Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 7477 |
|---|---|
| ensemblid | ENSG00000188064.10 |
| hgncid | 12787 |
| symbol | WNT7B |
| name | Wnt family member 7B |
| refseq_nuc | NM_058238.3 |
| refseq_prot | NP_478679.1 |
| ensembl_nuc | ENST00000339464.9 |
| ensembl_prot | ENSP00000341032.4 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 45920366 |
| end | 45977162 |
| strand | - |
| ver | v1.2 |
| region | chr22:45920366-45977162 |
| region5000 | chr22:45915366-45982162 |
| regionname0 | WNT7B_chr22_45920366_45977162 |
| regionname5000 | WNT7B_chr22_45915366_45982162 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 349 | 348 | 90 | 70 | 122 | 18 | 46 | 86 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0002 | 0/0 | 349 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0003 | 0/0 | 146 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1050 | 323 | 71 | 68 | 119 | 18 | 45 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| c0002 | 0/0 | 1050 | 9 | 8 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| c0003 | 0/0 | 1050 | 4 | 4 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| c0004 | 0/0 | 1050 | 2 | 2 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| c0005 | 0/0 | 1050 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| c0006 | 0/0 | 1050 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| c0007 | 0/0 | 1050 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| c0008 | 0/0 | 1050 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| c0009 | 0/0 | 1050 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| c0010 | 0/0 | 1050 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| c0011 | 0/0 | 1050 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| c0012 | 0/0 | 1050 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| c0013 | 0/0 | 1050 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| c0014 | 0/0 | 1050 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| c0015 | 0/0 | 1050 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| c0016 | 0/0 | 1050 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 2899 | 93 | 21 | 20 | 32 | 5 | 14 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0002 | 0/0 | 2899 | 83 | 1 | 10 | 59 | 5 | 8 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0003 | 0/0 | 2899 | 19 | 1 | 1 | 14 | 0 | 3 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0004 | 0/0 | 2899 | 16 | 0 | 5 | 3 | 0 | 8 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0005 | 0/1 | 2889 | 12 | 3 | 5 | 0 | 0 | 3 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0006 | 0/0 | 2889 | 11 | 2 | 8 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0007 | 0/0 | 2875 | 10 | 8 | 2 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0008 | 0/0 | 2899 | 5 | 0 | 0 | 4 | 1 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0009 | 0/0 | 2875 | 5 | 5 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0010 | 0/0 | 2901 | 4 | 0 | 1 | 0 | 1 | 2 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0011 | 0/0 | 2901 | 4 | 0 | 0 | 1 | 2 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0012 | 0/0 | 2899 | 4 | 4 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0013 | 0/0 | 2889 | 4 | 0 | 2 | 0 | 1 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0014 | 0/0 | 2899 | 4 | 4 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0015 | 0/0 | 2899 | 3 | 0 | 0 | 3 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0016 | 0/0 | 2899 | 3 | 0 | 0 | 3 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0017 | 0/0 | 2875 | 3 | 3 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0018 | 0/0 | 2899 | 3 | 2 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0019 | 0/0 | 2899 | 3 | 3 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0020 | 0/0 | 2899 | 3 | 3 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0021 | 0/0 | 2899 | 3 | 3 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0022 | 0/0 | 2889 | 2 | 0 | 2 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0023 | 0/0 | 2875 | 2 | 2 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0024 | 0/0 | 2899 | 2 | 2 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0025 | 0/0 | 2899 | 2 | 2 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0026 | 0/0 | 2889 | 2 | 0 | 0 | 0 | 1 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0027 | 0/0 | 2889 | 2 | 1 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0028 | 0/0 | 2889 | 2 | 0 | 2 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0029 | 0/0 | 2899 | 2 | 2 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0030 | 0/0 | 2875 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0031 | 0/0 | 2899 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0032 | 0/0 | 2899 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0033 | 0/0 | 2899 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0034 | 0/0 | 2875 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0035 | 0/0 | 2899 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0036 | 0/0 | 2889 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0037 | 0/0 | 2899 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0038 | 0/0 | 2899 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0039 | 0/0 | 2889 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0040 | 0/0 | 2899 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0041 | 0/0 | 2899 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0042 | 0/0 | 2899 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0043 | 0/0 | 2899 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0044 | 0/0 | 2899 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0045 | 0/0 | 2899 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0046 | 0/0 | 2899 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0047 | 0/0 | 2889 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0048 | 0/0 | 2899 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0049 | 0/0 | 2899 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0050 | 0/0 | 2901 | 1 | 0 | 0 | 0 | 1 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0051 | 0/0 | 2889 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0052 | 0/0 | 2899 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0053 | 0/0 | 2899 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0054 | 0/0 | 2899 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0055 | 0/0 | 2899 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0056 | 0/0 | 2875 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0057 | 0/0 | 2899 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0058 | 0/0 | 2899 | 1 | 0 | 0 | 0 | 1 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0059 | 0/0 | 2899 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0060 | 0/0 | 2887 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0061 | 0/0 | 2899 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0062 | 0/0 | 2899 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0063 | 0/0 | 2899 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0064 | 0/0 | 2899 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0065 | 0/0 | 2899 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0066 | 0/0 | 2875 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0067 | 0/0 | 2899 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| t0068 | 0/0 | 2899 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| 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 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0207 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0301 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1050 | 323 | 71 | 68 | 119 | 18 | 45 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0002 | 0/0 | 1050 | 9 | 8 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0003 | 0/0 | 1050 | 4 | 4 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0004 | 0/0 | 1050 | 2 | 2 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0005 | 0/0 | 1050 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0007 | 0/0 | 1050 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0008 | 0/0 | 1050 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0009 | 0/0 | 1050 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0010 | 0/0 | 1050 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0011 | 0/0 | 1050 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0012 | 0/0 | 1050 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0013 | 0/0 | 1050 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0014 | 0/0 | 1050 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0016 | 0/0 | 1050 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0002c0015 | 0/0 | 1050 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0003c0006 | 0/0 | 1050 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3948 | 89 | 19 | 19 | 31 | 5 | 14 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0002 | 0/0 | 3948 | 80 | 1 | 10 | 57 | 5 | 7 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0003 | 0/0 | 3948 | 19 | 1 | 1 | 14 | 0 | 3 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0004 | 0/0 | 3948 | 16 | 0 | 5 | 3 | 0 | 8 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0005 | 0/1 | 3938 | 12 | 3 | 5 | 0 | 0 | 3 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0006 | 0/0 | 3938 | 11 | 2 | 8 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0007 | 0/0 | 3924 | 7 | 5 | 2 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0008 | 0/0 | 3948 | 5 | 0 | 0 | 4 | 1 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0009 | 0/0 | 3924 | 4 | 4 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0010 | 0/0 | 3950 | 4 | 0 | 1 | 0 | 1 | 2 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0011 | 0/0 | 3950 | 4 | 0 | 0 | 1 | 2 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0012 | 0/0 | 3948 | 4 | 4 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0013 | 0/0 | 3938 | 4 | 0 | 2 | 0 | 1 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0014 | 0/0 | 3948 | 3 | 3 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0015 | 0/0 | 3948 | 3 | 0 | 0 | 3 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0016 | 0/0 | 3948 | 3 | 0 | 0 | 3 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0017 | 0/0 | 3924 | 3 | 3 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0018 | 0/0 | 3948 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0019 | 0/0 | 3948 | 3 | 3 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0020 | 0/0 | 3948 | 2 | 2 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0022 | 0/0 | 3938 | 2 | 0 | 2 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0023 | 0/0 | 3924 | 2 | 2 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0024 | 0/0 | 3948 | 2 | 2 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0025 | 0/0 | 3948 | 2 | 2 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0026 | 0/0 | 3938 | 2 | 0 | 0 | 0 | 1 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0027 | 0/0 | 3938 | 2 | 1 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0028 | 0/0 | 3938 | 2 | 0 | 2 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0029 | 0/0 | 3948 | 2 | 2 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0031 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0032 | 0/0 | 3948 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0033 | 0/0 | 3948 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0035 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0036 | 0/0 | 3938 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0038 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0039 | 0/0 | 3938 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0041 | 0/0 | 3948 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0042 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0043 | 0/0 | 3948 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0044 | 0/0 | 3948 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0045 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0046 | 0/0 | 3948 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0047 | 0/0 | 3938 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0048 | 0/0 | 3948 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0050 | 0/0 | 3950 | 1 | 0 | 0 | 0 | 1 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0051 | 0/0 | 3938 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0055 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0056 | 0/0 | 3924 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0057 | 0/0 | 3948 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0058 | 0/0 | 3948 | 1 | 0 | 0 | 0 | 1 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0059 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0060 | 0/0 | 3936 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0061 | 0/0 | 3948 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0062 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0063 | 0/0 | 3948 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0065 | 0/0 | 3948 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0066 | 0/0 | 3924 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0067 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0001t0068 | 0/0 | 3948 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0002t0001 | 0/0 | 3948 | 2 | 2 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0002t0007 | 0/0 | 3924 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0002t0014 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0002t0018 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0002t0020 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0002t0030 | 0/0 | 3924 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0002t0037 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0002t0052 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0003t0021 | 0/0 | 3948 | 2 | 2 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0003t0040 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0003t0053 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0004t0007 | 0/0 | 3924 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0004t0034 | 0/0 | 3924 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0005t0001 | 0/0 | 3948 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0007t0054 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0008t0002 | 0/0 | 3948 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0009t0002 | 0/0 | 3948 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0010t0002 | 0/0 | 3948 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0011t0049 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0012t0001 | 0/0 | 3948 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0013t0021 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0014t0018 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0001c0016t0007 | 0/0 | 3924 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0002c0015t0009 | 0/0 | 3924 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| a0003c0006t0064 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | copy fasta | chr22 | 45915366 | 45982162 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0207 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0003g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0004g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0004g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0004g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0004g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0004g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0004g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0004g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0004g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0004g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0004g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0004g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0004g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0004g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0004g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0004g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0005g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0005g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0005g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0005g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0005g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0005g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0005g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0005g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0005g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0005g0301 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0005g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0005g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0006g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0006g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0006g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0006g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0006g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0006g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0006g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0006g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0006g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0006g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0006g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0007g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0007g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0007g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0007g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0007g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0007g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0007g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0008g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0008g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0008g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0008g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0008g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0009g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0009g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0009g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0009g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0010g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0010g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0010g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0010g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0011g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0011g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0011g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0011g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0012g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0012g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0012g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0012g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0013g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0013g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0013g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0013g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0014g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0014g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0014g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0015g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0015g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0015g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0016g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0016g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0016g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0017g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0017g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0017g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0018g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0019g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0019g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0019g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0020g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0020g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0022g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0022g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0023g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0023g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0024g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0024g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0025g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0025g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0026g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0026g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0027g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0027g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0028g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0028g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0029g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0029g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0031g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0032g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0033g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0035g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0036g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0038g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0039g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0041g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0042g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0043g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0044g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0045g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0046g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0047g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0048g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0050g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0051g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0055g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0056g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0057g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0058g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0059g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0060g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0061g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0062g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0063g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0065g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0066g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0067g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0068g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0002t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0002t0007g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0002t0014g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0002t0018g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0002t0020g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0002t0030g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0002t0037g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0002t0052g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0003t0021g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0003t0021g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0003t0040g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0003t0053g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0004t0007g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0004t0034g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0005t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0007t0054g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0008t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0009t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0010t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0011t0049g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0012t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0013t0021g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0014t0018g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0016t0007g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0002c0015t0009g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0003c0006t0064g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0166 | EUR | GBR | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0177 | EUR | GBR | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0082 | EUR | GBR | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0054 | EUR | GBR | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0028 | EUR | FIN | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG00280 | hp2 | a0001 | c0001 | t0010 | g0029 | EUR | FIN | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG00323 | hp1 | a0001 | c0001 | t0011 | g0164 | EUR | FIN | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0179 | EUR | FIN | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | CHS | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | CHS | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | CHS | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | CHS | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | CHS | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG00597 | hp1 | a0001 | c0010 | t0002 | g0097 | EAS | CHS | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | CHS | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | CHS | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | CHS | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG00621 | hp1 | a0001 | c0001 | t0004 | g0275 | EAS | CHS | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | CHS | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0203 | AMR | PUR | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0335 | AMR | PUR | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG00642 | hp1 | a0001 | c0002 | t0030 | g0003 | AMR | PUR | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0100 | AMR | PUR | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | CHS | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | CHS | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG00733 | hp2 | a0001 | c0001 | t0013 | g0318 | AMR | PUR | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG00735 | hp1 | a0001 | c0001 | t0039 | g0074 | AMR | PUR | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0215 | AMR | PUR | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG00738 | hp2 | a0001 | c0012 | t0001 | g0255 | AMR | PUR | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | PUR | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG00741 | hp2 | a0001 | c0001 | t0004 | g0173 | AMR | PUR | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01069 | hp1 | a0001 | c0001 | t0006 | g0059 | AMR | PUR | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | PUR | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01081 | hp1 | a0001 | c0001 | t0013 | g0317 | AMR | PUR | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0101 | AMR | PUR | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01099 | hp1 | a0001 | c0001 | t0027 | g0256 | AMR | PUR | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01106 | hp1 | a0001 | c0001 | t0051 | g0307 | AMR | PUR | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0323 | AMR | PUR | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01167 | hp2 | a0001 | c0001 | t0007 | g0161 | AMR | PUR | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01169 | hp1 | a0001 | c0001 | t0007 | g0162 | AMR | PUR | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01169 | hp2 | a0001 | c0001 | t0033 | g0036 | AMR | PUR | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01175 | hp1 | a0001 | c0001 | t0060 | g0316 | AMR | PUR | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01175 | hp2 | a0001 | c0001 | t0010 | g0089 | AMR | PUR | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0095 | AMR | PUR | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01192 | hp2 | a0001 | c0001 | t0057 | g0296 | AMR | PUR | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01243 | hp1 | a0001 | c0001 | t0048 | g0326 | AMR | PUR | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01243 | hp2 | a0001 | c0001 | t0018 | g0327 | AMR | PUR | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01255 | hp1 | a0001 | c0001 | t0005 | g0149 | AMR | CLM | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0300 | AMR | CLM | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01256 | hp1 | a0001 | c0001 | t0022 | g0030 | AMR | CLM | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01256 | hp2 | a0001 | c0001 | t0028 | g0297 | AMR | CLM | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01258 | hp1 | a0001 | c0001 | t0028 | g0298 | AMR | CLM | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0081 | AMR | CLM | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01346 | hp1 | a0001 | c0001 | t0006 | g0117 | AMR | CLM | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01346 | hp2 | a0001 | c0001 | t0022 | g0093 | AMR | CLM | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01358 | hp2 | a0001 | c0001 | t0005 | g0249 | AMR | CLM | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | CLM | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | CLM | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01433 | hp2 | a0001 | c0001 | t0065 | g0347 | AMR | CLM | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01496 | hp1 | a0001 | c0001 | t0006 | g0121 | AMR | CLM | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01496 | hp2 | a0001 | c0001 | t0068 | g0348 | AMR | CLM | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0106 | EUR | IBS | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01515 | hp2 | a0001 | c0001 | t0058 | g0236 | EUR | IBS | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01516 | hp1 | a0001 | c0001 | t0050 | g0235 | EUR | IBS | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0308 | EUR | IBS | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0105 | EUR | IBS | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0309 | EUR | IBS | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01884 | hp1 | a0001 | c0003 | t0021 | g0311 | AFR | ACB | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01884 | hp2 | a0001 | c0001 | t0027 | g0209 | AFR | ACB | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01891 | hp1 | a0001 | c0001 | t0042 | g0013 | AFR | ACB | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01891 | hp2 | a0001 | c0011 | t0049 | g0330 | AFR | ACB | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01928 | hp1 | a0001 | c0001 | t0005 | g0279 | AMR | PEL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01928 | hp2 | a0001 | c0001 | t0006 | g0109 | AMR | PEL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0302 | AMR | PEL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0108 | AMR | PEL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01943 | hp1 | a0001 | c0001 | t0063 | g0344 | AMR | PEL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0077 | AMR | PEL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01952 | hp1 | a0001 | c0001 | t0006 | g0107 | AMR | PEL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0062 | AMR | PEL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | PEL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0102 | AMR | PEL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01978 | hp2 | a0001 | c0001 | t0006 | g0088 | AMR | PEL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0119 | AMR | PEL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01981 | hp2 | a0001 | c0001 | t0006 | g0090 | AMR | PEL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0110 | AMR | PEL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02004 | hp2 | a0001 | c0001 | t0005 | g0304 | AMR | PEL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | KHV | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02015 | hp2 | a0001 | c0001 | t0004 | g0168 | EAS | KHV | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | KHV | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02055 | hp1 | a0001 | c0001 | t0007 | g0315 | AFR | ACB | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0325 | AFR | ACB | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02056 | hp1 | a0001 | c0001 | t0008 | g0142 | EAS | KHV | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02056 | hp2 | a0001 | c0001 | t0008 | g0134 | EAS | KHV | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02071 | hp1 | a0001 | c0005 | t0001 | g0199 | EAS | KHV | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | KHV | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | KHV | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | KHV | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | KHV | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02145 | hp1 | a0001 | c0001 | t0055 | g0176 | AFR | ACB | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02145 | hp2 | a0001 | c0001 | t0023 | g0014 | AFR | ACB | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02148 | hp2 | a0001 | c0001 | t0006 | g0025 | AMR | PEL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02155 | hp1 | a0001 | c0001 | t0043 | g0103 | EAS | CDX | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | CDX | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | CDX | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | CDX | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02257 | hp2 | a0001 | c0003 | t0021 | g0229 | AFR | ACB | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02258 | hp1 | a0001 | c0004 | t0034 | g0011 | AFR | ACB | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02258 | hp2 | a0001 | c0002 | t0020 | g0336 | AFR | ACB | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02280 | hp1 | a0001 | c0001 | t0035 | g0018 | AFR | ACB | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02280 | hp2 | a0001 | c0001 | t0024 | g0010 | AFR | ACB | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02293 | hp1 | a0001 | c0001 | t0005 | g0202 | AMR | PEL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0306 | AMR | PEL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0303 | AMR | PEL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02300 | hp2 | a0001 | c0001 | t0004 | g0204 | AMR | PEL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02451 | hp2 | a0001 | c0001 | t0020 | g0158 | AFR | ACB | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02572 | hp1 | a0001 | c0003 | t0053 | g0310 | AFR | GWD | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0283 | AFR | GWD | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0044 | SAS | PJL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02622 | hp1 | a0001 | c0001 | t0059 | g0156 | AFR | GWD | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | GWD | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02630 | hp1 | a0001 | c0001 | t0019 | g0332 | AFR | GWD | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02647 | hp1 | a0001 | c0001 | t0019 | g0290 | AFR | GWD | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02647 | hp2 | a0001 | c0001 | t0020 | g0225 | AFR | GWD | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02683 | hp1 | a0001 | c0001 | t0005 | g0293 | SAS | PJL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0281 | SAS | PJL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02698 | hp1 | a0001 | c0001 | t0044 | g0147 | SAS | PJL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02698 | hp2 | a0001 | c0001 | t0004 | g0178 | SAS | PJL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02723 | hp1 | a0001 | c0001 | t0031 | g0004 | AFR | GWD | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02723 | hp2 | a0001 | c0003 | t0040 | g0046 | AFR | GWD | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02735 | hp1 | a0001 | c0001 | t0004 | g0171 | SAS | PJL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02735 | hp2 | a0001 | c0001 | t0046 | g0190 | SAS | PJL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02738 | hp1 | a0001 | c0001 | t0004 | g0200 | SAS | PJL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0053 | SAS | PJL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02809 | hp1 | a0001 | c0001 | t0038 | g0009 | AFR | GWD | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02809 | hp2 | a0001 | c0001 | t0006 | g0120 | AFR | GWD | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02818 | hp1 | a0001 | c0001 | t0005 | g0333 | AFR | GWD | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02818 | hp2 | a0001 | c0001 | t0009 | g0285 | AFR | GWD | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02886 | hp1 | a0001 | c0001 | t0012 | g0331 | AFR | GWD | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02886 | hp2 | a0001 | c0001 | t0025 | g0160 | AFR | GWD | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02895 | hp1 | a0001 | c0001 | t0017 | g0247 | AFR | GWD | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02895 | hp2 | a0001 | c0001 | t0047 | g0251 | AFR | GWD | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | GWD | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02897 | hp2 | a0001 | c0001 | t0017 | g0248 | AFR | GWD | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02965 | hp1 | a0001 | c0001 | t0007 | g0314 | AFR | ESN | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02965 | hp2 | a0001 | c0001 | t0014 | g0324 | AFR | ESN | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | ESN | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02970 | hp2 | a0001 | c0001 | t0062 | g0339 | AFR | ESN | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | ESN | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02976 | hp2 | a0001 | c0001 | t0066 | g0345 | AFR | ESN | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0094 | SAS | PJL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0232 | SAS | PJL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG03041 | hp1 | a0002 | c0015 | t0009 | g0228 | AFR | GWD | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG03041 | hp2 | a0001 | c0001 | t0009 | g0250 | AFR | GWD | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG03098 | hp1 | a0001 | c0002 | t0018 | g0157 | AFR | MSL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | MSL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG03130 | hp1 | a0001 | c0002 | t0014 | g0274 | AFR | ESN | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG03130 | hp2 | a0001 | c0007 | t0054 | g0334 | AFR | ESN | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG03139 | hp1 | a0001 | c0014 | t0018 | g0260 | AFR | ESN | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG03139 | hp2 | a0001 | c0001 | t0014 | g0254 | AFR | ESN | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG03195 | hp1 | a0001 | c0001 | t0025 | g0322 | AFR | ESN | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG03195 | hp2 | a0003 | c0006 | t0064 | g0343 | AFR | ESN | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG03209 | hp1 | a0001 | c0001 | t0067 | g0346 | AFR | MSL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG03209 | hp2 | a0001 | c0002 | t0037 | g0015 | AFR | MSL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG03225 | hp1 | a0001 | c0001 | t0014 | g0313 | AFR | MSL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG03225 | hp2 | a0001 | c0001 | t0029 | g0319 | AFR | MSL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG03239 | hp1 | a0001 | c0001 | t0005 | g0227 | SAS | PJL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG03453 | hp1 | a0001 | c0001 | t0024 | g0099 | AFR | MSL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG03453 | hp2 | a0001 | c0001 | t0012 | g0329 | AFR | MSL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG03486 | hp1 | a0001 | c0001 | t0009 | g0268 | AFR | MSL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | MSL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0221 | SAS | PJL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0287 | SAS | PJL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG03491 | hp1 | a0001 | c0001 | t0004 | g0186 | SAS | PJL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0087 | SAS | PJL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0086 | SAS | PJL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0222 | SAS | PJL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG03516 | hp1 | a0001 | c0001 | t0023 | g0017 | AFR | ESN | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0320 | AFR | ESN | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG03540 | hp1 | a0001 | c0001 | t0017 | g0257 | AFR | GWD | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG03540 | hp2 | a0001 | c0016 | t0007 | g0280 | AFR | GWD | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG03579 | hp1 | a0001 | c0001 | t0056 | g0226 | AFR | MSL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0288 | AFR | MSL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0078 | SAS | PJL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0266 | SAS | PJL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG03669 | hp2 | a0001 | c0001 | t0013 | g0286 | SAS | PJL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG03688 | hp1 | a0001 | c0001 | t0061 | g0273 | SAS | STU | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | STU | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG03704 | hp2 | a0001 | c0001 | t0011 | g0155 | SAS | PJL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG03710 | hp1 | a0001 | c0001 | t0005 | g0180 | SAS | PJL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0211 | SAS | BEB | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0006 | SAS | BEB | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0068 | SAS | BEB | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | BEB | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG03927 | hp1 | a0001 | c0001 | t0010 | g0063 | SAS | BEB | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG03927 | hp2 | a0001 | c0001 | t0010 | g0007 | SAS | BEB | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0277 | SAS | STU | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0083 | SAS | STU | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0026 | SAS | BEB | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG04184 | hp2 | a0001 | c0001 | t0036 | g0128 | SAS | BEB | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | STU | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG04199 | hp2 | a0001 | c0008 | t0002 | g0072 | SAS | STU | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG04204 | hp1 | a0001 | c0001 | t0026 | g0340 | SAS | STU | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG04204 | hp2 | a0001 | c0001 | t0032 | g0005 | SAS | STU | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | STU | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | STU | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | YRI | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18522 | hp2 | a0001 | c0001 | t0019 | g0244 | AFR | YRI | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0065 | EAS | CHB | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | CHB | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | CHB | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | CHB | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18906 | hp1 | a0001 | c0001 | t0012 | g0159 | AFR | YRI | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18906 | hp2 | a0001 | c0001 | t0007 | g0321 | AFR | YRI | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18943 | hp2 | a0001 | c0001 | t0015 | g0129 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18966 | hp1 | a0001 | c0001 | t0016 | g0032 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18969 | hp2 | a0001 | c0001 | t0016 | g0034 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18970 | hp1 | a0001 | c0001 | t0011 | g0189 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18980 | hp2 | a0001 | c0001 | t0008 | g0141 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18997 | hp2 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18999 | hp2 | a0001 | c0001 | t0004 | g0169 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0132 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA19007 | hp2 | a0001 | c0001 | t0015 | g0027 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0341 | AFR | LWK | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0163 | AFR | LWK | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | LWK | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA19043 | hp2 | a0001 | c0001 | t0012 | g0259 | AFR | LWK | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA19057 | hp1 | a0001 | c0001 | t0041 | g0130 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA19066 | hp1 | a0001 | c0001 | t0016 | g0035 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA19070 | hp1 | a0001 | c0009 | t0002 | g0067 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA19079 | hp1 | a0001 | c0001 | t0015 | g0033 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA19085 | hp2 | a0001 | c0001 | t0008 | g0039 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0139 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA19091 | hp1 | a0001 | c0001 | t0006 | g0124 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA19240 | hp1 | a0001 | c0013 | t0021 | g0337 | AFR | YRI | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA19240 | hp2 | a0001 | c0001 | t0007 | g0252 | AFR | YRI | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA20129 | hp1 | a0001 | c0002 | t0052 | g0338 | AFR | ASW | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA20129 | hp2 | a0001 | c0001 | t0045 | g0258 | AFR | ASW | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA20752 | hp1 | a0001 | c0001 | t0008 | g0122 | EUR | TSI | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA20752 | hp2 | a0001 | c0001 | t0011 | g0233 | EUR | TSI | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA20805 | hp1 | a0001 | c0001 | t0026 | g0198 | EUR | TSI | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA20805 | hp2 | a0001 | c0001 | t0013 | g0151 | EUR | TSI | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02109 | hp1 | a0001 | c0001 | t0006 | g0073 | AFR | ACB | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02109 | hp2 | a0001 | c0001 | t0007 | g0328 | AFR | ACB | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | ACB | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02486 | hp2 | a0001 | c0001 | t0009 | g0282 | AFR | ACB | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02559 | hp1 | a0001 | c0001 | t0029 | g0240 | AFR | ACB | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG02559 | hp2 | a0001 | c0004 | t0007 | g0342 | AFR | ACB | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | MSL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG03471 | hp2 | a0001 | c0002 | t0007 | g0230 | AFR | MSL | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0098 | EAS | JPT | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0114 | AFR | USA | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0224 | AFR | USA | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | LWK | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | LWK | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0005 | g0301 | REF | REF | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0207 | REF | REF | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:45931228
