.hp1 HG02559.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.883-25379_883-2537 others(6): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125019831 | |||||
| chr6:125019831
|
A | G | 61 | a0001c0001t0001g0058a0001c0001t0001g0084a0001c0001t0001g0107others(58): Show | 62 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.883-25380A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125019831 | ||||||
| chr6:125019833
|
T | C | 3 | a0001c0001t0001g0209a0001c0001t0005g0202a0001c0001t0015g0207 | 3 | NA18983.hp2 NA19004.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.883-25378T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125019833 | ||||||
| chr6:125019833
|
T | G | 240 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0048others(237): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.883-25378T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125019833 | ||||||
| chr6:125019836
|
G | C | 3 | a0001c0003t0010g0266a0002c0002t0071g0038a0006c0009t0001g0265 | 3 | HG02922.hp2 HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.883-25375G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125019836 | ||||||
| chr6:125019837
|
G | C | 1 | a0001c0001t0001g0048 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.883-25374G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125019837 | ||||||
| chr6:125019843
|
G | A | 1 | a0001c0001t0001g0072 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.883-25368G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125019843 | ||||||
| chr6:125020193
|
G | A | 98 | a0001c0001t0001g0058a0001c0001t0001g0084a0001c0001t0001g0102others(95): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.883-25018G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125020193 | ||||||
| chr6:125020335
|
A | G | 1 | a0001c0001t0023g0250 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.883-24876A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125020335 | ||||||
| chr6:125020373
|
G | A | 1 | a0011c0011t0079g0036 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.883-24838G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125020373 | ||||||
| chr6:125020431
|
T | G | 1 | a0001c0001t0061g0253 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.883-24780T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125020431 | ||||||
| chr6:125020935
|
T | A | 1 | a0001c0001t0015g0207 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.883-24276T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125020935 | ||||||
| chr6:125020984
|
A | G | 98 | a0001c0001t0001g0058a0001c0001t0001g0084a0001c0001t0001g0102others(95): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.883-24227A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125020984 | ||||||
| chr6:125021268
|
CT | C | 128 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0084others(125): Show | 129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.883-23927delT | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125021268 | |||||
| chr6:125021268
|
CTT | C | 63 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0048others(60): Show | 64 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.883-23928_883-2392 others(6): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125021268 | |||||
| chr6:125021327
|
C | T | 2 | a0001c0003t0008g0187a0001c0003t0008g0188 | 2 | HG01243.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.883-23884C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125021327 | ||||||
| chr6:125021480
|
T | C | 1 | a0001c0001t0001g0052 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.883-23731T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125021480 | ||||||
| chr6:125021481
|
G | C | 1 | a0001c0001t0001g0052 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.883-23730G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125021481 | ||||||
| chr6:125021482
|
G | T | 1 | a0001c0001t0001g0052 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.883-23729G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125021482 | ||||||
| chr6:125021512
|
A | G | 140 | a0001c0001t0001g0058a0001c0001t0001g0084a0001c0001t0001g0102others(137): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.883-23699A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125021512 | ||||||
| chr6:125021512
|
A | T | 65 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0048others(62): Show | 66 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.883-23699A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125021512 | ||||||
| chr6:125021565
|
A | G | 205 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0048others(202): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.883-23646A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125021565 | ||||||
| chr6:125021581
|
A | G | 2 | a0002c0002t0013g0011a0006c0009t0001g0194 | 2 | HG01106.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.883-23630A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125021581 | ||||||
| chr6:125021629
|
G | A | 8 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(5): Show | 8 | HG00423.hp1 HG01243.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.883-23582G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125021629 | ||||||
| chr6:125021728
|
C | A | 1 | a0001c0001t0012g0065 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.883-23483C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125021728 | ||||||
| chr6:125021748
|
A | G | 14 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(11): Show | 14 | HG00099.hp2 HG00639.hp1 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.883-23463A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125021748 | ||||||
| chr6:125021854
|
C | A | 2 | a0001c0001t0001g0200a0001c0001t0005g0081 | 2 | HG01433.hp1 HG01928.hp1 |
intron_variant | MODIFIER | c.883-23357C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125021854 | ||||||
| chr6:125021959
|
G | A | 2 | a0001c0001t0017g0101a0001c0001t0041g0099 | 2 | HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.883-23252G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125021959 | ||||||
| chr6:125022139
|
C | T | 6 | a0001c0001t0003g0255a0001c0001t0006g0003a0001c0001t0006g0191others(3): Show | 6 | HG02486.hp1 HG02559.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.883-23072C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125022139 | ||||||
| chr6:125022381
|
A | G | 3 | a0001c0003t0010g0266a0002c0002t0071g0038a0006c0009t0001g0265 | 3 | HG02922.hp2 HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.883-22830A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125022381 | ||||||
| chr6:125022389
|
C | T | 3 | a0001c0003t0010g0266a0002c0002t0071g0038a0006c0009t0001g0265 | 3 | HG02922.hp2 HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.883-22822C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125022389 | ||||||
| chr6:125022451
|
G | T | 97 | a0001c0001t0001g0058a0001c0001t0001g0084a0001c0001t0001g0102others(94): Show | 98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
intron_variant | MODIFIER | c.883-22760G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125022451 | ||||||
| chr6:125022717
|
G | A | 6 | a0001c0001t0003g0255a0001c0001t0006g0003a0001c0001t0006g0191others(3): Show | 6 | HG02486.hp1 HG02559.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.883-22494G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125022717 | ||||||
| chr6:125022992
|
C | A | 204 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0048others(201): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.883-22219C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125022992 | ||||||
| chr6:125023059
|
T | C | 98 | a0001c0001t0001g0058a0001c0001t0001g0084a0001c0001t0001g0102others(95): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.883-22152T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125023059 | ||||||
| chr6:125023133
|
C | T | 2 | a0001c0001t0010g0145a0001c0001t0022g0132 | 2 | HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.883-22078C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125023133 | ||||||
| chr6:125023150
|
T | G | 224 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0048others(221): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.883-22061T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125023150 | ||||||
| chr6:125023367
|
T | C | 23 | a0001c0001t0003g0169a0001c0001t0003g0172a0001c0001t0003g0176others(20): Show | 23 | HG01257.hp1 HG01258.hp2 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.883-21844T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125023367 | ||||||
| chr6:125023409
|
G | A | 224 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0048others(221): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.883-21802G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125023409 | ||||||
| chr6:125023428
|
G | T | 224 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0048others(221): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.883-21783G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125023428 | ||||||
| chr6:125023678
|
C | T | 2 | a0002c0002t0029g0005a0002c0006t0013g0010 | 2 | NA19065.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.883-21533C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125023678 | ||||||
| chr6:125023754
|
A | G | 1 | a0001c0001t0004g0046 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.883-21457A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125023754 | ||||||
| chr6:125023912
|
G | C | 1 | a0001c0001t0005g0082 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.883-21299G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125023912 | ||||||
| chr6:125024228
|
G | A | 1 | a0011c0011t0079g0036 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.883-20983G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125024228 | ||||||
| chr6:125024362
|
C | T | 4 | a0001c0001t0001g0052a0001c0001t0001g0064a0001c0001t0002g0056others(1): Show | 4 | NA18942.hp1 NA19057.hp2 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.883-20849C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125024362 | ||||||
| chr6:125024416
|
C | T | 53 | a0001c0001t0001g0044a0001c0001t0001g0051a0001c0001t0001g0052others(50): Show | 54 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.883-20795C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125024416 | ||||||
| chr6:125024492
|
C | T | 113 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0048others(110): Show | 114 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.883-20719C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125024492 | ||||||
| chr6:125024493
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.883-20718G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125024493 | ||||||
| chr6:125024584
|
G | A | 1 | a0001c0001t0017g0254 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.883-20627G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125024584 | ||||||
| chr6:125024632
|
A | G | 1 | a0001c0001t0003g0115 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.883-20579A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125024632 | ||||||
| chr6:125024635
|
T | G | 19 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(16): Show | 19 | HG00099.hp2 HG00735.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.883-20576T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125024635 | ||||||
| chr6:125024706
|
T | C | 1 | a0001c0001t0004g0075 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.883-20505T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125024706 | ||||||
| chr6:125024719
|
C | CA | 10 | a0001c0001t0001g0244a0001c0001t0003g0169a0001c0001t0019g0239others(7): Show | 10 | HG00741.hp1 HG00741.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.883-20471dupA | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125024719 | |||||
| chr6:125024719
|
CA | C | 84 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0050others(81): Show | 85 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.883-20471delA | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125024719 | |||||
| chr6:125024719
|
CAA | C | 6 | a0001c0001t0003g0255a0001c0001t0006g0191a0001c0001t0010g0163others(3): Show | 6 | HG01891.hp2 HG02559.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.883-20472_883-2047 others(6): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125024719 | |||||
| chr6:125024721
|
A | C | 1 | a0001c0001t0001g0200 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.883-20490A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125024721 | ||||||
| chr6:125024929
|
G | C | 1 | a0001c0001t0002g0234 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.883-20282G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125024929 | ||||||
| chr6:125025038
|
C | T | 21 | a0001c0001t0003g0169a0001c0001t0003g0172a0001c0001t0003g0176others(18): Show | 21 | HG01257.hp1 HG01258.hp2 HG01346.hp1 others(18): Show |
intron_variant | MODIFIER | c.883-20173C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125025038 | ||||||
| chr6:125025367
|
TTTTTTGT others(4): Show |
T | 2 | a0001c0001t0001g0158a0003c0004t0011g0157 | 2 | HG00741.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.883-19839_883-1982 others(15): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125025367 | |||||
| chr6:125025521
|
G | C | 19 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(16): Show | 19 | HG00099.hp2 HG00735.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.883-19690G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125025521 | ||||||
| chr6:125025576
|
A | AAGGG | 65 | a0001c0001t0001g0043a0001c0001t0001g0158a0001c0001t0001g0228others(62): Show | 65 | HG00423.hp1 HG00741.hp1 HG01243.hp1 others(62): Show |
intron_variant | MODIFIER | c.883-19617_883-1961 others(8): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125025576 | |||||
| chr6:125025666
|
T | G | 145 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0048others(142): Show | 146 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.883-19545T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125025666 | ||||||
| chr6:125025755
|
AGGAG | A | 15 | a0001c0001t0001g0051a0001c0001t0003g0169a0001c0001t0003g0172others(12): Show | 15 | HG01346.hp2 HG02055.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.883-19436_883-1943 others(8): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125025755 | |||||
| chr6:125025802
|
T | C | 6 | a0001c0001t0010g0145a0001c0001t0017g0101a0001c0001t0021g0133others(3): Show | 6 | HG02622.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.883-19409T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125025802 | ||||||
| chr6:125025817
|
T | C | 16 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(13): Show | 16 | HG00099.hp2 HG00735.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.883-19394T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125025817 | ||||||
| chr6:125025862
|
C | T | 1 | a0001c0001t0003g0240 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.883-19349C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125025862 | ||||||
| chr6:125025877
|
T | G | 1 | a0002c0002t0075g0040 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.883-19334T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125025877 | ||||||
| chr6:125025993
|
C | T | 1 | a0001c0001t0001g0077 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.883-19218C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125025993 | ||||||
| chr6:125026353
|
G | T | 19 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(16): Show | 19 | HG00099.hp2 HG00735.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.883-18858G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125026353 | ||||||
| chr6:125026533
|
T | C | 5 | a0001c0001t0006g0174a0001c0001t0008g0182a0001c0001t0022g0180others(2): Show | 5 | HG02055.hp2 HG02109.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-18678T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125026533 | ||||||
| chr6:125026545
|
C | T | 1 | a0001c0001t0056g0112 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.883-18666C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125026545 | ||||||
| chr6:125026547
|
T | A | 16 | a0001c0001t0003g0169a0001c0001t0003g0172a0001c0001t0003g0176others(13): Show | 16 | HG02055.hp2 HG02109.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.883-18664T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125026547 | ||||||
| chr6:125026550
|
C | T | 6 | a0001c0001t0010g0145a0001c0001t0017g0101a0001c0001t0021g0133others(3): Show | 6 | HG02622.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.883-18661C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125026550 | ||||||
| chr6:125026656
|
A | T | 246 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(243): Show | 248 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.883-18555A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125026656 | ||||||
| chr6:125026702
|
G | C | 1 | a0001c0001t0001g0107 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.883-18509G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125026702 | ||||||
| chr6:125026781
|
A | G | 13 | a0001c0001t0001g0263a0001c0001t0004g0183a0001c0001t0004g0227others(10): Show | 13 | HG00140.hp2 HG01192.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.883-18430A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125026781 | ||||||
| chr6:125026901
|
A | C | 1 | a0001c0001t0003g0002 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.883-18310A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125026901 | ||||||
| chr6:125026911
|
G | A | 6 | a0001c0001t0003g0255a0001c0001t0006g0003a0001c0001t0006g0191others(3): Show | 6 | HG02486.hp1 HG02559.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.883-18300G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125026911 | ||||||
| chr6:125026918
|
G | A | 2 | a0001c0001t0001g0231a0001c0001t0002g0087 | 2 | HG00323.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.883-18293G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125026918 | ||||||
| chr6:125026944
|
G | A | 1 | a0001c0001t0003g0115 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.883-18267G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125026944 | ||||||
| chr6:125026995
|
A | T | 246 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(243): Show | 248 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.883-18216A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125026995 | ||||||
| chr6:125027007
|
C | T | 251 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(248): Show | 253 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.883-18204C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125027007 | ||||||
| chr6:125027033
|
A | T | 1 | a0001c0012t0031g0256 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.883-18178A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125027033 | ||||||
| chr6:125027294
|
C | T | 182 | a0001c0001t0001g0044a0001c0001t0001g0047a0001c0001t0001g0048others(179): Show | 184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.883-17917C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125027294 | ||||||
| chr6:125027300
|
T | C | 246 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(243): Show | 248 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.883-17911T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125027300 | ||||||
| chr6:125027352
|
