Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MHRNF others(344): Show |
chr22 | 45915366 | 45982162 |
| a0002 | 0/0 | 349 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | MHRNF others(344): Show |
chr22 | 45915366 | 45982162 |
| a0003 | 0/0 | 146 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | MHRNF others(141): Show |
chr22 | 45915366 | 45982162 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1047 | 323 | 71 | 68 | 119 | 18 | 45 | WNT7B_chr22_45915366_45982162 | WNT7B | ATGCA others(1042): Show |
chr22 | 45915366 | 45982162 | ||
| a0001c0002 | 0/0 | 1047 | 9 | 8 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | ATGCA others(1042): Show |
chr22 | 45915366 | 45982162 | ||
| a0001c0003 | 0/0 | 1047 | 4 | 4 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | ATGCA others(1042): Show |
chr22 | 45915366 | 45982162 | ||
| a0001c0004 | 0/0 | 1047 | 2 | 2 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | ATGCA others(1042): Show |
chr22 | 45915366 | 45982162 | ||
| a0001c0005 | 0/0 | 1047 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | ATGCA others(1042): Show |
chr22 | 45915366 | 45982162 | ||
| a0001c0007 | 0/0 | 1047 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | ATGCA others(1042): Show |
chr22 | 45915366 | 45982162 | ||
| a0001c0008 | 0/0 | 1047 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | ATGCA others(1042): Show |
chr22 | 45915366 | 45982162 | ||
| a0001c0009 | 0/0 | 1047 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | ATGCA others(1042): Show |
chr22 | 45915366 | 45982162 | ||
| a0001c0010 | 0/0 | 1047 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | ATGCA others(1042): Show |
chr22 | 45915366 | 45982162 | ||
| a0001c0011 | 0/0 | 1047 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | ATGCA others(1042): Show |
chr22 | 45915366 | 45982162 | ||
| a0001c0012 | 0/0 | 1047 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | ATGCA others(1042): Show |
chr22 | 45915366 | 45982162 | ||
| a0001c0013 | 0/0 | 1047 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | ATGCA others(1042): Show |
chr22 | 45915366 | 45982162 | ||
| a0001c0014 | 0/0 | 1047 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | ATGCA others(1042): Show |
chr22 | 45915366 | 45982162 | ||
| a0001c0016 | 0/0 | 1047 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | ATGCA others(1042): Show |
chr22 | 45915366 | 45982162 | ||
| a0002c0015 | 0/0 | 1047 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | ATGCA others(1042): Show |
chr22 | 45915366 | 45982162 | ||
| a0003c0006 | 0/0 | 1047 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | ATGCA others(1042): Show |
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 | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0002 | 0/0 | 3948 | 80 | 1 | 10 | 57 | 5 | 7 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0003 | 0/0 | 3948 | 19 | 1 | 1 | 14 | 0 | 3 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0004 | 0/0 | 3948 | 16 | 0 | 5 | 3 | 0 | 8 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0005 | 0/1 | 3938 | 12 | 3 | 5 | 0 | 0 | 3 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3933): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0006 | 0/0 | 3938 | 11 | 2 | 8 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3933): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0007 | 0/0 | 3924 | 7 | 5 | 2 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3919): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0008 | 0/0 | 3948 | 5 | 0 | 0 | 4 | 1 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0009 | 0/0 | 3924 | 4 | 4 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3919): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0010 | 0/0 | 3948 | 4 | 0 | 1 | 0 | 1 | 2 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0011 | 0/0 | 3948 | 4 | 0 | 0 | 1 | 2 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0012 | 0/0 | 3948 | 4 | 4 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0013 | 0/0 | 3938 | 4 | 0 | 2 | 0 | 1 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3933): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0014 | 0/0 | 3948 | 3 | 3 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0015 | 0/0 | 3948 | 3 | 0 | 0 | 3 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0016 | 0/0 | 3948 | 3 | 0 | 0 | 3 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0017 | 0/0 | 3924 | 3 | 3 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3919): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0018 | 0/0 | 3948 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0019 | 0/0 | 3948 | 3 | 3 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0020 | 0/0 | 3948 | 2 | 2 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0022 | 0/0 | 3938 | 2 | 0 | 2 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3933): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0023 | 0/0 | 3924 | 2 | 2 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3919): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0024 | 0/0 | 3948 | 2 | 2 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0025 | 0/0 | 3948 | 2 | 2 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0026 | 0/0 | 3938 | 2 | 0 | 0 | 0 | 1 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3933): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0027 | 0/0 | 3938 | 2 | 1 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3933): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0028 | 0/0 | 3938 | 2 | 0 | 2 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3933): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0029 | 0/0 | 3948 | 2 | 2 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0031 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0032 | 0/0 | 3948 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0033 | 0/0 | 3948 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0035 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0036 | 0/0 | 3938 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3933): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0038 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0039 | 0/0 | 3938 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3933): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0041 | 0/0 | 3948 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0042 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0043 | 0/0 | 3948 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0044 | 0/0 | 3948 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0045 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0046 | 0/0 | 3948 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0047 | 0/0 | 3938 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3933): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0048 | 0/0 | 3948 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0049 | 0/0 | 3948 | 1 | 0 | 0 | 0 | 1 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0051 | 0/0 | 3938 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3933): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0055 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0056 | 0/0 | 3924 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3919): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0057 | 0/0 | 3948 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0058 | 0/0 | 3948 | 1 | 0 | 0 | 0 | 1 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0059 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0060 | 0/0 | 3936 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3931): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0061 | 0/0 | 3948 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0062 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0063 | 0/0 | 3948 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0065 | 0/0 | 3948 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0066 | 0/0 | 3924 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3919): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0067 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0001t0068 | 0/0 | 3948 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0002t0001 | 0/0 | 3948 | 2 | 2 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0002t0007 | 0/0 | 3924 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3919): Show |