|
C | T | 1 | a0003 | 1 | HG03195.hp2 | stop_gained | HIGH | c.440G>A | p.Trp147* | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/4 | 848/3948 | 440/1050 | 147/349 | chr22 | 45931228 | ||
| chr22:45931242
|
G | C | 1 | a0002 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.426C>G | p.Asn142Lys | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/4 | 834/3948 | 426/1050 | 142/349 | chr22 | 45931242 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:45922859
|
C | T | 1 | a0001c0009 | 1 | NA19070.hp1 | synonymous_variant | LOW | c.1047G>A | p.Lys349Lys | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 1455/3948 | 1047/1050 | 349/349 | chr22 | 45922859 | ||
| chr22:45922877
|
G | A | 1 | a0001c0010 | 1 | HG00597.hp1 | synonymous_variant | LOW | c.1029C>T | p.Thr343Thr | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 1437/3948 | 1029/1050 | 343/349 | chr22 | 45922877 | ||
| chr22:45923000
|
G | A | 1 | a0001c0011 | 1 | HG01891.hp2 | synonymous_variant | LOW | c.906C>T | p.Asp302Asp | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 1314/3948 | 906/1050 | 302/349 | chr22 | 45923000 | ||
| chr22:45923012
|
C | T | 1 | a0001c0014 | 1 | HG03139.hp1 | synonymous_variant | LOW | c.894G>A | p.Ser298Ser | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 1302/3948 | 894/1050 | 298/349 | chr22 | 45923012 | ||
| chr22:45923054
|
C | T | 1 | a0001c0008 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.852G>A | p.Thr284Thr | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 1260/3948 | 852/1050 | 284/349 | chr22 | 45923054 | ||
| chr22:45923156
|
G | T | 2 | a0001c0003a0001c0013 | 5 | HG01884.hp1 HG02257.hp2 HG02572.hp1 others(2): Show |
synonymous_variant | LOW | c.750C>A | p.Thr250Thr | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 1158/3948 | 750/1050 | 250/349 | chr22 | 45923156 | ||
| chr22:45923204
|
C | T | 1 | a0001c0007 | 1 | HG03130.hp2 | synonymous_variant | LOW | c.702G>A | p.Ala234Ala | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 1110/3948 | 702/1050 | 234/349 | chr22 | 45923204 | ||
| chr22:45931122
|
C | T | 1 | a0001c0007 | 1 | HG03130.hp2 | synonymous_variant | LOW | c.546G>A | p.Leu182Leu | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/4 | 954/3948 | 546/1050 | 182/349 | chr22 | 45931122 | ||
| chr22:45931308
|
G | A | 1 | a0001c0012 | 1 | HG00738.hp2 | synonymous_variant | LOW | c.360C>T | p.Thr120Thr | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/4 | 768/3948 | 360/1050 | 120/349 | chr22 | 45931308 | ||
| chr22:45931347
|
C | A | 1 | a0001c0004 | 2 | HG02258.hp1 HG02559.hp2 |
synonymous_variant | LOW | c.321G>T | p.Thr107Thr | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/4 | 729/3948 | 321/1050 | 107/349 | chr22 | 45931347 | ||
| chr22:45949945
|
G | A | 4 | a0001c0002a0001c0013a0001c0014others(1): Show | 12 | HG00642.hp1 HG02258.hp2 HG03041.hp1 others(9): Show |
synonymous_variant | LOW | c.273C>T | p.Thr91Thr | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/4 | 681/3948 | 273/1050 | 91/349 | chr22 | 45949945 | ||
| chr22:45950020
|
C | T | 1 | a0001c0005 | 1 | HG02071.hp1 | synonymous_variant | LOW | c.198G>A | p.Ala66Ala | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/4 | 606/3948 | 198/1050 | 66/349 | chr22 | 45950020 | ||
| chr22:45950050
|
G | A | 1 | a0001c0016 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.168C>T | p.Pro56Pro | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/4 | 576/3948 | 168/1050 | 56/349 | chr22 | 45950050 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:45920422
|
C | G | 1 | a0001c0001t0058 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2434G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 2434 | chr22 | 45920422 | |||||
| chr22:45920451
|
G | A | 3 | a0001c0001t0048a0001c0001t0059a0001c0002t0052 | 3 | HG01243.hp1 HG02622.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2405C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 2405 | chr22 | 45920451 | |||||
| chr22:45920544
|
G | A | 3 | a0001c0001t0010a0001c0001t0011a0001c0001t0050 | 9 | HG00280.hp2 HG00323.hp1 HG01175.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2312C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 2312 | chr22 | 45920544 | |||||
| chr22:45920618
|
G | A | 2 | a0001c0001t0020a0001c0002t0020 | 3 | HG02258.hp2 HG02451.hp2 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2238C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 2238 | chr22 | 45920618 | |||||
| chr22:45920628
|
C | T | 4 | a0001c0001t0010a0001c0001t0011a0001c0001t0050others(1): Show | 10 | HG00280.hp2 HG00323.hp1 HG01175.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2228G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 2228 | chr22 | 45920628 | |||||
| chr22:45920674
|
GAGGGATG others(17): Show |
G | 12 | a0001c0001t0007a0001c0001t0009a0001c0001t0017others(9): Show | 24 | HG00642.hp1 HG01167.hp2 HG01169.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2158_*2181delGACC others(20): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 2158 | chr22 | 45920674 | |||||
| chr22:45920687
|
G | A | 3 | a0001c0001t0010a0001c0001t0011a0001c0001t0050 | 9 | HG00280.hp2 HG00323.hp1 HG01175.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2169C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 2169 | chr22 | 45920687 | |||||
| chr22:45920696
|
G | A | 3 | a0001c0001t0010a0001c0001t0011a0001c0001t0050 | 9 | HG00280.hp2 HG00323.hp1 HG01175.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2160C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 2160 | chr22 | 45920696 | |||||
| chr22:45920698
|
C | G | 3 | a0001c0001t0010a0001c0001t0011a0001c0001t0050 | 9 | HG00280.hp2 HG00323.hp1 HG01175.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2158G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 2158 | chr22 | 45920698 | |||||
| chr22:45920699
|
A | G | 3 | a0001c0001t0010a0001c0001t0011a0001c0001t0050 | 9 | HG00280.hp2 HG00323.hp1 HG01175.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2157T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 2157 | chr22 | 45920699 | |||||
| chr22:45920699
|
AGGGATGG others(5): Show |
A | 1 | a0001c0001t0060 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2145_*2156delCCAT others(8): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 2145 | chr22 | 45920699 | |||||
| chr22:45920723
|
A | G | 3 | a0001c0001t0010a0001c0001t0011a0001c0001t0050 | 9 | HG00280.hp2 HG00323.hp1 HG01175.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2133T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 2133 | chr22 | 45920723 | |||||
| chr22:45920730
|
A | G | 3 | a0001c0001t0010a0001c0001t0011a0001c0001t0050 | 9 | HG00280.hp2 HG00323.hp1 HG01175.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2126T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 2126 | chr22 | 45920730 | |||||
| chr22:45920734
|
G | A | 1 | a0001c0011t0049 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2122C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 2122 | chr22 | 45920734 | |||||
| chr22:45920735
|
AGGGATGG others(3): Show |
A | 11 | a0001c0001t0005a0001c0001t0006a0001c0001t0013others(8): Show | 39 | HG00733.hp2 HG00735.hp1 HG01069.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*2111_*2120delATCC others(6): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 2111 | chr22 | 45920735 | |||||
| chr22:45920742
|
G | A | 3 | a0001c0001t0010a0001c0001t0011a0001c0001t0050 | 9 | HG00280.hp2 HG00323.hp1 HG01175.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2114C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 2114 | chr22 | 45920742 | |||||
| chr22:45920745
|
T | TGA | 3 | a0001c0001t0010a0001c0001t0011a0001c0001t0050 | 9 | HG00280.hp2 HG00323.hp1 HG01175.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2110_*2111insTC | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 2110 | chr22 | 45920745 | |||||
| chr22:45920925
|
T | G | 4 | a0001c0001t0010a0001c0001t0011a0001c0001t0039others(1): Show | 10 | HG00280.hp2 HG00323.hp1 HG00735.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1931A>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 1931 | chr22 | 45920925 | |||||
| chr22:45920982
|
C | T | 1 | a0001c0001t0045 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1874G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 1874 | chr22 | 45920982 | |||||
| chr22:45920983
|
G | A | 5 | a0001c0001t0003a0001c0001t0004a0001c0001t0015others(2): Show | 42 | HG00621.hp1 HG00639.hp1 HG00642.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1873C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 1873 | chr22 | 45920983 | |||||
| chr22:45920999
|
A | G | 8 | a0001c0001t0018a0001c0001t0042a0001c0001t0048others(5): Show | 8 | HG01243.hp1 HG01243.hp2 HG01433.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1857T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 1857 | chr22 | 45920999 | |||||
| chr22:45921052
|
A | C | 3 | a0001c0001t0031a0001c0001t0038a0001c0001t0062 | 3 | HG02723.hp1 HG02809.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1804T>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 1804 | chr22 | 45921052 | |||||
| chr22:45921192
|
C | T | 4 | a0001c0001t0012a0001c0001t0025a0001c0001t0035others(1): Show | 8 | HG02280.hp1 HG02886.hp1 HG02886.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1664G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 1664 | chr22 | 45921192 | |||||
| chr22:45921261
|
T | G | 1 | a0001c0002t0037 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1595A>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 1595 | chr22 | 45921261 | |||||
| chr22:45921310
|
G | T | 2 | a0001c0001t0031a0001c0001t0038 | 2 | HG02723.hp1 HG02809.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1546C>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 1546 | chr22 | 45921310 | |||||
| chr22:45921326
|
G | A | 1 | a0001c0002t0037 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1530C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 1530 | chr22 | 45921326 | |||||
| chr22:45921379
|
G | T | 6 | a0001c0001t0003a0001c0001t0004a0001c0001t0008others(3): Show | 45 | HG00621.hp1 HG00639.hp1 HG00642.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1477C>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 1477 | chr22 | 45921379 | |||||
| chr22:45921505
|
C | T | 1 | a0001c0001t0025 | 2 | HG02886.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1351G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 1351 | chr22 | 45921505 | |||||
| chr22:45921610
|
G | A | 6 | a0001c0001t0003a0001c0001t0004a0001c0001t0008others(3): Show | 43 | HG00621.hp1 HG00639.hp1 HG00642.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*1246C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 1246 | chr22 | 45921610 | |||||
| chr22:45921635
|
G | A | 1 | a0001c0001t0061 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1221C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 1221 | chr22 | 45921635 | |||||
| chr22:45921683
|
G | A | 1 | a0001c0002t0052 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1173C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 1173 | chr22 | 45921683 | |||||
| chr22:45921710
|
C | T | 3 | a0001c0001t0019a0001c0001t0020a0001c0002t0020 | 6 | HG02258.hp2 HG02451.hp2 HG02630.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1146G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 1146 | chr22 | 45921710 | |||||
| chr22:45921711
|
G | A | 1 | a0001c0001t0029 | 2 | HG02559.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1145C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 1145 | chr22 | 45921711 | |||||
| chr22:45921746
|
G | A | 1 | a0001c0001t0028 | 2 | HG01256.hp2 HG01258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1110C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 1110 | chr22 | 45921746 | |||||
| chr22:45921779
|
G | T | 1 | a0001c0001t0041 | 1 | NA19057.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1077C>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 1077 | chr22 | 45921779 | |||||
| chr22:45921780
|
A | T | 1 | a0001c0001t0041 | 1 | NA19057.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1076T>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 1076 | chr22 | 45921780 | |||||
| chr22:45921781
|
G | T | 1 | a0001c0001t0041 | 1 | NA19057.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1075C>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 1075 | chr22 | 45921781 | |||||
| chr22:45921782
|
A | T | 1 | a0001c0001t0041 | 1 | NA19057.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1074T>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 1074 | chr22 | 45921782 | |||||
| chr22:45921783
|
C | G | 1 | a0001c0001t0041 | 1 | NA19057.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1073G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 1073 | chr22 | 45921783 | |||||
| chr22:45921789
|
C | T | 1 | a0001c0002t0037 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1067G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 1067 | chr22 | 45921789 | |||||
| chr22:45921805
|
A | G | 58 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(55): Show | 155 | HG00280.hp2 HG00323.hp1 HG00621.hp1 others(152): Show |
3_prime_UTR_variant | MODIFIER | c.*1051T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 1051 | chr22 | 45921805 | |||||
| chr22:45921822
|
A | G | 1 | a0001c0003t0053 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1034T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 1034 | chr22 | 45921822 | |||||
| chr22:45921823
|
C | A | 1 | a0001c0003t0053 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1033G>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 1033 | chr22 | 45921823 | |||||
| chr22:45921909
|
C | T | 6 | a0001c0001t0013a0001c0001t0017a0001c0001t0022others(3): Show | 12 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*947G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 947 | chr22 | 45921909 | |||||
| chr22:45921981
|
G | T | 1 | a0001c0001t0047 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*875C>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 875 | chr22 | 45921981 | |||||
| chr22:45922040
|
T | C | 26 | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(23): Show | 79 | HG00621.hp1 HG00639.hp1 HG00642.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*816A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 816 | chr22 | 45922040 | |||||
| chr22:45922091
|
G | A | 2 | a0001c0001t0039a0001c0001t0051 | 2 | HG00735.hp1 HG01106.hp1 |
3_prime_UTR_variant | MODIFIER | c.*765C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 765 | chr22 | 45922091 | |||||
| chr22:45922092
|
G | A | 1 | a0001c0002t0052 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*764C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 764 | chr22 | 45922092 | |||||
| chr22:45922156
|
C | A | 3 | a0001c0001t0019a0001c0001t0020a0001c0002t0020 | 6 | HG02258.hp2 HG02451.hp2 HG02630.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*700G>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 700 | chr22 | 45922156 | |||||
| chr22:45922256
|
C | G | 1 | a0001c0001t0027 | 2 | HG01099.hp1 HG01884.hp2 |
3_prime_UTR_variant | MODIFIER | c.*600G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 600 | chr22 | 45922256 | |||||
| chr22:45922279
|
T | G | 58 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(55): Show | 155 | HG00280.hp2 HG00323.hp1 HG00621.hp1 others(152): Show |
3_prime_UTR_variant | MODIFIER | c.*577A>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 577 | chr22 | 45922279 | |||||
| chr22:45922298
|
G | C | 10 | a0001c0001t0003a0001c0001t0004a0001c0001t0008others(7): Show | 50 | HG00621.hp1 HG00639.hp1 HG00642.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*558C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 558 | chr22 | 45922298 | |||||
| chr22:45922332
|
C | T | 1 | a0001c0001t0055 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*524G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 524 | chr22 | 45922332 | |||||
| chr22:45922405
|
A | G | 21 | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(18): Show | 71 | HG00621.hp1 HG00639.hp1 HG00642.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*451T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 451 | chr22 | 45922405 | |||||
| chr22:45922419
|
C | T | 1 | a0001c0007t0054 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*437G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 437 | chr22 | 45922419 | |||||
| chr22:45922480
|
G | C | 4 | a0001c0003t0021a0001c0003t0040a0001c0003t0053others(1): Show | 5 | HG01884.hp1 HG02257.hp2 HG02572.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*376C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 376 | chr22 | 45922480 | |||||
| chr22:45922582
|
C | T | 3 | a0001c0001t0010a0001c0001t0011a0001c0001t0015 | 11 | HG00280.hp2 HG00323.hp1 HG01175.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*274G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 274 | chr22 | 45922582 | |||||
| chr22:45922599
|
A | G | 60 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(57): Show | 158 | HG00280.hp2 HG00323.hp1 HG00621.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*257T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 257 | chr22 | 45922599 | |||||
| chr22:45922644
|
G | A | 2 | a0001c0001t0042a0001c0001t0068 | 2 | HG01496.hp2 HG01891.hp1 |
3_prime_UTR_variant | MODIFIER | c.*212C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 212 | chr22 | 45922644 | |||||
| chr22:45922701
|
G | A | 1 | a0001c0001t0043 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*155C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 155 | chr22 | 45922701 | |||||
| chr22:45922713
|
C | T | 6 | a0001c0001t0007a0001c0002t0007a0001c0002t0030others(3): Show | 12 | HG00642.hp1 HG01167.hp2 HG01169.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*143G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 143 | chr22 | 45922713 | |||||
| chr22:45922752
|
C | T | 1 | a0001c0001t0033 | 1 | HG01169.hp2 | 3_prime_UTR_variant | MODIFIER | c.*104G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 104 | chr22 | 45922752 | |||||
| chr22:45922846
|
G | A | 1 | a0001c0001t0062 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 4/4 | 10 | chr22 | 45922846 | |||||
| chr22:45976767
|
G | C | 2 | a0001c0001t0063a0003c0006t0064 | 2 | HG01943.hp1 HG03195.hp2 |
5_prime_UTR_variant | MODIFIER | c.-13C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/4 | 13 | chr22 | 45976767 | |||||
| chr22:45976812
|
C | T | 1 | a0001c0001t0044 | 1 | HG02698.hp1 | 5_prime_UTR_variant | MODIFIER | c.-58G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/4 | 58 | chr22 | 45976812 | |||||
| chr22:45977012
|
C | G | 1 | a0001c0001t0032 | 1 | HG04204.hp2 | 5_prime_UTR_variant | MODIFIER | c.-258G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/4 | 258 | chr22 | 45977012 | |||||
| chr22:45977054
|
G | A | 4 | a0001c0001t0065a0001c0001t0066a0001c0001t0067others(1): Show | 4 | HG01433.hp2 HG01496.hp2 HG02976.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-300C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/4 | 300 | chr22 | 45977054 | |||||
| chr22:45977088
|
C | T | 25 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(22): Show | 146 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(143): Show |
5_prime_UTR_variant | MODIFIER | c.-334G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/4 | 334 | chr22 | 45977088 | |||||
| chr22:45977128
|
A | C | 2 | a0001c0001t0031a0001c0002t0030 | 2 | HG00642.hp1 HG02723.hp1 |
5_prime_UTR_variant | MODIFIER | c.-374T>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/4 | 374 | chr22 | 45977128 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:45923389
|
T | C | 21 | a0001c0001t0007g0161a0001c0001t0007g0162a0001c0001t0007g0252others(18): Show | 21 | HG00642.hp1 HG01167.hp2 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.571-54A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45923389 | ||||||
| chr22:45923408
|
C | T | 1 | a0001c0001t0062g0339 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.571-73G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45923408 | ||||||
| chr22:45923425
|
A | G | 3 | a0001c0001t0014g0254a0001c0001t0014g0313a0001c0001t0063g0344 | 3 | HG01943.hp1 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.571-90T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45923425 | ||||||
| chr22:45923481
|
C | G | 39 | a0001c0001t0007g0161a0001c0001t0007g0162a0001c0001t0007g0252others(36): Show | 39 | HG00642.hp1 HG01167.hp2 HG01169.hp1 others(36): Show |
intron_variant | MODIFIER | c.571-146G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45923481 | ||||||
| chr22:45923496
|
C | T | 2 | a0001c0001t0039g0074a0001c0001t0051g0307 | 2 | HG00735.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.571-161G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45923496 | ||||||
| chr22:45923527
|
C | G | 1 | a0001c0001t0067g0346 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.571-192G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45923527 | ||||||
| chr22:45923557
|
G | A | 1 | a0001c0001t0019g0244 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.571-222C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45923557 | ||||||
| chr22:45923567
|
A | G | 5 | a0001c0001t0009g0268a0001c0001t0031g0004a0001c0001t0038g0009others(2): Show | 5 | HG02723.hp1 HG02809.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.571-232T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45923567 | ||||||
| chr22:45923753
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.571-418A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45923753 | ||||||
| chr22:45923842
|
T | A | 137 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0040others(134): Show | 137 | HG00621.hp1 HG00639.hp1 HG00642.hp1 others(134): Show |
intron_variant | MODIFIER | c.571-507A>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45923842 | ||||||
| chr22:45923866
|
T | G | 1 | a0001c0001t0016g0034 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.571-531A>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45923866 | ||||||
| chr22:45923868
|
G | T | 1 | a0001c0001t0016g0034 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.571-533C>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45923868 | ||||||
| chr22:45923869
|
C | G | 1 | a0001c0001t0016g0034 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.571-534G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45923869 | ||||||
| chr22:45923943
|
C | T | 1 | a0001c0001t0035g0018 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.571-608G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45923943 | ||||||
| chr22:45923950
|
G | A | 5 | a0001c0001t0009g0268a0001c0001t0031g0004a0001c0001t0038g0009others(2): Show | 5 | HG02723.hp1 HG02809.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.571-615C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45923950 | ||||||
| chr22:45923996
|
C | T | 1 | a0001c0001t0001g0278 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.571-661G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45923996 | ||||||
| chr22:45924003
|
G | T | 5 | a0001c0001t0009g0268a0001c0001t0031g0004a0001c0001t0038g0009others(2): Show | 5 | HG02723.hp1 HG02809.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.571-668C>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45924003 | ||||||
| chr22:45924012
|
T | C | 1 | a0001c0014t0018g0260 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.571-677A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45924012 | ||||||
| chr22:45924083
|
G | A | 11 | a0001c0001t0009g0268a0001c0001t0019g0244a0001c0001t0019g0290others(8): Show | 11 | HG02258.hp2 HG02451.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.571-748C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45924083 | ||||||
| chr22:45924098
|
T | C | 1 | a0001c0001t0016g0034 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.571-763A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45924098 | ||||||
| chr22:45924099
|
G | T | 1 | a0001c0001t0016g0034 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.571-764C>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45924099 | ||||||
| chr22:45924100
|
C | G | 1 | a0001c0001t0016g0034 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.571-765G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45924100 | ||||||
| chr22:45924157
|
A | G | 3 | a0001c0001t0020g0158a0001c0001t0020g0225a0001c0002t0020g0336 | 3 | HG02258.hp2 HG02451.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.571-822T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45924157 | ||||||
| chr22:45924395
|
A | G | 144 | a0001c0001t0001g0212a0001c0001t0001g0214a0001c0001t0001g0306others(141): Show | 144 | HG00621.hp1 HG00639.hp1 HG00642.hp1 others(141): Show |
intron_variant | MODIFIER | c.571-1060T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45924395 | ||||||
| chr22:45924546
|
G | A | 1 | a0001c0001t0005g0283 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.571-1211C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45924546 | ||||||
| chr22:45924655
|
A | G | 70 | a0001c0001t0001g0214a0001c0001t0003g0006a0001c0001t0003g0019others(67): Show | 70 | HG00621.hp1 HG00639.hp1 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.571-1320T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45924655 | ||||||
| chr22:45924655
|
AGGTGGGC others(456): Show |
A | 1 | a0001c0001t0006g0073 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.571-1783_571-1321d others(2): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45924655 | ||||||
| chr22:45924661
|
G | T | 2 | a0001c0001t0001g0150a0001c0001t0057g0296 | 2 | HG00733.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.571-1326C>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45924661 | ||||||
| chr22:45924776
|
G | A | 2 | a0001c0001t0042g0013a0001c0001t0068g0348 | 2 | HG01496.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.571-1441C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45924776 | ||||||
| chr22:45924800
|
A | G | 90 | a0001c0001t0001g0214a0001c0001t0003g0006a0001c0001t0003g0019others(87): Show | 90 | HG00621.hp1 HG00639.hp1 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.571-1465T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45924800 | ||||||
| chr22:45924852
|
G | A | 12 | a0001c0001t0001g0284a0001c0001t0010g0007a0001c0001t0010g0029others(9): Show | 12 | HG00280.hp2 HG00323.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.571-1517C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45924852 | ||||||
| chr22:45924882
|
G | T | 1 | a0001c0001t0033g0036 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.571-1547C>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45924882 | ||||||
| chr22:45924913
|
A | G | 11 | a0001c0001t0010g0007a0001c0001t0010g0029a0001c0001t0010g0063others(8): Show | 11 | HG00280.hp2 HG00323.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.571-1578T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45924913 | ||||||
| chr22:45924939
|
T | C | 89 | a0001c0001t0001g0214a0001c0001t0003g0006a0001c0001t0003g0019others(86): Show | 89 | HG00621.hp1 HG00639.hp1 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.571-1604A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45924939 | ||||||
| chr22:45924944
|
G | C | 1 | a0001c0001t0001g0191 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.571-1609C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45924944 | ||||||
| chr22:45924961
|
T | C | 4 | a0001c0001t0009g0268a0001c0001t0031g0004a0001c0001t0038g0009others(1): Show | 4 | HG02723.hp1 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.571-1626A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45924961 | ||||||
| chr22:45924965
|
T | C | 4 | a0001c0001t0009g0268a0001c0001t0031g0004a0001c0001t0038g0009others(1): Show | 4 | HG02723.hp1 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.571-1630A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45924965 | ||||||
| chr22:45924992
|
G | A | 46 | a0001c0001t0001g0214a0001c0001t0003g0006a0001c0001t0003g0019others(43): Show | 46 | HG00621.hp1 HG00639.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.571-1657C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45924992 | ||||||
| chr22:45925017
|
A | G | 46 | a0001c0001t0001g0214a0001c0001t0003g0006a0001c0001t0003g0019others(43): Show | 46 | HG00621.hp1 HG00639.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.571-1682T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45925017 | ||||||
| chr22:45925117
|
TGGGTGGG others(55): Show |
T | 1 | a0001c0001t0044g0147 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.571-1844_571-1783d others(64): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45925117 | ||||||
| chr22:45925167
|
TCAGGTGG others(23): Show |
T | 1 | a0001c0001t0002g0051 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.571-1862_571-1833d others(32): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45925167 | ||||||
| chr22:45925236
|
G | A | 2 | a0001c0001t0039g0074a0001c0001t0051g0307 | 2 | HG00735.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.571-1901C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45925236 | ||||||
| chr22:45925310
|
T | C | 164 | a0001c0001t0001g0212a0001c0001t0001g0214a0001c0001t0001g0284others(161): Show | 164 | HG00280.hp2 HG00323.hp1 HG00621.hp1 others(161): Show |
intron_variant | MODIFIER | c.571-1975A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45925310 | ||||||
| chr22:45925317
|
C | T | 67 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0167others(64): Show | 67 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.571-1982G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45925317 | ||||||
| chr22:45925333
|
C | T | 1 | a0001c0001t0003g0006 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.571-1998G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45925333 | ||||||
| chr22:45925633
|
T | C | 1 | a0001c0001t0009g0268 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.571-2298A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45925633 | ||||||
| chr22:45925686
|
T | C | 164 | a0001c0001t0001g0212a0001c0001t0001g0214a0001c0001t0001g0284others(161): Show | 164 | HG00280.hp2 HG00323.hp1 HG00621.hp1 others(161): Show |
intron_variant | MODIFIER | c.571-2351A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45925686 | ||||||
| chr22:45925736
|
G | A | 2 | a0001c0001t0002g0028a0001c0001t0060g0316 | 2 | HG00280.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.571-2401C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45925736 | ||||||
| chr22:45925742
|
C | G | 1 | a0001c0001t0002g0064 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.571-2407G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45925742 | ||||||
| chr22:45925809
|
C | G | 1 | a0001c0001t0002g0022 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.571-2474G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45925809 | ||||||
| chr22:45925957
|
T | G | 3 | a0001c0001t0007g0321a0001c0002t0030g0003a0001c0016t0007g0280 | 3 | HG00642.hp1 HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.571-2622A>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45925957 | ||||||
| chr22:45926053
|
C | T | 1 | a0001c0001t0062g0339 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.571-2718G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45926053 | ||||||
| chr22:45926114
|
C | T | 62 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0167others(59): Show | 62 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.571-2779G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45926114 | ||||||
| chr22:45926228
|
C | T | 1 | a0001c0001t0041g0130 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.571-2893G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45926228 | ||||||
| chr22:45926263
|
G | A | 7 | a0001c0001t0001g0299a0001c0001t0001g0303a0001c0001t0001g0305others(4): Show | 7 | HG01361.hp2 HG01975.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.571-2928C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45926263 | ||||||
| chr22:45926285
|
C | G | 1 | a0001c0001t0035g0018 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.571-2950G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45926285 | ||||||
| chr22:45926382
|
G | A | 59 | a0001c0001t0001g0214a0001c0001t0003g0006a0001c0001t0003g0019others(56): Show | 59 | HG00621.hp1 HG00639.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.571-3047C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45926382 | ||||||
| chr22:45926400
|
G | A | 1 | a0001c0001t0029g0240 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.571-3065C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45926400 | ||||||
| chr22:45926580
|
G | A | 59 | a0001c0001t0001g0214a0001c0001t0003g0006a0001c0001t0003g0019others(56): Show | 59 | HG00621.hp1 HG00639.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.571-3245C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45926580 | ||||||
| chr22:45926633
|
G | T | 7 | a0001c0001t0018g0327a0001c0001t0042g0013a0001c0001t0048g0326others(4): Show | 7 | HG01243.hp1 HG01243.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.571-3298C>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45926633 | ||||||
| chr22:45926687
|
G | A | 1 | a0001c0001t0002g0076 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.571-3352C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45926687 | ||||||
| chr22:45926694
|
G | A | 1 | a0001c0002t0018g0157 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.571-3359C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45926694 | ||||||
| chr22:45926697
|
C | T | 65 | a0001c0001t0001g0214a0001c0001t0003g0006a0001c0001t0003g0019others(62): Show | 65 | HG00621.hp1 HG00639.hp1 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.571-3362G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45926697 | ||||||
| chr22:45926698
|
CTAAG | C | 65 | a0001c0001t0001g0214a0001c0001t0003g0006a0001c0001t0003g0019others(62): Show | 65 | HG00621.hp1 HG00639.hp1 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.571-3367_571-3364d others(6): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45926698 | ||||||
| chr22:45926747
|
G | A | 2 | a0001c0001t0005g0288a0001c0001t0006g0120 | 2 | HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.571-3412C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45926747 | ||||||
| chr22:45926768
|
C | T | 1 | a0001c0001t0061g0273 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.571-3433G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45926768 | ||||||
| chr22:45926828
|
G | A | 35 | a0001c0001t0005g0149a0001c0001t0005g0180a0001c0001t0005g0202others(32): Show | 35 | HG01069.hp1 HG01255.hp1 HG01256.hp2 others(32): Show |
intron_variant | MODIFIER | c.571-3493C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45926828 | ||||||
| chr22:45926883
|
C | T | 1 | a0001c0001t0002g0053 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.571-3548G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45926883 | ||||||
| chr22:45926898
|
G | A | 4 | a0001c0001t0001g0212a0001c0001t0001g0306a0001c0001t0002g0102others(1): Show | 4 | HG01934.hp2 HG01975.hp2 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.571-3563C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45926898 | ||||||
| chr22:45926935
|
A | C | 1 | a0001c0001t0002g0123 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.571-3600T>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45926935 | ||||||
| chr22:45926951
|
C | T | 3 | a0001c0001t0001g0174a0001c0001t0002g0048a0001c0001t0002g0066 | 3 | NA19004.hp2 NA19057.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.571-3616G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45926951 | ||||||
| chr22:45926961
|
G | A | 46 | a0001c0001t0001g0214a0001c0001t0003g0006a0001c0001t0003g0019others(43): Show | 46 | HG00621.hp1 HG00639.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.571-3626C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45926961 | ||||||
| chr22:45927104
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.571-3769C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45927104 | ||||||
| chr22:45927130
|
A | C | 3 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0292 | 3 | HG02486.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.571-3795T>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45927130 | ||||||
| chr22:45927208
|
G | A | 34 | a0001c0001t0005g0149a0001c0001t0005g0180a0001c0001t0005g0202others(31): Show | 34 | HG01069.hp1 HG01255.hp1 HG01256.hp2 others(31): Show |
intron_variant | MODIFIER | c.571-3873C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45927208 | ||||||
| chr22:45927261
|
C | T | 3 | a0001c0001t0029g0240a0001c0001t0029g0319a0001c0001t0059g0156 | 3 | HG02559.hp1 HG02622.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.570+3837G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45927261 | ||||||
| chr22:45927265
|
C | T | 8 | a0001c0001t0018g0327a0001c0001t0042g0013a0001c0001t0048g0326others(5): Show | 8 | HG01243.hp1 HG01243.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.570+3833G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45927265 | ||||||
| chr22:45927276
|
C | T | 8 | a0001c0001t0018g0327a0001c0001t0042g0013a0001c0001t0048g0326others(5): Show | 8 | HG01243.hp1 HG01243.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.570+3822G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45927276 | ||||||
| chr22:45927296
|
C | T | 1 | a0001c0011t0049g0330 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.570+3802G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45927296 | ||||||
| chr22:45927300
|
C | T | 1 | a0001c0001t0062g0339 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.570+3798G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45927300 | ||||||
| chr22:45927301
|
G | A | 4 | a0001c0001t0001g0181a0001c0001t0001g0205a0001c0001t0001g0206others(1): Show | 4 | NA18967.hp1 NA18995.hp2 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.570+3797C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45927301 | ||||||
| chr22:45927303
|
C | T | 1 | a0001c0001t0002g0038 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.570+3795G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45927303 | ||||||
| chr22:45927310
|
GGAGCTTG others(14): Show |
G | 1 | a0001c0001t0003g0139 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.570+3767_570+3787d others(23): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45927310 | ||||||
| chr22:45927361
|
G | A | 1 | a0001c0001t0019g0244 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.570+3737C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45927361 | ||||||
| chr22:45927363
|
C | T | 30 | a0001c0001t0005g0149a0001c0001t0005g0180a0001c0001t0005g0202others(27): Show | 30 | HG01069.hp1 HG01255.hp1 HG01256.hp2 others(27): Show |
intron_variant | MODIFIER | c.570+3735G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45927363 | ||||||
| chr22:45927364
|
G | A | 47 | a0001c0001t0001g0214a0001c0001t0002g0138a0001c0001t0003g0006others(44): Show | 47 | HG00423.hp1 HG00621.hp1 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.570+3734C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45927364 | ||||||
| chr22:45927444
|
C | T | 1 | a0001c0002t0030g0003 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.570+3654G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45927444 | ||||||
| chr22:45927445
|
G | A | 10 | a0001c0001t0001g0172a0001c0001t0002g0069a0001c0001t0004g0171others(7): Show | 10 | HG02145.hp2 HG02280.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.570+3653C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45927445 | ||||||
| chr22:45927455
|
C | T | 2 | a0001c0001t0014g0324a0001c0001t0024g0099 | 2 | HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.570+3643G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45927455 | ||||||
| chr22:45927462
|