C | T | 14 | a0001c0001t0003g0169a0001c0001t0003g0172a0001c0001t0003g0176others(11): Show | 14 | HG02055.hp2 HG02109.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.883-17859C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125027352 | ||||||
| chr6:125027578
|
C | T | 1 | a0001c0001t0036g0232 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.883-17633C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125027578 | ||||||
| chr6:125027781
|
A | G | 33 | a0001c0001t0001g0043a0001c0001t0001g0228a0001c0001t0001g0236others(30): Show | 33 | HG00423.hp1 HG01243.hp1 HG01257.hp1 others(30): Show |
intron_variant | MODIFIER | c.883-17430A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125027781 | ||||||
| chr6:125027862
|
C | T | 246 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(243): Show | 248 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.883-17349C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125027862 | ||||||
| chr6:125027911
|
G | A | 54 | a0001c0001t0001g0044a0001c0001t0001g0048a0001c0001t0001g0050others(51): Show | 55 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.883-17300G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125027911 | ||||||
| chr6:125027958
|
A | AT | 3 | a0001c0001t0026g0168a0001c0001t0045g0161a0001c0001t0046g0196 | 3 | HG03130.hp1 HG03486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.883-17247dupT | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125027958 | |||||
| chr6:125028034
|
A | G | 246 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(243): Show | 248 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.883-17177A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125028034 | ||||||
| chr6:125028273
|
C | T | 1 | a0001c0001t0005g0130 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.883-16938C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125028273 | ||||||
| chr6:125028315
|
G | T | 2 | a0001c0001t0001g0158a0003c0004t0011g0157 | 2 | HG00741.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.883-16896G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125028315 | ||||||
| chr6:125028361
|
A | G | 1 | a0001c0001t0067g0199 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.883-16850A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125028361 | ||||||
| chr6:125028414
|
C | T | 246 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(243): Show | 248 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.883-16797C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125028414 | ||||||
| chr6:125028423
|
A | G | 3 | a0001c0001t0026g0168a0001c0001t0045g0161a0001c0001t0046g0196 | 3 | HG03130.hp1 HG03486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.883-16788A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125028423 | ||||||
| chr6:125028630
|
TA | T | 3 | a0001c0001t0006g0156a0001c0003t0008g0131a0001c0003t0008g0175 | 3 | HG03471.hp2 HG06807.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.883-16577delA | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125028630 | |||||
| chr6:125028741
|
T | G | 61 | a0001c0001t0001g0043a0001c0001t0001g0228a0001c0001t0002g0059others(58): Show | 61 | HG00423.hp1 HG01243.hp1 HG01257.hp1 others(58): Show |
intron_variant | MODIFIER | c.883-16470T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125028741 | ||||||
| chr6:125028989
|
A | G | 246 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(243): Show | 248 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.883-16222A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125028989 | ||||||
| chr6:125029282
|
C | T | 1 | a0001c0001t0010g0163 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.883-15929C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125029282 | ||||||
| chr6:125029286
|
G | T | 184 | a0001c0001t0001g0044a0001c0001t0001g0047a0001c0001t0001g0048others(181): Show | 186 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.883-15925G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125029286 | ||||||
| chr6:125029479
|
G | A | 1 | a0001c0003t0008g0193 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.883-15732G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125029479 | ||||||
| chr6:125029542
|
G | C | 1 | a0001c0001t0004g0242 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.883-15669G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125029542 | ||||||
| chr6:125029665
|
A | G | 6 | a0001c0001t0006g0147a0001c0001t0006g0191a0001c0001t0039g0179others(3): Show | 6 | HG01884.hp1 HG02109.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.883-15546A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125029665 | ||||||
| chr6:125029671
|
T | A | 1 | a0001c0001t0021g0133 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.883-15540T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125029671 | ||||||
| chr6:125030028
|
C | T | 4 | a0001c0001t0063g0091a0002c0002t0029g0005a0002c0006t0013g0010others(1): Show | 4 | NA18970.hp2 NA19002.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.883-15183C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125030028 | ||||||
| chr6:125030032
|
A | T | 2 | a0001c0003t0010g0266a0006c0009t0001g0265 | 2 | HG02922.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.883-15179A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125030032 | ||||||
| chr6:125030052
|
A | C | 2 | a0001c0001t0010g0145a0001c0001t0022g0132 | 2 | HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.883-15159A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125030052 | ||||||
| chr6:125030070
|
A | G | 23 | a0001c0001t0001g0263a0001c0001t0003g0002a0001c0001t0004g0155others(20): Show | 24 | HG00140.hp2 HG01192.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.883-15141A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125030070 | ||||||
| chr6:125030075
|
A | G | 1 | a0001c0001t0043g0004 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.883-15136A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125030075 | ||||||
| chr6:125030251
|
G | T | 2 | a0001c0001t0002g0066a0002c0002t0009g0014 | 2 | HG00735.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.883-14960G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125030251 | ||||||
| chr6:125030356
|
A | T | 1 | a0001c0001t0004g0155 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.883-14855A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125030356 | ||||||
| chr6:125030516
|
A | G | 2 | a0001c0001t0021g0133a0001c0001t0033g0134 | 2 | HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.883-14695A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125030516 | ||||||
| chr6:125030765
|
G | A | 10 | a0001c0001t0003g0169a0001c0001t0003g0172a0001c0001t0003g0176others(7): Show | 10 | HG02109.hp1 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.883-14446G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125030765 | ||||||
| chr6:125030784
|
T | A | 3 | a0001c0001t0010g0145a0001c0001t0021g0133a0001c0001t0033g0134 | 3 | HG02622.hp1 HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.883-14427T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125030784 | ||||||
| chr6:125030836
|
GA | G | 3 | a0001c0001t0006g0147a0005c0007t0006g0094a0005c0007t0021g0095 | 3 | HG01884.hp1 HG02109.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.883-14374delA | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125030836 | ||||||
| chr6:125030848
|
A | G | 10 | a0001c0001t0001g0152a0001c0001t0001g0158a0001c0001t0001g0216others(7): Show | 10 | HG00741.hp1 HG01358.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.883-14363A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125030848 | ||||||
| chr6:125030891
|
G | A | 2 | a0001c0003t0008g0131a0001c0003t0008g0175 | 2 | HG03471.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.883-14320G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125030891 | ||||||
| chr6:125030912
|
T | G | 1 | a0001c0001t0022g0042 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.883-14299T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125030912 | ||||||
| chr6:125031031
|
C | T | 130 | a0001c0001t0001g0044a0001c0001t0001g0048a0001c0001t0001g0050others(127): Show | 131 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.883-14180C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125031031 | ||||||
| chr6:125031086
|
C | T | 62 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0070others(59): Show | 63 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.883-14125C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125031086 | ||||||
| chr6:125031215
|
G | A | 112 | a0001c0001t0001g0044a0001c0001t0001g0048a0001c0001t0001g0050others(109): Show | 113 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.883-13996G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125031215 | ||||||
| chr6:125031244
|
G | C | 238 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(235): Show | 240 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.883-13967G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125031244 | ||||||
| chr6:125031412
|
C | T | 15 | a0001c0001t0001g0047a0001c0001t0001g0241a0001c0001t0002g0055others(12): Show | 15 | HG01106.hp1 HG02055.hp1 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.883-13799C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125031412 | ||||||
| chr6:125031626
|
T | A | 10 | a0001c0001t0001g0152a0001c0001t0001g0158a0001c0001t0001g0216others(7): Show | 10 | HG00741.hp1 HG01358.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.883-13585T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125031626 | ||||||
| chr6:125031719
|
A | G | 1 | a0006c0009t0001g0194 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.883-13492A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125031719 | ||||||
| chr6:125031884
|
T | G | 102 | a0001c0001t0001g0043a0001c0001t0001g0047a0001c0001t0001g0063others(99): Show | 103 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(100): Show |
intron_variant | MODIFIER | c.883-13327T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125031884 | ||||||
| chr6:125031885
|
T | C | 102 | a0001c0001t0001g0043a0001c0001t0001g0047a0001c0001t0001g0063others(99): Show | 103 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(100): Show |
intron_variant | MODIFIER | c.883-13326T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125031885 | ||||||
| chr6:125031892
|
A | G | 1 | a0001c0003t0008g0193 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.883-13319A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125031892 | ||||||
| chr6:125031943
|
C | T | 1 | a0001c0001t0046g0196 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.883-13268C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125031943 | ||||||
| chr6:125031997
|
A | G | 15 | a0001c0001t0001g0047a0001c0001t0001g0241a0001c0001t0002g0055others(12): Show | 15 | HG01106.hp1 HG02055.hp1 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.883-13214A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125031997 | ||||||
| chr6:125032094
|
C | T | 15 | a0001c0001t0001g0047a0001c0001t0001g0241a0001c0001t0002g0055others(12): Show | 15 | HG01106.hp1 HG02055.hp1 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.883-13117C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125032094 | ||||||
| chr6:125032340
|
A | G | 4 | a0001c0003t0008g0151a0001c0003t0008g0187a0001c0003t0008g0188others(1): Show | 4 | HG01243.hp1 HG02280.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.883-12871A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125032340 | ||||||
| chr6:125032664
|
A | G | 1 | a0001c0001t0005g0061 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.883-12547A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125032664 | ||||||
| chr6:125032812
|
A | C | 2 | a0001c0001t0001g0210a0001c0001t0001g0217 | 2 | HG00408.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.883-12399A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125032812 | ||||||
| chr6:125033008
|
A | C | 139 | a0001c0001t0001g0044a0001c0001t0001g0048a0001c0001t0001g0050others(136): Show | 140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.883-12203A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125033008 | ||||||
| chr6:125033106
|
T | C | 15 | a0001c0001t0001g0047a0001c0001t0001g0241a0001c0001t0002g0055others(12): Show | 15 | HG01106.hp1 HG02055.hp1 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.883-12105T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125033106 | ||||||
| chr6:125033128
|
G | A | 15 | a0001c0001t0004g0155a0001c0001t0004g0183a0001c0001t0006g0003others(12): Show | 15 | HG00140.hp2 HG02486.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.883-12083G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125033128 | ||||||
| chr6:125033221
|
T | C | 139 | a0001c0001t0001g0044a0001c0001t0001g0048a0001c0001t0001g0050others(136): Show | 140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.883-11990T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125033221 | ||||||
| chr6:125033444
|
G | A | 1 | a0001c0001t0006g0264 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.883-11767G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125033444 | ||||||
| chr6:125033449
|
G | GT | 56 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0070others(53): Show | 57 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.883-11756dupT | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125033449 | |||||
| chr6:125033505
|
C | T | 78 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0070others(75): Show | 79 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.883-11706C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125033505 | ||||||
| chr6:125033516
|
A | G | 1 | a0001c0001t0012g0220 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.883-11695A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125033516 | ||||||
| chr6:125033571
|
C | T | 68 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0070others(65): Show | 69 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.883-11640C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125033571 | ||||||
| chr6:125033644
|
G | A | 3 | a0001c0001t0026g0168a0001c0001t0045g0161a0001c0001t0046g0196 | 3 | HG03130.hp1 HG03486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.883-11567G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125033644 | ||||||
| chr6:125033646
|
AATAAACA others(9): Show |
A | 1 | a0001c0003t0008g0193 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.883-11562_883-1154 others(20): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125033646 | |||||
| chr6:125033655
|
A | G | 1 | a0001c0001t0002g0249 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.883-11556A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125033655 | ||||||
| chr6:125033825
|
T | C | 3 | a0001c0001t0001g0152a0001c0001t0001g0216a0001c0001t0004g0046 | 3 | HG01358.hp2 HG04228.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.883-11386T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125033825 | ||||||
| chr6:125033891
|
G | C | 1 | a0001c0001t0002g0087 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.883-11320G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125033891 | ||||||
| chr6:125034150
|
A | G | 1 | a0001c0001t0023g0250 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.883-11061A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125034150 | ||||||
| chr6:125034155
|
T | C | 1 | a0001c0001t0023g0250 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.883-11056T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125034155 | ||||||
| chr6:125034229
|
G | A | 1 | a0002c0002t0071g0038 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.883-10982G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125034229 | ||||||
| chr6:125034370
|
G | A | 15 | a0001c0001t0001g0047a0001c0001t0001g0241a0001c0001t0002g0055others(12): Show | 15 | HG01106.hp1 HG02055.hp1 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.883-10841G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125034370 | ||||||
| chr6:125034477
|
G | C | 1 | a0001c0003t0008g0193 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.883-10734G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125034477 | ||||||
| chr6:125034513
|
C | T | 54 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0070others(51): Show | 55 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.883-10698C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125034513 | ||||||
| chr6:125034514
|
G | A | 1 | a0001c0001t0002g0234 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.883-10697G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125034514 | ||||||
| chr6:125034515
|
A | G | 23 | a0001c0001t0001g0047a0001c0001t0001g0241a0001c0001t0002g0055others(20): Show | 23 | HG01106.hp1 HG01884.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.883-10696A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125034515 | ||||||
| chr6:125034604
|
T | A | 5 | a0001c0001t0006g0003a0001c0001t0021g0159a0001c0001t0026g0160others(2): Show | 5 | HG02486.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-10607T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125034604 | ||||||
| chr6:125034645
|
G | T | 138 | a0001c0001t0001g0044a0001c0001t0001g0048a0001c0001t0001g0050others(135): Show | 139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.883-10566G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125034645 | ||||||
| chr6:125034764
|
C | T | 1 | a0001c0003t0008g0193 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.883-10447C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125034764 | ||||||
| chr6:125034772
|
A | G | 7 | a0001c0001t0006g0147a0001c0001t0010g0163a0001c0003t0010g0266others(4): Show | 7 | HG01884.hp1 HG01891.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.883-10439A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125034772 | ||||||
| chr6:125034850
|
G | C | 1 | a0001c0003t0008g0193 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.883-10361G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125034850 | ||||||
| chr6:125034894
|
C | G | 1 | a0002c0002t0071g0038 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.883-10317C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125034894 | ||||||
| chr6:125034915
|
C | A | 137 | a0001c0001t0001g0044a0001c0001t0001g0048a0001c0001t0001g0050others(134): Show | 138 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.883-10296C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125034915 | ||||||
| chr6:125035015
|
T | C | 12 | a0001c0001t0003g0169a0001c0001t0003g0172a0001c0001t0003g0176others(9): Show | 12 | HG02109.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.883-10196T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125035015 | ||||||
| chr6:125035022
|
G | T | 1 | a0001c0001t0001g0244 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.883-10189G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125035022 | ||||||
| chr6:125035086
|
G | A | 4 | a0001c0001t0003g0169a0001c0001t0003g0176a0001c0001t0003g0178others(1): Show | 4 | HG02451.hp1 HG02572.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.883-10125G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125035086 | ||||||
| chr6:125035104
|
C | T | 1 | a0001c0001t0010g0163 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.883-10107C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125035104 | ||||||
| chr6:125035247
|
