| geneid | 9671 |
|---|---|
| ensemblid | ENSG00000075035.10 |
| hgncid | 29117 |
| symbol | WSCD2 |
| name | WSC domain containing 2 |
| refseq_nuc | NM_014653.4 |
| refseq_prot | NP_055468.2 |
| ensembl_nuc | ENST00000547525.6 |
| ensembl_prot | ENSP00000448047.1 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 108129288 |
| end | 108250537 |
| strand | + |
| ver | v1.2 |
| region | chr12:108129288-108250537 |
| region5000 | chr12:108124288-108255537 |
| regionname0 | WSCD2_chr12_108129288_108250537 |
| regionname5000 | WSCD2_chr12_108124288_108255537 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 565 | 229 | 84 | 50 | 56 | 13 | 25 | 40 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0002 | 0/1 | 565 | 47 | 2 | 11 | 25 | 1 | 7 | 18 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0003 | 0/0 | 565 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0004 | 0/0 | 565 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0005 | 0/0 | 565 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0006 | 0/0 | 565 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0007 | 0/0 | 565 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 1698 | 220 | 78 | 48 | 55 | 13 | 25 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| c0002 | 0/1 | 1698 | 46 | 2 | 11 | 24 | 1 | 7 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| c0003 | 0/0 | 1698 | 7 | 6 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| c0004 | 0/0 | 1698 | 4 | 4 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| c0005 | 0/0 | 1698 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| c0006 | 0/0 | 1698 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| c0007 | 0/0 | 1698 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| c0008 | 0/0 | 1698 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| c0009 | 0/0 | 1698 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| c0010 | 0/0 | 1698 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| c0011 | 0/0 | 1698 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| 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 | 3385 | 41 | 6 | 10 | 14 | 2 | 9 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0002 | 0/0 | 3387 | 24 | 1 | 2 | 16 | 0 | 5 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0003 | 0/0 | 3387 | 18 | 4 | 4 | 9 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0004 | 1/1 | 3385 | 15 | 6 | 3 | 3 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0005 | 0/0 | 3387 | 12 | 0 | 5 | 5 | 0 | 2 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0006 | 0/0 | 3391 | 11 | 1 | 4 | 6 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0007 | 0/0 | 3387 | 8 | 1 | 3 | 2 | 1 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0008 | 0/0 | 3387 | 8 | 0 | 1 | 4 | 3 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0009 | 0/0 | 3391 | 8 | 0 | 1 | 7 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0010 | 0/0 | 3387 | 7 | 7 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0011 | 0/0 | 3385 | 7 | 7 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0012 | 0/0 | 3385 | 6 | 1 | 1 | 0 | 1 | 3 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0013 | 0/0 | 3389 | 6 | 3 | 1 | 2 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0014 | 0/0 | 3385 | 6 | 0 | 5 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0015 | 0/0 | 3395 | 5 | 2 | 1 | 0 | 1 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0016 | 0/0 | 3385 | 4 | 4 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0017 | 0/0 | 3393 | 4 | 2 | 1 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0018 | 0/0 | 3385 | 4 | 2 | 1 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0019 | 0/0 | 3395 | 4 | 0 | 1 | 0 | 1 | 2 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0020 | 0/0 | 3387 | 3 | 0 | 0 | 1 | 0 | 2 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0021 | 0/0 | 3389 | 3 | 3 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0022 | 0/0 | 3389 | 3 | 2 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0023 | 0/0 | 3387 | 3 | 0 | 0 | 3 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0024 | 0/0 | 3395 | 3 | 0 | 0 | 0 | 1 | 2 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0025 | 0/0 | 3389 | 3 | 3 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0026 | 0/0 | 3387 | 3 | 0 | 2 | 0 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0027 | 0/0 | 3387 | 2 | 2 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0028 | 0/0 | 3386 | 2 | 0 | 2 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0029 | 0/0 | 3389 | 2 | 0 | 2 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0030 | 0/0 | 3399 | 2 | 2 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0031 | 0/0 | 3387 | 2 | 1 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0032 | 0/0 | 3387 | 2 | 0 | 2 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0033 | 0/0 | 3391 | 2 | 1 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0034 | 0/0 | 3389 | 2 | 2 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0035 | 0/0 | 3387 | 2 | 1 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0036 | 0/0 | 3389 | 2 | 2 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0037 | 0/0 | 3389 | 2 | 2 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0038 | 0/0 | 3393 | 2 | 1 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0039 | 0/0 | 3387 | 2 | 0 | 0 | 2 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0040 | 0/0 | 3389 | 2 | 1 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0041 | 0/0 | 3387 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0042 | 0/0 | 3395 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0043 | 0/0 | 3387 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0044 | 0/0 | 3387 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0045 | 0/0 | 3385 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0046 | 0/0 | 3393 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0047 | 0/0 | 3387 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0048 | 0/0 | 3387 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0049 | 0/0 | 3387 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0050 | 0/0 | 3385 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0051 | 0/0 | 3385 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0052 | 0/0 | 3387 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0053 | 0/0 | 3396 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0054 | 0/0 | 3387 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0055 | 0/0 | 3387 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0056 | 0/0 | 3425 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0057 | 0/0 | 3389 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0058 | 0/0 | 3387 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0059 | 0/0 | 3391 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0060 | 0/0 | 3401 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0061 | 0/0 | 3387 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0062 | 0/0 | 3387 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0063 | 0/0 | 3387 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0064 | 0/0 | 3389 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0065 | 0/0 | 3385 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0066 | 0/0 | 3386 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0067 | 0/0 | 3387 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0068 | 0/0 | 3389 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0069 | 0/0 | 3389 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0070 | 0/0 | 3391 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0071 | 0/0 | 3385 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0072 | 0/0 | 3389 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0073 | 0/0 | 3385 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0074 | 0/0 | 3389 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0075 | 0/0 | 3387 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0076 | 0/0 | 3387 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| t0077 | 0/0 | 3391 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0002 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0167 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0173 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1698 | 220 | 78 | 48 | 55 | 13 | 25 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0003 | 0/0 | 1698 | 7 | 6 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0008 | 0/0 | 1698 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0010 | 0/0 | 1698 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0002c0002 | 0/1 | 1698 | 46 | 2 | 11 | 24 | 1 | 7 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0002c0009 | 0/0 | 1698 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0003c0004 | 0/0 | 1698 | 4 | 4 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0004c0005 | 0/0 | 1698 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0005c0006 | 0/0 | 1698 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0006c0007 | 0/0 | 1698 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0007c0011 | 0/0 | 1698 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5082 | 23 | 5 | 7 | 4 | 2 | 5 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0002 | 0/0 | 5084 | 15 | 0 | 1 | 12 | 0 | 2 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0003 | 0/0 | 5084 | 12 | 4 | 2 | 6 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0004 | 1/0 | 5082 | 12 | 5 | 3 | 2 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0005 | 0/0 | 5084 | 11 | 0 | 4 | 5 | 0 | 2 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0006 | 0/0 | 5088 | 11 | 1 | 4 | 6 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0007 | 0/0 | 5084 | 8 | 1 | 3 | 2 | 1 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0008 | 0/0 | 5084 | 8 | 0 | 1 | 4 | 3 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0009 | 0/0 | 5088 | 3 | 0 | 1 | 2 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0010 | 0/0 | 5084 | 7 | 7 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0011 | 0/0 | 5082 | 7 | 7 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0012 | 0/0 | 5082 | 5 | 0 | 1 | 0 | 1 | 3 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0013 | 0/0 | 5086 | 4 | 3 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0014 | 0/0 | 5082 | 6 | 0 | 5 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0015 | 0/0 | 5092 | 5 | 2 | 1 | 0 | 1 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0016 | 0/0 | 5082 | 2 | 2 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0017 | 0/0 | 5090 | 2 | 1 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0018 | 0/0 | 5082 | 3 | 2 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0019 | 0/0 | 5092 | 3 | 0 | 0 | 0 | 1 | 2 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0020 | 0/0 | 5084 | 3 | 0 | 0 | 1 | 0 | 2 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0021 | 0/0 | 5086 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0022 | 0/0 | 5086 | 3 | 2 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0023 | 0/0 | 5084 | 2 | 0 | 0 | 2 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0024 | 0/0 | 5092 | 3 | 0 | 0 | 0 | 1 | 2 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0025 | 0/0 | 5086 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0026 | 0/0 | 5084 | 3 | 0 | 2 | 0 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0027 | 0/0 | 5084 | 2 | 2 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0028 | 0/0 | 5083 | 2 | 0 | 2 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0029 | 0/0 | 5086 | 2 | 0 | 2 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0030 | 0/0 | 5096 | 2 | 2 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0032 | 0/0 | 5084 | 2 | 0 | 2 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0033 | 0/0 | 5088 | 2 | 1 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0034 | 0/0 | 5086 | 2 | 2 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0035 | 0/0 | 5084 | 2 | 1 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0036 | 0/0 | 5086 | 2 | 2 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0037 | 0/0 | 5086 | 2 | 2 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0039 | 0/0 | 5084 | 2 | 0 | 0 | 2 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0040 | 0/0 | 5086 | 2 | 1 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0041 | 0/0 | 5084 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0042 | 0/0 | 5092 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0043 | 0/0 | 5084 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0044 | 0/0 | 5084 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0045 | 0/0 | 5082 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0046 | 0/0 | 5090 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0047 | 0/0 | 5084 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0048 | 0/0 | 5084 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0050 | 0/0 | 5082 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0051 | 0/0 | 5082 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0052 | 0/0 | 5084 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0053 | 0/0 | 5093 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0054 | 0/0 | 5084 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0055 | 0/0 | 5084 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0056 | 0/0 | 5122 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0057 | 0/0 | 5086 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0058 | 0/0 | 5084 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0059 | 0/0 | 5088 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0060 | 0/0 | 5098 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0061 | 0/0 | 5084 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0062 | 0/0 | 5084 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0063 | 0/0 | 5084 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0064 | 0/0 | 5086 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0065 | 0/0 | 5082 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0066 | 0/0 | 5083 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0067 | 0/0 | 5084 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0069 | 0/0 | 5086 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0070 | 0/0 | 5088 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0071 | 0/0 | 5082 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0072 | 0/0 | 5086 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0073 | 0/0 | 5082 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0075 | 0/0 | 5084 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0001t0076 | 0/0 | 5084 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0003t0012 | 0/0 | 5082 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0003t0016 | 0/0 | 5082 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0003t0021 | 0/0 | 5086 | 2 | 2 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0003t0031 | 0/0 | 5084 | 2 | 1 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0003t0038 | 0/0 | 5090 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0008t0019 | 0/0 | 5092 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0001c0010t0049 | 0/0 | 5084 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0002c0002t0001 | 0/0 | 5082 | 17 | 1 | 3 | 9 | 0 | 4 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0002c0002t0002 | 0/0 | 5084 | 9 | 1 | 1 | 4 | 0 | 3 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0002c0002t0003 | 0/0 | 5084 | 6 | 0 | 2 | 3 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0002c0002t0004 | 0/1 | 5082 | 2 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0002c0002t0009 | 0/0 | 5088 | 5 | 0 | 0 | 5 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0002c0002t0013 | 0/0 | 5086 | 2 | 0 | 0 | 2 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0002c0002t0017 | 0/0 | 5090 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0002c0002t0018 | 0/0 | 5082 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0002c0002t0038 | 0/0 | 5090 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0002c0002t0068 | 0/0 | 5086 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0002c0002t0077 | 0/0 | 5088 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0002c0009t0001 | 0/0 | 5082 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0003c0004t0017 | 0/0 | 5090 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0003c0004t0025 | 0/0 | 5086 | 2 | 2 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0003c0004t0074 | 0/0 | 5086 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0004c0005t0005 | 0/0 | 5084 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0005c0006t0016 | 0/0 | 5082 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0006c0007t0023 | 0/0 | 5084 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| a0007c0011t0004 | 0/0 | 5082 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | copy fasta | chr12 | 108124288 | 108255537 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0003g0002 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0004g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0004g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0004g0167 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0004g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0004g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0004g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0005g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0005g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0005g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0005g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0005g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0005g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0005g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0005g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0005g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0005g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0005g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0006g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0006g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0006g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0006g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0006g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0006g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0006g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0006g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0006g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0006g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0007g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0007g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0007g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0007g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0007g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0007g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0007g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0007g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0008g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0008g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0008g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0008g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0008g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0008g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0008g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0009g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0009g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0009g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0010g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0010g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0010g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0010g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0010g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0010g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0010g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0011g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0011g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0011g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0011g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0011g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0011g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0012g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0012g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0012g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0012g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0012g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0013g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0013g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0013g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0013g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0014g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0014g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0014g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0014g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0014g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0014g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0015g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0015g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0015g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0015g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0015g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0016g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0016g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0017g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0017g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0018g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0018g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0018g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0019g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0019g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0019g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0020g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0020g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0020g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0021g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0022g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0022g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0022g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0023g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0023g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0024g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0024g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0024g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0025g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0026g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0026g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0026g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0027g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0028g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0028g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0029g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0029g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0030g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0030g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0032g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0032g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0033g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0033g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0034g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0034g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0035g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0035g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0036g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0036g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0037g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0037g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0039g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0039g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0040g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0040g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0041g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0042g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0043g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0044g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0045g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0046g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0047g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0048g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0050g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0051g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0052g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0053g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0054g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0055g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0056g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0057g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0058g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0059g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0060g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0061g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0062g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0063g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0064g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0065g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0066g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0067g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0069g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0070g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0071g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0072g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0073g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0075g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0001t0076g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0003t0012g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0003t0016g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0003t0021g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0003t0021g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0003t0031g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0003t0031g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0003t0038g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0008t0019g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0001c0010t0049g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0002c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0002c0002t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0002c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0002c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0002c0002t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0002c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0002c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0002c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0002c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0002c0002t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0002c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0002c0002t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0002c0002t0003g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0002c0002t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0002c0002t0003g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0002c0002t0003g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0002c0002t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0002c0002t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0002c0002t0004g0173 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0002c0002t0009g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0002c0002t0009g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0002c0002t0009g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0002c0002t0009g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0002c0002t0009g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0002c0002t0013g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0002c0002t0013g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0002c0002t0017g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0002c0002t0018g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0002c0002t0038g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0002c0002t0068g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0002c0002t0077g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0002c0009t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0003c0004t0017g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0003c0004t0025g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0003c0004t0025g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0003c0004t0074g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0004c0005t0005g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0005c0006t0016g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0006c0007t0023g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| a0007c0011t0004g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0168 | EUR | GBR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG00099 | hp2 | a0001 | c0001 | t0062 | g0034 | EUR | GBR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG00140 | hp1 | a0001 | c0001 | t0024 | g0015 | EUR | GBR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG00140 | hp2 | a0001 | c0001 | t0012 | g0024 | EUR | GBR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG00280 | hp1 | a0001 | c0001 | t0008 | g0021 | EUR | FIN | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG00280 | hp2 | a0002 | c0002 | t0003 | g0251 | EUR | FIN | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG00323 | hp1 | a0001 | c0001 | t0008 | g0012 | EUR | FIN | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG00323 | hp2 | a0001 | c0001 | t0026 | g0093 | EUR | FIN | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0133 | EAS | CHS | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | CHS | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG00438 | hp1 | a0006 | c0007 | t0023 | g0020 | EAS | CHS | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG00438 | hp2 | a0001 | c0001 | t0009 | g0194 | EAS | CHS | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG00558 | hp1 | a0002 | c0002 | t0003 | g0184 | EAS | CHS | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG00558 | hp2 | a0002 | c0002 | t0009 | g0132 | EAS | CHS | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG00597 | hp1 | a0002 | c0002 | t0002 | g0218 | EAS | CHS | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | CHS | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | CHS | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG00609 | hp2 | a0001 | c0001 | t0020 | g0273 | EAS | CHS | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG00639 | hp1 | a0001 | c0001 | t0013 | g0213 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG00639 | hp2 | a0001 | c0001 | t0009 | g0100 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG00642 | hp1 | a0001 | c0001 | t0007 | g0013 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG00642 | hp2 | a0001 | c0001 | t0005 | g0088 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG00733 | hp2 | a0004 | c0005 | t0005 | g0171 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG00735 | hp1 | a0002 | c0002 | t0018 | g0082 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG00735 | hp2 | a0001 | c0001 | t0006 | g0165 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0212 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG00738 | hp2 | a0001 | c0001 | t0053 | g0121 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01069 | hp1 | a0002 | c0002 | t0017 | g0038 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0069 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01074 | hp1 | a0002 | c0002 | t0003 | g0196 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0064 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01081 | hp2 | a0002 | c0002 | t0068 | g0214 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01099 | hp1 | a0001 | c0001 | t0015 | g0237 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01099 | hp2 | a0002 | c0002 | t0002 | g0270 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01109 | hp1 | a0001 | c0001 | t0064 | g0277 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01109 | hp2 | a0001 | c0001 | t0006 | g0170 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01167 | hp1 | a0001 | c0001 | t0040 | g0221 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01167 | hp2 | a0001 | c0001 | t0029 | g0235 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01168 | hp2 | a0001 | c0008 | t0019 | g0229 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01169 | hp1 | a0001 | c0001 | t0029 | g0236 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01175 | hp2 | a0002 | c0002 | t0003 | g0250 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01192 | hp1 | a0001 | c0001 | t0008 | g0026 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0195 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01243 | hp2 | a0001 | c0003 | t0031 | g0051 | AMR | PUR | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01256 | hp1 | a0001 | c0001 | t0005 | g0163 | AMR | CLM | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01256 | hp2 | a0001 | c0001 | t0007 | g0027 | AMR | CLM | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01257 | hp1 | a0001 | c0001 | t0032 | g0035 | AMR | CLM | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01257 | hp2 | a0001 | c0001 | t0005 | g0115 | AMR | CLM | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01258 | hp1 | a0001 | c0001 | t0005 | g0116 | AMR | CLM | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01258 | hp2 | a0001 | c0001 | t0007 | g0028 | AMR | CLM | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01261 | hp1 | a0001 | c0001 | t0069 | g0272 | AMR | CLM | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01261 | hp2 | a0002 | c0002 | t0077 | g0094 | AMR | CLM | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0169 | AMR | CLM | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01346 | hp2 | a0001 | c0001 | t0014 | g0140 | AMR | CLM | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01358 | hp1 | a0001 | c0001 | t0032 | g0036 | AMR | CLM | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01358 | hp2 | a0002 | c0002 | t0001 | g0207 | AMR | CLM | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01361 | hp1 | a0001 | c0001 | t0006 | g0117 | AMR | CLM | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01361 | hp2 | a0001 | c0001 | t0026 | g0092 | AMR | CLM | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01433 | hp1 | a0001 | c0001 | t0014 | g0136 | AMR | CLM | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01433 | hp2 | a0001 | c0001 | t0026 | g0095 | AMR | CLM | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01515 | hp1 | a0001 | c0001 | t0019 | g0083 | EUR | IBS | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0148 | EUR | IBS | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01516 | hp1 | a0001 | c0001 | t0015 | g0089 | EUR | IBS | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01516 | hp2 | a0001 | c0001 | t0007 | g0014 | EUR | IBS | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01884 | hp1 | a0001 | c0001 | t0010 | g0113 | AFR | ACB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01891 | hp1 | a0001 | c0001 | t0044 | g0160 | AFR | ACB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | ACB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01943 | hp1 | a0001 | c0001 | t0012 | g0040 | AMR | PEL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01943 | hp2 | a0001 | c0001 | t0035 | g0259 | AMR | PEL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01952 | hp1 | a0001 | c0001 | t0014 | g0209 | AMR | PEL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01952 | hp2 | a0001 | c0001 | t0006 | g0166 | AMR | PEL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01978 | hp1 | a0001 | c0001 | t0004 | g0122 | AMR | PEL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01981 | hp1 | a0001 | c0001 | t0028 | g0240 | AMR | PEL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01981 | hp2 | a0001 | c0001 | t0004 | g0114 | AMR | PEL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01993 | hp1 | a0001 | c0001 | t0014 | g0135 | AMR | PEL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG01993 | hp2 | a0001 | c0001 | t0028 | g0172 | AMR | PEL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | KHV | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02015 | hp2 | a0002 | c0002 | t0013 | g0192 | EAS | KHV | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0234 | AFR | ACB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02055 | hp2 | a0001 | c0001 | t0015 | g0156 | AFR | ACB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02080 | hp1 | a0002 | c0002 | t0009 | g0223 | EAS | KHV | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0178 | EAS | KHV | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02135 | hp1 | a0001 | c0001 | t0004 | g0124 | EAS | KHV | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02135 | hp2 | a0001 | c0001 | t0075 | g0141 | EAS | KHV | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02145 | hp1 | a0002 | c0002 | t0001 | g0206 | AFR | ACB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02145 | hp2 | a0001 | c0001 | t0010 | g0159 | AFR | ACB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02148 | hp1 | a0001 | c0001 | t0022 | g0241 | AMR | PEL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02148 | hp2 | a0002 | c0002 | t0038 | g0074 | AMR | PEL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02165 | hp1 | a0002 | c0002 | t0013 | g0193 | EAS | CDX | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | CDX | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0112 | AFR | ACB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02257 | hp2 | a0001 | c0001 | t0016 | g0044 | AFR | ACB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02258 | hp1 | a0002 | c0002 | t0002 | g0203 | AFR | ACB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02258 | hp2 | a0001 | c0001 | t0043 | g0004 | AFR | ACB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02273 | hp1 | a0001 | c0001 | t0014 | g0144 | AMR | PEL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02280 | hp1 | a0001 | c0001 | t0021 | g0085 | AFR | ACB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02280 | hp2 | a0001 | c0001 | t0010 | g0262 | AFR | ACB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02451 | hp1 | a0001 | c0003 | t0031 | g0050 | AFR | ACB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02451 | hp2 | a0001 | c0001 | t0071 | g0249 | AFR | ACB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0225 | EAS | KHV | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0215 | EAS | KHV | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02572 | hp1 | a0001 | c0001 | t0011 | g0128 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02572 | hp2 | a0001 | c0001 | t0036 | g0068 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02615 | hp1 | a0001 | c0003 | t0021 | g0245 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02615 | hp2 | a0001 | c0001 | t0010 | g0084 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02622 | hp1 | a0001 | c0001 | t0030 | g0162 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02622 | hp2 | a0001 | c0001 | t0037 | g0062 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02630 | hp1 | a0001 | c0001 | t0052 | g0131 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02630 | hp2 | a0001 | c0001 | t0011 | g0090 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02647 | hp1 | a0001 | c0001 | t0018 | g0059 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02647 | hp2 | a0001 | c0003 | t0038 | g0063 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02683 | hp1 | a0001 | c0001 | t0012 | g0041 | SAS | PJL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02683 | hp2 | a0001 | c0001 | t0005 | g0091 | SAS | PJL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02717 | hp1 | a0001 | c0001 | t0045 | g0232 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02717 | hp2 | a0001 | c0001 | t0070 | g0269 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02723 | hp1 | a0001 | c0001 | t0033 | g0049 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0066 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02735 | hp1 | a0001 | c0001 | t0020 | g0164 | SAS | PJL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02735 | hp2 | a0002 | c0002 | t0002 | g0216 | SAS | PJL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02738 | hp1 | a0001 | c0001 | t0066 | g0072 | SAS | PJL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02738 | hp2 | a0001 | c0001 | t0020 | g0265 | SAS | PJL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02809 | hp1 | a0001 | c0001 | t0006 | g0086 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02809 | hp2 | a0001 | c0003 | t0012 | g0045 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02818 | hp1 | a0001 | c0001 | t0042 | g0157 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02818 | hp2 | a0001 | c0001 | t0017 | g0023 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02886 | hp1 | a0001 | c0001 | t0018 | g0060 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02886 | hp2 | a0001 | c0001 | t0035 | g0233 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02895 | hp1 | a0001 | c0001 | t0034 | g0031 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02895 | hp2 | a0001 | c0001 | t0027 | g0005 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02896 | hp1 | a0001 | c0001 | t0011 | g0006 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0161 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02897 | hp1 | a0001 | c0001 | t0011 | g0006 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02897 | hp2 | a0001 | c0001 | t0027 | g0005 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02922 | hp1 | a0001 | c0001 | t0011 | g0056 | AFR | ESN | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02922 | hp2 | a0001 | c0001 | t0007 | g0048 | AFR | ESN | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02965 | hp1 | a0001 | c0001 | t0011 | g0125 | AFR | ESN | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02965 | hp2 | a0001 | c0001 | t0037 | g0099 | AFR | ESN | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02970 | hp1 | a0001 | c0001 | t0063 | g0276 | AFR | ESN | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02970 | hp2 | a0001 | c0001 | t0040 | g0222 | AFR | ESN | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02976 | hp1 | a0001 | c0001 | t0013 | g0255 | AFR | ESN | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02976 | hp2 | a0001 | c0001 | t0073 | g0061 | AFR | ESN | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG03017 | hp1 | a0001 | c0001 | t0012 | g0025 | SAS | PJL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG03017 | hp2 | a0001 | c0001 | t0019 | g0137 | SAS | PJL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG03041 | hp1 | a0001 | c0001 | t0010 | g0129 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG03041 | hp2 | a0001 | c0001 | t0013 | g0256 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG03098 | hp1 | a0003 | c0004 | t0017 | g0052 | AFR | MSL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG03098 | hp2 | a0001 | c0001 | t0016 | g0278 | AFR | MSL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG03130 | hp1 | a0001 | c0001 | t0060 | g0274 | AFR | ESN | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG03130 | hp2 | a0001 | c0001 | t0011 | g0127 | AFR | ESN | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG03139 | hp1 | a0001 | c0001 | t0010 | g0238 | AFR | ESN | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG03195 | hp1 | a0001 | c0001 | t0051 | g0158 | AFR | ESN | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG03195 | hp2 | a0001 | c0001 | t0050 | g0098 | AFR | ESN | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG03209 | hp1 | a0001 | c0001 | t0034 | g0032 | AFR | MSL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG03209 | hp2 | a0001 | c0001 | t0030 | g0130 | AFR | MSL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0065 | AFR | MSL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG03225 | hp2 | a0003 | c0004 | t0025 | g0054 | AFR | MSL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0150 | SAS | PJL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG03239 | hp2 | a0001 | c0001 | t0012 | g0030 | SAS | PJL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG03453 | hp1 | a0001 | c0001 | t0036 | g0261 | AFR | MSL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG03453 | hp2 | a0003 | c0004 | t0074 | g0226 | AFR | MSL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG03486 | hp1 | a0001 | c0003 | t0021 | g0266 | AFR | MSL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG03486 | hp2 | a0001 | c0001 | t0054 | g0126 | AFR | MSL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG03490 | hp1 | a0001 | c0001 | t0017 | g0011 | SAS | PJL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG03490 | hp2 | a0001 | c0001 | t0024 | g0042 | SAS | PJL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG03492 | hp1 | a0001 | c0001 | t0024 | g0029 | SAS | PJL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0220 | SAS | PJL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG03516 | hp1 | a0001 | c0001 | t0057 | g0047 | AFR | ESN | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | ESN | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG03540 | hp1 | a0001 | c0001 | t0022 | g0151 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG03540 | hp2 | a0001 | c0001 | t0013 | g0257 | AFR | GWD | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG03579 | hp1 | a0001 | c0001 | t0022 | g0155 | AFR | MSL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG03579 | hp2 | a0001 | c0001 | t0025 | g0033 | AFR | MSL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | STU | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG03688 | hp2 | a0001 | c0001 | t0047 | g0263 | SAS | STU | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG03704 | hp1 | a0001 | c0001 | t0019 | g0078 | SAS | PJL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0219 | SAS | PJL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG03710 | hp1 | a0001 | c0001 | t0018 | g0217 | SAS | PJL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | BEB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG03831 | hp2 | a0002 | c0002 | t0002 | g0224 | SAS | BEB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | BEB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | BEB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG03927 | hp1 | a0001 | c0001 | t0005 | g0264 | SAS | BEB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG03927 | hp2 | a0001 | c0001 | t0007 | g0039 | SAS | BEB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG03942 | hp1 | a0001 | c0001 | t0056 | g0016 | SAS | BEB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0076 | SAS | BEB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0188 | SAS | BEB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0179 | SAS | BEB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG04204 | hp1 | a0002 | c0002 | t0002 | g0147 | SAS | STU | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG04204 | hp2 | a0001 | c0001 | t0015 | g0174 | SAS | STU | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0110 | AFR | YRI | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA18522 | hp2 | a0001 | c0001 | t0067 | g0067 | AFR | YRI | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | CHB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA18612 | hp2 | a0001 | c0001 | t0008 | g0018 | EAS | CHB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | CHB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | CHB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA18906 | hp1 | a0001 | c0001 | t0065 | g0275 | AFR | YRI | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0248 | AFR | YRI | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA18940 | hp1 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA18940 | hp2 | a0001 | c0001 | t0003 | g0267 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA18941 | hp1 | a0001 | c0001 | t0006 | g0118 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA18941 | hp2 | a0001 | c0001 | t0023 | g0017 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA18944 | hp1 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0186 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0145 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA18946 | hp1 | a0001 | c0001 | t0005 | g0119 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA18946 | hp2 | a0002 | c0002 | t0002 | g0271 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA18948 | hp1 | a0002 | c0002 | t0003 | g0268 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA18948 | hp2 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA18949 | hp1 | a0001 | c0001 | t0005 | g0120 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA18949 | hp2 | a0002 | c0002 | t0002 | g0183 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA18951 | hp1 | a0001 | c0001 | t0059 | g0019 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA18952 | hp1 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA18952 | hp2 | a0001 | c0001 | t0006 | g0243 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA18953 | hp1 | a0001 | c0001 | t0055 | g0244 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA18953 | hp2 | a0002 | c0002 | t0009 | g0246 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0199 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA18959 | hp2 | a0001 | c0001 | t0005 | g0123 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA18960 | hp2 | a0001 | c0001 | t0033 | g0008 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA18971 | hp2 | a0002 | c0002 | t0009 | g0200 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA18978 | hp1 | a0002 | c0009 | t0001 | g0185 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA18981 | hp1 | a0001 | c0001 | t0007 | g0009 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA18982 | hp1 | a0002 | c0002 | t0004 | g0071 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA18982 | hp2 | a0001 | c0001 | t0039 | g0189 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA18984 | hp1 | a0002 | c0002 | t0001 | g0208 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA18994 | hp1 | a0001 | c0001 | t0039 | g0190 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA18994 | hp2 | a0001 | c0001 | t0048 | g0177 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA18998 | hp1 | a0001 | c0001 | t0023 | g0022 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA18998 | hp2 | a0001 | c0001 | t0076 | g0210 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA19000 | hp1 | a0001 | c0001 | t0007 | g0037 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0253 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA19009 | hp2 | a0001 | c0001 | t0014 | g0153 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA19012 | hp1 | a0001 | c0001 | t0006 | g0175 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0109 | AFR | LWK | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA19043 | hp2 | a0001 | c0001 | t0046 | g0152 | AFR | LWK | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA19064 | hp1 | a0001 | c0001 | t0005 | g0176 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA19064 | hp2 | a0002 | c0002 | t0002 | g0231 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA19068 | hp1 | a0001 | c0001 | t0008 | g0007 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA19068 | hp2 | a0002 | c0002 | t0009 | g0187 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA19079 | hp1 | a0002 | c0002 | t0001 | g0211 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA19079 | hp2 | a0001 | c0001 | t0006 | g0242 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA19081 | hp1 | a0001 | c0001 | t0005 | g0070 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA19081 | hp2 | a0002 | c0002 | t0001 | g0204 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA19087 | hp1 | a0001 | c0001 | t0009 | g0134 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA19087 | hp2 | a0002 | c0002 | t0001 | g0180 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA19088 | hp1 | a0001 | c0010 | t0049 | g0239 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA19088 | hp2 | a0002 | c0002 | t0003 | g0202 | EAS | JPT | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA20129 | hp1 | a0005 | c0006 | t0016 | g0046 | AFR | ASW | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA20129 | hp2 | a0007 | c0011 | t0004 | g0097 | AFR | ASW | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA20752 | hp1 | a0001 | c0001 | t0008 | g0010 | EUR | TSI | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0107 | EUR | TSI | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02109 | hp1 | a0001 | c0001 | t0061 | g0260 | AFR | ACB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02109 | hp2 | a0003 | c0004 | t0025 | g0053 | AFR | ACB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02486 | hp1 | a0001 | c0003 | t0016 | g0055 | AFR | ACB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | MSL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG03471 | hp2 | a0001 | c0001 | t0010 | g0004 | AFR | MSL | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG06807 | hp1 | a0001 | c0001 | t0041 | g0111 | AFR | USA | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| HG06807 | hp2 | a0001 | c0001 | t0015 | g0087 | AFR | USA | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA21309 | hp1 | a0001 | c0001 | t0058 | g0043 | AFR | LWK | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| NA21309 | hp2 | a0001 | c0001 | t0072 | g0108 | AFR | LWK | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0004 | g0173 | REF | REF | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0004 | g0167 | REF | REF | WSCD2_chr12_108124288_108255537 | WSCD2 | chr12 | 108124288 | 108255537 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:108195981
|
C | T | 1 | a0007 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.149C>T | p.Ala50Val | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/9 | 1339/5082 | 149/1698 | 50/565 | chr12 | 108195981 | ||
| chr12:108196134
|
G | A | 1 | a0004 | 1 | HG00733.hp2 | missense_variant | MODERATE | c.302G>A | p.Arg101Lys | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/9 | 1492/5082 | 302/1698 | 101/565 | chr12 | 108196134 | ||
| chr12:108196188
|
T | C | 1 | a0003 | 4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
missense_variant | MODERATE | c.356T>C | p.Val119Ala | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/9 | 1546/5082 | 356/1698 | 119/565 | chr12 | 108196188 | ||
| chr12:108224769
|
G | A | 1 | a0005 | 1 | NA20129.hp1 | missense_variant | MODERATE | c.713G>A | p.Arg238His | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 5/9 | 1903/5082 | 713/1698 | 238/565 | chr12 | 108224769 | ||
| chr12:108224853
|
C | T | 1 | a0002 | 47 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(44): Show |
missense_variant | MODERATE | c.797C>T | p.Thr266Ile | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 5/9 | 1987/5082 | 797/1698 | 266/565 | chr12 | 108224853 | ||
| chr12:108227106
|
G | C | 1 | a0006 | 1 | HG00438.hp1 | missense_variant | MODERATE | c.921G>C | p.Glu307Asp | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/9 | 2111/5082 | 921/1698 | 307/565 | chr12 | 108227106 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:108195985
|
C | T | 1 | a0001c0010 | 1 | NA19088.hp1 | synonymous_variant | LOW | c.153C>T | p.Asn51Asn | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/9 | 1343/5082 | 153/1698 | 51/565 | chr12 | 108195985 | ||
| chr12:108210151
|
C | T | 1 | a0002c0009 | 1 | NA18978.hp1 | synonymous_variant | LOW | c.528C>T | p.Gly176Gly | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/9 | 1718/5082 | 528/1698 | 176/565 | chr12 | 108210151 | ||
| chr12:108224776
|
C | G | 1 | a0001c0008 | 1 | HG01168.hp2 | synonymous_variant | LOW | c.720C>G | p.Pro240Pro | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 5/9 | 1910/5082 | 720/1698 | 240/565 | chr12 | 108224776 | ||
| chr12:108224839
|
C | T | 1 | a0001c0003 | 7 | HG01243.hp2 HG02451.hp1 HG02486.hp1 others(4): Show |
synonymous_variant | LOW | c.783C>T | p.Cys261Cys | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 5/9 | 1973/5082 | 783/1698 | 261/565 | chr12 | 108224839 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:108129413
|
C | T | 3 | a0001c0001t0026a0001c0001t0040a0002c0002t0077 | 6 | HG00323.hp2 HG01167.hp1 HG01261.hp2 others(3): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-1065C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/9 | chr12 | 108129413 | ||||||
| chr12:108129421
|
C | T | 37 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(34): Show | 137 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(134): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-1057C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/9 | chr12 | 108129421 | ||||||
| chr12:108129437
|
C | T | 1 | a0001c0001t0062 | 1 | HG00099.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-1041C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/9 | chr12 | 108129437 | ||||||
| chr12:108129442
|
C | A | 1 | a0001c0001t0062 | 1 | HG00099.hp2 | 5_prime_UTR_variant | MODIFIER | c.-1036C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/9 | 66391 | chr12 | 108129442 | |||||
| chr12:108129444
|
C | T | 34 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(31): Show | 134 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(131): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-1034C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/9 | chr12 | 108129444 | ||||||
| chr12:108129471
|
A | G | 3 | a0001c0001t0035a0001c0001t0036a0001c0001t0061 | 5 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-1007A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/9 | 66362 | chr12 | 108129471 | |||||
| chr12:108129559
|
C | G | 3 | a0001c0001t0063a0001c0001t0064a0001c0001t0065 | 3 | HG01109.hp1 HG02970.hp1 NA18906.hp1 |
5_prime_UTR_variant | MODIFIER | c.-919C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/9 | 66274 | chr12 | 108129559 | |||||
| chr12:108129744
|
G | T | 2 | a0001c0001t0014a0001c0001t0076 | 7 | HG01346.hp2 HG01433.hp1 HG01952.hp1 others(4): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-734G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/9 | chr12 | 108129744 | ||||||
| chr12:108129891
|
A | C | 28 | a0001c0001t0007a0001c0001t0008a0001c0001t0012others(25): Show | 56 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(53): Show |
5_prime_UTR_variant | MODIFIER | c.-587A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/9 | 65942 | chr12 | 108129891 | |||||
| chr12:108195393
|
G | A | 1 | a0001c0001t0027 | 2 | HG02895.hp2 HG02897.hp2 |
5_prime_UTR_variant | MODIFIER | c.-440G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/9 | 440 | chr12 | 108195393 | |||||
| chr12:108195637
|
A | G | 1 | a0001c0001t0075 | 1 | HG02135.hp2 | 5_prime_UTR_variant | MODIFIER | c.-196A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/9 | 196 | chr12 | 108195637 | |||||
| chr12:108195763
|
C | G | 1 | a0001c0001t0065 | 1 | NA18906.hp1 | 5_prime_UTR_variant | MODIFIER | c.-70C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/9 | 70 | chr12 | 108195763 | |||||
| chr12:108248357
|
G | T | 2 | a0001c0001t0039a0001c0001t0055 | 3 | NA18953.hp1 NA18982.hp2 NA18994.hp1 |
3_prime_UTR_variant | MODIFIER | c.*14G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 14 | chr12 | 108248357 | |||||
| chr12:108248385
|
C | T | 1 | a0001c0001t0075 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*42C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 42 | chr12 | 108248385 | |||||
| chr12:108248623
|
C | T | 36 | a0001c0001t0006a0001c0001t0009a0001c0001t0011others(33): Show | 79 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*280C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 280 | chr12 | 108248623 | |||||
| chr12:108248821
|
C | T | 1 | a0001c0001t0072 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*478C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 478 | chr12 | 108248821 | |||||
| chr12:108248988
|
C | A | 1 | a0001c0001t0050 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*645C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 645 | chr12 | 108248988 | |||||
| chr12:108249043
|
A | G | 1 | a0001c0001t0071 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*700A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 700 | chr12 | 108249043 | |||||
| chr12:108249113
|
C | A | 12 | a0001c0001t0010a0001c0001t0027a0001c0001t0028others(9): Show | 22 | HG00099.hp2 HG01243.hp2 HG01257.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*770C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 770 | chr12 | 108249113 | |||||
| chr12:108249114
|
C | A | 12 | a0001c0001t0010a0001c0001t0027a0001c0001t0028others(9): Show | 22 | HG00099.hp2 HG01243.hp2 HG01257.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*771C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 771 | chr12 | 108249114 | |||||
| chr12:108249115
|
TCA | T | 12 | a0001c0001t0010a0001c0001t0027a0001c0001t0028others(9): Show | 22 | HG00099.hp2 HG01243.hp2 HG01257.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*773_*774delCA | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 773 | chr12 | 108249115 | |||||
| chr12:108249280
|
G | A | 31 | a0001c0001t0006a0001c0001t0009a0001c0001t0011others(28): Show | 72 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*937G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 937 | chr12 | 108249280 | |||||
| chr12:108249295
|
G | T | 12 | a0001c0001t0010a0001c0001t0027a0001c0001t0028others(9): Show | 22 | HG00099.hp2 HG01257.hp1 HG01358.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*952G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 952 | chr12 | 108249295 | |||||
| chr12:108249339
|
A | G | 1 | a0001c0001t0043 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*996A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 996 | chr12 | 108249339 | |||||
| chr12:108249400
|
T | C | 2 | a0001c0001t0044a0001c0001t0061 | 2 | HG01891.hp1 HG02109.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1057T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 1057 | chr12 | 108249400 | |||||
| chr12:108249641
|
A | C | 3 | a0001c0001t0023a0001c0010t0049a0006c0007t0023 | 4 | HG00438.hp1 NA18941.hp2 NA18998.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1298A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 1298 | chr12 | 108249641 | |||||
| chr12:108249689
|
G | T | 1 | a0001c0001t0048 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1346G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 1346 | chr12 | 108249689 | |||||
| chr12:108249776
|
C | T | 25 | a0001c0001t0006a0001c0001t0009a0001c0001t0013others(22): Show | 59 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*1433C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 1433 | chr12 | 108249776 | |||||
| chr12:108249779
|
C | G | 1 | a0001c0001t0047 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1436C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 1436 | chr12 | 108249779 | |||||
| chr12:108249927
|
AT | A | 2 | a0001c0001t0028a0001c0001t0066 | 3 | HG01981.hp1 HG01993.hp2 HG02738.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1589delT | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 1589 | INFO_REALIGN_3_PRIME | chr12 | 108249927 | ||||
| chr12:108249999
|
A | AGAAGGAA others(33): Show |
1 | a0001c0001t0056 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1658_*1659insAGGA others(36): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 1659 | INFO_REALIGN_3_PRIME | chr12 | 108249999 | ||||
| chr12:108250171
|
A | AGT | 13 | a0001c0001t0002a0001c0001t0005a0001c0001t0007others(10): Show | 53 | HG00597.hp1 HG00597.hp2 HG00609.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*1855_*1856dupGT | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 1857 | INFO_REALIGN_3_PRIME | chr12 | 108250171 | ||||
| chr12:108250171
|
A | AGTGT | 27 | a0001c0001t0010a0001c0001t0013a0001c0001t0021others(24): Show | 49 | HG00099.hp2 HG00639.hp1 HG01081.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*1853_*1856dupGTGT | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 1857 | INFO_REALIGN_3_PRIME | chr12 | 108250171 | ||||
| chr12:108250171
|
A | AGTGTGT | 5 | a0001c0001t0006a0001c0001t0009a0001c0001t0059others(2): Show | 21 | HG00438.hp2 HG00558.hp2 HG00639.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1851_*1856dupGTGT others(2): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 1857 | INFO_REALIGN_3_PRIME | chr12 | 108250171 | ||||
| chr12:108250171
|
A | AGTGTGTG others(1): Show |
6 | a0001c0001t0017a0001c0001t0046a0001c0003t0038others(3): Show | 7 | HG01069.hp1 HG02148.hp2 HG02647.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1849_*1856dupGTGT others(4): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 1857 | INFO_REALIGN_3_PRIME | chr12 | 108250171 | ||||
| chr12:108250171
|
A | AGTGTGTG others(3): Show |
4 | a0001c0001t0015a0001c0001t0019a0001c0001t0024others(1): Show | 12 | HG00140.hp1 HG01099.hp1 HG01168.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1847_*1856dupGTGT others(6): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 1857 | INFO_REALIGN_3_PRIME | chr12 | 108250171 | ||||
| chr12:108250171
|
A | AGTGTGTG others(5): Show |
1 | a0001c0001t0042 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1845_*1856dupGTGT others(8): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 1857 | INFO_REALIGN_3_PRIME | chr12 | 108250171 | ||||
| chr12:108250171
|
A | AGTGTGTG others(7): Show |
1 | a0001c0001t0030 | 2 | HG02622.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1843_*1856dupGTGT others(10): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 1857 | INFO_REALIGN_3_PRIME | chr12 | 108250171 | ||||
| chr12:108250171
|
A | AGTGTGTG others(9): Show |
1 | a0001c0001t0060 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1841_*1856dupGTGT others(12): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 1857 | INFO_REALIGN_3_PRIME | chr12 | 108250171 | ||||
| chr12:108250198
|
G | A | 1 | a0001c0001t0045 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1855G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 1855 | chr12 | 108250198 | |||||
| chr12:108250199
|
T | TGTGTGTG others(4): Show |
1 | a0001c0001t0053 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1856_*1857insGTGT others(7): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 1857 | chr12 | 108250199 | |||||
| chr12:108250200
|
A | G | 24 | a0001c0001t0003a0001c0001t0008a0001c0001t0011others(21): Show | 64 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*1857A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 1857 | chr12 | 108250200 | |||||
| chr12:108250201
|
T | A | 1 | a0001c0001t0045 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1858T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 1858 | chr12 | 108250201 | |||||
| chr12:108250202
|
G | A | 7 | a0001c0001t0011a0001c0001t0016a0001c0001t0018others(4): Show | 16 | HG00735.hp1 HG02257.hp2 HG02486.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1859G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 1859 | chr12 | 108250202 | |||||
| chr12:108250202
|
G | C | 2 | a0001c0001t0041a0001c0001t0067 | 2 | HG06807.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1859G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 1859 | chr12 | 108250202 | |||||
| chr12:108250202
|
G | GTA | 12 | a0001c0001t0003a0001c0001t0008a0001c0001t0020others(9): Show | 41 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1859_*1860insTA | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 1860 | chr12 | 108250202 | |||||
| chr12:108250202
|
G | GTGTA | 2 | a0001c0001t0040a0001c0001t0069 | 3 | HG01167.hp1 HG01261.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1859_*1860insTGTA | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 1860 | chr12 | 108250202 | |||||
| chr12:108250202
|
G | GTGTGTA | 2 | a0001c0001t0033a0001c0001t0070 | 3 | HG02717.hp2 HG02723.hp1 NA18960.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1859_*1860insTGTG others(2): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 1860 | chr12 | 108250202 | |||||
| chr12:108250203
|
A | T | 23 | a0001c0001t0003a0001c0001t0008a0001c0001t0011others(20): Show | 63 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*1860A>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 1860 | chr12 | 108250203 | |||||
| chr12:108250381
|
T | A | 1 | a0001c0001t0045 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2038T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 2038 | chr12 | 108250381 | |||||
| chr12:108250412
|
T | C | 73 | a0001c0001t0003a0001c0001t0006a0001c0001t0008others(70): Show | 160 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(157): Show |
3_prime_UTR_variant | MODIFIER | c.*2069T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 2069 | chr12 | 108250412 | |||||
| chr12:108250476
|
T | C | 10 | a0001c0001t0011a0001c0001t0016a0001c0001t0018others(7): Show | 19 | HG00735.hp1 HG02257.hp2 HG02486.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2133T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 9/9 | 2133 | chr12 | 108250476 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:108129976
|
G | A | 39 | a0001c0001t0007g0009a0001c0001t0007g0013a0001c0001t0007g0014others(36): Show | 40 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(37): Show |
intron_variant | MODIFIER | c.-552+50G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108129976 | ||||||
| chr12:108130261
|
G | T | 45 | a0001c0001t0007g0009a0001c0001t0007g0013a0001c0001t0007g0014others(42): Show | 46 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(43): Show |
intron_variant | MODIFIER | c.-552+335G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108130261 | ||||||
| chr12:108130329
|
T | A | 56 | a0001c0001t0007g0009a0001c0001t0007g0013a0001c0001t0007g0014others(53): Show | 57 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(54): Show |
intron_variant | MODIFIER | c.-552+403T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108130329 | ||||||
| chr12:108130342
|
G | A | 5 | a0001c0001t0007g0048a0001c0001t0033g0049a0001c0001t0057g0047others(2): Show | 5 | HG02723.hp1 HG02809.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+416G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108130342 | ||||||
| chr12:108130475
|
G | GGT | 33 | a0001c0001t0001g0252a0001c0001t0001g0254a0001c0001t0001g0258others(30): Show | 35 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.-552+594_-552+595d others(4): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108130475 | |||||
| chr12:108130475
|
G | GGTGT | 11 | a0001c0001t0003g0267a0001c0001t0005g0264a0001c0001t0010g0262others(8): Show | 11 | HG02257.hp2 HG02280.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.-552+592_-552+595d others(6): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108130475 | |||||
| chr12:108130475
|
G | GTGT | 3 | a0001c0001t0069g0272a0002c0002t0002g0270a0002c0002t0002g0271 | 3 | HG01099.hp2 HG01261.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.-552+549_-552+550i others(5): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108130475 | ||||||
| chr12:108130475
|
GGT | G | 53 | a0001c0001t0001g0107a0001c0001t0001g0139a0001c0001t0001g0148others(50): Show | 53 | HG00423.hp1 HG00558.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.-552+594_-552+595d others(4): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108130475 | |||||
| chr12:108130475
|
GGTGT | G | 16 | a0001c0001t0001g0096a0001c0001t0002g0102a0001c0001t0002g0103others(13): Show | 16 | HG00639.hp2 HG01069.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.-552+592_-552+595d others(6): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108130475 | |||||
| chr12:108130475
|
GGTGTGT | G | 32 | a0001c0001t0005g0088a0001c0001t0005g0091a0001c0001t0006g0086others(29): Show | 32 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.-552+590_-552+595d others(8): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108130475 | |||||
| chr12:108130475
|
GGTGTGTG others(1): Show |
G | 27 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0001g0079others(24): Show | 28 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(25): Show |
intron_variant | MODIFIER | c.-552+588_-552+595d others(10): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108130475 | |||||
| chr12:108130475
|
GGTGTGTG others(3): Show |
G | 2 | a0001c0001t0002g0069a0001c0001t0060g0274 | 2 | HG01069.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-552+586_-552+595d others(12): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108130475 | |||||
| chr12:108130475
|
GGTGTGTG others(5): Show |
G | 13 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0003g0002others(10): Show | 14 | HG01081.hp1 HG01175.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-552+584_-552+595d others(14): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108130475 | |||||
| chr12:108130475
|
GGTGTGTG others(15): Show |
G | 4 | a0001c0001t0007g0009a0001c0001t0008g0001a0001c0001t0008g0007others(1): Show | 5 | NA18944.hp1 NA18952.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+574_-552+595d others(24): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108130475 | |||||
| chr12:108130479
|
T | G | 1 | a0001c0001t0011g0056 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-552+553T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108130479 | ||||||
| chr12:108130481
|
T | G | 1 | a0001c0001t0023g0022 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-552+555T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108130481 | ||||||
| chr12:108130483
|
T | G | 6 | a0001c0001t0008g0018a0001c0001t0008g0021a0001c0001t0020g0273others(3): Show | 6 | HG00280.hp1 HG00438.hp1 HG00609.hp2 others(3): Show |
intron_variant | MODIFIER | c.-552+557T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108130483 | ||||||
| chr12:108130485
|
T | G | 7 | a0001c0001t0007g0013a0001c0001t0007g0014a0001c0001t0008g0010others(4): Show | 7 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(4): Show |
intron_variant | MODIFIER | c.-552+559T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108130485 | ||||||
| chr12:108130499
|
T | G | 4 | a0001c0001t0007g0009a0001c0001t0008g0001a0001c0001t0008g0007others(1): Show | 5 | NA18944.hp1 NA18952.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+573T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108130499 | ||||||
| chr12:108130765
|
G | A | 1 | a0001c0001t0001g0154 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-552+839G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108130765 | ||||||
| chr12:108130834
|
A | G | 53 | a0001c0001t0007g0009a0001c0001t0007g0013a0001c0001t0007g0014others(50): Show | 54 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(51): Show |
intron_variant | MODIFIER | c.-552+908A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108130834 | ||||||
| chr12:108130931
|
A | G | 53 | a0001c0001t0007g0009a0001c0001t0007g0013a0001c0001t0007g0014others(50): Show | 54 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(51): Show |
intron_variant | MODIFIER | c.-552+1005A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108130931 | ||||||
| chr12:108130957
|
A | G | 53 | a0001c0001t0007g0009a0001c0001t0007g0013a0001c0001t0007g0014others(50): Show | 54 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(51): Show |
intron_variant | MODIFIER | c.-552+1031A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108130957 | ||||||
| chr12:108130962
|
C | T | 3 | a0001c0001t0032g0035a0001c0001t0032g0036a0001c0001t0062g0034 | 3 | HG00099.hp2 HG01257.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.-552+1036C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108130962 | ||||||
| chr12:108131072
|
T | C | 1 | a0001c0001t0001g0107 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-552+1146T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108131072 | ||||||
| chr12:108131095
|
C | T | 58 | a0001c0001t0007g0009a0001c0001t0007g0013a0001c0001t0007g0014others(55): Show | 59 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(56): Show |
intron_variant | MODIFIER | c.-552+1169C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108131095 | ||||||
| chr12:108131133
|
G | A | 58 | a0001c0001t0007g0009a0001c0001t0007g0013a0001c0001t0007g0014others(55): Show | 59 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(56): Show |
intron_variant | MODIFIER | c.-552+1207G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108131133 | ||||||
| chr12:108131648
|
G | A | 1 | a0001c0001t0072g0108 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-552+1722G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108131648 | ||||||
| chr12:108131649
|
A | G | 1 | a0001c0001t0072g0108 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-552+1723A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108131649 | ||||||
| chr12:108131668
|
A | G | 59 | a0001c0001t0007g0009a0001c0001t0007g0013a0001c0001t0007g0014others(56): Show | 60 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(57): Show |
intron_variant | MODIFIER | c.-552+1742A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108131668 | ||||||
| chr12:108131738
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-552+1812G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108131738 | ||||||
| chr12:108131756
|
C | T | 59 | a0001c0001t0007g0009a0001c0001t0007g0013a0001c0001t0007g0014others(56): Show | 60 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(57): Show |
intron_variant | MODIFIER | c.-552+1830C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108131756 | ||||||
| chr12:108131818
|
C | G | 59 | a0001c0001t0007g0009a0001c0001t0007g0013a0001c0001t0007g0014others(56): Show | 60 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(57): Show |
intron_variant | MODIFIER | c.-552+1892C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108131818 | ||||||
| chr12:108131823
|
A | C | 1 | a0001c0001t0016g0278 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-552+1897A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108131823 | ||||||
| chr12:108131898
|
A | G | 1 | a0001c0001t0014g0153 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-552+1972A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108131898 | ||||||
| chr12:108131950
|
C | T | 8 | a0001c0001t0007g0048a0001c0001t0033g0049a0001c0001t0057g0047others(5): Show | 8 | HG01243.hp2 HG02451.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-552+2024C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108131950 | ||||||
| chr12:108132036
|
T | TTG | 5 | a0001c0001t0035g0233a0001c0001t0035g0259a0001c0001t0036g0068others(2): Show | 5 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+2124_-552+212 others(6): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108132036 | |||||
| chr12:108132041
|
TG | T | 3 | a0001c0001t0022g0151a0001c0001t0045g0232a0001c0001t0046g0152 | 3 | HG02717.hp1 HG03540.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-552+2116delG | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108132041 | ||||||
| chr12:108132135
|
A | AT | 133 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(130): Show | 134 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.-552+2216dupT | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108132135 | |||||
| chr12:108132147
|
G | A | 8 | a0001c0001t0007g0048a0001c0001t0033g0049a0001c0001t0057g0047others(5): Show | 8 | HG01243.hp2 HG02451.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-552+2221G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108132147 | ||||||
| chr12:108132296
|
A | G | 216 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(213): Show | 219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.-552+2370A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108132296 | ||||||
| chr12:108132529
|
C | T | 135 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(132): Show | 136 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.-552+2603C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108132529 | ||||||
| chr12:108132559
|
T | C | 240 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(237): Show | 244 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.-552+2633T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108132559 | ||||||
| chr12:108132608
|
C | T | 60 | a0001c0001t0007g0009a0001c0001t0007g0013a0001c0001t0007g0014others(57): Show | 61 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(58): Show |
intron_variant | MODIFIER | c.-552+2682C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108132608 | ||||||
| chr12:108132629
|
CAT | C | 4 | a0001c0001t0063g0276a0001c0001t0064g0277a0001c0001t0065g0275others(1): Show | 4 | HG01109.hp1 HG02970.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.-552+2704_-552+270 others(6): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108132629 | ||||||
| chr12:108132669
|
C | G | 59 | a0001c0001t0007g0009a0001c0001t0007g0013a0001c0001t0007g0014others(56): Show | 60 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(57): Show |
intron_variant | MODIFIER | c.-552+2743C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108132669 | ||||||
| chr12:108132694
|
T | C | 2 | a0001c0001t0016g0278a0001c0001t0060g0274 | 2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-552+2768T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108132694 | ||||||
| chr12:108132721
|
A | G | 59 | a0001c0001t0007g0009a0001c0001t0007g0013a0001c0001t0007g0014others(56): Show | 60 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(57): Show |
intron_variant | MODIFIER | c.-552+2795A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108132721 | ||||||
| chr12:108132759
|
G | A | 59 | a0001c0001t0007g0009a0001c0001t0007g0013a0001c0001t0007g0014others(56): Show | 60 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(57): Show |
intron_variant | MODIFIER | c.-552+2833G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108132759 | ||||||
| chr12:108132778
|
G | A | 7 | a0001c0001t0011g0006a0001c0001t0011g0125a0001c0001t0011g0127others(4): Show | 8 | HG02280.hp1 HG02572.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-552+2852G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108132778 | ||||||
| chr12:108132827
|
A | G | 5 | a0001c0001t0005g0088a0001c0001t0005g0091a0001c0001t0011g0090others(2): Show | 5 | HG00642.hp2 HG01516.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+2901A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108132827 | ||||||
| chr12:108132914
|
A | G | 3 | a0001c0001t0063g0276a0001c0001t0064g0277a0001c0001t0065g0275 | 3 | HG01109.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-552+2988A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108132914 | ||||||
| chr12:108133018
|
C | T | 1 | a0001c0001t0057g0047 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-552+3092C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108133018 | ||||||
| chr12:108133073
|
G | A | 59 | a0001c0001t0007g0009a0001c0001t0007g0013a0001c0001t0007g0014others(56): Show | 60 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(57): Show |
intron_variant | MODIFIER | c.-552+3147G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108133073 | ||||||
| chr12:108133180
|
G | A | 1 | a0001c0001t0004g0234 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-552+3254G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108133180 | ||||||
| chr12:108133240
|
G | A | 1 | a0001c0001t0011g0125 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-552+3314G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108133240 | ||||||
| chr12:108133294
|
G | A | 1 | a0001c0001t0004g0114 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-552+3368G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108133294 | ||||||
| chr12:108133319
|
C | T | 1 | a0001c0001t0046g0152 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-552+3393C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108133319 | ||||||
| chr12:108133320
|
G | A | 59 | a0001c0001t0007g0009a0001c0001t0007g0013a0001c0001t0007g0014others(56): Show | 60 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(57): Show |
intron_variant | MODIFIER | c.-552+3394G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108133320 | ||||||
| chr12:108133374
|
C | T | 4 | a0001c0001t0026g0092a0001c0001t0026g0093a0001c0001t0026g0095others(1): Show | 4 | HG00323.hp2 HG01261.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.-552+3448C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108133374 | ||||||
| chr12:108133411
|
G | T | 5 | a0001c0001t0002g0102a0001c0001t0002g0103a0001c0001t0002g0104others(2): Show | 5 | HG02015.hp1 HG02165.hp2 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.-552+3485G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108133411 | ||||||
| chr12:108133539
|
C | T | 2 | a0001c0001t0016g0278a0001c0001t0060g0274 | 2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-552+3613C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108133539 | ||||||
| chr12:108133540
|
C | T | 1 | a0002c0002t0004g0071 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-552+3614C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108133540 | ||||||
| chr12:108133623
|
C | T | 1 | a0001c0001t0004g0124 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-552+3697C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108133623 | ||||||
| chr12:108133686
|
C | T | 41 | a0001c0001t0007g0009a0001c0001t0007g0013a0001c0001t0007g0014others(38): Show | 42 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(39): Show |
intron_variant | MODIFIER | c.-552+3760C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108133686 | ||||||
| chr12:108133716
|
G | A | 3 | a0001c0001t0063g0276a0001c0001t0064g0277a0001c0001t0065g0275 | 3 | HG01109.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-552+3790G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108133716 | ||||||
| chr12:108133784
|
G | A | 192 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(189): Show | 194 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.-552+3858G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108133784 | ||||||
| chr12:108133807
|
G | A | 1 | a0003c0004t0017g0052 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-552+3881G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108133807 | ||||||
| chr12:108134392
|
C | G | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG01074.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.-552+4466C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108134392 | ||||||
| chr12:108134413
|
C | T | 1 | a0001c0001t0022g0151 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-552+4487C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108134413 | ||||||
| chr12:108134470
|
A | G | 2 | a0001c0001t0016g0278a0001c0001t0060g0274 | 2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-552+4544A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108134470 | ||||||
| chr12:108134494
|
T | G | 1 | a0001c0001t0012g0025 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-552+4568T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108134494 | ||||||
| chr12:108134512
|
C | T | 1 | a0002c0002t0002g0231 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-552+4586C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108134512 | ||||||
| chr12:108134618
|
A | G | 1 | a0001c0001t0004g0234 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-552+4692A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108134618 | ||||||
| chr12:108134734
|
G | A | 2 | a0001c0001t0010g0004a0001c0001t0043g0004 | 2 | HG02258.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-552+4808G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108134734 | ||||||
| chr12:108134809
|
A | T | 2 | a0001c0001t0016g0278a0001c0001t0060g0274 | 2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-552+4883A>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108134809 | ||||||
| chr12:108134937
|
G | A | 1 | a0001c0001t0022g0151 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-552+5011G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108134937 | ||||||
| chr12:108135055
|
G | A | 1 | a0001c0001t0004g0109 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-552+5129G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108135055 | ||||||
| chr12:108135083
|
A | G | 3 | a0003c0004t0017g0052a0003c0004t0025g0053a0003c0004t0025g0054 | 3 | HG02109.hp2 HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-552+5157A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108135083 | ||||||
| chr12:108135126
|
TTCCA | T | 11 | a0001c0001t0007g0048a0001c0001t0033g0049a0001c0001t0057g0047others(8): Show | 11 | HG01109.hp1 HG01243.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-552+5204_-552+520 others(8): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108135126 | |||||
| chr12:108135166
|
A | ATCCATCC others(1): Show |
12 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0003g0002others(9): Show | 13 | HG01081.hp1 HG01175.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.-552+5243_-552+524 others(12): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108135166 | |||||
| chr12:108135308
|
A | G | 41 | a0001c0001t0007g0009a0001c0001t0007g0013a0001c0001t0007g0014others(38): Show | 42 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(39): Show |
intron_variant | MODIFIER | c.-552+5382A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108135308 | ||||||
| chr12:108135313
|
A | G | 7 | a0001c0001t0011g0006a0001c0001t0011g0125a0001c0001t0011g0127others(4): Show | 8 | HG02280.hp1 HG02572.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-552+5387A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108135313 | ||||||
| chr12:108135471
|
C | T | 2 | a0001c0001t0045g0232a0001c0001t0046g0152 | 2 | HG02717.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-552+5545C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108135471 | ||||||
| chr12:108135481
|
T | A | 1 | a0001c0001t0017g0023 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-552+5555T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108135481 | ||||||
| chr12:108135565
|
C | T | 3 | a0001c0001t0063g0276a0001c0001t0064g0277a0001c0001t0065g0275 | 3 | HG01109.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-552+5639C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108135565 | ||||||
| chr12:108135594
|
G | A | 5 | a0001c0001t0035g0233a0001c0001t0035g0259a0001c0001t0036g0068others(2): Show | 5 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+5668G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108135594 | ||||||
| chr12:108135789
|
C | T | 1 | a0002c0002t0002g0147 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-552+5863C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108135789 | ||||||
| chr12:108135808
|
C | T | 1 | a0001c0001t0030g0162 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-552+5882C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108135808 | ||||||
| chr12:108135864
|
G | GA | 203 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(200): Show | 205 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.-552+5938_-552+593 others(5): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108135864 | ||||||
| chr12:108135865
|
G | C | 203 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(200): Show | 205 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.-552+5939G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108135865 | ||||||
| chr12:108135988
|
C | T | 2 | a0001c0001t0016g0278a0001c0001t0060g0274 | 2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-552+6062C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108135988 | ||||||
| chr12:108136012
|
G | A | 1 | a0001c0001t0072g0108 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-552+6086G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108136012 | ||||||
| chr12:108136064
|
G | A | 1 | a0002c0002t0002g0270 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-552+6138G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108136064 | ||||||
| chr12:108136306
|
C | T | 3 | a0001c0001t0011g0056a0001c0001t0016g0044a0001c0001t0058g0043 | 3 | HG02257.hp2 HG02922.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-552+6380C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108136306 | ||||||