A | G | 29 | a0001c0001t0001g0212a0001c0001t0001g0306a0001c0001t0002g0102others(26): Show | 29 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.570+3636T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45927462 | ||||||
| chr22:45927540
|
G | A | 3 | a0001c0001t0001g0217a0001c0001t0001g0234a0001c0001t0002g0112 | 3 | NA18952.hp1 NA19079.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.570+3558C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45927540 | ||||||
| chr22:45927746
|
AT | A | 60 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0292others(57): Show | 60 | HG00642.hp1 HG01069.hp1 HG01167.hp2 others(57): Show |
intron_variant | MODIFIER | c.570+3351delA | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45927746 | ||||||
| chr22:45927768
|
C | T | 3 | a0001c0001t0014g0324a0001c0001t0024g0099a0001c0002t0014g0274 | 3 | HG02965.hp2 HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.570+3330G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45927768 | ||||||
| chr22:45927788
|
C | T | 3 | a0001c0001t0014g0324a0001c0001t0024g0099a0001c0002t0014g0274 | 3 | HG02965.hp2 HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.570+3310G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45927788 | ||||||
| chr22:45927820
|
C | T | 1 | a0001c0002t0018g0157 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.570+3278G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45927820 | ||||||
| chr22:45927837
|
G | A | 1 | a0001c0002t0018g0157 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.570+3261C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45927837 | ||||||
| chr22:45927889
|
C | A | 30 | a0001c0001t0005g0149a0001c0001t0005g0180a0001c0001t0005g0202others(27): Show | 30 | HG01069.hp1 HG01255.hp1 HG01256.hp2 others(27): Show |
intron_variant | MODIFIER | c.570+3209G>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45927889 | ||||||
| chr22:45927892
|
T | A | 30 | a0001c0001t0005g0149a0001c0001t0005g0180a0001c0001t0005g0202others(27): Show | 30 | HG01069.hp1 HG01255.hp1 HG01256.hp2 others(27): Show |
intron_variant | MODIFIER | c.570+3206A>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45927892 | ||||||
| chr22:45927896
|
A | C | 7 | a0001c0001t0018g0327a0001c0001t0042g0013a0001c0001t0048g0326others(4): Show | 7 | HG01243.hp1 HG01243.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.570+3202T>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45927896 | ||||||
| chr22:45927972
|
T | A | 52 | a0001c0001t0001g0214a0001c0001t0002g0138a0001c0001t0003g0006others(49): Show | 52 | HG00423.hp1 HG00621.hp1 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.570+3126A>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45927972 | ||||||
| chr22:45927981
|
C | T | 4 | a0001c0001t0001g0216a0001c0001t0001g0242a0001c0001t0001g0243others(1): Show | 4 | HG01109.hp1 HG01167.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.570+3117G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45927981 | ||||||
| chr22:45928037
|
C | G | 1 | a0001c0002t0018g0157 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.570+3061G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45928037 | ||||||
| chr22:45928138
|
C | T | 1 | a0001c0001t0002g0102 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.570+2960G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45928138 | ||||||
| chr22:45928152
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.570+2946C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45928152 | ||||||
| chr22:45928157
|
G | A | 1 | a0001c0002t0018g0157 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.570+2941C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45928157 | ||||||
| chr22:45928193
|
C | T | 37 | a0001c0001t0001g0188a0001c0001t0001g0238a0001c0001t0001g0271others(34): Show | 38 | HG00280.hp2 HG00323.hp1 HG01175.hp2 others(35): Show |
intron_variant | MODIFIER | c.570+2905G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45928193 | ||||||
| chr22:45928194
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.570+2904C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45928194 | ||||||
| chr22:45928253
|
C | T | 1 | a0001c0001t0001g0312 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.570+2845G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45928253 | ||||||
| chr22:45928265
|
C | T | 32 | a0001c0001t0005g0149a0001c0001t0005g0180a0001c0001t0005g0202others(29): Show | 32 | HG01069.hp1 HG01255.hp1 HG01256.hp2 others(29): Show |
intron_variant | MODIFIER | c.570+2833G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45928265 | ||||||
| chr22:45928291
|
A | G | 11 | a0001c0001t0010g0007a0001c0001t0010g0029a0001c0001t0010g0063others(8): Show | 11 | HG00280.hp2 HG00323.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.570+2807T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45928291 | ||||||
| chr22:45928352
|
G | A | 1 | a0001c0001t0045g0258 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.570+2746C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45928352 | ||||||
| chr22:45928376
|
C | T | 2 | a0001c0001t0001g0263a0001c0001t0045g0258 | 2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.570+2722G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45928376 | ||||||
| chr22:45928403
|
C | T | 1 | a0001c0001t0017g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.570+2695G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45928403 | ||||||
| chr22:45928404
|
G | A | 89 | a0001c0001t0001g0167a0001c0001t0001g0175a0001c0001t0001g0214others(86): Show | 89 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.570+2694C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45928404 | ||||||
| chr22:45928411
|
T | G | 1 | a0001c0001t0005g0180 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.570+2687A>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45928411 | ||||||
| chr22:45928479
|
G | A | 1 | a0001c0001t0001g0284 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.570+2619C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45928479 | ||||||
| chr22:45928495
|
C | T | 1 | a0001c0002t0037g0015 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.570+2603G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45928495 | ||||||
| chr22:45928495
|
CCCACCGG others(31): Show |
C | 2 | a0001c0001t0042g0013a0001c0001t0068g0348 | 2 | HG01496.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.570+2565_570+2602d others(40): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45928495 | ||||||
| chr22:45928496
|
C | T | 5 | a0001c0003t0021g0229a0001c0003t0021g0311a0001c0003t0040g0046others(2): Show | 5 | HG01884.hp1 HG02257.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.570+2602G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45928496 | ||||||
| chr22:45928497
|
C | T | 1 | a0001c0001t0019g0244 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.570+2601G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45928497 | ||||||
| chr22:45928500
|
C | T | 22 | a0001c0001t0005g0249a0001c0001t0005g0301a0001c0001t0006g0073others(19): Show | 22 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.570+2598G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45928500 | ||||||
| chr22:45928502
|
G | A | 1 | a0001c0002t0018g0157 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.570+2596C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45928502 | ||||||
| chr22:45928573
|
C | T | 1 | a0001c0001t0002g0082 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.570+2525G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45928573 | ||||||
| chr22:45928593
|
C | A | 104 | a0001c0001t0001g0167a0001c0001t0001g0175a0001c0001t0001g0188others(101): Show | 104 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.570+2505G>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45928593 | ||||||
| chr22:45928612
|
C | T | 99 | a0001c0001t0001g0167a0001c0001t0001g0175a0001c0001t0001g0212others(96): Show | 99 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.570+2486G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45928612 | ||||||
| chr22:45928634
|
T | TCTCCCCA others(14): Show |
24 | a0001c0001t0001g0212a0001c0001t0001g0306a0001c0001t0002g0102others(21): Show | 24 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.570+2463_570+2464i others(23): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45928634 | ||||||
| chr22:45928634
|
T | TCTCCCCA others(14): Show |
118 | a0001c0001t0001g0167a0001c0001t0001g0175a0001c0001t0001g0188others(115): Show | 119 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.570+2463_570+2464i others(23): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45928634 | ||||||
| chr22:45928671
|
C | T | 11 | a0001c0001t0001g0188a0001c0001t0001g0238a0001c0001t0001g0271others(8): Show | 12 | HG01256.hp1 HG02451.hp1 HG02683.hp2 others(9): Show |
intron_variant | MODIFIER | c.570+2427G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45928671 | ||||||
| chr22:45928727
|
A | G | 2 | a0001c0001t0008g0039a0001c0001t0008g0142 | 2 | HG02056.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.570+2371T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45928727 | ||||||
| chr22:45928745
|
A | C | 143 | a0001c0001t0001g0167a0001c0001t0001g0175a0001c0001t0001g0188others(140): Show | 144 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.570+2353T>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45928745 | ||||||
| chr22:45928761
|
T | G | 6 | a0001c0001t0019g0244a0001c0001t0019g0290a0001c0001t0019g0332others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.570+2337A>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45928761 | ||||||
| chr22:45928811
|
A | C | 1 | a0001c0001t0002g0024 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.570+2287T>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45928811 | ||||||
| chr22:45928828
|
C | T | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.570+2270G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45928828 | ||||||
| chr22:45928829
|
G | A | 8 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0292others(5): Show | 8 | HG02486.hp1 HG02723.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.570+2269C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45928829 | ||||||
| chr22:45928837
|
T | G | 33 | a0001c0001t0001g0265a0001c0001t0005g0149a0001c0001t0005g0180others(30): Show | 33 | HG01069.hp1 HG01255.hp1 HG01256.hp2 others(30): Show |
intron_variant | MODIFIER | c.570+2261A>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45928837 | ||||||
| chr22:45928853
|
ATACCGCA others(3): Show |
A | 100 | a0001c0001t0001g0167a0001c0001t0001g0175a0001c0001t0001g0212others(97): Show | 100 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.570+2235_570+2244d others(12): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45928853 | ||||||
| chr22:45928854
|
T | C | 43 | a0001c0001t0001g0188a0001c0001t0001g0238a0001c0001t0001g0271others(40): Show | 44 | HG00280.hp2 HG00323.hp1 HG01175.hp2 others(41): Show |
intron_variant | MODIFIER | c.570+2244A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45928854 | ||||||
| chr22:45928857
|
C | T | 42 | a0001c0001t0001g0188a0001c0001t0001g0238a0001c0001t0001g0271others(39): Show | 43 | HG00280.hp2 HG00323.hp1 HG01175.hp2 others(40): Show |
intron_variant | MODIFIER | c.570+2241G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45928857 | ||||||
| chr22:45928867
|
G | T | 100 | a0001c0001t0001g0167a0001c0001t0001g0175a0001c0001t0001g0212others(97): Show | 100 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.570+2231C>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45928867 | ||||||
| chr22:45928868
|
A | G | 100 | a0001c0001t0001g0167a0001c0001t0001g0175a0001c0001t0001g0212others(97): Show | 100 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.570+2230T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45928868 | ||||||
| chr22:45928958
|
CCCACAAG others(21): Show |
C | 36 | a0001c0001t0001g0188a0001c0001t0001g0238a0001c0001t0001g0271others(33): Show | 37 | HG00280.hp2 HG00323.hp1 HG01175.hp2 others(34): Show |
intron_variant | MODIFIER | c.570+2112_570+2139d others(30): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45928958 | ||||||
| chr22:45928974
|
C | T | 19 | a0001c0001t0001g0212a0001c0001t0001g0306a0001c0001t0002g0102others(16): Show | 19 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.570+2124G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45928974 | ||||||
| chr22:45928987
|
C | T | 3 | a0001c0001t0018g0327a0001c0001t0048g0326a0001c0002t0052g0338 | 3 | HG01243.hp1 HG01243.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.570+2111G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45928987 | ||||||
| chr22:45929053
|
G | C | 155 | a0001c0001t0001g0167a0001c0001t0001g0175a0001c0001t0001g0188others(152): Show | 156 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.570+2045C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929053 | ||||||
| chr22:45929065
|
C | T | 1 | a0001c0001t0038g0009 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.570+2033G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929065 | ||||||
| chr22:45929071
|
C | T | 6 | a0001c0001t0019g0244a0001c0001t0019g0290a0001c0001t0019g0332others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.570+2027G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929071 | ||||||
| chr22:45929072
|
G | A | 1 | a0001c0001t0002g0104 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.570+2026C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929072 | ||||||
| chr22:45929077
|
T | C | 1 | a0001c0001t0004g0300 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.570+2021A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929077 | ||||||
| chr22:45929141
|
C | T | 5 | a0001c0001t0001g0271a0001c0001t0001g0281a0001c0001t0002g0083others(2): Show | 5 | HG01256.hp1 HG02451.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.570+1957G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929141 | ||||||
| chr22:45929188
|
G | T | 1 | a0001c0001t0001g0284 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.570+1910C>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929188 | ||||||
| chr22:45929266
|
G | A | 7 | a0001c0001t0018g0327a0001c0001t0042g0013a0001c0001t0048g0326others(4): Show | 7 | HG01243.hp1 HG01243.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.570+1832C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929266 | ||||||
| chr22:45929283
|
T | G | 1 | a0001c0001t0062g0339 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.570+1815A>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929283 | ||||||
| chr22:45929287
|
T | C | 7 | a0001c0001t0018g0327a0001c0001t0042g0013a0001c0001t0048g0326others(4): Show | 7 | HG01243.hp1 HG01243.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.570+1811A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929287 | ||||||
| chr22:45929362
|
A | C | 1 | a0001c0001t0001g0265 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.570+1736T>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929362 | ||||||
| chr22:45929372
|
C | A | 1 | a0001c0001t0002g0094 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.570+1726G>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929372 | ||||||
| chr22:45929375
|
TCCACCCA others(113): Show |
T | 6 | a0001c0001t0019g0244a0001c0001t0019g0290a0001c0001t0019g0332others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.570+1603_570+1722d others(2): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929375 | ||||||
| chr22:45929387
|
CCCATCCA others(29): Show |
C | 4 | a0001c0001t0005g0249a0001c0001t0005g0301a0001c0001t0006g0073others(1): Show | 4 | HG01099.hp1 HG01358.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.570+1675_570+1710d others(38): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929387 | ||||||
| chr22:45929398
|
TTCCATCC others(17): Show |
T | 9 | a0001c0001t0012g0159a0001c0001t0012g0259a0001c0001t0012g0329others(6): Show | 9 | HG01243.hp1 HG01243.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.570+1676_570+1699d others(26): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929398 | ||||||
| chr22:45929473
|
C | T | 32 | a0001c0001t0005g0149a0001c0001t0005g0180a0001c0001t0005g0202others(29): Show | 32 | HG01069.hp1 HG01255.hp1 HG01256.hp2 others(29): Show |
intron_variant | MODIFIER | c.570+1625G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929473 | ||||||
| chr22:45929475
|
T | TCCATCCA others(1): Show |
115 | a0001c0001t0001g0167a0001c0001t0001g0175a0001c0001t0001g0188others(112): Show | 116 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(113): Show |
intron_variant | MODIFIER | c.570+1622_570+1623i others(10): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929475 | ||||||
| chr22:45929481
|
T | C | 32 | a0001c0001t0001g0212a0001c0001t0001g0284a0001c0001t0001g0306others(29): Show | 32 | HG00280.hp2 HG00323.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.570+1617A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929481 | ||||||
| chr22:45929482
|
G | A | 32 | a0001c0001t0001g0212a0001c0001t0001g0284a0001c0001t0001g0306others(29): Show | 32 | HG00280.hp2 HG00323.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.570+1616C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929482 | ||||||
| chr22:45929483
|
T | C | 32 | a0001c0001t0001g0212a0001c0001t0001g0284a0001c0001t0001g0306others(29): Show | 32 | HG00280.hp2 HG00323.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.570+1615A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929483 | ||||||
| chr22:45929484
|
A | C | 32 | a0001c0001t0001g0212a0001c0001t0001g0284a0001c0001t0001g0306others(29): Show | 32 | HG00280.hp2 HG00323.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.570+1614T>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929484 | ||||||
| chr22:45929487
|
TCCAC | T | 8 | a0001c0001t0001g0299a0001c0001t0001g0303a0001c0001t0001g0305others(5): Show | 8 | HG00609.hp1 HG01361.hp2 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.570+1607_570+1610d others(6): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929487 | ||||||
| chr22:45929488
|
C | CTGTA | 32 | a0001c0001t0001g0212a0001c0001t0001g0284a0001c0001t0001g0306others(29): Show | 32 | HG00280.hp2 HG00323.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.570+1609_570+1610i others(6): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929488 | ||||||
| chr22:45929491
|
C | CCCATCTG others(5): Show |
56 | a0001c0001t0001g0188a0001c0001t0001g0238a0001c0001t0001g0271others(53): Show | 57 | HG01069.hp1 HG01255.hp1 HG01256.hp1 others(54): Show |
intron_variant | MODIFIER | c.570+1606_570+1607i others(14): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929491 | ||||||
| chr22:45929491
|
C | T | 32 | a0001c0001t0001g0212a0001c0001t0001g0284a0001c0001t0001g0306others(29): Show | 32 | HG00280.hp2 HG00323.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.570+1607G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929491 | ||||||
| chr22:45929495
|
C | T | 1 | a0001c0002t0018g0157 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.570+1603G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929495 | ||||||
| chr22:45929497
|
C | T | 1 | a0001c0002t0018g0157 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.570+1601G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929497 | ||||||
| chr22:45929498
|
A | G | 1 | a0001c0002t0018g0157 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.570+1600T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929498 | ||||||
| chr22:45929499
|
C | T | 1 | a0001c0002t0018g0157 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.570+1599G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929499 | ||||||
| chr22:45929500
|
C | A | 1 | a0001c0002t0018g0157 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.570+1598G>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929500 | ||||||
| chr22:45929503
|
C | T | 1 | a0001c0002t0018g0157 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.570+1595G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929503 | ||||||
| chr22:45929514
|
T | A | 1 | a0001c0002t0018g0157 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.570+1584A>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929514 | ||||||
| chr22:45929517
|
C | T | 1 | a0001c0002t0018g0157 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.570+1581G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929517 | ||||||
| chr22:45929520
|
C | A | 1 | a0001c0002t0018g0157 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.570+1578G>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929520 | ||||||
| chr22:45929525
|
T | C | 1 | a0001c0002t0018g0157 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.570+1573A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929525 | ||||||
| chr22:45929526
|
T | A | 1 | a0001c0002t0018g0157 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.570+1572A>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929526 | ||||||
| chr22:45929527
|
T | C | 1 | a0001c0002t0018g0157 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.570+1571A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929527 | ||||||
| chr22:45929547
|
ACCATCCT others(5): Show |
A | 4 | a0001c0001t0029g0240a0001c0001t0029g0319a0001c0001t0059g0156others(1): Show | 4 | HG02559.hp1 HG02622.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.570+1539_570+1550d others(14): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929547 | ||||||
| chr22:45929551
|
T | C | 2 | a0001c0001t0042g0013a0001c0001t0068g0348 | 2 | HG01496.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.570+1547A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929551 | ||||||
| chr22:45929600
|
C | G | 1 | a0001c0001t0007g0321 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.570+1498G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929600 | ||||||
| chr22:45929608
|
C | T | 1 | a0001c0001t0041g0130 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.570+1490G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929608 | ||||||
| chr22:45929619
|
C | CCCATCCT others(21): Show |
4 | a0001c0001t0009g0268a0001c0001t0031g0004a0001c0001t0038g0009others(1): Show | 4 | HG02723.hp1 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.570+1451_570+1478d others(30): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929619 | ||||||
| chr22:45929619
|
C | T | 6 | a0001c0001t0019g0244a0001c0001t0019g0290a0001c0001t0019g0332others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.570+1479G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929619 | ||||||
| chr22:45929619
|
CCCATCCT others(21): Show |
C | 28 | a0001c0001t0005g0149a0001c0001t0005g0180a0001c0001t0005g0202others(25): Show | 28 | HG01069.hp1 HG01255.hp1 HG01256.hp2 others(25): Show |
intron_variant | MODIFIER | c.570+1451_570+1478d others(30): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929619 | ||||||
| chr22:45929628
|
CCATCCAT others(1): Show |
C | 20 | a0001c0001t0001g0212a0001c0001t0001g0306a0001c0001t0002g0102others(17): Show | 20 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.570+1462_570+1469d others(10): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929628 | ||||||
| chr22:45929628
|
CCATCCAT others(9): Show |
C | 1 | a0001c0001t0001g0303 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.570+1454_570+1469d others(18): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929628 | ||||||
| chr22:45929630
|
A | C | 36 | a0001c0001t0001g0188a0001c0001t0001g0238a0001c0001t0001g0271others(33): Show | 37 | HG00280.hp2 HG00323.hp1 HG01175.hp2 others(34): Show |
intron_variant | MODIFIER | c.570+1468T>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929630 | ||||||
| chr22:45929631
|
T | C | 6 | a0001c0001t0019g0244a0001c0001t0019g0290a0001c0001t0019g0332others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.570+1467A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929631 | ||||||
| chr22:45929632
|
CCATG | C | 6 | a0001c0001t0019g0244a0001c0001t0019g0290a0001c0001t0019g0332others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.570+1462_570+1465d others(6): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929632 | ||||||
| chr22:45929632
|
CCATGCAT others(5): Show |
C | 1 | a0001c0001t0012g0331 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.570+1454_570+1465d others(14): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929632 | ||||||
| chr22:45929636
|
G | A | 36 | a0001c0001t0001g0188a0001c0001t0001g0238a0001c0001t0001g0271others(33): Show | 37 | HG00280.hp2 HG00323.hp1 HG01175.hp2 others(34): Show |
intron_variant | MODIFIER | c.570+1462C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929636 | ||||||
| chr22:45929638
|
A | T | 36 | a0001c0001t0001g0188a0001c0001t0001g0238a0001c0001t0001g0271others(33): Show | 37 | HG00280.hp2 HG00323.hp1 HG01175.hp2 others(34): Show |
intron_variant | MODIFIER | c.570+1460T>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929638 | ||||||
| chr22:45929639
|
T | C | 26 | a0001c0001t0001g0212a0001c0001t0001g0306a0001c0001t0002g0102others(23): Show | 26 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.570+1459A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929639 | ||||||
| chr22:45929641
|
C | T | 2 | a0001c0001t0019g0290a0001c0001t0019g0332 | 2 | HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.570+1457G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929641 | ||||||
| chr22:45929642
|
A | G | 6 | a0001c0001t0019g0244a0001c0001t0019g0290a0001c0001t0019g0332others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.570+1456T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929642 | ||||||
| chr22:45929643
|
C | T | 36 | a0001c0001t0001g0188a0001c0001t0001g0238a0001c0001t0001g0271others(33): Show | 37 | HG00280.hp2 HG00323.hp1 HG01175.hp2 others(34): Show |
intron_variant | MODIFIER | c.570+1455G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929643 | ||||||
| chr22:45929644
|
T | C | 62 | a0001c0001t0001g0188a0001c0001t0001g0212a0001c0001t0001g0238others(59): Show | 63 | HG00280.hp2 HG00323.hp1 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.570+1454A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929644 | ||||||
| chr22:45929646
|
A | G | 20 | a0001c0001t0001g0212a0001c0001t0001g0306a0001c0001t0002g0102others(17): Show | 20 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.570+1452T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929646 | ||||||
| chr22:45929647
|
T | C | 56 | a0001c0001t0001g0188a0001c0001t0001g0212a0001c0001t0001g0238others(53): Show | 57 | HG00280.hp2 HG00323.hp1 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.570+1451A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929647 | ||||||
| chr22:45929650
|
A | T | 6 | a0001c0001t0019g0244a0001c0001t0019g0290a0001c0001t0019g0332others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.570+1448T>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929650 | ||||||
| chr22:45929652
|
CCTTCCAC others(20): Show |
C | 32 | a0001c0001t0001g0188a0001c0001t0001g0238a0001c0001t0001g0271others(29): Show | 33 | HG00280.hp2 HG00323.hp1 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.570+1419_570+1445d others(29): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929652 | ||||||
| chr22:45929653
|
C | CCATT | 4 | a0001c0001t0014g0324a0001c0001t0024g0099a0001c0002t0014g0274others(1): Show | 4 | HG01891.hp2 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.570+1444_570+1445i others(6): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929653 | ||||||
| chr22:45929654
|
T | C | 6 | a0001c0001t0019g0244a0001c0001t0019g0290a0001c0001t0019g0332others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.570+1444A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929654 | ||||||
| chr22:45929658
|
A | C | 20 | a0001c0001t0001g0212a0001c0001t0001g0306a0001c0001t0002g0102others(17): Show | 20 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.570+1440T>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929658 | ||||||
| chr22:45929659
|
C | T | 24 | a0001c0001t0001g0212a0001c0001t0001g0306a0001c0001t0002g0102others(21): Show | 24 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.570+1439G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929659 | ||||||
| chr22:45929662
|
ACCC | A | 6 | a0001c0001t0019g0244a0001c0001t0019g0290a0001c0001t0019g0332others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.570+1433_570+1435d others(5): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929662 | ||||||
| chr22:45929662
|
ACCCG | A | 4 | a0001c0001t0014g0324a0001c0001t0024g0099a0001c0002t0014g0274others(1): Show | 4 | HG01891.hp2 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.570+1432_570+1435d others(6): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929662 | ||||||
| chr22:45929663
|
C | T | 20 | a0001c0001t0001g0212a0001c0001t0001g0306a0001c0001t0002g0102others(17): Show | 20 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.570+1435G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929663 | ||||||
| chr22:45929664
|
C | A | 20 | a0001c0001t0001g0212a0001c0001t0001g0306a0001c0001t0002g0102others(17): Show | 20 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.570+1434G>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929664 | ||||||
| chr22:45929666
|
G | T | 26 | a0001c0001t0001g0212a0001c0001t0001g0306a0001c0001t0002g0102others(23): Show | 26 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.570+1432C>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929666 | ||||||
| chr22:45929667
|
C | T | 24 | a0001c0001t0001g0212a0001c0001t0001g0306a0001c0001t0002g0102others(21): Show | 24 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.570+1431G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929667 | ||||||
| chr22:45929671
|
TC | T | 6 | a0001c0001t0019g0244a0001c0001t0019g0290a0001c0001t0019g0332others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.570+1426delG | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929671 | ||||||
| chr22:45929673
|
C | T | 10 | a0001c0001t0014g0324a0001c0001t0019g0244a0001c0001t0019g0290others(7): Show | 10 | HG01891.hp2 HG02258.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.570+1425G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929673 | ||||||
| chr22:45929674
|
T | A | 20 | a0001c0001t0001g0212a0001c0001t0001g0306a0001c0001t0002g0102others(17): Show | 20 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.570+1424A>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929674 | ||||||
| chr22:45929675
|
T | C | 20 | a0001c0001t0001g0212a0001c0001t0001g0306a0001c0001t0002g0102others(17): Show | 20 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.570+1423A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929675 | ||||||
| chr22:45929677
|
CCT | C | 4 | a0001c0001t0014g0324a0001c0001t0024g0099a0001c0002t0014g0274others(1): Show | 4 | HG01891.hp2 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.570+1419_570+1420d others(4): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929677 | ||||||
| chr22:45929678
|
C | A | 26 | a0001c0001t0001g0212a0001c0001t0001g0306a0001c0001t0002g0102others(23): Show | 26 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.570+1420G>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929678 | ||||||
| chr22:45929682
|
A | C | 20 | a0001c0001t0001g0212a0001c0001t0001g0306a0001c0001t0002g0102others(17): Show | 20 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.570+1416T>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929682 | ||||||
| chr22:45929683
|
T | A | 20 | a0001c0001t0001g0212a0001c0001t0001g0306a0001c0001t0002g0102others(17): Show | 20 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.570+1415A>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929683 | ||||||
| chr22:45929683
|
T | C | 6 | a0001c0001t0019g0244a0001c0001t0019g0290a0001c0001t0019g0332others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.570+1415A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929683 | ||||||
| chr22:45929683
|
TA | T | 36 | a0001c0001t0001g0188a0001c0001t0001g0238a0001c0001t0001g0271others(33): Show | 37 | HG00280.hp2 HG00323.hp1 HG01175.hp2 others(34): Show |
intron_variant | MODIFIER | c.570+1414delT | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929683 | ||||||
| chr22:45929684
|
A | C | 6 | a0001c0001t0019g0244a0001c0001t0019g0290a0001c0001t0019g0332others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.570+1414T>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929684 | ||||||
| chr22:45929684
|
A | T | 20 | a0001c0001t0001g0212a0001c0001t0001g0306a0001c0001t0002g0102others(17): Show | 20 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.570+1414T>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929684 | ||||||
| chr22:45929685
|
C | T | 56 | a0001c0001t0001g0188a0001c0001t0001g0212a0001c0001t0001g0238others(53): Show | 57 | HG00280.hp2 HG00323.hp1 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.570+1413G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929685 | ||||||
| chr22:45929686
|
T | G | 6 | a0001c0001t0019g0244a0001c0001t0019g0290a0001c0001t0019g0332others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.570+1412A>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929686 | ||||||
| chr22:45929688
|
C | G | 6 | a0001c0001t0019g0244a0001c0001t0019g0290a0001c0001t0019g0332others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.570+1410G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929688 | ||||||
| chr22:45929689
|
C | A | 6 | a0001c0001t0019g0244a0001c0001t0019g0290a0001c0001t0019g0332others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.570+1409G>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929689 | ||||||
| chr22:45929695
|
C | CCCATCCC others(13): Show |
31 | a0001c0001t0003g0006a0001c0001t0005g0149a0001c0001t0005g0180others(28): Show | 31 | HG01069.hp1 HG01255.hp1 HG01256.hp2 others(28): Show |
intron_variant | MODIFIER | c.570+1402_570+1403i others(22): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929695 | ||||||
| chr22:45929695
|
C | CCCATCCC others(29): Show |
36 | a0001c0001t0001g0167a0001c0001t0001g0175a0001c0001t0001g0214others(33): Show | 36 | HG00544.hp2 HG00639.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.570+1402_570+1403i others(38): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929695 | ||||||
| chr22:45929695
|
C | CCCATCCT others(9): Show |
4 | a0001c0001t0004g0173a0001c0001t0004g0204a0001c0001t0004g0221others(1): Show | 4 | HG00741.hp2 HG02300.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.570+1402_570+1403i others(18): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929695 | ||||||
| chr22:45929695
|
C | T | 56 | a0001c0001t0001g0188a0001c0001t0001g0212a0001c0001t0001g0238others(53): Show | 57 | HG00280.hp2 HG00323.hp1 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.570+1403G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929695 | ||||||
| chr22:45929696
|
C | T | 6 | a0001c0001t0019g0244a0001c0001t0019g0290a0001c0001t0019g0332others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.570+1402G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929696 | ||||||
| chr22:45929701
|
T | C | 6 | a0001c0001t0019g0244a0001c0001t0019g0290a0001c0001t0019g0332others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.570+1397A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929701 | ||||||
| chr22:45929702
|
T | A | 6 | a0001c0001t0019g0244a0001c0001t0019g0290a0001c0001t0019g0332others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.570+1396A>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929702 | ||||||
| chr22:45929705
|
CATCCACC others(5): Show |
C | 3 | a0001c0001t0014g0254a0001c0001t0014g0313a0001c0001t0063g0344 | 3 | HG01943.hp1 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.570+1381_570+1392d others(14): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929705 | ||||||
| chr22:45929707
|
T | C | 6 | a0001c0001t0019g0244a0001c0001t0019g0290a0001c0001t0019g0332others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.570+1391A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929707 | ||||||
| chr22:45929709
|
C | T | 6 | a0001c0001t0019g0244a0001c0001t0019g0290a0001c0001t0019g0332others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.570+1389G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929709 | ||||||
| chr22:45929713
|
C | T | 2 | a0001c0001t0009g0268a0002c0015t0009g0228 | 2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.570+1385G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929713 | ||||||
| chr22:45929714
|
G | A | 6 | a0001c0001t0019g0244a0001c0001t0019g0290a0001c0001t0019g0332others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.570+1384C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929714 | ||||||
| chr22:45929716
|
G | C | 6 | a0001c0001t0019g0244a0001c0001t0019g0290a0001c0001t0019g0332others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.570+1382C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929716 | ||||||
| chr22:45929717
|
A | C | 6 | a0001c0001t0019g0244a0001c0001t0019g0290a0001c0001t0019g0332others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.570+1381T>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929717 | ||||||
| chr22:45929718
|
A | T | 6 | a0001c0001t0019g0244a0001c0001t0019g0290a0001c0001t0019g0332others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.570+1380T>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929718 | ||||||
| chr22:45929727
|
C | T | 6 | a0001c0001t0019g0244a0001c0001t0019g0290a0001c0001t0019g0332others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.570+1371G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929727 | ||||||
| chr22:45929728
|
C | T | 6 | a0001c0001t0019g0244a0001c0001t0019g0290a0001c0001t0019g0332others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.570+1370G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929728 | ||||||
| chr22:45929731
|
TCCAC | T | 15 | a0001c0001t0001g0188a0001c0001t0001g0238a0001c0001t0001g0271others(12): Show | 16 | HG01256.hp1 HG02451.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.570+1363_570+1366d others(6): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929731 | ||||||
| chr22:45929740
|
C | T | 2 | a0001c0001t0002g0085a0001c0001t0002g0146 | 2 | NA18941.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.570+1358G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929740 | ||||||
| chr22:45929741
|
G | A | 2 | a0001c0001t0014g0313a0001c0001t0063g0344 | 2 | HG01943.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.570+1357C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929741 | ||||||
| chr22:45929743
|
T | C | 1 | a0001c0001t0011g0155 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.570+1355A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929743 | ||||||
| chr22:45929801
|
C | CATCTACC others(9): Show |
86 | a0001c0001t0001g0167a0001c0001t0001g0175a0001c0001t0001g0188others(83): Show | 87 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.570+1296_570+1297i others(18): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929801 | ||||||
| chr22:45929806
|
A | ACCCACTC others(9): Show |
19 | a0001c0001t0001g0212a0001c0001t0001g0306a0001c0001t0002g0102others(16): Show | 19 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.570+1291_570+1292i others(18): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929806 | ||||||
| chr22:45929809
|
C | CACTCATC others(5): Show |
6 | a0001c0001t0019g0244a0001c0001t0019g0290a0001c0001t0019g0332others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.570+1288_570+1289i others(14): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929809 | ||||||
| chr22:45929811
|
T | C | 6 | a0001c0001t0019g0244a0001c0001t0019g0290a0001c0001t0019g0332others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.570+1287A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929811 | ||||||
| chr22:45929817
|
T | C | 6 | a0001c0001t0019g0244a0001c0001t0019g0290a0001c0001t0019g0332others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.570+1281A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929817 | ||||||
| chr22:45929840
|
ACATCCAC others(77): Show |
A | 1 | a0001c0001t0001g0154 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.570+1174_570+1257d others(86): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929840 | ||||||
| chr22:45929864
|
C | CCATTCAT others(1): Show |
141 | a0001c0001t0001g0167a0001c0001t0001g0175a0001c0001t0001g0188others(138): Show | 142 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.570+1233_570+1234i others(10): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929864 | ||||||
| chr22:45929864
|
C | CCATTCAT others(21): Show |
6 | a0001c0001t0019g0244a0001c0001t0019g0290a0001c0001t0019g0332others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.570+1233_570+1234i others(30): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929864 | ||||||
| chr22:45929868
|
C | T | 1 | a0001c0002t0018g0157 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.570+1230G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929868 | ||||||
| chr22:45929872
|
C | A | 1 | a0001c0002t0018g0157 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.570+1226G>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929872 | ||||||
| chr22:45929875
|
A | T | 1 | a0001c0002t0018g0157 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.570+1223T>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929875 | ||||||
| chr22:45929876
|
CCATCTAC others(5): Show |
C | 1 | a0001c0002t0018g0157 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.570+1210_570+1221d others(14): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929876 | ||||||
| chr22:45929877
|
CATCTACC others(4): Show |
C | 5 | a0001c0001t0009g0268a0001c0001t0031g0004a0001c0001t0038g0009others(2): Show | 5 | HG02723.hp1 HG02809.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.570+1210_570+1220d others(13): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929877 | ||||||
| chr22:45929900
|
C | A | 1 | a0001c0002t0018g0157 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.570+1198G>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929900 | ||||||
| chr22:45929901
|
T | C | 1 | a0001c0002t0018g0157 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.570+1197A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929901 | ||||||
| chr22:45929910
|
ATCCATCT others(25): Show |
A | 1 | a0001c0002t0018g0157 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.570+1156_570+1187d others(34): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929910 | ||||||
| chr22:45929916
|
C | T | 26 | a0001c0001t0001g0188a0001c0001t0001g0238a0001c0001t0001g0271others(23): Show | 27 | HG00280.hp2 HG00323.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.570+1182G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929916 | ||||||
| chr22:45929923
|
C | CCCACTCA others(5): Show |
53 | a0001c0001t0001g0188a0001c0001t0001g0212a0001c0001t0001g0238others(50): Show | 54 | HG00280.hp2 HG00323.hp1 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.570+1174_570+1175i others(14): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929923 | ||||||
| chr22:45929931
|
C | T | 53 | a0001c0001t0001g0188a0001c0001t0001g0212a0001c0001t0001g0238others(50): Show | 54 | HG00280.hp2 HG00323.hp1 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.570+1167G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929931 | ||||||
| chr22:45929939
|
T | TACATCTA others(1): Show |
53 | a0001c0001t0001g0188a0001c0001t0001g0212a0001c0001t0001g0238others(50): Show | 54 | HG00280.hp2 HG00323.hp1 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.570+1158_570+1159i others(10): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929939 | ||||||
| chr22:45929942
|
T | A | 53 | a0001c0001t0001g0188a0001c0001t0001g0212a0001c0001t0001g0238others(50): Show | 54 | HG00280.hp2 HG00323.hp1 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.570+1156A>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929942 | ||||||