G | A | 15 | a0001c0001t0001g0047a0001c0001t0001g0241a0001c0001t0002g0055others(12): Show | 15 | HG01106.hp1 HG02055.hp1 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.883-9964G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125035247 | ||||||
| chr6:125035501
|
T | G | 1 | a0001c0001t0026g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.883-9710T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125035501 | ||||||
| chr6:125035520
|
T | C | 15 | a0001c0001t0001g0047a0001c0001t0001g0241a0001c0001t0002g0055others(12): Show | 15 | HG01106.hp1 HG02055.hp1 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.883-9691T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125035520 | ||||||
| chr6:125035732
|
T | C | 1 | a0002c0006t0078g0007 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.883-9479T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125035732 | ||||||
| chr6:125035755
|
A | G | 15 | a0001c0001t0001g0047a0001c0001t0001g0241a0001c0001t0002g0055others(12): Show | 15 | HG01106.hp1 HG02055.hp1 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.883-9456A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125035755 | ||||||
| chr6:125036129
|
G | A | 4 | a0001c0001t0006g0156a0001c0001t0048g0162a0001c0003t0008g0131others(1): Show | 4 | HG03041.hp2 HG03471.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.883-9082G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125036129 | ||||||
| chr6:125036371
|
G | T | 1 | a0002c0002t0077g0034 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.883-8840G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125036371 | ||||||
| chr6:125036432
|
G | A | 6 | a0001c0001t0001g0158a0001c0001t0008g0182a0001c0001t0017g0254others(3): Show | 6 | HG00741.hp1 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.883-8779G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125036432 | ||||||
| chr6:125036496
|
C | T | 15 | a0001c0001t0001g0047a0001c0001t0001g0241a0001c0001t0002g0055others(12): Show | 15 | HG01106.hp1 HG02055.hp1 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.883-8715C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125036496 | ||||||
| chr6:125036523
|
G | T | 1 | a0001c0001t0035g0140 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.883-8688G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125036523 | ||||||
| chr6:125036553
|
A | G | 1 | a0001c0003t0008g0193 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.883-8658A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125036553 | ||||||
| chr6:125036660
|
G | A | 1 | a0001c0001t0017g0154 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.883-8551G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125036660 | ||||||
| chr6:125036773
|
G | A | 22 | a0001c0001t0001g0047a0001c0001t0001g0241a0001c0001t0002g0055others(19): Show | 22 | HG01106.hp1 HG01884.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.883-8438G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125036773 | ||||||
| chr6:125036838
|
C | T | 1 | a0001c0003t0008g0193 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.883-8373C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125036838 | ||||||
| chr6:125036844
|
A | G | 54 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0070others(51): Show | 55 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.883-8367A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125036844 | ||||||
| chr6:125036891
|
T | G | 15 | a0001c0001t0001g0047a0001c0001t0001g0241a0001c0001t0002g0055others(12): Show | 15 | HG01106.hp1 HG02055.hp1 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.883-8320T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125036891 | ||||||
| chr6:125036925
|
A | C | 1 | a0001c0001t0004g0155 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.883-8286A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125036925 | ||||||
| chr6:125036926
|
G | A | 54 | a0001c0001t0001g0043a0001c0001t0001g0063a0001c0001t0001g0070others(51): Show | 55 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.883-8285G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125036926 | ||||||
| chr6:125037037
|
G | A | 1 | a0002c0002t0071g0038 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.883-8174G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125037037 | ||||||
| chr6:125037077
|
GA | G | 15 | a0001c0001t0001g0047a0001c0001t0001g0241a0001c0001t0002g0055others(12): Show | 15 | HG01106.hp1 HG02055.hp1 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.883-8121delA | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125037077 | |||||
| chr6:125037181
|
A | T | 1 | a0001c0001t0005g0081 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.883-8030A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125037181 | ||||||
| chr6:125037326
|
C | G | 1 | a0001c0001t0001g0200 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.883-7885C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125037326 | ||||||
| chr6:125037541
|
G | A | 1 | a0001c0003t0008g0193 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.883-7670G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125037541 | ||||||
| chr6:125037626
|
G | T | 2 | a0001c0001t0005g0061a0001c0001t0062g0197 | 2 | NA18988.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.883-7585G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125037626 | ||||||
| chr6:125037737
|
A | T | 1 | a0001c0001t0019g0119 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.883-7474A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125037737 | ||||||
| chr6:125037767
|
C | G | 10 | a0001c0001t0001g0152a0001c0001t0001g0158a0001c0001t0001g0216others(7): Show | 10 | HG00741.hp1 HG01358.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.883-7444C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125037767 | ||||||
| chr6:125037953
|
G | A | 16 | a0001c0001t0001g0047a0001c0001t0001g0241a0001c0001t0002g0055others(13): Show | 16 | HG01106.hp1 HG02055.hp1 HG02132.hp1 others(13): Show |
intron_variant | MODIFIER | c.883-7258G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125037953 | ||||||
| chr6:125037955
|
C | A | 16 | a0001c0001t0001g0047a0001c0001t0001g0241a0001c0001t0002g0055others(13): Show | 16 | HG01106.hp1 HG02055.hp1 HG02132.hp1 others(13): Show |
intron_variant | MODIFIER | c.883-7256C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125037955 | ||||||
| chr6:125038242
|
T | G | 257 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(254): Show | 259 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.883-6969T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125038242 | ||||||
| chr6:125038243
|
T | A | 257 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(254): Show | 259 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.883-6968T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125038243 | ||||||
| chr6:125038547
|
G | T | 5 | a0001c0001t0001g0063a0001c0001t0001g0080a0001c0001t0001g0200others(2): Show | 5 | HG01928.hp1 HG01952.hp1 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.883-6664G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125038547 | ||||||
| chr6:125038739
|
A | G | 1 | a0001c0001t0002g0067 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.883-6472A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125038739 | ||||||
| chr6:125038895
|
G | A | 15 | a0001c0001t0001g0047a0001c0001t0001g0241a0001c0001t0002g0055others(12): Show | 15 | HG01106.hp1 HG02055.hp1 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.883-6316G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125038895 | ||||||
| chr6:125039053
|
A | C | 140 | a0001c0001t0001g0044a0001c0001t0001g0048a0001c0001t0001g0050others(137): Show | 141 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.883-6158A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125039053 | ||||||
| chr6:125039332
|
A | G | 1 | a0001c0001t0022g0132 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.883-5879A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125039332 | ||||||
| chr6:125039443
|
C | G | 1 | a0006c0009t0001g0194 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.883-5768C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125039443 | ||||||
| chr6:125039516
|
A | C | 238 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0047others(235): Show | 240 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.883-5695A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125039516 | ||||||
| chr6:125039562
|
A | G | 17 | a0001c0001t0001g0047a0001c0001t0001g0241a0001c0001t0002g0055others(14): Show | 17 | HG01106.hp1 HG02055.hp1 HG02132.hp1 others(14): Show |
intron_variant | MODIFIER | c.883-5649A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125039562 | ||||||
| chr6:125039861
|
C | T | 101 | a0001c0001t0001g0044a0001c0001t0001g0048a0001c0001t0001g0050others(98): Show | 102 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.883-5350C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125039861 | ||||||
| chr6:125039908
|
A | G | 1 | a0001c0001t0015g0252 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.883-5303A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125039908 | ||||||
| chr6:125040119
|
T | A | 15 | a0001c0001t0001g0047a0001c0001t0001g0241a0001c0001t0002g0055others(12): Show | 15 | HG01106.hp1 HG02055.hp1 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.883-5092T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125040119 | ||||||
| chr6:125040267
|
C | T | 135 | a0001c0001t0001g0044a0001c0001t0001g0048a0001c0001t0001g0050others(132): Show | 136 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.883-4944C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125040267 | ||||||
| chr6:125040406
|
C | T | 3 | a0001c0001t0010g0145a0001c0001t0021g0133a0001c0001t0033g0134 | 3 | HG02622.hp1 HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.883-4805C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125040406 | ||||||
| chr6:125040422
|
C | T | 1 | a0001c0001t0005g0208 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.883-4789C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125040422 | ||||||
| chr6:125040734
|
A | G | 1 | a0001c0001t0022g0180 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.883-4477A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125040734 | ||||||
| chr6:125040938
|
A | G | 1 | a0001c0003t0008g0193 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.883-4273A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125040938 | ||||||
| chr6:125040964
|
A | T | 1 | a0002c0006t0013g0010 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.883-4247A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125040964 | ||||||
| chr6:125040967
|
A | G | 1 | a0006c0009t0001g0194 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.883-4244A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125040967 | ||||||
| chr6:125041047
|
T | C | 10 | a0001c0001t0001g0152a0001c0001t0001g0158a0001c0001t0001g0216others(7): Show | 10 | HG00741.hp1 HG01358.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.883-4164T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125041047 | ||||||
| chr6:125041395
|
C | G | 1 | a0001c0003t0008g0193 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.883-3816C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125041395 | ||||||
| chr6:125041414
|
A | T | 1 | a0001c0001t0005g0130 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.883-3797A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125041414 | ||||||
| chr6:125041437
|
A | G | 15 | a0001c0001t0001g0047a0001c0001t0001g0241a0001c0001t0002g0055others(12): Show | 15 | HG01106.hp1 HG02055.hp1 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.883-3774A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125041437 | ||||||
| chr6:125041478
|
T | C | 1 | a0001c0001t0015g0045 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.883-3733T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125041478 | ||||||
| chr6:125041583
|
C | T | 1 | a0001c0001t0062g0197 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.883-3628C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125041583 | ||||||
| chr6:125042454
|
A | T | 1 | a0001c0003t0008g0193 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.883-2757A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125042454 | ||||||
| chr6:125042557
|
T | C | 1 | a0001c0001t0004g0117 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.883-2654T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125042557 | ||||||
| chr6:125042744
|
C | A | 21 | a0001c0001t0001g0047a0001c0001t0001g0241a0001c0001t0002g0055others(18): Show | 21 | HG01106.hp1 HG01884.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.883-2467C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125042744 | ||||||
| chr6:125042927
|
T | G | 12 | a0001c0001t0003g0169a0001c0001t0003g0172a0001c0001t0003g0176others(9): Show | 12 | HG02109.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.883-2284T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125042927 | ||||||
| chr6:125042993
|
A | C | 2 | a0002c0002t0009g0012a0002c0002t0009g0013 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.883-2218A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125042993 | ||||||
| chr6:125043056
|
T | C | 7 | a0001c0001t0001g0158a0001c0001t0008g0182a0001c0001t0017g0254others(4): Show | 7 | HG00741.hp1 HG01891.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.883-2155T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125043056 | ||||||
| chr6:125043388
|
G | A | 1 | a0001c0001t0052g0049 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.883-1823G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125043388 | ||||||
| chr6:125043412
|
A | G | 1 | a0002c0002t0071g0038 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.883-1799A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125043412 | ||||||
| chr6:125043504
|
C | G | 2 | a0001c0001t0001g0231a0002c0002t0009g0025 | 2 | HG00323.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.883-1707C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125043504 | ||||||
| chr6:125043561
|
A | G | 1 | a0001c0001t0012g0126 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.883-1650A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125043561 | ||||||
| chr6:125043712
|
G | A | 4 | a0001c0001t0002g0086a0002c0002t0007g0026a0002c0002t0009g0024others(1): Show | 4 | HG01981.hp2 HG03669.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.883-1499G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125043712 | ||||||
| chr6:125043859
|
A | G | 137 | a0001c0001t0001g0044a0001c0001t0001g0048a0001c0001t0001g0050others(134): Show | 138 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.883-1352A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125043859 | ||||||
| chr6:125043959
|
A | G | 1 | a0001c0001t0019g0239 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.883-1252A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125043959 | ||||||
| chr6:125044058
|
GT | G | 141 | a0001c0001t0001g0044a0001c0001t0001g0048a0001c0001t0001g0050others(138): Show | 142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.883-1142delT | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125044058 | |||||
| chr6:125044149
|
C | T | 134 | a0001c0001t0001g0044a0001c0001t0001g0048a0001c0001t0001g0050others(131): Show | 135 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.883-1062C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125044149 | ||||||
| chr6:125044327
|
C | T | 131 | a0001c0001t0001g0044a0001c0001t0001g0048a0001c0001t0001g0050others(128): Show | 131 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.883-884C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125044327 | ||||||
| chr6:125044402
|
T | C | 3 | a0001c0001t0001g0158a0001c0001t0008g0182a0001c0001t0022g0180 | 3 | HG01891.hp1 HG02055.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.883-809T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125044402 | ||||||
| chr6:125044486
|
T | G | 78 | a0001c0001t0001g0043a0001c0001t0001g0058a0001c0001t0001g0063others(75): Show | 80 | HG00408.hp1 HG00408.hp2 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.883-725T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125044486 | ||||||
| chr6:125044502
|
A | T | 153 | a0001c0001t0001g0044a0001c0001t0001g0048a0001c0001t0001g0050others(150): Show | 153 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.883-709A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125044502 | ||||||
| chr6:125044541
|
A | T | 1 | a0001c0001t0041g0099 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.883-670A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125044541 | ||||||
| chr6:125044620
|
G | T | 128 | a0001c0001t0001g0044a0001c0001t0001g0048a0001c0001t0001g0050others(125): Show | 128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.883-591G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125044620 | ||||||
| chr6:125044716
|
A | G | 1 | a0001c0001t0068g0245 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.883-495A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125044716 | ||||||
| chr6:125045143
|
C | CA | 18 | a0001c0001t0001g0047a0001c0001t0001g0209a0001c0001t0002g0055others(15): Show | 18 | HG01106.hp1 HG02056.hp1 HG02132.hp1 others(15): Show |
intron_variant | MODIFIER | c.883-57dupA | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125045143 | |||||
| chr6:125045143
|
CA | C | 72 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0058others(69): Show | 74 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.883-57delA | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125045143 | |||||
| chr6:125045179
|
T | G | 1 | a0001c0001t0054g0181 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.883-32T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125045179 | ||||||
| chr6:125045784
|
T | C | 13 | a0001c0001t0001g0057a0001c0001t0001g0104a0001c0001t0001g0105others(10): Show | 13 | HG01243.hp2 HG01261.hp1 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.1116+340T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125045784 | ||||||
| chr6:125045955
|
G | A | 69 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0058others(66): Show | 71 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.1116+511G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125045955 | ||||||
| chr6:125046237
|
G | A | 3 | a0001c0001t0001g0084a0001c0001t0001g0125a0001c0001t0012g0126 | 3 | HG00140.hp1 HG02486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1116+793G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125046237 | ||||||
| chr6:125046277
|
G | A | 1 | a0001c0001t0002g0056 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1116+833G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125046277 | ||||||
| chr6:125046307
|
A | G | 1 | a0001c0001t0002g0221 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1116+863A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125046307 | ||||||
| chr6:125046510
|
C | G | 11 | a0001c0001t0003g0169a0001c0001t0003g0172a0001c0001t0003g0176others(8): Show | 11 | HG02109.hp1 HG02280.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1116+1066C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125046510 | ||||||
| chr6:125046647
|
T | C | 1 | a0001c0001t0016g0222 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1116+1203T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125046647 | ||||||
| chr6:125046727
|