| chr12:108136318
|
T | G | 1 | a0001c0001t0002g0179 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-552+6392T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108136318 | ||||||
| chr12:108136334
|
G | GTCCCTTC others(19): Show |
1 | a0001c0001t0016g0278 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-552+6412_-552+641 others(30): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108136334 | |||||
| chr12:108136334
|
G | GTCCCTTC others(19): Show |
197 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(194): Show | 199 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.-552+6412_-552+641 others(30): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108136334 | |||||
| chr12:108136371
|
C | G | 1 | a0001c0001t0072g0108 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-552+6445C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108136371 | ||||||
| chr12:108136510
|
G | A | 1 | a0002c0002t0001g0180 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-552+6584G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108136510 | ||||||
| chr12:108136722
|
CCCGTGTT others(46): Show |
C | 3 | a0001c0001t0025g0033a0001c0001t0034g0031a0001c0001t0034g0032 | 3 | HG02895.hp1 HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-552+6797_-552+684 others(57): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108136722 | ||||||
| chr12:108136745
|
C | T | 5 | a0001c0001t0005g0088a0001c0001t0005g0091a0001c0001t0011g0090others(2): Show | 5 | HG00642.hp2 HG01516.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+6819C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108136745 | ||||||
| chr12:108136746
|
G | C | 58 | a0001c0001t0007g0009a0001c0001t0007g0013a0001c0001t0007g0014others(55): Show | 59 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(56): Show |
intron_variant | MODIFIER | c.-552+6820G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108136746 | ||||||
| chr12:108136760
|
C | A | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG01074.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.-552+6834C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108136760 | ||||||
| chr12:108136760
|
C | T | 1 | a0001c0001t0033g0049 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-552+6834C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108136760 | ||||||
| chr12:108136804
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-552+6878C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108136804 | ||||||
| chr12:108136904
|
G | T | 11 | a0001c0001t0007g0048a0001c0001t0033g0049a0001c0001t0057g0047others(8): Show | 11 | HG01109.hp1 HG01243.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-552+6978G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108136904 | ||||||
| chr12:108137076
|
C | G | 9 | a0001c0001t0005g0088a0001c0001t0005g0091a0001c0001t0006g0086others(6): Show | 9 | HG00642.hp2 HG01516.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-552+7150C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108137076 | ||||||
| chr12:108137086
|
C | T | 1 | a0001c0001t0056g0016 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-552+7160C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108137086 | ||||||
| chr12:108137214
|
A | C | 1 | a0001c0001t0016g0278 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-552+7288A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108137214 | ||||||
| chr12:108137245
|
T | C | 5 | a0001c0001t0035g0233a0001c0001t0035g0259a0001c0001t0036g0068others(2): Show | 5 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+7319T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108137245 | ||||||
| chr12:108137270
|
T | C | 46 | a0001c0001t0007g0009a0001c0001t0007g0013a0001c0001t0007g0014others(43): Show | 47 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(44): Show |
intron_variant | MODIFIER | c.-552+7344T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108137270 | ||||||
| chr12:108137336
|
C | T | 3 | a0003c0004t0017g0052a0003c0004t0025g0053a0003c0004t0025g0054 | 3 | HG02109.hp2 HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-552+7410C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108137336 | ||||||
| chr12:108137640
|
G | A | 3 | a0001c0001t0063g0276a0001c0001t0064g0277a0001c0001t0065g0275 | 3 | HG01109.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-552+7714G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108137640 | ||||||
| chr12:108137700
|
G | A | 1 | a0002c0002t0009g0132 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-552+7774G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108137700 | ||||||
| chr12:108137742
|
T | G | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG03688.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-552+7816T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108137742 | ||||||
| chr12:108137824
|
G | T | 61 | a0001c0001t0007g0009a0001c0001t0007g0013a0001c0001t0007g0014others(58): Show | 62 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(59): Show |
intron_variant | MODIFIER | c.-552+7898G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108137824 | ||||||
| chr12:108137883
|
C | T | 1 | a0001c0001t0072g0108 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-552+7957C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108137883 | ||||||
| chr12:108138273
|
A | G | 15 | a0001c0001t0007g0048a0001c0001t0016g0278a0001c0001t0022g0151others(12): Show | 15 | HG01109.hp1 HG01243.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.-552+8347A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108138273 | ||||||
| chr12:108138376
|
G | A | 5 | a0001c0001t0035g0233a0001c0001t0035g0259a0001c0001t0036g0068others(2): Show | 5 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+8450G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108138376 | ||||||
| chr12:108138494
|
G | A | 1 | a0001c0001t0016g0278 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-552+8568G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108138494 | ||||||
| chr12:108138504
|
A | G | 2 | a0001c0001t0002g0146a0002c0002t0002g0147 | 2 | HG04204.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.-552+8578A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108138504 | ||||||
| chr12:108138523
|
G | A | 4 | a0001c0001t0017g0023a0001c0001t0025g0033a0001c0001t0034g0031others(1): Show | 4 | HG02818.hp2 HG02895.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-552+8597G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108138523 | ||||||
| chr12:108138682
|
C | G | 3 | a0001c0001t0063g0276a0001c0001t0064g0277a0001c0001t0065g0275 | 3 | HG01109.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-552+8756C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108138682 | ||||||
| chr12:108138732
|
C | T | 133 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(130): Show | 134 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.-552+8806C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108138732 | ||||||
| chr12:108138800
|
G | A | 1 | a0001c0001t0022g0151 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-552+8874G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108138800 | ||||||
| chr12:108138915
|
A | G | 4 | a0001c0001t0006g0086a0001c0001t0010g0129a0001c0003t0021g0245others(1): Show | 4 | HG02615.hp1 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-552+8989A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108138915 | ||||||
| chr12:108139026
|
G | A | 1 | a0005c0006t0016g0046 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-552+9100G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108139026 | ||||||
| chr12:108139077
|
A | G | 10 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0001g0230others(7): Show | 10 | HG01168.hp2 HG01169.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.-552+9151A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108139077 | ||||||
| chr12:108139086
|
G | A | 6 | a0001c0001t0003g0133a0002c0002t0001g0186a0002c0002t0002g0183others(3): Show | 6 | HG00423.hp1 HG00558.hp1 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.-552+9160G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108139086 | ||||||
| chr12:108139128
|
A | G | 5 | a0001c0001t0035g0233a0001c0001t0035g0259a0001c0001t0036g0068others(2): Show | 5 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+9202A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108139128 | ||||||
| chr12:108139220
|
T | G | 8 | a0001c0001t0007g0048a0001c0001t0033g0049a0001c0001t0057g0047others(5): Show | 8 | HG01243.hp2 HG02451.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-552+9294T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108139220 | ||||||
| chr12:108139287
|
G | A | 1 | a0001c0001t0002g0247 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-552+9361G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108139287 | ||||||
| chr12:108139447
|
G | A | 1 | a0002c0002t0002g0147 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-552+9521G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108139447 | ||||||
| chr12:108139566
|
C | A | 1 | a0001c0001t0060g0274 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-552+9640C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108139566 | ||||||
| chr12:108139800
|
A | C | 1 | a0001c0001t0052g0131 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-552+9874A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108139800 | ||||||
| chr12:108139860
|
G | A | 1 | a0001c0001t0060g0274 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-552+9934G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108139860 | ||||||
| chr12:108139944
|
A | C | 41 | a0001c0001t0007g0009a0001c0001t0007g0013a0001c0001t0007g0014others(38): Show | 42 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(39): Show |
intron_variant | MODIFIER | c.-552+10018A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108139944 | ||||||
| chr12:108140119
|
G | A | 38 | a0001c0001t0007g0009a0001c0001t0007g0013a0001c0001t0007g0014others(35): Show | 39 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(36): Show |
intron_variant | MODIFIER | c.-552+10193G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108140119 | ||||||
| chr12:108140210
|
C | T | 1 | a0001c0001t0003g0101 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-552+10284C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108140210 | ||||||
| chr12:108140262
|
G | A | 15 | a0001c0001t0007g0048a0001c0001t0016g0278a0001c0001t0022g0151others(12): Show | 15 | HG01109.hp1 HG01243.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.-552+10336G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108140262 | ||||||
| chr12:108140285
|
C | T | 5 | a0001c0001t0035g0233a0001c0001t0035g0259a0001c0001t0036g0068others(2): Show | 5 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+10359C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108140285 | ||||||
| chr12:108140381
|
C | T | 1 | a0002c0002t0001g0145 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-552+10455C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108140381 | ||||||
| chr12:108140924
|
C | T | 1 | a0001c0001t0012g0025 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-552+10998C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108140924 | ||||||
| chr12:108141025
|
T | C | 1 | a0001c0001t0027g0005 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-552+11099T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108141025 | ||||||
| chr12:108141080
|
G | A | 1 | a0001c0001t0008g0026 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-552+11154G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108141080 | ||||||
| chr12:108141134
|
G | A | 5 | a0001c0001t0035g0233a0001c0001t0035g0259a0001c0001t0036g0068others(2): Show | 5 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+11208G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108141134 | ||||||
| chr12:108141196
|
A | G | 1 | a0001c0001t0009g0100 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-552+11270A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108141196 | ||||||
| chr12:108141238
|
G | A | 13 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0254others(10): Show | 14 | HG01081.hp1 HG01175.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-552+11312G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108141238 | ||||||
| chr12:108141282
|
G | A | 1 | a0001c0001t0016g0278 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-552+11356G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108141282 | ||||||
| chr12:108141452
|
A | C | 1 | a0001c0001t0003g0225 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-552+11526A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108141452 | ||||||
| chr12:108141536
|
A | G | 209 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(206): Show | 211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.-552+11610A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108141536 | ||||||
| chr12:108141581
|
G | A | 8 | a0001c0001t0007g0048a0001c0001t0033g0049a0001c0001t0057g0047others(5): Show | 8 | HG01243.hp2 HG02451.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-552+11655G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108141581 | ||||||
| chr12:108141607
|
G | A | 2 | a0001c0001t0002g0102a0001c0001t0002g0103 | 2 | HG02015.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.-552+11681G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108141607 | ||||||
| chr12:108141777
|
A | G | 16 | a0001c0001t0007g0048a0001c0001t0016g0278a0001c0001t0022g0151others(13): Show | 16 | HG01109.hp1 HG01243.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.-552+11851A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108141777 | ||||||
| chr12:108141833
|
A | G | 9 | a0001c0001t0005g0088a0001c0001t0005g0091a0001c0001t0006g0086others(6): Show | 9 | HG00642.hp2 HG01516.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-552+11907A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108141833 | ||||||
| chr12:108141872
|
C | T | 4 | a0003c0004t0017g0052a0003c0004t0025g0053a0003c0004t0025g0054others(1): Show | 4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-552+11946C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108141872 | ||||||
| chr12:108141915
|
G | C | 8 | a0001c0001t0011g0056a0001c0001t0016g0044a0001c0001t0035g0233others(5): Show | 8 | HG01943.hp2 HG02109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-552+11989G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108141915 | ||||||
| chr12:108142081
|
C | T | 169 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(166): Show | 171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.-552+12155C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108142081 | ||||||
| chr12:108142260
|
T | C | 3 | a0001c0001t0011g0056a0001c0001t0016g0044a0001c0001t0058g0043 | 3 | HG02257.hp2 HG02922.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-552+12334T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108142260 | ||||||
| chr12:108142553
|
C | T | 1 | a0002c0002t0001g0145 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-552+12627C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108142553 | ||||||
| chr12:108142729
|
A | C | 1 | a0001c0001t0060g0274 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-552+12803A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108142729 | ||||||
| chr12:108142950
|
G | A | 5 | a0001c0001t0035g0233a0001c0001t0035g0259a0001c0001t0036g0068others(2): Show | 5 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+13024G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108142950 | ||||||
| chr12:108142983
|
A | G | 1 | a0001c0001t0014g0144 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-552+13057A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108142983 | ||||||
| chr12:108143010
|
C | T | 3 | a0001c0001t0011g0056a0001c0001t0016g0044a0001c0001t0058g0043 | 3 | HG02257.hp2 HG02922.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-552+13084C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108143010 | ||||||
| chr12:108143128
|
C | T | 1 | a0001c0001t0020g0265 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-552+13202C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108143128 | ||||||
| chr12:108143191
|
A | G | 222 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(219): Show | 225 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.-552+13265A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108143191 | ||||||
| chr12:108143555
|
T | C | 1 | a0001c0001t0020g0273 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-552+13629T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108143555 | ||||||
| chr12:108143837
|
A | G | 1 | a0001c0001t0060g0274 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-552+13911A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108143837 | ||||||
| chr12:108143848
|
G | A | 1 | a0002c0002t0009g0187 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-552+13922G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108143848 | ||||||
| chr12:108143879
|
G | A | 1 | a0002c0002t0001g0188 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-552+13953G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108143879 | ||||||
| chr12:108143893
|
C | T | 5 | a0001c0001t0035g0233a0001c0001t0035g0259a0001c0001t0036g0068others(2): Show | 5 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+13967C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108143893 | ||||||
| chr12:108143933
|
C | A | 4 | a0003c0004t0017g0052a0003c0004t0025g0053a0003c0004t0025g0054others(1): Show | 4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-552+14007C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108143933 | ||||||
| chr12:108144010
|
C | T | 1 | a0001c0001t0003g0143 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-552+14084C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108144010 | ||||||
| chr12:108144218
|
C | T | 5 | a0001c0001t0005g0088a0001c0001t0005g0091a0001c0001t0011g0090others(2): Show | 5 | HG00642.hp2 HG01516.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+14292C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108144218 | ||||||
| chr12:108144250
|
G | A | 2 | a0001c0001t0030g0130a0001c0001t0052g0131 | 2 | HG02630.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-552+14324G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108144250 | ||||||
| chr12:108144271
|
G | T | 1 | a0001c0001t0016g0278 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-552+14345G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108144271 | ||||||
| chr12:108144282
|
G | A | 170 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(167): Show | 171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.-552+14356G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108144282 | ||||||
| chr12:108144390
|
C | T | 5 | a0001c0001t0035g0233a0001c0001t0035g0259a0001c0001t0036g0068others(2): Show | 5 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+14464C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108144390 | ||||||
| chr12:108144419
|
A | T | 3 | a0001c0001t0010g0084a0001c0001t0010g0113a0001c0001t0010g0159 | 3 | HG01884.hp1 HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-552+14493A>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108144419 | ||||||
| chr12:108144424
|
T | C | 1 | a0001c0001t0060g0274 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-552+14498T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108144424 | ||||||
| chr12:108144524
|
A | G | 185 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(182): Show | 186 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.-552+14598A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108144524 | ||||||
| chr12:108144667
|
T | A | 4 | a0003c0004t0017g0052a0003c0004t0025g0053a0003c0004t0025g0054others(1): Show | 4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-552+14741T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108144667 | ||||||
| chr12:108144786
|
A | G | 1 | a0001c0001t0019g0083 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-552+14860A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108144786 | ||||||
| chr12:108145054
|
C | A | 5 | a0001c0001t0035g0233a0001c0001t0035g0259a0001c0001t0036g0068others(2): Show | 5 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+15128C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108145054 | ||||||
| chr12:108145215
|
C | T | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG01074.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.-552+15289C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108145215 | ||||||
| chr12:108145501
|
C | T | 185 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(182): Show | 186 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.-552+15575C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108145501 | ||||||
| chr12:108145502
|
G | A | 9 | a0001c0001t0005g0088a0001c0001t0005g0091a0001c0001t0006g0086others(6): Show | 9 | HG00642.hp2 HG01516.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-552+15576G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108145502 | ||||||
| chr12:108145996
|
G | A | 1 | a0001c0001t0027g0005 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-552+16070G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108145996 | ||||||
| chr12:108146334
|
C | T | 171 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(168): Show | 172 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.-552+16408C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108146334 | ||||||
| chr12:108146588
|
G | A | 19 | a0001c0001t0007g0009a0001c0001t0007g0013a0001c0001t0007g0014others(16): Show | 20 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(17): Show |
intron_variant | MODIFIER | c.-552+16662G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108146588 | ||||||
| chr12:108146666
|
G | A | 1 | a0001c0001t0016g0278 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-552+16740G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108146666 | ||||||
| chr12:108146710
|
G | A | 5 | a0001c0001t0005g0088a0001c0001t0005g0091a0001c0001t0011g0090others(2): Show | 5 | HG00642.hp2 HG01516.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+16784G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108146710 | ||||||
| chr12:108146809
|
C | T | 169 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(166): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.-552+16883C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108146809 | ||||||
| chr12:108146840
|
A | G | 5 | a0001c0001t0022g0151a0001c0001t0030g0130a0001c0001t0045g0232others(2): Show | 5 | HG02630.hp1 HG02717.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+16914A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108146840 | ||||||
| chr12:108146856
|
G | T | 3 | a0001c0001t0015g0237a0001c0001t0029g0235a0001c0001t0029g0236 | 3 | HG01099.hp1 HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-552+16930G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108146856 | ||||||
| chr12:108146987
|
G | C | 1 | a0001c0001t0037g0062 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-552+17061G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108146987 | ||||||
| chr12:108147051
|
G | T | 1 | a0002c0002t0002g0224 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-552+17125G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108147051 | ||||||
| chr12:108147100
|
G | A | 1 | a0001c0001t0066g0072 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-552+17174G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108147100 | ||||||
| chr12:108147476
|
G | A | 1 | a0001c0003t0038g0063 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-552+17550G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108147476 | ||||||
| chr12:108147580
|
C | T | 1 | a0001c0001t0012g0030 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-552+17654C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108147580 | ||||||
| chr12:108147598
|
C | T | 3 | a0001c0001t0001g0252a0001c0001t0003g0253a0002c0002t0009g0223 | 3 | HG02080.hp1 NA19000.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.-552+17672C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108147598 | ||||||
| chr12:108147635
|
G | T | 3 | a0001c0001t0069g0272a0002c0002t0003g0251a0002c0002t0003g0268 | 3 | HG00280.hp2 HG01261.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.-552+17709G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108147635 | ||||||
| chr12:108147689
|
CA | C | 3 | a0001c0001t0001g0080a0001c0001t0001g0081a0002c0002t0018g0082 | 3 | HG00733.hp1 HG00735.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.-552+17765delA | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108147689 | |||||
| chr12:108147691
|
A | T | 3 | a0001c0001t0001g0080a0001c0001t0001g0081a0002c0002t0018g0082 | 3 | HG00733.hp1 HG00735.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.-552+17765A>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108147691 | ||||||
| chr12:108147692
|
T | G | 3 | a0001c0001t0001g0080a0001c0001t0001g0081a0002c0002t0018g0082 | 3 | HG00733.hp1 HG00735.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.-552+17766T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108147692 | ||||||
| chr12:108147857
|
A | G | 2 | a0001c0001t0040g0221a0001c0001t0040g0222 | 2 | HG01167.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-552+17931A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108147857 | ||||||
| chr12:108147993
|
G | A | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG01074.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.-552+18067G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108147993 | ||||||
| chr12:108148109
|
C | T | 2 | a0001c0001t0016g0278a0001c0001t0060g0274 | 2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-552+18183C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108148109 | ||||||
| chr12:108148277
|
G | A | 5 | a0001c0001t0005g0088a0001c0001t0005g0091a0001c0001t0011g0090others(2): Show | 5 | HG00642.hp2 HG01516.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+18351G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108148277 | ||||||
| chr12:108148352
|
C | A | 1 | a0001c0001t0065g0275 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-552+18426C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108148352 | ||||||
| chr12:108148447
|
T | C | 1 | a0002c0002t0009g0246 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-552+18521T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108148447 | ||||||
| chr12:108148458
|
C | T | 1 | a0001c0001t0060g0274 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-552+18532C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108148458 | ||||||
| chr12:108148667
|
G | T | 1 | a0001c0001t0002g0142 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-552+18741G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108148667 | ||||||
| chr12:108148787
|
T | C | 4 | a0001c0001t0011g0056a0001c0001t0016g0044a0001c0001t0027g0005others(1): Show | 5 | HG02257.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+18861T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108148787 | ||||||
| chr12:108148814
|
C | A | 168 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(165): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.-552+18888C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108148814 | ||||||
| chr12:108148956
|
C | T | 4 | a0001c0001t0007g0013a0001c0001t0007g0014a0001c0001t0012g0024others(1): Show | 4 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(1): Show |
intron_variant | MODIFIER | c.-552+19030C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108148956 | ||||||
| chr12:108148975
|
A | G | 2 | a0001c0001t0016g0278a0001c0001t0060g0274 | 2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-552+19049A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108148975 | ||||||
| chr12:108149047
|
A | G | 14 | a0001c0001t0007g0027a0001c0001t0007g0028a0001c0001t0007g0039others(11): Show | 14 | HG00099.hp2 HG01069.hp1 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.-552+19121A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108149047 | ||||||
| chr12:108149080
|
T | C | 5 | a0001c0001t0035g0233a0001c0001t0035g0259a0001c0001t0036g0068others(2): Show | 5 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+19154T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108149080 | ||||||
| chr12:108149222
|
G | A | 1 | a0001c0001t0065g0275 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-552+19296G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108149222 | ||||||
| chr12:108149360
|
A | G | 2 | a0001c0001t0016g0278a0001c0001t0060g0274 | 2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-552+19434A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108149360 | ||||||
| chr12:108149489
|
A | G | 1 | a0001c0001t0060g0274 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-552+19563A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108149489 | ||||||
| chr12:108149571
|
TGCTCAG | T | 5 | a0001c0001t0035g0233a0001c0001t0035g0259a0001c0001t0036g0068others(2): Show | 5 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+19648_-552+19 others(12): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108149571 | |||||
| chr12:108149675
|
C | T | 1 | a0001c0001t0060g0274 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-552+19749C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108149675 | ||||||
| chr12:108149746
|
T | A | 5 | a0001c0001t0035g0233a0001c0001t0035g0259a0001c0001t0036g0068others(2): Show | 5 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+19820T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108149746 | ||||||
| chr12:108149805
|
T | A | 240 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(237): Show | 244 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.-552+19879T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108149805 | ||||||
| chr12:108149825
|
G | A | 1 | a0001c0001t0046g0152 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-552+19899G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108149825 | ||||||
| chr12:108149852
|
C | G | 9 | a0001c0001t0007g0048a0001c0001t0016g0278a0001c0001t0035g0233others(6): Show | 9 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-552+19926C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108149852 | ||||||
| chr12:108149988
|
G | T | 3 | a0001c0001t0011g0056a0001c0001t0016g0044a0001c0001t0058g0043 | 3 | HG02257.hp2 HG02922.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-552+20062G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108149988 | ||||||
| chr12:108150118
|
AGGGT | A | 4 | a0001c0001t0011g0056a0001c0001t0016g0044a0001c0001t0027g0005others(1): Show | 5 | HG02257.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+20195_-552+20 others(10): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108150118 | |||||
| chr12:108150172
|
A | T | 2 | a0001c0001t0033g0049a0001c0003t0012g0045 | 2 | HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-552+20246A>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108150172 | ||||||
| chr12:108150188
|
G | A | 1 | a0002c0002t0002g0231 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-552+20262G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108150188 | ||||||
| chr12:108150211
|
G | A | 1 | a0001c0001t0003g0064 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-552+20285G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108150211 | ||||||
| chr12:108150212
|
A | G | 1 | a0001c0001t0003g0064 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-552+20286A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108150212 | ||||||
| chr12:108150214
|
C | A | 1 | a0001c0001t0003g0064 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-552+20288C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108150214 | ||||||
| chr12:108150379
|
G | A | 1 | a0001c0001t0060g0274 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-552+20453G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108150379 | ||||||
| chr12:108150598
|
G | A | 1 | a0001c0001t0023g0017 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-552+20672G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108150598 | ||||||
| chr12:108150669
|
C | T | 2 | a0001c0001t0007g0048a0001c0001t0057g0047 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-552+20743C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108150669 | ||||||
| chr12:108150878
|
C | G | 6 | a0001c0001t0026g0092a0001c0001t0026g0093a0001c0001t0026g0095others(3): Show | 6 | HG00323.hp2 HG01167.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.-552+20952C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108150878 | ||||||
| chr12:108150964
|
G | C | 1 | a0001c0001t0008g0018 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-552+21038G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108150964 | ||||||
| chr12:108150991
|
C | T | 1 | a0002c0002t0009g0187 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-552+21065C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108150991 | ||||||
| chr12:108151283
|
C | T | 5 | a0001c0001t0022g0151a0001c0001t0033g0049a0001c0001t0045g0232others(2): Show | 5 | HG02717.hp1 HG02723.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+21357C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108151283 | ||||||
| chr12:108151353
|
C | T | 1 | a0001c0001t0022g0151 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-552+21427C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108151353 | ||||||
| chr12:108151461
|
G | T | 2 | a0001c0001t0003g0143a0002c0002t0002g0231 | 2 | NA18981.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.-552+21535G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108151461 | ||||||
| chr12:108151488
|
G | A | 1 | a0001c0001t0037g0099 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-552+21562G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108151488 | ||||||
| chr12:108151611
|
T | C | 2 | a0001c0001t0007g0048a0001c0001t0057g0047 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-552+21685T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108151611 | ||||||
| chr12:108151707
|
C | A | 5 | a0001c0001t0022g0151a0001c0001t0033g0049a0001c0001t0045g0232others(2): Show | 5 | HG02717.hp1 HG02723.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+21781C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108151707 | ||||||
| chr12:108151849
|
A | G | 1 | a0002c0002t0001g0220 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-552+21923A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108151849 | ||||||
| chr12:108151960
|
G | A | 4 | a0001c0001t0012g0025a0001c0001t0012g0030a0001c0001t0012g0040others(1): Show | 4 | HG01943.hp1 HG02683.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.-552+22034G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108151960 | ||||||
| chr12:108152013
|
C | T | 1 | a0001c0001t0004g0178 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-552+22087C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108152013 | ||||||
| chr12:108152014
|
G | A | 4 | a0001c0001t0011g0056a0001c0001t0016g0044a0001c0001t0027g0005others(1): Show | 5 | HG02257.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+22088G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108152014 | ||||||
| chr12:108152102
|
G | A | 1 | a0001c0001t0037g0099 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-552+22176G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108152102 | ||||||
| chr12:108152103
|
A | G | 199 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(196): Show | 201 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.-552+22177A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108152103 | ||||||
| chr12:108152208
|
A | C | 81 | a0001c0001t0001g0079a0001c0001t0001g0139a0001c0001t0001g0154others(78): Show | 81 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.-552+22282A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108152208 | ||||||
| chr12:108152292
|
A | G | 1 | a0001c0001t0073g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-552+22366A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108152292 | ||||||
| chr12:108152582
|
G | A | 3 | a0001c0003t0016g0055a0001c0003t0031g0050a0001c0003t0031g0051 | 3 | HG01243.hp2 HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-552+22656G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108152582 | ||||||
| chr12:108152734
|
A | G | 1 | a0001c0001t0005g0264 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-552+22808A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108152734 | ||||||
| chr12:108152741
|
T | C | 1 | a0001c0001t0012g0024 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-552+22815T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108152741 | ||||||
| chr12:108152761
|
A | C | 1 | a0001c0001t0007g0048 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-552+22835A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108152761 | ||||||
| chr12:108152762
|
C | T | 1 | a0001c0001t0014g0153 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-552+22836C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108152762 | ||||||
| chr12:108152766
|
G | A | 162 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(159): Show | 163 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.-552+22840G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108152766 | ||||||
| chr12:108152824
|
C | G | 9 | a0001c0001t0005g0088a0001c0001t0005g0091a0001c0001t0006g0086others(6): Show | 9 | HG00642.hp2 HG01516.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-552+22898C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108152824 | ||||||
| chr12:108153015
|
A | T | 12 | a0001c0001t0022g0151a0001c0001t0030g0130a0001c0001t0033g0049others(9): Show | 12 | HG02109.hp2 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.-552+23089A>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108153015 | ||||||
| chr12:108153101
|
T | TCAAA | 15 | a0001c0001t0001g0073a0001c0001t0002g0179a0001c0001t0007g0014others(12): Show | 16 | HG00140.hp1 HG01168.hp1 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.-552+23200_-552+23 others(10): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108153101 | |||||
| chr12:108153101
|
T | TCAAACAA others(1): Show |
61 | a0001c0001t0001g0075a0001c0001t0001g0079a0001c0001t0001g0080others(58): Show | 62 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.-552+23196_-552+23 others(14): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108153101 | |||||
| chr12:108153101
|
T | TCAAACAA others(5): Show |
85 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0139others(82): Show | 85 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.-552+23192_-552+23 others(18): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108153101 | |||||
| chr12:108153101
|
T | TCAAACAA others(9): Show |
5 | a0001c0001t0007g0039a0001c0001t0024g0029a0001c0001t0024g0042others(2): Show | 5 | HG03239.hp1 HG03490.hp2 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.-552+23188_-552+23 others(22): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108153101 | |||||
| chr12:108153101
|
TCAAA | T | 13 | a0001c0001t0005g0088a0001c0001t0005g0091a0001c0001t0006g0086others(10): Show | 13 | HG00642.hp2 HG01243.hp2 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.-552+23200_-552+23 others(10): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108153101 | |||||
| chr12:108153418
|
T | C | 1 | a0001c0001t0001g0227 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-552+23492T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108153418 | ||||||
| chr12:108153462
|
G | A | 1 | a0001c0001t0026g0092 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-552+23536G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108153462 | ||||||
| chr12:108153569
|
T | C | 3 | a0001c0001t0063g0276a0001c0001t0064g0277a0001c0001t0065g0275 | 3 | HG01109.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-552+23643T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108153569 | ||||||
| chr12:108153587
|
A | G | 198 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(195): Show | 200 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.-552+23661A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108153587 | ||||||
| chr12:108153619
|
C | T | 5 | a0001c0001t0002g0077a0001c0001t0002g0146a0001c0001t0003g0101others(2): Show | 5 | HG00597.hp2 HG04204.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.-552+23693C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108153619 | ||||||
| chr12:108153844
|
C | T | 1 | a0006c0007t0023g0020 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-552+23918C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108153844 | ||||||
| chr12:108153966
|
G | A | 1 | a0001c0001t0003g0065 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-552+24040G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108153966 | ||||||
| chr12:108154020
|
G | A | 1 | a0002c0002t0003g0196 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-552+24094G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108154020 | ||||||
| chr12:108154057
|
A | G | 198 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(195): Show | 200 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.-552+24131A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108154057 | ||||||
| chr12:108154125
|
G | A | 196 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(193): Show | 198 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.-552+24199G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108154125 | ||||||
| chr12:108154151
|
T | A | 1 | a0001c0001t0002g0197 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-552+24225T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108154151 | ||||||
| chr12:108154208
|
C | A | 12 | a0001c0001t0022g0151a0001c0001t0030g0130a0001c0001t0033g0049others(9): Show | 12 | HG02109.hp2 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.-552+24282C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108154208 | ||||||
| chr12:108154242
|
G | T | 186 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(183): Show | 188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.-552+24316G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108154242 | ||||||
| chr12:108154387
|
G | A | 1 | a0001c0001t0001g0252 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-552+24461G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108154387 | ||||||
| chr12:108154451
|
C | T | 1 | a0002c0002t0002g0218 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-552+24525C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108154451 | ||||||
| chr12:108154513
|
T | C | 198 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(195): Show | 200 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.-552+24587T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108154513 | ||||||
| chr12:108154768
|
A | G | 1 | a0001c0001t0001g0191 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-552+24842A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108154768 | ||||||
| chr12:108154898
|
A | G | 12 | a0001c0001t0022g0151a0001c0001t0030g0130a0001c0001t0033g0049others(9): Show | 12 | HG02109.hp2 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.-552+24972A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108154898 | ||||||
| chr12:108155009
|
G | A | 1 | a0001c0001t0034g0031 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-552+25083G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108155009 | ||||||
| chr12:108155139
|
C | A | 4 | a0001c0001t0033g0049a0001c0001t0045g0232a0001c0001t0046g0152others(1): Show | 4 | HG02717.hp1 HG02723.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-552+25213C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108155139 | ||||||
| chr12:108155147
|
A | C | 198 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(195): Show | 200 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.-552+25221A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108155147 | ||||||
| chr12:108155155
|
C | T | 196 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(193): Show | 198 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.-552+25229C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108155155 | ||||||
| chr12:108155320
|
C | G | 162 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(159): Show | 163 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.-552+25394C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108155320 | ||||||
| chr12:108155373
|
C | T | 3 | a0001c0001t0032g0035a0001c0001t0032g0036a0001c0001t0062g0034 | 3 | HG00099.hp2 HG01257.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.-552+25447C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108155373 | ||||||
| chr12:108156098
|
G | A | 1 | a0002c0002t0001g0220 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-552+26172G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108156098 | ||||||
| chr12:108156131
|
C | T | 1 | a0001c0001t0010g0129 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-552+26205C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108156131 | ||||||
| chr12:108156190
|
C | T | 2 | a0001c0001t0033g0049a0001c0003t0012g0045 | 2 | HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-552+26264C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108156190 | ||||||
| chr12:108156212
|
G | A | 1 | a0001c0001t0005g0163 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-552+26286G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108156212 | ||||||
| chr12:108156402
|
A | G | 1 | a0001c0001t0025g0033 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-552+26476A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108156402 | ||||||
| chr12:108156539
|
G | A | 12 | a0001c0001t0005g0088a0001c0001t0006g0086a0001c0001t0010g0129others(9): Show | 12 | HG00642.hp2 HG01243.hp2 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.-552+26613G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108156539 | ||||||
| chr12:108156598
|
T | A | 1 | a0001c0001t0001g0252 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-552+26672T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108156598 | ||||||
| chr12:108156659
|
A | G | 1 | a0001c0001t0018g0217 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-552+26733A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108156659 | ||||||
| chr12:108157024
|