chr22 | 45915366 | 45982162 |
| a0001c0002t0014 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0002t0018 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0002t0020 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0002t0030 | 0/0 | 3924 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3919): Show |
chr22 | 45915366 | 45982162 |
| a0001c0002t0037 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0002t0052 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0003t0021 | 0/0 | 3948 | 2 | 2 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0003t0040 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0003t0053 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0004t0007 | 0/0 | 3924 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3919): Show |
chr22 | 45915366 | 45982162 |
| a0001c0004t0034 | 0/0 | 3924 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3919): Show |
chr22 | 45915366 | 45982162 |
| a0001c0005t0001 | 0/0 | 3948 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0007t0054 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0008t0002 | 0/0 | 3948 | 1 | 0 | 0 | 0 | 0 | 1 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0009t0002 | 0/0 | 3948 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0010t0002 | 0/0 | 3948 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0011t0050 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0012t0001 | 0/0 | 3948 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0013t0021 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0014t0018 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| a0001c0016t0007 | 0/0 | 3924 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3919): Show |
chr22 | 45915366 | 45982162 |
| a0002c0015t0009 | 0/0 | 3924 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3919): Show |
chr22 | 45915366 | 45982162 |
| a0003c0006t0064 | 0/0 | 3948 | 1 | 1 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | GAGTC others(3943): Show |
chr22 | 45915366 | 45982162 |
| actghapid | grch38/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 |
| a0001c0001t0001g0200 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0202 | 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 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0275 | 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 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0001g0300 | 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 |
| a0001c0001t0004g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0004g0205 | 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 |
| a0001c0001t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0004g0301 | 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 |
| a0001c0001t0005g0203 | 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 |
| a0001c0001t0005g0294 | 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 |
| a0001c0001t0028g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| a0001c0001t0028g0299 | 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 |
| a0001c0001t0049g0235 | 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 |
| a0001c0001t0057g0297 | 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 |
| a0001c0011t0050g0330 | 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 | g0276 | 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 | g0204 | 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 | g0295 | 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 | g0297 | 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 | g0301 | 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 | g0298 | AMR | CLM | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| HG01258 | hp1 | a0001 | c0001 | t0028 | g0299 | 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 | t0049 | 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 | t0050 | 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 | g0300 | 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 | g0202 | 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 | g0203 | 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 | g0205 | 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 | g0201 | 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 | g0206 | 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 | g0296 | 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 | g0207 | 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 | g0275 | 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 | a0001 | c0001 | t0005 | g0294 | REF | REF | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0200 | REF | REF | WNT7B_chr22_45915366_45982162 | WNT7B | chr22 | 45915366 | 45982162 |
| view | 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 |
| view | 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 | a0001c0003 a0001c0013 |
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 | a0001c0002 a0001c0013 a0001c0014 others(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 |
| view | 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 | a0001c0001t0048 a0001c0001t0059 a0001c0002t0052 |
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 | a0001c0001t0010 a0001c0001t0011 a0001c0001t0049 |
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 | a0001c0001t0020 a0001c0002t0020 |
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 | a0001c0001t0010 a0001c0001t0011 a0001c0001t0049 others(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 | a0001c0001t0007 a0001c0001t0009 a0001c0001t0017 others(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 | a0001c0001t0010 a0001c0001t0011 a0001c0001t0049 |
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 | a0001c0001t0010 a0001c0001t0011 a0001c0001t0049 |
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 | a0001c0001t0010 a0001c0001t0011 a0001c0001t0049 |
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 | a0001c0001t0010 a0001c0001t0011 a0001c0001t0049 |
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 | a0001c0001t0010 a0001c0001t0011 a0001c0001t0049 |
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 | a0001c0001t0010 a0001c0001t0011 a0001c0001t0049 |
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 | a0001c0011t0050 | 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 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0013 others(8): Show |