G | A | 1 | a0002c0002t0007g0023 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1116+1283G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125046727 | ||||||
| chr6:125046854
|
T | G | 1 | a0002c0006t0078g0007 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1116+1410T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125046854 | ||||||
| chr6:125046857
|
C | T | 92 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0001g0051others(89): Show | 92 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.1116+1413C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125046857 | ||||||
| chr6:125047134
|
G | A | 71 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0058others(68): Show | 73 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.1116+1690G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125047134 | ||||||
| chr6:125047265
|
T | C | 3 | a0001c0001t0006g0147a0005c0007t0006g0094a0005c0007t0021g0095 | 3 | HG01884.hp1 HG02109.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1116+1821T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125047265 | ||||||
| chr6:125047278
|
T | C | 3 | a0001c0001t0006g0147a0005c0007t0006g0094a0005c0007t0021g0095 | 3 | HG01884.hp1 HG02109.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1116+1834T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125047278 | ||||||
| chr6:125047320
|
T | C | 1 | a0001c0001t0001g0084 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1116+1876T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125047320 | ||||||
| chr6:125047328
|
G | A | 70 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0058others(67): Show | 72 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.1116+1884G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125047328 | ||||||
| chr6:125047502
|
G | A | 13 | a0001c0001t0001g0047a0001c0001t0002g0055a0001c0001t0010g0145others(10): Show | 13 | HG01106.hp1 HG02056.hp1 HG02132.hp1 others(10): Show |
intron_variant | MODIFIER | c.1116+2058G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125047502 | ||||||
| chr6:125047532
|
T | A | 1 | a0001c0001t0004g0155 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1116+2088T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125047532 | ||||||
| chr6:125047532
|
T | G | 27 | a0001c0001t0003g0255a0001c0001t0004g0183a0001c0001t0006g0003others(24): Show | 27 | HG00140.hp2 HG00741.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.1116+2088T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125047532 | ||||||
| chr6:125047563
|
G | A | 69 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0058others(66): Show | 71 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.1116+2119G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125047563 | ||||||
| chr6:125047610
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1116+2166T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125047610 | ||||||
| chr6:125048216
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1116+2772C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125048216 | ||||||
| chr6:125048466
|
A | T | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG01243.hp2 HG01934.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.1116+3022A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125048466 | ||||||
| chr6:125048528
|
T | C | 68 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0058others(65): Show | 69 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.1116+3084T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125048528 | ||||||
| chr6:125048552
|
T | C | 1 | a0001c0001t0001g0263 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1116+3108T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125048552 | ||||||
| chr6:125048590
|
T | C | 2 | a0002c0002t0009g0012a0002c0002t0009g0013 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1116+3146T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125048590 | ||||||
| chr6:125048608
|
G | A | 11 | a0001c0001t0003g0169a0001c0001t0003g0172a0001c0001t0003g0176others(8): Show | 11 | HG02109.hp1 HG02280.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1116+3164G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125048608 | ||||||
| chr6:125048650
|
GAGTA | G | 3 | a0001c0001t0006g0177a0001c0001t0010g0163a0001c0001t0045g0161 | 3 | HG01891.hp2 HG02630.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1116+3210_1116+321 others(8): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 125048650 | |||||
| chr6:125048720
|
C | T | 1 | a0001c0008t0003g0001 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1116+3276C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125048720 | ||||||
| chr6:125048891
|
C | T | 9 | a0001c0001t0003g0169a0001c0001t0003g0172a0001c0001t0003g0176others(6): Show | 9 | HG02109.hp1 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1116+3447C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125048891 | ||||||
| chr6:125049115
|
G | A | 1 | a0001c0001t0010g0195 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1116+3671G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125049115 | ||||||
| chr6:125049480
|
T | C | 118 | a0001c0001t0001g0044a0001c0001t0001g0058a0001c0001t0001g0070others(115): Show | 120 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.1116+4036T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125049480 | ||||||
| chr6:125049572
|
G | A | 1 | a0001c0001t0002g0066 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1116+4128G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125049572 | ||||||
| chr6:125049643
|
CACACATA others(22): Show |
C | 34 | a0001c0001t0001g0158a0001c0001t0001g0209a0001c0001t0001g0244others(31): Show | 34 | HG00741.hp1 HG01884.hp1 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.1116+4200_1116+422 others(33): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125049643 | ||||||
| chr6:125049658
|
C | G | 1 | a0001c0001t0001g0064 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1116+4214C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125049658 | ||||||
| chr6:125049706
|
T | C | 56 | a0001c0001t0001g0158a0001c0001t0001g0209a0001c0001t0001g0244others(53): Show | 56 | HG00741.hp1 HG01106.hp1 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.1116+4262T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125049706 | ||||||
| chr6:125049765
|
A | G | 28 | a0001c0001t0002g0066a0001c0001t0003g0172a0001c0001t0004g0227others(25): Show | 28 | HG00735.hp1 HG00741.hp1 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.1116+4321A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125049765 | ||||||
| chr6:125049791
|
A | G | 6 | a0001c0001t0001g0084a0001c0001t0025g0142a0001c0001t0025g0165others(3): Show | 6 | HG00140.hp2 HG00741.hp2 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.1116+4347A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125049791 | ||||||
| chr6:125049839
|
A | G | 13 | a0001c0001t0006g0177a0001c0001t0006g0251a0001c0001t0010g0195others(10): Show | 13 | HG01884.hp2 HG02630.hp2 HG03041.hp2 others(10): Show |
intron_variant | MODIFIER | c.1116+4395A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125049839 | ||||||
| chr6:125049851
|
G | A | 2 | a0001c0001t0010g0163a0011c0011t0079g0036 | 2 | HG01891.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1116+4407G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125049851 | ||||||
| chr6:125049883
|
T | C | 1 | a0001c0001t0008g0182 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1116+4439T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125049883 | ||||||
| chr6:125049885
|
A | C | 1 | a0001c0003t0008g0193 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1116+4441A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125049885 | ||||||
| chr6:125050155
|
G | A | 36 | a0001c0001t0003g0172a0001c0001t0003g0255a0001c0001t0004g0075others(33): Show | 36 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(33): Show |
intron_variant | MODIFIER | c.1116+4711G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125050155 | ||||||
| chr6:125050157
|
G | A | 7 | a0001c0001t0017g0101a0001c0001t0017g0154a0001c0001t0017g0254others(4): Show | 7 | HG01884.hp2 HG02258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1116+4713G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125050157 | ||||||
| chr6:125050184
|
G | T | 96 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0158others(93): Show | 97 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.1116+4740G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125050184 | ||||||
| chr6:125050187
|
T | G | 96 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0158others(93): Show | 97 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.1116+4743T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125050187 | ||||||
| chr6:125050317
|
C | T | 17 | a0001c0001t0004g0075a0001c0001t0004g0123a0001c0001t0034g0146others(14): Show | 18 | HG01243.hp1 HG02280.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.1116+4873C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125050317 | ||||||
| chr6:125050320
|
C | T | 1 | a0002c0002t0071g0038 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1116+4876C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125050320 | ||||||
| chr6:125050473
|
A | C | 3 | a0001c0001t0023g0250a0001c0001t0043g0004a0001c0001t0068g0245 | 3 | HG02486.hp1 HG03098.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1116+5029A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125050473 | ||||||
| chr6:125050478
|
C | T | 12 | a0002c0002t0070g0039a0003c0004t0011g0149a0003c0004t0011g0150others(9): Show | 12 | HG00741.hp1 HG02055.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1116+5034C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125050478 | ||||||
| chr6:125050517
|
A | G | 3 | a0001c0001t0008g0182a0001c0001t0022g0132a0001c0001t0022g0180 | 3 | HG02055.hp2 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1116+5073A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125050517 | ||||||
| chr6:125050654
|
A | G | 13 | a0001c0001t0010g0195a0002c0002t0070g0039a0003c0004t0011g0149others(10): Show | 13 | HG00741.hp1 HG02055.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1116+5210A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125050654 | ||||||
| chr6:125050669
|
A | G | 1 | a0001c0001t0005g0214 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1116+5225A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125050669 | ||||||
| chr6:125050985
|
A | G | 155 | a0001c0001t0001g0047a0001c0001t0001g0102a0001c0001t0001g0135others(152): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.1116+5541A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125050985 | ||||||
| chr6:125051054
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1116+5610G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125051054 | ||||||
| chr6:125051280
|
T | C | 122 | a0001c0001t0001g0047a0001c0001t0001g0102a0001c0001t0001g0209others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(121): Show |
intron_variant | MODIFIER | c.1116+5836T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125051280 | ||||||
| chr6:125051441
|
A | G | 3 | a0001c0001t0019g0076a0001c0001t0019g0119a0001c0001t0019g0239 | 3 | HG02056.hp1 NA18971.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.1116+5997A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125051441 | ||||||
| chr6:125051721
|
T | A | 1 | a0001c0001t0036g0232 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1117-6221T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125051721 | ||||||
| chr6:125051756
|
T | C | 10 | a0003c0004t0011g0149a0003c0004t0011g0150a0003c0004t0011g0157others(7): Show | 10 | HG00741.hp1 HG02055.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1117-6186T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125051756 | ||||||
| chr6:125051891
|
C | T | 1 | a0001c0001t0054g0181 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1117-6051C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125051891 | ||||||
| chr6:125051920
|
C | T | 9 | a0001c0001t0001g0051a0001c0001t0001g0057a0001c0001t0001g0069others(6): Show | 9 | HG01255.hp1 HG01261.hp1 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.1117-6022C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125051920 | ||||||
| chr6:125052284
|
T | G | 3 | a0001c0001t0008g0182a0001c0001t0022g0132a0001c0001t0022g0180 | 3 | HG02055.hp2 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1117-5658T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125052284 | ||||||
| chr6:125052284
|
T | TTG | 8 | a0001c0001t0001g0047a0001c0001t0001g0052a0001c0001t0002g0087others(5): Show | 8 | HG01981.hp1 HG02523.hp1 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.1117-5623_1117-562 others(6): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 125052284 | |||||
| chr6:125052284
|
T | TTGTG | 11 | a0001c0001t0004g0183a0001c0001t0014g0060a0001c0001t0024g0170others(8): Show | 11 | HG00140.hp2 HG00741.hp2 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.1117-5625_1117-562 others(8): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 125052284 | |||||
| chr6:125052284
|
T | TTGTGTG | 7 | a0001c0001t0003g0002a0001c0001t0003g0115a0001c0001t0003g0198others(4): Show | 8 | HG00735.hp2 HG02970.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.1117-5627_1117-562 others(10): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 125052284 | |||||
| chr6:125052284
|
T | TTGTGTGT others(1): Show |
19 | a0001c0001t0003g0169a0001c0001t0003g0172a0001c0001t0003g0176others(16): Show | 19 | HG01891.hp2 HG02055.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1117-5629_1117-562 others(12): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 125052284 | |||||
| chr6:125052284
|
T | TTGTGTGT others(3): Show |
12 | a0001c0001t0010g0145a0001c0001t0021g0133a0001c0001t0021g0159others(9): Show | 12 | HG00741.hp1 HG02083.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1117-5631_1117-562 others(14): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 125052284 | |||||
| chr6:125052284
|
T | TTGTGTGT others(5): Show |
1 | a0001c0001t0039g0179 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1117-5633_1117-562 others(16): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 125052284 | |||||
| chr6:125052284
|
T | TTGTGTGT others(7): Show |
2 | a0001c0001t0010g0153a0011c0011t0079g0036 | 2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1117-5635_1117-562 others(18): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 125052284 | |||||
| chr6:125052288
|
G | A | 10 | a0001c0001t0003g0255a0001c0001t0006g0003a0001c0001t0006g0147others(7): Show | 10 | HG01884.hp1 HG02109.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1117-5654G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125052288 | ||||||
| chr6:125052292
|
G | GTA | 3 | a0001c0001t0008g0182a0001c0001t0022g0132a0001c0001t0022g0180 | 3 | HG02055.hp2 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1117-5649_1117-564 others(6): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 125052292 | |||||
| chr6:125052306
|
GTGTGTGT others(2): Show |
G | 19 | a0001c0001t0034g0146a0001c0003t0008g0131a0001c0003t0008g0175others(16): Show | 20 | HG00639.hp1 HG01243.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.1117-5635_1117-562 others(13): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125052306 | ||||||
| chr6:125052318
|
G | T | 20 | a0001c0001t0034g0146a0001c0003t0008g0131a0001c0003t0008g0151others(17): Show | 21 | HG00639.hp1 HG01243.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.1117-5624G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125052318 | ||||||
| chr6:125052320
|
G | GTGTGTGT | 3 | a0001c0001t0017g0254a0001c0001t0045g0161a0001c0001t0051g0173 | 3 | HG02258.hp2 HG02809.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1117-5622_1117-562 others(11): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125052320 | ||||||
| chr6:125052320
|
G | GTGTGTGT others(2): Show |
7 | a0001c0001t0003g0255a0001c0001t0006g0003a0001c0001t0006g0147others(4): Show | 7 | HG01884.hp1 HG02109.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1117-5622_1117-562 others(13): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125052320 | ||||||
| chr6:125052320
|
G | GTGTGTGT others(6): Show |
1 | a0002c0002t0071g0038 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1117-5622_1117-562 others(17): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125052320 | ||||||
| chr6:125052320
|
G | T | 20 | a0001c0001t0034g0146a0001c0003t0008g0131a0001c0003t0008g0151others(17): Show | 21 | HG00639.hp1 HG01243.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.1117-5622G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125052320 | ||||||
| chr6:125052321
|
G | A | 20 | a0001c0001t0034g0146a0001c0003t0008g0131a0001c0003t0008g0151others(17): Show | 21 | HG00639.hp1 HG01243.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.1117-5621G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125052321 | ||||||
| chr6:125052321
|
G | T | 1 | a0002c0002t0073g0030 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1117-5621G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125052321 | ||||||
| chr6:125052323
|
T | G | 17 | a0001c0001t0003g0255a0001c0001t0006g0003a0001c0001t0006g0147others(14): Show | 17 | HG01884.hp1 HG01884.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1117-5619T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125052323 | ||||||
| chr6:125052325
|
T | G | 38 | a0001c0001t0003g0255a0001c0001t0006g0003a0001c0001t0006g0147others(35): Show | 39 | HG00639.hp1 HG01243.hp1 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.1117-5617T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125052325 | ||||||
| chr6:125052326
|
A | ATTTGTTT others(3): Show |
16 | a0001c0001t0008g0182a0001c0001t0010g0195a0001c0001t0022g0132others(13): Show | 16 | HG00741.hp1 HG02055.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.1117-5596_1117-558 others(14): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 125052326 | |||||
| chr6:125052326
|
A | G | 17 | a0001c0001t0003g0255a0001c0001t0006g0003a0001c0001t0006g0147others(14): Show | 17 | HG01884.hp1 HG01884.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1117-5616A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125052326 | ||||||
| chr6:125052326
|
A | T | 21 | a0001c0001t0034g0146a0001c0003t0008g0131a0001c0003t0008g0151others(18): Show | 22 | HG00639.hp1 HG01243.hp1 HG02280.hp1 others(19): Show |
intron_variant | MODIFIER | c.1117-5616A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125052326 | ||||||
| chr6:125052330
|
G | T | 17 | a0001c0001t0003g0255a0001c0001t0006g0003a0001c0001t0006g0147others(14): Show | 17 | HG01884.hp1 HG01884.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1117-5612G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125052330 | ||||||
| chr6:125052331
|
T | A | 17 | a0001c0001t0003g0255a0001c0001t0006g0003a0001c0001t0006g0147others(14): Show | 17 | HG01884.hp1 HG01884.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1117-5611T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125052331 | ||||||
| chr6:125052517
|
G | T | 3 | a0001c0001t0008g0182a0001c0001t0022g0132a0001c0001t0022g0180 | 3 | HG02055.hp2 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1117-5425G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125052517 | ||||||
| chr6:125052715
|