C | T | 4 | a0003c0004t0017g0052a0003c0004t0025g0053a0003c0004t0025g0054others(1): Show | 4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-552+27098C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108157024 | ||||||
| chr12:108157084
|
G | A | 6 | a0001c0003t0016g0055a0001c0003t0021g0245a0001c0003t0021g0266others(3): Show | 6 | HG01243.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-552+27158G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108157084 | ||||||
| chr12:108157126
|
T | C | 2 | a0001c0001t0006g0086a0001c0001t0010g0129 | 2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-552+27200T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108157126 | ||||||
| chr12:108157140
|
T | C | 4 | a0001c0001t0035g0259a0001c0001t0036g0068a0001c0001t0036g0261others(1): Show | 4 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.-552+27214T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108157140 | ||||||
| chr12:108157149
|
A | G | 13 | a0001c0001t0016g0278a0001c0001t0022g0151a0001c0001t0030g0130others(10): Show | 13 | HG02109.hp2 HG02630.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.-552+27223A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108157149 | ||||||
| chr12:108157210
|
C | G | 3 | a0001c0001t0063g0276a0001c0001t0064g0277a0001c0001t0065g0275 | 3 | HG01109.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-552+27284C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108157210 | ||||||
| chr12:108157216
|
A | G | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG01074.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.-552+27290A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108157216 | ||||||
| chr12:108157547
|
T | C | 15 | a0001c0001t0003g0002a0001c0001t0003g0064a0001c0001t0003g0065others(12): Show | 17 | HG01081.hp1 HG01175.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.-552+27621T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108157547 | ||||||
| chr12:108157653
|
G | A | 10 | a0001c0001t0022g0151a0001c0001t0033g0049a0001c0001t0045g0232others(7): Show | 10 | HG02109.hp2 HG02717.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.-552+27727G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108157653 | ||||||
| chr12:108158199
|
G | A | 11 | a0001c0001t0016g0278a0001c0001t0022g0151a0001c0001t0033g0049others(8): Show | 11 | HG02109.hp2 HG02717.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.-552+28273G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108158199 | ||||||
| chr12:108158256
|
C | T | 1 | a0001c0001t0020g0265 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-552+28330C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108158256 | ||||||
| chr12:108158278
|
C | T | 1 | a0001c0001t0037g0099 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-552+28352C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108158278 | ||||||
| chr12:108158787
|
G | A | 1 | a0005c0006t0016g0046 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-552+28861G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108158787 | ||||||
| chr12:108158805
|
A | G | 13 | a0001c0001t0016g0278a0001c0001t0022g0151a0001c0001t0030g0130others(10): Show | 13 | HG02109.hp2 HG02630.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.-552+28879A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108158805 | ||||||
| chr12:108159147
|
T | A | 4 | a0001c0001t0035g0259a0001c0001t0036g0068a0001c0001t0036g0261others(1): Show | 4 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.-552+29221T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108159147 | ||||||
| chr12:108159152
|
C | A | 2 | a0001c0003t0031g0050a0001c0003t0031g0051 | 2 | HG01243.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-552+29226C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108159152 | ||||||
| chr12:108159299
|
G | A | 1 | a0001c0001t0026g0093 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-552+29373G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108159299 | ||||||
| chr12:108159402
|
C | T | 1 | a0002c0002t0002g0216 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-552+29476C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108159402 | ||||||
| chr12:108159418
|
G | A | 2 | a0001c0001t0005g0115a0001c0001t0005g0116 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-552+29492G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108159418 | ||||||
| chr12:108159461
|
A | G | 1 | a0002c0002t0001g0215 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-552+29535A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108159461 | ||||||
| chr12:108159502
|
C | T | 3 | a0001c0001t0013g0213a0002c0002t0001g0212a0002c0002t0068g0214 | 3 | HG00639.hp1 HG00738.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.-552+29576C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108159502 | ||||||
| chr12:108159504
|
G | A | 3 | a0001c0001t0004g0114a0001c0001t0020g0164a0001c0010t0049g0239 | 3 | HG01981.hp2 HG02735.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.-552+29578G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108159504 | ||||||
| chr12:108159537
|
G | T | 4 | a0001c0001t0005g0088a0001c0001t0011g0090a0001c0001t0015g0087others(1): Show | 4 | HG00642.hp2 HG01516.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.-552+29611G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108159537 | ||||||
| chr12:108159609
|
T | A | 6 | a0001c0003t0016g0055a0001c0003t0021g0245a0001c0003t0021g0266others(3): Show | 6 | HG01243.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-552+29683T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108159609 | ||||||
| chr12:108159728
|
G | A | 1 | a0001c0001t0016g0278 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-552+29802G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108159728 | ||||||
| chr12:108159836
|
G | T | 1 | a0002c0002t0009g0223 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-552+29910G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108159836 | ||||||
| chr12:108159882
|
C | T | 3 | a0001c0001t0063g0276a0001c0001t0064g0277a0001c0001t0065g0275 | 3 | HG01109.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-552+29956C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108159882 | ||||||
| chr12:108159903
|
G | A | 10 | a0001c0001t0022g0151a0001c0001t0033g0049a0001c0001t0045g0232others(7): Show | 10 | HG02109.hp2 HG02717.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.-552+29977G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108159903 | ||||||
| chr12:108159989
|
T | C | 2 | a0001c0001t0033g0049a0001c0003t0012g0045 | 2 | HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-552+30063T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108159989 | ||||||
| chr12:108160052
|
A | G | 1 | a0001c0001t0018g0060 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-552+30126A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108160052 | ||||||
| chr12:108160272
|
T | G | 1 | a0001c0001t0015g0087 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-552+30346T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108160272 | ||||||
| chr12:108160350
|
A | G | 12 | a0001c0001t0022g0151a0001c0001t0030g0130a0001c0001t0033g0049others(9): Show | 12 | HG02109.hp2 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.-552+30424A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108160350 | ||||||
| chr12:108160649
|
C | A | 1 | a0001c0001t0016g0278 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-552+30723C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108160649 | ||||||
| chr12:108161342
|
T | C | 165 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(162): Show | 166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.-552+31416T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108161342 | ||||||
| chr12:108161465
|
G | A | 1 | a0001c0001t0028g0240 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-552+31539G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108161465 | ||||||
| chr12:108161481
|
G | A | 1 | a0001c0001t0037g0099 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-552+31555G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108161481 | ||||||
| chr12:108161637
|
A | G | 1 | a0001c0001t0011g0090 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-552+31711A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108161637 | ||||||
| chr12:108161773
|
T | C | 2 | a0001c0001t0002g0198a0001c0001t0003g0225 | 2 | HG02523.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.-552+31847T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108161773 | ||||||
| chr12:108162062
|
A | G | 200 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(197): Show | 202 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.-552+32136A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108162062 | ||||||
| chr12:108162129
|
G | A | 1 | a0002c0002t0001g0199 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-552+32203G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108162129 | ||||||
| chr12:108162435
|
T | G | 162 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(159): Show | 163 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.-552+32509T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108162435 | ||||||
| chr12:108162514
|
C | T | 1 | a0002c0002t0002g0231 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-552+32588C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108162514 | ||||||
| chr12:108162624
|
G | A | 1 | a0001c0001t0022g0151 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-551-32658G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108162624 | ||||||
| chr12:108162649
|
G | A | 78 | a0001c0001t0001g0139a0001c0001t0001g0154a0001c0001t0001g0181others(75): Show | 78 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.-551-32633G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108162649 | ||||||
| chr12:108162838
|
T | G | 1 | a0001c0001t0039g0189 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-551-32444T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108162838 | ||||||
| chr12:108162900
|
T | G | 1 | a0006c0007t0023g0020 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-551-32382T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108162900 | ||||||
| chr12:108163134
|
T | C | 4 | a0001c0001t0011g0056a0001c0001t0016g0044a0001c0001t0027g0005others(1): Show | 5 | HG02257.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-551-32148T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108163134 | ||||||
| chr12:108163143
|
G | A | 1 | a0001c0001t0016g0278 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-551-32139G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108163143 | ||||||
| chr12:108163450
|
A | G | 12 | a0001c0001t0022g0151a0001c0001t0030g0130a0001c0001t0033g0049others(9): Show | 12 | HG02109.hp2 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.-551-31832A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108163450 | ||||||
| chr12:108163556
|
C | A | 4 | a0001c0001t0006g0117a0001c0001t0006g0165a0001c0001t0006g0166others(1): Show | 4 | HG00735.hp2 HG01361.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.-551-31726C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108163556 | ||||||
| chr12:108163558
|
T | C | 1 | a0002c0002t0009g0200 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-551-31724T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108163558 | ||||||
| chr12:108163605
|
G | A | 1 | a0001c0001t0037g0099 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-551-31677G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108163605 | ||||||
| chr12:108163609
|
G | A | 162 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(159): Show | 163 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.-551-31673G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108163609 | ||||||
| chr12:108163644
|
T | A | 1 | a0002c0002t0001g0212 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-551-31638T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108163644 | ||||||
| chr12:108163712
|
A | G | 8 | a0001c0001t0003g0002a0001c0001t0003g0064a0001c0001t0003g0065others(5): Show | 9 | HG01081.hp1 HG01175.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-551-31570A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108163712 | ||||||
| chr12:108163853
|
G | GT | 12 | a0001c0001t0022g0151a0001c0001t0030g0130a0001c0001t0033g0049others(9): Show | 12 | HG02109.hp2 HG02630.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.-551-31422dupT | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108163853 | |||||
| chr12:108164009
|
TGATGGCT others(8): Show |
T | 1 | a0001c0001t0003g0143 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-551-31272_-551-31 others(21): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108164009 | ||||||
| chr12:108164137
|
TC | T | 7 | a0001c0001t0004g0114a0001c0001t0004g0169a0001c0001t0004g0178others(4): Show | 7 | HG01167.hp2 HG01257.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.-551-31143delC | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108164137 | |||||
| chr12:108164138
|
C | CT | 11 | a0001c0001t0002g0142a0001c0001t0002g0201a0001c0001t0004g0112others(8): Show | 11 | HG01361.hp1 HG02257.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.-551-31144_-551-31 others(7): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108164138 | ||||||
| chr12:108164138
|
C | CTT | 5 | a0001c0001t0002g0198a0001c0001t0003g0225a0001c0001t0003g0267others(2): Show | 5 | HG00597.hp1 HG02523.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-551-31144_-551-31 others(8): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108164138 | ||||||
| chr12:108164138
|
C | CTTTTTT | 3 | a0001c0001t0013g0255a0001c0001t0033g0049a0001c0003t0012g0045 | 3 | HG02723.hp1 HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-551-31144_-551-31 others(12): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108164138 | ||||||
| chr12:108164138
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001g0079 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-551-31144_-551-31 others(16): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108164138 | ||||||
| chr12:108164138
|
C | CTTTTTTT others(4): Show |
3 | a0001c0001t0008g0007a0001c0001t0063g0276a0001c0001t0065g0275 | 3 | HG02970.hp1 NA18906.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.-551-31144_-551-31 others(17): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108164138 | ||||||
| chr12:108164138
|
C | CTTTTTTT others(6): Show |
18 | a0001c0001t0001g0057a0001c0001t0001g0080a0001c0001t0001g0096others(15): Show | 18 | HG00597.hp2 HG00733.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.-551-31144_-551-31 others(19): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108164138 | ||||||
| chr12:108164138
|
C | CTTTTTTT others(7): Show |
16 | a0001c0001t0001g0058a0001c0001t0001g0073a0001c0001t0001g0075others(13): Show | 16 | HG00280.hp1 HG01168.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.-551-31144_-551-31 others(20): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108164138 | ||||||
| chr12:108164138
|
C | CTTTTTTT others(8): Show |
22 | a0001c0001t0001g0081a0001c0001t0001g0148a0001c0001t0001g0154others(19): Show | 22 | HG00609.hp1 HG00609.hp2 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.-551-31144_-551-31 others(21): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108164138 | ||||||
| chr12:108164138
|
C | CTTTTTTT others(9): Show |
46 | a0001c0001t0001g0149a0001c0001t0001g0182a0001c0001t0001g0205others(43): Show | 47 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(44): Show |
intron_variant | MODIFIER | c.-551-31144_-551-31 others(22): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108164138 | ||||||
| chr12:108164138
|
C | CTTTTTTT others(10): Show |
31 | a0001c0001t0001g0139a0001c0001t0001g0252a0001c0001t0002g0197others(28): Show | 31 | HG00438.hp1 HG00738.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.-551-31144_-551-31 others(23): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108164138 | ||||||
| chr12:108164138
|
C | CTTTTTTT others(11): Show |
10 | a0001c0001t0001g0227a0001c0001t0004g0234a0001c0001t0007g0037others(7): Show | 10 | HG01261.hp1 HG01358.hp1 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.-551-31144_-551-31 others(24): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108164138 | ||||||
| chr12:108164138
|
C | CTTTTTTT others(12): Show |
3 | a0001c0001t0001g0230a0001c0001t0009g0194a0002c0002t0003g0250 | 3 | HG00438.hp2 HG01175.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.-551-31144_-551-31 others(25): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108164138 | ||||||
| chr12:108164138
|
C | CTTTTTTT others(13): Show |
1 | a0001c0001t0026g0093 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-551-31144_-551-31 others(26): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108164138 | ||||||
| chr12:108164138
|
C | CTTTTTTT others(15): Show |
2 | a0001c0001t0075g0141a0002c0002t0003g0251 | 2 | HG00280.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.-551-31144_-551-31 others(28): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108164138 | ||||||
| chr12:108164138
|
CCT | C | 21 | a0001c0001t0003g0002a0001c0001t0003g0064a0001c0001t0003g0065others(18): Show | 23 | HG00099.hp1 HG01081.hp1 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.-551-31143_-551-31 others(8): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108164138 | ||||||
| chr12:108164138
|
CCTT | C | 7 | a0001c0001t0003g0066a0001c0001t0016g0278a0001c0001t0027g0005others(4): Show | 8 | HG02109.hp2 HG02723.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-551-31143_-551-31 others(9): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108164138 | ||||||
| chr12:108164138
|
CCTTTTT | C | 3 | a0001c0003t0016g0055a0001c0003t0031g0050a0001c0003t0031g0051 | 3 | HG01243.hp2 HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-551-31143_-551-31 others(12): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108164138 | ||||||
| chr12:108164138
|
CCTTTTTT | C | 3 | a0001c0003t0021g0245a0001c0003t0021g0266a0005c0006t0016g0046 | 3 | HG02615.hp1 HG03486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-551-31143_-551-31 others(13): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108164138 | ||||||
| chr12:108164138
|
CCTTTTTT others(3): Show |
C | 7 | a0001c0001t0005g0088a0001c0001t0005g0091a0001c0001t0006g0086others(4): Show | 7 | HG00642.hp2 HG01516.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-551-31143_-551-31 others(16): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108164138 | ||||||
| chr12:108164139
|
C | T | 229 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(226): Show | 231 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.-551-31143C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108164139 | ||||||
| chr12:108164162
|
T | TTTTTTTT others(7): Show |
1 | a0001c0001t0019g0083 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-551-31120_-551-31 others(20): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108164162 | ||||||
| chr12:108164567
|
A | G | 2 | a0002c0002t0001g0195a0002c0002t0017g0038 | 2 | HG01069.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.-551-30715A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108164567 | ||||||
| chr12:108164617
|
C | G | 1 | a0001c0001t0012g0030 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-551-30665C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108164617 | ||||||
| chr12:108164908
|
G | A | 1 | a0001c0003t0038g0063 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-551-30374G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108164908 | ||||||
| chr12:108165045
|
G | A | 1 | a0003c0004t0025g0053 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-551-30237G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108165045 | ||||||
| chr12:108165123
|
G | T | 3 | a0001c0001t0063g0276a0001c0001t0064g0277a0001c0001t0065g0275 | 3 | HG01109.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-551-30159G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108165123 | ||||||
| chr12:108165139
|
G | T | 25 | a0001c0001t0003g0002a0001c0001t0003g0064a0001c0001t0003g0065others(22): Show | 27 | HG00642.hp2 HG01081.hp1 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.-551-30143G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108165139 | ||||||
| chr12:108165680
|
C | T | 152 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0001g0079others(149): Show | 153 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.-551-29602C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108165680 | ||||||
| chr12:108165986
|
T | G | 1 | a0001c0001t0006g0086 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-551-29296T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108165986 | ||||||
| chr12:108166099
|
T | C | 2 | a0001c0001t0006g0086a0001c0001t0010g0129 | 2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-551-29183T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108166099 | ||||||
| chr12:108166331
|
A | G | 1 | a0001c0001t0022g0151 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-551-28951A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108166331 | ||||||
| chr12:108166550
|
G | A | 160 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(157): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-551-28732G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108166550 | ||||||
| chr12:108166716
|
C | T | 173 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(170): Show | 175 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.-551-28566C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108166716 | ||||||
| chr12:108166724
|
T | TCTCTTCT others(11): Show |
1 | a0001c0001t0002g0146 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-551-28558_-551-28 others(24): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108166724 | ||||||
| chr12:108166726
|
C | T | 1 | a0001c0001t0002g0146 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-551-28556C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108166726 | ||||||
| chr12:108166741
|
T | C | 1 | a0001c0001t0001g0081 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-551-28541T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108166741 | ||||||
| chr12:108166745
|
C | CTTCTTCT others(8): Show |
1 | a0002c0002t0001g0204 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-551-28532_-551-28 others(21): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166745 | |||||
| chr12:108166745
|
C | CTTCTTTC others(3): Show |
1 | a0002c0002t0009g0223 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-551-28529_-551-28 others(16): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166745 | |||||
| chr12:108166745
|
C | CTTTCTTT others(10): Show |
1 | a0001c0001t0071g0249 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-551-28535_-551-28 others(23): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166745 | |||||
| chr12:108166745
|
C | T | 3 | a0001c0001t0001g0081a0001c0001t0002g0146a0001c0001t0033g0008 | 3 | HG01243.hp1 NA18960.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.-551-28537C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108166745 | ||||||
| chr12:108166745
|
CTTCTTTC others(10): Show |
C | 5 | a0001c0001t0005g0088a0001c0001t0005g0091a0001c0001t0011g0090others(2): Show | 5 | HG00642.hp2 HG01516.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-551-28518_-551-28 others(23): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166745 | |||||
| chr12:108166748
|
CTTTCTTT others(6): Show |
C | 1 | a0001c0001t0037g0099 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-551-28518_-551-28 others(19): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166748 | |||||
| chr12:108166756
|
CTTTCT | C | 5 | a0001c0001t0006g0086a0001c0001t0009g0194a0001c0001t0010g0129others(2): Show | 5 | HG00438.hp2 HG01433.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-551-28518_-551-28 others(11): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166756 | |||||
| chr12:108166760
|
C | T | 2 | a0001c0001t0008g0001a0001c0001t0008g0007 | 3 | NA18944.hp1 NA18952.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.-551-28522C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108166760 | ||||||
| chr12:108166760
|
CT | C | 16 | a0001c0001t0001g0073a0001c0001t0001g0139a0001c0001t0007g0037others(13): Show | 16 | HG00438.hp1 HG01168.hp1 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.-551-28518delT | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166760 | |||||
| chr12:108166761
|
T | TCTTTCTT others(2): Show |
2 | a0001c0001t0008g0001a0001c0001t0008g0007 | 3 | NA18944.hp1 NA18952.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.-551-28521_-551-28 others(15): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108166761 | ||||||
| chr12:108166761
|
T | TTTC | 20 | a0001c0001t0001g0191a0001c0001t0001g0252a0001c0001t0002g0069others(17): Show | 20 | HG00280.hp1 HG00323.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.-551-28519_-551-28 others(9): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166761 | |||||
| chr12:108166761
|
T | TTTCTTTC | 22 | a0001c0001t0001g0075a0001c0001t0001g0107a0001c0001t0001g0154others(19): Show | 22 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.-551-28519_-551-28 others(13): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166761 | |||||
| chr12:108166761
|
T | TTTCTTTC others(22): Show |
1 | a0001c0001t0027g0005 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-551-28519_-551-28 others(35): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166761 | |||||
| chr12:108166761
|
T | TTTCTTTC others(4): Show |
38 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0182others(35): Show | 38 | HG00099.hp2 HG00609.hp1 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.-551-28519_-551-28 others(17): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166761 | |||||
| chr12:108166761
|
T | TTTCTTTC others(8): Show |
36 | a0001c0001t0001g0081a0001c0001t0001g0148a0001c0001t0001g0149others(33): Show | 36 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(33): Show |
intron_variant | MODIFIER | c.-551-28519_-551-28 others(21): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166761 | |||||
| chr12:108166761
|
T | TTTCTTTC others(12): Show |
20 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0181others(17): Show | 20 | HG00558.hp1 HG00639.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.-551-28519_-551-28 others(25): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166761 | |||||
| chr12:108166761
|
T | TTTCTTTC others(16): Show |
8 | a0001c0001t0002g0142a0001c0001t0007g0009a0001c0001t0052g0131others(5): Show | 8 | HG01081.hp2 HG02148.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-551-28519_-551-28 others(29): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166761 | |||||
| chr12:108166761
|
T | TTTCTTTC others(20): Show |
8 | a0001c0001t0002g0102a0001c0001t0002g0197a0001c0001t0003g0143others(5): Show | 8 | HG01943.hp2 HG02109.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.-551-28519_-551-28 others(33): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166761 | |||||
| chr12:108166761
|
T | TTTCTTTC others(24): Show |
4 | a0001c0001t0002g0076a0001c0001t0002g0103a0001c0001t0007g0048others(1): Show | 4 | HG01109.hp1 HG02015.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-551-28519_-551-28 others(37): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166761 | |||||
| chr12:108166761
|
T | TTTTC | 5 | a0001c0001t0004g0109a0001c0001t0006g0117a0001c0001t0006g0165others(2): Show | 5 | HG00735.hp2 HG01361.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.-551-28495_-551-28 others(10): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166761 | |||||
| chr12:108166761
|
T | TTTTTCTT others(10): Show |
1 | a0001c0001t0065g0275 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-551-28518_-551-28 others(23): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166761 | |||||
| chr12:108166761
|
T | TTTTTCTT others(14): Show |
1 | a0001c0003t0021g0266 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-551-28518_-551-28 others(27): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166761 | |||||
| chr12:108166761
|
T | TTTTTCTT others(18): Show |
1 | a0001c0003t0031g0051 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-551-28518_-551-28 others(31): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166761 | |||||
| chr12:108166761
|
T | TTTTTCTT others(22): Show |
4 | a0001c0001t0016g0278a0001c0003t0021g0245a0001c0003t0031g0050others(1): Show | 4 | HG02451.hp1 HG02615.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-551-28518_-551-28 others(35): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166761 | |||||
| chr12:108166761
|
T | TTTTTCTT others(30): Show |
1 | a0001c0003t0016g0055 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-551-28518_-551-28 others(43): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166761 | |||||
| chr12:108166761
|
TTTTC | T | 3 | a0001c0001t0003g0248a0001c0001t0004g0168a0001c0001t0006g0118 | 3 | HG00099.hp1 NA18906.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.-551-28495_-551-28 others(10): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166761 | |||||
| chr12:108166787
|
T | G | 1 | a0001c0001t0035g0259 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-551-28495T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108166787 | ||||||
| chr12:108166791
|
G | GTCTT | 6 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0254others(3): Show | 6 | HG01884.hp2 HG01891.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-551-28479_-551-28 others(10): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166791 | |||||
| chr12:108166791
|
G | T | 5 | a0001c0001t0007g0048a0001c0001t0027g0005a0001c0001t0063g0276others(2): Show | 6 | HG01109.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-551-28491G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108166791 | ||||||
| chr12:108166805
|
C | CTT | 3 | a0001c0001t0027g0005a0001c0001t0064g0277a0001c0001t0065g0275 | 4 | HG01109.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-551-28476_-551-28 others(8): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166805 | |||||
| chr12:108166805
|
C | CTTTCTTT others(19): Show |
1 | a0001c0001t0063g0276 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-551-28476_-551-28 others(32): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166805 | |||||
| chr12:108166807
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-551-28475C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108166807 | ||||||
| chr12:108166811
|
T | G | 1 | a0002c0002t0001g0208 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-551-28471T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108166811 | ||||||
| chr12:108166817
|
C | CT | 6 | a0001c0001t0005g0088a0001c0001t0005g0091a0001c0001t0011g0090others(3): Show | 6 | HG00642.hp2 HG01516.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-551-28451dupT | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108166817 | |||||
| chr12:108166851
|
G | A | 1 | a0001c0001t0022g0151 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-551-28431G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108166851 | ||||||
| chr12:108166873
|
A | G | 188 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(185): Show | 190 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.-551-28409A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108166873 | ||||||
| chr12:108166890
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-551-28392C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108166890 | ||||||
| chr12:108166905
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-551-28377G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108166905 | ||||||
| chr12:108167153
|
G | T | 11 | a0001c0001t0016g0278a0001c0001t0027g0005a0001c0001t0063g0276others(8): Show | 12 | HG01109.hp1 HG01243.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-551-28129G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108167153 | ||||||
| chr12:108167167
|
C | T | 1 | a0001c0001t0048g0177 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-551-28115C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108167167 | ||||||
| chr12:108167358
|
T | G | 2 | a0001c0001t0018g0059a0001c0001t0018g0060 | 2 | HG02647.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-551-27924T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108167358 | ||||||
| chr12:108167413
|
A | G | 1 | a0002c0002t0038g0074 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-551-27869A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108167413 | ||||||
| chr12:108167653
|
C | T | 8 | a0001c0001t0005g0070a0001c0001t0005g0176a0001c0001t0006g0003others(5): Show | 9 | NA18940.hp1 NA18948.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.-551-27629C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108167653 | ||||||
| chr12:108167946
|
G | A | 4 | a0001c0001t0017g0023a0001c0001t0025g0033a0001c0001t0034g0031others(1): Show | 4 | HG02818.hp2 HG02895.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-551-27336G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108167946 | ||||||
| chr12:108168003
|
A | T | 1 | a0001c0001t0022g0151 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-551-27279A>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108168003 | ||||||
| chr12:108168193
|
T | A | 1 | a0002c0002t0013g0192 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-551-27089T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108168193 | ||||||
| chr12:108168197
|
G | A | 1 | a0001c0001t0020g0265 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-551-27085G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108168197 | ||||||
| chr12:108168490
|
G | C | 1 | a0002c0009t0001g0185 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-551-26792G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108168490 | ||||||
| chr12:108168533
|
CACTT | C | 160 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(157): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-551-26741_-551-26 others(10): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108168533 | |||||
| chr12:108168626
|
A | G | 1 | a0001c0001t0037g0099 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-551-26656A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108168626 | ||||||
| chr12:108168684
|
G | T | 4 | a0001c0001t0012g0025a0001c0001t0012g0030a0001c0001t0012g0040others(1): Show | 4 | HG01943.hp1 HG02683.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.-551-26598G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108168684 | ||||||
| chr12:108168774
|
A | G | 2 | a0001c0001t0033g0049a0001c0003t0012g0045 | 2 | HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-551-26508A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108168774 | ||||||
| chr12:108169056
|
A | T | 4 | a0001c0001t0006g0086a0001c0001t0010g0129a0001c0001t0045g0232others(1): Show | 4 | HG02717.hp1 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-551-26226A>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108169056 | ||||||
| chr12:108169500
|
G | A | 5 | a0001c0001t0008g0018a0001c0001t0023g0017a0001c0001t0023g0022others(2): Show | 5 | HG00438.hp1 NA18612.hp2 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.-551-25782G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108169500 | ||||||
| chr12:108169880
|
T | TA | 4 | a0001c0003t0021g0245a0001c0003t0021g0266a0001c0003t0031g0050others(1): Show | 4 | HG01243.hp2 HG02451.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.-551-25400dupA | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108169880 | |||||
| chr12:108169908
|
C | G | 1 | a0001c0001t0037g0099 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-551-25374C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108169908 | ||||||
| chr12:108169909
|
G | A | 1 | a0001c0001t0002g0069 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-551-25373G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108169909 | ||||||
| chr12:108170036
|
C | T | 1 | a0001c0001t0017g0023 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-551-25246C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108170036 | ||||||
| chr12:108170171
|
GA | G | 152 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0001g0079others(149): Show | 153 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.-551-25109delA | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108170171 | |||||
| chr12:108170173
|
A | T | 152 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0001g0079others(149): Show | 153 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.-551-25109A>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108170173 | ||||||
| chr12:108170174
|
C | A | 1 | a0001c0001t0016g0278 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-551-25108C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108170174 | ||||||
| chr12:108170376
|
A | AATG | 5 | a0001c0001t0005g0088a0001c0001t0005g0091a0001c0001t0011g0090others(2): Show | 5 | HG00642.hp2 HG01516.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-551-24896_-551-24 others(9): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108170376 | |||||
| chr12:108170445
|
A | AATG | 3 | a0001c0001t0011g0056a0001c0001t0016g0044a0001c0001t0058g0043 | 3 | HG02257.hp2 HG02922.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-551-24817_-551-24 others(9): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108170445 | |||||
| chr12:108170468
|
G | T | 2 | a0001c0001t0007g0048a0001c0001t0057g0047 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-551-24814G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108170468 | ||||||
| chr12:108170586
|
T | C | 4 | a0001c0001t0035g0259a0001c0001t0036g0068a0001c0001t0036g0261others(1): Show | 4 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.-551-24696T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108170586 | ||||||
| chr12:108170703
|
G | A | 2 | a0001c0001t0016g0278a0002c0002t0009g0132 | 2 | HG00558.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-551-24579G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108170703 | ||||||
| chr12:108170793
|
A | G | 1 | a0001c0001t0005g0091 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-551-24489A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108170793 | ||||||
| chr12:108171025
|
G | A | 1 | a0002c0002t0018g0082 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-551-24257G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108171025 | ||||||
| chr12:108171119
|
G | A | 5 | a0001c0001t0005g0088a0001c0001t0005g0091a0001c0001t0011g0090others(2): Show | 5 | HG00642.hp2 HG01516.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-551-24163G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108171119 | ||||||
| chr12:108171267
|
G | C | 217 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(214): Show | 221 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.-551-24015G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108171267 | ||||||
| chr12:108171300
|
G | A | 28 | a0001c0001t0003g0002a0001c0001t0003g0064a0001c0001t0003g0065others(25): Show | 30 | HG01081.hp1 HG01175.hp1 HG02109.hp2 others(27): Show |
intron_variant | MODIFIER | c.-551-23982G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108171300 | ||||||
| chr12:108171335
|
CA | C | 205 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(202): Show | 209 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.-551-23945delA | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108171335 | |||||
| chr12:108171383
|
A | T | 1 | a0002c0002t0002g0224 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-551-23899A>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108171383 | ||||||
| chr12:108171447
|
T | A | 5 | a0001c0001t0022g0151a0001c0001t0027g0005a0001c0001t0063g0276others(2): Show | 6 | HG01109.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-551-23835T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108171447 | ||||||
| chr12:108171512
|
C | T | 1 | a0001c0001t0002g0198 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-551-23770C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108171512 | ||||||
| chr12:108171841
|
A | G | 1 | a0001c0001t0037g0099 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-551-23441A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108171841 | ||||||
| chr12:108171963
|
A | G | 175 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(172): Show | 177 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.-551-23319A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108171963 | ||||||
| chr12:108172010
|
C | A | 2 | a0001c0001t0004g0114a0001c0010t0049g0239 | 2 | HG01981.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.-551-23272C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108172010 | ||||||
| chr12:108172073
|
G | T | 8 | a0001c0001t0006g0086a0001c0001t0010g0129a0001c0001t0030g0130others(5): Show | 8 | HG02630.hp1 HG02723.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-551-23209G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108172073 | ||||||
| chr12:108172238
|
G | A | 3 | a0001c0001t0015g0237a0001c0001t0029g0235a0001c0001t0029g0236 | 3 | HG01099.hp1 HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-551-23044G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108172238 | ||||||
| chr12:108172405
|
T | C | 1 | a0002c0002t0002g0271 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-551-22877T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108172405 | ||||||
| chr12:108172476
|
T | C | 1 | a0002c0002t0001g0145 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-551-22806T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108172476 | ||||||
| chr12:108172601
|
G | A | 172 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(169): Show | 174 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.-551-22681G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108172601 | ||||||
| chr12:108172659
|
C | T | 6 | a0001c0001t0016g0278a0001c0001t0022g0151a0001c0001t0027g0005others(3): Show | 7 | HG01109.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-551-22623C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108172659 | ||||||
| chr12:108172746
|
G | A | 11 | a0001c0001t0016g0278a0001c0001t0022g0151a0001c0001t0027g0005others(8): Show | 12 | HG01109.hp1 HG01243.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-551-22536G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108172746 | ||||||
| chr12:108173074
|
C | T | 2 | a0001c0001t0007g0048a0001c0001t0057g0047 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-551-22208C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108173074 | ||||||
| chr12:108173178
|
C | A | 1 | a0002c0002t0001g0220 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-551-22104C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108173178 | ||||||
| chr12:108173419
|
G | T | 161 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(158): Show | 162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.-551-21863G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108173419 | ||||||
| chr12:108173546
|
A | G | 175 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(172): Show | 177 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.-551-21736A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108173546 | ||||||
| chr12:108173606
|
C | T | 7 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0254others(4): Show | 7 | HG01884.hp2 HG01891.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-551-21676C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108173606 | ||||||
| chr12:108173607
|
A | G | 213 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(210): Show | 217 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.-551-21675A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108173607 | ||||||
| chr12:108173716
|
A | G | 1 | a0002c0002t0018g0082 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-551-21566A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108173716 | ||||||
| chr12:108173804
|
G | T | 1 | a0001c0001t0002g0197 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-551-21478G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108173804 | ||||||
| chr12:108173805
|
G | GCT | 9 | a0001c0001t0002g0069a0001c0001t0002g0077a0001c0001t0002g0106others(6): Show | 9 | HG00323.hp1 HG00597.hp2 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.-551-21472_-551-21 others(8): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108173805 | |||||
| chr12:108173805
|
G | GCTCT | 82 | a0001c0001t0001g0073a0001c0001t0001g0079a0001c0001t0001g0107others(79): Show | 83 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.-551-21474_-551-21 others(10): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108173805 | |||||
| chr12:108173810
|
C | CTCTCTCT others(11): Show |
1 | a0001c0001t0027g0005 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-551-21471_-551-21 others(24): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108173810 | |||||
| chr12:108173810
|
C | CTCTCTG | 39 | a0001c0001t0001g0075a0001c0001t0001g0080a0001c0001t0001g0081others(36): Show | 39 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(36): Show |
intron_variant | MODIFIER | c.-551-21471_-551-21 others(12): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108173810 | |||||
| chr12:108173810
|
C | CTCTCTGT others(1): Show |
18 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0096others(15): Show | 18 | HG00735.hp1 HG01074.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.-551-21471_-551-21 others(14): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108173810 | |||||
| chr12:108173810
|
C | CTCTCTGT others(3): Show |
5 | a0001c0001t0003g0133a0001c0001t0018g0060a0002c0002t0003g0184others(2): Show | 5 | HG00423.hp1 HG00558.hp1 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.-551-21471_-551-21 others(16): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108173810 | |||||
| chr12:108173810
|
C | CTCTCTGT others(7): Show |
2 | a0001c0001t0018g0059a0005c0006t0016g0046 | 2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-551-21471_-551-21 others(20): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108173810 | |||||
| chr12:108173810
|
C | CTCTCTGT others(9): Show |
1 | a0001c0001t0022g0151 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-551-21471_-551-21 others(22): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108173810 | |||||
| chr12:108173810
|
C | CTCTCTGT others(11): Show |
1 | a0001c0001t0064g0277 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-551-21471_-551-21 others(24): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108173810 | |||||