38 | HG00733.hp2 HG00735.hp1 HG01069.hp1 others(35): 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 | a0001c0001t0010 a0001c0001t0011 a0001c0001t0049 |
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 | a0001c0001t0010 a0001c0001t0011 a0001c0001t0049 |
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 | a0001c0001t0010 a0001c0001t0011 a0001c0001t0039 others(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 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0015 others(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 | a0001c0001t0018 a0001c0001t0042 a0001c0001t0048 others(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 | a0001c0001t0031 a0001c0001t0038 a0001c0001t0062 |
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 | a0001c0001t0012 a0001c0001t0025 a0001c0001t0035 others(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 | a0001c0001t0031 a0001c0001t0038 |
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 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0008 others(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 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0008 others(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 | a0001c0001t0019 a0001c0001t0020 a0001c0002t0020 |
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 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(55): Show |
154 | HG00280.hp2 HG00323.hp1 HG00621.hp1 others(151): 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 | a0001c0001t0013 a0001c0001t0017 a0001c0001t0022 others(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 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 others(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 | a0001c0001t0039 a0001c0001t0051 |
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 | a0001c0001t0019 a0001c0001t0020 a0001c0002t0020 |
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 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(55): Show |
154 | HG00280.hp2 HG00323.hp1 HG00621.hp1 others(151): 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 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0008 others(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 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 others(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 | a0001c0003t0021 a0001c0003t0040 a0001c0003t0053 others(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 | a0001c0001t0010 a0001c0001t0011 a0001c0001t0015 |
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 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(57): Show |
157 | HG00280.hp2 HG00323.hp1 HG00621.hp1 others(154): 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 | a0001c0001t0042 a0001c0001t0068 |
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 | a0001c0001t0007 a0001c0002t0007 a0001c0002t0030 others(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 | a0001c0001t0063 a0003c0006t0064 |
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 | a0001c0001t0065 a0001c0001t0066 a0001c0001t0067 others(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 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(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 | a0001c0001t0031 a0001c0002t0030 |
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 |
| view | 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 | a0001c0001t0007g0161 a0001c0001t0007g0162 a0001c0001t0007g0252 others(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 | a0001c0001t0014g0254 a0001c0001t0014g0313 a0001c0001t0063g0344 |
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 | a0001c0001t0007g0161 a0001c0001t0007g0162 a0001c0001t0007g0252 others(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 | a0001c0001t0039g0074 a0001c0001t0051g0307 |
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 | a0001c0001t0009g0268 a0001c0001t0031g0004 a0001c0001t0038g0009 others(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 | 136 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0040 others(133): Show |
136 | HG00621.hp1 HG00639.hp1 HG00642.hp1 others(133): 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 | a0001c0001t0009g0268 a0001c0001t0031g0004 a0001c0001t0038g0009 others(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 | a0001c0001t0009g0268 a0001c0001t0031g0004 a0001c0001t0038g0009 others(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 | a0001c0001t0009g0268 a0001c0001t0019g0244 a0001c0001t0019g0290 others(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 | a0001c0001t0020g0158 a0001c0001t0020g0225 a0001c0002t0020g0336 |
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 | 143 | a0001c0001t0001g0212 a0001c0001t0001g0214 a0001c0001t0001g0306 others(140): Show |
143 | HG00621.hp1 HG00639.hp1 HG00642.hp1 others(140): 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 | a0001c0001t0001g0214 a0001c0001t0003g0006 a0001c0001t0003g0019 others(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 | a0001c0001t0001g0150 a0001c0001t0057g0297 |
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 | a0001c0001t0042g0013 a0001c0001t0068g0348 |
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 | a0001c0001t0001g0214 a0001c0001t0003g0006 a0001c0001t0003g0019 others(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 | a0001c0001t0001g0284 a0001c0001t0010g0007 a0001c0001t0010g0029 others(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 | a0001c0001t0010g0007 a0001c0001t0010g0029 a0001c0001t0010g0063 others(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 | a0001c0001t0001g0214 a0001c0001t0003g0006 a0001c0001t0003g0019 others(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 | a0001c0001t0009g0268 a0001c0001t0031g0004 a0001c0001t0038g0009 others(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 | a0001c0001t0009g0268 a0001c0001t0031g0004 a0001c0001t0038g0009 others(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 | a0001c0001t0001g0214 a0001c0001t0003g0006 a0001c0001t0003g0019 others(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 | a0001c0001t0001g0214 a0001c0001t0003g0006 a0001c0001t0003g0019 others(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 | a0001c0001t0039g0074 a0001c0001t0051g0307 |
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 | 163 | a0001c0001t0001g0212 a0001c0001t0001g0214 a0001c0001t0001g0284 others(160): Show |
163 | HG00280.hp2 HG00323.hp1 HG00621.hp1 others(160): 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 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0167 others(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 | 163 | a0001c0001t0001g0212 a0001c0001t0001g0214 a0001c0001t0001g0284 others(160): Show |
163 | HG00280.hp2 HG00323.hp1 HG00621.hp1 others(160): 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 | a0001c0001t0002g0028 a0001c0001t0060g0316 |
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 | a0001c0001t0007g0321 a0001c0002t0030g0003 a0001c0016t0007g0280 |