| chr22:45929943
|
T | C | 54 | a0001c0001t0001g0188a0001c0001t0001g0212a0001c0001t0001g0238others(51): Show | 55 | HG00280.hp2 HG00323.hp1 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.570+1155A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929943 | ||||||
| chr22:45929948
|
C | CCATCCAC others(21): Show |
143 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0167others(140): Show | 143 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.570+1149_570+1150i others(30): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929948 | ||||||
| chr22:45929948
|
C | G | 54 | a0001c0001t0001g0188a0001c0001t0001g0212a0001c0001t0001g0238others(51): Show | 55 | HG00280.hp2 HG00323.hp1 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.570+1150G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929948 | ||||||
| chr22:45929954
|
A | C | 5 | a0001c0001t0019g0244a0001c0001t0019g0332a0001c0001t0020g0158others(2): Show | 5 | HG02258.hp2 HG02451.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.570+1144T>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929954 | ||||||
| chr22:45929957
|
C | T | 1 | a0001c0001t0019g0290 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.570+1141G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929957 | ||||||
| chr22:45929960
|
A | T | 5 | a0001c0001t0019g0244a0001c0001t0019g0332a0001c0001t0020g0158others(2): Show | 5 | HG02258.hp2 HG02451.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.570+1138T>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929960 | ||||||
| chr22:45929964
|
C | CTACCCAC others(17): Show |
1 | a0001c0002t0037g0015 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.570+1133_570+1134i others(26): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929964 | ||||||
| chr22:45929965
|
T | C | 5 | a0001c0001t0019g0244a0001c0001t0019g0332a0001c0001t0020g0158others(2): Show | 5 | HG02258.hp2 HG02451.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.570+1133A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929965 | ||||||
| chr22:45929967
|
T | C | 33 | a0001c0001t0005g0149a0001c0001t0005g0180a0001c0001t0005g0202others(30): Show | 33 | HG01069.hp1 HG01255.hp1 HG01256.hp2 others(30): Show |
intron_variant | MODIFIER | c.570+1131A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929967 | ||||||
| chr22:45929968
|
C | A | 5 | a0001c0001t0019g0244a0001c0001t0019g0332a0001c0001t0020g0158others(2): Show | 5 | HG02258.hp2 HG02451.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.570+1130G>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929968 | ||||||
| chr22:45929971
|
T | C | 1 | a0001c0001t0019g0290 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.570+1127A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929971 | ||||||
| chr22:45929975
|
T | TGCATCCA others(46): Show |
1 | a0001c0001t0019g0290 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.570+1122_570+1123i others(55): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929975 | ||||||
| chr22:45929977
|
C | A | 1 | a0001c0001t0019g0290 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.570+1121G>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929977 | ||||||
| chr22:45929977
|
C | CACTTATA others(70): Show |
5 | a0001c0001t0019g0244a0001c0001t0019g0332a0001c0001t0020g0158others(2): Show | 5 | HG02258.hp2 HG02451.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.570+1120_570+1121i others(79): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929977 | ||||||
| chr22:45929980
|
C | T | 6 | a0001c0001t0019g0244a0001c0001t0019g0290a0001c0001t0019g0332others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.570+1118G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929980 | ||||||
| chr22:45929982
|
A | C | 1 | a0001c0001t0065g0347 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.570+1116T>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929982 | ||||||
| chr22:45930027
|
A | G | 1 | a0001c0001t0004g0200 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.570+1071T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45930027 | ||||||
| chr22:45930066
|
T | C | 3 | a0001c0001t0003g0068a0001c0001t0004g0200a0001c0001t0004g0300 | 3 | HG01255.hp2 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.570+1032A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45930066 | ||||||
| chr22:45930078
|
C | T | 4 | a0001c0001t0001g0271a0001c0001t0001g0281a0001c0001t0002g0083others(1): Show | 4 | HG01256.hp1 HG02451.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.570+1020G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45930078 | ||||||
| chr22:45930116
|
T | C | 15 | a0001c0001t0001g0188a0001c0001t0001g0238a0001c0001t0001g0271others(12): Show | 16 | HG01256.hp1 HG02451.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.570+982A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45930116 | ||||||
| chr22:45930137
|
A | G | 143 | a0001c0001t0001g0167a0001c0001t0001g0175a0001c0001t0001g0188others(140): Show | 144 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.570+961T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45930137 | ||||||
| chr22:45930139
|
C | A | 55 | a0001c0001t0001g0188a0001c0001t0001g0212a0001c0001t0001g0238others(52): Show | 56 | HG00280.hp2 HG00323.hp1 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.570+959G>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45930139 | ||||||
| chr22:45930147
|
G | A | 1 | a0001c0001t0001g0206 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.570+951C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45930147 | ||||||
| chr22:45930162
|
C | A | 2 | a0001c0001t0006g0107a0001c0001t0006g0109 | 2 | HG01928.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.570+936G>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45930162 | ||||||
| chr22:45930162
|
C | G | 2 | a0001c0001t0001g0231a0001c0001t0002g0041 | 2 | NA18747.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.570+936G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45930162 | ||||||
| chr22:45930167
|
A | G | 1 | a0001c0001t0008g0039 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.570+931T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45930167 | ||||||
| chr22:45930191
|
A | G | 48 | a0001c0001t0001g0167a0001c0001t0001g0175a0001c0001t0001g0214others(45): Show | 48 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.570+907T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45930191 | ||||||
| chr22:45930221
|
G | C | 29 | a0001c0001t0005g0149a0001c0001t0005g0180a0001c0001t0005g0202others(26): Show | 29 | HG01069.hp1 HG01255.hp1 HG01256.hp2 others(26): Show |
intron_variant | MODIFIER | c.570+877C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45930221 | ||||||
| chr22:45930240
|
G | A | 55 | a0001c0001t0001g0188a0001c0001t0001g0212a0001c0001t0001g0238others(52): Show | 56 | HG00280.hp2 HG00323.hp1 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.570+858C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45930240 | ||||||
| chr22:45930255
|
G | T | 56 | a0001c0001t0001g0188a0001c0001t0001g0212a0001c0001t0001g0238others(53): Show | 57 | HG00280.hp2 HG00323.hp1 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.570+843C>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45930255 | ||||||
| chr22:45930263
|
C | G | 2 | a0001c0001t0001g0208a0001c0001t0002g0137 | 2 | HG00673.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.570+835G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45930263 | ||||||
| chr22:45930278
|
A | G | 32 | a0001c0001t0005g0149a0001c0001t0005g0180a0001c0001t0005g0202others(29): Show | 32 | HG01069.hp1 HG01255.hp1 HG01256.hp2 others(29): Show |
intron_variant | MODIFIER | c.570+820T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45930278 | ||||||
| chr22:45930299
|
T | C | 1 | a0001c0001t0017g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.570+799A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45930299 | ||||||
| chr22:45930303
|
T | G | 4 | a0001c0001t0009g0268a0001c0001t0031g0004a0001c0001t0038g0009others(1): Show | 4 | HG02723.hp1 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.570+795A>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45930303 | ||||||
| chr22:45930325
|
G | A | 8 | a0001c0001t0002g0022a0001c0001t0008g0142a0001c0001t0019g0244others(5): Show | 8 | HG02056.hp1 HG02258.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.570+773C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45930325 | ||||||
| chr22:45930348
|
A | G | 143 | a0001c0001t0001g0167a0001c0001t0001g0175a0001c0001t0001g0188others(140): Show | 144 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.570+750T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45930348 | ||||||
| chr22:45930392
|
G | A | 61 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0182others(58): Show | 61 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.570+706C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45930392 | ||||||
| chr22:45930397
|
C | T | 20 | a0001c0001t0005g0149a0001c0001t0005g0180a0001c0001t0005g0202others(17): Show | 20 | HG01069.hp1 HG01255.hp1 HG01256.hp2 others(17): Show |
intron_variant | MODIFIER | c.570+701G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45930397 | ||||||
| chr22:45930454
|
C | T | 2 | a0001c0001t0017g0247a0001c0001t0017g0248 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.570+644G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45930454 | ||||||
| chr22:45930459
|
A | G | 270 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0167others(267): Show | 271 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.570+639T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45930459 | ||||||
| chr22:45930581
|
G | A | 15 | a0001c0001t0001g0241a0001c0001t0001g0245a0001c0001t0001g0246others(12): Show | 15 | HG01109.hp2 HG01243.hp1 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.570+517C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45930581 | ||||||
| chr22:45930586
|
G | A | 30 | a0001c0001t0005g0149a0001c0001t0005g0180a0001c0001t0005g0202others(27): Show | 30 | HG01069.hp1 HG01255.hp1 HG01256.hp2 others(27): Show |
intron_variant | MODIFIER | c.570+512C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45930586 | ||||||
| chr22:45930602
|
G | A | 1 | a0001c0001t0010g0007 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.570+496C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45930602 | ||||||
| chr22:45930684
|
G | C | 2 | a0001c0001t0001g0269a0001c0001t0001g0270 | 2 | HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.570+414C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45930684 | ||||||
| chr22:45930704
|
C | G | 2 | a0001c0001t0007g0161a0001c0001t0007g0162 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.570+394G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45930704 | ||||||
| chr22:45930711
|
G | C | 104 | a0001c0001t0001g0167a0001c0001t0001g0175a0001c0001t0001g0188others(101): Show | 105 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.570+387C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45930711 | ||||||
| chr22:45930730
|
G | T | 155 | a0001c0001t0001g0167a0001c0001t0001g0175a0001c0001t0001g0188others(152): Show | 156 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.570+368C>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45930730 | ||||||
| chr22:45930740
|
G | A | 107 | a0001c0001t0001g0167a0001c0001t0001g0175a0001c0001t0001g0188others(104): Show | 108 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.570+358C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45930740 | ||||||
| chr22:45930757
|
G | A | 32 | a0001c0001t0005g0149a0001c0001t0005g0180a0001c0001t0005g0202others(29): Show | 32 | HG01069.hp1 HG01255.hp1 HG01256.hp2 others(29): Show |
intron_variant | MODIFIER | c.570+341C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45930757 | ||||||
| chr22:45930791
|
G | C | 143 | a0001c0001t0001g0167a0001c0001t0001g0175a0001c0001t0001g0188others(140): Show | 144 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.570+307C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45930791 | ||||||
| chr22:45930795
|
C | G | 1 | a0001c0002t0037g0015 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.570+303G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45930795 | ||||||
| chr22:45930828
|
C | A | 1 | a0001c0001t0065g0347 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.570+270G>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45930828 | ||||||
| chr22:45931019
|
G | A | 1 | a0001c0001t0029g0319 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.570+79C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45931019 | ||||||
| chr22:45931069
|
G | A | 1 | a0001c0002t0018g0157 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.570+29C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45931069 | ||||||
| chr22:45931386
|
G | A | 1 | a0001c0001t0004g0300 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.299-17C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45931386 | ||||||
| chr22:45931392
|
A | G | 14 | a0001c0001t0001g0188a0001c0001t0001g0238a0001c0001t0001g0271others(11): Show | 15 | HG01256.hp1 HG02451.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.299-23T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45931392 | ||||||
| chr22:45931430
|
G | A | 8 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0292others(5): Show | 8 | HG02486.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.299-61C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45931430 | ||||||
| chr22:45931495
|
G | GC | 6 | a0001c0001t0001g0175a0001c0001t0003g0006a0001c0001t0003g0139others(3): Show | 6 | HG00544.hp2 HG00738.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.299-127dupG | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45931495 | ||||||
| chr22:45931568
|
ACCTGGTA others(30): Show |
A | 1 | a0001c0001t0065g0347 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.299-236_299-200del others(37): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45931568 | ||||||
| chr22:45931603
|
GTGCCTGG others(30): Show |
G | 11 | a0001c0001t0010g0007a0001c0001t0010g0029a0001c0001t0010g0063others(8): Show | 11 | HG00280.hp2 HG00323.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.299-271_299-235del others(37): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45931603 | ||||||
| chr22:45931660
|
C | G | 47 | a0001c0001t0001g0167a0001c0001t0001g0175a0001c0001t0002g0138others(44): Show | 47 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.299-291G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45931660 | ||||||
| chr22:45931664
|
C | T | 1 | a0001c0001t0020g0158 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.299-295G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45931664 | ||||||
| chr22:45931719
|
C | A | 1 | a0001c0001t0001g0210 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.299-350G>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45931719 | ||||||
| chr22:45931771
|
T | C | 1 | a0001c0002t0037g0015 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.299-402A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45931771 | ||||||
| chr22:45931789
|
G | C | 4 | a0001c0001t0001g0271a0001c0001t0001g0281a0001c0001t0002g0083others(1): Show | 4 | HG01256.hp1 HG02451.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-420C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45931789 | ||||||
| chr22:45931896
|
G | A | 1 | a0001c0002t0018g0157 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.299-527C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45931896 | ||||||
| chr22:45931896
|
G | C | 2 | a0001c0001t0014g0313a0001c0001t0063g0344 | 2 | HG01943.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.299-527C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45931896 | ||||||
| chr22:45931942
|
A | C | 2 | a0001c0001t0014g0313a0001c0001t0063g0344 | 2 | HG01943.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.299-573T>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45931942 | ||||||
| chr22:45931951
|
G | C | 3 | a0001c0001t0001g0174a0001c0001t0002g0048a0001c0001t0002g0066 | 3 | NA19004.hp2 NA19057.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.299-582C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45931951 | ||||||
| chr22:45931975
|
C | T | 3 | a0001c0001t0001g0220a0001c0001t0001g0265a0001c0001t0044g0147 | 3 | HG00735.hp2 HG02698.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.299-606G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45931975 | ||||||
| chr22:45931977
|
G | A | 103 | a0001c0001t0001g0167a0001c0001t0001g0175a0001c0001t0001g0188others(100): Show | 104 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.299-608C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45931977 | ||||||
| chr22:45931988
|
G | A | 38 | a0001c0001t0001g0306a0001c0001t0003g0139a0001c0001t0004g0169others(35): Show | 38 | HG01069.hp1 HG01243.hp1 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.299-619C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45931988 | ||||||
| chr22:45932002
|
G | A | 1 | a0001c0001t0002g0055 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.299-633C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45932002 | ||||||
| chr22:45932026
|
A | C | 1 | a0001c0001t0002g0094 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.299-657T>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45932026 | ||||||
| chr22:45932134
|
G | C | 2 | a0001c0001t0014g0313a0001c0001t0063g0344 | 2 | HG01943.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.299-765C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45932134 | ||||||
| chr22:45932207
|
G | T | 1 | a0001c0001t0002g0146 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.299-838C>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45932207 | ||||||
| chr22:45932292
|
G | A | 1 | a0001c0001t0004g0232 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.299-923C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45932292 | ||||||
| chr22:45932320
|
G | A | 1 | a0001c0001t0059g0156 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.299-951C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45932320 | ||||||
| chr22:45932416
|
A | ACC | 60 | a0001c0001t0001g0188a0001c0001t0001g0238a0001c0001t0001g0271others(57): Show | 61 | HG01069.hp1 HG01099.hp1 HG01255.hp1 others(58): Show |
intron_variant | MODIFIER | c.299-1049_299-1048d others(4): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45932416 | ||||||
| chr22:45932419
|
C | A | 2 | a0001c0001t0031g0004a0001c0001t0038g0009 | 2 | HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.299-1050G>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45932419 | ||||||
| chr22:45932448
|
T | C | 5 | a0001c0001t0042g0013a0001c0001t0048g0326a0001c0001t0065g0347others(2): Show | 5 | HG01243.hp1 HG01433.hp2 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.299-1079A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45932448 | ||||||
| chr22:45932558
|
C | T | 1 | a0001c0001t0003g0078 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.299-1189G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45932558 | ||||||
| chr22:45932567
|
T | G | 57 | a0001c0001t0001g0188a0001c0001t0001g0238a0001c0001t0001g0271others(54): Show | 58 | HG01069.hp1 HG01255.hp1 HG01256.hp1 others(55): Show |
intron_variant | MODIFIER | c.299-1198A>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45932567 | ||||||
| chr22:45932571
|
T | C | 1 | a0001c0002t0037g0015 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.299-1202A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45932571 | ||||||
| chr22:45932582
|
T | G | 2 | a0001c0002t0018g0157a0001c0011t0049g0330 | 2 | HG01891.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.299-1213A>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45932582 | ||||||
| chr22:45932606
|
C | G | 58 | a0001c0001t0001g0167a0001c0001t0001g0175a0001c0001t0001g0212others(55): Show | 58 | HG00544.hp2 HG00639.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.299-1237G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45932606 | ||||||
| chr22:45932606
|
C | T | 2 | a0001c0001t0001g0276a0001c0009t0002g0067 | 2 | NA19065.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.299-1237G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45932606 | ||||||
| chr22:45932674
|
T | C | 8 | a0001c0001t0001g0148a0001c0001t0002g0008a0001c0001t0002g0023others(5): Show | 8 | HG00423.hp2 HG00597.hp2 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.299-1305A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45932674 | ||||||
| chr22:45932684
|
G | A | 3 | a0001c0001t0005g0301a0001c0001t0006g0073a0001c0001t0027g0256 | 3 | HG01099.hp1 HG02109.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.299-1315C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45932684 | ||||||
| chr22:45932704
|
G | A | 2 | a0001c0002t0018g0157a0001c0011t0049g0330 | 2 | HG01891.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.299-1335C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45932704 | ||||||
| chr22:45932819
|
C | G | 30 | a0001c0001t0001g0306a0001c0001t0005g0149a0001c0001t0005g0180others(27): Show | 30 | HG01069.hp1 HG01255.hp1 HG01256.hp2 others(27): Show |
intron_variant | MODIFIER | c.299-1450G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45932819 | ||||||
| chr22:45932861
|
CAGCACCC others(3): Show |
C | 2 | a0001c0001t0042g0013a0001c0001t0068g0348 | 2 | HG01496.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.299-1502_299-1493d others(12): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45932861 | ||||||
| chr22:45932879
|
G | A | 3 | a0001c0001t0003g0068a0001c0001t0004g0200a0001c0001t0004g0300 | 3 | HG01255.hp2 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.299-1510C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45932879 | ||||||
| chr22:45932902
|
C | T | 1 | a0001c0001t0068g0348 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.299-1533G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45932902 | ||||||
| chr22:45932974
|
T | C | 134 | a0001c0001t0001g0167a0001c0001t0001g0175a0001c0001t0001g0188others(131): Show | 135 | HG00280.hp2 HG00323.hp1 HG00544.hp2 others(132): Show |
intron_variant | MODIFIER | c.299-1605A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45932974 | ||||||
| chr22:45933046
|
G | A | 2 | a0001c0001t0014g0313a0001c0001t0063g0344 | 2 | HG01943.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.299-1677C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45933046 | ||||||
| chr22:45933104
|
C | T | 2 | a0001c0001t0007g0321a0001c0002t0030g0003 | 2 | HG00642.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.299-1735G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45933104 | ||||||
| chr22:45933169
|
C | A | 1 | a0001c0002t0037g0015 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.299-1800G>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45933169 | ||||||
| chr22:45933169
|
C | T | 1 | a0001c0001t0059g0156 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.299-1800G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45933169 | ||||||
| chr22:45933176
|
G | C | 2 | a0001c0002t0018g0157a0001c0011t0049g0330 | 2 | HG01891.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.299-1807C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45933176 | ||||||
| chr22:45933185
|
A | G | 4 | a0001c0001t0002g0021a0001c0001t0002g0037a0001c0001t0002g0049others(1): Show | 4 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-1816T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45933185 | ||||||
| chr22:45933194
|
C | T | 1 | a0001c0003t0021g0311 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.299-1825G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45933194 | ||||||
| chr22:45933231
|
G | A | 1 | a0001c0001t0001g0267 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.299-1862C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45933231 | ||||||
| chr22:45933264
|
C | T | 2 | a0001c0001t0009g0268a0001c0001t0062g0339 | 2 | HG02970.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.299-1895G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45933264 | ||||||
| chr22:45933269
|
C | T | 129 | a0001c0001t0001g0167a0001c0001t0001g0175a0001c0001t0001g0188others(126): Show | 130 | HG00280.hp2 HG00323.hp1 HG00544.hp2 others(127): Show |
intron_variant | MODIFIER | c.299-1900G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45933269 | ||||||
| chr22:45933345
|
C | T | 2 | a0001c0001t0018g0327a0001c0001t0048g0326 | 2 | HG01243.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.299-1976G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45933345 | ||||||
| chr22:45933351
|
T | A | 2 | a0001c0002t0018g0157a0001c0011t0049g0330 | 2 | HG01891.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.299-1982A>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45933351 | ||||||
| chr22:45933383
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.299-2014C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45933383 | ||||||
| chr22:45933450
|
G | A | 5 | a0001c0003t0021g0229a0001c0003t0021g0311a0001c0003t0040g0046others(2): Show | 5 | HG01884.hp1 HG02257.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.299-2081C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45933450 | ||||||
| chr22:45933648
|
T | C | 2 | a0001c0001t0014g0313a0001c0001t0063g0344 | 2 | HG01943.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.299-2279A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45933648 | ||||||
| chr22:45933731
|
G | A | 4 | a0001c0001t0019g0244a0001c0001t0019g0290a0001c0001t0019g0332others(1): Show | 4 | HG02630.hp1 HG02647.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-2362C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45933731 | ||||||
| chr22:45933784
|
G | A | 13 | a0001c0001t0001g0241a0001c0001t0001g0269a0001c0001t0009g0268others(10): Show | 13 | HG01243.hp1 HG01433.hp2 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.299-2415C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45933784 | ||||||
| chr22:45933876
|
G | C | 1 | a0001c0001t0065g0347 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.299-2507C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45933876 | ||||||
| chr22:45933917
|
C | T | 5 | a0001c0001t0001g0325a0001c0001t0020g0225a0001c0002t0014g0274others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.299-2548G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45933917 | ||||||
| chr22:45933938
|
T | C | 145 | a0001c0001t0001g0167a0001c0001t0001g0175a0001c0001t0001g0188others(142): Show | 146 | HG00280.hp2 HG00323.hp1 HG00544.hp2 others(143): Show |
intron_variant | MODIFIER | c.299-2569A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45933938 | ||||||
| chr22:45933966
|
C | T | 4 | a0001c0002t0018g0157a0001c0011t0049g0330a0001c0016t0007g0280others(1): Show | 4 | HG01891.hp2 HG03041.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-2597G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45933966 | ||||||
| chr22:45933999
|
A | G | 1 | a0001c0001t0002g0112 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.299-2630T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45933999 | ||||||
| chr22:45934047
|
G | A | 20 | a0001c0001t0001g0241a0001c0001t0009g0268a0001c0001t0019g0290others(17): Show | 20 | HG01243.hp1 HG01433.hp2 HG01496.hp2 others(17): Show |
intron_variant | MODIFIER | c.299-2678C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45934047 | ||||||
| chr22:45934056
|
G | A | 1 | a0001c0001t0001g0191 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.299-2687C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45934056 | ||||||
| chr22:45934099
|
C | T | 1 | a0001c0001t0019g0244 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.299-2730G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45934099 | ||||||
| chr22:45934191
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.299-2822C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45934191 | ||||||
| chr22:45934313
|
G | A | 2 | a0001c0001t0001g0308a0001c0001t0001g0309 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.299-2944C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45934313 | ||||||
| chr22:45934394
|
G | C | 1 | a0001c0001t0048g0326 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.299-3025C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45934394 | ||||||
| chr22:45934639
|
G | A | 1 | a0001c0001t0002g0083 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.299-3270C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45934639 | ||||||
| chr22:45934679
|
C | T | 1 | a0001c0001t0013g0151 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.299-3310G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45934679 | ||||||
| chr22:45934713
|
T | C | 2 | a0001c0001t0019g0244a0001c0007t0054g0334 | 2 | HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.299-3344A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45934713 | ||||||
| chr22:45934801
|
A | C | 2 | a0001c0001t0014g0313a0001c0001t0063g0344 | 2 | HG01943.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.299-3432T>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45934801 | ||||||
| chr22:45934901
|
G | A | 2 | a0001c0001t0001g0269a0001c0001t0001g0270 | 2 | HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.299-3532C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45934901 | ||||||
| chr22:45934925
|
T | C | 136 | a0001c0001t0001g0167a0001c0001t0001g0175a0001c0001t0001g0188others(133): Show | 137 | HG00280.hp2 HG00323.hp1 HG00544.hp2 others(134): Show |
intron_variant | MODIFIER | c.299-3556A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45934925 | ||||||
| chr22:45934999
|
G | A | 1 | a0001c0003t0053g0310 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.299-3630C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45934999 | ||||||
| chr22:45935001
|
T | C | 7 | a0001c0001t0001g0299a0001c0001t0001g0303a0001c0001t0001g0305others(4): Show | 7 | HG01361.hp2 HG01975.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.299-3632A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45935001 | ||||||
| chr22:45935098
|
G | A | 2 | a0001c0001t0014g0313a0001c0001t0063g0344 | 2 | HG01943.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.299-3729C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45935098 | ||||||
| chr22:45935151
|
C | A | 16 | a0001c0001t0001g0241a0001c0001t0009g0268a0001c0001t0031g0004others(13): Show | 16 | HG01243.hp1 HG01433.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.299-3782G>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45935151 | ||||||
| chr22:45935181
|
G | T | 4 | a0001c0001t0019g0244a0001c0001t0019g0290a0001c0001t0019g0332others(1): Show | 4 | HG02630.hp1 HG02647.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-3812C>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45935181 | ||||||
| chr22:45935208
|
G | A | 1 | a0001c0001t0068g0348 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.299-3839C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45935208 | ||||||
| chr22:45935243
|
T | C | 3 | a0001c0001t0001g0341a0001c0002t0001g0163a0001c0002t0001g0224 | 3 | NA19030.hp1 NA19030.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.299-3874A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45935243 | ||||||
| chr22:45935304
|
G | A | 1 | a0001c0001t0058g0236 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.299-3935C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45935304 | ||||||
| chr22:45935368
|
C | T | 1 | a0001c0001t0062g0339 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.299-3999G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45935368 | ||||||
| chr22:45935536
|
C | T | 1 | a0001c0001t0001g0181 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.299-4167G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45935536 | ||||||
| chr22:45935537
|
G | A | 7 | a0001c0001t0009g0268a0001c0001t0031g0004a0001c0001t0038g0009others(4): Show | 7 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.299-4168C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45935537 | ||||||
| chr22:45935618
|
G | A | 2 | a0001c0001t0014g0313a0001c0001t0063g0344 | 2 | HG01943.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.299-4249C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45935618 | ||||||
| chr22:45935629
|
G | A | 6 | a0001c0001t0001g0241a0001c0001t0048g0326a0001c0001t0065g0347others(3): Show | 6 | HG01243.hp1 HG01433.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.299-4260C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45935629 | ||||||
| chr22:45935697
|
G | T | 1 | a0001c0002t0037g0015 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.299-4328C>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45935697 | ||||||
| chr22:45935762
|
T | A | 2 | a0001c0001t0002g0080a0001c0001t0002g0126 | 2 | NA18983.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.299-4393A>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45935762 | ||||||
| chr22:45935779
|
C | T | 37 | a0001c0001t0001g0167a0001c0001t0001g0175a0001c0001t0001g0214others(34): Show | 37 | HG00544.hp2 HG00639.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.299-4410G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45935779 | ||||||
| chr22:45935915
|
C | T | 4 | a0001c0001t0025g0322a0001c0002t0018g0157a0001c0011t0049g0330others(1): Show | 4 | HG01891.hp2 HG03041.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-4546G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45935915 | ||||||
| chr22:45935999
|
G | A | 1 | a0001c0001t0056g0226 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.299-4630C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45935999 | ||||||
| chr22:45936091
|
G | T | 3 | a0001c0002t0018g0157a0001c0011t0049g0330a0002c0015t0009g0228 | 3 | HG01891.hp2 HG03041.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.299-4722C>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45936091 | ||||||
| chr22:45936109
|
T | G | 1 | a0001c0001t0002g0083 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.299-4740A>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45936109 | ||||||
| chr22:45936147
|
C | T | 4 | a0001c0001t0025g0322a0001c0001t0029g0240a0001c0001t0029g0319others(1): Show | 4 | HG02559.hp1 HG02622.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-4778G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45936147 | ||||||
| chr22:45936190
|
C | T | 1 | a0001c0001t0041g0130 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.299-4821G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45936190 | ||||||
| chr22:45936254
|
C | G | 26 | a0001c0001t0001g0241a0001c0001t0009g0268a0001c0001t0010g0007others(23): Show | 26 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(23): Show |
intron_variant | MODIFIER | c.299-4885G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45936254 | ||||||
| chr22:45936319
|
T | C | 1 | a0001c0001t0001g0263 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.299-4950A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45936319 | ||||||
| chr22:45936352
|
C | T | 1 | a0001c0001t0058g0236 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.299-4983G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45936352 | ||||||
| chr22:45936439
|
C | T | 2 | a0001c0001t0001g0302a0001c0001t0002g0062 | 2 | HG01934.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.299-5070G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45936439 | ||||||
| chr22:45936457
|
C | T | 1 | a0001c0001t0002g0044 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.299-5088G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45936457 | ||||||
| chr22:45936544
|
C | T | 1 | a0001c0001t0050g0235 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.299-5175G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45936544 | ||||||
| chr22:45936573
|
C | T | 1 | a0001c0001t0002g0091 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.299-5204G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45936573 | ||||||
| chr22:45936583
|
C | T | 11 | a0001c0001t0001g0188a0001c0001t0001g0238a0001c0001t0001g0271others(8): Show | 12 | HG01256.hp1 HG02451.hp1 HG02683.hp2 others(9): Show |
intron_variant | MODIFIER | c.299-5214G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45936583 | ||||||
| chr22:45936756
|
C | G | 1 | a0001c0001t0001g0269 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.299-5387G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45936756 | ||||||
| chr22:45936933
|
A | G | 103 | a0001c0001t0001g0167a0001c0001t0001g0175a0001c0001t0001g0212others(100): Show | 103 | HG00280.hp2 HG00323.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.299-5564T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45936933 | ||||||
| chr22:45936941
|
C | T | 3 | a0001c0002t0018g0157a0001c0011t0049g0330a0002c0015t0009g0228 | 3 | HG01891.hp2 HG03041.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.299-5572G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45936941 | ||||||
| chr22:45936965
|
C | T | 11 | a0001c0001t0009g0268a0001c0001t0012g0159a0001c0001t0012g0259others(8): Show | 11 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.299-5596G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45936965 | ||||||
| chr22:45937034
|
C | T | 71 | a0001c0001t0001g0167a0001c0001t0001g0175a0001c0001t0001g0214others(68): Show | 71 | HG00544.hp2 HG00639.hp1 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.299-5665G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45937034 | ||||||
| chr22:45937507
|
C | T | 7 | a0001c0001t0001g0241a0001c0001t0018g0327a0001c0001t0048g0326others(4): Show | 7 | HG01243.hp1 HG01243.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.299-6138G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45937507 | ||||||
| chr22:45937574
|
A | T | 61 | a0001c0001t0001g0212a0001c0001t0001g0241a0001c0001t0002g0102others(58): Show | 61 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.299-6205T>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45937574 | ||||||
| chr22:45937586
|
T | TG | 40 | a0001c0001t0001g0212a0001c0001t0001g0241a0001c0001t0002g0102others(37): Show | 40 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.299-6218dupC | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45937586 | ||||||
| chr22:45937611
|
G | C | 1 | a0001c0001t0002g0038 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.299-6242C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45937611 | ||||||
| chr22:45937645
|
G | C | 1 | a0001c0001t0012g0329 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.299-6276C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45937645 | ||||||
| chr22:45937729
|
G | A | 3 | a0001c0001t0012g0159a0001c0001t0012g0259a0001c0001t0012g0329 | 3 | HG03453.hp2 NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.299-6360C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45937729 | ||||||
| chr22:45937745
|
G | A | 4 | a0001c0001t0003g0065a0001c0001t0003g0111a0001c0001t0003g0139others(1): Show | 4 | HG00621.hp1 NA18612.hp1 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-6376C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45937745 | ||||||
| chr22:45937775
|
T | A | 45 | a0001c0001t0001g0212a0001c0001t0002g0102a0001c0001t0002g0108others(42): Show | 45 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.299-6406A>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45937775 | ||||||
| chr22:45937913
|
G | A | 2 | a0001c0001t0019g0290a0001c0001t0019g0332 | 2 | HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.299-6544C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45937913 | ||||||
| chr22:45937995
|
C | T | 1 | a0001c0001t0008g0141 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.299-6626G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45937995 | ||||||
| chr22:45938004
|
G | A | 4 | a0001c0003t0021g0229a0001c0003t0021g0311a0001c0003t0040g0046others(1): Show | 4 | HG01884.hp1 HG02257.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-6635C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45938004 | ||||||
| chr22:45938105
|
T | C | 1 | a0001c0001t0068g0348 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.299-6736A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45938105 | ||||||
| chr22:45938125
|
G | A | 3 | a0001c0002t0018g0157a0001c0011t0049g0330a0002c0015t0009g0228 | 3 | HG01891.hp2 HG03041.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.299-6756C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45938125 | ||||||
| chr22:45938253
|
G | T | 114 | a0001c0001t0001g0167a0001c0001t0001g0175a0001c0001t0001g0188others(111): Show | 115 | HG00280.hp2 HG00323.hp1 HG00544.hp2 others(112): Show |
intron_variant | MODIFIER | c.299-6884C>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45938253 | ||||||
| chr22:45938301
|
C | T | 2 | a0001c0001t0001g0242a0001c0001t0001g0243 | 2 | HG01109.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.299-6932G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45938301 | ||||||
| chr22:45938302
|
G | A | 2 | a0001c0001t0013g0286a0001c0003t0021g0311 | 2 | HG01884.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.299-6933C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45938302 | ||||||
| chr22:45938354
|
T | C | 204 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0167others(201): Show | 205 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(202): Show |
intron_variant | MODIFIER | c.299-6985A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45938354 | ||||||
| chr22:45938365
|
T | G | 2 | a0001c0001t0025g0160a0001c0001t0025g0322 | 2 | HG02886.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.299-6996A>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45938365 | ||||||
| chr22:45938394
|
C | T | 13 | a0001c0001t0009g0268a0001c0001t0019g0244a0001c0001t0019g0290others(10): Show | 13 | HG01891.hp2 HG02258.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.299-7025G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45938394 | ||||||
| chr22:45938401
|
T | C | 15 | a0001c0001t0009g0268a0001c0001t0014g0324a0001c0001t0019g0244others(12): Show | 15 | HG01891.hp2 HG02258.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.299-7032A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45938401 | ||||||
| chr22:45938412
|
G | A | 15 | a0001c0001t0009g0268a0001c0001t0014g0324a0001c0001t0019g0244others(12): Show | 15 | HG01891.hp2 HG02258.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.299-7043C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45938412 | ||||||
| chr22:45938465
|
C | A | 3 | a0001c0001t0019g0244a0001c0001t0019g0290a0001c0001t0019g0332 | 3 | HG02630.hp1 HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.299-7096G>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45938465 | ||||||
| chr22:45938510
|
G | A | 1 | a0001c0001t0003g0056 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.299-7141C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45938510 | ||||||
| chr22:45938536
|
C | A | 3 | a0001c0001t0018g0327a0001c0001t0048g0326a0001c0014t0018g0260 | 3 | HG01243.hp1 HG01243.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.299-7167G>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45938536 | ||||||
| chr22:45938559
|
C | G | 15 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0284others(12): Show | 15 | HG01884.hp1 HG02257.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.299-7190G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45938559 | ||||||
| chr22:45938587
|
A | C | 152 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0167others(149): Show | 152 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.299-7218T>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45938587 | ||||||
| chr22:45938603
|