A | G | 2 | a0001c0001t0045g0161a0002c0002t0071g0038 | 2 | HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1117-5227A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125052715 | ||||||
| chr6:125052926
|
A | C | 3 | a0001c0001t0012g0062a0001c0001t0012g0201a0001c0001t0012g0220 | 3 | HG01981.hp1 HG02735.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1117-5016A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125052926 | ||||||
| chr6:125053092
|
C | A | 1 | a0001c0001t0004g0242 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1117-4850C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125053092 | ||||||
| chr6:125053210
|
T | G | 12 | a0001c0001t0003g0255a0001c0001t0006g0003a0001c0001t0006g0147others(9): Show | 12 | HG01884.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1117-4732T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125053210 | ||||||
| chr6:125053320
|
A | G | 134 | a0001c0001t0001g0047a0001c0001t0001g0102a0001c0001t0001g0135others(131): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.1117-4622A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125053320 | ||||||
| chr6:125053473
|
A | G | 3 | a0001c0001t0008g0182a0001c0001t0022g0132a0001c0001t0022g0180 | 3 | HG02055.hp2 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1117-4469A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125053473 | ||||||
| chr6:125053636
|
TC | T | 13 | a0001c0001t0010g0195a0002c0002t0070g0039a0003c0004t0011g0149others(10): Show | 13 | HG00741.hp1 HG02055.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1117-4304delC | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 125053636 | |||||
| chr6:125053644
|
C | T | 13 | a0001c0001t0010g0195a0002c0002t0070g0039a0003c0004t0011g0149others(10): Show | 13 | HG00741.hp1 HG02055.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1117-4298C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125053644 | ||||||
| chr6:125053674
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1117-4268A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125053674 | ||||||
| chr6:125053730
|
G | A | 5 | a0001c0001t0021g0159a0001c0001t0026g0160a0001c0001t0026g0168others(2): Show | 5 | HG02809.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1117-4212G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125053730 | ||||||
| chr6:125053883
|
C | T | 12 | a0001c0001t0003g0002a0001c0001t0003g0115a0001c0001t0003g0169others(9): Show | 13 | HG00735.hp2 HG02083.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1117-4059C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125053883 | ||||||
| chr6:125054124
|
G | A | 16 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0002g0066others(13): Show | 16 | HG00099.hp2 HG00140.hp1 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.1117-3818G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125054124 | ||||||
| chr6:125054151
|
T | C | 13 | a0001c0001t0010g0195a0002c0002t0070g0039a0003c0004t0011g0149others(10): Show | 13 | HG00741.hp1 HG02055.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1117-3791T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125054151 | ||||||
| chr6:125054333
|
G | A | 13 | a0001c0001t0010g0195a0002c0002t0070g0039a0003c0004t0011g0149others(10): Show | 13 | HG00741.hp1 HG02055.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1117-3609G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125054333 | ||||||
| chr6:125054343
|
G | A | 1 | a0002c0002t0071g0038 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1117-3599G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125054343 | ||||||
| chr6:125054346
|
G | A | 1 | a0001c0001t0010g0195 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1117-3596G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125054346 | ||||||
| chr6:125054366
|
C | A | 1 | a0001c0001t0004g0046 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1117-3576C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125054366 | ||||||
| chr6:125054414
|
C | G | 10 | a0001c0001t0017g0101a0001c0001t0017g0154a0001c0001t0017g0254others(7): Show | 10 | HG01884.hp2 HG02258.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1117-3528C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125054414 | ||||||
| chr6:125054603
|
A | G | 3 | a0001c0001t0008g0182a0001c0001t0022g0132a0001c0001t0022g0180 | 3 | HG02055.hp2 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1117-3339A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125054603 | ||||||
| chr6:125054755
|
T | C | 1 | a0001c0001t0069g0118 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1117-3187T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125054755 | ||||||
| chr6:125054869
|
C | A | 5 | a0001c0001t0021g0159a0001c0001t0026g0160a0001c0001t0026g0168others(2): Show | 5 | HG02809.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1117-3073C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125054869 | ||||||
| chr6:125054955
|
T | A | 2 | a0001c0001t0001g0109a0001c0001t0001g0210 | 2 | HG00609.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1117-2987T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125054955 | ||||||
| chr6:125054956
|
A | C | 96 | a0001c0001t0001g0047a0001c0001t0001g0102a0001c0001t0001g0209others(93): Show | 96 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.1117-2986A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125054956 | ||||||
| chr6:125054958
|
G | A | 3 | a0001c0001t0008g0182a0001c0001t0022g0132a0001c0001t0022g0180 | 3 | HG02055.hp2 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1117-2984G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125054958 | ||||||
| chr6:125055265
|
C | T | 13 | a0001c0001t0010g0195a0002c0002t0070g0039a0003c0004t0011g0149others(10): Show | 13 | HG00741.hp1 HG02055.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1117-2677C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125055265 | ||||||
| chr6:125055353
|
T | C | 1 | a0001c0001t0024g0184 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1117-2589T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125055353 | ||||||
| chr6:125055486
|
C | T | 2 | a0001c0001t0016g0083a0001c0001t0016g0222 | 2 | HG02602.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1117-2456C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125055486 | ||||||
| chr6:125055490
|
T | A | 1 | a0001c0003t0008g0175 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1117-2452T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125055490 | ||||||
| chr6:125055543
|
G | A | 3 | a0001c0001t0008g0182a0001c0001t0022g0132a0001c0001t0022g0180 | 3 | HG02055.hp2 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1117-2399G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125055543 | ||||||
| chr6:125055683
|
A | G | 1 | a0001c0001t0002g0164 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1117-2259A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125055683 | ||||||
| chr6:125055694
|
G | A | 20 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0002g0066others(17): Show | 20 | HG00099.hp2 HG00140.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.1117-2248G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125055694 | ||||||
| chr6:125055733
|
A | G | 1 | a0002c0002t0073g0030 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1117-2209A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125055733 | ||||||
| chr6:125055748
|
T | A | 3 | a0001c0001t0008g0182a0001c0001t0022g0132a0001c0001t0022g0180 | 3 | HG02055.hp2 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1117-2194T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125055748 | ||||||
| chr6:125055767
|
TTTCA | T | 5 | a0001c0001t0021g0159a0001c0001t0026g0160a0001c0001t0026g0168others(2): Show | 5 | HG02809.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1117-2168_1117-216 others(8): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 125055767 | |||||
| chr6:125055843
|
G | A | 3 | a0001c0001t0008g0182a0001c0001t0022g0132a0001c0001t0022g0180 | 3 | HG02055.hp2 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1117-2099G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125055843 | ||||||
| chr6:125056330
|
T | G | 1 | a0001c0001t0001g0106 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1117-1612T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125056330 | ||||||
| chr6:125056339
|
A | G | 9 | a0001c0001t0010g0145a0001c0001t0010g0148a0001c0001t0010g0153others(6): Show | 9 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1117-1603A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125056339 | ||||||
| chr6:125056579
|
G | T | 2 | a0001c0001t0024g0170a0001c0001t0033g0134 | 2 | HG02970.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1117-1363G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125056579 | ||||||
| chr6:125057040
|
T | C | 3 | a0001c0001t0008g0182a0001c0001t0022g0132a0001c0001t0022g0180 | 3 | HG02055.hp2 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1117-902T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125057040 | ||||||
| chr6:125057218
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1117-724C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125057218 | ||||||
| chr6:125057222
|
C | A | 1 | a0005c0007t0021g0095 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1117-720C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125057222 | ||||||
| chr6:125057362
|
C | A | 79 | a0001c0001t0001g0047a0001c0001t0001g0102a0001c0001t0001g0209others(76): Show | 79 | HG00099.hp1 HG00639.hp2 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.1117-580C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125057362 | ||||||
| chr6:125057428
|
C | T | 1 | a0001c0001t0004g0227 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1117-514C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125057428 | ||||||
| chr6:125057769
|
A | G | 69 | a0001c0001t0001g0047a0001c0001t0001g0102a0001c0001t0001g0209others(66): Show | 69 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.1117-173A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125057769 | ||||||
| chr6:125057821
|
T | C | 20 | a0001c0001t0034g0146a0001c0003t0008g0131a0001c0003t0008g0151others(17): Show | 21 | HG00639.hp1 HG01243.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.1117-121T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125057821 | ||||||
| chr6:125058280
|
C | A | 148 | a0001c0001t0001g0047a0001c0001t0001g0135a0001c0001t0001g0137others(145): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.1281+174C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125058280 | ||||||
| chr6:125058283
|
G | A | 1 | a0002c0002t0071g0038 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1281+177G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125058283 | ||||||
| chr6:125058445
|
C | A | 1 | a0001c0001t0004g0183 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1281+339C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125058445 | ||||||
| chr6:125058490
|
C | T | 5 | a0001c0001t0021g0159a0001c0001t0026g0160a0001c0001t0026g0168others(2): Show | 5 | HG02809.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1281+384C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125058490 | ||||||
| chr6:125058788
|
C | T | 95 | a0001c0001t0001g0047a0001c0001t0001g0102a0001c0001t0001g0209others(92): Show | 95 | HG00099.hp1 HG00639.hp2 HG00642.hp2 others(92): Show |
intron_variant | MODIFIER | c.1281+682C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125058788 | ||||||
| chr6:125058789
|
T | C | 1 | a0001c0001t0001g0247 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1281+683T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125058789 | ||||||
| chr6:125058798
|
A | G | 1 | a0001c0001t0010g0195 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1281+692A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125058798 | ||||||
| chr6:125058850
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1281+744A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125058850 | ||||||
| chr6:125059143
|
GA | G | 9 | a0001c0001t0010g0145a0001c0001t0010g0148a0001c0001t0010g0153others(6): Show | 9 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1281+1041delA | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125059143 | |||||
| chr6:125059227
|
T | C | 13 | a0001c0001t0010g0195a0002c0002t0070g0039a0003c0004t0011g0149others(10): Show | 13 | HG00741.hp1 HG02055.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1281+1121T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125059227 | ||||||
| chr6:125059299
|
G | T | 1 | a0001c0001t0068g0245 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1281+1193G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125059299 | ||||||
| chr6:125059402
|
C | G | 12 | a0001c0001t0001g0109a0001c0001t0001g0210a0003c0004t0011g0149others(9): Show | 12 | HG00609.hp2 HG00741.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1281+1296C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125059402 | ||||||
| chr6:125059477
|
A | C | 1 | a0001c0001t0001g0108 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1281+1371A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125059477 | ||||||
| chr6:125059567
|
T | C | 1 | a0001c0001t0043g0004 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1281+1461T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125059567 | ||||||
| chr6:125059623
|
T | C | 9 | a0001c0001t0010g0145a0001c0001t0010g0148a0001c0001t0010g0153others(6): Show | 9 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1281+1517T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125059623 | ||||||
| chr6:125059747
|
A | G | 2 | a0001c0001t0001g0120a0001c0001t0057g0246 | 2 | NA18968.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.1281+1641A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125059747 | ||||||
| chr6:125059992
|
G | C | 1 | a0010c0013t0030g0192 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1281+1886G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125059992 | ||||||
| chr6:125060304
|
A | G | 1 | a0001c0001t0001g0048 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1281+2198A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125060304 | ||||||
| chr6:125060356
|
T | TAC | 29 | a0001c0001t0001g0050a0001c0001t0001g0116a0001c0001t0001g0135others(26): Show | 29 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.1281+2274_1281+227 others(6): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125060356 | |||||
| chr6:125060356
|
T | TACACACA others(3): Show |
1 | a0001c0001t0033g0134 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1281+2266_1281+227 others(14): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125060356 | |||||
| chr6:125060356
|
TAC | T | 106 | a0001c0001t0001g0047a0001c0001t0001g0102a0001c0001t0001g0209others(103): Show | 107 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.1281+2274_1281+227 others(6): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125060356 | |||||
| chr6:125060382
|
T | C | 18 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0002g0066others(15): Show | 18 | HG00099.hp2 HG00140.hp1 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.1281+2276T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125060382 | ||||||
| chr6:125060596
|
C | A | 29 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0002g0066others(26): Show | 29 | HG00099.hp2 HG00140.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.1281+2490C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125060596 | ||||||
| chr6:125060633
|
C | T | 5 | a0001c0001t0021g0159a0001c0001t0026g0160a0001c0001t0026g0168others(2): Show | 5 | HG02809.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1281+2527C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125060633 | ||||||
| chr6:125060892
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1281+2786C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125060892 | ||||||
| chr6:125060977
|
T | C | 108 | a0001c0001t0001g0047a0001c0001t0001g0102a0001c0001t0001g0241others(105): Show | 109 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(106): Show |
intron_variant | MODIFIER | c.1281+2871T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125060977 | ||||||
| chr6:125061242
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1281+3136G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125061242 | ||||||
| chr6:125061521
|
A | G | 4 | a0002c0002t0013g0011a0002c0002t0077g0034a0006c0009t0001g0194others(1): Show | 4 | HG01106.hp1 HG01934.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1281+3415A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125061521 | ||||||
| chr6:125061525
|
T | A | 18 | a0001c0001t0010g0145a0001c0001t0010g0148a0001c0001t0010g0153others(15): Show | 18 | HG01891.hp2 HG02109.hp1 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.1281+3419T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125061525 | ||||||
| chr6:125061552
|
A | G | 26 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0004g0046others(23): Show | 26 | HG00099.hp2 HG00140.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.1281+3446A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125061552 | ||||||
| chr6:125061629
|
G | A | 18 | a0001c0001t0010g0145a0001c0001t0010g0148a0001c0001t0010g0153others(15): Show | 18 | HG01891.hp2 HG02109.hp1 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.1281+3523G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125061629 | ||||||
| chr6:125061705
|
C | A | 3 | a0001c0001t0023g0250a0001c0001t0068g0245a0001c0003t0023g0143 | 3 | HG02451.hp2 HG03098.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1281+3599C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125061705 | ||||||
| chr6:125061792
|
T | C | 83 | a0001c0001t0001g0047a0001c0001t0001g0102a0001c0001t0001g0135others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(80): Show |
intron_variant | MODIFIER | c.1281+3686T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125061792 | ||||||
| chr6:125061804
|
G | A | 100 | a0001c0001t0001g0047a0001c0001t0001g0102a0001c0001t0001g0135others(97): Show | 100 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(97): Show |
intron_variant | MODIFIER | c.1281+3698G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125061804 | ||||||
| chr6:125061844
|
TTTTC | T | 5 | a0001c0001t0021g0159a0001c0001t0026g0160a0001c0001t0026g0168others(2): Show | 5 | HG02809.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1281+3746_1281+374 others(8): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125061844 | |||||
| chr6:125062000
|
A | G | 55 | a0001c0001t0001g0047a0001c0001t0001g0102a0001c0001t0002g0055others(52): Show | 55 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.1281+3894A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125062000 | ||||||
| chr6:125062252
|
C | T | 18 | a0001c0001t0010g0145a0001c0001t0010g0148a0001c0001t0010g0153others(15): Show | 18 | HG01891.hp2 HG02109.hp1 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.1281+4146C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125062252 | ||||||
| chr6:125062360
|
T | C | 18 | a0001c0001t0010g0145a0001c0001t0010g0148a0001c0001t0010g0153others(15): Show | 18 | HG01891.hp2 HG02109.hp1 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.1281+4254T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125062360 | ||||||
| chr6:125062416
|
ATACT | A | 10 | a0001c0001t0023g0250a0003c0004t0011g0149a0003c0004t0011g0150others(7): Show | 10 | HG00741.hp1 HG02055.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1281+4318_1281+432 others(8): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125062416 | |||||