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 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0167 others(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 | a0001c0001t0001g0300 a0001c0001t0001g0303 a0001c0001t0001g0305 others(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 | a0001c0001t0001g0214 a0001c0001t0003g0006 a0001c0001t0003g0019 others(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 | a0001c0001t0001g0214 a0001c0001t0003g0006 a0001c0001t0003g0019 others(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 | a0001c0001t0018g0327 a0001c0001t0042g0013 a0001c0001t0048g0326 others(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 | a0001c0001t0001g0214 a0001c0001t0003g0006 a0001c0001t0003g0019 others(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 | a0001c0001t0001g0214 a0001c0001t0003g0006 a0001c0001t0003g0019 others(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 | a0001c0001t0005g0288 a0001c0001t0006g0120 |
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 | a0001c0001t0005g0149 a0001c0001t0005g0180 a0001c0001t0005g0203 others(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 | a0001c0001t0001g0212 a0001c0001t0001g0306 a0001c0001t0002g0102 others(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 | a0001c0001t0001g0174 a0001c0001t0002g0048 a0001c0001t0002g0066 |
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 | a0001c0001t0001g0214 a0001c0001t0003g0006 a0001c0001t0003g0019 others(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 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0292 |
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 | a0001c0001t0005g0149 a0001c0001t0005g0180 a0001c0001t0005g0203 others(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 | a0001c0001t0029g0240 a0001c0001t0029g0319 a0001c0001t0059g0156 |
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 | a0001c0001t0018g0327 a0001c0001t0042g0013 a0001c0001t0048g0326 others(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 | a0001c0001t0018g0327 a0001c0001t0042g0013 a0001c0001t0048g0326 others(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 | a0001c0011t0050g0330 | 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 | a0001c0001t0001g0181 a0001c0001t0001g0206 a0001c0001t0001g0207 others(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 | a0001c0001t0005g0149 a0001c0001t0005g0180 a0001c0001t0005g0203 others(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 | a0001c0001t0001g0214 a0001c0001t0002g0138 a0001c0001t0003g0006 others(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 | a0001c0001t0001g0172 a0001c0001t0002g0069 a0001c0001t0004g0171 others(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 | a0001c0001t0014g0324 a0001c0001t0024g0099 |
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 | 28 | a0001c0001t0001g0212 a0001c0001t0001g0306 a0001c0001t0002g0102 others(25): Show |
28 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(25): 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 | a0001c0001t0001g0217 a0001c0001t0001g0234 a0001c0001t0002g0112 |
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 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0292 others(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 | a0001c0001t0014g0324 a0001c0001t0024g0099 a0001c0002t0014g0274 |
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 | a0001c0001t0014g0324 a0001c0001t0024g0099 a0001c0002t0014g0274 |
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 | a0001c0001t0005g0149 a0001c0001t0005g0180 a0001c0001t0005g0203 others(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 | a0001c0001t0005g0149 a0001c0001t0005g0180 a0001c0001t0005g0203 others(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 | a0001c0001t0018g0327 a0001c0001t0042g0013 a0001c0001t0048g0326 others(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 | a0001c0001t0001g0214 a0001c0001t0002g0138 a0001c0001t0003g0006 others(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 | a0001c0001t0001g0216 a0001c0001t0001g0242 a0001c0001t0001g0243 others(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 | a0001c0001t0001g0188 a0001c0001t0001g0238 a0001c0001t0001g0271 others(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 | a0001c0001t0005g0149 a0001c0001t0005g0180 a0001c0001t0005g0203 others(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 | a0001c0001t0010g0007 a0001c0001t0010g0029 a0001c0001t0010g0063 others(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 | a0001c0001t0001g0263 a0001c0001t0045g0258 |
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 | a0001c0001t0001g0167 a0001c0001t0001g0175 a0001c0001t0001g0214 others(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 | a0001c0001t0042g0013 a0001c0001t0068g0348 |
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 | a0001c0003t0021g0229 a0001c0003t0021g0311 a0001c0003t0040g0046 others(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 | 21 | a0001c0001t0005g0249 a0001c0001t0006g0073 a0001c0001t0013g0151 others(18): Show |
21 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(18): 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 | a0001c0001t0001g0167 a0001c0001t0001g0175 a0001c0001t0001g0188 others(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 | 98 | a0001c0001t0001g0167 a0001c0001t0001g0175 a0001c0001t0001g0212 others(95): Show |
98 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(95): 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 |
23 | a0001c0001t0001g0212 a0001c0001t0001g0306 a0001c0001t0002g0102 others(20): Show |
23 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(20): 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 | a0001c0001t0001g0167 a0001c0001t0001g0175 a0001c0001t0001g0188 others(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 | a0001c0001t0001g0188 a0001c0001t0001g0238 a0001c0001t0001g0271 others(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 | a0001c0001t0008g0039 a0001c0001t0008g0142 |
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 | 142 | a0001c0001t0001g0167 a0001c0001t0001g0175 a0001c0001t0001g0188 others(139): Show |
143 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(140): 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 | a0001c0001t0019g0244 a0001c0001t0019g0290 a0001c0001t0019g0332 others(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 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0292 others(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 | a0001c0001t0001g0265 a0001c0001t0005g0149 a0001c0001t0005g0180 others(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 | 99 | a0001c0001t0001g0167 a0001c0001t0001g0175 a0001c0001t0001g0212 others(96): Show |
99 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(96): 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 | a0001c0001t0001g0188 a0001c0001t0001g0238 a0001c0001t0001g0271 others(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 | a0001c0001t0001g0188 a0001c0001t0001g0238 a0001c0001t0001g0271 others(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 | 99 | a0001c0001t0001g0167 a0001c0001t0001g0175 a0001c0001t0001g0212 others(96): Show |
99 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.570+2231C>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45928867 | |||||||
| chr22:45928868 | A | G | 99 | a0001c0001t0001g0167 a0001c0001t0001g0175 a0001c0001t0001g0212 others(96): Show |
99 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(96): 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 | a0001c0001t0001g0188 a0001c0001t0001g0238 a0001c0001t0001g0271 others(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 | 18 | a0001c0001t0001g0212 a0001c0001t0001g0306 a0001c0001t0002g0102 others(15): Show |