A | T | 152 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0167others(149): Show | 152 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.299-7234T>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45938603 | ||||||
| chr22:45938845
|
T | C | 4 | a0001c0001t0001g0341a0001c0001t0012g0259a0001c0002t0001g0163others(1): Show | 4 | NA19030.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-7476A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45938845 | ||||||
| chr22:45938850
|
T | C | 164 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0167others(161): Show | 164 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.299-7481A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45938850 | ||||||
| chr22:45938861
|
A | G | 4 | a0001c0001t0014g0324a0001c0001t0024g0099a0001c0002t0014g0274others(1): Show | 4 | HG01891.hp2 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-7492T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45938861 | ||||||
| chr22:45938871
|
T | C | 1 | a0001c0001t0001g0295 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.299-7502A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45938871 | ||||||
| chr22:45938914
|
C | A | 2 | a0001c0004t0007g0342a0001c0004t0034g0011 | 2 | HG02258.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.299-7545G>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45938914 | ||||||
| chr22:45939126
|
G | A | 4 | a0001c0001t0019g0244a0001c0001t0019g0290a0001c0001t0019g0332others(1): Show | 4 | HG02630.hp1 HG02647.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-7757C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45939126 | ||||||
| chr22:45939189
|
G | A | 1 | a0001c0001t0003g0078 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.299-7820C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45939189 | ||||||
| chr22:45939229
|
G | T | 4 | a0001c0001t0014g0324a0001c0001t0024g0099a0001c0002t0014g0274others(1): Show | 4 | HG01891.hp2 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-7860C>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45939229 | ||||||
| chr22:45939274
|
A | G | 2 | a0001c0001t0001g0308a0001c0001t0001g0309 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.299-7905T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45939274 | ||||||
| chr22:45939398
|
A | G | 1 | a0001c0002t0018g0157 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.299-8029T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45939398 | ||||||
| chr22:45939479
|
C | T | 7 | a0001c0001t0009g0268a0001c0001t0031g0004a0001c0001t0038g0009others(4): Show | 7 | HG02258.hp1 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.299-8110G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45939479 | ||||||
| chr22:45939484
|
T | TACAGTGT others(10): Show |
1 | a0001c0001t0001g0197 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.299-8116_299-8115i others(19): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45939484 | ||||||
| chr22:45939542
|
C | G | 37 | a0001c0001t0001g0167a0001c0001t0001g0175a0001c0001t0001g0214others(34): Show | 37 | HG00544.hp2 HG00639.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.299-8173G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45939542 | ||||||
| chr22:45939568
|
C | T | 2 | a0001c0001t0001g0208a0001c0001t0002g0137 | 2 | HG00673.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.299-8199G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45939568 | ||||||
| chr22:45939632
|
A | AAC | 130 | a0001c0001t0001g0150a0001c0001t0001g0152a0001c0001t0001g0153others(127): Show | 131 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.299-8265_299-8264d others(4): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45939632 | ||||||
| chr22:45939632
|
A | AACAC | 6 | a0001c0001t0001g0192a0001c0001t0004g0221a0001c0001t0004g0222others(3): Show | 6 | HG02257.hp1 HG02886.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.299-8267_299-8264d others(6): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45939632 | ||||||
| chr22:45939632
|
A | AACACAC | 36 | a0001c0001t0001g0175a0001c0001t0001g0213a0001c0001t0001g0276others(33): Show | 36 | HG00544.hp2 HG00639.hp1 HG01361.hp2 others(33): Show |
intron_variant | MODIFIER | c.299-8269_299-8264d others(8): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45939632 | ||||||
| chr22:45939632
|
A | AACACACA others(1): Show |
26 | a0001c0001t0001g0184a0001c0001t0001g0238a0001c0001t0001g0284others(23): Show | 26 | HG00597.hp2 HG00642.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.299-8271_299-8264d others(10): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45939632 | ||||||
| chr22:45939632
|
A | AACACACA others(3): Show |
57 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0174others(54): Show | 58 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.299-8273_299-8264d others(12): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45939632 | ||||||
| chr22:45939632
|
A | AACACACA others(5): Show |
19 | a0001c0001t0001g0148a0001c0001t0001g0219a0001c0001t0001g0266others(16): Show | 19 | HG00423.hp2 HG01243.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.299-8275_299-8264d others(14): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45939632 | ||||||
| chr22:45939632
|
A | AACACACA others(7): Show |
10 | a0001c0001t0001g0201a0001c0001t0001g0223a0001c0001t0001g0272others(7): Show | 10 | HG02080.hp1 HG02155.hp1 HG03017.hp2 others(7): Show |
intron_variant | MODIFIER | c.299-8277_299-8264d others(16): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45939632 | ||||||
| chr22:45939632
|
A | AACACACA others(9): Show |
2 | a0001c0001t0009g0250a0001c0001t0063g0344 | 2 | HG01943.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.299-8279_299-8264d others(18): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45939632 | ||||||
| chr22:45939632
|
A | AACACACA others(11): Show |
1 | a0001c0001t0068g0348 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.299-8264_299-8263i others(20): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45939632 | ||||||
| chr22:45939632
|
A | AACACACC others(10): Show |
1 | a0001c0001t0001g0208 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.299-8264_299-8263i others(19): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45939632 | ||||||
| chr22:45939632
|
A | ACACACAC others(4): Show |
1 | a0001c0001t0002g0083 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.299-8264_299-8263i others(13): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45939632 | ||||||
| chr22:45939632
|
A | ACACACAC others(8): Show |
1 | a0001c0001t0055g0176 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.299-8264_299-8263i others(17): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45939632 | ||||||
| chr22:45939637
|
ACACACAC others(5): Show |
A | 2 | a0001c0001t0019g0290a0001c0001t0019g0332 | 2 | HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.299-8280_299-8269d others(14): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45939637 | ||||||
| chr22:45939641
|
ACACACAC others(1): Show |
A | 6 | a0001c0001t0001g0263a0001c0001t0012g0159a0001c0001t0012g0329others(3): Show | 6 | HG02451.hp2 HG02895.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.299-8280_299-8273d others(10): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45939641 | ||||||
| chr22:45939645
|
A | ACACACAC others(1): Show |
3 | a0001c0001t0029g0240a0001c0001t0029g0319a0001c0001t0059g0156 | 3 | HG02559.hp1 HG02622.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.299-8277_299-8276i others(10): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45939645 | ||||||
| chr22:45939647
|
A | ACACT | 4 | a0001c0001t0001g0253a0001c0001t0002g0031a0001c0001t0003g0006others(1): Show | 4 | HG01069.hp2 HG02896.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-8279_299-8278i others(6): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45939647 | ||||||
| chr22:45939647
|
ACT | A | 17 | a0001c0001t0002g0084a0001c0001t0005g0249a0001c0001t0005g0288others(14): Show | 17 | HG01358.hp2 HG02109.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.299-8280_299-8279d others(4): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45939647 | ||||||
| chr22:45939649
|
T | A | 179 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0167others(176): Show | 180 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.299-8280A>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45939649 | ||||||
| chr22:45939655
|
A | T | 2 | a0001c0001t0005g0149a0001c0001t0006g0121 | 2 | HG01255.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.299-8286T>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45939655 | ||||||
| chr22:45939670
|
C | CACACACA others(3): Show |
1 | a0001c0001t0002g0023 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.299-8302_299-8301i others(12): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45939670 | ||||||
| chr22:45939671
|
A | ACACACAC others(4): Show |
1 | a0001c0001t0001g0212 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.299-8303_299-8302i others(13): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45939671 | ||||||
| chr22:45939672
|
A | C | 3 | a0001c0001t0001g0231a0001c0001t0002g0051a0001c0001t0009g0268 | 3 | HG00609.hp1 HG03486.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.299-8303T>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45939672 | ||||||
| chr22:45939676
|
T | C | 1 | a0001c0004t0007g0342 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.299-8307A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45939676 | ||||||
| chr22:45939692
|
T | C | 3 | a0001c0001t0029g0240a0001c0001t0029g0319a0001c0001t0059g0156 | 3 | HG02559.hp1 HG02622.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.299-8323A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45939692 | ||||||
| chr22:45939743
|
TTGGGCCC others(465): Show |
T | 1 | a0001c0001t0001g0197 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.299-8846_299-8375d others(2): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45939743 | ||||||
| chr22:45939780
|
C | T | 2 | a0001c0001t0014g0313a0001c0001t0063g0344 | 2 | HG01943.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.299-8411G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45939780 | ||||||
| chr22:45940114
|
G | A | 1 | a0001c0002t0020g0336 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.299-8745C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45940114 | ||||||
| chr22:45940190
|
G | A | 13 | a0001c0001t0001g0284a0001c0001t0014g0254a0001c0001t0019g0244others(10): Show | 13 | HG01884.hp1 HG02257.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.299-8821C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45940190 | ||||||
| chr22:45940323
|
C | A | 39 | a0001c0001t0001g0212a0001c0001t0001g0261a0001c0001t0001g0262others(36): Show | 39 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.299-8954G>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45940323 | ||||||
| chr22:45940390
|
T | A | 1 | a0001c0001t0002g0094 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.299-9021A>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45940390 | ||||||
| chr22:45940422
|
A | G | 95 | a0001c0001t0001g0167a0001c0001t0001g0175a0001c0001t0001g0212others(92): Show | 95 | HG00544.hp2 HG00639.hp1 HG00642.hp2 others(92): Show |
intron_variant | MODIFIER | c.299-9053T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45940422 | ||||||
| chr22:45940463
|
C | T | 36 | a0001c0001t0001g0167a0001c0001t0001g0175a0001c0001t0001g0214others(33): Show | 36 | HG00544.hp2 HG00639.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.299-9094G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45940463 | ||||||
| chr22:45940559
|
G | A | 31 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0284others(28): Show | 31 | HG01884.hp1 HG01891.hp2 HG02257.hp2 others(28): Show |
intron_variant | MODIFIER | c.299-9190C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45940559 | ||||||
| chr22:45940561
|
G | A | 1 | a0001c0010t0002g0097 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.299-9192C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45940561 | ||||||
| chr22:45940624
|
C | T | 1 | a0001c0001t0026g0340 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.299-9255G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45940624 | ||||||
| chr22:45940675
|
G | A | 5 | a0001c0002t0037g0015a0001c0003t0021g0229a0001c0003t0021g0311others(2): Show | 5 | HG01884.hp1 HG02257.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.298+9245C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45940675 | ||||||
| chr22:45940755
|
G | C | 7 | a0001c0001t0018g0327a0001c0001t0020g0225a0001c0001t0065g0347others(4): Show | 7 | HG01243.hp2 HG01433.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.298+9165C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45940755 | ||||||
| chr22:45940854
|
C | G | 2 | a0001c0001t0014g0313a0001c0001t0063g0344 | 2 | HG01943.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.298+9066G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45940854 | ||||||
| chr22:45941000
|
T | G | 1 | a0001c0001t0002g0113 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.298+8920A>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45941000 | ||||||
| chr22:45941001
|
T | C | 2 | a0001c0001t0009g0268a0001c0003t0053g0310 | 2 | HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.298+8919A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45941001 | ||||||
| chr22:45941163
|
C | G | 131 | a0001c0001t0001g0148a0001c0001t0001g0154a0001c0001t0001g0174others(128): Show | 132 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.298+8757G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45941163 | ||||||
| chr22:45941177
|
G | A | 1 | a0001c0002t0030g0003 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.298+8743C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45941177 | ||||||
| chr22:45941231
|
C | T | 3 | a0001c0001t0001g0197a0001c0001t0001g0284a0001c0001t0068g0348 | 3 | HG01496.hp2 HG02622.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.298+8689G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45941231 | ||||||
| chr22:45941238
|
G | A | 116 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0172others(113): Show | 117 | HG00280.hp1 HG00408.hp2 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.298+8682C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45941238 | ||||||
| chr22:45941281
|
G | A | 4 | a0001c0001t0031g0004a0001c0001t0038g0009a0001c0002t0052g0338others(1): Show | 4 | HG02559.hp2 HG02723.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.298+8639C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45941281 | ||||||
| chr22:45941317
|
C | T | 1 | a0001c0001t0014g0254 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.298+8603G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45941317 | ||||||
| chr22:45941411
|
TGAGCCAG others(2): Show |
T | 7 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0320others(4): Show | 7 | HG02896.hp2 HG02897.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.298+8500_298+8508d others(11): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45941411 | ||||||
| chr22:45941440
|
G | T | 3 | a0001c0001t0001g0241a0001c0001t0001g0323a0001c0001t0002g0012 | 3 | HG01109.hp2 HG03098.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.298+8480C>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45941440 | ||||||
| chr22:45941509
|
C | CA | 17 | a0001c0001t0001g0194a0001c0001t0001g0196a0001c0001t0001g0213others(14): Show | 17 | HG00735.hp2 HG00738.hp2 HG01978.hp1 others(14): Show |
intron_variant | MODIFIER | c.298+8410dupT | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45941509 | ||||||
| chr22:45941509
|
C | CAA | 8 | a0001c0001t0001g0271a0001c0001t0005g0283a0001c0001t0007g0161others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.298+8409_298+8410d others(4): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45941509 | ||||||
| chr22:45941509
|
CA | C | 34 | a0001c0001t0001g0152a0001c0001t0001g0216a0001c0001t0001g0261others(31): Show | 34 | HG00323.hp1 HG01099.hp1 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.298+8410delT | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45941509 | ||||||
| chr22:45941509
|
CAA | C | 8 | a0001c0001t0012g0159a0001c0001t0012g0329a0001c0001t0017g0257others(5): Show | 8 | HG01243.hp1 HG01496.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.298+8409_298+8410d others(4): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45941509 | ||||||
| chr22:45941509
|
CAAA | C | 10 | a0001c0001t0014g0324a0001c0001t0024g0099a0001c0001t0031g0004others(7): Show | 10 | HG01433.hp2 HG01891.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.298+8408_298+8410d others(5): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45941509 | ||||||
| chr22:45941527
|
A | G | 3 | a0001c0002t0014g0274a0001c0002t0020g0336a0001c0014t0018g0260 | 3 | HG02258.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.298+8393T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45941527 | ||||||
| chr22:45941529
|
A | G | 1 | a0001c0001t0009g0282 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.298+8391T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45941529 | ||||||
| chr22:45941597
|
G | A | 1 | a0001c0001t0001g0263 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.298+8323C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45941597 | ||||||
| chr22:45941744
|
G | A | 106 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0174others(103): Show | 106 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.298+8176C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45941744 | ||||||
| chr22:45941751
|
A | T | 6 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0325others(3): Show | 6 | HG01884.hp1 HG02055.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.298+8169T>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45941751 | ||||||
| chr22:45941808
|
G | A | 3 | a0001c0001t0068g0348a0001c0002t0018g0157a0001c0003t0053g0310 | 3 | HG01496.hp2 HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.298+8112C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45941808 | ||||||
| chr22:45941849
|
G | C | 269 | a0001c0001t0001g0148a0001c0001t0001g0150a0001c0001t0001g0152others(266): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.298+8071C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45941849 | ||||||
| chr22:45941890
|
G | A | 1 | a0001c0001t0004g0215 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.298+8030C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45941890 | ||||||
| chr22:45941948
|
G | C | 2 | a0001c0001t0001g0246a0001c0001t0001g0253 | 2 | HG02896.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.298+7972C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45941948 | ||||||
| chr22:45942108
|
C | T | 3 | a0001c0001t0009g0268a0001c0002t0007g0230a0001c0002t0052g0338 | 3 | HG03471.hp2 HG03486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.298+7812G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45942108 | ||||||
| chr22:45942165
|
C | T | 19 | a0001c0001t0001g0241a0001c0001t0001g0245a0001c0001t0001g0278others(16): Show | 19 | HG01109.hp2 HG01943.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.298+7755G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45942165 | ||||||
| chr22:45942195
|
C | T | 1 | a0001c0001t0067g0346 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.298+7725G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45942195 | ||||||
| chr22:45942226
|
C | T | 1 | a0001c0001t0048g0326 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.298+7694G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45942226 | ||||||
| chr22:45942373
|
C | A | 3 | a0001c0001t0059g0156a0001c0003t0053g0310a0001c0007t0054g0334 | 3 | HG02572.hp1 HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.298+7547G>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45942373 | ||||||
| chr22:45942450
|
G | A | 1 | a0001c0001t0068g0348 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.298+7470C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45942450 | ||||||
| chr22:45942509
|
A | C | 1 | a0001c0001t0009g0282 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.298+7411T>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45942509 | ||||||
| chr22:45942577
|
T | C | 127 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0174others(124): Show | 127 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.298+7343A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45942577 | ||||||
| chr22:45942645
|
G | GCACCTAA others(1): Show |
8 | a0001c0001t0001g0320a0001c0001t0007g0252a0001c0001t0009g0250others(5): Show | 8 | HG02258.hp2 HG03041.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.298+7267_298+7274d others(10): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45942645 | ||||||
| chr22:45942676
|
T | C | 37 | a0001c0001t0001g0170a0001c0001t0001g0172a0001c0001t0001g0177others(34): Show | 37 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.298+7244A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45942676 | ||||||
| chr22:45942772
|
C | T | 4 | a0001c0001t0001g0241a0001c0001t0001g0323a0001c0001t0002g0012others(1): Show | 4 | HG01109.hp2 HG03098.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.298+7148G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45942772 | ||||||
| chr22:45942773
|
G | A | 1 | a0001c0001t0025g0322 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.298+7147C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45942773 | ||||||
| chr22:45942792
|
G | A | 117 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0174others(114): Show | 117 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.298+7128C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45942792 | ||||||
| chr22:45942793
|
T | A | 112 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0174others(109): Show | 112 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.298+7127A>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45942793 | ||||||
| chr22:45942810
|
A | C | 1 | a0001c0001t0002g0135 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.298+7110T>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45942810 | ||||||
| chr22:45942827
|
C | T | 2 | a0001c0001t0008g0039a0001c0001t0008g0142 | 2 | HG02056.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.298+7093G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45942827 | ||||||
| chr22:45942855
|
C | CTG | 92 | a0001c0001t0001g0150a0001c0001t0001g0152a0001c0001t0001g0153others(89): Show | 93 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.298+7063_298+7064d others(4): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45942855 | ||||||
| chr22:45942855
|
CTG | C | 3 | a0001c0001t0029g0240a0001c0002t0018g0157a0001c0007t0054g0334 | 3 | HG02559.hp1 HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.298+7063_298+7064d others(4): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45942855 | ||||||
| chr22:45942863
|
G | T | 103 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0174others(100): Show | 103 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.298+7057C>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45942863 | ||||||
| chr22:45942872
|
C | T | 1 | a0001c0001t0009g0282 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.298+7048G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45942872 | ||||||
| chr22:45942877
|
G | A | 300 | a0001c0001t0001g0148a0001c0001t0001g0150a0001c0001t0001g0152others(297): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.298+7043C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45942877 | ||||||
| chr22:45942879
|
G | C | 4 | a0001c0001t0001g0195a0001c0001t0002g0095a0001c0001t0013g0317others(1): Show | 4 | HG00733.hp2 HG01081.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.298+7041C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45942879 | ||||||
| chr22:45942891
|
G | A | 4 | a0001c0001t0001g0241a0001c0001t0001g0323a0001c0001t0002g0012others(1): Show | 4 | HG01109.hp2 HG03098.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.298+7029C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45942891 | ||||||
| chr22:45942898
|
T | C | 3 | a0001c0001t0029g0240a0001c0002t0018g0157a0001c0007t0054g0334 | 3 | HG02559.hp1 HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.298+7022A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45942898 | ||||||
| chr22:45942900
|
C | T | 2 | a0001c0001t0009g0282a0001c0001t0012g0331 | 2 | HG02486.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.298+7020G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45942900 | ||||||
| chr22:45942902
|
C | T | 1 | a0001c0001t0031g0004 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.298+7018G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45942902 | ||||||
| chr22:45942903
|
G | A | 3 | a0001c0001t0001g0148a0001c0001t0001g0234a0001c0001t0002g0061 | 3 | HG00423.hp2 NA19010.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.298+7017C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45942903 | ||||||
| chr22:45942904
|
C | T | 1 | a0001c0001t0029g0240 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.298+7016G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45942904 | ||||||
| chr22:45942906
|
T | C | 2 | a0001c0001t0014g0254a0001c0001t0017g0257 | 2 | HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.298+7014A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45942906 | ||||||
| chr22:45942922
|
G | A | 140 | a0001c0001t0001g0148a0001c0001t0001g0153a0001c0001t0001g0166others(137): Show | 140 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.298+6998C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45942922 | ||||||
| chr22:45942923
|
T | TGTGTGCA others(49): Show |
4 | a0001c0001t0001g0184a0001c0001t0002g0069a0001c0001t0002g0112others(1): Show | 4 | NA18951.hp1 NA18952.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.298+6996_298+6997i others(58): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45942923 | ||||||
| chr22:45942923
|
TGTGTGCA others(51): Show |
T | 1 | a0001c0001t0048g0326 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.298+6939_298+6996d others(60): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45942923 | ||||||
| chr22:45942946
|
ATG | A | 106 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0174others(103): Show | 106 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.298+6972_298+6973d others(4): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45942946 | ||||||
| chr22:45942961
|
ATG | A | 3 | a0001c0001t0001g0292a0001c0001t0005g0288a0001c0001t0006g0120 | 3 | HG02486.hp1 HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.298+6957_298+6958d others(4): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45942961 | ||||||
| chr22:45942972
|
C | T | 5 | a0001c0001t0012g0159a0001c0001t0012g0329a0001c0001t0014g0313others(2): Show | 5 | HG02257.hp2 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.298+6948G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45942972 | ||||||
| chr22:45943008
|
G | A | 4 | a0001c0001t0001g0241a0001c0001t0001g0323a0001c0001t0002g0012others(1): Show | 4 | HG01109.hp2 HG03098.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.298+6912C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45943008 | ||||||
| chr22:45943012
|
A | AGTGTGCA others(51): Show |
1 | a0001c0001t0001g0213 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.298+6907_298+6908i others(60): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45943012 | ||||||
| chr22:45943012
|
A | C | 112 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0174others(109): Show | 112 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.298+6908T>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45943012 | ||||||
| chr22:45943034
|
C | CAGTGTGC others(14): Show |
10 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0320others(7): Show | 10 | HG02258.hp2 HG02559.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.298+6885_298+6886i others(23): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45943034 | ||||||
| chr22:45943034
|
C | T | 55 | a0001c0001t0001g0170a0001c0001t0001g0172a0001c0001t0001g0177others(52): Show | 55 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.298+6886G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45943034 | ||||||
| chr22:45943036
|
C | T | 5 | a0001c0002t0007g0230a0001c0002t0030g0003a0001c0002t0037g0015others(2): Show | 5 | HG00642.hp1 HG03209.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.298+6884G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45943036 | ||||||
| chr22:45943041
|
G | A | 4 | a0001c0001t0001g0284a0001c0001t0001g0341a0001c0001t0012g0259others(1): Show | 4 | HG01943.hp1 HG02622.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.298+6879C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45943041 | ||||||
| chr22:45943051
|
CATGT | C | 3 | a0001c0002t0014g0274a0001c0002t0020g0336a0001c0014t0018g0260 | 3 | HG02258.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.298+6865_298+6868d others(6): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45943051 | ||||||
| chr22:45943081
|
G | A | 1 | a0001c0001t0005g0333 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.298+6839C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45943081 | ||||||
| chr22:45943089
|
G | T | 9 | a0001c0002t0001g0163a0001c0002t0001g0224a0001c0002t0007g0230others(6): Show | 9 | HG00642.hp1 HG03041.hp1 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.298+6831C>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45943089 | ||||||
| chr22:45943107
|
A | G | 10 | a0001c0001t0017g0257a0001c0002t0001g0163a0001c0002t0001g0224others(7): Show | 10 | HG00642.hp1 HG03041.hp1 HG03098.hp1 others(7): Show |
intron_variant | MODIFIER | c.298+6813T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45943107 | ||||||
| chr22:45943129
|
C | G | 9 | a0001c0002t0001g0163a0001c0002t0001g0224a0001c0002t0007g0230others(6): Show | 9 | HG00642.hp1 HG03041.hp1 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.298+6791G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45943129 | ||||||
| chr22:45943167
|
C | T | 178 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0170others(175): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.298+6753G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45943167 | ||||||
| chr22:45943169
|
T | C | 2 | a0001c0001t0001g0153a0001c0001t0002g0113 | 2 | NA18941.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.298+6751A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45943169 | ||||||
| chr22:45943238
|
A | C | 196 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0170others(193): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.298+6682T>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45943238 | ||||||
| chr22:45943345
|
G | A | 2 | a0001c0001t0014g0254a0001c0001t0017g0257 | 2 | HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.298+6575C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45943345 | ||||||
| chr22:45943349
|
G | A | 4 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0325others(1): Show | 4 | HG01496.hp2 HG02055.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.298+6571C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45943349 | ||||||
| chr22:45943356
|
C | T | 5 | a0001c0001t0014g0324a0001c0001t0024g0099a0001c0001t0029g0240others(2): Show | 5 | HG01891.hp2 HG02559.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.298+6564G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45943356 | ||||||
| chr22:45943370
|
C | T | 5 | a0001c0001t0014g0324a0001c0001t0024g0099a0001c0001t0029g0240others(2): Show | 5 | HG01891.hp2 HG02559.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.298+6550G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45943370 | ||||||
| chr22:45943379
|
G | A | 7 | a0001c0002t0001g0163a0001c0002t0001g0224a0001c0002t0007g0230others(4): Show | 7 | HG00642.hp1 HG03041.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.298+6541C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45943379 | ||||||
| chr22:45943387
|
T | A | 1 | a0001c0001t0001g0325 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.298+6533A>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45943387 | ||||||
| chr22:45943405
|
G | C | 188 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0170others(185): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.298+6515C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45943405 | ||||||
| chr22:45943481
|
C | G | 15 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0284others(12): Show | 15 | HG01891.hp2 HG01943.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.298+6439G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45943481 | ||||||
| chr22:45943481
|
C | T | 1 | a0001c0001t0001g0234 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.298+6439G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45943481 | ||||||
| chr22:45943533
|
G | C | 3 | a0001c0001t0031g0004a0001c0001t0047g0251a0001c0001t0065g0347 | 3 | HG01433.hp2 HG02723.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.298+6387C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45943533 | ||||||
| chr22:45943562
|
T | C | 4 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0320others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.298+6358A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45943562 | ||||||
| chr22:45943566
|
T | C | 3 | a0001c0001t0024g0099a0001c0001t0029g0240a0001c0007t0054g0334 | 3 | HG02559.hp1 HG03130.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.298+6354A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45943566 | ||||||
| chr22:45943623
|
G | A | 3 | a0001c0001t0019g0290a0001c0001t0019g0332a0001c0001t0020g0225 | 3 | HG02630.hp1 HG02647.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.298+6297C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45943623 | ||||||
| chr22:45943670
|
T | C | 1 | a0001c0001t0001g0223 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.298+6250A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45943670 | ||||||
| chr22:45943671
|
T | TG | 5 | a0001c0001t0014g0254a0001c0001t0017g0257a0001c0001t0019g0244others(2): Show | 5 | HG02559.hp2 HG02809.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.298+6248dupC | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45943671 | ||||||
| chr22:45943827
|
G | A | 4 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0325others(1): Show | 4 | HG01496.hp2 HG02055.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.298+6093C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45943827 | ||||||
| chr22:45943908
|
C | T | 1 | a0001c0001t0002g0095 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.298+6012G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45943908 | ||||||
| chr22:45943959
|
G | A | 6 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0284others(3): Show | 6 | HG01943.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.298+5961C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45943959 | ||||||
| chr22:45943982
|
G | C | 3 | a0001c0002t0014g0274a0001c0002t0020g0336a0001c0014t0018g0260 | 3 | HG02258.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.298+5938C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45943982 | ||||||
| chr22:45944010
|
G | A | 2 | a0001c0001t0001g0308a0001c0001t0001g0309 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.298+5910C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45944010 | ||||||
| chr22:45944050
|
C | A | 3 | a0001c0002t0014g0274a0001c0002t0020g0336a0001c0014t0018g0260 | 3 | HG02258.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.298+5870G>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45944050 | ||||||
| chr22:45944108
|
A | C | 196 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0167others(193): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.298+5812T>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45944108 | ||||||
| chr22:45944125
|
G | A | 7 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0284others(4): Show | 7 | HG01943.hp1 HG02622.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.298+5795C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45944125 | ||||||
| chr22:45944199
|
C | G | 7 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0284others(4): Show | 7 | HG01943.hp1 HG02622.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.298+5721G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45944199 | ||||||
| chr22:45944207
|
T | C | 7 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0284others(4): Show | 7 | HG01943.hp1 HG02622.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.298+5713A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45944207 | ||||||
| chr22:45944236
|
T | C | 3 | a0001c0001t0019g0290a0001c0001t0019g0332a0001c0001t0020g0225 | 3 | HG02630.hp1 HG02647.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.298+5684A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45944236 | ||||||
| chr22:45944328
|
C | T | 5 | a0001c0001t0014g0324a0001c0001t0024g0099a0001c0001t0029g0240others(2): Show | 5 | HG01891.hp2 HG02559.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.298+5592G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45944328 | ||||||
| chr22:45944393
|
G | C | 3 | a0001c0001t0031g0004a0001c0001t0047g0251a0001c0001t0065g0347 | 3 | HG01433.hp2 HG02723.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.298+5527C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45944393 | ||||||
| chr22:45944398
|
C | A | 1 | a0001c0001t0001g0154 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.298+5522G>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45944398 | ||||||
| chr22:45944424
|
G | A | 1 | a0001c0001t0001g0281 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.298+5496C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45944424 | ||||||
| chr22:45944467
|
G | A | 1 | a0001c0001t0059g0156 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.298+5453C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45944467 | ||||||
| chr22:45944470
|
G | A | 1 | a0001c0001t0001g0325 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.298+5450C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45944470 | ||||||
| chr22:45944658
|
C | T | 116 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0174others(113): Show | 116 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.298+5262G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45944658 | ||||||
| chr22:45944719
|
C | A | 5 | a0001c0001t0001g0196a0001c0001t0002g0081a0001c0001t0002g0101others(2): Show | 5 | HG01081.hp2 HG01258.hp2 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.298+5201G>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45944719 | ||||||
| chr22:45944757
|
A | G | 7 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0284others(4): Show | 7 | HG01943.hp1 HG02622.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.298+5163T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45944757 | ||||||
| chr22:45944760
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.298+5160G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45944760 | ||||||
| chr22:45944820
|
C | T | 3 | a0001c0001t0014g0324a0001c0001t0024g0099a0001c0011t0049g0330 | 3 | HG01891.hp2 HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.298+5100G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45944820 | ||||||
| chr22:45944821
|
G | A | 9 | a0001c0002t0001g0163a0001c0002t0001g0224a0001c0002t0007g0230others(6): Show | 9 | HG00642.hp1 HG03041.hp1 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.298+5099C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45944821 | ||||||
| chr22:45944822
|
C | T | 3 | a0001c0001t0019g0244a0001c0001t0038g0009a0001c0004t0007g0342 | 3 | HG02559.hp2 HG02809.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.298+5098G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45944822 | ||||||
| chr22:45944837
|
G | A | 159 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0174others(156): Show | 159 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.298+5083C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45944837 | ||||||
| chr22:45944885
|
A | G | 38 | a0001c0001t0001g0170a0001c0001t0001g0172a0001c0001t0001g0177others(35): Show | 38 | HG00099.hp2 HG00639.hp2 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.298+5035T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45944885 | ||||||
| chr22:45945003
|
C | T | 9 | a0001c0002t0001g0163a0001c0002t0001g0224a0001c0002t0007g0230others(6): Show | 9 | HG00642.hp1 HG03041.hp1 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.298+4917G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45945003 | ||||||
| chr22:45945024
|
A | G | 2 | a0001c0001t0001g0167a0001c0001t0001g0175 | 2 | HG00544.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.298+4896T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45945024 | ||||||
| chr22:45945026
|
G | A | 6 | a0001c0001t0019g0244a0001c0001t0038g0009a0001c0002t0014g0274others(3): Show | 6 | HG02258.hp2 HG02559.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.298+4894C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45945026 | ||||||
| chr22:45945088
|
A | AT | 17 | a0001c0001t0019g0290a0001c0001t0019g0332a0001c0001t0020g0225others(14): Show | 17 | HG00642.hp1 HG01433.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.298+4831dupA | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45945088 | ||||||
| chr22:45945088
|
AT | A | 6 | a0001c0001t0001g0184a0001c0001t0001g0287a0001c0001t0003g0111others(3): Show | 6 | HG00323.hp1 HG02109.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.298+4831delA | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45945088 | ||||||
| chr22:45945106
|
G | A | 4 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0325others(1): Show | 4 | HG01496.hp2 HG02055.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.298+4814C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45945106 | ||||||
| chr22:45945177
|
G | A | 116 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0174others(113): Show | 116 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.298+4743C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45945177 | ||||||
| chr22:45945225
|
A | G | 1 | a0001c0001t0002g0028 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.298+4695T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45945225 | ||||||
| chr22:45945284
|
C | T | 13 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0284others(10): Show | 13 | HG01891.hp2 HG01943.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.298+4636G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45945284 | ||||||
| chr22:45945285
|
G | A | 2 | a0001c0001t0002g0061a0001c0001t0002g0123 | 2 | NA18940.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.298+4635C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45945285 | ||||||
| chr22:45945516
|
T | C | 5 | a0001c0001t0001g0263a0001c0001t0005g0283a0001c0001t0005g0333others(2): Show | 5 | HG01243.hp1 HG02572.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.298+4404A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45945516 | ||||||
| chr22:45945606
|
A | C | 6 | a0001c0001t0014g0324a0001c0001t0017g0257a0001c0001t0024g0099others(3): Show | 6 | HG01891.hp2 HG02559.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.298+4314T>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45945606 | ||||||
| chr22:45945627
|
G | C | 1 | a0001c0001t0017g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.298+4293C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45945627 | ||||||
| chr22:45945672
|
C | A | 3 | a0001c0001t0031g0004a0001c0001t0047g0251a0001c0001t0065g0347 | 3 | HG01433.hp2 HG02723.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.298+4248G>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45945672 | ||||||
| chr22:45945699
|