| chr12:108173810
|
C | CTCTCTGT others(13): Show |
2 | a0001c0001t0063g0276a0001c0001t0065g0275 | 2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-551-21471_-551-21 others(26): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108173810 | |||||
| chr12:108173810
|
C | CTCTGTG | 3 | a0001c0001t0035g0259a0001c0001t0036g0068a0001c0001t0061g0260 | 3 | HG01943.hp2 HG02109.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-551-21471_-551-21 others(12): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108173810 | |||||
| chr12:108173810
|
C | CTCTGTGT others(1): Show |
3 | a0001c0001t0007g0048a0001c0001t0036g0261a0002c0002t0002g0270 | 3 | HG01099.hp2 HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-551-21471_-551-21 others(14): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108173810 | |||||
| chr12:108173810
|
C | CTG | 17 | a0001c0001t0004g0110a0001c0001t0004g0122a0001c0001t0004g0178others(14): Show | 17 | HG01257.hp2 HG01258.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.-551-21428_-551-21 others(8): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108173810 | |||||
| chr12:108173810
|
C | CTGTG | 8 | a0001c0001t0004g0109a0001c0001t0005g0070a0001c0001t0006g0003others(5): Show | 9 | HG02280.hp2 HG03139.hp1 HG06807.hp1 others(6): Show |
intron_variant | MODIFIER | c.-551-21430_-551-21 others(10): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108173810 | |||||
| chr12:108173810
|
C | CTGTGTG | 7 | a0001c0001t0004g0168a0001c0001t0028g0240a0001c0001t0037g0099others(4): Show | 7 | HG00099.hp1 HG01981.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.-551-21432_-551-21 others(12): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108173810 | |||||
| chr12:108173810
|
C | CTGTGTGT others(1): Show |
4 | a0001c0001t0016g0278a0001c0001t0033g0049a0003c0004t0025g0054others(1): Show | 4 | HG02723.hp1 HG03098.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-551-21434_-551-21 others(14): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108173810 | |||||
| chr12:108173810
|
C | CTGTGTGT others(3): Show |
1 | a0001c0003t0012g0045 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-551-21436_-551-21 others(16): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108173810 | |||||
| chr12:108173810
|
C | CTGTGTGT others(5): Show |
5 | a0001c0001t0011g0056a0001c0001t0015g0087a0001c0001t0016g0044others(2): Show | 5 | HG01243.hp2 HG02257.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-551-21438_-551-21 others(18): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108173810 | |||||
| chr12:108173810
|
C | CTGTGTGT others(7): Show |
6 | a0001c0001t0005g0088a0001c0001t0011g0090a0001c0001t0052g0131others(3): Show | 6 | HG00642.hp2 HG02451.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-551-21440_-551-21 others(20): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108173810 | |||||
| chr12:108173810
|
C | CTGTGTGT others(9): Show |
2 | a0001c0001t0015g0089a0001c0001t0030g0130 | 2 | HG01516.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-551-21442_-551-21 others(22): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108173810 | |||||
| chr12:108173810
|
C | CTGTGTGT others(11): Show |
1 | a0001c0001t0010g0129 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-551-21444_-551-21 others(24): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108173810 | |||||
| chr12:108173810
|
C | CTGTGTGT others(13): Show |
1 | a0001c0001t0006g0086 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-551-21446_-551-21 others(26): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108173810 | |||||
| chr12:108173810
|
C | CTGTGTGT others(19): Show |
1 | a0001c0001t0005g0091 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-551-21452_-551-21 others(32): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108173810 | |||||
| chr12:108173810
|
C | G | 1 | a0001c0001t0046g0152 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-551-21472C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108173810 | ||||||
| chr12:108173810
|
CTG | C | 16 | a0001c0001t0003g0002a0001c0001t0003g0064a0001c0001t0003g0065others(13): Show | 18 | HG01081.hp1 HG01109.hp2 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.-551-21428_-551-21 others(8): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108173810 | |||||
| chr12:108173810
|
CTGTG | C | 4 | a0001c0001t0004g0112a0001c0001t0004g0114a0001c0001t0039g0189others(1): Show | 4 | HG01981.hp2 HG02257.hp1 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.-551-21430_-551-21 others(10): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108173810 | |||||
| chr12:108173812
|
G | C | 19 | a0001c0001t0001g0252a0001c0001t0002g0069a0001c0001t0002g0077others(16): Show | 19 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(16): Show |
intron_variant | MODIFIER | c.-551-21470G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108173812 | ||||||
| chr12:108173814
|
G | C | 3 | a0001c0001t0002g0179a0001c0001t0040g0222a0001c0001t0066g0072 | 3 | HG02738.hp1 HG02970.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.-551-21468G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108173814 | ||||||
| chr12:108174007
|
C | T | 4 | a0001c0001t0022g0151a0001c0001t0063g0276a0001c0001t0064g0277others(1): Show | 4 | HG01109.hp1 HG02970.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-551-21275C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108174007 | ||||||
| chr12:108174105
|
C | T | 1 | a0001c0001t0008g0026 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-551-21177C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108174105 | ||||||
| chr12:108174245
|
A | G | 176 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(173): Show | 178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.-551-21037A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108174245 | ||||||
| chr12:108174260
|
G | A | 1 | a0002c0002t0001g0150 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-551-21022G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108174260 | ||||||
| chr12:108174474
|
A | G | 1 | a0003c0004t0017g0052 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-551-20808A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108174474 | ||||||
| chr12:108174662
|
T | C | 2 | a0001c0001t0007g0048a0001c0001t0057g0047 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-551-20620T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108174662 | ||||||
| chr12:108174691
|
T | C | 4 | a0001c0003t0021g0245a0001c0003t0021g0266a0001c0003t0031g0050others(1): Show | 4 | HG01243.hp2 HG02451.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.-551-20591T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108174691 | ||||||
| chr12:108174791
|
G | A | 1 | a0001c0001t0037g0099 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-551-20491G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108174791 | ||||||
| chr12:108174875
|
G | A | 5 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0254others(2): Show | 5 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.-551-20407G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108174875 | ||||||
| chr12:108174908
|
G | C | 2 | a0001c0001t0007g0048a0001c0001t0057g0047 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-551-20374G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108174908 | ||||||
| chr12:108174962
|
G | A | 3 | a0001c0001t0018g0059a0001c0001t0018g0060a0005c0006t0016g0046 | 3 | HG02647.hp1 HG02886.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-551-20320G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108174962 | ||||||
| chr12:108175001
|
G | A | 1 | a0001c0001t0017g0023 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-551-20281G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108175001 | ||||||
| chr12:108175055
|
C | T | 1 | a0001c0001t0003g0065 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-551-20227C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108175055 | ||||||
| chr12:108175420
|
T | C | 7 | a0001c0001t0005g0088a0001c0001t0005g0091a0001c0001t0011g0090others(4): Show | 7 | HG00642.hp2 HG01516.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-551-19862T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108175420 | ||||||
| chr12:108175449
|
T | C | 5 | a0001c0001t0005g0119a0001c0001t0005g0120a0001c0001t0005g0123others(2): Show | 5 | NA18941.hp1 NA18946.hp1 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.-551-19833T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108175449 | ||||||
| chr12:108175455
|
C | A | 14 | a0001c0001t0003g0002a0001c0001t0003g0064a0001c0001t0003g0065others(11): Show | 16 | HG01081.hp1 HG01175.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.-551-19827C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108175455 | ||||||
| chr12:108175527
|
C | T | 153 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0001g0079others(150): Show | 154 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.-551-19755C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108175527 | ||||||
| chr12:108175631
|
T | C | 2 | a0001c0001t0015g0156a0001c0001t0022g0155 | 2 | HG02055.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-551-19651T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108175631 | ||||||
| chr12:108175643
|
C | T | 1 | a0001c0001t0056g0016 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-551-19639C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108175643 | ||||||
| chr12:108175678
|
T | C | 1 | a0002c0002t0009g0187 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-551-19604T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108175678 | ||||||
| chr12:108175692
|
A | C | 5 | a0001c0003t0016g0055a0001c0003t0021g0245a0001c0003t0021g0266others(2): Show | 5 | HG01243.hp2 HG02451.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-551-19590A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108175692 | ||||||
| chr12:108175870
|
C | T | 1 | a0001c0001t0037g0099 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-551-19412C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108175870 | ||||||
| chr12:108175925
|
C | T | 1 | a0002c0002t0001g0150 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-551-19357C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108175925 | ||||||
| chr12:108175980
|
C | T | 1 | a0002c0002t0001g0188 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-551-19302C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108175980 | ||||||
| chr12:108176121
|
G | A | 21 | a0001c0001t0003g0002a0001c0001t0003g0064a0001c0001t0003g0065others(18): Show | 23 | HG01081.hp1 HG01175.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.-551-19161G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108176121 | ||||||
| chr12:108176134
|
C | T | 9 | a0001c0001t0007g0013a0001c0001t0007g0014a0001c0001t0008g0010others(6): Show | 9 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-551-19148C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108176134 | ||||||
| chr12:108176234
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-551-19048T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108176234 | ||||||
| chr12:108176247
|
A | G | 192 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(189): Show | 196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.-551-19035A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108176247 | ||||||
| chr12:108176325
|
T | G | 2 | a0001c0001t0007g0048a0001c0001t0057g0047 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-551-18957T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108176325 | ||||||
| chr12:108176508
|
A | G | 4 | a0001c0001t0001g0075a0001c0001t0001g0080a0001c0001t0001g0081others(1): Show | 4 | HG00733.hp1 HG00735.hp1 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.-551-18774A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108176508 | ||||||
| chr12:108176814
|
GT | G | 169 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(166): Show | 171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.-551-18459delT | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108176814 | |||||
| chr12:108176895
|
C | T | 2 | a0001c0001t0018g0059a0001c0001t0018g0060 | 2 | HG02647.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-551-18387C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108176895 | ||||||
| chr12:108177037
|
A | G | 2 | a0001c0001t0006g0086a0001c0001t0010g0129 | 2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-551-18245A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108177037 | ||||||
| chr12:108177379
|
C | T | 21 | a0001c0001t0003g0002a0001c0001t0003g0064a0001c0001t0003g0065others(18): Show | 23 | HG01081.hp1 HG01175.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.-551-17903C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108177379 | ||||||
| chr12:108177448
|
C | G | 1 | a0001c0001t0019g0137 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-551-17834C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108177448 | ||||||
| chr12:108177660
|
C | T | 1 | a0001c0001t0058g0043 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-551-17622C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108177660 | ||||||
| chr12:108177791
|
C | T | 1 | a0001c0001t0016g0278 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-551-17491C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108177791 | ||||||
| chr12:108177807
|
G | A | 1 | a0001c0001t0007g0048 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-551-17475G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108177807 | ||||||
| chr12:108177944
|
G | A | 3 | a0001c0001t0018g0059a0001c0001t0018g0060a0005c0006t0016g0046 | 3 | HG02647.hp1 HG02886.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-551-17338G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108177944 | ||||||
| chr12:108178126
|
T | C | 1 | a0001c0001t0001g0154 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-551-17156T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108178126 | ||||||
| chr12:108178342
|
C | A | 5 | a0001c0001t0005g0119a0001c0001t0005g0120a0001c0001t0005g0123others(2): Show | 5 | NA18941.hp1 NA18946.hp1 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.-551-16940C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108178342 | ||||||
| chr12:108178343
|
C | A | 32 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0205others(29): Show | 32 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.-551-16939C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108178343 | ||||||
| chr12:108178375
|
T | C | 3 | a0001c0001t0011g0056a0001c0001t0016g0044a0001c0001t0058g0043 | 3 | HG02257.hp2 HG02922.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-551-16907T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108178375 | ||||||
| chr12:108178393
|
C | T | 1 | a0001c0001t0058g0043 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-551-16889C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108178393 | ||||||
| chr12:108178423
|
C | T | 1 | a0001c0001t0008g0010 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-551-16859C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108178423 | ||||||
| chr12:108178424
|
G | A | 21 | a0001c0001t0003g0002a0001c0001t0003g0064a0001c0001t0003g0065others(18): Show | 23 | HG01081.hp1 HG01175.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.-551-16858G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108178424 | ||||||
| chr12:108178461
|
C | T | 1 | a0001c0001t0002g0077 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-551-16821C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108178461 | ||||||
| chr12:108178577
|
C | A | 3 | a0001c0001t0011g0056a0001c0001t0016g0044a0001c0001t0058g0043 | 3 | HG02257.hp2 HG02922.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-551-16705C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108178577 | ||||||
| chr12:108178577
|
C | T | 1 | a0001c0001t0001g0154 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-551-16705C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108178577 | ||||||
| chr12:108178582
|
A | G | 1 | a0002c0002t0001g0208 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-551-16700A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108178582 | ||||||
| chr12:108178739
|
G | A | 217 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(214): Show | 221 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.-551-16543G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108178739 | ||||||
| chr12:108178797
|
C | G | 6 | a0001c0001t0006g0086a0001c0001t0010g0129a0001c0001t0033g0049others(3): Show | 6 | HG02723.hp1 HG02809.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-551-16485C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108178797 | ||||||
| chr12:108178868
|
C | G | 1 | a0001c0003t0031g0051 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-551-16414C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108178868 | ||||||
| chr12:108178869
|
G | A | 1 | a0001c0001t0028g0172 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-551-16413G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108178869 | ||||||
| chr12:108178942
|
C | T | 20 | a0001c0001t0003g0002a0001c0001t0003g0064a0001c0001t0003g0065others(17): Show | 22 | HG01081.hp1 HG01175.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.-551-16340C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108178942 | ||||||
| chr12:108179058
|
C | A | 1 | a0002c0002t0001g0186 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-551-16224C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108179058 | ||||||
| chr12:108179219
|
A | G | 1 | a0001c0001t0009g0100 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-551-16063A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108179219 | ||||||
| chr12:108179265
|
G | C | 18 | a0001c0001t0005g0088a0001c0001t0005g0091a0001c0001t0011g0090others(15): Show | 18 | HG00642.hp2 HG01109.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.-551-16017G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108179265 | ||||||
| chr12:108179266
|
G | T | 18 | a0001c0001t0005g0088a0001c0001t0005g0091a0001c0001t0011g0090others(15): Show | 18 | HG00642.hp2 HG01109.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.-551-16016G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108179266 | ||||||
| chr12:108179284
|
G | A | 2 | a0001c0001t0006g0175a0001c0001t0006g0242 | 2 | NA19012.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.-551-15998G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108179284 | ||||||
| chr12:108179453
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-551-15829G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108179453 | ||||||
| chr12:108179520
|
C | T | 2 | a0001c0001t0033g0049a0001c0003t0012g0045 | 2 | HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-551-15762C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108179520 | ||||||
| chr12:108179767
|
A | G | 1 | a0001c0001t0051g0158 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-551-15515A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108179767 | ||||||
| chr12:108179913
|
G | A | 10 | a0001c0001t0001g0075a0001c0001t0001g0079a0001c0001t0001g0080others(7): Show | 10 | HG00733.hp1 HG01069.hp2 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.-551-15369G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108179913 | ||||||
| chr12:108180050
|
CA | C | 178 | a0001c0001t0001g0075a0001c0001t0001g0079a0001c0001t0001g0080others(175): Show | 180 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.-551-15215delA | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108180050 | |||||
| chr12:108180050
|
CAA | C | 10 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(7): Show | 10 | HG01168.hp1 HG01884.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.-551-15216_-551-15 others(8): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108180050 | |||||
| chr12:108180055
|
A | C | 6 | a0001c0001t0004g0109a0001c0001t0004g0110a0001c0001t0004g0112others(3): Show | 7 | HG02257.hp1 NA18522.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.-551-15227A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108180055 | ||||||
| chr12:108180501
|
T | G | 11 | a0001c0001t0001g0075a0001c0001t0001g0079a0001c0001t0001g0080others(8): Show | 11 | HG00733.hp1 HG01069.hp2 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.-551-14781T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108180501 | ||||||
| chr12:108180624
|
C | G | 5 | a0001c0003t0016g0055a0001c0003t0021g0245a0001c0003t0021g0266others(2): Show | 5 | HG01243.hp2 HG02451.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-551-14658C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108180624 | ||||||
| chr12:108180672
|
G | T | 2 | a0001c0001t0063g0276a0001c0001t0064g0277 | 2 | HG01109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-551-14610G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108180672 | ||||||
| chr12:108180829
|
C | T | 2 | a0001c0001t0007g0048a0001c0001t0057g0047 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-551-14453C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108180829 | ||||||
| chr12:108181048
|
G | T | 4 | a0001c0001t0011g0056a0001c0001t0016g0044a0001c0001t0058g0043others(1): Show | 4 | HG02257.hp2 HG02647.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-551-14234G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108181048 | ||||||
| chr12:108181122
|
T | G | 7 | a0001c0001t0004g0109a0001c0001t0004g0110a0001c0001t0004g0112others(4): Show | 7 | HG00639.hp1 HG01099.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.-551-14160T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108181122 | ||||||
| chr12:108181196
|
C | T | 1 | a0001c0001t0006g0086 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-551-14086C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108181196 | ||||||
| chr12:108181230
|
C | A | 1 | a0001c0001t0006g0243 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-551-14052C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108181230 | ||||||
| chr12:108181257
|
G | A | 4 | a0001c0001t0006g0117a0001c0001t0006g0165a0001c0001t0006g0166others(1): Show | 4 | HG00735.hp2 HG01361.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.-551-14025G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108181257 | ||||||
| chr12:108181260
|
G | A | 2 | a0001c0001t0004g0178a0001c0001t0005g0264 | 2 | HG02080.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-551-14022G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108181260 | ||||||
| chr12:108181285
|
C | T | 1 | a0001c0001t0065g0275 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-551-13997C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108181285 | ||||||
| chr12:108181491
|
A | G | 1 | a0002c0002t0003g0196 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-551-13791A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108181491 | ||||||
| chr12:108181786
|
A | G | 200 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(197): Show | 203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.-551-13496A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108181786 | ||||||
| chr12:108181817
|
C | T | 1 | a0001c0001t0020g0265 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-551-13465C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108181817 | ||||||
| chr12:108181834
|
C | A | 2 | a0001c0001t0018g0059a0001c0001t0018g0060 | 2 | HG02647.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-551-13448C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108181834 | ||||||
| chr12:108181834
|
C | G | 1 | a0005c0006t0016g0046 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-551-13448C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108181834 | ||||||
| chr12:108182215
|
A | C | 169 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(166): Show | 171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.-551-13067A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108182215 | ||||||
| chr12:108182221
|
A | G | 200 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(197): Show | 203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.-551-13061A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108182221 | ||||||
| chr12:108182425
|
C | T | 2 | a0002c0002t0001g0207a0002c0002t0002g0203 | 2 | HG01358.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.-551-12857C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108182425 | ||||||
| chr12:108182784
|
G | A | 189 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(186): Show | 192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.-551-12498G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108182784 | ||||||
| chr12:108182839
|
GT | G | 17 | a0001c0001t0011g0006a0001c0001t0011g0125a0001c0001t0011g0127others(14): Show | 18 | HG01109.hp1 HG01243.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.-551-12432delT | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108182839 | |||||
| chr12:108183013
|
GGGTCCAC others(1): Show |
G | 189 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(186): Show | 192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.-551-12266_-551-12 others(14): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108183013 | |||||
| chr12:108183046
|
A | G | 200 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(197): Show | 203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.-551-12236A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108183046 | ||||||
| chr12:108183082
|
C | A | 1 | a0007c0011t0004g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-551-12200C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108183082 | ||||||
| chr12:108183353
|
A | G | 1 | a0001c0001t0024g0015 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-551-11929A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108183353 | ||||||
| chr12:108183610
|
A | G | 200 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(197): Show | 203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.-551-11672A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108183610 | ||||||
| chr12:108183628
|
G | A | 2 | a0001c0001t0007g0048a0001c0001t0057g0047 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-551-11654G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108183628 | ||||||
| chr12:108183640
|
C | T | 1 | a0001c0003t0016g0055 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-551-11642C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108183640 | ||||||
| chr12:108183649
|
A | G | 7 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0254others(4): Show | 7 | HG01884.hp2 HG01891.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-551-11633A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108183649 | ||||||
| chr12:108183651
|
C | A | 11 | a0001c0001t0010g0238a0001c0001t0010g0262a0001c0001t0011g0056others(8): Show | 11 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-551-11631C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108183651 | ||||||
| chr12:108183770
|
C | T | 8 | a0001c0001t0011g0006a0001c0001t0011g0125a0001c0001t0011g0127others(5): Show | 9 | HG02280.hp1 HG02572.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.-551-11512C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108183770 | ||||||
| chr12:108184146
|
C | G | 200 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(197): Show | 203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.-551-11136C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108184146 | ||||||
| chr12:108184206
|
A | G | 200 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(197): Show | 203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.-551-11076A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108184206 | ||||||
| chr12:108184246
|
G | A | 4 | a0001c0001t0004g0161a0001c0001t0022g0151a0001c0001t0030g0162others(1): Show | 4 | HG01891.hp1 HG02622.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-551-11036G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108184246 | ||||||
| chr12:108184277
|
G | C | 1 | a0001c0001t0015g0089 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-551-11005G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108184277 | ||||||
| chr12:108184386
|
G | T | 8 | a0001c0001t0005g0091a0001c0001t0006g0086a0001c0001t0010g0129others(5): Show | 8 | HG02630.hp1 HG02683.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-551-10896G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108184386 | ||||||
| chr12:108184453
|
C | A | 8 | a0001c0001t0005g0091a0001c0001t0006g0086a0001c0001t0010g0129others(5): Show | 8 | HG02630.hp1 HG02683.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-551-10829C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108184453 | ||||||
| chr12:108184476
|
G | A | 1 | a0001c0001t0065g0275 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-551-10806G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108184476 | ||||||
| chr12:108184491
|
C | T | 9 | a0001c0001t0011g0006a0001c0001t0011g0125a0001c0001t0011g0127others(6): Show | 10 | HG02280.hp1 HG02572.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.-551-10791C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108184491 | ||||||
| chr12:108184729
|
A | G | 1 | a0001c0001t0060g0274 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-551-10553A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108184729 | ||||||
| chr12:108185111
|
T | C | 204 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(201): Show | 207 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.-551-10171T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108185111 | ||||||
| chr12:108185406
|
G | A | 1 | a0001c0001t0005g0091 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-551-9876G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108185406 | ||||||
| chr12:108185605
|
G | A | 189 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(186): Show | 192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.-551-9677G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108185605 | ||||||
| chr12:108185619
|
C | T | 2 | a0001c0001t0010g0238a0001c0001t0010g0262 | 2 | HG02280.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-551-9663C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108185619 | ||||||
| chr12:108185670
|
G | A | 1 | a0002c0002t0001g0188 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-551-9612G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108185670 | ||||||
| chr12:108185730
|
T | C | 9 | a0001c0001t0011g0006a0001c0001t0011g0125a0001c0001t0011g0127others(6): Show | 10 | HG02280.hp1 HG02572.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.-551-9552T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108185730 | ||||||
| chr12:108186017
|
G | A | 1 | a0001c0001t0027g0005 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-551-9265G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108186017 | ||||||
| chr12:108186041
|
C | T | 1 | a0001c0001t0072g0108 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-551-9241C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108186041 | ||||||
| chr12:108186312
|
G | A | 4 | a0001c0001t0035g0259a0001c0001t0036g0068a0001c0001t0036g0261others(1): Show | 4 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.-551-8970G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108186312 | ||||||
| chr12:108186347
|
C | T | 4 | a0003c0004t0017g0052a0003c0004t0025g0053a0003c0004t0025g0054others(1): Show | 4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-551-8935C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108186347 | ||||||
| chr12:108186413
|
C | T | 189 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(186): Show | 192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.-551-8869C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108186413 | ||||||
| chr12:108186597
|
C | T | 189 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(186): Show | 192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.-551-8685C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108186597 | ||||||
| chr12:108186598
|
G | A | 1 | a0001c0001t0046g0152 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-551-8684G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108186598 | ||||||
| chr12:108186843
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-551-8439G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108186843 | ||||||
| chr12:108186901
|
C | T | 189 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(186): Show | 192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.-551-8381C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108186901 | ||||||
| chr12:108186949
|
C | G | 11 | a0001c0001t0010g0238a0001c0001t0010g0262a0001c0001t0011g0056others(8): Show | 11 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-551-8333C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108186949 | ||||||
| chr12:108187169
|
G | A | 189 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(186): Show | 192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.-551-8113G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108187169 | ||||||
| chr12:108187317
|
T | A | 1 | a0001c0001t0017g0011 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-551-7965T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108187317 | ||||||
| chr12:108187325
|
C | A | 2 | a0001c0001t0004g0110a0001c0001t0004g0112 | 2 | HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-551-7957C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108187325 | ||||||
| chr12:108187618
|
A | G | 169 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(166): Show | 171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.-551-7664A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108187618 | ||||||
| chr12:108187636
|
AGT | A | 3 | a0001c0001t0010g0238a0001c0001t0010g0262a0007c0011t0004g0097 | 3 | HG02280.hp2 HG03139.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-551-7643_-551-764 others(6): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108187636 | |||||
| chr12:108187827
|
G | A | 1 | a0001c0001t0006g0175 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-551-7455G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108187827 | ||||||
| chr12:108187922
|
C | G | 189 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(186): Show | 192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.-551-7360C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108187922 | ||||||
| chr12:108188025
|
C | T | 1 | a0001c0001t0003g0248 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-551-7257C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108188025 | ||||||
| chr12:108188351
|
G | A | 4 | a0001c0001t0035g0259a0001c0001t0036g0068a0001c0001t0036g0261others(1): Show | 4 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.-551-6931G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108188351 | ||||||
| chr12:108188521
|
G | A | 52 | a0001c0001t0001g0075a0001c0001t0001g0079a0001c0001t0001g0080others(49): Show | 52 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.-551-6761G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108188521 | ||||||
| chr12:108188629
|
A | T | 3 | a0001c0001t0001g0252a0001c0001t0003g0253a0002c0002t0009g0223 | 3 | HG02080.hp1 NA19000.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.-551-6653A>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108188629 | ||||||
| chr12:108188840
|
T | C | 20 | a0001c0001t0007g0048a0001c0001t0011g0006a0001c0001t0011g0125others(17): Show | 21 | HG01243.hp2 HG01943.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.-551-6442T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108188840 | ||||||
| chr12:108188910
|
C | A | 2 | a0001c0001t0015g0156a0001c0001t0022g0155 | 2 | HG02055.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-551-6372C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108188910 | ||||||
| chr12:108188922
|
T | C | 1 | a0001c0001t0046g0152 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-551-6360T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108188922 | ||||||
| chr12:108189039
|
G | A | 1 | a0001c0001t0046g0152 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-551-6243G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108189039 | ||||||
| chr12:108189141
|
T | C | 4 | a0001c0001t0035g0259a0001c0001t0036g0068a0001c0001t0036g0261others(1): Show | 4 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.-551-6141T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108189141 | ||||||
| chr12:108189233
|
C | T | 1 | a0001c0001t0046g0152 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-551-6049C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108189233 | ||||||
| chr12:108189239
|
C | T | 8 | a0001c0001t0010g0238a0001c0001t0010g0262a0001c0001t0011g0056others(5): Show | 8 | HG02257.hp2 HG02280.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-551-6043C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108189239 | ||||||
| chr12:108189240
|
G | A | 169 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(166): Show | 171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.-551-6042G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108189240 | ||||||
| chr12:108189313
|
G | A | 5 | a0001c0003t0016g0055a0001c0003t0021g0245a0001c0003t0021g0266others(2): Show | 5 | HG01243.hp2 HG02451.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-551-5969G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108189313 | ||||||
| chr12:108189367
|
C | G | 1 | a0001c0001t0017g0011 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-551-5915C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108189367 | ||||||
| chr12:108189453
|
T | C | 1 | a0001c0001t0037g0099 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-551-5829T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108189453 | ||||||
| chr12:108189484
|
G | C | 4 | a0003c0004t0017g0052a0003c0004t0025g0053a0003c0004t0025g0054others(1): Show | 4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-551-5798G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108189484 | ||||||
| chr12:108189662
|
G | T | 1 | a0001c0001t0019g0078 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-551-5620G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108189662 | ||||||
| chr12:108189702
|
G | T | 1 | a0001c0001t0046g0152 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-551-5580G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108189702 | ||||||
| chr12:108189821
|
A | G | 212 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(209): Show | 215 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.-551-5461A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108189821 | ||||||
| chr12:108189896
|
AT | A | 10 | a0001c0001t0001g0075a0001c0001t0001g0079a0001c0001t0001g0080others(7): Show | 10 | HG00733.hp1 HG01069.hp2 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.-551-5384delT | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108189896 | |||||
| chr12:108190098
|
G | A | 7 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0254others(4): Show | 7 | HG01884.hp2 HG01891.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-551-5184G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108190098 | ||||||
| chr12:108190184
|
C | T | 1 | a0002c0002t0001g0186 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-551-5098C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108190184 | ||||||
| chr12:108190196
|
G | A | 2 | a0001c0001t0063g0276a0001c0001t0064g0277 | 2 | HG01109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-551-5086G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108190196 | ||||||
| chr12:108190290
|
G | A | 169 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(166): Show | 171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.-551-4992G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108190290 | ||||||
| chr12:108190366
|
T | G | 2 | a0001c0001t0063g0276a0001c0001t0064g0277 | 2 | HG01109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-551-4916T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108190366 | ||||||
| chr12:108190527
|
G | T | 1 | a0001c0001t0012g0025 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-551-4755G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108190527 | ||||||
| chr12:108190837
|
G | A | 1 | a0002c0002t0001g0219 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-551-4445G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108190837 | ||||||
| chr12:108191013
|
C | T | 4 | a0001c0001t0035g0259a0001c0001t0036g0068a0001c0001t0036g0261others(1): Show | 4 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.-551-4269C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108191013 | ||||||
| chr12:108191104
|
T | G | 2 | a0001c0001t0007g0048a0001c0001t0057g0047 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-551-4178T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108191104 | ||||||
| chr12:108191111
|
G | A | 2 | a0001c0001t0007g0048a0001c0001t0057g0047 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-551-4171G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108191111 | ||||||
| chr12:108191242
|
A | G | 7 | a0001c0001t0010g0238a0001c0001t0010g0262a0001c0001t0011g0056others(4): Show | 7 | HG02257.hp2 HG02280.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-551-4040A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108191242 | ||||||
| chr12:108191367
|
G | A | 1 | a0001c0001t0046g0152 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-551-3915G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108191367 | ||||||
| chr12:108191473
|
G | A | 4 | a0001c0001t0017g0023a0001c0001t0025g0033a0001c0001t0034g0031others(1): Show | 4 | HG02818.hp2 HG02895.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-551-3809G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108191473 | ||||||
| chr12:108191525
|
G | A | 1 | a0001c0001t0041g0111 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-551-3757G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108191525 | ||||||
| chr12:108191573
|
G | A | 1 | a0001c0001t0001g0258 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-551-3709G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108191573 | ||||||
| chr12:108191592
|
T | G | 2 | a0001c0001t0007g0048a0001c0001t0057g0047 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-551-3690T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108191592 | ||||||
| chr12:108191768
|
G | A | 1 | a0001c0001t0051g0158 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-551-3514G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108191768 | ||||||
| chr12:108191863
|
C | T | 8 | a0001c0001t0005g0091a0001c0001t0006g0086a0001c0001t0010g0129others(5): Show | 8 | HG02630.hp1 HG02683.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-551-3419C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108191863 | ||||||
| chr12:108191878
|
C | T | 1 | a0001c0001t0053g0121 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-551-3404C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108191878 | ||||||
| chr12:108192050
|
A | G | 189 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(186): Show | 192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.-551-3232A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108192050 | ||||||
| chr12:108192119
|
C | G | 2 | a0001c0001t0006g0086a0001c0001t0010g0129 | 2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-551-3163C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108192119 | ||||||
| chr12:108192155
|
T | A | 2 | a0001c0001t0063g0276a0001c0001t0064g0277 | 2 | HG01109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-551-3127T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108192155 | ||||||
| chr12:108192205
|
A | G | 7 | a0001c0001t0010g0238a0001c0001t0010g0262a0001c0001t0011g0056others(4): Show | 7 | HG02257.hp2 HG02280.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-551-3077A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108192205 | ||||||
| chr12:108192272
|
G | A | 161 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0001g0079others(158): Show | 162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.-551-3010G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108192272 | ||||||
| chr12:108192461
|
C | T | 8 | a0001c0001t0005g0091a0001c0001t0006g0086a0001c0001t0010g0129others(5): Show | 8 | HG02630.hp1 HG02683.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-551-2821C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108192461 | ||||||
| chr12:108192513
|
C | T | 4 | a0001c0001t0004g0161a0001c0001t0022g0151a0001c0001t0030g0162others(1): Show | 4 | HG01891.hp1 HG02622.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-551-2769C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108192513 | ||||||
| chr12:108192529
|
T | A | 17 | a0001c0001t0005g0088a0001c0001t0007g0027a0001c0001t0007g0028others(14): Show | 17 | HG00099.hp2 HG00642.hp2 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.-551-2753T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108192529 | ||||||
| chr12:108192529
|
T | G | 8 | a0001c0001t0003g0248a0001c0001t0006g0170a0001c0001t0026g0092others(5): Show | 8 | HG00323.hp2 HG01109.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.-551-2753T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108192529 | ||||||
| chr12:108192554
|
T | C | 196 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(193): Show | 199 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.-551-2728T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108192554 | ||||||
| chr12:108192773
|
A | G | 212 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(209): Show | 215 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.-551-2509A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108192773 | ||||||
| chr12:108193025
|
T | C | 1 | a0001c0001t0026g0092 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-551-2257T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108193025 | ||||||
| chr12:108193213
|
C | T | 189 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(186): Show | 192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.-551-2069C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108193213 | ||||||
| chr12:108193229
|
A | G | 7 | a0001c0001t0010g0238a0001c0001t0010g0262a0001c0001t0011g0056others(4): Show | 7 | HG02257.hp2 HG02280.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-551-2053A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108193229 | ||||||