18 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(15): 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 | a0001c0001t0018g0327 a0001c0001t0048g0326 a0001c0002t0052g0338 |
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 | 154 | a0001c0001t0001g0167 a0001c0001t0001g0175 a0001c0001t0001g0188 others(151): Show |
155 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(152): 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 | a0001c0001t0019g0244 a0001c0001t0019g0290 a0001c0001t0019g0332 others(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 | a0001c0001t0004g0301 | 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 | a0001c0001t0001g0271 a0001c0001t0001g0281 a0001c0001t0002g0083 others(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 | a0001c0001t0018g0327 a0001c0001t0042g0013 a0001c0001t0048g0326 others(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 | a0001c0001t0018g0327 a0001c0001t0042g0013 a0001c0001t0048g0326 others(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 | a0001c0001t0019g0244 a0001c0001t0019g0290 a0001c0001t0019g0332 others(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 | 3 | a0001c0001t0005g0249 a0001c0001t0006g0073 a0001c0001t0027g0256 |
3 | HG01099.hp1 HG01358.hp2 HG02109.hp1 |
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 | a0001c0001t0012g0159 a0001c0001t0012g0259 a0001c0001t0012g0329 others(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 | a0001c0001t0005g0149 a0001c0001t0005g0180 a0001c0001t0005g0203 others(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 | a0001c0001t0001g0167 a0001c0001t0001g0175 a0001c0001t0001g0188 others(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 | 31 | a0001c0001t0001g0212 a0001c0001t0001g0284 a0001c0001t0001g0306 others(28): Show |
31 | HG00280.hp2 HG00323.hp1 HG00733.hp2 others(28): Show |
intron_variant | MODIFIER | c.570+1617A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929481 | |||||||
| chr22:45929482 | G | A | 31 | a0001c0001t0001g0212 a0001c0001t0001g0284 a0001c0001t0001g0306 others(28): Show |
31 | HG00280.hp2 HG00323.hp1 HG00733.hp2 others(28): Show |
intron_variant | MODIFIER | c.570+1616C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929482 | |||||||
| chr22:45929483 | T | C | 31 | a0001c0001t0001g0212 a0001c0001t0001g0284 a0001c0001t0001g0306 others(28): Show |
31 | HG00280.hp2 HG00323.hp1 HG00733.hp2 others(28): Show |
intron_variant | MODIFIER | c.570+1615A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929483 | |||||||
| chr22:45929484 | A | C | 31 | a0001c0001t0001g0212 a0001c0001t0001g0284 a0001c0001t0001g0306 others(28): Show |
31 | HG00280.hp2 HG00323.hp1 HG00733.hp2 others(28): 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 | a0001c0001t0001g0300 a0001c0001t0001g0303 a0001c0001t0001g0305 others(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 | 31 | a0001c0001t0001g0212 a0001c0001t0001g0284 a0001c0001t0001g0306 others(28): Show |
31 | HG00280.hp2 HG00323.hp1 HG00733.hp2 others(28): 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 | a0001c0001t0001g0188 a0001c0001t0001g0238 a0001c0001t0001g0271 others(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 | 31 | a0001c0001t0001g0212 a0001c0001t0001g0284 a0001c0001t0001g0306 others(28): Show |
31 | HG00280.hp2 HG00323.hp1 HG00733.hp2 others(28): 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 | a0001c0001t0029g0240 a0001c0001t0029g0319 a0001c0001t0059g0156 others(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 | a0001c0001t0042g0013 a0001c0001t0068g0348 |
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 | a0001c0001t0009g0268 a0001c0001t0031g0004 a0001c0001t0038g0009 others(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 | a0001c0001t0019g0244 a0001c0001t0019g0290 a0001c0001t0019g0332 others(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 | a0001c0001t0005g0149 a0001c0001t0005g0180 a0001c0001t0005g0203 others(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 | 19 | a0001c0001t0001g0212 a0001c0001t0001g0306 a0001c0001t0002g0102 others(16): Show |
19 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(16): 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 | a0001c0001t0001g0188 a0001c0001t0001g0238 a0001c0001t0001g0271 others(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 | a0001c0001t0019g0244 a0001c0001t0019g0290 a0001c0001t0019g0332 others(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 | a0001c0001t0019g0244 a0001c0001t0019g0290 a0001c0001t0019g0332 others(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 | a0001c0001t0001g0188 a0001c0001t0001g0238 a0001c0001t0001g0271 others(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 | a0001c0001t0001g0188 a0001c0001t0001g0238 a0001c0001t0001g0271 others(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 | 25 | a0001c0001t0001g0212 a0001c0001t0001g0306 a0001c0001t0002g0102 others(22): Show |
25 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(22): 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 | a0001c0001t0019g0290 a0001c0001t0019g0332 |
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 | a0001c0001t0019g0244 a0001c0001t0019g0290 a0001c0001t0019g0332 others(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 | a0001c0001t0001g0188 a0001c0001t0001g0238 a0001c0001t0001g0271 others(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 | 61 | a0001c0001t0001g0188 a0001c0001t0001g0212 a0001c0001t0001g0238 others(58): Show |
62 | HG00280.hp2 HG00323.hp1 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.570+1454A>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929644 | |||||||
| chr22:45929646 | A | G | 19 | a0001c0001t0001g0212 a0001c0001t0001g0306 a0001c0001t0002g0102 others(16): Show |
19 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.570+1452T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929646 | |||||||
| chr22:45929647 | T | C | 55 | a0001c0001t0001g0188 a0001c0001t0001g0212 a0001c0001t0001g0238 others(52): Show |
56 | HG00280.hp2 HG00323.hp1 HG00733.hp2 others(53): 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 | a0001c0001t0019g0244 a0001c0001t0019g0290 a0001c0001t0019g0332 others(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 | a0001c0001t0001g0188 a0001c0001t0001g0238 a0001c0001t0001g0271 others(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 | a0001c0001t0014g0324 a0001c0001t0024g0099 a0001c0002t0014g0274 others(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 | a0001c0001t0019g0244 a0001c0001t0019g0290 a0001c0001t0019g0332 others(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 | 19 | a0001c0001t0001g0212 a0001c0001t0001g0306 a0001c0001t0002g0102 others(16): Show |
19 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.570+1440T>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929658 | |||||||
| chr22:45929659 | C | T | 23 | a0001c0001t0001g0212 a0001c0001t0001g0306 a0001c0001t0002g0102 others(20): Show |
23 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(20): 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 | a0001c0001t0019g0244 a0001c0001t0019g0290 a0001c0001t0019g0332 others(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 | a0001c0001t0014g0324 a0001c0001t0024g0099 a0001c0002t0014g0274 others(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 | 19 | a0001c0001t0001g0212 a0001c0001t0001g0306 a0001c0001t0002g0102 others(16): Show |