G | C | 1 | a0001c0001t0017g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.298+4221C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45945699 | ||||||
| chr22:45945797
|
G | C | 1 | a0001c0002t0001g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.298+4123C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45945797 | ||||||
| chr22:45945833
|
C | T | 1 | a0001c0001t0006g0124 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.298+4087G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45945833 | ||||||
| chr22:45945863
|
C | T | 1 | a0001c0001t0058g0236 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.298+4057G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45945863 | ||||||
| chr22:45945887
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.298+4033G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45945887 | ||||||
| chr22:45945957
|
G | A | 8 | a0001c0001t0001g0303a0001c0001t0001g0306a0001c0001t0002g0077others(5): Show | 8 | HG00639.hp1 HG01255.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.298+3963C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45945957 | ||||||
| chr22:45946007
|
A | G | 181 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0170others(178): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.298+3913T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45946007 | ||||||
| chr22:45946064
|
C | CT | 158 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0170others(155): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.298+3855dupA | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45946064 | ||||||
| chr22:45946302
|
C | T | 1 | a0001c0001t0019g0290 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.298+3618G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45946302 | ||||||
| chr22:45946340
|
C | G | 4 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0320others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.298+3580G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45946340 | ||||||
| chr22:45946375
|
T | C | 1 | a0001c0001t0002g0053 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.298+3545A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45946375 | ||||||
| chr22:45946406
|
T | C | 204 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0170others(201): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.298+3514A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45946406 | ||||||
| chr22:45946529
|
C | T | 2 | a0001c0001t0002g0086a0001c0001t0002g0087 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.298+3391G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45946529 | ||||||
| chr22:45946676
|
AGGCGAGC others(9): Show |
A | 12 | a0001c0001t0001g0241a0001c0001t0001g0269a0001c0001t0001g0270others(9): Show | 12 | HG01109.hp2 HG01496.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.298+3228_298+3243d others(18): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45946676 | ||||||
| chr22:45946680
|
G | A | 1 | a0001c0004t0007g0342 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.298+3240C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45946680 | ||||||
| chr22:45946723
|
C | A | 3 | a0001c0001t0001g0284a0001c0001t0001g0341a0001c0001t0063g0344 | 3 | HG01943.hp1 HG02622.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.298+3197G>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45946723 | ||||||
| chr22:45946746
|
T | A | 4 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0320others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.298+3174A>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45946746 | ||||||
| chr22:45946933
|
C | T | 1 | a0001c0001t0025g0160 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.298+2987G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45946933 | ||||||
| chr22:45947058
|
G | A | 4 | a0001c0001t0002g0127a0001c0001t0003g0050a0001c0001t0003g0096others(1): Show | 4 | HG02015.hp2 NA18990.hp1 NA19087.hp2 others(1): Show |
intron_variant | MODIFIER | c.298+2862C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45947058 | ||||||
| chr22:45947069
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.298+2851C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45947069 | ||||||
| chr22:45947108
|
G | A | 11 | a0001c0001t0001g0241a0001c0001t0001g0269a0001c0001t0001g0270others(8): Show | 11 | HG01109.hp2 HG01496.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.298+2812C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45947108 | ||||||
| chr22:45947110
|
A | G | 1 | a0001c0001t0020g0158 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.298+2810T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45947110 | ||||||
| chr22:45947246
|
C | T | 1 | a0001c0003t0053g0310 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.298+2674G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45947246 | ||||||
| chr22:45947288
|
A | T | 4 | a0001c0001t0001g0284a0001c0001t0001g0341a0001c0001t0027g0256others(1): Show | 4 | HG01099.hp1 HG01943.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.298+2632T>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45947288 | ||||||
| chr22:45947717
|
G | A | 1 | a0001c0001t0017g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.298+2203C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45947717 | ||||||
| chr22:45947877
|
C | T | 12 | a0001c0001t0001g0241a0001c0001t0001g0269a0001c0001t0001g0270others(9): Show | 12 | HG01109.hp2 HG01496.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.298+2043G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45947877 | ||||||
| chr22:45947944
|
G | A | 1 | a0001c0001t0014g0254 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.298+1976C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45947944 | ||||||
| chr22:45948047
|
C | A | 3 | a0001c0001t0014g0324a0001c0001t0024g0099a0001c0011t0049g0330 | 3 | HG01891.hp2 HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.298+1873G>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45948047 | ||||||
| chr22:45948105
|
G | T | 1 | a0001c0001t0041g0130 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.298+1815C>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45948105 | ||||||
| chr22:45948107
|
G | A | 1 | a0001c0001t0059g0156 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.298+1813C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45948107 | ||||||
| chr22:45948124
|
C | T | 4 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0320others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.298+1796G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45948124 | ||||||
| chr22:45948218
|
G | A | 3 | a0001c0001t0031g0004a0001c0001t0047g0251a0001c0001t0065g0347 | 3 | HG01433.hp2 HG02723.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.298+1702C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45948218 | ||||||
| chr22:45948258
|
G | A | 1 | a0001c0001t0001g0306 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.298+1662C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45948258 | ||||||
| chr22:45948354
|
G | A | 2 | a0001c0001t0002g0082a0001c0001t0010g0029 | 2 | HG00140.hp1 HG00280.hp2 |
intron_variant | MODIFIER | c.298+1566C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45948354 | ||||||
| chr22:45948358
|
G | A | 9 | a0001c0002t0001g0163a0001c0002t0001g0224a0001c0002t0007g0230others(6): Show | 9 | HG00642.hp1 HG03041.hp1 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.298+1562C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45948358 | ||||||
| chr22:45948373
|
G | A | 1 | a0001c0001t0031g0004 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.298+1547C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45948373 | ||||||
| chr22:45948431
|
C | T | 11 | a0001c0001t0001g0284a0001c0001t0001g0341a0001c0001t0012g0259others(8): Show | 11 | HG01099.hp1 HG01891.hp2 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.298+1489G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45948431 | ||||||
| chr22:45948436
|
C | T | 2 | a0001c0001t0002g0086a0001c0001t0002g0087 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.298+1484G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45948436 | ||||||
| chr22:45948460
|
G | T | 11 | a0001c0001t0001g0284a0001c0001t0001g0341a0001c0001t0012g0259others(8): Show | 11 | HG01099.hp1 HG01891.hp2 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.298+1460C>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45948460 | ||||||
| chr22:45948580
|
C | G | 25 | a0001c0001t0001g0241a0001c0001t0001g0269a0001c0001t0001g0270others(22): Show | 25 | HG01099.hp1 HG01109.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.298+1340G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45948580 | ||||||
| chr22:45948631
|
G | A | 4 | a0001c0001t0012g0259a0001c0001t0014g0254a0001c0001t0038g0009others(1): Show | 4 | HG02559.hp2 HG02809.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.298+1289C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45948631 | ||||||
| chr22:45948816
|
T | C | 1 | a0001c0005t0001g0199 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.298+1104A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45948816 | ||||||
| chr22:45948827
|
C | CT | 41 | a0001c0001t0001g0154a0001c0001t0001g0170a0001c0001t0001g0177others(38): Show | 41 | HG00099.hp2 HG00423.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.298+1092dupA | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45948827 | ||||||
| chr22:45948827
|
C | CTT | 6 | a0001c0001t0001g0185a0001c0001t0001g0191a0001c0001t0009g0268others(3): Show | 6 | HG02258.hp2 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.298+1091_298+1092d others(4): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45948827 | ||||||
| chr22:45948827
|
CT | C | 50 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0218others(47): Show | 50 | HG00099.hp1 HG00423.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.298+1092delA | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45948827 | ||||||
| chr22:45948827
|
CTT | C | 78 | a0001c0001t0001g0174a0001c0001t0001g0182a0001c0001t0001g0193others(75): Show | 78 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.298+1091_298+1092d others(4): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45948827 | ||||||
| chr22:45948827
|
CTTT | C | 14 | a0001c0001t0001g0184a0001c0001t0001g0265a0001c0001t0001g0271others(11): Show | 14 | HG01169.hp1 HG01243.hp2 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.298+1090_298+1092d others(5): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45948827 | ||||||
| chr22:45948827
|
CTTTTTT | C | 8 | a0001c0001t0001g0341a0001c0001t0012g0259a0001c0001t0014g0254others(5): Show | 8 | HG01099.hp1 HG01943.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.298+1087_298+1092d others(8): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45948827 | ||||||
| chr22:45948827
|
CTTTTTTT others(4): Show |
C | 3 | a0001c0001t0019g0290a0001c0001t0019g0332a0001c0001t0020g0225 | 3 | HG02630.hp1 HG02647.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.298+1082_298+1092d others(13): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45948827 | ||||||
| chr22:45948827
|
CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0011g0189a0001c0001t0013g0286 | 2 | HG03669.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.298+1081_298+1092d others(14): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45948827 | ||||||
| chr22:45948827
|
CTTTTTTT others(6): Show |
C | 6 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0325others(3): Show | 6 | HG01496.hp2 HG02055.hp2 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.298+1080_298+1092d others(15): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45948827 | ||||||
| chr22:45948827
|
CTTTTTTT others(10): Show |
C | 1 | a0001c0002t0018g0157 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.298+1076_298+1092d others(19): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45948827 | ||||||
| chr22:45948827
|
CTTTTTTT others(11): Show |
C | 16 | a0001c0001t0001g0263a0001c0001t0005g0283a0001c0001t0005g0333others(13): Show | 16 | HG00642.hp1 HG01243.hp1 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.298+1075_298+1092d others(20): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45948827 | ||||||
| chr22:45948832
|
T | C | 3 | a0001c0001t0014g0324a0001c0001t0024g0099a0001c0011t0049g0330 | 3 | HG01891.hp2 HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.298+1088A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45948832 | ||||||
| chr22:45948833
|
T | C | 1 | a0001c0001t0001g0284 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.298+1087A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45948833 | ||||||
| chr22:45948834
|
T | C | 8 | a0001c0001t0001g0341a0001c0001t0012g0259a0001c0001t0014g0254others(5): Show | 8 | HG01099.hp1 HG01943.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.298+1086A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45948834 | ||||||
| chr22:45948857
|
T | C | 1 | a0001c0001t0001g0263 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.298+1063A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45948857 | ||||||
| chr22:45948883
|
T | C | 12 | a0001c0001t0001g0284a0001c0001t0001g0341a0001c0001t0012g0259others(9): Show | 12 | HG01099.hp1 HG01891.hp2 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.298+1037A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45948883 | ||||||
| chr22:45948886
|
G | C | 185 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0174others(182): Show | 185 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.298+1034C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45948886 | ||||||
| chr22:45948892
|
T | C | 2 | a0001c0001t0005g0301a0001c0001t0006g0073 | 2 | HG02109.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.298+1028A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45948892 | ||||||
| chr22:45948908
|
C | T | 11 | a0001c0001t0001g0284a0001c0001t0001g0341a0001c0001t0012g0259others(8): Show | 11 | HG01099.hp1 HG01891.hp2 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.298+1012G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45948908 | ||||||
| chr22:45948935
|
G | A | 7 | a0001c0001t0001g0241a0001c0001t0001g0323a0001c0001t0002g0012others(4): Show | 7 | HG01109.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.298+985C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45948935 | ||||||
| chr22:45948950
|
G | A | 2 | a0001c0001t0025g0160a0001c0001t0025g0322 | 2 | HG02886.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.298+970C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45948950 | ||||||
| chr22:45948998
|
T | A | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+922A>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45948998 | ||||||
| chr22:45949120
|
C | T | 1 | a0001c0001t0017g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.298+800G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949120 | ||||||
| chr22:45949134
|
A | G | 12 | a0001c0001t0001g0284a0001c0001t0001g0341a0001c0001t0012g0259others(9): Show | 12 | HG01099.hp1 HG01891.hp2 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.298+786T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949134 | ||||||
| chr22:45949275
|
C | T | 2 | a0001c0001t0029g0240a0001c0007t0054g0334 | 2 | HG02559.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.298+645G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949275 | ||||||
| chr22:45949300
|
C | T | 2 | a0001c0001t0038g0009a0001c0004t0007g0342 | 2 | HG02559.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.298+620G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949300 | ||||||
| chr22:45949315
|
A | G | 1 | a0001c0003t0053g0310 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.298+605T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949315 | ||||||
| chr22:45949323
|
C | T | 3 | a0001c0001t0031g0004a0001c0001t0047g0251a0001c0001t0065g0347 | 3 | HG01433.hp2 HG02723.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.298+597G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949323 | ||||||
| chr22:45949331
|
G | A | 1 | a0001c0002t0020g0336 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.298+589C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949331 | ||||||
| chr22:45949368
|
T | C | 1 | a0001c0001t0012g0159 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.298+552A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949368 | ||||||
| chr22:45949528
|
G | C | 7 | a0001c0001t0001g0284a0001c0001t0012g0259a0001c0001t0014g0254others(4): Show | 7 | HG01943.hp1 HG02559.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.298+392C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949528 | ||||||
| chr22:45949548
|
G | A | 2 | a0001c0001t0005g0333a0001c0003t0021g0311 | 2 | HG01884.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.298+372C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949548 | ||||||
| chr22:45949550
|
G | A | 5 | a0001c0001t0001g0263a0001c0001t0005g0283a0001c0001t0005g0333others(2): Show | 5 | HG01243.hp1 HG02572.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.298+370C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949550 | ||||||
| chr22:45949609
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.298+311G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949609 | ||||||
| chr22:45949610
|
G | A | 5 | a0001c0001t0001g0263a0001c0001t0005g0283a0001c0001t0005g0333others(2): Show | 5 | HG01243.hp1 HG02572.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.298+310C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949610 | ||||||
| chr22:45949666
|
C | T | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+254G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949666 | ||||||
| chr22:45949676
|
C | T | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+244G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949676 | ||||||
| chr22:45949677
|
A | G | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+243T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949677 | ||||||
| chr22:45949682
|
C | T | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+238G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949682 | ||||||
| chr22:45949683
|
G | A | 1 | a0001c0001t0003g0078 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.298+237C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949683 | ||||||
| chr22:45949691
|
A | G | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+229T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949691 | ||||||
| chr22:45949692
|
C | G | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+228G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949692 | ||||||
| chr22:45949694
|
T | C | 31 | a0001c0001t0001g0241a0001c0001t0001g0269a0001c0001t0001g0270others(28): Show | 31 | HG01109.hp2 HG01358.hp2 HG01496.hp2 others(28): Show |
intron_variant | MODIFIER | c.298+226A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949694 | ||||||
| chr22:45949696
|
C | G | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+224G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949696 | ||||||
| chr22:45949697
|
A | G | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+223T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949697 | ||||||
| chr22:45949698
|
T | C | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+222A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949698 | ||||||
| chr22:45949702
|
C | G | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+218G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949702 | ||||||
| chr22:45949703
|
A | G | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+217T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949703 | ||||||
| chr22:45949704
|
C | G | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+216G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949704 | ||||||
| chr22:45949719
|
A | G | 4 | a0001c0001t0001g0284a0001c0001t0001g0341a0001c0001t0027g0256others(1): Show | 4 | HG01099.hp1 HG01943.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.298+201T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949719 | ||||||
| chr22:45949719
|
A | T | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+201T>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949719 | ||||||
| chr22:45949722
|
G | C | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+198C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949722 | ||||||
| chr22:45949727
|
C | G | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+193G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949727 | ||||||
| chr22:45949735
|
C | A | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+185G>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949735 | ||||||
| chr22:45949738
|
C | T | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+182G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949738 | ||||||
| chr22:45949739
|
A | T | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+181T>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949739 | ||||||
| chr22:45949742
|
A | G | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+178T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949742 | ||||||
| chr22:45949745
|
A | T | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+175T>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949745 | ||||||
| chr22:45949748
|
G | GCCTAAAT others(155): Show |
1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+171_298+172ins others(162): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949748 | ||||||
| chr22:45949755
|
C | G | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+165G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949755 | ||||||
| chr22:45949758
|
A | T | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+162T>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949758 | ||||||
| chr22:45949759
|
G | T | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+161C>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949759 | ||||||
| chr22:45949761
|
G | C | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+159C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949761 | ||||||
| chr22:45949764
|
A | T | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+156T>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949764 | ||||||
| chr22:45949766
|
G | GGCCCCTG others(4): Show |
1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+153_298+154ins others(11): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949766 | ||||||
| chr22:45949771
|
G | T | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+149C>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949771 | ||||||
| chr22:45949772
|
C | T | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+148G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949772 | ||||||
| chr22:45949773
|
A | G | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+147T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949773 | ||||||
| chr22:45949775
|
G | A | 17 | a0001c0001t0001g0278a0001c0001t0001g0292a0001c0001t0005g0249others(14): Show | 17 | HG01358.hp2 HG01884.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.298+145C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949775 | ||||||
| chr22:45949775
|
G | T | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+145C>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949775 | ||||||
| chr22:45949777
|
A | T | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+143T>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949777 | ||||||
| chr22:45949779
|
A | C | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+141T>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949779 | ||||||
| chr22:45949780
|
A | T | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+140T>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949780 | ||||||
| chr22:45949781
|
G | C | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+139C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949781 | ||||||
| chr22:45949783
|
G | C | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+137C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949783 | ||||||
| chr22:45949788
|
C | G | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+132G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949788 | ||||||
| chr22:45949797
|
A | T | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+123T>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949797 | ||||||
| chr22:45949798
|
A | C | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+122T>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949798 | ||||||
| chr22:45949801
|
A | C | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+119T>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949801 | ||||||
| chr22:45949803
|
A | C | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+117T>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949803 | ||||||
| chr22:45949805
|
T | A | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+115A>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949805 | ||||||
| chr22:45949814
|
A | T | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+106T>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949814 | ||||||
| chr22:45949815
|
G | C | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+105C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949815 | ||||||
| chr22:45949816
|
G | C | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+104C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949816 | ||||||
| chr22:45949818
|
G | C | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+102C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949818 | ||||||
| chr22:45949819
|
A | T | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+101T>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949819 | ||||||
| chr22:45949820
|
T | G | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+100A>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949820 | ||||||
| chr22:45949821
|
G | C | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+99C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949821 | ||||||
| chr22:45949826
|
C | G | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+94G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949826 | ||||||
| chr22:45949827
|
A | T | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+93T>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949827 | ||||||
| chr22:45949828
|
G | C | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+92C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949828 | ||||||
| chr22:45949829
|
A | C | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+91T>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949829 | ||||||
| chr22:45949830
|
A | C | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+90T>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949830 | ||||||
| chr22:45949832
|
A | C | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+88T>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949832 | ||||||
| chr22:45949833
|
G | T | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+87C>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949833 | ||||||
| chr22:45949834
|
C | T | 118 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0174others(115): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.298+86G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949834 | ||||||
| chr22:45949843
|
C | G | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+77G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949843 | ||||||
| chr22:45949844
|
T | A | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+76A>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949844 | ||||||
| chr22:45949850
|
T | C | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+70A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949850 | ||||||
| chr22:45949852
|
A | T | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+68T>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949852 | ||||||
| chr22:45949854
|
T | A | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+66A>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949854 | ||||||
| chr22:45949856
|
G | C | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+64C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949856 | ||||||
| chr22:45949857
|
G | C | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+63C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949857 | ||||||
| chr22:45949858
|
T | A | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+62A>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949858 | ||||||
| chr22:45949859
|
G | T | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+61C>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949859 | ||||||
| chr22:45949860
|
G | C | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+60C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949860 | ||||||
| chr22:45949863
|
T | A | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+57A>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949863 | ||||||
| chr22:45949869
|
A | ATTCCTCA others(92): Show |
1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+50_298+51insAC others(97): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949869 | ||||||
| chr22:45949870
|
C | G | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+50G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45949870 | ||||||
| chr22:45950241
|
G | A | 136 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0174others(133): Show | 136 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.72-95C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45950241 | ||||||
| chr22:45950258
|
G | A | 1 | a0001c0001t0017g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.72-112C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45950258 | ||||||
| chr22:45950325
|
C | T | 4 | a0001c0001t0012g0259a0001c0001t0014g0254a0001c0001t0038g0009others(1): Show | 4 | HG02559.hp2 HG02809.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-179G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45950325 | ||||||
| chr22:45950522
|
G | A | 1 | a0001c0001t0017g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.72-376C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45950522 | ||||||
| chr22:45950534
|
C | T | 1 | a0001c0002t0001g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.72-388G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45950534 | ||||||
| chr22:45950546
|
A | T | 4 | a0001c0001t0014g0254a0001c0001t0031g0004a0001c0001t0047g0251others(1): Show | 4 | HG01433.hp2 HG02723.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-400T>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45950546 | ||||||
| chr22:45950579
|
T | C | 1 | a0001c0001t0001g0152 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.72-433A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45950579 | ||||||
| chr22:45950601
|
A | G | 29 | a0001c0001t0001g0241a0001c0001t0001g0261a0001c0001t0001g0262others(26): Show | 29 | HG00642.hp1 HG01109.hp2 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.72-455T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45950601 | ||||||
| chr22:45950694
|
G | A | 26 | a0001c0001t0001g0241a0001c0001t0001g0261a0001c0001t0001g0262others(23): Show | 26 | HG00642.hp1 HG01109.hp2 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.72-548C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45950694 | ||||||
| chr22:45950697
|
C | G | 7 | a0001c0001t0001g0263a0001c0001t0005g0283a0001c0001t0005g0333others(4): Show | 7 | HG01243.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.72-551G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45950697 | ||||||
| chr22:45950699
|
C | A | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.72-553G>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45950699 | ||||||
| chr22:45950702
|
C | T | 29 | a0001c0001t0001g0241a0001c0001t0001g0261a0001c0001t0001g0262others(26): Show | 29 | HG00642.hp1 HG01099.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.72-556G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45950702 | ||||||
| chr22:45950703
|
G | A | 3 | a0001c0001t0001g0299a0001c0001t0001g0302a0001c0001t0002g0062 | 3 | HG01934.hp1 HG01952.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.72-557C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45950703 | ||||||
| chr22:45950723
|
AC | A | 4 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0320others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-578delG | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45950723 | ||||||
| chr22:45950766
|
A | T | 5 | a0001c0001t0001g0263a0001c0001t0005g0283a0001c0001t0005g0333others(2): Show | 5 | HG01243.hp1 HG02572.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-620T>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45950766 | ||||||
| chr22:45950848
|
G | C | 6 | a0001c0001t0001g0241a0001c0001t0001g0323a0001c0001t0002g0012others(3): Show | 6 | HG01109.hp2 HG02572.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.72-702C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45950848 | ||||||
| chr22:45950856
|
G | C | 1 | a0001c0001t0002g0080 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.72-710C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45950856 | ||||||
| chr22:45950904
|
C | T | 206 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0170others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.72-758G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45950904 | ||||||
| chr22:45950915
|
G | A | 4 | a0001c0001t0001g0192a0001c0001t0002g0028a0001c0001t0002g0031others(1): Show | 4 | HG00280.hp1 HG00738.hp2 HG01069.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-769C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45950915 | ||||||
| chr22:45950930
|
C | T | 172 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0170others(169): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.72-784G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45950930 | ||||||
| chr22:45950951
|
CACT | C | 3 | a0001c0001t0031g0004a0001c0001t0047g0251a0001c0001t0065g0347 | 3 | HG01433.hp2 HG02723.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.72-808_72-806delAG others(1): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45950951 | ||||||
| chr22:45951017
|
C | T | 1 | a0001c0001t0003g0139 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.72-871G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45951017 | ||||||
| chr22:45951075
|
G | A | 3 | a0001c0001t0014g0324a0001c0001t0024g0099a0001c0011t0049g0330 | 3 | HG01891.hp2 HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.72-929C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45951075 | ||||||
| chr22:45951119
|
G | C | 171 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0170others(168): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.72-973C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45951119 | ||||||
| chr22:45951141
|
G | C | 1 | a0001c0004t0034g0011 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.72-995C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45951141 | ||||||
| chr22:45951203
|
G | A | 5 | a0001c0001t0001g0263a0001c0001t0005g0283a0001c0001t0005g0333others(2): Show | 5 | HG01243.hp1 HG02572.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-1057C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45951203 | ||||||
| chr22:45951238
|
G | A | 1 | a0001c0001t0017g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.72-1092C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45951238 | ||||||
| chr22:45951320
|
G | A | 18 | a0001c0001t0001g0278a0001c0001t0001g0292a0001c0001t0005g0249others(15): Show | 18 | HG01358.hp2 HG01884.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.72-1174C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45951320 | ||||||
| chr22:45951336
|
C | T | 3 | a0001c0001t0014g0324a0001c0001t0024g0099a0001c0011t0049g0330 | 3 | HG01891.hp2 HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.72-1190G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45951336 | ||||||
| chr22:45951397
|
G | A | 18 | a0001c0001t0001g0278a0001c0001t0001g0292a0001c0001t0005g0249others(15): Show | 18 | HG01358.hp2 HG01884.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.72-1251C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45951397 | ||||||
| chr22:45951400
|
A | C | 4 | a0001c0001t0001g0241a0001c0001t0001g0323a0001c0001t0002g0012others(1): Show | 4 | HG01109.hp2 HG03098.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-1254T>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45951400 | ||||||
| chr22:45951423
|
C | CCATTTTT others(27): Show |
5 | a0001c0001t0001g0184a0001c0001t0001g0213a0001c0001t0002g0069others(2): Show | 5 | NA18951.hp1 NA18952.hp1 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.72-1278_72-1277ins others(34): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45951423 | ||||||
| chr22:45951458
|
C | T | 2 | a0001c0002t0014g0274a0001c0014t0018g0260 | 2 | HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.72-1312G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45951458 | ||||||
| chr22:45951511
|
C | T | 4 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0320others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-1365G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45951511 | ||||||
| chr22:45951578
|
C | T | 194 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0170others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.72-1432G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45951578 | ||||||
| chr22:45951594
|
T | C | 4 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0325others(1): Show | 4 | HG01496.hp2 HG02055.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.72-1448A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45951594 | ||||||
| chr22:45951639
|
T | C | 199 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0170others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.72-1493A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45951639 | ||||||
| chr22:45951640
|
G | A | 193 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0170others(190): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.72-1494C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45951640 | ||||||
| chr22:45951641
|
T | C | 193 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0170others(190): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.72-1495A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45951641 | ||||||
| chr22:45951664
|
T | C | 182 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0170others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.72-1518A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45951664 | ||||||
| chr22:45951724
|
G | A | 194 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0170others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.72-1578C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45951724 | ||||||
| chr22:45951732
|
G | A | 16 | a0001c0001t0001g0278a0001c0001t0001g0292a0001c0001t0005g0249others(13): Show | 16 | HG01358.hp2 HG01884.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.72-1586C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45951732 | ||||||
| chr22:45951771
|
G | C | 185 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0170others(182): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.72-1625C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45951771 | ||||||
| chr22:45951803
|
C | T | 191 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0170others(188): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.72-1657G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45951803 | ||||||
| chr22:45951833
|
C | T | 4 | a0001c0001t0012g0259a0001c0001t0014g0254a0001c0001t0038g0009others(1): Show | 4 | HG02559.hp2 HG02809.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-1687G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45951833 | ||||||
| chr22:45951846
|
C | T | 1 | a0001c0001t0017g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.72-1700G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45951846 | ||||||
| chr22:45951907
|
G | A | 1 | a0001c0001t0005g0279 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.72-1761C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45951907 | ||||||
| chr22:45951958
|
C | T | 1 | a0001c0001t0017g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.72-1812G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45951958 | ||||||
| chr22:45952042
|
C | T | 189 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0170others(186): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.72-1896G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45952042 | ||||||
| chr22:45952052
|
A | G | 1 | a0001c0001t0001g0152 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.72-1906T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45952052 | ||||||
| chr22:45952108
|
G | A | 2 | a0001c0001t0001g0210a0001c0001t0002g0058 | 2 | NA18952.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.72-1962C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45952108 | ||||||
| chr22:45952139
|
C | T | 1 | a0001c0001t0001g0213 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.72-1993G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45952139 | ||||||
| chr22:45952140
|
G | A | 31 | a0001c0001t0001g0194a0001c0001t0001g0196a0001c0001t0001g0234others(28): Show | 32 | HG00140.hp2 HG00609.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.72-1994C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45952140 | ||||||
| chr22:45952150
|
C | T | 24 | a0001c0001t0001g0241a0001c0001t0001g0269a0001c0001t0001g0270others(21): Show | 24 | HG01109.hp2 HG01358.hp2 HG01496.hp2 others(21): Show |
intron_variant | MODIFIER | c.72-2004G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45952150 | ||||||
| chr22:45952263
|
G | A | 20 | a0001c0001t0001g0241a0001c0001t0001g0278a0001c0001t0001g0292others(17): Show | 20 | HG01109.hp2 HG01358.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.72-2117C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45952263 | ||||||
| chr22:45952295
|
C | T | 4 | a0001c0001t0009g0268a0001c0001t0014g0324a0001c0001t0024g0099others(1): Show | 4 | HG01891.hp2 HG02965.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.72-2149G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45952295 | ||||||
| chr22:45952342
|
C | T | 3 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0320 | 3 | HG02896.hp2 HG02897.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.72-2196G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45952342 | ||||||
| chr22:45952411
|
C | A | 2 | a0001c0001t0001g0261a0001c0001t0001g0262 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.72-2265G>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45952411 | ||||||
| chr22:45952475
|
G | A | 24 | a0001c0001t0001g0241a0001c0001t0001g0269a0001c0001t0001g0270others(21): Show | 24 | HG01109.hp2 HG01358.hp2 HG01496.hp2 others(21): Show |
intron_variant | MODIFIER | c.72-2329C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45952475 | ||||||
| chr22:45952520
|
G | A | 1 | a0001c0001t0019g0244 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.72-2374C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45952520 | ||||||
| chr22:45952570
|
T | G | 1 | a0001c0001t0002g0126 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.72-2424A>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45952570 | ||||||
| chr22:45952577
|
C | T | 3 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0320 | 3 | HG02896.hp2 HG02897.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.72-2431G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45952577 | ||||||
| chr22:45952592
|