| chr12:108193277
|
C | T | 1 | a0001c0001t0037g0099 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-551-2005C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108193277 | ||||||
| chr12:108193350
|
G | T | 20 | a0001c0001t0007g0048a0001c0001t0011g0006a0001c0001t0011g0125others(17): Show | 21 | HG01243.hp2 HG01943.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.-551-1932G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108193350 | ||||||
| chr12:108193367
|
T | G | 1 | a0001c0001t0009g0100 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-551-1915T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108193367 | ||||||
| chr12:108193389
|
T | A | 4 | a0003c0004t0017g0052a0003c0004t0025g0053a0003c0004t0025g0054others(1): Show | 4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-551-1893T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108193389 | ||||||
| chr12:108193452
|
A | G | 1 | a0001c0001t0001g0107 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-551-1830A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108193452 | ||||||
| chr12:108193567
|
T | C | 3 | a0001c0001t0025g0033a0001c0001t0034g0031a0001c0001t0034g0032 | 3 | HG02895.hp1 HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-551-1715T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108193567 | ||||||
| chr12:108193596
|
A | AATGG | 189 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(186): Show | 191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.-551-1667_-551-166 others(8): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108193596 | |||||
| chr12:108193596
|
A | AATGGATG others(1): Show |
8 | a0001c0001t0011g0006a0001c0001t0011g0125a0001c0001t0011g0127others(5): Show | 9 | HG02280.hp1 HG02572.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.-551-1671_-551-166 others(12): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108193596 | |||||
| chr12:108193603
|
GGATGGAT others(9): Show |
G | 4 | a0003c0004t0017g0052a0003c0004t0025g0053a0003c0004t0025g0054others(1): Show | 4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-551-1664_-551-164 others(20): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 108193603 | |||||
| chr12:108193737
|
G | A | 1 | a0001c0003t0016g0055 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-551-1545G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108193737 | ||||||
| chr12:108193863
|
T | C | 1 | a0001c0003t0031g0051 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-551-1419T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108193863 | ||||||
| chr12:108193887
|
T | C | 1 | a0001c0001t0046g0152 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-551-1395T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108193887 | ||||||
| chr12:108194135
|
T | C | 1 | a0001c0001t0011g0090 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-551-1147T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108194135 | ||||||
| chr12:108194318
|
G | A | 1 | a0001c0001t0046g0152 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-551-964G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108194318 | ||||||
| chr12:108194353
|
A | G | 189 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(186): Show | 192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.-551-929A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108194353 | ||||||
| chr12:108194363
|
G | A | 20 | a0001c0001t0001g0139a0001c0001t0002g0198a0001c0001t0002g0201others(17): Show | 20 | HG00558.hp2 HG00597.hp1 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.-551-919G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108194363 | ||||||
| chr12:108194456
|
C | T | 7 | a0001c0001t0010g0238a0001c0001t0010g0262a0001c0001t0011g0056others(4): Show | 7 | HG02257.hp2 HG02280.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-551-826C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108194456 | ||||||
| chr12:108194516
|
A | G | 2 | a0002c0002t0001g0199a0002c0002t0003g0202 | 2 | NA18959.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.-551-766A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108194516 | ||||||
| chr12:108194534
|
A | T | 197 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(194): Show | 200 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.-551-748A>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108194534 | ||||||
| chr12:108194629
|
A | C | 1 | a0001c0001t0001g0075 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-551-653A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108194629 | ||||||
| chr12:108194651
|
T | C | 1 | a0001c0001t0037g0099 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-551-631T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108194651 | ||||||
| chr12:108194692
|
T | C | 197 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(194): Show | 200 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.-551-590T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108194692 | ||||||
| chr12:108194846
|
A | G | 7 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0254others(4): Show | 7 | HG01884.hp2 HG01891.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-551-436A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108194846 | ||||||
| chr12:108195060
|
ATCCAG | A | 15 | a0001c0001t0001g0096a0001c0001t0001g0191a0001c0001t0002g0077others(12): Show | 15 | HG00597.hp2 HG00639.hp2 HG02015.hp1 others(12): Show |
intron_variant | MODIFIER | c.-551-221_-551-217d others(7): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108195060 | ||||||
| chr12:108195077
|
C | T | 1 | a0001c0001t0002g0179 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-551-205C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108195077 | ||||||
| chr12:108195150
|
A | G | 205 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(202): Show | 208 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.-551-132A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 1/8 | chr12 | 108195150 | ||||||
| chr12:108196291
|
A | G | 2 | a0001c0001t0007g0048a0001c0001t0057g0047 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.382+77A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108196291 | ||||||
| chr12:108196404
|
G | A | 2 | a0001c0001t0041g0111a0001c0001t0067g0067 | 2 | HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.382+190G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108196404 | ||||||
| chr12:108196418
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.382+204C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108196418 | ||||||
| chr12:108196499
|
T | G | 1 | a0003c0004t0074g0226 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.382+285T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108196499 | ||||||
| chr12:108196892
|
A | G | 21 | a0001c0001t0001g0096a0001c0001t0001g0181a0001c0001t0001g0182others(18): Show | 21 | HG00423.hp2 HG00639.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.382+678A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108196892 | ||||||
| chr12:108196963
|
G | C | 21 | a0001c0001t0001g0096a0001c0001t0001g0181a0001c0001t0001g0182others(18): Show | 21 | HG00423.hp2 HG00639.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.382+749G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108196963 | ||||||
| chr12:108197107
|
T | C | 21 | a0001c0001t0001g0096a0001c0001t0001g0181a0001c0001t0001g0182others(18): Show | 21 | HG00423.hp2 HG00639.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.382+893T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108197107 | ||||||
| chr12:108197108
|
AAG | A | 21 | a0001c0001t0001g0096a0001c0001t0001g0181a0001c0001t0001g0182others(18): Show | 21 | HG00423.hp2 HG00639.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.382+896_382+897del others(2): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr12 | 108197108 | |||||
| chr12:108197112
|
T | A | 21 | a0001c0001t0001g0096a0001c0001t0001g0181a0001c0001t0001g0182others(18): Show | 21 | HG00423.hp2 HG00639.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.382+898T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108197112 | ||||||
| chr12:108197113
|
T | C | 21 | a0001c0001t0001g0096a0001c0001t0001g0181a0001c0001t0001g0182others(18): Show | 21 | HG00423.hp2 HG00639.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.382+899T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108197113 | ||||||
| chr12:108197114
|
A | C | 21 | a0001c0001t0001g0096a0001c0001t0001g0181a0001c0001t0001g0182others(18): Show | 21 | HG00423.hp2 HG00639.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.382+900A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108197114 | ||||||
| chr12:108197115
|
A | C | 21 | a0001c0001t0001g0096a0001c0001t0001g0181a0001c0001t0001g0182others(18): Show | 21 | HG00423.hp2 HG00639.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.382+901A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108197115 | ||||||
| chr12:108197228
|
A | G | 1 | a0002c0002t0001g0219 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.382+1014A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108197228 | ||||||
| chr12:108197356
|
C | T | 5 | a0001c0003t0016g0055a0001c0003t0021g0245a0001c0003t0021g0266others(2): Show | 5 | HG01243.hp2 HG02451.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.382+1142C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108197356 | ||||||
| chr12:108197403
|
AG | A | 167 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(164): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.382+1192delG | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr12 | 108197403 | |||||
| chr12:108197541
|
G | A | 4 | a0001c0001t0035g0259a0001c0001t0036g0068a0001c0001t0036g0261others(1): Show | 4 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.382+1327G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108197541 | ||||||
| chr12:108197572
|
A | G | 4 | a0001c0001t0004g0161a0001c0001t0022g0151a0001c0001t0030g0162others(1): Show | 4 | HG01891.hp1 HG02622.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.382+1358A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108197572 | ||||||
| chr12:108197841
|
C | T | 1 | a0001c0003t0016g0055 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.382+1627C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108197841 | ||||||
| chr12:108197943
|
G | A | 67 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0107others(64): Show | 69 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(66): Show |
intron_variant | MODIFIER | c.382+1729G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108197943 | ||||||
| chr12:108197994
|
A | T | 160 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(157): Show | 162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.382+1780A>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108197994 | ||||||
| chr12:108198025
|
C | T | 1 | a0001c0003t0031g0050 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.382+1811C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108198025 | ||||||
| chr12:108198167
|
C | A | 7 | a0001c0001t0010g0084a0001c0001t0010g0113a0001c0001t0010g0159others(4): Show | 7 | HG01884.hp1 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.382+1953C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108198167 | ||||||
| chr12:108198167
|
C | T | 42 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0148others(39): Show | 43 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(40): Show |
intron_variant | MODIFIER | c.382+1953C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108198167 | ||||||
| chr12:108198656
|
T | C | 4 | a0001c0001t0035g0259a0001c0001t0036g0068a0001c0001t0036g0261others(1): Show | 4 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.382+2442T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108198656 | ||||||
| chr12:108198826
|
C | T | 5 | a0001c0001t0006g0170a0001c0001t0026g0092a0001c0001t0026g0093others(2): Show | 5 | HG00323.hp2 HG01109.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.382+2612C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108198826 | ||||||
| chr12:108199013
|
C | T | 1 | a0001c0001t0003g0064 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.382+2799C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108199013 | ||||||
| chr12:108199055
|
G | A | 36 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0154others(33): Show | 37 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.382+2841G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108199055 | ||||||
| chr12:108199212
|
T | C | 2 | a0001c0001t0033g0049a0001c0003t0012g0045 | 2 | HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.382+2998T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108199212 | ||||||
| chr12:108199233
|
C | T | 1 | a0001c0001t0003g0133 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.382+3019C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108199233 | ||||||
| chr12:108199243
|
A | AT | 22 | a0001c0001t0001g0096a0001c0001t0001g0181a0001c0001t0001g0182others(19): Show | 22 | HG00423.hp2 HG00639.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.382+3033dupT | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr12 | 108199243 | |||||
| chr12:108199271
|
C | T | 4 | a0001c0001t0035g0259a0001c0001t0036g0068a0001c0001t0036g0261others(1): Show | 4 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.382+3057C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108199271 | ||||||
| chr12:108199420
|
C | T | 1 | a0001c0001t0034g0032 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.382+3206C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108199420 | ||||||
| chr12:108199604
|
G | A | 4 | a0003c0004t0017g0052a0003c0004t0025g0053a0003c0004t0025g0054others(1): Show | 4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.382+3390G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108199604 | ||||||
| chr12:108199680
|
T | G | 1 | a0001c0001t0005g0088 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.382+3466T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108199680 | ||||||
| chr12:108200092
|
T | A | 1 | a0001c0001t0004g0168 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.382+3878T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108200092 | ||||||
| chr12:108200266
|
T | A | 99 | a0001c0001t0001g0073a0001c0001t0001g0139a0001c0001t0001g0205others(96): Show | 100 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.382+4052T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108200266 | ||||||
| chr12:108200267
|
C | A | 99 | a0001c0001t0001g0073a0001c0001t0001g0139a0001c0001t0001g0205others(96): Show | 100 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.382+4053C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108200267 | ||||||
| chr12:108200292
|
G | C | 97 | a0001c0001t0001g0073a0001c0001t0001g0139a0001c0001t0001g0205others(94): Show | 98 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.382+4078G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108200292 | ||||||
| chr12:108200489
|
T | TTTCA | 42 | a0001c0001t0001g0075a0001c0001t0001g0079a0001c0001t0001g0080others(39): Show | 43 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.382+4291_382+4294d others(6): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr12 | 108200489 | |||||
| chr12:108200505
|
A | T | 2 | a0001c0001t0005g0115a0001c0001t0005g0116 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.382+4291A>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108200505 | ||||||
| chr12:108200730
|
GGGGACCC others(7): Show |
G | 2 | a0001c0001t0033g0049a0001c0003t0012g0045 | 2 | HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.382+4526_382+4539d others(16): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr12 | 108200730 | |||||
| chr12:108200923
|
GGGTGGTC others(4): Show |
G | 1 | a0001c0001t0003g0248 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.382+4712_382+4722d others(13): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr12 | 108200923 | |||||
| chr12:108200959
|
A | C | 1 | a0002c0002t0009g0223 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.382+4745A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108200959 | ||||||
| chr12:108201264
|
T | A | 17 | a0001c0001t0001g0096a0001c0001t0001g0181a0001c0001t0001g0182others(14): Show | 17 | HG00423.hp2 HG00639.hp2 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.383-5025T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108201264 | ||||||
| chr12:108201338
|
G | A | 1 | a0001c0001t0003g0248 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.383-4951G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108201338 | ||||||
| chr12:108201476
|
T | C | 1 | a0001c0001t0030g0130 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.383-4813T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108201476 | ||||||
| chr12:108201519
|
T | TG | 65 | a0001c0001t0001g0073a0001c0001t0001g0205a0001c0001t0001g0227others(62): Show | 65 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.383-4764dupG | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr12 | 108201519 | |||||
| chr12:108201602
|
C | T | 4 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0254others(1): Show | 4 | HG01884.hp2 HG01891.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.383-4687C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108201602 | ||||||
| chr12:108201760
|
T | C | 49 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0148others(46): Show | 50 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.383-4529T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108201760 | ||||||
| chr12:108201783
|
C | A | 14 | a0001c0001t0001g0075a0001c0001t0001g0079a0001c0001t0001g0080others(11): Show | 14 | HG00733.hp1 HG01069.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.383-4506C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108201783 | ||||||
| chr12:108201806
|
C | T | 4 | a0001c0001t0035g0259a0001c0001t0036g0068a0001c0001t0036g0261others(1): Show | 4 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.383-4483C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108201806 | ||||||
| chr12:108202011
|
C | T | 3 | a0001c0001t0004g0109a0001c0001t0004g0110a0001c0001t0004g0112 | 3 | HG02257.hp1 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.383-4278C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108202011 | ||||||
| chr12:108202062
|
C | A | 5 | a0001c0003t0016g0055a0001c0003t0021g0245a0001c0003t0021g0266others(2): Show | 5 | HG01243.hp2 HG02451.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.383-4227C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108202062 | ||||||
| chr12:108202103
|
G | A | 1 | a0002c0002t0001g0220 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.383-4186G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108202103 | ||||||
| chr12:108202121
|
C | T | 1 | a0002c0002t0001g0211 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.383-4168C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108202121 | ||||||
| chr12:108202136
|
CACGCTAA others(11): Show |
C | 6 | a0001c0001t0033g0049a0001c0003t0012g0045a0003c0004t0017g0052others(3): Show | 6 | HG02109.hp2 HG02723.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.383-4152_383-4135d others(20): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108202136 | ||||||
| chr12:108202197
|
C | G | 2 | a0001c0001t0015g0174a0001c0001t0020g0164 | 2 | HG02735.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.383-4092C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108202197 | ||||||
| chr12:108202330
|
T | C | 14 | a0001c0001t0001g0075a0001c0001t0001g0079a0001c0001t0001g0080others(11): Show | 14 | HG00733.hp1 HG01069.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.383-3959T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108202330 | ||||||
| chr12:108202346
|
A | G | 99 | a0001c0001t0001g0073a0001c0001t0001g0139a0001c0001t0001g0205others(96): Show | 100 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.383-3943A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108202346 | ||||||
| chr12:108202531
|
A | G | 110 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0001g0079others(107): Show | 111 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.383-3758A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108202531 | ||||||
| chr12:108202566
|
T | C | 10 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0254others(7): Show | 10 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.383-3723T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108202566 | ||||||
| chr12:108202622
|
C | T | 146 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(143): Show | 147 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.383-3667C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108202622 | ||||||
| chr12:108202726
|
G | A | 1 | a0002c0002t0068g0214 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.383-3563G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108202726 | ||||||
| chr12:108202758
|
G | A | 6 | a0001c0001t0035g0259a0001c0001t0036g0068a0001c0001t0036g0261others(3): Show | 6 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.383-3531G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108202758 | ||||||
| chr12:108203038
|
T | G | 4 | a0003c0004t0017g0052a0003c0004t0025g0053a0003c0004t0025g0054others(1): Show | 4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.383-3251T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108203038 | ||||||
| chr12:108203111
|
G | A | 17 | a0001c0001t0005g0088a0001c0001t0007g0027a0001c0001t0007g0028others(14): Show | 17 | HG00642.hp2 HG01192.hp1 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.383-3178G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108203111 | ||||||
| chr12:108203137
|
G | A | 2 | a0001c0001t0033g0049a0001c0003t0012g0045 | 2 | HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.383-3152G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108203137 | ||||||
| chr12:108203177
|
C | T | 4 | a0003c0004t0017g0052a0003c0004t0025g0053a0003c0004t0025g0054others(1): Show | 4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.383-3112C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108203177 | ||||||
| chr12:108203294
|
T | C | 1 | a0002c0002t0013g0193 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.383-2995T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108203294 | ||||||
| chr12:108203383
|
G | A | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG01074.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.383-2906G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108203383 | ||||||
| chr12:108203463
|
A | G | 4 | a0001c0001t0011g0056a0001c0001t0016g0044a0001c0001t0058g0043others(1): Show | 4 | HG02257.hp2 HG02647.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.383-2826A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108203463 | ||||||
| chr12:108203604
|
C | T | 2 | a0001c0001t0001g0080a0001c0001t0001g0081 | 2 | HG00733.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.383-2685C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108203604 | ||||||
| chr12:108203623
|
C | T | 2 | a0001c0001t0030g0130a0001c0001t0052g0131 | 2 | HG02630.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.383-2666C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108203623 | ||||||
| chr12:108203636
|
C | T | 4 | a0003c0004t0017g0052a0003c0004t0025g0053a0003c0004t0025g0054others(1): Show | 4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.383-2653C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108203636 | ||||||
| chr12:108203769
|
T | C | 138 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(135): Show | 139 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.383-2520T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108203769 | ||||||
| chr12:108203881
|
T | C | 6 | a0001c0001t0035g0259a0001c0001t0036g0068a0001c0001t0036g0261others(3): Show | 6 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.383-2408T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108203881 | ||||||
| chr12:108204237
|
T | A | 133 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(130): Show | 133 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.383-2052T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108204237 | ||||||
| chr12:108204259
|
C | T | 4 | a0003c0004t0017g0052a0003c0004t0025g0053a0003c0004t0025g0054others(1): Show | 4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.383-2030C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108204259 | ||||||
| chr12:108204359
|
C | G | 1 | a0001c0001t0056g0016 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.383-1930C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108204359 | ||||||
| chr12:108204384
|
T | C | 2 | a0001c0001t0007g0048a0001c0001t0057g0047 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.383-1905T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108204384 | ||||||
| chr12:108204496
|
C | T | 4 | a0003c0004t0017g0052a0003c0004t0025g0053a0003c0004t0025g0054others(1): Show | 4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.383-1793C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108204496 | ||||||
| chr12:108204497
|
G | A | 15 | a0001c0001t0001g0096a0001c0001t0001g0181a0001c0001t0001g0182others(12): Show | 15 | HG00423.hp2 HG00639.hp2 HG02015.hp1 others(12): Show |
intron_variant | MODIFIER | c.383-1792G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108204497 | ||||||
| chr12:108204506
|
A | C | 6 | a0001c0001t0001g0205a0001c0001t0003g0143a0001c0001t0008g0001others(3): Show | 7 | HG00609.hp2 NA18944.hp1 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.383-1783A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108204506 | ||||||
| chr12:108204542
|
G | A | 1 | a0001c0001t0005g0091 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.383-1747G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108204542 | ||||||
| chr12:108204690
|
T | G | 1 | a0002c0009t0001g0185 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.383-1599T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108204690 | ||||||
| chr12:108204764
|
G | A | 1 | a0001c0001t0012g0040 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.383-1525G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108204764 | ||||||
| chr12:108204822
|
A | G | 2 | a0001c0001t0033g0049a0001c0003t0012g0045 | 2 | HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.383-1467A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108204822 | ||||||
| chr12:108204910
|
A | G | 219 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(216): Show | 222 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.383-1379A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108204910 | ||||||
| chr12:108204999
|
C | CGA | 4 | a0003c0004t0017g0052a0003c0004t0025g0053a0003c0004t0025g0054others(1): Show | 4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.383-1290_383-1289i others(4): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108204999 | ||||||
| chr12:108205018
|
G | A | 4 | a0001c0001t0035g0259a0001c0001t0036g0068a0001c0001t0036g0261others(1): Show | 4 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.383-1271G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108205018 | ||||||
| chr12:108205101
|
C | T | 4 | a0003c0004t0017g0052a0003c0004t0025g0053a0003c0004t0025g0054others(1): Show | 4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.383-1188C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108205101 | ||||||
| chr12:108205159
|
G | C | 14 | a0001c0001t0001g0107a0001c0001t0005g0091a0001c0001t0011g0056others(11): Show | 14 | HG00099.hp2 HG01109.hp1 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.383-1130G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108205159 | ||||||
| chr12:108205178
|
C | G | 1 | a0007c0011t0004g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.383-1111C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108205178 | ||||||
| chr12:108205226
|
G | T | 1 | a0001c0001t0073g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.383-1063G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108205226 | ||||||
| chr12:108205252
|
A | G | 1 | a0001c0001t0005g0176 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.383-1037A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108205252 | ||||||
| chr12:108205255
|
T | A | 4 | a0003c0004t0017g0052a0003c0004t0025g0053a0003c0004t0025g0054others(1): Show | 4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.383-1034T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108205255 | ||||||
| chr12:108205287
|
C | T | 4 | a0001c0001t0035g0259a0001c0001t0036g0068a0001c0001t0036g0261others(1): Show | 4 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.383-1002C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108205287 | ||||||
| chr12:108205288
|
G | A | 2 | a0002c0002t0003g0268a0002c0002t0009g0132 | 2 | HG00558.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.383-1001G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108205288 | ||||||
| chr12:108205300
|
C | A | 5 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0254others(2): Show | 5 | HG01884.hp2 HG01891.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.383-989C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108205300 | ||||||
| chr12:108205313
|
C | T | 133 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(130): Show | 133 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.383-976C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108205313 | ||||||
| chr12:108205424
|
T | C | 1 | a0001c0001t0004g0122 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.383-865T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108205424 | ||||||
| chr12:108205531
|
G | GATTTATA | 4 | a0003c0004t0017g0052a0003c0004t0025g0053a0003c0004t0025g0054others(1): Show | 4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.383-754_383-748dup others(7): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr12 | 108205531 | |||||
| chr12:108205638
|
T | C | 1 | a0007c0011t0004g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.383-651T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108205638 | ||||||
| chr12:108205864
|
A | G | 2 | a0001c0001t0033g0049a0001c0003t0012g0045 | 2 | HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.383-425A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108205864 | ||||||
| chr12:108205988
|
T | C | 1 | a0001c0001t0003g0248 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.383-301T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108205988 | ||||||
| chr12:108205995
|
C | T | 2 | a0001c0001t0063g0276a0001c0001t0064g0277 | 2 | HG01109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.383-294C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108205995 | ||||||
| chr12:108206005
|
G | A | 1 | a0001c0001t0004g0178 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.383-284G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108206005 | ||||||
| chr12:108206035
|
T | C | 1 | a0002c0002t0001g0211 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.383-254T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108206035 | ||||||
| chr12:108206093
|
A | G | 4 | a0001c0001t0004g0161a0001c0001t0022g0151a0001c0001t0030g0162others(1): Show | 4 | HG01891.hp1 HG02622.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.383-196A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 2/8 | chr12 | 108206093 | ||||||
| chr12:108206416
|
C | T | 1 | a0001c0003t0016g0055 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.497+13C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108206416 | ||||||
| chr12:108206460
|
A | G | 133 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(130): Show | 133 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.497+57A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108206460 | ||||||
| chr12:108206511
|
C | T | 1 | a0001c0001t0073g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.497+108C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108206511 | ||||||
| chr12:108206528
|
T | C | 4 | a0003c0004t0017g0052a0003c0004t0025g0053a0003c0004t0025g0054others(1): Show | 4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.497+125T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108206528 | ||||||
| chr12:108206657
|
T | C | 1 | a0002c0002t0003g0196 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.497+254T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108206657 | ||||||
| chr12:108206698
|
A | T | 14 | a0001c0001t0001g0139a0001c0001t0002g0077a0001c0001t0004g0114others(11): Show | 14 | HG00597.hp2 HG01346.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.497+295A>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108206698 | ||||||
| chr12:108206739
|
C | A | 4 | a0003c0004t0017g0052a0003c0004t0025g0053a0003c0004t0025g0054others(1): Show | 4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.497+336C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108206739 | ||||||
| chr12:108206783
|
G | A | 4 | a0003c0004t0017g0052a0003c0004t0025g0053a0003c0004t0025g0054others(1): Show | 4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.497+380G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108206783 | ||||||
| chr12:108207043
|
T | C | 5 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0254others(2): Show | 5 | HG01884.hp2 HG01891.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.497+640T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108207043 | ||||||
| chr12:108207086
|
TA | T | 14 | a0001c0001t0001g0107a0001c0001t0005g0091a0001c0001t0011g0056others(11): Show | 14 | HG00099.hp2 HG01109.hp1 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.497+684delA | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108207086 | ||||||
| chr12:108207339
|
C | A | 128 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0001g0079others(125): Show | 128 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.497+936C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108207339 | ||||||
| chr12:108207351
|
T | C | 1 | a0001c0001t0070g0269 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.497+948T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108207351 | ||||||
| chr12:108207388
|
G | T | 1 | a0001c0001t0073g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.497+985G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108207388 | ||||||
| chr12:108207390
|
G | C | 4 | a0003c0004t0017g0052a0003c0004t0025g0053a0003c0004t0025g0054others(1): Show | 4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.497+987G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108207390 | ||||||
| chr12:108207533
|
C | CT | 16 | a0001c0001t0001g0096a0001c0001t0003g0002a0001c0001t0004g0124others(13): Show | 17 | HG00735.hp2 HG01175.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.497+1156dupT | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 108207533 | |||||
| chr12:108207533
|
C | CTTTT | 6 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0254others(3): Show | 6 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.497+1153_497+1156d others(6): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 108207533 | |||||
| chr12:108207533
|
CT | C | 99 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0001g0079others(96): Show | 100 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.497+1156delT | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 108207533 | |||||
| chr12:108207533
|
CTT | C | 22 | a0001c0001t0001g0080a0001c0001t0001g0107a0001c0001t0005g0091others(19): Show | 22 | HG00099.hp2 HG00323.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.497+1155_497+1156d others(4): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 108207533 | |||||
| chr12:108207627
|
T | C | 14 | a0001c0001t0001g0107a0001c0001t0005g0091a0001c0001t0011g0056others(11): Show | 14 | HG00099.hp2 HG01109.hp1 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.497+1224T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108207627 | ||||||
| chr12:108207737
|
G | A | 1 | a0003c0004t0017g0052 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.497+1334G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108207737 | ||||||
| chr12:108207892
|
T | A | 13 | a0001c0001t0001g0107a0001c0001t0005g0091a0001c0001t0011g0056others(10): Show | 13 | HG00099.hp2 HG01109.hp1 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.497+1489T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108207892 | ||||||
| chr12:108207912
|
G | T | 1 | a0001c0001t0011g0006 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.497+1509G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108207912 | ||||||
| chr12:108207939
|
T | C | 32 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0154others(29): Show | 33 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.497+1536T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108207939 | ||||||
| chr12:108207974
|
G | A | 1 | a0001c0001t0004g0122 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.497+1571G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108207974 | ||||||
| chr12:108208026
|
T | A | 14 | a0001c0001t0001g0107a0001c0001t0005g0091a0001c0001t0011g0056others(11): Show | 14 | HG00099.hp2 HG01109.hp1 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.497+1623T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108208026 | ||||||
| chr12:108208110
|
A | C | 127 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(124): Show | 127 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.497+1707A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108208110 | ||||||
| chr12:108208131
|
C | T | 1 | a0002c0002t0004g0173 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.497+1728C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108208131 | ||||||
| chr12:108208133
|
G | A | 127 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(124): Show | 127 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.497+1730G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108208133 | ||||||
| chr12:108208178
|
G | C | 1 | a0001c0001t0003g0143 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.497+1775G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108208178 | ||||||
| chr12:108208237
|
TA | T | 4 | a0001c0001t0035g0259a0001c0001t0036g0068a0001c0001t0036g0261others(1): Show | 4 | HG01943.hp2 HG02109.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.497+1836delA | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr12 | 108208237 | |||||
| chr12:108208269
|
G | T | 6 | a0001c0001t0008g0018a0001c0001t0023g0017a0001c0001t0023g0022others(3): Show | 6 | HG00438.hp1 NA18612.hp2 NA18941.hp2 others(3): Show |
intron_variant | MODIFIER | c.498-1852G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108208269 | ||||||
| chr12:108208378
|
A | G | 6 | a0002c0002t0001g0145a0002c0002t0001g0208a0002c0002t0001g0211others(3): Show | 6 | HG02015.hp2 HG02165.hp1 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.498-1743A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108208378 | ||||||
| chr12:108208468
|
T | A | 4 | a0003c0004t0017g0052a0003c0004t0025g0053a0003c0004t0025g0054others(1): Show | 4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.498-1653T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108208468 | ||||||
| chr12:108208538
|
T | C | 1 | a0001c0003t0031g0051 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.498-1583T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108208538 | ||||||
| chr12:108208634
|
A | T | 129 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(126): Show | 129 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.498-1487A>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108208634 | ||||||
| chr12:108208677
|
G | C | 4 | a0003c0004t0017g0052a0003c0004t0025g0053a0003c0004t0025g0054others(1): Show | 4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.498-1444G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108208677 | ||||||
| chr12:108208738
|
G | C | 5 | a0001c0001t0004g0109a0001c0001t0004g0110a0001c0001t0004g0112others(2): Show | 6 | HG02257.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.498-1383G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108208738 | ||||||
| chr12:108208796
|
T | C | 202 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(199): Show | 205 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.498-1325T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108208796 | ||||||
| chr12:108209078
|
C | A | 3 | a0002c0002t0001g0150a0002c0002t0001g0206a0002c0002t0001g0219 | 3 | HG02145.hp1 HG03239.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.498-1043C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108209078 | ||||||
| chr12:108209078
|
C | G | 104 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(101): Show | 104 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.498-1043C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108209078 | ||||||
| chr12:108209193
|
C | A | 113 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(110): Show | 113 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.498-928C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108209193 | ||||||
| chr12:108209239
|
A | G | 192 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(189): Show | 194 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.498-882A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108209239 | ||||||
| chr12:108209264
|
T | C | 133 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(130): Show | 133 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.498-857T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108209264 | ||||||
| chr12:108209432
|
G | A | 2 | a0001c0001t0010g0004a0001c0001t0043g0004 | 2 | HG02258.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.498-689G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108209432 | ||||||
| chr12:108209455
|
T | C | 4 | a0003c0004t0017g0052a0003c0004t0025g0053a0003c0004t0025g0054others(1): Show | 4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.498-666T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108209455 | ||||||
| chr12:108209583
|
A | G | 13 | a0001c0001t0011g0006a0001c0001t0011g0125a0001c0001t0011g0127others(10): Show | 14 | HG02280.hp1 HG02572.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.498-538A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108209583 | ||||||
| chr12:108209640
|
G | A | 3 | a0001c0001t0033g0049a0001c0003t0012g0045a0001c0003t0038g0063 | 3 | HG02647.hp2 HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.498-481G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108209640 | ||||||
| chr12:108209752
|
C | G | 20 | a0001c0001t0001g0107a0001c0001t0004g0109a0001c0001t0004g0110others(17): Show | 21 | HG00099.hp2 HG01943.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.498-369C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108209752 | ||||||
| chr12:108209882
|
T | C | 40 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0107others(37): Show | 41 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.498-239T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108209882 | ||||||
| chr12:108209922
|
G | A | 2 | a0001c0001t0040g0221a0001c0001t0040g0222 | 2 | HG01167.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.498-199G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108209922 | ||||||
| chr12:108209949
|
C | G | 1 | a0001c0001t0004g0168 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.498-172C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108209949 | ||||||
| chr12:108209991
|
C | T | 1 | a0001c0001t0051g0158 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.498-130C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 3/8 | chr12 | 108209991 | ||||||
| chr12:108210411
|
C | T | 1 | a0005c0006t0016g0046 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.682+106C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108210411 | ||||||
| chr12:108210445
|
A | G | 33 | a0001c0001t0001g0107a0001c0001t0004g0161a0001c0001t0005g0091others(30): Show | 33 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.682+140A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108210445 | ||||||
| chr12:108210455
|
C | G | 201 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(198): Show | 204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.682+150C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108210455 | ||||||
| chr12:108210603
|
G | A | 1 | a0001c0001t0003g0064 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.682+298G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108210603 | ||||||
| chr12:108210652
|
T | C | 2 | a0001c0001t0006g0086a0001c0001t0010g0129 | 2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.682+347T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108210652 | ||||||
| chr12:108210799
|
T | C | 34 | a0001c0001t0001g0107a0001c0001t0005g0091a0001c0001t0006g0086others(31): Show | 34 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.682+494T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108210799 | ||||||
| chr12:108210830
|
G | A | 4 | a0003c0004t0017g0052a0003c0004t0025g0053a0003c0004t0025g0054others(1): Show | 4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.682+525G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108210830 | ||||||
| chr12:108210931
|
C | T | 1 | a0001c0001t0008g0026 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.682+626C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108210931 | ||||||
| chr12:108211145
|
C | T | 1 | a0001c0001t0001g0252 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.682+840C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108211145 | ||||||
| chr12:108211250
|
G | A | 2 | a0001c0001t0041g0111a0001c0001t0067g0067 | 2 | HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.682+945G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108211250 | ||||||
| chr12:108211296
|
T | C | 1 | a0001c0003t0012g0045 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.682+991T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108211296 | ||||||
| chr12:108211296
|
T | G | 5 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0254others(2): Show | 5 | HG01884.hp2 HG01891.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.682+991T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108211296 | ||||||
| chr12:108211383
|
A | G | 2 | a0001c0001t0006g0086a0001c0001t0010g0129 | 2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.682+1078A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108211383 | ||||||
| chr12:108211435
|