19 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.570+1435G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929663 | |||||||
| chr22:45929664 | C | A | 19 | a0001c0001t0001g0212 a0001c0001t0001g0306 a0001c0001t0002g0102 others(16): Show |
19 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.570+1434G>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929664 | |||||||
| chr22:45929666 | G | T | 25 | a0001c0001t0001g0212 a0001c0001t0001g0306 a0001c0001t0002g0102 others(22): Show |
25 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.570+1432C>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929666 | |||||||
| chr22:45929667 | C | T | 23 | a0001c0001t0001g0212 a0001c0001t0001g0306 a0001c0001t0002g0102 others(20): Show |
23 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(20): 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 | a0001c0001t0019g0244 a0001c0001t0019g0290 a0001c0001t0019g0332 others(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 | a0001c0001t0014g0324 a0001c0001t0019g0244 a0001c0001t0019g0290 others(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 | 19 | a0001c0001t0001g0212 a0001c0001t0001g0306 a0001c0001t0002g0102 others(16): Show |
19 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.570+1424A>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929674 | |||||||
| chr22:45929675 | T | C | 19 | a0001c0001t0001g0212 a0001c0001t0001g0306 a0001c0001t0002g0102 others(16): Show |
19 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(16): 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 | a0001c0001t0014g0324 a0001c0001t0024g0099 a0001c0002t0014g0274 others(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 | 25 | a0001c0001t0001g0212 a0001c0001t0001g0306 a0001c0001t0002g0102 others(22): Show |
25 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.570+1420G>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929678 | |||||||
| chr22:45929682 | A | C | 19 | a0001c0001t0001g0212 a0001c0001t0001g0306 a0001c0001t0002g0102 others(16): Show |
19 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.570+1416T>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929682 | |||||||
| chr22:45929683 | T | A | 19 | a0001c0001t0001g0212 a0001c0001t0001g0306 a0001c0001t0002g0102 others(16): Show |
19 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(16): 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 | a0001c0001t0019g0244 a0001c0001t0019g0290 a0001c0001t0019g0332 others(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 | a0001c0001t0001g0188 a0001c0001t0001g0238 a0001c0001t0001g0271 others(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 | a0001c0001t0019g0244 a0001c0001t0019g0290 a0001c0001t0019g0332 others(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 | 19 | a0001c0001t0001g0212 a0001c0001t0001g0306 a0001c0001t0002g0102 others(16): Show |
19 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.570+1414T>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929684 | |||||||
| chr22:45929685 | C | T | 55 | a0001c0001t0001g0188 a0001c0001t0001g0212 a0001c0001t0001g0238 others(52): Show |
56 | HG00280.hp2 HG00323.hp1 HG00733.hp2 others(53): 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 | a0001c0001t0019g0244 a0001c0001t0019g0290 a0001c0001t0019g0332 others(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 | a0001c0001t0019g0244 a0001c0001t0019g0290 a0001c0001t0019g0332 others(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 | a0001c0001t0019g0244 a0001c0001t0019g0290 a0001c0001t0019g0332 others(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 | a0001c0001t0003g0006 a0001c0001t0005g0149 a0001c0001t0005g0180 others(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 | a0001c0001t0001g0167 a0001c0001t0001g0175 a0001c0001t0001g0214 others(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 | a0001c0001t0004g0173 a0001c0001t0004g0205 a0001c0001t0004g0221 others(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 | 55 | a0001c0001t0001g0188 a0001c0001t0001g0212 a0001c0001t0001g0238 others(52): Show |
56 | HG00280.hp2 HG00323.hp1 HG00733.hp2 others(53): 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 | a0001c0001t0019g0244 a0001c0001t0019g0290 a0001c0001t0019g0332 others(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 | a0001c0001t0019g0244 a0001c0001t0019g0290 a0001c0001t0019g0332 others(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 | a0001c0001t0019g0244 a0001c0001t0019g0290 a0001c0001t0019g0332 others(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 | a0001c0001t0014g0254 a0001c0001t0014g0313 a0001c0001t0063g0344 |
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 | a0001c0001t0019g0244 a0001c0001t0019g0290 a0001c0001t0019g0332 others(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 | a0001c0001t0019g0244 a0001c0001t0019g0290 a0001c0001t0019g0332 others(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 | a0001c0001t0009g0268 a0002c0015t0009g0228 |
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 | a0001c0001t0019g0244 a0001c0001t0019g0290 a0001c0001t0019g0332 others(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 | a0001c0001t0019g0244 a0001c0001t0019g0290 a0001c0001t0019g0332 others(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 | a0001c0001t0019g0244 a0001c0001t0019g0290 a0001c0001t0019g0332 others(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 | a0001c0001t0019g0244 a0001c0001t0019g0290 a0001c0001t0019g0332 others(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 | a0001c0001t0019g0244 a0001c0001t0019g0290 a0001c0001t0019g0332 others(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 | a0001c0001t0019g0244 a0001c0001t0019g0290 a0001c0001t0019g0332 others(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 | a0001c0001t0001g0188 a0001c0001t0001g0238 a0001c0001t0001g0271 others(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 | a0001c0001t0002g0085 a0001c0001t0002g0146 |
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 | a0001c0001t0014g0313 a0001c0001t0063g0344 |
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 | a0001c0001t0001g0167 a0001c0001t0001g0175 a0001c0001t0001g0188 others(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 |
18 | a0001c0001t0001g0212 a0001c0001t0001g0306 a0001c0001t0002g0102 others(15): Show |
18 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(15): 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 | a0001c0001t0019g0244 a0001c0001t0019g0290 a0001c0001t0019g0332 others(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 | a0001c0001t0019g0244 a0001c0001t0019g0290 a0001c0001t0019g0332 others(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 | a0001c0001t0019g0244 a0001c0001t0019g0290 a0001c0001t0019g0332 others(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 |
140 | a0001c0001t0001g0167 a0001c0001t0001g0175 a0001c0001t0001g0188 others(137): Show |