G | A | 5 | a0001c0001t0014g0324a0001c0001t0024g0099a0001c0002t0014g0274others(2): Show | 5 | HG01891.hp2 HG02965.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-2446C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45952592 | ||||||
| chr22:45952691
|
G | A | 33 | a0001c0001t0001g0241a0001c0001t0001g0269a0001c0001t0001g0270others(30): Show | 33 | HG01109.hp2 HG01358.hp2 HG01433.hp2 others(30): Show |
intron_variant | MODIFIER | c.72-2545C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45952691 | ||||||
| chr22:45952698
|
C | T | 1 | a0001c0003t0053g0310 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.72-2552G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45952698 | ||||||
| chr22:45952727
|
T | C | 187 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0170others(184): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.72-2581A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45952727 | ||||||
| chr22:45952762
|
T | C | 197 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0170others(194): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.72-2616A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45952762 | ||||||
| chr22:45952767
|
G | A | 1 | a0001c0001t0002g0038 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.72-2621C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45952767 | ||||||
| chr22:45952804
|
C | A | 111 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0174others(108): Show | 111 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.72-2658G>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45952804 | ||||||
| chr22:45952807
|
G | A | 4 | a0001c0001t0019g0290a0001c0001t0019g0332a0001c0001t0020g0225others(1): Show | 4 | HG02258.hp2 HG02630.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.72-2661C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45952807 | ||||||
| chr22:45952825
|
C | G | 3 | a0001c0001t0012g0259a0001c0001t0038g0009a0001c0004t0007g0342 | 3 | HG02559.hp2 HG02809.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.72-2679G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45952825 | ||||||
| chr22:45952866
|
C | T | 1 | a0001c0001t0004g0178 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.72-2720G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45952866 | ||||||
| chr22:45952956
|
T | C | 4 | a0001c0001t0009g0268a0001c0001t0059g0156a0001c0002t0014g0274others(1): Show | 4 | HG02622.hp1 HG03130.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.72-2810A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45952956 | ||||||
| chr22:45952975
|
G | A | 7 | a0001c0001t0001g0263a0001c0001t0005g0283a0001c0001t0005g0333others(4): Show | 7 | HG01243.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.72-2829C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45952975 | ||||||
| chr22:45953045
|
G | A | 180 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0170others(177): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.72-2899C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45953045 | ||||||
| chr22:45953062
|
G | A | 21 | a0001c0001t0001g0241a0001c0001t0001g0278a0001c0001t0001g0292others(18): Show | 21 | HG01109.hp2 HG01358.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.72-2916C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45953062 | ||||||
| chr22:45953089
|
G | C | 21 | a0001c0001t0001g0241a0001c0001t0001g0278a0001c0001t0001g0292others(18): Show | 21 | HG01109.hp2 HG01358.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.72-2943C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45953089 | ||||||
| chr22:45953114
|
C | T | 4 | a0001c0001t0009g0250a0001c0001t0023g0017a0001c0001t0056g0226others(1): Show | 4 | HG03041.hp2 HG03209.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.72-2968G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45953114 | ||||||
| chr22:45953119
|
TCACCGTG others(25): Show |
T | 6 | a0001c0001t0014g0324a0001c0001t0024g0099a0001c0001t0025g0160others(3): Show | 6 | HG01433.hp2 HG01891.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.72-3005_72-2974del others(32): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45953119 | ||||||
| chr22:45953119
|
TCACCGTG others(57): Show |
T | 11 | a0001c0001t0001g0184a0001c0001t0001g0213a0001c0001t0001g0261others(8): Show | 11 | HG02257.hp2 HG02451.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.72-3037_72-2974del others(64): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45953119 | ||||||
| chr22:45953130
|
G | A | 1 | a0001c0001t0005g0279 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.72-2984C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45953130 | ||||||
| chr22:45953134
|
CCGGCTTC others(85): Show |
C | 124 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0174others(121): Show | 124 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.72-3080_72-2989del others(92): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45953134 | ||||||
| chr22:45953134
|
CCGGCTTC others(113): Show |
C | 40 | a0001c0001t0001g0170a0001c0001t0001g0172a0001c0001t0001g0177others(37): Show | 40 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.72-3108_72-2989del | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45953134 | ||||||
| chr22:45953167
|
C | T | 11 | a0001c0001t0001g0263a0001c0001t0005g0283a0001c0001t0005g0333others(8): Show | 11 | HG01243.hp1 HG02559.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.72-3021G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45953167 | ||||||
| chr22:45953183
|
C | T | 11 | a0001c0001t0001g0263a0001c0001t0005g0283a0001c0001t0005g0333others(8): Show | 11 | HG01243.hp1 HG02559.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.72-3037G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45953183 | ||||||
| chr22:45953192
|
CCGTG | C | 11 | a0001c0001t0001g0263a0001c0001t0005g0283a0001c0001t0005g0333others(8): Show | 11 | HG01243.hp1 HG02559.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.72-3050_72-3047del others(4): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45953192 | ||||||
| chr22:45953198
|
C | T | 11 | a0001c0001t0001g0263a0001c0001t0005g0283a0001c0001t0005g0333others(8): Show | 11 | HG01243.hp1 HG02559.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.72-3052G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45953198 | ||||||
| chr22:45953199
|
T | C | 11 | a0001c0001t0001g0263a0001c0001t0005g0283a0001c0001t0005g0333others(8): Show | 11 | HG01243.hp1 HG02559.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.72-3053A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45953199 | ||||||
| chr22:45953199
|
TGGCTTCC others(21): Show |
T | 11 | a0001c0001t0001g0184a0001c0001t0001g0213a0001c0001t0001g0261others(8): Show | 11 | HG02257.hp2 HG02451.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.72-3081_72-3054del others(28): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45953199 | ||||||
| chr22:45953227
|
C | T | 124 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0174others(121): Show | 124 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.72-3081G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45953227 | ||||||
| chr22:45953255
|
C | T | 40 | a0001c0001t0001g0170a0001c0001t0001g0172a0001c0001t0001g0177others(37): Show | 40 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.72-3109G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45953255 | ||||||
| chr22:45953613
|
G | A | 2 | a0001c0001t0002g0043a0001c0001t0002g0052 | 2 | HG02040.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.72-3467C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45953613 | ||||||
| chr22:45953639
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.72-3493G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45953639 | ||||||
| chr22:45953723
|
T | TA | 51 | a0001c0001t0001g0170a0001c0001t0001g0172a0001c0001t0001g0177others(48): Show | 51 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.72-3578dupT | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45953723 | ||||||
| chr22:45953723
|
T | TAA | 82 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0174others(79): Show | 82 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.72-3579_72-3578dup others(2): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45953723 | ||||||
| chr22:45953723
|
TA | T | 54 | a0001c0001t0001g0153a0001c0001t0001g0241a0001c0001t0001g0261others(51): Show | 54 | HG01109.hp2 HG01167.hp2 HG01243.hp1 others(51): Show |
intron_variant | MODIFIER | c.72-3578delT | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45953723 | ||||||
| chr22:45953741
|
G | A | 1 | a0001c0001t0002g0123 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.72-3595C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45953741 | ||||||
| chr22:45953765
|
C | T | 1 | a0001c0001t0014g0254 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.72-3619G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45953765 | ||||||
| chr22:45953820
|
C | A | 1 | a0001c0003t0053g0310 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.72-3674G>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45953820 | ||||||
| chr22:45953821
|
G | A | 4 | a0001c0001t0009g0268a0001c0001t0063g0344a0001c0002t0014g0274others(1): Show | 4 | HG01943.hp1 HG03130.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.72-3675C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45953821 | ||||||
| chr22:45953874
|
A | G | 8 | a0001c0001t0012g0259a0001c0001t0014g0254a0001c0001t0014g0324others(5): Show | 8 | HG01891.hp2 HG02559.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.72-3728T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45953874 | ||||||
| chr22:45954073
|
G | A | 5 | a0001c0001t0001g0263a0001c0001t0005g0283a0001c0001t0005g0333others(2): Show | 5 | HG01243.hp1 HG02572.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-3927C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45954073 | ||||||
| chr22:45954095
|
T | G | 12 | a0001c0001t0001g0341a0001c0001t0007g0321a0001c0001t0062g0339others(9): Show | 12 | HG00642.hp1 HG02970.hp2 HG03041.hp1 others(9): Show |
intron_variant | MODIFIER | c.72-3949A>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45954095 | ||||||
| chr22:45954220
|
A | G | 25 | a0001c0001t0001g0241a0001c0001t0001g0269a0001c0001t0001g0270others(22): Show | 25 | HG01109.hp2 HG01358.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.72-4074T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45954220 | ||||||
| chr22:45954221
|
TAG | T | 41 | a0001c0001t0001g0170a0001c0001t0001g0172a0001c0001t0001g0177others(38): Show | 41 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.72-4077_72-4076del others(2): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45954221 | ||||||
| chr22:45954261
|
C | T | 3 | a0001c0001t0025g0160a0001c0001t0047g0251a0001c0001t0065g0347 | 3 | HG01433.hp2 HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.72-4115G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45954261 | ||||||
| chr22:45954396
|
C | T | 79 | a0001c0001t0001g0170a0001c0001t0001g0172a0001c0001t0001g0177others(76): Show | 79 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.72-4250G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45954396 | ||||||
| chr22:45954453
|
T | C | 3 | a0001c0001t0025g0160a0001c0001t0047g0251a0001c0001t0065g0347 | 3 | HG01433.hp2 HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.72-4307A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45954453 | ||||||
| chr22:45954547
|
G | A | 1 | a0001c0001t0002g0038 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.72-4401C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45954547 | ||||||
| chr22:45954646
|
A | G | 148 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0170others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.72-4500T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45954646 | ||||||
| chr22:45954765
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.72-4619C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45954765 | ||||||
| chr22:45954768
|
C | T | 150 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0170others(147): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.72-4622G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45954768 | ||||||
| chr22:45955079
|
G | A | 5 | a0001c0001t0012g0159a0001c0001t0012g0329a0001c0001t0014g0313others(2): Show | 5 | HG02257.hp2 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-4933C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45955079 | ||||||
| chr22:45955146
|
T | A | 49 | a0001c0001t0001g0170a0001c0001t0001g0172a0001c0001t0001g0177others(46): Show | 49 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.72-5000A>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45955146 | ||||||
| chr22:45955191
|
C | T | 96 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0174others(93): Show | 96 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.72-5045G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45955191 | ||||||
| chr22:45955200
|
C | G | 4 | a0001c0001t0002g0146a0001c0001t0003g0019a0001c0001t0003g0040others(1): Show | 4 | NA18941.hp1 NA18959.hp1 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-5054G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45955200 | ||||||
| chr22:45955213
|
G | A | 1 | a0001c0001t0009g0250 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.72-5067C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45955213 | ||||||
| chr22:45955229
|
G | C | 3 | a0001c0001t0014g0254a0001c0001t0038g0009a0001c0004t0007g0342 | 3 | HG02559.hp2 HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.72-5083C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45955229 | ||||||
| chr22:45955235
|
C | T | 2 | a0001c0001t0007g0161a0001c0001t0007g0162 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.72-5089G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45955235 | ||||||
| chr22:45955236
|
C | A | 12 | a0001c0001t0001g0341a0001c0001t0007g0321a0001c0001t0062g0339others(9): Show | 12 | HG00642.hp1 HG02970.hp2 HG03041.hp1 others(9): Show |
intron_variant | MODIFIER | c.72-5090G>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45955236 | ||||||
| chr22:45955274
|
G | A | 3 | a0001c0001t0002g0146a0001c0001t0003g0040a0001c0001t0003g0145 | 3 | NA18941.hp1 NA18985.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.72-5128C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45955274 | ||||||
| chr22:45955338
|
G | C | 3 | a0001c0001t0001g0299a0001c0001t0001g0302a0001c0001t0002g0062 | 3 | HG01934.hp1 HG01952.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.72-5192C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45955338 | ||||||
| chr22:45955469
|
C | T | 2 | a0001c0001t0020g0225a0001c0002t0020g0336 | 2 | HG02258.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.72-5323G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45955469 | ||||||
| chr22:45955470
|
G | A | 6 | a0001c0001t0014g0254a0001c0001t0025g0160a0001c0001t0038g0009others(3): Show | 6 | HG01433.hp2 HG02559.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.72-5324C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45955470 | ||||||
| chr22:45955481
|
C | T | 1 | a0001c0001t0007g0321 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.72-5335G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45955481 | ||||||
| chr22:45955490
|
T | C | 1 | a0001c0001t0010g0007 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.72-5344A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45955490 | ||||||
| chr22:45955505
|
G | A | 4 | a0001c0001t0014g0254a0001c0001t0025g0160a0001c0001t0047g0251others(1): Show | 4 | HG01433.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-5359C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45955505 | ||||||
| chr22:45955601
|
G | C | 78 | a0001c0001t0001g0170a0001c0001t0001g0172a0001c0001t0001g0177others(75): Show | 78 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.72-5455C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45955601 | ||||||
| chr22:45955602
|
G | A | 45 | a0001c0001t0001g0170a0001c0001t0001g0172a0001c0001t0001g0177others(42): Show | 45 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.72-5456C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45955602 | ||||||
| chr22:45955673
|
T | C | 2 | a0001c0001t0001g0284a0001c0001t0007g0252 | 2 | HG02622.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.72-5527A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45955673 | ||||||
| chr22:45955681
|
C | T | 7 | a0001c0001t0001g0238a0001c0001t0001g0276a0001c0001t0002g0002others(4): Show | 8 | HG00621.hp1 NA18986.hp2 NA18998.hp1 others(5): Show |
intron_variant | MODIFIER | c.72-5535G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45955681 | ||||||
| chr22:45955820
|
T | C | 4 | a0001c0001t0014g0324a0001c0001t0017g0257a0001c0001t0024g0099others(1): Show | 4 | HG01891.hp2 HG02965.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.72-5674A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45955820 | ||||||
| chr22:45955880
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.72-5734C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45955880 | ||||||
| chr22:45955903
|
C | T | 90 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0174others(87): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.72-5757G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45955903 | ||||||
| chr22:45955917
|
C | T | 1 | a0001c0001t0017g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.72-5771G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45955917 | ||||||
| chr22:45955918
|
G | A | 1 | a0001c0001t0005g0333 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.72-5772C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45955918 | ||||||
| chr22:45955932
|
G | T | 1 | a0001c0001t0005g0333 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.72-5786C>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45955932 | ||||||
| chr22:45955943
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.72-5797G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45955943 | ||||||
| chr22:45955944
|
G | A | 76 | a0001c0001t0001g0170a0001c0001t0001g0172a0001c0001t0001g0177others(73): Show | 76 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.72-5798C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45955944 | ||||||
| chr22:45955960
|
A | G | 1 | a0001c0001t0003g0065 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.72-5814T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45955960 | ||||||
| chr22:45955976
|
G | A | 24 | a0001c0001t0001g0241a0001c0001t0001g0261a0001c0001t0001g0262others(21): Show | 24 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.72-5830C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45955976 | ||||||
| chr22:45956082
|
C | G | 1 | a0001c0001t0001g0241 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.72-5936G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45956082 | ||||||
| chr22:45956165
|
G | A | 10 | a0001c0001t0001g0302a0001c0001t0002g0110a0001c0001t0004g0203others(7): Show | 10 | HG00639.hp1 HG01069.hp1 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.72-6019C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45956165 | ||||||
| chr22:45956185
|
G | A | 1 | a0001c0001t0004g0178 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.72-6039C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45956185 | ||||||
| chr22:45956252
|
C | T | 1 | a0001c0001t0035g0018 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.72-6106G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45956252 | ||||||
| chr22:45956257
|
A | G | 24 | a0001c0001t0001g0245a0001c0001t0001g0269a0001c0001t0001g0270others(21): Show | 24 | HG01106.hp1 HG01496.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.72-6111T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45956257 | ||||||
| chr22:45956294
|
C | T | 1 | a0001c0001t0011g0189 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.72-6148G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45956294 | ||||||
| chr22:45956402
|
G | A | 3 | a0001c0001t0001g0153a0001c0001t0002g0070a0001c0001t0002g0071 | 3 | NA18941.hp2 NA19000.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.72-6256C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45956402 | ||||||
| chr22:45956425
|
C | T | 1 | a0001c0001t0001g0294 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.72-6279G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45956425 | ||||||
| chr22:45956466
|
C | T | 2 | a0001c0001t0007g0315a0001c0001t0007g0328 | 2 | HG02055.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.72-6320G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45956466 | ||||||
| chr22:45956500
|
C | T | 2 | a0001c0001t0001g0246a0001c0001t0001g0253 | 2 | HG02896.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.72-6354G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45956500 | ||||||
| chr22:45956519
|
C | G | 1 | a0001c0001t0045g0258 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.72-6373G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45956519 | ||||||
| chr22:45956533
|
C | T | 1 | a0001c0001t0005g0180 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.72-6387G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45956533 | ||||||
| chr22:45956548
|
T | C | 4 | a0001c0001t0020g0225a0001c0002t0018g0157a0001c0007t0054g0334others(1): Show | 4 | HG02647.hp2 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-6402A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45956548 | ||||||
| chr22:45956575
|
T | C | 3 | a0001c0001t0001g0271a0001c0001t0020g0158a0001c0014t0018g0260 | 3 | HG02451.hp1 HG02451.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.72-6429A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45956575 | ||||||
| chr22:45956597
|
A | G | 15 | a0001c0001t0001g0263a0001c0001t0001g0278a0001c0001t0012g0259others(12): Show | 15 | HG01099.hp1 HG01496.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.72-6451T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45956597 | ||||||
| chr22:45956599
|
G | A | 1 | a0001c0002t0001g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.72-6453C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45956599 | ||||||
| chr22:45956715
|
G | A | 1 | a0001c0001t0039g0074 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.72-6569C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45956715 | ||||||
| chr22:45956777
|
A | G | 1 | a0001c0003t0021g0229 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.72-6631T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45956777 | ||||||
| chr22:45956825
|
C | T | 1 | a0001c0001t0002g0104 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.72-6679G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45956825 | ||||||
| chr22:45956833
|
C | A | 17 | a0001c0001t0001g0271a0001c0001t0001g0284a0001c0001t0005g0283others(14): Show | 17 | HG01243.hp1 HG02451.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.72-6687G>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45956833 | ||||||
| chr22:45956836
|
G | A | 22 | a0001c0001t0001g0165a0001c0001t0001g0241a0001c0001t0001g0261others(19): Show | 22 | HG00280.hp1 HG01069.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.72-6690C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45956836 | ||||||
| chr22:45956846
|
G | A | 60 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0153others(57): Show | 60 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(57): Show |
intron_variant | MODIFIER | c.72-6700C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45956846 | ||||||
| chr22:45956930
|
G | A | 2 | a0001c0001t0001g0214a0001c0001t0010g0063 | 2 | HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.72-6784C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45956930 | ||||||
| chr22:45956966
|
C | T | 7 | a0001c0001t0007g0161a0001c0001t0007g0162a0001c0001t0009g0268others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.72-6820G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45956966 | ||||||
| chr22:45957104
|
C | CA | 53 | a0001c0001t0001g0179a0001c0001t0001g0181a0001c0001t0001g0187others(50): Show | 53 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.72-6959dupT | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45957104 | ||||||
| chr22:45957104
|
C | CAA | 11 | a0001c0001t0001g0165a0001c0001t0001g0270a0001c0001t0001g0291others(8): Show | 11 | HG01109.hp2 HG02055.hp2 HG02698.hp2 others(8): Show |
intron_variant | MODIFIER | c.72-6960_72-6959dup others(2): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45957104 | ||||||
| chr22:45957104
|
C | CAAAAA | 6 | a0001c0001t0001g0177a0001c0001t0001g0312a0001c0001t0001g0335others(3): Show | 6 | HG00099.hp2 HG00639.hp2 HG00733.hp2 others(3): Show |
intron_variant | MODIFIER | c.72-6963_72-6959dup others(5): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45957104 | ||||||
| chr22:45957104
|
C | CAAAAAA | 9 | a0001c0001t0005g0333a0001c0001t0014g0254a0001c0001t0014g0324others(6): Show | 9 | HG00642.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.72-6964_72-6959dup others(6): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45957104 | ||||||
| chr22:45957104
|
C | CAAAAAAA | 6 | a0001c0001t0001g0195a0001c0001t0001g0261a0001c0001t0001g0262others(3): Show | 6 | HG00741.hp2 HG01433.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.72-6965_72-6959dup others(7): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45957104 | ||||||
| chr22:45957104
|
C | CAAAAAAA others(1): Show |
6 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0253others(3): Show | 6 | HG02559.hp1 HG02630.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.72-6966_72-6959dup others(8): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45957104 | ||||||
| chr22:45957104
|
CA | C | 7 | a0001c0001t0001g0278a0001c0001t0004g0171a0001c0001t0018g0327others(4): Show | 7 | HG00738.hp2 HG01243.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.72-6959delT | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45957104 | ||||||
| chr22:45957104
|
CAAAAAAA | C | 6 | a0001c0001t0001g0341a0001c0001t0035g0018a0001c0001t0042g0013others(3): Show | 6 | HG01891.hp1 HG02280.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.72-6965_72-6959del others(7): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45957104 | ||||||
| chr22:45957112
|
A | AG | 156 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(153): Show | 157 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.72-6967_72-6966ins others(1): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45957112 | ||||||
| chr22:45957113
|
A | G | 1 | a0001c0001t0010g0029 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.72-6967T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45957113 | ||||||
| chr22:45957166
|
C | G | 26 | a0001c0001t0001g0177a0001c0001t0001g0195a0001c0001t0001g0241others(23): Show | 26 | HG00099.hp2 HG00639.hp2 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.72-7020G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45957166 | ||||||
| chr22:45957260
|
AC | A | 147 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0153others(144): Show | 148 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.72-7115delG | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45957260 | ||||||
| chr22:45957293
|
C | T | 1 | a0001c0001t0001g0242 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.72-7147G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45957293 | ||||||
| chr22:45957406
|
G | A | 29 | a0001c0001t0001g0150a0001c0001t0001g0165a0001c0001t0001g0193others(26): Show | 29 | HG00733.hp1 HG01358.hp2 HG01433.hp2 others(26): Show |
intron_variant | MODIFIER | c.72-7260C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45957406 | ||||||
| chr22:45957455
|
G | A | 1 | a0001c0001t0020g0158 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.72-7309C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45957455 | ||||||
| chr22:45957479
|
T | A | 5 | a0001c0001t0007g0314a0001c0001t0007g0315a0001c0001t0007g0328others(2): Show | 5 | HG02055.hp1 HG02109.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-7333A>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45957479 | ||||||
| chr22:45957537
|
A | C | 2 | a0001c0001t0001g0241a0003c0006t0064g0343 | 2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.72-7391T>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45957537 | ||||||
| chr22:45957540
|
T | C | 53 | a0001c0001t0001g0150a0001c0001t0001g0165a0001c0001t0001g0170others(50): Show | 53 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.72-7394A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45957540 | ||||||
| chr22:45957682
|
C | CA | 18 | a0001c0001t0001g0166a0001c0001t0001g0181a0001c0001t0001g0191others(15): Show | 18 | HG00099.hp1 HG01081.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.72-7537dupT | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45957682 | ||||||
| chr22:45957682
|
C | CAA | 79 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0174others(76): Show | 80 | HG00140.hp1 HG00544.hp1 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.72-7538_72-7537dup others(2): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45957682 | ||||||
| chr22:45957682
|
C | CAAA | 56 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0167others(53): Show | 56 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.72-7539_72-7537dup others(3): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45957682 | ||||||
| chr22:45957682
|
C | CAAAA | 16 | a0001c0001t0001g0175a0001c0001t0001g0214a0001c0001t0002g0028others(13): Show | 16 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(13): Show |
intron_variant | MODIFIER | c.72-7540_72-7537dup others(4): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45957682 | ||||||
| chr22:45957682
|
C | CAAAAAAA | 9 | a0001c0001t0001g0312a0001c0001t0001g0335a0001c0001t0004g0173others(6): Show | 9 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.72-7543_72-7537dup others(7): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45957682 | ||||||
| chr22:45957682
|
C | CAAAAAAA others(3): Show |
6 | a0001c0001t0001g0253a0001c0001t0009g0282a0001c0001t0012g0259others(3): Show | 6 | HG02486.hp2 HG02622.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.72-7546_72-7537dup others(10): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45957682 | ||||||
| chr22:45957682
|
C | CAAAAAAA others(5): Show |
3 | a0001c0001t0001g0246a0001c0001t0001g0261a0001c0001t0029g0240 | 3 | HG02559.hp1 HG02897.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.72-7548_72-7537dup others(12): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45957682 | ||||||
| chr22:45957682
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0001g0262 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.72-7549_72-7537dup others(13): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45957682 | ||||||
| chr22:45957682
|
CA | C | 53 | a0001c0001t0001g0179a0001c0001t0001g0187a0001c0001t0001g0188others(50): Show | 53 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.72-7537delT | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45957682 | ||||||
| chr22:45957682
|
CAA | C | 18 | a0001c0001t0001g0150a0001c0001t0001g0170a0001c0001t0001g0284others(15): Show | 18 | HG00733.hp1 HG01243.hp1 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.72-7538_72-7537del others(2): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45957682 | ||||||
| chr22:45957682
|
CAAAAAAA others(4): Show |
C | 8 | a0001c0001t0001g0165a0001c0001t0001g0193a0001c0001t0001g0277others(5): Show | 8 | HG02040.hp1 HG02486.hp1 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.72-7547_72-7537del others(11): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45957682 | ||||||
| chr22:45957682
|
CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0001g0245a0001c0001t0002g0041 | 2 | HG02630.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.72-7548_72-7537del others(12): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45957682 | ||||||
| chr22:45957703
|
A | C | 19 | a0001c0001t0001g0150a0001c0001t0001g0170a0001c0001t0001g0263others(16): Show | 19 | HG00733.hp1 HG01358.hp1 HG01358.hp2 others(16): Show |
intron_variant | MODIFIER | c.72-7557T>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45957703 | ||||||
| chr22:45957723
|
G | A | 30 | a0001c0001t0001g0150a0001c0001t0001g0165a0001c0001t0001g0170others(27): Show | 30 | HG00733.hp1 HG01358.hp1 HG01358.hp2 others(27): Show |
intron_variant | MODIFIER | c.72-7577C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45957723 | ||||||
| chr22:45957739
|
G | A | 148 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0153others(145): Show | 149 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.72-7593C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45957739 | ||||||
| chr22:45957789
|
G | C | 1 | a0001c0001t0002g0135 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.72-7643C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45957789 | ||||||
| chr22:45957791
|
G | C | 3 | a0001c0001t0005g0293a0001c0001t0022g0093a0001c0001t0026g0340 | 3 | HG01346.hp2 HG02683.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.72-7645C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45957791 | ||||||
| chr22:45957816
|
C | T | 146 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0153others(143): Show | 147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.72-7670G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45957816 | ||||||
| chr22:45957846
|
C | T | 2 | a0001c0001t0001g0271a0001c0001t0001g0278 | 2 | HG02451.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.72-7700G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45957846 | ||||||
| chr22:45957892
|
G | A | 2 | a0001c0001t0001g0271a0001c0001t0001g0278 | 2 | HG02451.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.72-7746C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45957892 | ||||||
| chr22:45957982
|
G | A | 1 | a0001c0001t0005g0180 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.72-7836C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45957982 | ||||||
| chr22:45958114
|
C | T | 7 | a0001c0001t0005g0333a0001c0001t0014g0324a0001c0001t0017g0257others(4): Show | 7 | HG00642.hp1 HG01884.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.72-7968G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45958114 | ||||||
| chr22:45958224
|
C | T | 172 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0153others(169): Show | 173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.72-8078G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45958224 | ||||||
| chr22:45958226
|
T | G | 59 | a0001c0001t0001g0179a0001c0001t0001g0187a0001c0001t0001g0231others(56): Show | 59 | HG00323.hp1 HG00323.hp2 HG01109.hp2 others(56): Show |
intron_variant | MODIFIER | c.72-8080A>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45958226 | ||||||
| chr22:45958399
|
C | A | 1 | a0001c0002t0037g0015 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.72-8253G>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45958399 | ||||||
| chr22:45958444
|
G | A | 10 | a0001c0001t0001g0341a0001c0001t0014g0254a0001c0001t0019g0290others(7): Show | 10 | HG01891.hp1 HG02280.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.72-8298C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45958444 | ||||||
| chr22:45958705
|
A | G | 307 | a0001c0001t0001g0148a0001c0001t0001g0150a0001c0001t0001g0152others(304): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.72-8559T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45958705 | ||||||
| chr22:45958786
|
G | A | 6 | a0001c0001t0005g0333a0001c0001t0014g0324a0001c0001t0024g0099others(3): Show | 6 | HG00642.hp1 HG01884.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.72-8640C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45958786 | ||||||
| chr22:45958870
|
C | T | 7 | a0001c0001t0001g0165a0001c0001t0001g0291a0001c0001t0001g0292others(4): Show | 7 | HG01884.hp2 HG02486.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.72-8724G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45958870 | ||||||
| chr22:45958993
|
C | T | 1 | a0001c0001t0002g0047 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.72-8847G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45958993 | ||||||
| chr22:45959018
|
T | C | 45 | a0001c0001t0001g0177a0001c0001t0001g0195a0001c0001t0001g0241others(42): Show | 45 | HG00099.hp2 HG00639.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.72-8872A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45959018 | ||||||
| chr22:45959052
|
G | C | 69 | a0001c0001t0001g0150a0001c0001t0001g0165a0001c0001t0001g0170others(66): Show | 69 | HG00323.hp1 HG00323.hp2 HG00733.hp1 others(66): Show |
intron_variant | MODIFIER | c.72-8906C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45959052 | ||||||
| chr22:45959056
|
C | G | 6 | a0001c0001t0001g0341a0001c0001t0035g0018a0001c0001t0042g0013others(3): Show | 6 | HG01891.hp1 HG02280.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.72-8910G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45959056 | ||||||
| chr22:45959093
|
A | T | 2 | a0001c0001t0001g0294a0001c0001t0002g0028 | 2 | HG00280.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.72-8947T>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45959093 | ||||||
| chr22:45959260
|
G | A | 1 | a0001c0001t0059g0156 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.72-9114C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45959260 | ||||||
| chr22:45959264
|
G | A | 1 | a0001c0001t0001g0263 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.72-9118C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45959264 | ||||||
| chr22:45959265
|
T | G | 1 | a0001c0001t0014g0254 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.72-9119A>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45959265 | ||||||
| chr22:45959269
|
C | G | 45 | a0001c0001t0001g0166a0001c0001t0001g0234a0001c0001t0001g0241others(42): Show | 45 | HG00099.hp1 HG00735.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.72-9123G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45959269 | ||||||
| chr22:45959271
|
G | T | 2 | a0001c0001t0007g0161a0001c0001t0007g0162 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.72-9125C>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45959271 | ||||||
| chr22:45959350
|
C | T | 1 | a0001c0007t0054g0334 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.72-9204G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45959350 | ||||||
| chr22:45959395
|
G | T | 1 | a0001c0001t0002g0140 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.72-9249C>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45959395 | ||||||
| chr22:45959443
|
G | A | 1 | a0001c0001t0002g0016 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.72-9297C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45959443 | ||||||
| chr22:45959535
|
G | A | 1 | a0001c0001t0001g0210 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.72-9389C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45959535 | ||||||
| chr22:45959582
|
G | A | 2 | a0001c0001t0002g0115a0001c0001t0003g0096 | 2 | HG02165.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.72-9436C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45959582 | ||||||
| chr22:45959690
|
G | A | 1 | a0001c0001t0003g0132 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.72-9544C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45959690 | ||||||
| chr22:45959789
|
G | A | 1 | a0001c0001t0001g0241 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.72-9643C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45959789 | ||||||
| chr22:45959793
|
T | C | 1 | a0001c0001t0004g0215 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.72-9647A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45959793 | ||||||
| chr22:45959806
|
C | T | 2 | a0001c0001t0012g0329a0001c0001t0018g0327 | 2 | HG01243.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.72-9660G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45959806 | ||||||
| chr22:45959825
|
C | T | 1 | a0001c0004t0007g0342 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.72-9679G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45959825 | ||||||
| chr22:45959834
|
C | T | 2 | a0001c0001t0004g0173a0001c0001t0011g0164 | 2 | HG00323.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.72-9688G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45959834 | ||||||
| chr22:45959901
|
G | A | 1 | a0001c0001t0002g0126 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.72-9755C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45959901 | ||||||
| chr22:45959944
|
G | T | 1 | a0001c0001t0023g0014 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.72-9798C>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45959944 | ||||||
| chr22:45960161
|
C | G | 1 | a0001c0001t0001g0166 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.72-10015G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45960161 | ||||||
| chr22:45960180
|
G | A | 2 | a0001c0001t0014g0254a0001c0001t0027g0256 | 2 | HG01099.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.72-10034C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45960180 | ||||||
| chr22:45960196
|
C | T | 1 | a0001c0001t0063g0344 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.72-10050G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45960196 | ||||||
| chr22:45960262
|
G | A | 1 | a0001c0007t0054g0334 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.72-10116C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45960262 | ||||||
| chr22:45960289
|
C | T | 1 | a0001c0001t0025g0160 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.72-10143G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45960289 | ||||||
| chr22:45960300
|
G | C | 2 | a0001c0001t0001g0276a0001c0001t0004g0275 | 2 | HG00621.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.72-10154C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45960300 | ||||||
| chr22:45960399
|
A | C | 1 | a0003c0006t0064g0343 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.72-10253T>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45960399 | ||||||
| chr22:45960469
|
AC | A | 200 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0153others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.72-10324delG | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45960469 | ||||||
| chr22:45960554
|
T | C | 299 | a0001c0001t0001g0148a0001c0001t0001g0150a0001c0001t0001g0152others(296): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.72-10408A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45960554 | ||||||
| chr22:45960573
|
C | T | 3 | a0001c0001t0012g0329a0001c0001t0018g0327a0001c0014t0018g0260 | 3 | HG01243.hp2 HG03139.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.72-10427G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45960573 | ||||||
| chr22:45960594
|
C | G | 1 | a0001c0001t0001g0231 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.72-10448G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45960594 | ||||||
| chr22:45960631
|
G | A | 2 | a0001c0001t0001g0271a0001c0001t0005g0333 | 2 | HG02451.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.72-10485C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45960631 | ||||||
| chr22:45960674
|
C | T | 266 | a0001c0001t0001g0148a0001c0001t0001g0150a0001c0001t0001g0152others(263): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.72-10528G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45960674 | ||||||
| chr22:45960713
|
C | T | 1 | a0001c0001t0025g0160 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.72-10567G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45960713 | ||||||
| chr22:45960803
|
G | A | 7 | a0001c0001t0009g0282a0001c0001t0009g0285a0001c0001t0012g0159others(4): Show | 7 | HG01433.hp2 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.72-10657C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45960803 | ||||||