C | T | 8 | a0001c0001t0033g0049a0001c0003t0012g0045a0001c0003t0016g0055others(5): Show | 8 | HG01243.hp2 HG02451.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.682+1130C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108211435 | ||||||
| chr12:108211441
|
G | T | 1 | a0001c0001t0041g0111 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.682+1136G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108211441 | ||||||
| chr12:108211442
|
C | G | 1 | a0001c0001t0041g0111 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.682+1137C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108211442 | ||||||
| chr12:108211450
|
T | C | 34 | a0001c0001t0001g0107a0001c0001t0005g0091a0001c0001t0006g0086others(31): Show | 34 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.682+1145T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108211450 | ||||||
| chr12:108211575
|
G | A | 4 | a0003c0004t0017g0052a0003c0004t0025g0053a0003c0004t0025g0054others(1): Show | 4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.682+1270G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108211575 | ||||||
| chr12:108211630
|
C | CAT | 8 | a0001c0001t0004g0124a0001c0001t0005g0119a0001c0001t0005g0123others(5): Show | 8 | HG00738.hp2 HG02135.hp1 NA18941.hp1 others(5): Show |
intron_variant | MODIFIER | c.682+1345_682+1346d others(4): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108211630 | |||||
| chr12:108211630
|
C | CATAT | 32 | a0001c0001t0001g0154a0001c0001t0001g0205a0001c0001t0003g0143others(29): Show | 33 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.682+1343_682+1346d others(6): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108211630 | |||||
| chr12:108211630
|
C | CATATAT | 3 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0022g0151 | 3 | HG01074.hp2 HG01515.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.682+1341_682+1346d others(8): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108211630 | |||||
| chr12:108211630
|
C | CATATATA others(5): Show |
3 | a0003c0004t0025g0053a0003c0004t0025g0054a0003c0004t0074g0226 | 3 | HG02109.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.682+1335_682+1346d others(14): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108211630 | |||||
| chr12:108211630
|
C | CATATATA others(17): Show |
1 | a0001c0001t0016g0044 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.682+1338_682+1361d others(26): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108211630 | |||||
| chr12:108211630
|
C | CATATATA others(19): Show |
1 | a0001c0001t0058g0043 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.682+1336_682+1361d others(28): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108211630 | |||||
| chr12:108211630
|
C | CATATATA others(19): Show |
3 | a0001c0001t0006g0243a0001c0001t0011g0056a0001c0001t0055g0244 | 3 | HG02922.hp1 NA18952.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.682+1346_682+1347i others(28): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108211630 | |||||
| chr12:108211630
|
C | CATATATA others(31): Show |
1 | a0003c0004t0017g0052 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.682+1346_682+1347i others(40): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108211630 | |||||
| chr12:108211630
|
CAT | C | 135 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0001g0079others(132): Show | 136 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.682+1345_682+1346d others(4): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108211630 | |||||
| chr12:108211633
|
A | ATATATAT others(3): Show |
2 | a0001c0001t0007g0048a0001c0001t0057g0047 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.682+1337_682+1338i others(12): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108211633 | |||||
| chr12:108211649
|
A | G | 1 | a0002c0002t0003g0184 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.682+1344A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108211649 | ||||||
| chr12:108211650
|
T | TATAC | 8 | a0001c0001t0033g0049a0001c0003t0012g0045a0001c0003t0016g0055others(5): Show | 8 | HG01243.hp2 HG02451.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.682+1346_682+1347i others(6): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108211650 | |||||
| chr12:108211667
|
T | A | 2 | a0001c0001t0006g0086a0001c0001t0010g0129 | 2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.682+1362T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108211667 | ||||||
| chr12:108211746
|
C | T | 12 | a0001c0001t0033g0049a0001c0003t0012g0045a0001c0003t0016g0055others(9): Show | 12 | HG01243.hp2 HG02109.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.682+1441C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108211746 | ||||||
| chr12:108211794
|
G | C | 48 | a0001c0001t0001g0096a0001c0001t0001g0107a0001c0001t0001g0181others(45): Show | 48 | HG00099.hp2 HG00423.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.682+1489G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108211794 | ||||||
| chr12:108211803
|
G | A | 4 | a0001c0003t0021g0245a0001c0003t0021g0266a0001c0003t0031g0050others(1): Show | 4 | HG01243.hp2 HG02451.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.682+1498G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108211803 | ||||||
| chr12:108211820
|
A | AT | 86 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0001g0080others(83): Show | 87 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.682+1531dupT | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108211820 | |||||
| chr12:108211820
|
A | ATT | 12 | a0001c0001t0001g0079a0001c0001t0002g0179a0001c0001t0004g0109others(9): Show | 12 | HG00735.hp1 HG01074.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.682+1530_682+1531d others(4): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108211820 | |||||
| chr12:108211820
|
AT | A | 91 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0107others(88): Show | 93 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.682+1531delT | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108211820 | |||||
| chr12:108211837
|
G | T | 1 | a0001c0001t0004g0178 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.682+1532G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108211837 | ||||||
| chr12:108211948
|
C | T | 1 | a0001c0001t0006g0242 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.682+1643C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108211948 | ||||||
| chr12:108212106
|
C | G | 7 | a0001c0001t0001g0107a0001c0001t0005g0091a0001c0001t0030g0130others(4): Show | 7 | HG00099.hp2 HG01257.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.682+1801C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108212106 | ||||||
| chr12:108212200
|
T | C | 2 | a0001c0001t0006g0086a0001c0001t0010g0129 | 2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.682+1895T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108212200 | ||||||
| chr12:108212245
|
G | A | 1 | a0001c0001t0073g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.682+1940G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108212245 | ||||||
| chr12:108212251
|
A | T | 10 | a0001c0001t0011g0006a0001c0001t0011g0125a0001c0001t0011g0127others(7): Show | 11 | HG02280.hp1 HG02572.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.682+1946A>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108212251 | ||||||
| chr12:108212285
|
A | G | 19 | a0001c0001t0001g0107a0001c0001t0005g0091a0001c0001t0011g0056others(16): Show | 19 | HG00099.hp2 HG01109.hp1 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.682+1980A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108212285 | ||||||
| chr12:108212322
|
G | A | 1 | a0001c0001t0002g0069 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.682+2017G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108212322 | ||||||
| chr12:108212564
|
C | G | 4 | a0003c0004t0017g0052a0003c0004t0025g0053a0003c0004t0025g0054others(1): Show | 4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.682+2259C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108212564 | ||||||
| chr12:108212579
|
T | C | 19 | a0001c0001t0011g0006a0001c0001t0011g0056a0001c0001t0011g0125others(16): Show | 20 | HG01109.hp1 HG01943.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.682+2274T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108212579 | ||||||
| chr12:108212584
|
C | G | 11 | a0001c0001t0007g0013a0001c0001t0007g0014a0001c0001t0008g0010others(8): Show | 11 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(8): Show |
intron_variant | MODIFIER | c.682+2279C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108212584 | ||||||
| chr12:108212590
|
T | TTC | 3 | a0001c0001t0005g0115a0001c0001t0005g0116a0001c0008t0019g0229 | 3 | HG01168.hp2 HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.682+2308_682+2309d others(4): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108212590 | |||||
| chr12:108212590
|
TTCTC | T | 10 | a0001c0001t0011g0056a0001c0001t0016g0044a0001c0001t0035g0259others(7): Show | 10 | HG01109.hp1 HG01943.hp2 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.682+2306_682+2309d others(6): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108212590 | |||||
| chr12:108212609
|
TCTCTCA | T | 4 | a0001c0001t0001g0073a0001c0001t0001g0228a0001c0001t0001g0230others(1): Show | 4 | HG01168.hp1 HG01169.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.682+2306_682+2311d others(8): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108212609 | |||||
| chr12:108212611
|
T | A | 2 | a0001c0001t0006g0086a0001c0001t0010g0129 | 2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.682+2306T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108212611 | ||||||
| chr12:108212611
|
T | TCACACAC others(7): Show |
3 | a0001c0001t0033g0049a0001c0003t0012g0045a0001c0003t0038g0063 | 3 | HG02647.hp2 HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.682+2307_682+2308i others(16): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108212611 | |||||
| chr12:108212613
|
T | A | 6 | a0001c0001t0001g0107a0001c0001t0006g0086a0001c0001t0010g0129others(3): Show | 6 | HG02647.hp2 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.682+2308T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108212613 | ||||||
| chr12:108212613
|
T | TCA | 14 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0254others(11): Show | 15 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.682+2329_682+2330d others(4): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108212613 | |||||
| chr12:108212613
|
T | TCACA | 14 | a0001c0001t0001g0096a0001c0001t0001g0181a0001c0001t0001g0182others(11): Show | 14 | HG00423.hp2 HG00639.hp2 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.682+2327_682+2330d others(6): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108212613 | |||||
| chr12:108212613
|
T | TCACACAC others(9): Show |
5 | a0001c0003t0016g0055a0001c0003t0021g0245a0001c0003t0021g0266others(2): Show | 5 | HG01243.hp2 HG02451.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.682+2316_682+2317i others(18): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108212613 | |||||
| chr12:108212613
|
T | TCTCA | 30 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0154others(27): Show | 31 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(28): Show |
intron_variant | MODIFIER | c.682+2309_682+2310i others(6): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108212613 | |||||
| chr12:108212613
|
T | TCTCACA | 3 | a0001c0001t0007g0013a0001c0001t0007g0014a0001c0001t0073g0061 | 3 | HG00642.hp1 HG01516.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.682+2309_682+2310i others(8): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108212613 | |||||
| chr12:108212613
|
TCA | T | 86 | a0001c0001t0001g0075a0001c0001t0001g0079a0001c0001t0001g0080others(83): Show | 86 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.682+2329_682+2330d others(4): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108212613 | |||||
| chr12:108212615
|
A | T | 3 | a0001c0001t0004g0168a0001c0001t0014g0153a0001c0008t0019g0229 | 3 | HG00099.hp1 HG01168.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.682+2310A>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108212615 | ||||||
| chr12:108212616
|
C | CACACAG | 4 | a0003c0004t0017g0052a0003c0004t0025g0053a0003c0004t0025g0054others(1): Show | 4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.682+2316_682+2317i others(8): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108212616 | |||||
| chr12:108212618
|
C | CACAG | 10 | a0001c0001t0001g0107a0001c0001t0005g0091a0001c0001t0030g0130others(7): Show | 10 | HG00099.hp2 HG01257.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.682+2316_682+2317i others(6): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108212618 | |||||
| chr12:108212618
|
C | G | 3 | a0001c0001t0006g0086a0001c0001t0010g0129a0001c0001t0073g0061 | 3 | HG02809.hp1 HG02976.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.682+2313C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108212618 | ||||||
| chr12:108212640
|
G | GAC | 14 | a0001c0001t0001g0096a0001c0001t0001g0181a0001c0001t0001g0182others(11): Show | 14 | HG00423.hp2 HG00639.hp2 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.682+2348_682+2349d others(4): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108212640 | |||||
| chr12:108212728
|
C | T | 5 | a0001c0001t0004g0109a0001c0001t0004g0110a0001c0001t0004g0112others(2): Show | 6 | HG02257.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.682+2423C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108212728 | ||||||
| chr12:108212730
|
A | C | 30 | a0001c0001t0001g0107a0001c0001t0005g0091a0001c0001t0006g0086others(27): Show | 30 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.682+2425A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108212730 | ||||||
| chr12:108212949
|
A | G | 2 | a0001c0001t0027g0005a0001c0001t0037g0099 | 3 | HG02895.hp2 HG02897.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.682+2644A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108212949 | ||||||
| chr12:108212973
|
T | C | 27 | a0001c0001t0001g0107a0001c0001t0005g0091a0001c0001t0006g0086others(24): Show | 27 | HG00099.hp2 HG01109.hp1 HG01257.hp1 others(24): Show |
intron_variant | MODIFIER | c.682+2668T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108212973 | ||||||
| chr12:108213091
|
T | C | 1 | a0001c0001t0073g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.682+2786T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108213091 | ||||||
| chr12:108213179
|
C | G | 1 | a0002c0002t0001g0220 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.682+2874C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108213179 | ||||||
| chr12:108213272
|
G | A | 1 | a0002c0002t0001g0211 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.682+2967G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108213272 | ||||||
| chr12:108213597
|
A | C | 6 | a0001c0001t0001g0258a0001c0001t0002g0102a0001c0001t0002g0103others(3): Show | 6 | HG00423.hp2 HG02015.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.682+3292A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108213597 | ||||||
| chr12:108213601
|
G | T | 1 | a0001c0001t0073g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.682+3296G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108213601 | ||||||
| chr12:108213790
|
T | C | 1 | a0001c0001t0016g0044 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.682+3485T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108213790 | ||||||
| chr12:108213836
|
T | C | 1 | a0001c0001t0022g0151 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.682+3531T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108213836 | ||||||
| chr12:108213839
|
C | A | 95 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0001g0079others(92): Show | 95 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.682+3534C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108213839 | ||||||
| chr12:108213955
|
A | G | 42 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0148others(39): Show | 43 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(40): Show |
intron_variant | MODIFIER | c.682+3650A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108213955 | ||||||
| chr12:108214799
|
T | C | 1 | a0001c0001t0008g0021 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.682+4494T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108214799 | ||||||
| chr12:108214916
|
A | G | 1 | a0001c0001t0002g0076 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.682+4611A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108214916 | ||||||
| chr12:108215124
|
T | C | 2 | a0001c0001t0006g0086a0001c0001t0010g0129 | 2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.682+4819T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108215124 | ||||||
| chr12:108215191
|
G | T | 1 | a0001c0001t0004g0124 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.682+4886G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108215191 | ||||||
| chr12:108215361
|
G | A | 69 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0107others(66): Show | 70 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.682+5056G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108215361 | ||||||
| chr12:108215409
|
C | T | 69 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0107others(66): Show | 70 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.682+5104C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108215409 | ||||||
| chr12:108215555
|
C | A | 1 | a0002c0002t0001g0150 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.682+5250C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108215555 | ||||||
| chr12:108215637
|
T | C | 69 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0107others(66): Show | 70 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.682+5332T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108215637 | ||||||
| chr12:108215697
|
G | C | 22 | a0001c0001t0001g0107a0001c0001t0005g0091a0001c0001t0011g0056others(19): Show | 22 | HG00099.hp2 HG01109.hp1 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.682+5392G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108215697 | ||||||
| chr12:108215857
|
G | A | 66 | a0001c0001t0001g0073a0001c0001t0001g0227a0001c0001t0001g0228others(63): Show | 66 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.682+5552G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108215857 | ||||||
| chr12:108215921
|
T | A | 15 | a0001c0001t0005g0088a0001c0001t0007g0027a0001c0001t0007g0028others(12): Show | 15 | HG00642.hp2 HG01192.hp1 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.682+5616T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108215921 | ||||||
| chr12:108216108
|
A | G | 229 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(226): Show | 232 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.682+5803A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108216108 | ||||||
| chr12:108216474
|
C | G | 65 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0107others(62): Show | 66 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.682+6169C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108216474 | ||||||
| chr12:108216587
|
G | A | 159 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0075others(156): Show | 160 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.682+6282G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108216587 | ||||||
| chr12:108216623
|
G | A | 42 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0148others(39): Show | 43 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(40): Show |
intron_variant | MODIFIER | c.682+6318G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108216623 | ||||||
| chr12:108216706
|
C | A | 5 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0254others(2): Show | 5 | HG01884.hp2 HG01891.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.682+6401C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108216706 | ||||||
| chr12:108216725
|
A | G | 161 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0075others(158): Show | 162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.682+6420A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108216725 | ||||||
| chr12:108216821
|
G | A | 7 | a0001c0003t0012g0045a0001c0003t0016g0055a0001c0003t0021g0245others(4): Show | 7 | HG01243.hp2 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.682+6516G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108216821 | ||||||
| chr12:108216843
|
A | T | 202 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(199): Show | 205 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.682+6538A>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108216843 | ||||||
| chr12:108216849
|
G | A | 5 | a0001c0001t0004g0109a0001c0001t0004g0110a0001c0001t0004g0112others(2): Show | 6 | HG02257.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.682+6544G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108216849 | ||||||
| chr12:108216872
|
G | A | 90 | a0001c0001t0001g0075a0001c0001t0001g0079a0001c0001t0001g0080others(87): Show | 90 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.682+6567G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108216872 | ||||||
| chr12:108216899
|
T | C | 161 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0075others(158): Show | 162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.682+6594T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108216899 | ||||||
| chr12:108217554
|
G | A | 7 | a0001c0003t0012g0045a0001c0003t0016g0055a0001c0003t0021g0245others(4): Show | 7 | HG01243.hp2 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.683-7185G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108217554 | ||||||
| chr12:108217648
|
C | T | 168 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0075others(165): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.683-7091C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108217648 | ||||||
| chr12:108217697
|
T | C | 93 | a0001c0001t0001g0075a0001c0001t0001g0079a0001c0001t0001g0080others(90): Show | 93 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.683-7042T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108217697 | ||||||
| chr12:108217741
|
G | T | 2 | a0001c0001t0006g0086a0001c0001t0010g0129 | 2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.683-6998G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108217741 | ||||||
| chr12:108217762
|
C | G | 1 | a0001c0001t0002g0179 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.683-6977C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108217762 | ||||||
| chr12:108217799
|
C | T | 2 | a0001c0001t0006g0086a0001c0001t0010g0129 | 2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.683-6940C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108217799 | ||||||
| chr12:108217936
|
G | GCTGGATC others(8): Show |
161 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0075others(158): Show | 162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.683-6801_683-6800i others(17): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108217936 | |||||
| chr12:108218027
|
G | C | 202 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(199): Show | 205 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.683-6712G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108218027 | ||||||
| chr12:108218225
|
A | T | 3 | a0001c0003t0016g0055a0001c0003t0031g0050a0001c0003t0031g0051 | 3 | HG01243.hp2 HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.683-6514A>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108218225 | ||||||
| chr12:108218231
|
G | C | 1 | a0001c0001t0006g0117 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.683-6508G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108218231 | ||||||
| chr12:108218283
|
A | T | 5 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0254others(2): Show | 5 | HG01884.hp2 HG01891.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.683-6456A>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108218283 | ||||||
| chr12:108218459
|
A | G | 203 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(200): Show | 206 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.683-6280A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108218459 | ||||||
| chr12:108218464
|
T | A | 1 | a0002c0002t0003g0184 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.683-6275T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108218464 | ||||||
| chr12:108218524
|
A | G | 162 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0075others(159): Show | 163 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.683-6215A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108218524 | ||||||
| chr12:108218624
|
C | T | 43 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0148others(40): Show | 44 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(41): Show |
intron_variant | MODIFIER | c.683-6115C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108218624 | ||||||
| chr12:108219031
|
C | T | 1 | a0001c0008t0019g0229 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.683-5708C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108219031 | ||||||
| chr12:108219143
|
C | A | 1 | a0001c0003t0012g0045 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.683-5596C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108219143 | ||||||
| chr12:108219199
|
T | C | 5 | a0001c0001t0004g0109a0001c0001t0004g0110a0001c0001t0004g0112others(2): Show | 6 | HG02257.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.683-5540T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108219199 | ||||||
| chr12:108219331
|
C | T | 1 | a0002c0002t0002g0270 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.683-5408C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108219331 | ||||||
| chr12:108219374
|
G | A | 93 | a0001c0001t0001g0075a0001c0001t0001g0079a0001c0001t0001g0080others(90): Show | 93 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.683-5365G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108219374 | ||||||
| chr12:108219398
|
G | A | 2 | a0001c0001t0006g0086a0001c0001t0010g0129 | 2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.683-5341G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108219398 | ||||||
| chr12:108219418
|
A | G | 176 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0075others(173): Show | 177 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.683-5321A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108219418 | ||||||
| chr12:108219464
|
C | T | 1 | a0001c0001t0053g0121 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.683-5275C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108219464 | ||||||
| chr12:108219496
|
T | C | 1 | a0001c0001t0007g0037 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.683-5243T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108219496 | ||||||
| chr12:108219631
|
C | A | 1 | a0002c0002t0009g0246 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.683-5108C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108219631 | ||||||
| chr12:108219684
|
G | T | 15 | a0001c0001t0001g0073a0001c0001t0001g0227a0001c0001t0001g0228others(12): Show | 16 | HG01168.hp1 HG01169.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.683-5055G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108219684 | ||||||
| chr12:108219685
|
T | C | 15 | a0001c0001t0001g0073a0001c0001t0001g0227a0001c0001t0001g0228others(12): Show | 16 | HG01168.hp1 HG01169.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.683-5054T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108219685 | ||||||
| chr12:108219846
|
G | C | 4 | a0001c0001t0003g0143a0001c0001t0008g0001a0001c0001t0008g0007others(1): Show | 5 | NA18944.hp1 NA18952.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.683-4893G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108219846 | ||||||
| chr12:108219991
|
TG | T | 12 | a0001c0001t0001g0139a0001c0001t0002g0077a0001c0001t0004g0114others(9): Show | 12 | HG00597.hp2 HG01346.hp2 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.683-4747delG | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108219991 | ||||||
| chr12:108220023
|
C | T | 161 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0075others(158): Show | 162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.683-4716C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108220023 | ||||||
| chr12:108220052
|
C | G | 4 | a0003c0004t0017g0052a0003c0004t0025g0053a0003c0004t0025g0054others(1): Show | 4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.683-4687C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108220052 | ||||||
| chr12:108220126
|
T | A | 160 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0075others(157): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.683-4613T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108220126 | ||||||
| chr12:108220184
|
CA | C | 4 | a0001c0003t0012g0045a0001c0003t0021g0245a0001c0003t0021g0266others(1): Show | 4 | HG02615.hp1 HG02647.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.683-4553delA | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108220184 | |||||
| chr12:108220269
|
T | C | 162 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0075others(159): Show | 163 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.683-4470T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108220269 | ||||||
| chr12:108220287
|
C | T | 161 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0075others(158): Show | 162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.683-4452C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108220287 | ||||||
| chr12:108220538
|
G | A | 67 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0107others(64): Show | 68 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(65): Show |
intron_variant | MODIFIER | c.683-4201G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108220538 | ||||||
| chr12:108220563
|
T | G | 7 | a0001c0003t0012g0045a0001c0003t0016g0055a0001c0003t0021g0245others(4): Show | 7 | HG01243.hp2 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.683-4176T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108220563 | ||||||
| chr12:108220704
|
T | A | 7 | a0001c0003t0012g0045a0001c0003t0016g0055a0001c0003t0021g0245others(4): Show | 7 | HG01243.hp2 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.683-4035T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108220704 | ||||||
| chr12:108220836
|
C | A | 1 | a0001c0001t0011g0125 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.683-3903C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108220836 | ||||||
| chr12:108220951
|
C | T | 7 | a0001c0001t0001g0107a0001c0001t0005g0091a0001c0001t0030g0130others(4): Show | 7 | HG00099.hp2 HG01257.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.683-3788C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108220951 | ||||||
| chr12:108220971
|
T | G | 162 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0075others(159): Show | 163 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.683-3768T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108220971 | ||||||
| chr12:108221058
|
T | A | 2 | a0001c0001t0006g0086a0001c0001t0010g0129 | 2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.683-3681T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108221058 | ||||||
| chr12:108221123
|
A | G | 1 | a0001c0001t0045g0232 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.683-3616A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108221123 | ||||||
| chr12:108221176
|
G | A | 1 | a0001c0001t0003g0101 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.683-3563G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108221176 | ||||||
| chr12:108221180
|
G | A | 161 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0075others(158): Show | 162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.683-3559G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108221180 | ||||||
| chr12:108221293
|
G | A | 7 | a0001c0003t0012g0045a0001c0003t0016g0055a0001c0003t0021g0245others(4): Show | 7 | HG01243.hp2 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.683-3446G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108221293 | ||||||
| chr12:108221571
|
C | T | 1 | a0001c0001t0016g0278 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.683-3168C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108221571 | ||||||
| chr12:108221678
|
C | T | 2 | a0001c0003t0012g0045a0001c0003t0038g0063 | 2 | HG02647.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.683-3061C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108221678 | ||||||
| chr12:108221694
|
A | G | 176 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0075others(173): Show | 177 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.683-3045A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108221694 | ||||||
| chr12:108221695
|
A | C | 176 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0075others(173): Show | 177 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.683-3044A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108221695 | ||||||
| chr12:108221789
|
G | A | 2 | a0001c0001t0027g0005a0001c0001t0037g0099 | 3 | HG02895.hp2 HG02897.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.683-2950G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108221789 | ||||||
| chr12:108221848
|
C | A | 1 | a0001c0003t0016g0055 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.683-2891C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108221848 | ||||||
| chr12:108222058
|
A | G | 2 | a0002c0002t0001g0207a0002c0002t0002g0203 | 2 | HG01358.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.683-2681A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108222058 | ||||||
| chr12:108222157
|
T | A | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG01074.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.683-2582T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108222157 | ||||||
| chr12:108222320
|
A | C | 1 | a0001c0001t0003g0253 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.683-2419A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108222320 | ||||||
| chr12:108222346
|
G | A | 1 | a0001c0001t0045g0232 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.683-2393G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108222346 | ||||||
| chr12:108222413
|
G | A | 1 | a0001c0001t0004g0161 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.683-2326G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108222413 | ||||||
| chr12:108222487
|
A | G | 1 | a0001c0001t0005g0070 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.683-2252A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108222487 | ||||||
| chr12:108222709
|
G | T | 1 | a0001c0001t0011g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.683-2030G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108222709 | ||||||
| chr12:108222717
|
C | T | 7 | a0001c0001t0003g0267a0001c0001t0005g0070a0001c0001t0005g0176others(4): Show | 8 | NA18940.hp1 NA18940.hp2 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.683-2022C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108222717 | ||||||
| chr12:108222724
|
C | T | 1 | a0001c0001t0005g0163 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.683-2015C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108222724 | ||||||
| chr12:108222767
|
A | G | 175 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0075others(172): Show | 176 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.683-1972A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108222767 | ||||||
| chr12:108222845
|
T | C | 1 | a0001c0001t0073g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.683-1894T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108222845 | ||||||
| chr12:108222875
|
G | C | 1 | a0001c0001t0035g0233 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.683-1864G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108222875 | ||||||
| chr12:108222905
|
T | C | 2 | a0001c0001t0030g0130a0001c0001t0052g0131 | 2 | HG02630.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.683-1834T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108222905 | ||||||
| chr12:108222958
|
G | A | 1 | a0001c0001t0002g0146 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.683-1781G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108222958 | ||||||
| chr12:108222982
|
G | A | 1 | a0001c0001t0026g0092 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.683-1757G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108222982 | ||||||
| chr12:108222992
|
T | C | 2 | a0002c0002t0001g0188a0002c0002t0002g0224 | 2 | HG03831.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.683-1747T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108222992 | ||||||
| chr12:108223120
|
A | G | 4 | a0001c0003t0012g0045a0001c0003t0021g0245a0001c0003t0021g0266others(1): Show | 4 | HG02615.hp1 HG02647.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.683-1619A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108223120 | ||||||
| chr12:108223608
|
T | C | 176 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0075others(173): Show | 177 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.683-1131T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108223608 | ||||||
| chr12:108223934
|
G | T | 1 | a0001c0001t0013g0256 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.683-805G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108223934 | ||||||
| chr12:108223978
|
G | A | 1 | a0001c0001t0045g0232 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.683-761G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108223978 | ||||||
| chr12:108224237
|
A | G | 69 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0107others(66): Show | 70 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.683-502A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108224237 | ||||||
| chr12:108224240
|
ACTTTTCC others(14): Show |
A | 69 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0107others(66): Show | 70 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.683-497_683-477del others(21): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr12 | 108224240 | |||||
| chr12:108224304
|
C | T | 2 | a0001c0001t0005g0115a0001c0001t0005g0116 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.683-435C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108224304 | ||||||
| chr12:108224321
|
C | A | 1 | a0002c0002t0013g0192 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.683-418C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108224321 | ||||||
| chr12:108224454
|
A | G | 4 | a0001c0001t0012g0025a0001c0001t0012g0030a0001c0001t0012g0040others(1): Show | 4 | HG01943.hp1 HG02683.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.683-285A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108224454 | ||||||
| chr12:108224476
|
A | G | 176 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0075others(173): Show | 177 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.683-263A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108224476 | ||||||
| chr12:108224514
|
G | A | 2 | a0002c0002t0001g0138a0002c0002t0001g0180 | 2 | NA18964.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.683-225G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108224514 | ||||||
| chr12:108224555
|
A | G | 1 | a0001c0001t0004g0109 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.683-184A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 4/8 | chr12 | 108224555 | ||||||
| chr12:108224957
|
C | T | 4 | a0003c0004t0017g0052a0003c0004t0025g0053a0003c0004t0025g0054others(1): Show | 4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.804+97C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 5/8 | chr12 | 108224957 | ||||||
| chr12:108224992
|
G | A | 23 | a0001c0001t0001g0107a0001c0001t0005g0091a0001c0001t0011g0056others(20): Show | 23 | HG00099.hp2 HG01109.hp1 HG01257.hp1 others(20): Show |
intron_variant | MODIFIER | c.804+132G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 5/8 | chr12 | 108224992 | ||||||
| chr12:108225018
|
G | A | 1 | a0001c0001t0002g0179 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.804+158G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 5/8 | chr12 | 108225018 | ||||||
| chr12:108225065
|
A | G | 176 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0075others(173): Show | 177 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.804+205A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 5/8 | chr12 | 108225065 | ||||||
| chr12:108225075
|
G | GT | 176 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0075others(173): Show | 177 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.804+218dupT | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 108225075 | |||||
| chr12:108225285
|
G | A | 176 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0075others(173): Show | 177 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.804+425G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 5/8 | chr12 | 108225285 | ||||||
| chr12:108225566
|
C | G | 175 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0075others(172): Show | 176 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.804+706C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 5/8 | chr12 | 108225566 | ||||||
| chr12:108225586
|
C | T | 7 | a0001c0003t0012g0045a0001c0003t0016g0055a0001c0003t0021g0245others(4): Show | 7 | HG01243.hp2 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.804+726C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 5/8 | chr12 | 108225586 | ||||||
| chr12:108225618
|
T | TG | 176 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0075others(173): Show | 177 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.804+760dupG | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 108225618 | |||||
| chr12:108225691
|
C | G | 1 | a0001c0001t0013g0257 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.804+831C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 5/8 | chr12 | 108225691 | ||||||
| chr12:108225834
|
G | T | 1 | a0001c0001t0003g0064 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.804+974G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 5/8 | chr12 | 108225834 | ||||||
| chr12:108225910
|
C | A | 5 | a0001c0001t0004g0109a0001c0001t0004g0110a0001c0001t0004g0112others(2): Show | 6 | HG02257.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.804+1050C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 5/8 | chr12 | 108225910 | ||||||
| chr12:108225920
|
G | C | 32 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0154others(29): Show | 33 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.804+1060G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 5/8 | chr12 | 108225920 | ||||||
| chr12:108226040
|
C | A | 23 | a0001c0001t0001g0107a0001c0001t0005g0091a0001c0001t0011g0056others(20): Show | 23 | HG00099.hp2 HG01109.hp1 HG01257.hp1 others(20): Show |
intron_variant | MODIFIER | c.805-950C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 5/8 | chr12 | 108226040 | ||||||
| chr12:108226244
|
G | A | 67 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0107others(64): Show | 68 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(65): Show |
intron_variant | MODIFIER | c.805-746G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 5/8 | chr12 | 108226244 | ||||||
| chr12:108226265
|
C | T | 13 | a0001c0001t0001g0139a0001c0001t0002g0077a0001c0001t0004g0114others(10): Show | 13 | HG00597.hp2 HG01346.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.805-725C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 5/8 | chr12 | 108226265 | ||||||
| chr12:108226333
|
G | C | 1 | a0001c0001t0073g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.805-657G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 5/8 | chr12 | 108226333 | ||||||
| chr12:108226469
|
G | T | 11 | a0001c0001t0011g0056a0001c0001t0016g0044a0001c0001t0025g0033others(8): Show | 11 | HG01109.hp1 HG01943.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.805-521G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 5/8 | chr12 | 108226469 | ||||||
| chr12:108226625
|
T | C | 69 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0107others(66): Show | 70 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.805-365T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 5/8 | chr12 | 108226625 | ||||||
| chr12:108226797
|
T | C | 2 | a0001c0001t0004g0124a0001c0001t0026g0095 | 2 | HG01433.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.805-193T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 5/8 | chr12 | 108226797 | ||||||
| chr12:108226913
|
C | A | 2 | a0001c0001t0007g0048a0001c0001t0057g0047 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.805-77C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 5/8 | chr12 | 108226913 | ||||||
| chr12:108227480
|
G | A | 7 | a0001c0003t0012g0045a0001c0003t0016g0055a0001c0003t0021g0245others(4): Show | 7 | HG01243.hp2 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.979+316G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108227480 | ||||||
| chr12:108227533
|
C | T | 43 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0148others(40): Show | 44 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(41): Show |
intron_variant | MODIFIER | c.979+369C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108227533 | ||||||
| chr12:108227641
|
A | C | 176 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0075others(173): Show | 177 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.979+477A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108227641 | ||||||
| chr12:108227660
|
C | A | 1 | a0001c0001t0071g0249 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.979+496C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108227660 | ||||||
| chr12:108227660
|
C | T | 1 | a0001c0001t0045g0232 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.979+496C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108227660 | ||||||
| chr12:108227700
|
G | C | 1 | a0001c0001t0045g0232 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.979+536G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108227700 | ||||||
| chr12:108227727
|
G | GTGA | 95 | a0001c0001t0001g0075a0001c0001t0001g0079a0001c0001t0001g0080others(92): Show | 95 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.979+587_979+589dup others(3): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 108227727 | |||||
| chr12:108227727
|