| chr6:125062420
|
T | C | 2 | a0001c0001t0003g0198a0001c0001t0003g0240 | 2 | HG00735.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1281+4314T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125062420 | ||||||
| chr6:125062447
|
C | T | 2 | a0001c0001t0045g0161a0002c0002t0071g0038 | 2 | HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1281+4341C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125062447 | ||||||
| chr6:125062513
|
A | G | 15 | a0001c0001t0010g0145a0001c0001t0010g0148a0001c0001t0010g0153others(12): Show | 15 | HG01891.hp2 HG02109.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.1281+4407A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125062513 | ||||||
| chr6:125062559
|
T | A | 1 | a0001c0001t0034g0146 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1281+4453T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125062559 | ||||||
| chr6:125062610
|
C | T | 13 | a0001c0001t0003g0002a0001c0001t0003g0085a0001c0001t0003g0115others(10): Show | 15 | HG00642.hp1 HG00735.hp2 HG02083.hp1 others(12): Show |
intron_variant | MODIFIER | c.1281+4504C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125062610 | ||||||
| chr6:125062625
|
G | A | 1 | a0001c0003t0065g0167 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1281+4519G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125062625 | ||||||
| chr6:125062664
|
T | C | 1 | a0001c0001t0019g0119 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1281+4558T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125062664 | ||||||
| chr6:125062757
|
A | G | 9 | a0001c0001t0008g0182a0001c0003t0008g0131a0001c0003t0008g0151others(6): Show | 9 | HG01243.hp1 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1281+4651A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125062757 | ||||||
| chr6:125062765
|
C | T | 12 | a0001c0001t0001g0072a0001c0001t0005g0061a0001c0001t0005g0081others(9): Show | 12 | HG00408.hp2 HG00423.hp2 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.1281+4659C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125062765 | ||||||
| chr6:125062796
|
G | A | 1 | a0001c0001t0003g0172 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1281+4690G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125062796 | ||||||
| chr6:125062809
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1281+4703C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125062809 | ||||||
| chr6:125062835
|
C | G | 3 | a0001c0001t0021g0133a0001c0001t0033g0134a0001c0001t0034g0146 | 3 | HG02970.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1281+4729C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125062835 | ||||||
| chr6:125062891
|
T | G | 19 | a0001c0001t0010g0145a0001c0001t0010g0148a0001c0001t0010g0153others(16): Show | 19 | HG01891.hp2 HG02109.hp1 HG02622.hp1 others(16): Show |
intron_variant | MODIFIER | c.1281+4785T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125062891 | ||||||
| chr6:125062925
|
T | C | 1 | a0001c0001t0002g0237 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1281+4819T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125062925 | ||||||
| chr6:125063057
|
C | T | 5 | a0001c0001t0021g0159a0001c0001t0026g0160a0001c0001t0026g0168others(2): Show | 5 | HG02809.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1281+4951C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125063057 | ||||||
| chr6:125063073
|
T | C | 15 | a0001c0001t0010g0145a0001c0001t0010g0148a0001c0001t0010g0153others(12): Show | 15 | HG01891.hp2 HG02109.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.1281+4967T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125063073 | ||||||
| chr6:125063080
|
A | T | 9 | a0001c0001t0008g0182a0001c0003t0008g0131a0001c0003t0008g0151others(6): Show | 9 | HG01243.hp1 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1281+4974A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125063080 | ||||||
| chr6:125063111
|
A | G | 2 | a0001c0001t0001g0102a0001c0001t0002g0211 | 2 | HG01074.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1281+5005A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125063111 | ||||||
| chr6:125063276
|
C | T | 1 | a0002c0002t0071g0038 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1281+5170C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125063276 | ||||||
| chr6:125063360
|
C | T | 1 | a0001c0001t0002g0086 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1281+5254C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125063360 | ||||||
| chr6:125063373
|
T | C | 1 | a0002c0002t0027g0019 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1281+5267T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125063373 | ||||||
| chr6:125063442
|
C | T | 18 | a0001c0001t0010g0145a0001c0001t0010g0148a0001c0001t0010g0153others(15): Show | 18 | HG01891.hp2 HG02109.hp1 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.1281+5336C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125063442 | ||||||
| chr6:125063443
|
G | A | 2 | a0001c0001t0002g0205a0002c0002t0009g0025 | 2 | HG01070.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.1281+5337G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125063443 | ||||||
| chr6:125063578
|
C | T | 1 | a0001c0001t0039g0179 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1281+5472C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125063578 | ||||||
| chr6:125063677
|
TATAAC | T | 83 | a0001c0001t0001g0047a0001c0001t0001g0135a0001c0001t0001g0137others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(80): Show |
intron_variant | MODIFIER | c.1281+5578_1281+558 others(9): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125063677 | |||||
| chr6:125063688
|
A | G | 5 | a0001c0001t0022g0042a0001c0001t0022g0132a0001c0001t0022g0180others(2): Show | 5 | HG02647.hp2 HG02886.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1281+5582A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125063688 | ||||||
| chr6:125063778
|
A | C | 1 | a0011c0011t0079g0036 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1281+5672A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125063778 | ||||||
| chr6:125064018
|
T | C | 1 | a0001c0001t0038g0204 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1281+5912T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125064018 | ||||||
| chr6:125064324
|
G | A | 82 | a0001c0001t0001g0047a0001c0001t0001g0102a0001c0001t0001g0135others(79): Show | 82 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(79): Show |
intron_variant | MODIFIER | c.1281+6218G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125064324 | ||||||
| chr6:125064350
|
T | C | 2 | a0001c0001t0001g0135a0001c0001t0001g0137 | 2 | HG00099.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1281+6244T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125064350 | ||||||
| chr6:125064504
|
C | T | 1 | a0001c0001t0002g0237 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1281+6398C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125064504 | ||||||
| chr6:125064663
|
A | C | 2 | a0002c0002t0070g0039a0010c0013t0030g0192 | 2 | HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1281+6557A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125064663 | ||||||
| chr6:125064729
|
A | T | 9 | a0001c0001t0008g0182a0001c0003t0008g0131a0001c0003t0008g0151others(6): Show | 9 | HG01243.hp1 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1281+6623A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125064729 | ||||||
| chr6:125064739
|
C | A | 2 | a0001c0001t0001g0135a0001c0001t0001g0137 | 2 | HG00099.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1281+6633C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125064739 | ||||||
| chr6:125064745
|
A | C | 1 | a0001c0001t0001g0108 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1281+6639A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125064745 | ||||||
| chr6:125064791
|
T | G | 2 | a0001c0001t0016g0083a0001c0001t0016g0222 | 2 | HG02602.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1281+6685T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125064791 | ||||||
| chr6:125064806
|
A | G | 1 | a0002c0002t0007g0015 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1281+6700A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125064806 | ||||||
| chr6:125064931
|
C | G | 19 | a0001c0001t0010g0145a0001c0001t0010g0148a0001c0001t0010g0153others(16): Show | 19 | HG01891.hp2 HG02109.hp1 HG02622.hp1 others(16): Show |
intron_variant | MODIFIER | c.1281+6825C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125064931 | ||||||
| chr6:125064947
|
A | G | 1 | a0001c0001t0025g0142 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1281+6841A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125064947 | ||||||
| chr6:125065057
|
C | T | 6 | a0001c0001t0004g0155a0001c0001t0015g0045a0001c0001t0015g0207others(3): Show | 6 | NA18942.hp2 NA18943.hp1 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.1281+6951C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125065057 | ||||||
| chr6:125065084
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1281+6978G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125065084 | ||||||
| chr6:125065103
|
G | A | 5 | a0001c0001t0003g0169a0001c0001t0003g0176a0001c0001t0003g0178others(2): Show | 5 | HG02451.hp1 HG02572.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1281+6997G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125065103 | ||||||
| chr6:125065163
|
C | T | 1 | a0001c0001t0038g0204 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1281+7057C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125065163 | ||||||
| chr6:125065166
|
T | C | 156 | a0001c0001t0001g0047a0001c0001t0001g0102a0001c0001t0001g0135others(153): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.1281+7060T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125065166 | ||||||
| chr6:125065269
|
C | T | 1 | a0001c0003t0013g0186 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1281+7163C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125065269 | ||||||
| chr6:125065290
|
C | CA | 33 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0003g0255others(30): Show | 33 | HG00140.hp2 HG00741.hp2 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.1281+7204dupA | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125065290 | |||||
| chr6:125065290
|
C | CAA | 11 | a0001c0001t0010g0145a0001c0001t0010g0148a0001c0001t0010g0153others(8): Show | 11 | HG01891.hp2 HG02109.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1281+7203_1281+720 others(6): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125065290 | |||||
| chr6:125065317
|
G | C | 102 | a0001c0001t0001g0047a0001c0001t0001g0102a0001c0001t0001g0135others(99): Show | 102 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(99): Show |
intron_variant | MODIFIER | c.1281+7211G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125065317 | ||||||
| chr6:125065527
|
C | T | 3 | a0001c0001t0021g0133a0001c0001t0033g0134a0001c0001t0034g0146 | 3 | HG02970.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1281+7421C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125065527 | ||||||
| chr6:125065541
|
G | A | 1 | a0001c0001t0022g0132 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1281+7435G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125065541 | ||||||
| chr6:125065580
|
A | G | 19 | a0001c0001t0010g0145a0001c0001t0010g0148a0001c0001t0010g0153others(16): Show | 19 | HG01891.hp2 HG02109.hp1 HG02622.hp1 others(16): Show |
intron_variant | MODIFIER | c.1281+7474A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125065580 | ||||||
| chr6:125065831
|
G | A | 9 | a0003c0004t0011g0149a0003c0004t0011g0150a0003c0004t0011g0157others(6): Show | 9 | HG00741.hp1 HG02055.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1281+7725G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125065831 | ||||||
| chr6:125066016
|
C | G | 1 | a0001c0001t0001g0152 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1281+7910C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125066016 | ||||||
| chr6:125066034
|
C | T | 10 | a0001c0001t0010g0145a0001c0001t0010g0148a0001c0001t0010g0153others(7): Show | 10 | HG01891.hp2 HG02109.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1281+7928C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125066034 | ||||||
| chr6:125066158
|
G | C | 11 | a0001c0001t0006g0003a0001c0001t0006g0147a0001c0001t0006g0156others(8): Show | 11 | HG01884.hp1 HG02109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1281+8052G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125066158 | ||||||
| chr6:125066252
|
T | C | 5 | a0001c0001t0010g0163a0001c0001t0010g0195a0001c0003t0010g0259others(2): Show | 5 | HG01891.hp2 HG02922.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1281+8146T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125066252 | ||||||
| chr6:125066329
|
T | C | 162 | a0001c0001t0001g0047a0001c0001t0001g0102a0001c0001t0001g0135others(159): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.1281+8223T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125066329 | ||||||
| chr6:125066404
|
C | T | 1 | a0001c0003t0023g0143 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1281+8298C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125066404 | ||||||
| chr6:125066447
|
G | A | 1 | a0001c0003t0023g0143 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1281+8341G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125066447 | ||||||
| chr6:125066466
|
C | T | 1 | a0001c0001t0024g0184 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1281+8360C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125066466 | ||||||
| chr6:125066727
|
T | C | 16 | a0001c0001t0010g0145a0001c0001t0010g0148a0001c0001t0010g0153others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.1281+8621T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125066727 | ||||||
| chr6:125066737
|
GA | G | 15 | a0001c0001t0010g0145a0001c0001t0010g0148a0001c0001t0010g0153others(12): Show | 15 | HG01891.hp2 HG02109.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.1281+8632delA | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125066737 | ||||||
| chr6:125066995
|
A | AG | 163 | a0001c0001t0001g0047a0001c0001t0001g0102a0001c0001t0001g0135others(160): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.1281+8891dupG | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125066995 | |||||
| chr6:125067001
|
A | G | 92 | a0001c0001t0001g0047a0001c0001t0001g0102a0001c0001t0001g0135others(89): Show | 92 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(89): Show |
intron_variant | MODIFIER | c.1281+8895A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125067001 | ||||||
| chr6:125067020
|
C | A | 29 | a0001c0001t0008g0182a0001c0001t0021g0133a0001c0001t0021g0159others(26): Show | 29 | HG00741.hp1 HG01243.hp1 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.1281+8914C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125067020 | ||||||
| chr6:125067048
|
T | A | 1 | a0001c0003t0064g0189 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1281+8942T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125067048 | ||||||
| chr6:125067054
|
G | C | 91 | a0001c0001t0001g0047a0001c0001t0001g0135a0001c0001t0001g0137others(88): Show | 91 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(88): Show |
intron_variant | MODIFIER | c.1281+8948G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125067054 | ||||||
| chr6:125067127
|
T | C | 1 | a0001c0001t0002g0237 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1281+9021T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125067127 | ||||||
| chr6:125067135
|
C | T | 1 | a0001c0001t0068g0245 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1281+9029C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125067135 | ||||||
| chr6:125067560
|
G | A | 2 | a0006c0009t0001g0194a0006c0009t0001g0265 | 2 | HG02257.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1282-9097G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125067560 | ||||||
| chr6:125067607
|
A | G | 16 | a0001c0001t0010g0145a0001c0001t0010g0148a0001c0001t0010g0153others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.1282-9050A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125067607 | ||||||
| chr6:125067632
|
G | A | 1 | a0001c0001t0003g0085 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1282-9025G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125067632 | ||||||
| chr6:125067783
|
T | C | 16 | a0001c0001t0010g0145a0001c0001t0010g0148a0001c0001t0010g0153others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.1282-8874T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125067783 | ||||||
| chr6:125067820
|
G | A | 1 | a0001c0001t0001g0084 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1282-8837G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125067820 | ||||||
| chr6:125067953
|
A | G | 16 | a0001c0001t0010g0145a0001c0001t0010g0148a0001c0001t0010g0153others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.1282-8704A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125067953 | ||||||
| chr6:125068065
|
A | G | 55 | a0001c0001t0003g0002a0001c0001t0003g0085a0001c0001t0003g0115others(52): Show | 57 | HG00642.hp1 HG00735.hp2 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.1282-8592A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125068065 | ||||||
| chr6:125068153
|
C | A | 16 | a0001c0001t0010g0145a0001c0001t0010g0148a0001c0001t0010g0153others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.1282-8504C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125068153 | ||||||
| chr6:125068280
|
C | T | 1 | a0002c0002t0070g0039 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1282-8377C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125068280 | ||||||
| chr6:125068449
|
G | T | 2 | a0001c0001t0001g0231a0009c0014t0001g0127 | 2 | HG00323.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.1282-8208G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125068449 | ||||||
| chr6:125068666
|
T | A | 1 | a0001c0001t0001g0108 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1282-7991T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125068666 | ||||||
| chr6:125068709
|
A | G | 2 | a0001c0001t0001g0074a0001c0001t0001g0216 | 2 | HG01255.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.1282-7948A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125068709 | ||||||
| chr6:125068920
|
A | G | 1 | a0001c0001t0006g0003 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1282-7737A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125068920 | ||||||
| chr6:125068963
|
G | A | 16 | a0001c0001t0010g0145a0001c0001t0010g0148a0001c0001t0010g0153others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.1282-7694G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125068963 | ||||||
| chr6:125069213
|
A | C | 1 | a0001c0001t0004g0183 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1282-7444A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125069213 | ||||||
| chr6:125069239
|
A | G | 1 | a0006c0009t0001g0194 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1282-7418A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125069239 | ||||||
| chr6:125069287
|
T | C | 2 | a0001c0001t0045g0161a0002c0002t0071g0038 | 2 | HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1282-7370T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125069287 | ||||||