141 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(138): 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 | a0001c0001t0019g0244 a0001c0001t0019g0290 a0001c0001t0019g0332 others(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 | a0001c0001t0009g0268 a0001c0001t0031g0004 a0001c0001t0038g0009 others(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 | a0001c0001t0001g0188 a0001c0001t0001g0238 a0001c0001t0001g0271 others(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 |
52 | a0001c0001t0001g0188 a0001c0001t0001g0212 a0001c0001t0001g0238 others(49): Show |
53 | HG00280.hp2 HG00323.hp1 HG00733.hp2 others(50): 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 | 52 | a0001c0001t0001g0188 a0001c0001t0001g0212 a0001c0001t0001g0238 others(49): Show |
53 | HG00280.hp2 HG00323.hp1 HG00733.hp2 others(50): 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 |
52 | a0001c0001t0001g0188 a0001c0001t0001g0212 a0001c0001t0001g0238 others(49): Show |
53 | HG00280.hp2 HG00323.hp1 HG00733.hp2 others(50): 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 | 52 | a0001c0001t0001g0188 a0001c0001t0001g0212 a0001c0001t0001g0238 others(49): Show |
53 | HG00280.hp2 HG00323.hp1 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.570+1156A>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45929942 | |||||||
| chr22:45929943 | T | C | 53 | a0001c0001t0001g0188 a0001c0001t0001g0212 a0001c0001t0001g0238 others(50): Show |
54 | HG00280.hp2 HG00323.hp1 HG00733.hp2 others(51): 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 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0167 others(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 | 53 | a0001c0001t0001g0188 a0001c0001t0001g0212 a0001c0001t0001g0238 others(50): Show |
54 | HG00280.hp2 HG00323.hp1 HG00733.hp2 others(51): 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 | a0001c0001t0019g0244 a0001c0001t0019g0332 a0001c0001t0020g0158 others(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 | a0001c0001t0019g0244 a0001c0001t0019g0332 a0001c0001t0020g0158 others(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 | a0001c0001t0019g0244 a0001c0001t0019g0332 a0001c0001t0020g0158 others(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 | a0001c0001t0005g0149 a0001c0001t0005g0180 a0001c0001t0005g0203 others(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 | a0001c0001t0019g0244 a0001c0001t0019g0332 a0001c0001t0020g0158 others(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 | a0001c0001t0019g0244 a0001c0001t0019g0332 a0001c0001t0020g0158 others(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 | a0001c0001t0019g0244 a0001c0001t0019g0290 a0001c0001t0019g0332 others(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 | a0001c0001t0004g0201 | 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 | a0001c0001t0003g0068 a0001c0001t0004g0201 a0001c0001t0004g0301 |
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 | a0001c0001t0001g0271 a0001c0001t0001g0281 a0001c0001t0002g0083 others(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 | a0001c0001t0001g0188 a0001c0001t0001g0238 a0001c0001t0001g0271 others(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 | 142 | a0001c0001t0001g0167 a0001c0001t0001g0175 a0001c0001t0001g0188 others(139): Show |
143 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.570+961T>C | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45930137 | |||||||
| chr22:45930139 | C | A | 54 | a0001c0001t0001g0188 a0001c0001t0001g0212 a0001c0001t0001g0238 others(51): Show |
55 | HG00280.hp2 HG00323.hp1 HG00733.hp2 others(52): 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 | a0001c0001t0001g0207 | 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 | a0001c0001t0006g0107 a0001c0001t0006g0109 |
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 | a0001c0001t0001g0231 a0001c0001t0002g0041 |
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 | a0001c0001t0001g0167 a0001c0001t0001g0175 a0001c0001t0001g0214 others(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 | a0001c0001t0005g0149 a0001c0001t0005g0180 a0001c0001t0005g0203 others(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 | 54 | a0001c0001t0001g0188 a0001c0001t0001g0212 a0001c0001t0001g0238 others(51): Show |
55 | HG00280.hp2 HG00323.hp1 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.570+858C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45930240 | |||||||
| chr22:45930255 | G | T | 55 | a0001c0001t0001g0188 a0001c0001t0001g0212 a0001c0001t0001g0238 others(52): Show |
56 | HG00280.hp2 HG00323.hp1 HG00733.hp2 others(53): 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 | a0001c0001t0001g0208 a0001c0001t0002g0137 |
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 | a0001c0001t0005g0149 a0001c0001t0005g0180 a0001c0001t0005g0203 others(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 | a0001c0001t0009g0268 a0001c0001t0031g0004 a0001c0001t0038g0009 others(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 | a0001c0001t0002g0022 a0001c0001t0008g0142 a0001c0001t0019g0244 others(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 | 142 | a0001c0001t0001g0167 a0001c0001t0001g0175 a0001c0001t0001g0188 others(139): Show |
143 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(140): 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 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0182 others(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 | a0001c0001t0005g0149 a0001c0001t0005g0180 a0001c0001t0005g0203 others(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 | a0001c0001t0017g0247 a0001c0001t0017g0248 |
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 | 269 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0167 others(266): Show |
270 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(267): 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 | a0001c0001t0001g0241 a0001c0001t0001g0245 a0001c0001t0001g0246 others(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 | a0001c0001t0005g0149 a0001c0001t0005g0180 a0001c0001t0005g0203 others(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 | a0001c0001t0001g0269 a0001c0001t0001g0270 |
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 | a0001c0001t0007g0161 a0001c0001t0007g0162 |
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 | 103 | a0001c0001t0001g0167 a0001c0001t0001g0175 a0001c0001t0001g0188 others(100): Show |
104 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.570+387C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45930711 | |||||||
| chr22:45930730 | G | T | 154 | a0001c0001t0001g0167 a0001c0001t0001g0175 a0001c0001t0001g0188 others(151): Show |
155 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.570+368C>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 3/3 | chr22 | 45930730 | |||||||
| chr22:45930740 | G | A | 106 | a0001c0001t0001g0167 a0001c0001t0001g0175 a0001c0001t0001g0188 others(103): Show |
107 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(104): 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 | a0001c0001t0005g0149 a0001c0001t0005g0180 a0001c0001t0005g0203 others(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 | 142 | a0001c0001t0001g0167 a0001c0001t0001g0175 a0001c0001t0001g0188 others(139): Show |