G | GTGATAA | 3 | a0001c0001t0011g0056a0001c0001t0016g0044a0001c0001t0058g0043 | 3 | HG02257.hp2 HG02922.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.979+567_979+568ins others(6): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 108227727 | |||||
| chr12:108227727
|
G | GTGATGA | 75 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0096others(72): Show | 76 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(73): Show |
intron_variant | MODIFIER | c.979+584_979+589dup others(6): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 108227727 | |||||
| chr12:108227727
|
G | GTGATGAT others(8): Show |
2 | a0001c0001t0006g0086a0001c0001t0010g0129 | 2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.979+575_979+589dup others(15): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 108227727 | |||||
| chr12:108227845
|
C | T | 5 | a0001c0001t0004g0109a0001c0001t0004g0110a0001c0001t0004g0112others(2): Show | 6 | HG02257.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.979+681C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108227845 | ||||||
| chr12:108227887
|
C | T | 175 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0075others(172): Show | 176 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.979+723C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108227887 | ||||||
| chr12:108228103
|
G | A | 1 | a0001c0001t0044g0160 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.979+939G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108228103 | ||||||
| chr12:108228134
|
C | A | 4 | a0001c0003t0012g0045a0001c0003t0021g0245a0001c0003t0021g0266others(1): Show | 4 | HG02615.hp1 HG02647.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.979+970C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108228134 | ||||||
| chr12:108228147
|
A | T | 1 | a0001c0008t0019g0229 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.979+983A>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108228147 | ||||||
| chr12:108228165
|
G | C | 175 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0075others(172): Show | 176 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.979+1001G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108228165 | ||||||
| chr12:108228181
|
T | A | 6 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0013g0213others(3): Show | 6 | HG00639.hp1 HG01074.hp2 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.979+1017T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108228181 | ||||||
| chr12:108228295
|
C | T | 5 | a0003c0004t0017g0052a0003c0004t0025g0053a0003c0004t0025g0054others(2): Show | 5 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.979+1131C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108228295 | ||||||
| chr12:108228315
|
T | A | 176 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0075others(173): Show | 177 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.979+1151T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108228315 | ||||||
| chr12:108228358
|
C | T | 1 | a0001c0001t0051g0158 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.979+1194C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108228358 | ||||||
| chr12:108228415
|
T | C | 1 | a0002c0002t0001g0180 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.979+1251T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108228415 | ||||||
| chr12:108228565
|
T | C | 1 | a0007c0011t0004g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.979+1401T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108228565 | ||||||
| chr12:108228725
|
G | A | 1 | a0002c0002t0003g0250 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.979+1561G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108228725 | ||||||
| chr12:108228907
|
G | T | 1 | a0001c0001t0073g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.979+1743G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108228907 | ||||||
| chr12:108228956
|
A | C | 2 | a0001c0001t0030g0130a0001c0001t0052g0131 | 2 | HG02630.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.979+1792A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108228956 | ||||||
| chr12:108229050
|
T | A | 9 | a0001c0001t0006g0086a0001c0001t0010g0129a0001c0003t0012g0045others(6): Show | 9 | HG01243.hp2 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.979+1886T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108229050 | ||||||
| chr12:108229076
|
C | A | 2 | a0002c0002t0001g0138a0002c0002t0001g0180 | 2 | NA18964.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.979+1912C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108229076 | ||||||
| chr12:108229106
|
G | T | 197 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(194): Show | 199 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.979+1942G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108229106 | ||||||
| chr12:108229111
|
G | A | 1 | a0001c0001t0006g0086 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.979+1947G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108229111 | ||||||
| chr12:108229265
|
C | G | 2 | a0001c0001t0035g0259a0001c0001t0061g0260 | 2 | HG01943.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.979+2101C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108229265 | ||||||
| chr12:108229724
|
T | C | 1 | a0002c0002t0002g0183 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.979+2560T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108229724 | ||||||
| chr12:108229783
|
T | G | 1 | a0001c0001t0008g0018 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.979+2619T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108229783 | ||||||
| chr12:108229790
|
G | C | 4 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0254others(1): Show | 4 | HG01884.hp2 HG01891.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.979+2626G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108229790 | ||||||
| chr12:108229865
|
G | GA | 17 | a0001c0001t0001g0096a0001c0001t0001g0181a0001c0001t0001g0182others(14): Show | 17 | HG00423.hp2 HG00438.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.979+2718dupA | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 108229865 | |||||
| chr12:108229865
|
GAA | G | 44 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0148others(41): Show | 45 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(42): Show |
intron_variant | MODIFIER | c.979+2717_979+2718d others(4): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 108229865 | |||||
| chr12:108229866
|
A | G | 1 | a0001c0001t0011g0056 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.979+2702A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108229866 | ||||||
| chr12:108229903
|
G | A | 1 | a0002c0002t0009g0223 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.979+2739G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108229903 | ||||||
| chr12:108229949
|
T | C | 2 | a0001c0001t0041g0111a0001c0001t0067g0067 | 2 | HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.980-2782T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108229949 | ||||||
| chr12:108229959
|
A | G | 45 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0148others(42): Show | 46 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(43): Show |
intron_variant | MODIFIER | c.980-2772A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108229959 | ||||||
| chr12:108229976
|
T | C | 43 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0148others(40): Show | 44 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(41): Show |
intron_variant | MODIFIER | c.980-2755T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108229976 | ||||||
| chr12:108230030
|
G | A | 1 | a0002c0002t0001g0150 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.980-2701G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108230030 | ||||||
| chr12:108230249
|
G | A | 219 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(216): Show | 222 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.980-2482G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108230249 | ||||||
| chr12:108230441
|
C | T | 57 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0148others(54): Show | 59 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.980-2290C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108230441 | ||||||
| chr12:108230451
|
C | G | 43 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0148others(40): Show | 44 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(41): Show |
intron_variant | MODIFIER | c.980-2280C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108230451 | ||||||
| chr12:108230501
|
G | A | 43 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0148others(40): Show | 44 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(41): Show |
intron_variant | MODIFIER | c.980-2230G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108230501 | ||||||
| chr12:108230593
|
G | A | 5 | a0001c0001t0004g0109a0001c0001t0004g0110a0001c0001t0004g0112others(2): Show | 6 | HG02257.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.980-2138G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108230593 | ||||||
| chr12:108230763
|
G | A | 2 | a0001c0001t0004g0161a0001c0001t0044g0160 | 2 | HG01891.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.980-1968G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108230763 | ||||||
| chr12:108230769
|
T | C | 7 | a0001c0003t0012g0045a0001c0003t0016g0055a0001c0003t0021g0245others(4): Show | 7 | HG01243.hp2 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.980-1962T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108230769 | ||||||
| chr12:108230812
|
C | T | 1 | a0001c0001t0057g0047 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.980-1919C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108230812 | ||||||
| chr12:108230920
|
C | G | 4 | a0003c0004t0017g0052a0003c0004t0025g0053a0003c0004t0025g0054others(1): Show | 4 | HG02109.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.980-1811C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108230920 | ||||||
| chr12:108230940
|
T | C | 1 | a0001c0001t0004g0169 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.980-1791T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108230940 | ||||||
| chr12:108230952
|
G | C | 2 | a0001c0001t0003g0064a0001c0001t0037g0062 | 2 | HG01081.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.980-1779G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108230952 | ||||||
| chr12:108231255
|
C | G | 2 | a0001c0001t0006g0086a0001c0001t0010g0129 | 2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.980-1476C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108231255 | ||||||
| chr12:108231308
|
C | T | 44 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0148others(41): Show | 45 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(42): Show |
intron_variant | MODIFIER | c.980-1423C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108231308 | ||||||
| chr12:108231685
|
G | A | 275 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(272): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.980-1046G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108231685 | ||||||
| chr12:108231894
|
C | G | 49 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0148others(46): Show | 51 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(48): Show |
intron_variant | MODIFIER | c.980-837C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108231894 | ||||||
| chr12:108232196
|
C | G | 1 | a0002c0002t0003g0202 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.980-535C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108232196 | ||||||
| chr12:108232463
|
C | A | 1 | a0001c0001t0066g0072 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.980-268C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108232463 | ||||||
| chr12:108232654
|
G | A | 44 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0148others(41): Show | 45 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(42): Show |
intron_variant | MODIFIER | c.980-77G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108232654 | ||||||
| chr12:108232694
|
C | G | 12 | a0001c0001t0004g0109a0001c0001t0004g0110a0001c0001t0004g0112others(9): Show | 13 | HG01243.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.980-37C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 6/8 | chr12 | 108232694 | ||||||
| chr12:108232950
|
C | T | 1 | a0001c0001t0017g0023 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1144+55C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108232950 | ||||||
| chr12:108233047
|
A | AC | 14 | a0001c0001t0002g0197a0001c0001t0004g0109a0001c0001t0004g0110others(11): Show | 15 | HG01243.hp2 HG02145.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1144+159dupC | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 108233047 | |||||
| chr12:108233052
|
C | A | 44 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0148others(41): Show | 45 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(42): Show |
intron_variant | MODIFIER | c.1144+157C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108233052 | ||||||
| chr12:108233055
|
A | C | 1 | a0001c0001t0045g0232 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1144+160A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108233055 | ||||||
| chr12:108233055
|
A | G | 12 | a0001c0001t0004g0109a0001c0001t0004g0110a0001c0001t0004g0112others(9): Show | 13 | HG01243.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1144+160A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108233055 | ||||||
| chr12:108233085
|
A | G | 57 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0148others(54): Show | 59 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.1144+190A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108233085 | ||||||
| chr12:108233292
|
A | G | 1 | a0002c0002t0018g0082 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1144+397A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108233292 | ||||||
| chr12:108233402
|
C | T | 14 | a0001c0001t0004g0109a0001c0001t0004g0110a0001c0001t0004g0112others(11): Show | 15 | HG01243.hp2 HG02257.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1144+507C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108233402 | ||||||
| chr12:108233619
|
A | C | 46 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0148others(43): Show | 47 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(44): Show |
intron_variant | MODIFIER | c.1144+724A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108233619 | ||||||
| chr12:108233650
|
A | AT | 43 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0148others(40): Show | 44 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(41): Show |
intron_variant | MODIFIER | c.1144+765dupT | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 108233650 | |||||
| chr12:108233672
|
T | C | 3 | a0001c0003t0016g0055a0001c0003t0031g0050a0001c0003t0031g0051 | 3 | HG01243.hp2 HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1144+777T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108233672 | ||||||
| chr12:108233676
|
G | A | 12 | a0001c0001t0004g0109a0001c0001t0004g0110a0001c0001t0004g0112others(9): Show | 13 | HG01243.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1144+781G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108233676 | ||||||
| chr12:108234011
|
C | T | 13 | a0001c0001t0004g0109a0001c0001t0004g0110a0001c0001t0004g0112others(10): Show | 14 | HG01243.hp2 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1144+1116C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108234011 | ||||||
| chr12:108234192
|
G | A | 1 | a0002c0009t0001g0185 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1144+1297G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108234192 | ||||||
| chr12:108234217
|
G | A | 2 | a0001c0001t0006g0175a0001c0001t0006g0242 | 2 | NA19012.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1144+1322G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108234217 | ||||||
| chr12:108234272
|
G | A | 1 | a0001c0001t0066g0072 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1144+1377G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108234272 | ||||||
| chr12:108234290
|
T | C | 93 | a0001c0001t0001g0075a0001c0001t0001g0079a0001c0001t0001g0080others(90): Show | 93 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.1144+1395T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108234290 | ||||||
| chr12:108234539
|
C | T | 13 | a0001c0001t0001g0096a0001c0001t0001g0181a0001c0001t0001g0182others(10): Show | 13 | HG00639.hp2 HG02015.hp1 HG02165.hp2 others(10): Show |
intron_variant | MODIFIER | c.1144+1644C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108234539 | ||||||
| chr12:108234842
|
G | A | 2 | a0001c0001t0027g0005a0001c0001t0037g0099 | 3 | HG02895.hp2 HG02897.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1144+1947G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108234842 | ||||||
| chr12:108234864
|
A | G | 2 | a0001c0001t0030g0130a0001c0001t0052g0131 | 2 | HG02630.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1144+1969A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108234864 | ||||||
| chr12:108234955
|
G | A | 2 | a0001c0001t0037g0062a0002c0002t0001g0180 | 2 | HG02622.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1144+2060G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108234955 | ||||||
| chr12:108234977
|
G | A | 1 | a0001c0001t0019g0137 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1144+2082G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108234977 | ||||||
| chr12:108235019
|
C | T | 12 | a0001c0001t0004g0109a0001c0001t0004g0110a0001c0001t0004g0112others(9): Show | 13 | HG01243.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1144+2124C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108235019 | ||||||
| chr12:108235199
|
A | G | 1 | a0002c0002t0003g0184 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1144+2304A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108235199 | ||||||
| chr12:108235238
|
T | C | 1 | a0001c0001t0045g0232 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1144+2343T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108235238 | ||||||
| chr12:108235316
|
G | A | 1 | a0001c0001t0037g0099 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1144+2421G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108235316 | ||||||
| chr12:108235317
|
G | A | 13 | a0001c0001t0001g0096a0001c0001t0001g0181a0001c0001t0001g0182others(10): Show | 13 | HG00639.hp2 HG02015.hp1 HG02165.hp2 others(10): Show |
intron_variant | MODIFIER | c.1144+2422G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108235317 | ||||||
| chr12:108235325
|
G | T | 13 | a0001c0001t0004g0109a0001c0001t0004g0110a0001c0001t0004g0112others(10): Show | 14 | HG01243.hp2 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1144+2430G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108235325 | ||||||
| chr12:108235524
|
C | G | 1 | a0002c0002t0001g0206 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1144+2629C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108235524 | ||||||
| chr12:108235792
|
T | G | 1 | a0001c0001t0002g0179 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1144+2897T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108235792 | ||||||
| chr12:108235874
|
G | A | 1 | a0002c0002t0001g0220 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1144+2979G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108235874 | ||||||
| chr12:108235882
|
A | G | 202 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(199): Show | 205 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.1144+2987A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108235882 | ||||||
| chr12:108235965
|
G | A | 1 | a0001c0003t0031g0050 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1144+3070G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108235965 | ||||||
| chr12:108236003
|
G | A | 50 | a0001c0001t0001g0252a0001c0001t0001g0258a0001c0001t0003g0253others(47): Show | 50 | HG00280.hp2 HG00423.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.1144+3108G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108236003 | ||||||
| chr12:108236004
|
C | A | 1 | a0001c0001t0045g0232 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1144+3109C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108236004 | ||||||
| chr12:108236011
|
C | T | 1 | a0001c0001t0041g0111 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1144+3116C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108236011 | ||||||
| chr12:108236051
|
G | A | 1 | a0001c0001t0045g0232 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1144+3156G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108236051 | ||||||
| chr12:108236531
|
C | T | 1 | a0001c0001t0073g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1144+3636C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108236531 | ||||||
| chr12:108236553
|
C | T | 1 | a0001c0003t0016g0055 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1144+3658C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108236553 | ||||||
| chr12:108236582
|
TTC | T | 54 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0148others(51): Show | 56 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.1144+3703_1144+370 others(6): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 108236582 | |||||
| chr12:108236600
|
A | C | 1 | a0007c0011t0004g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1144+3705A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108236600 | ||||||
| chr12:108236837
|
C | T | 13 | a0001c0001t0004g0109a0001c0001t0004g0110a0001c0001t0004g0112others(10): Show | 14 | HG01243.hp2 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1145-3507C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108236837 | ||||||
| chr12:108237066
|
C | T | 1 | a0006c0007t0023g0020 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1145-3278C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108237066 | ||||||
| chr12:108237212
|
C | T | 186 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(183): Show | 188 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.1145-3132C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108237212 | ||||||
| chr12:108237270
|
G | A | 145 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0001g0079others(142): Show | 146 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.1145-3074G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108237270 | ||||||
| chr12:108237417
|
G | T | 1 | a0001c0001t0022g0241 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1145-2927G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108237417 | ||||||
| chr12:108237439
|
G | A | 41 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0148others(38): Show | 42 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.1145-2905G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108237439 | ||||||
| chr12:108237505
|
C | T | 16 | a0001c0001t0001g0073a0001c0001t0001g0227a0001c0001t0001g0228others(13): Show | 17 | HG01168.hp1 HG01169.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1145-2839C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108237505 | ||||||
| chr12:108237783
|
C | G | 2 | a0001c0001t0015g0156a0001c0001t0022g0155 | 2 | HG02055.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1145-2561C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108237783 | ||||||
| chr12:108238525
|
G | A | 1 | a0001c0001t0073g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1145-1819G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108238525 | ||||||
| chr12:108238698
|
T | A | 1 | a0001c0001t0073g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1145-1646T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108238698 | ||||||
| chr12:108238866
|
G | A | 3 | a0003c0004t0025g0053a0003c0004t0025g0054a0003c0004t0074g0226 | 3 | HG02109.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1145-1478G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108238866 | ||||||
| chr12:108239245
|
C | T | 6 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0013g0213others(3): Show | 6 | HG00639.hp1 HG01074.hp2 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.1145-1099C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108239245 | ||||||
| chr12:108239281
|
T | C | 28 | a0001c0001t0001g0154a0001c0001t0001g0205a0001c0001t0002g0142others(25): Show | 29 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(26): Show |
intron_variant | MODIFIER | c.1145-1063T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108239281 | ||||||
| chr12:108239486
|
C | T | 2 | a0001c0001t0032g0035a0001c0001t0032g0036 | 2 | HG01257.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.1145-858C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108239486 | ||||||
| chr12:108239515
|
C | T | 1 | a0001c0001t0072g0108 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1145-829C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108239515 | ||||||
| chr12:108239563
|
A | G | 278 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(275): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.1145-781A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108239563 | ||||||
| chr12:108239582
|
C | T | 12 | a0001c0001t0011g0056a0001c0001t0016g0044a0001c0001t0025g0033others(9): Show | 12 | HG01109.hp1 HG01943.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1145-762C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108239582 | ||||||
| chr12:108239719
|
T | C | 4 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0254others(1): Show | 4 | HG01884.hp2 HG01891.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1145-625T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108239719 | ||||||
| chr12:108239735
|
G | A | 163 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0075others(160): Show | 165 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.1145-609G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108239735 | ||||||
| chr12:108239766
|
C | G | 220 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(217): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1145-578C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108239766 | ||||||
| chr12:108239872
|
C | A | 101 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0075others(98): Show | 102 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.1145-472C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108239872 | ||||||
| chr12:108239996
|
C | G | 146 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(143): Show | 148 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.1145-348C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108239996 | ||||||
| chr12:108240001
|
G | A | 5 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0013g0213others(2): Show | 5 | HG00639.hp1 HG01074.hp2 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.1145-343G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108240001 | ||||||
| chr12:108240026
|
C | G | 1 | a0001c0001t0001g0080 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1145-318C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108240026 | ||||||
| chr12:108240091
|
A | C | 1 | a0001c0001t0005g0264 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1145-253A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108240091 | ||||||
| chr12:108240228
|
C | T | 1 | a0002c0002t0018g0082 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1145-116C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 7/8 | chr12 | 108240228 | ||||||
| chr12:108240554
|
G | C | 1 | a0001c0001t0072g0108 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1345+10G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108240554 | ||||||
| chr12:108240963
|
T | C | 1 | a0007c0011t0004g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1345+419T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108240963 | ||||||
| chr12:108241081
|
A | G | 168 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0001g0079others(165): Show | 171 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.1345+537A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108241081 | ||||||
| chr12:108241108
|
ATCATTTC others(34): Show |
A | 1 | a0001c0001t0056g0016 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1345+568_1345+608d others(43): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr12 | 108241108 | |||||
| chr12:108241319
|
G | A | 15 | a0001c0001t0001g0096a0001c0001t0001g0181a0001c0001t0001g0182others(12): Show | 15 | HG00597.hp1 HG00597.hp2 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.1345+775G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108241319 | ||||||
| chr12:108241455
|
C | T | 169 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0001g0079others(166): Show | 172 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.1345+911C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108241455 | ||||||
| chr12:108241652
|
C | A | 6 | a0001c0001t0037g0062a0001c0003t0016g0055a0001c0003t0021g0245others(3): Show | 6 | HG01243.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1345+1108C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108241652 | ||||||
| chr12:108241683
|
G | A | 110 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0075others(107): Show | 111 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.1345+1139G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108241683 | ||||||
| chr12:108241699
|
T | C | 50 | a0001c0001t0002g0105a0001c0001t0002g0146a0001c0001t0002g0179others(47): Show | 52 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.1345+1155T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108241699 | ||||||
| chr12:108241723
|
A | C | 1 | a0001c0001t0033g0049 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1345+1179A>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108241723 | ||||||
| chr12:108241839
|
G | A | 2 | a0001c0001t0010g0129a0007c0011t0004g0097 | 2 | HG03041.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1345+1295G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108241839 | ||||||
| chr12:108241868
|
T | A | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG01074.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.1345+1324T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108241868 | ||||||
| chr12:108242004
|
T | C | 1 | a0001c0001t0003g0253 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1345+1460T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108242004 | ||||||
| chr12:108242038
|
G | A | 6 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0254others(3): Show | 6 | HG01884.hp2 HG01891.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1345+1494G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108242038 | ||||||
| chr12:108242100
|
G | A | 1 | a0003c0004t0025g0053 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1345+1556G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108242100 | ||||||
| chr12:108242149
|
G | C | 1 | a0001c0001t0011g0056 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1345+1605G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108242149 | ||||||
| chr12:108242155
|
C | T | 4 | a0001c0001t0004g0124a0001c0001t0012g0025a0001c0001t0012g0030others(1): Show | 4 | HG01943.hp1 HG02135.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.1345+1611C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108242155 | ||||||
| chr12:108242236
|
T | A | 2 | a0001c0001t0010g0129a0007c0011t0004g0097 | 2 | HG03041.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1345+1692T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108242236 | ||||||
| chr12:108242293
|
G | A | 46 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0205others(43): Show | 48 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(45): Show |
intron_variant | MODIFIER | c.1345+1749G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108242293 | ||||||
| chr12:108242384
|
A | G | 1 | a0001c0010t0049g0239 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1345+1840A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108242384 | ||||||
| chr12:108242396
|
G | T | 18 | a0001c0001t0001g0096a0001c0001t0001g0181a0001c0001t0001g0182others(15): Show | 18 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.1345+1852G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108242396 | ||||||
| chr12:108242536
|
A | G | 85 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0096others(82): Show | 87 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1345+1992A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108242536 | ||||||
| chr12:108242544
|
G | A | 8 | a0001c0001t0033g0049a0001c0001t0045g0232a0001c0001t0054g0126others(5): Show | 8 | HG01243.hp2 HG02451.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1345+2000G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108242544 | ||||||
| chr12:108242555
|
C | T | 3 | a0001c0001t0002g0179a0001c0001t0005g0115a0001c0001t0005g0116 | 3 | HG01257.hp2 HG01258.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1345+2011C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108242555 | ||||||
| chr12:108242606
|
G | C | 1 | a0001c0001t0073g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1345+2062G>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108242606 | ||||||
| chr12:108242654
|
G | A | 2 | a0001c0001t0010g0129a0007c0011t0004g0097 | 2 | HG03041.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1345+2110G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108242654 | ||||||
| chr12:108242689
|
G | A | 75 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0254others(72): Show | 77 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.1345+2145G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108242689 | ||||||
| chr12:108242789
|
C | T | 3 | a0002c0002t0001g0145a0002c0002t0001g0208a0002c0002t0009g0200 | 3 | NA18945.hp1 NA18971.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.1345+2245C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108242789 | ||||||
| chr12:108242843
|
A | G | 113 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(110): Show | 116 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.1345+2299A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108242843 | ||||||
| chr12:108242862
|
C | T | 79 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0096others(76): Show | 81 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.1345+2318C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108242862 | ||||||
| chr12:108243117
|
C | T | 1 | a0001c0001t0073g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1345+2573C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108243117 | ||||||
| chr12:108243118
|
T | C | 1 | a0001c0001t0073g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1345+2574T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108243118 | ||||||
| chr12:108243120
|
T | C | 1 | a0001c0001t0073g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1345+2576T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108243120 | ||||||
| chr12:108243124
|
G | A | 18 | a0001c0001t0001g0096a0001c0001t0001g0181a0001c0001t0001g0182others(15): Show | 18 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.1345+2580G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108243124 | ||||||
| chr12:108243151
|
T | G | 3 | a0001c0001t0007g0039a0001c0001t0024g0029a0001c0001t0024g0042 | 3 | HG03490.hp2 HG03492.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1345+2607T>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108243151 | ||||||
| chr12:108243255
|
T | C | 6 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0254others(3): Show | 6 | HG01884.hp2 HG01891.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1345+2711T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108243255 | ||||||
| chr12:108243330
|
C | T | 77 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0096others(74): Show | 79 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.1345+2786C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108243330 | ||||||
| chr12:108243399
|
G | A | 1 | a0001c0001t0004g0178 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1345+2855G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108243399 | ||||||
| chr12:108243439
|
G | T | 1 | a0002c0002t0004g0071 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1345+2895G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108243439 | ||||||
| chr12:108243691
|
C | T | 1 | a0001c0001t0030g0130 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1345+3147C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108243691 | ||||||
| chr12:108243727
|
G | A | 3 | a0001c0003t0016g0055a0001c0003t0031g0050a0001c0003t0031g0051 | 3 | HG01243.hp2 HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1345+3183G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108243727 | ||||||
| chr12:108243792
|
G | A | 6 | a0001c0001t0025g0033a0001c0001t0035g0259a0001c0001t0036g0068others(3): Show | 6 | HG01891.hp1 HG01943.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1345+3248G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108243792 | ||||||
| chr12:108243935
|
A | G | 79 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0096others(76): Show | 81 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.1345+3391A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108243935 | ||||||
| chr12:108244145
|
G | A | 1 | a0002c0002t0002g0270 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1345+3601G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108244145 | ||||||
| chr12:108244171
|
G | T | 46 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0205others(43): Show | 48 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(45): Show |
intron_variant | MODIFIER | c.1345+3627G>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108244171 | ||||||
| chr12:108244224
|
G | A | 53 | a0001c0001t0002g0105a0001c0001t0002g0146a0001c0001t0002g0179others(50): Show | 55 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.1345+3680G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108244224 | ||||||
| chr12:108244386
|
A | G | 6 | a0001c0001t0025g0033a0001c0001t0035g0259a0001c0001t0036g0068others(3): Show | 6 | HG01891.hp1 HG01943.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1346-3605A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108244386 | ||||||
| chr12:108244409
|
G | A | 1 | a0005c0006t0016g0046 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1346-3582G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108244409 | ||||||
| chr12:108244469
|
C | T | 2 | a0001c0001t0007g0048a0001c0001t0057g0047 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1346-3522C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108244469 | ||||||
| chr12:108244582
|
G | A | 1 | a0001c0001t0073g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1346-3409G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108244582 | ||||||
| chr12:108244604
|
C | T | 1 | a0001c0001t0067g0067 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1346-3387C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108244604 | ||||||
| chr12:108244636
|
G | A | 1 | a0001c0001t0044g0160 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1346-3355G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108244636 | ||||||
| chr12:108244659
|
A | G | 1 | a0001c0001t0018g0059 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1346-3332A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108244659 | ||||||
| chr12:108245137
|
T | C | 2 | a0001c0001t0029g0235a0001c0001t0029g0236 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1346-2854T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108245137 | ||||||
| chr12:108245216
|
G | A | 266 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(263): Show | 271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.1346-2775G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108245216 | ||||||
| chr12:108245239
|
C | CT | 106 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(103): Show | 109 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.1346-2751dupT | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr12 | 108245239 | |||||
| chr12:108245286
|
A | G | 2 | a0001c0001t0007g0027a0001c0001t0007g0028 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1346-2705A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108245286 | ||||||
| chr12:108245893
|
A | G | 116 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(113): Show | 119 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.1346-2098A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108245893 | ||||||
| chr12:108245915
|
C | T | 6 | a0001c0001t0001g0205a0001c0001t0003g0143a0001c0001t0008g0001others(3): Show | 7 | HG00609.hp2 NA18944.hp1 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.1346-2076C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108245915 | ||||||
| chr12:108245951
|
T | A | 2 | a0001c0001t0010g0004a0001c0001t0043g0004 | 2 | HG02258.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1346-2040T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108245951 | ||||||
| chr12:108246096
|
T | A | 1 | a0001c0001t0002g0076 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1346-1895T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108246096 | ||||||
| chr12:108246179
|
C | T | 1 | a0001c0001t0010g0129 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1346-1812C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108246179 | ||||||
| chr12:108246190
|
C | T | 1 | a0001c0001t0012g0040 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1346-1801C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108246190 | ||||||
| chr12:108246336
|
C | T | 1 | a0001c0001t0017g0011 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1346-1655C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108246336 | ||||||
| chr12:108246388
|
G | A | 5 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0254others(2): Show | 5 | HG01884.hp2 HG01891.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1346-1603G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108246388 | ||||||
| chr12:108246402
|
CTTGTGAG others(3): Show |
C | 2 | a0001c0001t0010g0129a0007c0011t0004g0097 | 2 | HG03041.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1346-1588_1346-157 others(14): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108246402 | ||||||
| chr12:108246405
|
G | A | 1 | a0001c0001t0060g0274 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1346-1586G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108246405 | ||||||
| chr12:108246521
|
C | G | 20 | a0001c0001t0001g0073a0001c0001t0001g0227a0001c0001t0001g0228others(17): Show | 21 | HG01167.hp1 HG01168.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.1346-1470C>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108246521 | ||||||
| chr12:108246536
|
C | T | 1 | a0001c0001t0051g0158 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1346-1455C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108246536 | ||||||
| chr12:108246537
|
C | T | 3 | a0001c0001t0001g0075a0001c0001t0004g0122a0002c0002t0038g0074 | 3 | HG01978.hp1 HG02148.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.1346-1454C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108246537 | ||||||
| chr12:108246686
|
C | A | 1 | a0001c0001t0010g0129 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1346-1305C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108246686 | ||||||
| chr12:108246687
|
A | G | 2 | a0001c0001t0011g0056a0001c0001t0015g0156 | 2 | HG02055.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1346-1304A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108246687 | ||||||
| chr12:108246737
|
AGAT | A | 17 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(14): Show | 17 | HG01167.hp1 HG01168.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.1346-1247_1346-124 others(7): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr12 | 108246737 | |||||
| chr12:108246787
|
C | T | 2 | a0001c0001t0037g0099a0001c0001t0073g0061 | 2 | HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1346-1204C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108246787 | ||||||
| chr12:108246931
|
T | C | 2 | a0002c0002t0001g0195a0002c0002t0001g0212 | 2 | HG00738.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1346-1060T>C | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108246931 | ||||||
| chr12:108247000
|
A | G | 1 | a0001c0001t0026g0093 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1346-991A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108247000 | ||||||
| chr12:108247014
|
G | A | 269 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(266): Show | 274 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.1346-977G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108247014 | ||||||
| chr12:108247233
|
G | A | 2 | a0001c0001t0044g0160a0001c0001t0061g0260 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1346-758G>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108247233 | ||||||
| chr12:108247352
|
CAT | C | 6 | a0001c0001t0021g0085a0001c0001t0037g0062a0001c0001t0046g0152others(3): Show | 6 | HG01109.hp1 HG02280.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1346-637_1346-636d others(4): Show |
WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr12 | 108247352 | |||||
| chr12:108247356
|
A | G | 1 | a0001c0001t0021g0085 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1346-635A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108247356 | ||||||
| chr12:108247533
|
A | G | 1 | a0001c0001t0010g0129 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1346-458A>G | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108247533 | ||||||
| chr12:108247595
|
A | T | 1 | a0007c0011t0004g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1346-396A>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108247595 | ||||||
| chr12:108247814
|
C | A | 3 | a0001c0001t0001g0096a0001c0001t0001g0181a0001c0001t0001g0182 | 3 | HG03688.hp1 HG03831.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1346-177C>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108247814 | ||||||
| chr12:108247847
|
T | A | 2 | a0001c0001t0001g0079a0001c0001t0056g0016 | 2 | HG03834.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1346-144T>A | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108247847 | ||||||
| chr12:108247954
|
C | T | 1 | a0001c0003t0031g0050 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1346-37C>T | WSCD2 | ENSG00000075035.10 | transcript | ENST00000547525.6 | protein_coding | 8/8 | chr12 | 108247954 |