| chr6:125069538
|
C | A | 15 | a0001c0001t0003g0002a0001c0001t0003g0085a0001c0001t0003g0115others(12): Show | 17 | HG00642.hp1 HG00735.hp2 HG02083.hp1 others(14): Show |
intron_variant | MODIFIER | c.1282-7119C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125069538 | ||||||
| chr6:125069547
|
G | A | 89 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0002g0055others(86): Show | 89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
intron_variant | MODIFIER | c.1282-7110G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125069547 | ||||||
| chr6:125069679
|
G | A | 2 | a0002c0002t0009g0012a0002c0002t0009g0013 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1282-6978G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125069679 | ||||||
| chr6:125069831
|
A | G | 9 | a0001c0001t0008g0182a0001c0003t0008g0131a0001c0003t0008g0151others(6): Show | 9 | HG01243.hp1 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1282-6826A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125069831 | ||||||
| chr6:125069858
|
A | AT | 14 | a0001c0001t0003g0002a0001c0001t0003g0085a0001c0001t0003g0115others(11): Show | 16 | HG00642.hp1 HG00735.hp2 HG02083.hp1 others(13): Show |
intron_variant | MODIFIER | c.1282-6791dupT | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125069858 | |||||
| chr6:125069889
|
C | T | 1 | a0001c0001t0004g0155 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1282-6768C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125069889 | ||||||
| chr6:125069922
|
G | A | 14 | a0001c0001t0003g0002a0001c0001t0003g0085a0001c0001t0003g0115others(11): Show | 16 | HG00642.hp1 HG00735.hp2 HG02083.hp1 others(13): Show |
intron_variant | MODIFIER | c.1282-6735G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125069922 | ||||||
| chr6:125070008
|
T | A | 9 | a0003c0004t0011g0149a0003c0004t0011g0150a0003c0004t0011g0157others(6): Show | 9 | HG00741.hp1 HG02055.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1282-6649T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125070008 | ||||||
| chr6:125070033
|
C | T | 3 | a0001c0001t0023g0250a0001c0001t0068g0245a0001c0003t0023g0143 | 3 | HG02451.hp2 HG03098.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1282-6624C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125070033 | ||||||
| chr6:125070258
|
T | A | 161 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0002g0055others(158): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.1282-6399T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125070258 | ||||||
| chr6:125070462
|
C | T | 6 | a0001c0001t0001g0043a0001c0001t0001g0128a0001c0001t0052g0049others(3): Show | 6 | HG02056.hp2 NA18747.hp2 NA18994.hp1 others(3): Show |
intron_variant | MODIFIER | c.1282-6195C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125070462 | ||||||
| chr6:125070500
|
A | T | 3 | a0001c0001t0023g0250a0001c0001t0068g0245a0001c0003t0023g0143 | 3 | HG02451.hp2 HG03098.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1282-6157A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125070500 | ||||||
| chr6:125070507
|
A | G | 1 | a0001c0001t0002g0221 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1282-6150A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125070507 | ||||||
| chr6:125070541
|
G | A | 9 | a0003c0004t0011g0149a0003c0004t0011g0150a0003c0004t0011g0157others(6): Show | 9 | HG00741.hp1 HG02055.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1282-6116G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125070541 | ||||||
| chr6:125070547
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1282-6110G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125070547 | ||||||
| chr6:125070549
|
A | G | 29 | a0001c0001t0008g0182a0001c0001t0021g0133a0001c0001t0021g0159others(26): Show | 29 | HG00741.hp1 HG01243.hp1 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.1282-6108A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125070549 | ||||||
| chr6:125070839
|
A | T | 2 | a0001c0001t0024g0170a0008c0015t0053g0248 | 2 | HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1282-5818A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125070839 | ||||||
| chr6:125070942
|
T | C | 3 | a0001c0001t0001g0152a0001c0001t0001g0231a0009c0014t0001g0127 | 3 | HG00323.hp1 HG02083.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1282-5715T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125070942 | ||||||
| chr6:125070947
|
G | T | 90 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0002g0055others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.1282-5710G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125070947 | ||||||
| chr6:125070948
|
T | C | 1 | a0001c0001t0015g0225 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1282-5709T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125070948 | ||||||
| chr6:125071045
|
A | T | 3 | a0001c0001t0001g0080a0001c0001t0001g0105a0001c0001t0001g0212 | 3 | HG01952.hp1 HG02273.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.1282-5612A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125071045 | ||||||
| chr6:125071129
|
C | A | 29 | a0001c0001t0008g0182a0001c0001t0021g0133a0001c0001t0021g0159others(26): Show | 29 | HG00741.hp1 HG01243.hp1 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.1282-5528C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125071129 | ||||||
| chr6:125071148
|
G | A | 1 | a0001c0001t0001g0043 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1282-5509G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125071148 | ||||||
| chr6:125071208
|
A | G | 1 | a0001c0001t0001g0209 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1282-5449A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125071208 | ||||||
| chr6:125071231
|
C | A | 1 | a0001c0001t0001g0215 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1282-5426C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125071231 | ||||||
| chr6:125071253
|
T | C | 161 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0002g0055others(158): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.1282-5404T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125071253 | ||||||
| chr6:125071260
|
T | A | 1 | a0003c0004t0011g0157 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1282-5397T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125071260 | ||||||
| chr6:125071335
|
G | A | 1 | a0001c0001t0021g0133 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1282-5322G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125071335 | ||||||
| chr6:125071344
|
C | T | 2 | a0001c0001t0016g0083a0001c0001t0016g0222 | 2 | HG02602.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1282-5313C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125071344 | ||||||
| chr6:125071365
|
C | T | 1 | a0001c0001t0039g0179 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1282-5292C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125071365 | ||||||
| chr6:125071454
|
A | C | 1 | a0001c0012t0031g0256 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1282-5203A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125071454 | ||||||
| chr6:125071482
|
ATATGTGT others(1): Show |
A | 6 | a0001c0001t0017g0101a0001c0001t0017g0154a0001c0001t0017g0254others(3): Show | 6 | HG01884.hp2 HG02258.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1282-5173_1282-516 others(12): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125071482 | |||||
| chr6:125071484
|
A | ATG | 14 | a0001c0001t0001g0063a0001c0001t0001g0072a0001c0001t0001g0108others(11): Show | 14 | HG00408.hp2 HG00423.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.1282-5121_1282-512 others(6): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125071484 | |||||
| chr6:125071484
|
A | ATGTG | 7 | a0001c0001t0005g0082a0001c0001t0005g0208a0001c0001t0005g0218others(4): Show | 7 | NA18946.hp2 NA18975.hp1 NA18989.hp2 others(4): Show |
intron_variant | MODIFIER | c.1282-5123_1282-512 others(8): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125071484 | |||||
| chr6:125071484
|
A | ATGTGTGT others(3): Show |
2 | a0001c0001t0014g0060a0001c0001t0057g0246 | 2 | NA19010.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1282-5129_1282-512 others(14): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125071484 | |||||
| chr6:125071484
|
ATG | A | 38 | a0001c0001t0001g0043a0001c0001t0001g0047a0001c0001t0001g0057others(35): Show | 38 | HG00323.hp1 HG00609.hp2 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.1282-5121_1282-512 others(6): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125071484 | |||||
| chr6:125071484
|
ATGTG | A | 39 | a0001c0001t0001g0044a0001c0001t0001g0051a0001c0001t0001g0052others(36): Show | 39 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(36): Show |
intron_variant | MODIFIER | c.1282-5123_1282-512 others(8): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125071484 | |||||
| chr6:125071484
|
ATGTGTG | A | 74 | a0001c0001t0001g0050a0001c0001t0001g0116a0001c0001t0002g0055others(71): Show | 74 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.1282-5125_1282-512 others(10): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125071484 | |||||
| chr6:125071484
|
ATGTGTGT others(1): Show |
A | 28 | a0001c0001t0003g0002a0001c0001t0003g0085a0001c0001t0003g0115others(25): Show | 30 | HG00642.hp1 HG00735.hp2 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.1282-5127_1282-512 others(12): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125071484 | |||||
| chr6:125071484
|
ATGTGTGT others(3): Show |
A | 3 | a0001c0001t0046g0196a0001c0003t0008g0131a0002c0002t0071g0038 | 3 | HG03130.hp1 HG03209.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1282-5129_1282-512 others(14): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125071484 | |||||
| chr6:125071484
|
ATGTGTGT others(5): Show |
A | 14 | a0001c0001t0021g0133a0001c0001t0021g0159a0001c0001t0026g0160others(11): Show | 14 | HG00741.hp1 HG02630.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.1282-5131_1282-512 others(16): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125071484 | |||||
| chr6:125071484
|
ATGTGTGT others(7): Show |
A | 11 | a0001c0001t0008g0182a0001c0003t0008g0151a0001c0003t0008g0175others(8): Show | 11 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1282-5133_1282-512 others(18): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125071484 | |||||
| chr6:125071484
|
ATGTGTGT others(9): Show |
A | 1 | a0001c0001t0023g0250 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1282-5135_1282-512 others(20): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125071484 | |||||
| chr6:125071484
|
ATGTGTGT others(13): Show |
A | 4 | a0001c0001t0001g0104a0001c0001t0001g0235a0001c0001t0006g0177others(1): Show | 4 | HG01243.hp2 HG01993.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1282-5139_1282-512 others(24): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125071484 | |||||
| chr6:125071528
|
G | A | 4 | a0001c0001t0024g0170a0001c0001t0040g0261a0002c0002t0027g0019others(1): Show | 4 | HG00738.hp2 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1282-5129G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125071528 | ||||||
| chr6:125071530
|
G | A | 80 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0002g0055others(77): Show | 80 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(77): Show |
intron_variant | MODIFIER | c.1282-5127G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125071530 | ||||||
| chr6:125071532
|
G | A | 89 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0002g0055others(86): Show | 89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
intron_variant | MODIFIER | c.1282-5125G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125071532 | ||||||
| chr6:125071534
|
G | A | 103 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0002g0055others(100): Show | 103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
intron_variant | MODIFIER | c.1282-5123G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125071534 | ||||||
| chr6:125071536
|
G | A | 131 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0002g0055others(128): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.1282-5121G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125071536 | ||||||
| chr6:125071538
|
A | G | 1 | a0001c0001t0001g0108 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1282-5119A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125071538 | ||||||
| chr6:125071689
|
C | A | 1 | a0001c0003t0008g0151 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1282-4968C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125071689 | ||||||
| chr6:125071810
|
A | G | 90 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0002g0055others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.1282-4847A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125071810 | ||||||
| chr6:125071828
|
G | A | 161 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0002g0055others(158): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.1282-4829G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125071828 | ||||||
| chr6:125072028
|
C | A | 1 | a0001c0001t0001g0070 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1282-4629C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125072028 | ||||||
| chr6:125072041
|
G | T | 22 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0004g0046others(19): Show | 22 | HG00099.hp2 HG00140.hp1 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.1282-4616G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125072041 | ||||||
| chr6:125072060
|
A | G | 90 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0002g0055others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.1282-4597A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125072060 | ||||||
| chr6:125072261
|
A | G | 1 | a0001c0001t0037g0139 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1282-4396A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125072261 | ||||||
| chr6:125072278
|
T | A | 15 | a0001c0001t0003g0002a0001c0001t0003g0085a0001c0001t0003g0115others(12): Show | 17 | HG00642.hp1 HG00735.hp2 HG02083.hp1 others(14): Show |
intron_variant | MODIFIER | c.1282-4379T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125072278 | ||||||
| chr6:125072450
|
A | G | 1 | a0010c0013t0030g0192 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1282-4207A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125072450 | ||||||
| chr6:125072626
|
T | A | 1 | a0001c0001t0024g0184 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1282-4031T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125072626 | ||||||
| chr6:125072654
|
T | C | 11 | a0001c0001t0045g0161a0002c0002t0071g0038a0003c0004t0011g0149others(8): Show | 11 | HG00741.hp1 HG02055.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1282-4003T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125072654 | ||||||
| chr6:125072669
|
C | T | 1 | a0001c0001t0023g0250 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1282-3988C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125072669 | ||||||
| chr6:125072854
|
C | CAG | 161 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0002g0055others(158): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.1282-3802_1282-380 others(6): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125072854 | |||||
| chr6:125072972
|
G | A | 1 | a0001c0012t0031g0256 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1282-3685G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125072972 | ||||||
| chr6:125073012
|
G | A | 6 | a0001c0001t0021g0133a0001c0001t0021g0159a0001c0001t0026g0160others(3): Show | 6 | HG02809.hp1 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1282-3645G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125073012 | ||||||
| chr6:125073049
|
G | A | 1 | a0001c0001t0040g0261 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1282-3608G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125073049 | ||||||
| chr6:125073453
|
G | A | 11 | a0001c0001t0006g0003a0001c0001t0006g0147a0001c0001t0006g0156others(8): Show | 11 | HG01884.hp1 HG02109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1282-3204G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125073453 | ||||||
| chr6:125073609
|
A | G | 161 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0002g0055others(158): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.1282-3048A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125073609 | ||||||
| chr6:125073628
|
C | T | 101 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0002g0055others(98): Show | 101 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(98): Show |
intron_variant | MODIFIER | c.1282-3029C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125073628 | ||||||
| chr6:125073676
|
A | C | 90 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0002g0055others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.1282-2981A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125073676 | ||||||
| chr6:125073942
|
A | T | 1 | a0001c0001t0050g0041 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1282-2715A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125073942 | ||||||
| chr6:125074000
|
T | C | 90 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0002g0055others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.1282-2657T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125074000 | ||||||
| chr6:125074044
|
A | T | 101 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0002g0055others(98): Show | 101 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(98): Show |
intron_variant | MODIFIER | c.1282-2613A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125074044 | ||||||
| chr6:125074048
|
G | C | 101 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0002g0055others(98): Show | 101 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(98): Show |
intron_variant | MODIFIER | c.1282-2609G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125074048 | ||||||
| chr6:125074198
|
G | A | 30 | a0001c0001t0001g0063a0001c0001t0001g0072a0001c0001t0001g0093others(27): Show | 30 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.1282-2459G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125074198 | ||||||
| chr6:125074226
|
T | C | 1 | a0001c0012t0031g0256 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1282-2431T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125074226 | ||||||
| chr6:125074297
|
G | GTAGA | 21 | a0001c0001t0001g0231a0001c0001t0002g0059a0001c0001t0002g0086others(18): Show | 22 | HG00323.hp1 HG00741.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.1282-2308_1282-230 others(8): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125074297 | |||||
| chr6:125074297
|
G | GTAGATAG others(1): Show |
3 | a0001c0001t0002g0141a0001c0001t0004g0123a0001c0001t0022g0180 | 3 | HG01169.hp1 HG03540.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1282-2312_1282-230 others(12): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125074297 | |||||
| chr6:125074297
|
GTAGA | G | 96 | a0001c0001t0001g0050a0001c0001t0001g0057a0001c0001t0001g0064others(93): Show | 96 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(93): Show |
intron_variant | MODIFIER | c.1282-2308_1282-230 others(8): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125074297 | |||||
| chr6:125074297
|