| chr22:45960888
|
G | C | 1 | a0001c0001t0027g0256 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.72-10742C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45960888 | ||||||
| chr22:45961019
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.72-10873C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45961019 | ||||||
| chr22:45961039
|
C | T | 7 | a0001c0001t0009g0282a0001c0001t0009g0285a0001c0001t0012g0159others(4): Show | 7 | HG01433.hp2 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.72-10893G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45961039 | ||||||
| chr22:45961074
|
T | C | 7 | a0001c0001t0009g0282a0001c0001t0009g0285a0001c0001t0012g0159others(4): Show | 7 | HG01433.hp2 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.72-10928A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45961074 | ||||||
| chr22:45961154
|
C | T | 1 | a0001c0001t0002g0041 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.72-11008G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45961154 | ||||||
| chr22:45961212
|
G | A | 1 | a0001c0001t0062g0339 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.72-11066C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45961212 | ||||||
| chr22:45961232
|
T | C | 2 | a0001c0001t0068g0348a0001c0002t0014g0274 | 2 | HG01496.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.72-11086A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45961232 | ||||||
| chr22:45961271
|
C | T | 3 | a0001c0001t0012g0329a0001c0001t0018g0327a0001c0014t0018g0260 | 3 | HG01243.hp2 HG03139.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.72-11125G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45961271 | ||||||
| chr22:45961283
|
C | G | 1 | a0001c0001t0002g0020 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.72-11137G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45961283 | ||||||
| chr22:45961408
|
G | A | 3 | a0001c0001t0012g0329a0001c0001t0018g0327a0001c0014t0018g0260 | 3 | HG01243.hp2 HG03139.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.72-11262C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45961408 | ||||||
| chr22:45961477
|
C | T | 3 | a0001c0001t0016g0032a0001c0001t0016g0034a0001c0001t0016g0035 | 3 | NA18966.hp1 NA18969.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.72-11331G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45961477 | ||||||
| chr22:45961768
|
C | T | 3 | a0001c0001t0001g0223a0001c0001t0004g0221a0001c0001t0004g0222 | 3 | HG03490.hp1 HG03492.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.72-11622G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45961768 | ||||||
| chr22:45961809
|
G | A | 1 | a0001c0001t0059g0156 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.72-11663C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45961809 | ||||||
| chr22:45961884
|
C | T | 2 | a0001c0001t0006g0073a0001c0008t0002g0072 | 2 | HG02109.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.72-11738G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45961884 | ||||||
| chr22:45961897
|
A | G | 276 | a0001c0001t0001g0148a0001c0001t0001g0150a0001c0001t0001g0152others(273): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.72-11751T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45961897 | ||||||
| chr22:45962029
|
C | T | 2 | a0001c0001t0007g0161a0001c0001t0007g0162 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.72-11883G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45962029 | ||||||
| chr22:45962061
|
G | A | 2 | a0001c0001t0068g0348a0001c0002t0014g0274 | 2 | HG01496.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.72-11915C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45962061 | ||||||
| chr22:45962157
|
G | C | 1 | a0001c0001t0005g0301 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.72-12011C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45962157 | ||||||
| chr22:45962316
|
GAGCCTCA others(20): Show |
G | 1 | a0001c0001t0005g0227 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.72-12197_72-12171d others(29): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45962316 | ||||||
| chr22:45962412
|
G | C | 1 | a0001c0007t0054g0334 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.72-12266C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45962412 | ||||||
| chr22:45962542
|
C | T | 14 | a0001c0001t0001g0241a0001c0001t0001g0245a0001c0001t0001g0246others(11): Show | 14 | HG02451.hp1 HG02559.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.72-12396G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45962542 | ||||||
| chr22:45962555
|
C | T | 3 | a0001c0001t0012g0329a0001c0001t0018g0327a0001c0014t0018g0260 | 3 | HG01243.hp2 HG03139.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.72-12409G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45962555 | ||||||
| chr22:45962620
|
T | C | 3 | a0001c0001t0012g0329a0001c0001t0018g0327a0001c0014t0018g0260 | 3 | HG01243.hp2 HG03139.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.72-12474A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45962620 | ||||||
| chr22:45962703
|
T | C | 14 | a0001c0001t0001g0241a0001c0001t0001g0245a0001c0001t0001g0246others(11): Show | 14 | HG02451.hp1 HG02559.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.72-12557A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45962703 | ||||||
| chr22:45962762
|
T | TCCTGGC | 6 | a0001c0001t0009g0282a0001c0001t0009g0285a0001c0001t0012g0159others(3): Show | 6 | HG01433.hp2 HG02486.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.72-12622_72-12617d others(8): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45962762 | ||||||
| chr22:45962866
|
G | T | 202 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0153others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.72-12720C>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45962866 | ||||||
| chr22:45962909
|
T | C | 1 | a0001c0003t0053g0310 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.72-12763A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45962909 | ||||||
| chr22:45962951
|
G | A | 1 | a0001c0001t0003g0040 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.72-12805C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45962951 | ||||||
| chr22:45963121
|
C | T | 6 | a0001c0001t0001g0341a0001c0001t0002g0070a0001c0001t0002g0071others(3): Show | 6 | HG01891.hp1 HG02280.hp1 NA19000.hp2 others(3): Show |
intron_variant | MODIFIER | c.72-12975G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45963121 | ||||||
| chr22:45963145
|
C | G | 1 | a0001c0007t0054g0334 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.72-12999G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45963145 | ||||||
| chr22:45963257
|
C | T | 2 | a0001c0001t0001g0278a0001c0001t0001g0320 | 2 | HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.72-13111G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45963257 | ||||||
| chr22:45963319
|
C | T | 7 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0325others(4): Show | 7 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.72-13173G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45963319 | ||||||
| chr22:45963388
|
C | G | 1 | a0001c0001t0002g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.72-13242G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45963388 | ||||||
| chr22:45963388
|
C | T | 1 | a0001c0001t0003g0100 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.72-13242G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45963388 | ||||||
| chr22:45963467
|
G | A | 3 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0325 | 3 | HG02055.hp2 HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.71+13217C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45963467 | ||||||
| chr22:45963486
|
C | A | 3 | a0001c0001t0002g0140a0001c0001t0008g0141a0001c0001t0008g0142 | 3 | HG02056.hp1 NA18980.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.71+13198G>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45963486 | ||||||
| chr22:45963507
|
G | A | 1 | a0001c0001t0067g0346 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.71+13177C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45963507 | ||||||
| chr22:45963564
|
G | C | 1 | a0001c0001t0001g0278 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.71+13120C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45963564 | ||||||
| chr22:45963591
|
G | A | 1 | a0001c0001t0003g0098 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.71+13093C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45963591 | ||||||
| chr22:45963680
|
C | T | 1 | a0001c0001t0003g0068 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.71+13004G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45963680 | ||||||
| chr22:45963811
|
A | G | 38 | a0001c0001t0001g0241a0001c0001t0001g0245a0001c0001t0001g0246others(35): Show | 38 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.71+12873T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45963811 | ||||||
| chr22:45963884
|
T | C | 7 | a0001c0001t0002g0012a0001c0001t0023g0014a0001c0001t0024g0010others(4): Show | 7 | HG02145.hp2 HG02258.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.71+12800A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45963884 | ||||||
| chr22:45963928
|
C | T | 1 | a0001c0001t0018g0327 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.71+12756G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45963928 | ||||||
| chr22:45963943
|
C | T | 2 | a0001c0002t0014g0274a0001c0002t0018g0157 | 2 | HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.71+12741G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45963943 | ||||||
| chr22:45964116
|
A | G | 347 | a0001c0001t0001g0148a0001c0001t0001g0150a0001c0001t0001g0152others(344): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.71+12568T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45964116 | ||||||
| chr22:45964203
|
G | A | 105 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0174others(102): Show | 105 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.71+12481C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45964203 | ||||||
| chr22:45964252
|
C | A | 2 | a0001c0001t0009g0250a0001c0002t0001g0163 | 2 | HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.71+12432G>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45964252 | ||||||
| chr22:45964292
|
A | C | 14 | a0001c0001t0001g0271a0001c0001t0001g0341a0001c0001t0012g0259others(11): Show | 14 | HG00642.hp1 HG01243.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.71+12392T>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45964292 | ||||||
| chr22:45964354
|
C | G | 175 | a0001c0001t0001g0150a0001c0001t0001g0152a0001c0001t0001g0165others(172): Show | 176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.71+12330G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45964354 | ||||||
| chr22:45964370
|
T | C | 23 | a0001c0001t0001g0292a0001c0001t0001g0320a0001c0001t0001g0323others(20): Show | 23 | HG01109.hp2 HG01167.hp2 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.71+12314A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45964370 | ||||||
| chr22:45964385
|
G | A | 11 | a0001c0001t0001g0253a0001c0001t0001g0278a0001c0001t0001g0284others(8): Show | 11 | HG01243.hp1 HG01243.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.71+12299C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45964385 | ||||||
| chr22:45964422
|
C | A | 1 | a0001c0001t0001g0212 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.71+12262G>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45964422 | ||||||
| chr22:45964424
|
C | T | 49 | a0001c0001t0001g0148a0001c0001t0001g0166a0001c0001t0001g0167others(46): Show | 49 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.71+12260G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45964424 | ||||||
| chr22:45964521
|
G | A | 7 | a0001c0001t0002g0113a0001c0001t0002g0115a0001c0001t0002g0116others(4): Show | 7 | HG01346.hp1 HG01981.hp1 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.71+12163C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45964521 | ||||||
| chr22:45964522
|
C | T | 3 | a0001c0001t0001g0172a0001c0001t0004g0171a0001c0001t0013g0286 | 3 | HG02735.hp1 HG03239.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.71+12162G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45964522 | ||||||
| chr22:45964582
|
C | T | 1 | a0001c0001t0001g0267 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.71+12102G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45964582 | ||||||
| chr22:45964719
|
GC | G | 6 | a0001c0001t0002g0012a0001c0001t0023g0014a0001c0001t0024g0010others(3): Show | 6 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.71+11964delG | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45964719 | ||||||
| chr22:45964725
|
G | C | 1 | a0001c0001t0005g0227 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.71+11959C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45964725 | ||||||
| chr22:45964745
|
A | ACACCAGA others(14): Show |
1 | a0001c0001t0005g0227 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.71+11938_71+11939i others(23): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45964745 | ||||||
| chr22:45964762
|
G | A | 2 | a0001c0001t0001g0277a0001c0001t0026g0340 | 2 | HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.71+11922C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45964762 | ||||||
| chr22:45964766
|
C | T | 1 | a0001c0001t0005g0227 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.71+11918G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45964766 | ||||||
| chr22:45964839
|
C | T | 1 | a0001c0001t0006g0120 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.71+11845G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45964839 | ||||||
| chr22:45964860
|
G | A | 1 | a0001c0001t0020g0158 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.71+11824C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45964860 | ||||||
| chr22:45964892
|
C | T | 164 | a0001c0001t0001g0277a0001c0001t0001g0291a0001c0001t0001g0292others(161): Show | 166 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.71+11792G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45964892 | ||||||
| chr22:45964919
|
C | T | 2 | a0001c0001t0001g0269a0001c0001t0001g0270 | 2 | HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.71+11765G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45964919 | ||||||
| chr22:45965003
|
C | A | 2 | a0001c0001t0001g0277a0001c0001t0026g0340 | 2 | HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.71+11681G>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45965003 | ||||||
| chr22:45965173
|
G | A | 2 | a0001c0001t0003g0125a0001c0001t0006g0124 | 2 | NA18951.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.71+11511C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45965173 | ||||||
| chr22:45965226
|
G | A | 2 | a0001c0001t0007g0161a0001c0001t0007g0162 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.71+11458C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45965226 | ||||||
| chr22:45965325
|
C | A | 185 | a0001c0001t0001g0150a0001c0001t0001g0170a0001c0001t0001g0220others(182): Show | 187 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.71+11359G>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45965325 | ||||||
| chr22:45965408
|
G | A | 1 | a0001c0004t0007g0342 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.71+11276C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45965408 | ||||||
| chr22:45965549
|
G | A | 4 | a0001c0001t0065g0347a0001c0001t0066g0345a0001c0001t0067g0346others(1): Show | 4 | HG01433.hp2 HG01496.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.71+11135C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45965549 | ||||||
| chr22:45965678
|
G | A | 1 | a0001c0001t0005g0333 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.71+11006C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45965678 | ||||||
| chr22:45965713
|
G | A | 1 | a0001c0001t0002g0126 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.71+10971C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45965713 | ||||||
| chr22:45965887
|
C | T | 2 | a0001c0001t0025g0160a0003c0006t0064g0343 | 2 | HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.71+10797G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45965887 | ||||||
| chr22:45965961
|
A | G | 5 | a0001c0001t0005g0333a0001c0001t0007g0161a0001c0001t0007g0162others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.71+10723T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45965961 | ||||||
| chr22:45966006
|
G | A | 1 | a0001c0001t0002g0127 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.71+10678C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45966006 | ||||||
| chr22:45966220
|
G | A | 1 | a0001c0001t0001g0213 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.71+10464C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45966220 | ||||||
| chr22:45966237
|
G | C | 1 | a0001c0001t0009g0250 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.71+10447C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45966237 | ||||||
| chr22:45966305
|
C | T | 2 | a0001c0001t0001g0277a0001c0001t0026g0340 | 2 | HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.71+10379G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45966305 | ||||||
| chr22:45966380
|
C | T | 4 | a0001c0001t0065g0347a0001c0001t0066g0345a0001c0001t0067g0346others(1): Show | 4 | HG01433.hp2 HG01496.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.71+10304G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45966380 | ||||||
| chr22:45966516
|
A | G | 240 | a0001c0001t0001g0150a0001c0001t0001g0170a0001c0001t0001g0220others(237): Show | 242 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.71+10168T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45966516 | ||||||
| chr22:45966581
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.71+10103G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45966581 | ||||||
| chr22:45966673
|
A | G | 1 | a0001c0001t0051g0307 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.71+10011T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45966673 | ||||||
| chr22:45966703
|
C | T | 1 | a0001c0001t0001g0263 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.71+9981G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45966703 | ||||||
| chr22:45966706
|
C | T | 5 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0271others(2): Show | 5 | HG02451.hp1 HG02970.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.71+9978G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45966706 | ||||||
| chr22:45966844
|
C | T | 2 | a0001c0001t0001g0261a0001c0001t0001g0262 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.71+9840G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45966844 | ||||||
| chr22:45966872
|
G | A | 4 | a0001c0001t0001g0263a0001c0002t0020g0336a0001c0002t0052g0338others(1): Show | 4 | HG02258.hp2 NA19240.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.71+9812C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45966872 | ||||||
| chr22:45966913
|
G | A | 2 | a0001c0001t0012g0329a0001c0011t0049g0330 | 2 | HG01891.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.71+9771C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45966913 | ||||||
| chr22:45966916
|
C | T | 1 | a0001c0001t0002g0026 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.71+9768G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45966916 | ||||||
| chr22:45966942
|
C | CT | 148 | a0001c0001t0001g0281a0001c0001t0002g0001a0001c0001t0002g0002others(145): Show | 150 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.71+9741dupA | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45966942 | ||||||
| chr22:45967208
|
C | G | 1 | a0001c0001t0006g0025 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.71+9476G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45967208 | ||||||
| chr22:45967295
|
C | A | 1 | a0001c0001t0001g0214 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.71+9389G>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45967295 | ||||||
| chr22:45967306
|
G | A | 1 | a0001c0001t0012g0331 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.71+9378C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45967306 | ||||||
| chr22:45967397
|
G | A | 2 | a0001c0001t0001g0281a0001c0001t0036g0128 | 2 | HG02683.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.71+9287C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45967397 | ||||||
| chr22:45967401
|
C | T | 1 | a0001c0001t0062g0339 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.71+9283G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45967401 | ||||||
| chr22:45967454
|
GGCTCCCA others(44): Show |
G | 231 | a0001c0001t0001g0150a0001c0001t0001g0220a0001c0001t0001g0263others(228): Show | 233 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.71+9179_71+9229del others(51): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45967454 | ||||||
| chr22:45967609
|
C | T | 2 | a0001c0001t0007g0161a0001c0001t0007g0162 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.71+9075G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45967609 | ||||||
| chr22:45967811
|
G | A | 3 | a0001c0001t0001g0150a0001c0001t0005g0149a0001c0001t0013g0151 | 3 | HG00733.hp1 HG01255.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.71+8873C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45967811 | ||||||
| chr22:45967859
|
A | G | 181 | a0001c0001t0001g0272a0001c0001t0001g0276a0001c0001t0001g0277others(178): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.71+8825T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45967859 | ||||||
| chr22:45968020
|
G | C | 6 | a0001c0001t0001g0302a0001c0001t0001g0303a0001c0001t0001g0305others(3): Show | 6 | HG01361.hp2 HG01928.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.71+8664C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45968020 | ||||||
| chr22:45968029
|
C | G | 1 | a0001c0001t0004g0168 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.71+8655G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45968029 | ||||||
| chr22:45968162
|
TAGTCTGG others(35): Show |
T | 3 | a0001c0002t0020g0336a0001c0002t0052g0338a0001c0013t0021g0337 | 3 | HG02258.hp2 NA19240.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.71+8480_71+8521del others(42): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45968162 | ||||||
| chr22:45968207
|
T | G | 3 | a0001c0002t0020g0336a0001c0002t0052g0338a0001c0013t0021g0337 | 3 | HG02258.hp2 NA19240.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.71+8477A>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45968207 | ||||||
| chr22:45968239
|
T | C | 1 | a0001c0001t0001g0281 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.71+8445A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45968239 | ||||||
| chr22:45968281
|
G | A | 139 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0008others(136): Show | 141 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.71+8403C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45968281 | ||||||
| chr22:45968288
|
T | A | 1 | a0001c0001t0002g0133 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.71+8396A>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45968288 | ||||||
| chr22:45968311
|
C | T | 155 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0271others(152): Show | 157 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.71+8373G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45968311 | ||||||
| chr22:45968478
|
G | C | 1 | a0001c0001t0004g0215 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.71+8206C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45968478 | ||||||
| chr22:45968550
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.71+8134G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45968550 | ||||||
| chr22:45968557
|
T | C | 3 | a0001c0001t0001g0253a0001c0001t0007g0252a0001c0001t0047g0251 | 3 | HG02895.hp2 HG02896.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.71+8127A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45968557 | ||||||
| chr22:45968625
|
C | T | 1 | a0001c0004t0007g0342 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.71+8059G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45968625 | ||||||
| chr22:45968632
|
G | A | 1 | a0001c0001t0001g0306 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.71+8052C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45968632 | ||||||
| chr22:45968750
|
G | T | 1 | a0001c0001t0003g0019 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.71+7934C>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45968750 | ||||||
| chr22:45969052
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.71+7632G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45969052 | ||||||
| chr22:45969223
|
C | A | 1 | a0001c0001t0015g0129 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.71+7461G>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45969223 | ||||||
| chr22:45969288
|
C | T | 4 | a0001c0001t0065g0347a0001c0001t0066g0345a0001c0001t0067g0346others(1): Show | 4 | HG01433.hp2 HG01496.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.71+7396G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45969288 | ||||||
| chr22:45969335
|
C | G | 6 | a0001c0001t0005g0333a0001c0001t0007g0161a0001c0001t0007g0162others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.71+7349G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45969335 | ||||||
| chr22:45969389
|
A | G | 1 | a0001c0001t0009g0285 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.71+7295T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45969389 | ||||||
| chr22:45969621
|
C | T | 35 | a0001c0001t0001g0263a0001c0001t0001g0272a0001c0001t0001g0276others(32): Show | 35 | HG00621.hp1 HG00733.hp2 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.71+7063G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45969621 | ||||||
| chr22:45969677
|
G | T | 137 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0008others(134): Show | 139 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.71+7007C>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45969677 | ||||||
| chr22:45969687
|
C | T | 2 | a0001c0001t0001g0284a0001c0001t0019g0332 | 2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.71+6997G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45969687 | ||||||
| chr22:45969750
|
G | A | 37 | a0001c0001t0001g0263a0001c0001t0001g0272a0001c0001t0001g0276others(34): Show | 37 | HG00621.hp1 HG00733.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.71+6934C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45969750 | ||||||
| chr22:45969946
|
A | C | 3 | a0001c0001t0020g0158a0001c0001t0059g0156a0001c0002t0018g0157 | 3 | HG02451.hp2 HG02622.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.71+6738T>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45969946 | ||||||
| chr22:45970048
|
G | A | 8 | a0001c0001t0001g0281a0001c0001t0002g0012a0001c0001t0023g0014others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.71+6636C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45970048 | ||||||
| chr22:45970058
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.71+6626G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45970058 | ||||||
| chr22:45970080
|
C | G | 1 | a0001c0016t0007g0280 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.71+6604G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45970080 | ||||||
| chr22:45970247
|
G | C | 218 | a0001c0001t0001g0150a0001c0001t0001g0216a0001c0001t0001g0220others(215): Show | 220 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.71+6437C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45970247 | ||||||
| chr22:45970285
|
C | T | 99 | a0001c0001t0001g0150a0001c0001t0001g0220a0001c0001t0001g0269others(96): Show | 99 | HG00621.hp1 HG00639.hp2 HG00733.hp1 others(96): Show |
intron_variant | MODIFIER | c.71+6399G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45970285 | ||||||
| chr22:45970300
|
T | C | 3 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0219 | 3 | NA19004.hp1 NA19011.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.71+6384A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45970300 | ||||||
| chr22:45970362
|
G | A | 1 | a0001c0001t0041g0130 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.71+6322C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45970362 | ||||||
| chr22:45970381
|
G | A | 1 | a0001c0001t0002g0131 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.71+6303C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45970381 | ||||||
| chr22:45970431
|
GGCACCAC others(3): Show |
G | 96 | a0001c0001t0001g0150a0001c0001t0001g0220a0001c0001t0001g0269others(93): Show | 96 | HG00621.hp1 HG00639.hp2 HG00733.hp1 others(93): Show |
intron_variant | MODIFIER | c.71+6243_71+6252del others(10): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45970431 | ||||||
| chr22:45970489
|
T | C | 2 | a0001c0001t0001g0261a0001c0001t0001g0262 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.71+6195A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45970489 | ||||||
| chr22:45970541
|
C | A | 1 | a0001c0001t0014g0254 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.71+6143G>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45970541 | ||||||
| chr22:45970545
|
C | G | 1 | a0001c0001t0011g0164 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.71+6139G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45970545 | ||||||
| chr22:45970570
|
C | G | 2 | a0001c0001t0023g0017a0001c0001t0035g0018 | 2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.71+6114G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45970570 | ||||||
| chr22:45970841
|
C | T | 3 | a0001c0001t0001g0223a0001c0001t0004g0221a0001c0001t0004g0222 | 3 | HG03490.hp1 HG03492.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.71+5843G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45970841 | ||||||
| chr22:45970863
|
G | A | 1 | a0001c0001t0019g0332 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.71+5821C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45970863 | ||||||
| chr22:45970865
|
G | T | 2 | a0001c0001t0001g0269a0001c0001t0001g0270 | 2 | HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.71+5819C>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45970865 | ||||||
| chr22:45970921
|
G | A | 4 | a0001c0001t0065g0347a0001c0001t0066g0345a0001c0001t0067g0346others(1): Show | 4 | HG01433.hp2 HG01496.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.71+5763C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45970921 | ||||||
| chr22:45970968
|
C | T | 3 | a0001c0001t0002g0135a0001c0001t0002g0137a0001c0001t0003g0136 | 3 | HG00609.hp2 NA18983.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.71+5716G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45970968 | ||||||
| chr22:45971110
|
G | A | 3 | a0001c0001t0001g0281a0001c0001t0005g0283a0001c0016t0007g0280 | 3 | HG02572.hp2 HG02683.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.71+5574C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45971110 | ||||||
| chr22:45971126
|
G | A | 3 | a0001c0002t0020g0336a0001c0002t0052g0338a0001c0013t0021g0337 | 3 | HG02258.hp2 NA19240.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.71+5558C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45971126 | ||||||
| chr22:45971205
|
G | C | 1 | a0001c0001t0063g0344 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.71+5479C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45971205 | ||||||
| chr22:45971264
|
G | A | 88 | a0001c0001t0001g0150a0001c0001t0001g0269a0001c0001t0001g0270others(85): Show | 88 | HG00621.hp1 HG00639.hp2 HG00733.hp1 others(85): Show |
intron_variant | MODIFIER | c.71+5420C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45971264 | ||||||
| chr22:45971456
|
C | T | 1 | a0001c0001t0009g0282 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.71+5228G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45971456 | ||||||
| chr22:45971503
|
C | T | 1 | a0001c0001t0009g0268 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.71+5181G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45971503 | ||||||
| chr22:45971568
|
C | T | 2 | a0001c0001t0001g0281a0001c0016t0007g0280 | 2 | HG02683.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.71+5116G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45971568 | ||||||
| chr22:45971631
|
G | T | 1 | a0001c0001t0001g0272 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.71+5053C>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45971631 | ||||||
| chr22:45971908
|
G | A | 3 | a0001c0002t0020g0336a0001c0002t0052g0338a0001c0013t0021g0337 | 3 | HG02258.hp2 NA19240.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.71+4776C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45971908 | ||||||
| chr22:45971973
|
G | A | 2 | a0001c0001t0002g0002a0001c0001t0003g0132 | 3 | NA18986.hp2 NA18998.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.71+4711C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45971973 | ||||||
| chr22:45972006
|
G | C | 1 | a0001c0001t0063g0344 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.71+4678C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45972006 | ||||||
| chr22:45972030
|
G | A | 1 | a0001c0001t0063g0344 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.71+4654C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45972030 | ||||||
| chr22:45972169
|
G | A | 1 | a0001c0001t0005g0333 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.71+4515C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45972169 | ||||||
| chr22:45972202
|
G | A | 1 | a0001c0001t0002g0133 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.71+4482C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45972202 | ||||||
| chr22:45972250
|
T | C | 280 | a0001c0001t0001g0150a0001c0001t0001g0223a0001c0001t0001g0231others(277): Show | 282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.71+4434A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45972250 | ||||||
| chr22:45972339
|
G | A | 1 | a0001c0001t0001g0263 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.71+4345C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45972339 | ||||||
| chr22:45972468
|
A | G | 1 | a0001c0001t0005g0279 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.71+4216T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45972468 | ||||||
| chr22:45972471
|
C | G | 2 | a0001c0001t0059g0156a0001c0002t0018g0157 | 2 | HG02622.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.71+4213G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45972471 | ||||||
| chr22:45972548
|
C | G | 1 | a0001c0001t0002g0016 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.71+4136G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45972548 | ||||||
| chr22:45972598
|
C | A | 1 | a0001c0001t0008g0134 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.71+4086G>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45972598 | ||||||
| chr22:45972604
|
G | A | 1 | a0001c0001t0005g0333 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.71+4080C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45972604 | ||||||
| chr22:45972650
|
G | C | 1 | a0001c0012t0001g0255 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.71+4034C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45972650 | ||||||
| chr22:45972668
|
T | C | 3 | a0001c0001t0002g0135a0001c0001t0002g0137a0001c0001t0003g0136 | 3 | HG00609.hp2 NA18983.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.71+4016A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45972668 | ||||||
| chr22:45972894
|
G | A | 2 | a0001c0001t0002g0138a0001c0001t0003g0139 | 2 | HG00423.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.71+3790C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45972894 | ||||||
| chr22:45972909
|
G | A | 3 | a0001c0001t0002g0140a0001c0001t0008g0141a0001c0001t0008g0142 | 3 | HG02056.hp1 NA18980.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.71+3775C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45972909 | ||||||
| chr22:45972996
|
A | T | 1 | a0001c0001t0044g0147 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.71+3688T>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45972996 | ||||||
| chr22:45973100
|
C | T | 2 | a0001c0001t0059g0156a0001c0002t0018g0157 | 2 | HG02622.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.71+3584G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45973100 | ||||||
| chr22:45973223
|
C | T | 1 | a0001c0002t0001g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.71+3461G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45973223 | ||||||
| chr22:45973497
|
A | C | 9 | a0001c0001t0001g0272a0001c0001t0001g0276a0001c0001t0001g0277others(6): Show | 9 | HG00621.hp1 HG02559.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.71+3187T>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45973497 | ||||||
| chr22:45973563
|
A | G | 1 | a0001c0001t0061g0273 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.71+3121T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45973563 | ||||||
| chr22:45973616
|
G | A | 8 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0263others(5): Show | 8 | HG01099.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.71+3068C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45973616 | ||||||
| chr22:45973665
|
C | T | 1 | a0001c0001t0062g0339 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.71+3019G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45973665 | ||||||
| chr22:45973745
|
G | C | 3 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0266 | 3 | HG03654.hp2 HG03669.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.71+2939C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45973745 | ||||||
| chr22:45973777
|
C | G | 224 | a0001c0001t0001g0150a0001c0001t0001g0272a0001c0001t0001g0276others(221): Show | 226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.71+2907G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45973777 | ||||||
| chr22:45973835
|
T | C | 2 | a0001c0001t0001g0154a0001c0001t0011g0155 | 2 | HG02602.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.71+2849A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45973835 | ||||||
| chr22:45973898
|
C | CT | 234 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0271others(231): Show | 236 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.71+2785_71+2786ins others(1): Show |
WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45973898 | ||||||
| chr22:45973927
|
G | A | 1 | a0001c0001t0001g0267 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.71+2757C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45973927 | ||||||
| chr22:45973969
|
T | C | 4 | a0001c0001t0002g0143a0001c0001t0002g0146a0001c0001t0003g0144others(1): Show | 4 | NA18941.hp1 NA18994.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.71+2715A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45973969 | ||||||
| chr22:45974183
|
C | T | 1 | a0001c0001t0001g0272 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.71+2501G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45974183 | ||||||
| chr22:45974371
|
C | T | 1 | a0003c0006t0064g0343 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.71+2313G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45974371 | ||||||
| chr22:45974479
|
G | C | 1 | a0001c0001t0009g0268 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.71+2205C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45974479 | ||||||
| chr22:45974624
|
G | C | 3 | a0001c0002t0020g0336a0001c0002t0052g0338a0001c0013t0021g0337 | 3 | HG02258.hp2 NA19240.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.71+2060C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45974624 | ||||||
| chr22:45974744
|
G | A | 3 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0271 | 3 | HG02451.hp1 HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.71+1940C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45974744 | ||||||
| chr22:45974885
|
T | C | 228 | a0001c0001t0001g0150a0001c0001t0001g0154a0001c0001t0001g0272others(225): Show | 230 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.71+1799A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45974885 | ||||||
| chr22:45974909
|
G | A | 3 | a0001c0001t0020g0158a0001c0001t0059g0156a0001c0002t0018g0157 | 3 | HG02451.hp2 HG02622.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.71+1775C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45974909 | ||||||
| chr22:45974984
|
A | G | 7 | a0001c0001t0020g0158a0001c0001t0059g0156a0001c0001t0065g0347others(4): Show | 7 | HG01433.hp2 HG01496.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.71+1700T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45974984 | ||||||
| chr22:45975035
|
G | A | 1 | a0001c0001t0062g0339 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.71+1649C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45975035 | ||||||
| chr22:45975199
|
A | G | 140 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0002g0001others(137): Show | 142 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.71+1485T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45975199 | ||||||
| chr22:45975508
|
C | T | 7 | a0001c0001t0002g0012a0001c0001t0023g0014a0001c0001t0024g0010others(4): Show | 7 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.71+1176G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45975508 | ||||||
| chr22:45975578
|
G | A | 1 | a0001c0001t0026g0340 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.71+1106C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45975578 | ||||||
| chr22:45975689
|
C | G | 1 | a0001c0001t0001g0152 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.71+995G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45975689 | ||||||
| chr22:45975702
|
C | T | 4 | a0001c0001t0065g0347a0001c0001t0066g0345a0001c0001t0067g0346others(1): Show | 4 | HG01433.hp2 HG01496.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.71+982G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45975702 | ||||||
| chr22:45975703
|
G | T | 1 | a0001c0001t0002g0008 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.71+981C>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45975703 | ||||||
| chr22:45975766
|
C | G | 1 | a0001c0001t0010g0007 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.71+918G>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45975766 | ||||||
| chr22:45975863
|
C | T | 1 | a0001c0001t0003g0006 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.71+821G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45975863 | ||||||
| chr22:45976039
|
G | C | 1 | a0001c0001t0001g0341 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.71+645C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45976039 | ||||||
| chr22:45976092
|
C | T | 3 | a0001c0001t0001g0150a0001c0001t0005g0149a0001c0001t0013g0151 | 3 | HG00733.hp1 HG01255.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.71+592G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45976092 | ||||||
| chr22:45976148
|
T | C | 1 | a0001c0004t0007g0342 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.71+536A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45976148 | ||||||
| chr22:45976343
|
A | G | 2 | a0001c0001t0001g0150a0001c0001t0005g0149 | 2 | HG00733.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.71+341T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45976343 | ||||||
| chr22:45976639
|
G | T | 1 | a0001c0001t0001g0148 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.71+45C>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45976639 | ||||||
| chr22:45976640
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.71+44G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45976640 |