GTAGATAG others(1): Show |
G | 31 | a0001c0001t0001g0080a0001c0001t0001g0093a0001c0001t0001g0106others(28): Show | 31 | HG00408.hp2 HG00609.hp2 HG01346.hp1 others(28): Show |
intron_variant | MODIFIER | c.1282-2312_1282-230 others(12): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125074297 | |||||
| chr6:125074297
|
GTAGATAG others(5): Show |
G | 30 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0063others(27): Show | 30 | HG00423.hp1 HG00738.hp1 HG01433.hp1 others(27): Show |
intron_variant | MODIFIER | c.1282-2316_1282-230 others(16): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125074297 | |||||
| chr6:125074297
|
GTAGATAG others(9): Show |
G | 1 | a0001c0001t0017g0254 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1282-2320_1282-230 others(20): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125074297 | |||||
| chr6:125074317
|
A | ATAGGTAG others(13): Show |
1 | a0001c0001t0033g0134 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1282-2337_1282-233 others(24): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125074317 | |||||
| chr6:125074388
|
T | G | 15 | a0001c0001t0010g0145a0001c0001t0010g0148a0001c0001t0010g0153others(12): Show | 15 | HG01891.hp2 HG02109.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.1282-2269T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125074388 | ||||||
| chr6:125074533
|
A | C | 11 | a0001c0001t0006g0003a0001c0001t0006g0147a0001c0001t0006g0156others(8): Show | 11 | HG01884.hp1 HG02109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1282-2124A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125074533 | ||||||
| chr6:125074585
|
C | T | 1 | a0005c0007t0006g0094 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1282-2072C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125074585 | ||||||
| chr6:125075070
|
A | G | 159 | a0001c0001t0002g0055a0001c0001t0002g0056a0001c0001t0002g0059others(156): Show | 161 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.1282-1587A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125075070 | ||||||
| chr6:125075188
|
G | A | 1 | a0003c0004t0011g0150 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1282-1469G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125075188 | ||||||
| chr6:125075235
|
T | A | 104 | a0001c0001t0002g0055a0001c0001t0002g0056a0001c0001t0002g0059others(101): Show | 104 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.1282-1422T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125075235 | ||||||
| chr6:125075406
|
C | A | 1 | a0001c0001t0040g0261 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1282-1251C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125075406 | ||||||
| chr6:125075407
|
G | A | 1 | a0001c0008t0003g0001 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1282-1250G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125075407 | ||||||
| chr6:125075528
|
C | T | 1 | a0001c0001t0002g0098 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1282-1129C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125075528 | ||||||
| chr6:125075764
|
C | T | 157 | a0001c0001t0002g0055a0001c0001t0002g0056a0001c0001t0002g0059others(154): Show | 159 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.1282-893C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125075764 | ||||||
| chr6:125075781
|
C | T | 11 | a0001c0001t0006g0003a0001c0001t0006g0147a0001c0001t0006g0156others(8): Show | 11 | HG01884.hp1 HG02109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1282-876C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125075781 | ||||||
| chr6:125075790
|
C | A | 14 | a0001c0001t0023g0250a0001c0001t0045g0161a0001c0001t0068g0245others(11): Show | 14 | HG00741.hp1 HG02055.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1282-867C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125075790 | ||||||
| chr6:125075847
|
G | A | 102 | a0001c0001t0002g0055a0001c0001t0002g0056a0001c0001t0002g0059others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.1282-810G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125075847 | ||||||
| chr6:125075899
|
C | G | 25 | a0001c0001t0006g0003a0001c0001t0006g0147a0001c0001t0006g0156others(22): Show | 25 | HG00741.hp1 HG01884.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.1282-758C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125075899 | ||||||
| chr6:125075940
|
A | G | 1 | a0001c0001t0001g0244 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1282-717A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125075940 | ||||||
| chr6:125076034
|
A | T | 1 | a0001c0001t0017g0254 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1282-623A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125076034 | ||||||
| chr6:125076066
|
C | T | 30 | a0001c0001t0003g0002a0001c0001t0003g0085a0001c0001t0003g0115others(27): Show | 32 | HG00642.hp1 HG00735.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.1282-591C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125076066 | ||||||
| chr6:125076144
|
A | C | 11 | a0001c0001t0006g0003a0001c0001t0006g0147a0001c0001t0006g0156others(8): Show | 11 | HG01884.hp1 HG02109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1282-513A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125076144 | ||||||
| chr6:125076414
|
A | G | 102 | a0001c0001t0002g0055a0001c0001t0002g0056a0001c0001t0002g0059others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.1282-243A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125076414 | ||||||
| chr6:125076594
|
C | T | 1 | a0001c0012t0031g0256 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1282-63C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125076594 | ||||||
| chr6:125076907
|
G | A | 1 | a0001c0012t0031g0256 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1483+49G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125076907 | ||||||
| chr6:125077167
|
G | A | 1 | a0001c0001t0024g0184 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1483+309G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125077167 | ||||||
| chr6:125077173
|
T | C | 6 | a0001c0001t0004g0071a0001c0001t0004g0075a0001c0001t0004g0096others(3): Show | 6 | HG02080.hp2 NA18948.hp1 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.1483+315T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125077173 | ||||||
| chr6:125077228
|
T | C | 14 | a0001c0001t0023g0250a0001c0001t0045g0161a0001c0001t0068g0245others(11): Show | 14 | HG00741.hp1 HG02055.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1483+370T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125077228 | ||||||
| chr6:125077409
|
A | G | 3 | a0001c0001t0023g0250a0001c0001t0068g0245a0001c0003t0023g0143 | 3 | HG02451.hp2 HG03098.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1483+551A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125077409 | ||||||
| chr6:125077456
|
G | A | 3 | a0001c0001t0022g0042a0001c0001t0022g0132a0001c0001t0022g0180 | 3 | HG02647.hp2 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1483+598G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125077456 | ||||||
| chr6:125077556
|
C | T | 14 | a0001c0001t0003g0002a0001c0001t0003g0085a0001c0001t0003g0115others(11): Show | 16 | HG00642.hp1 HG00735.hp2 HG02083.hp1 others(13): Show |
intron_variant | MODIFIER | c.1483+698C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125077556 | ||||||
| chr6:125077621
|
G | A | 5 | a0001c0001t0022g0042a0001c0001t0022g0132a0001c0001t0022g0180others(2): Show | 5 | HG02647.hp2 HG02886.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1483+763G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125077621 | ||||||
| chr6:125077721
|
CT | C | 5 | a0001c0001t0015g0045a0001c0001t0015g0207a0001c0001t0015g0225others(2): Show | 5 | NA18942.hp2 NA18943.hp1 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.1483+864delT | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125077721 | ||||||
| chr6:125077886
|
C | T | 9 | a0003c0004t0011g0149a0003c0004t0011g0150a0003c0004t0011g0157others(6): Show | 9 | HG00741.hp1 HG02055.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1483+1028C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125077886 | ||||||
| chr6:125077937
|
T | C | 2 | a0002c0002t0070g0039a0010c0013t0030g0192 | 2 | HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1483+1079T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125077937 | ||||||
| chr6:125077971
|
A | G | 1 | a0001c0003t0064g0189 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1483+1113A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125077971 | ||||||
| chr6:125078061
|
A | G | 15 | a0001c0001t0003g0002a0001c0001t0003g0085a0001c0001t0003g0115others(12): Show | 17 | HG00642.hp1 HG00735.hp2 HG02083.hp1 others(14): Show |
intron_variant | MODIFIER | c.1483+1203A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125078061 | ||||||
| chr6:125078081
|
G | A | 1 | a0001c0001t0010g0195 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1483+1223G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125078081 | ||||||
| chr6:125078224
|
C | T | 11 | a0001c0001t0006g0003a0001c0001t0006g0147a0001c0001t0006g0156others(8): Show | 11 | HG01884.hp1 HG02109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1483+1366C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125078224 | ||||||
| chr6:125078384
|
C | T | 11 | a0001c0001t0006g0003a0001c0001t0006g0147a0001c0001t0006g0156others(8): Show | 11 | HG01884.hp1 HG02109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1483+1526C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125078384 | ||||||
| chr6:125078442
|
C | T | 19 | a0001c0001t0003g0169a0001c0001t0003g0176a0001c0001t0003g0178others(16): Show | 19 | HG00741.hp1 HG02055.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.1483+1584C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125078442 | ||||||
| chr6:125078546
|
C | G | 162 | a0001c0001t0002g0055a0001c0001t0002g0056a0001c0001t0002g0059others(159): Show | 164 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.1483+1688C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125078546 | ||||||
| chr6:125078605
|
C | T | 1 | a0002c0002t0077g0034 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1483+1747C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125078605 | ||||||
| chr6:125078713
|
T | C | 5 | a0001c0001t0022g0042a0001c0001t0022g0132a0001c0001t0022g0180others(2): Show | 5 | HG02647.hp2 HG02886.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1483+1855T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125078713 | ||||||
| chr6:125078824
|
G | A | 14 | a0001c0001t0003g0002a0001c0001t0003g0085a0001c0001t0003g0115others(11): Show | 16 | HG00642.hp1 HG00735.hp2 HG02083.hp1 others(13): Show |
intron_variant | MODIFIER | c.1483+1966G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125078824 | ||||||
| chr6:125078981
|
C | T | 2 | a0001c0001t0016g0083a0001c0001t0016g0222 | 2 | HG02602.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1483+2123C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125078981 | ||||||
| chr6:125079065
|
G | A | 1 | a0001c0001t0038g0204 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1483+2207G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125079065 | ||||||
| chr6:125079141
|
G | A | 14 | a0001c0001t0003g0002a0001c0001t0003g0085a0001c0001t0003g0115others(11): Show | 16 | HG00642.hp1 HG00735.hp2 HG02083.hp1 others(13): Show |
intron_variant | MODIFIER | c.1483+2283G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125079141 | ||||||
| chr6:125079329
|
T | C | 12 | a0001c0001t0043g0004a0001c0001t0045g0161a0002c0002t0071g0038others(9): Show | 12 | HG00741.hp1 HG02055.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.1484-2107T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125079329 | ||||||
| chr6:125079382
|
C | T | 5 | a0001c0001t0002g0055a0001c0001t0002g0056a0001c0001t0002g0098others(2): Show | 5 | HG02132.hp1 NA18952.hp2 NA18956.hp1 others(2): Show |
intron_variant | MODIFIER | c.1484-2054C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125079382 | ||||||
| chr6:125079438
|
T | TA | 17 | a0001c0001t0003g0085a0001c0001t0008g0182a0001c0001t0021g0133others(14): Show | 17 | HG00642.hp1 HG01243.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1484-1983dupA | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr6 | 125079438 | |||||
| chr6:125079792
|
A | G | 15 | a0001c0001t0023g0250a0001c0001t0043g0004a0001c0001t0045g0161others(12): Show | 15 | HG00741.hp1 HG02055.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1484-1644A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125079792 | ||||||
| chr6:125079833
|
T | C | 5 | a0001c0001t0015g0045a0001c0001t0015g0207a0001c0001t0015g0225others(2): Show | 5 | NA18942.hp2 NA18943.hp1 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.1484-1603T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125079833 | ||||||
| chr6:125079888
|
A | T | 15 | a0001c0001t0023g0250a0001c0001t0043g0004a0001c0001t0045g0161others(12): Show | 15 | HG00741.hp1 HG02055.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1484-1548A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125079888 | ||||||
| chr6:125080124
|
T | A | 3 | a0001c0001t0023g0250a0001c0001t0068g0245a0001c0003t0023g0143 | 3 | HG02451.hp2 HG03098.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1484-1312T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125080124 | ||||||
| chr6:125080174
|
C | G | 1 | a0001c0001t0001g0213 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1484-1262C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125080174 | ||||||
| chr6:125080355
|
C | G | 14 | a0001c0001t0003g0002a0001c0001t0003g0085a0001c0001t0003g0115others(11): Show | 16 | HG00642.hp1 HG00735.hp2 HG02083.hp1 others(13): Show |
intron_variant | MODIFIER | c.1484-1081C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125080355 | ||||||
| chr6:125080418
|
C | T | 10 | a0001c0001t0043g0004a0003c0004t0011g0149a0003c0004t0011g0150others(7): Show | 10 | HG00741.hp1 HG02055.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1484-1018C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125080418 | ||||||
| chr6:125080574
|
C | T | 1 | a0001c0001t0055g0073 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1484-862C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125080574 | ||||||
| chr6:125080575
|
G | A | 3 | a0001c0001t0023g0250a0001c0001t0068g0245a0001c0003t0023g0143 | 3 | HG02451.hp2 HG03098.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1484-861G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125080575 | ||||||
| chr6:125080686
|
G | C | 3 | a0001c0001t0023g0250a0001c0001t0068g0245a0001c0003t0023g0143 | 3 | HG02451.hp2 HG03098.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1484-750G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125080686 | ||||||
| chr6:125081542
|
A | T | 1 | a0001c0001t0033g0134 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1555+35A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 5/5 | chr6 | 125081542 | ||||||
| chr6:125081565
|
C | T | 134 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0002g0055others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.1555+58C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 5/5 | chr6 | 125081565 | ||||||
| chr6:125081625
|
T | G | 1 | a0001c0001t0017g0254 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1555+118T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 5/5 | chr6 | 125081625 | ||||||
| chr6:125081732
|
C | T | 134 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0002g0055others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.1555+225C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 5/5 | chr6 | 125081732 | ||||||
| chr6:125081733
|
C | G | 3 | a0001c0001t0017g0101a0001c0001t0017g0154a0002c0002t0073g0030 | 3 | HG01884.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1555+226C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 5/5 | chr6 | 125081733 | ||||||
| chr6:125081863
|
C | T | 26 | a0001c0001t0006g0003a0001c0001t0006g0147a0001c0001t0006g0156others(23): Show | 26 | HG00741.hp1 HG01884.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1555+356C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 5/5 | chr6 | 125081863 | ||||||
| chr6:125082133
|
A | G | 48 | a0001c0001t0002g0055a0001c0001t0002g0056a0001c0001t0002g0059others(45): Show | 48 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.1555+626A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 5/5 | chr6 | 125082133 | ||||||
| chr6:125082203
|
A | T | 1 | a0001c0003t0064g0189 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1556-661A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 5/5 | chr6 | 125082203 | ||||||
| chr6:125082248
|
T | C | 93 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0002g0055others(90): Show | 93 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(90): Show |
intron_variant | MODIFIER | c.1556-616T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 5/5 | chr6 | 125082248 | ||||||
| chr6:125082293
|
G | T | 2 | a0001c0001t0012g0065a0001c0001t0012g0126 | 2 | HG00140.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1556-571G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 5/5 | chr6 | 125082293 | ||||||
| chr6:125082320
|
G | A | 9 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0052others(6): Show | 9 | HG01255.hp1 HG01358.hp2 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.1556-544G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 5/5 | chr6 | 125082320 | ||||||
| chr6:125082347
|
T | C | 1 | a0001c0003t0064g0189 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1556-517T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 5/5 | chr6 | 125082347 | ||||||
| chr6:125082478
|
A | G | 1 | a0001c0003t0064g0189 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1556-386A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 5/5 | chr6 | 125082478 | ||||||
| chr6:125082545
|
T | A | 1 | a0001c0001t0001g0263 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1556-319T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 5/5 | chr6 | 125082545 | ||||||
| chr6:125082661
|
G | C | 2 | a0001c0001t0001g0050a0001c0001t0001g0116 | 2 | NA18956.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.1556-203G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 5/5 | chr6 | 125082661 | ||||||
| chr6:125082720
|
T | C | 15 | a0001c0001t0023g0250a0001c0001t0043g0004a0001c0001t0045g0161others(12): Show | 15 | HG00741.hp1 HG02055.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1556-144T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 5/5 | chr6 | 125082720 | ||||||
| chr6:125082771
|
C | T | 26 | a0001c0001t0006g0003a0001c0001t0006g0147a0001c0001t0006g0156others(23): Show | 26 | HG00741.hp1 HG01884.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1556-93C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 5/5 | chr6 | 125082771 | ||||||
| chr6:125082777
|
C | T | 26 | a0001c0001t0006g0003a0001c0001t0006g0147a0001c0001t0006g0156others(23): Show | 26 | HG00741.hp1 HG01884.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1556-87C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 5/5 | chr6 | 125082777 | ||||||
| chr6:125082793
|
A | C | 9 | a0001c0001t0010g0145a0001c0001t0010g0148a0001c0001t0010g0153others(6): Show | 9 | HG01891.hp2 HG02109.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1556-71A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 5/5 | chr6 | 125082793 |