143 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(140): 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 | a0001c0001t0004g0301 | 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 | a0001c0001t0001g0188 a0001c0001t0001g0238 a0001c0001t0001g0271 others(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 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0292 others(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 | a0001c0001t0001g0175 a0001c0001t0003g0006 a0001c0001t0003g0139 others(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 | a0001c0001t0010g0007 a0001c0001t0010g0029 a0001c0001t0010g0063 others(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 | a0001c0001t0001g0167 a0001c0001t0001g0175 a0001c0001t0002g0138 others(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 | a0001c0001t0001g0271 a0001c0001t0001g0281 a0001c0001t0002g0083 others(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 | a0001c0001t0014g0313 a0001c0001t0063g0344 |
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 | a0001c0001t0014g0313 a0001c0001t0063g0344 |
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 | a0001c0001t0001g0174 a0001c0001t0002g0048 a0001c0001t0002g0066 |
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 | a0001c0001t0001g0220 a0001c0001t0001g0265 a0001c0001t0044g0147 |
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 | 102 | a0001c0001t0001g0167 a0001c0001t0001g0175 a0001c0001t0001g0188 others(99): Show |
103 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(100): 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 | a0001c0001t0001g0306 a0001c0001t0003g0139 a0001c0001t0004g0169 others(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 | a0001c0001t0014g0313 a0001c0001t0063g0344 |
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 | 59 | a0001c0001t0001g0188 a0001c0001t0001g0238 a0001c0001t0001g0271 others(56): Show |
60 | HG01069.hp1 HG01099.hp1 HG01255.hp1 others(57): 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 | a0001c0001t0031g0004 a0001c0001t0038g0009 |
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 | a0001c0001t0042g0013 a0001c0001t0048g0326 a0001c0001t0065g0347 others(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 | a0001c0001t0001g0188 a0001c0001t0001g0238 a0001c0001t0001g0271 others(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 | a0001c0002t0018g0157 a0001c0011t0050g0330 |
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 | 57 | a0001c0001t0001g0167 a0001c0001t0001g0175 a0001c0001t0001g0212 others(54): Show |
57 | HG00544.hp2 HG00639.hp1 HG00642.hp2 others(54): 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 | a0001c0001t0001g0275 a0001c0009t0002g0067 |
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 | a0001c0001t0001g0148 a0001c0001t0002g0008 a0001c0001t0002g0023 others(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 | 2 | a0001c0001t0006g0073 a0001c0001t0027g0256 |
2 | HG01099.hp1 HG02109.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 | a0001c0002t0018g0157 a0001c0011t0050g0330 |
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 | a0001c0001t0001g0306 a0001c0001t0005g0149 a0001c0001t0005g0180 others(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 | a0001c0001t0042g0013 a0001c0001t0068g0348 |
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 | a0001c0001t0003g0068 a0001c0001t0004g0201 a0001c0001t0004g0301 |
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 | 133 | a0001c0001t0001g0167 a0001c0001t0001g0175 a0001c0001t0001g0188 others(130): Show |
134 | HG00280.hp2 HG00323.hp1 HG00544.hp2 others(131): 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 | a0001c0001t0014g0313 a0001c0001t0063g0344 |
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 | a0001c0001t0007g0321 a0001c0002t0030g0003 |
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 | a0001c0002t0018g0157 a0001c0011t0050g0330 |
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 | a0001c0001t0002g0021 a0001c0001t0002g0037 a0001c0001t0002g0049 others(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 | a0001c0001t0009g0268 a0001c0001t0062g0339 |
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 | 128 | a0001c0001t0001g0167 a0001c0001t0001g0175 a0001c0001t0001g0188 others(125): Show |
129 | HG00280.hp2 HG00323.hp1 HG00544.hp2 others(126): 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 | a0001c0001t0018g0327 a0001c0001t0048g0326 |
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 | a0001c0002t0018g0157 a0001c0011t0050g0330 |
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 | a0001c0003t0021g0229 a0001c0003t0021g0311 a0001c0003t0040g0046 others(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 | a0001c0001t0014g0313 a0001c0001t0063g0344 |
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 | a0001c0001t0019g0244 a0001c0001t0019g0290 a0001c0001t0019g0332 others(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 | a0001c0001t0001g0241 a0001c0001t0001g0269 a0001c0001t0009g0268 others(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 | a0001c0001t0001g0325 a0001c0001t0020g0225 a0001c0002t0014g0274 others(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 | 144 | a0001c0001t0001g0167 a0001c0001t0001g0175 a0001c0001t0001g0188 others(141): Show |
145 | HG00280.hp2 HG00323.hp1 HG00544.hp2 others(142): 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 | a0001c0002t0018g0157 a0001c0011t0050g0330 a0001c0016t0007g0280 others(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 | a0001c0001t0001g0241 a0001c0001t0009g0268 a0001c0001t0019g0290 others(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 | a0001c0001t0001g0308 a0001c0001t0001g0309 |
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 | a0001c0001t0019g0244 a0001c0007t0054g0334 |
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 | a0001c0001t0014g0313 a0001c0001t0063g0344 |
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 | a0001c0001t0001g0269 a0001c0001t0001g0270 |
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 | 135 | a0001c0001t0001g0167 a0001c0001t0001g0175 a0001c0001t0001g0188 others(132): Show |
136 | HG00280.hp2 HG00323.hp1 HG00544.hp2 others(133): 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 | a0001c0001t0001g0300 a0001c0001t0001g0303 a0001c0001t0001g0305 others(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 | a0001c0001t0014g0313 a0001c0001t0063g0344 |
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 | a0001c0001t0001g0241 a0001c0001t0009g0268 a0001c0001t0031g0004 others(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 | a0001c0001t0019g0244 a0001c0001t0019g0290 a0001c0001t0019g0332 others(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 | a0001c0001t0001g0341 a0001c0002t0001g0163 a0001c0002t0001g0224 |
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 | a0001c0001t0009g0268 a0001c0001t0031g0004 a0001c0001t0038g0009 others(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 | a0001c0001t0014g0313 a0001c0001t0063g0344 |
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 | a0001c0001t0001g0241 a0001c0001t0048g0326 a0001c0001t0065g0347 others(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 | a0001c0001t0002g0080 a0001c0001t0002g0126 |
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 | a0001c0001t0001g0167 a0001c0001t0001g0175 a0001c0001t0001g0214 others(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 | a0001c0001t0025g0322 a0001c0002t0018g0157 a0001c0011t0050g0330 others(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 | a0001c0002t0018g0157 a0001c0011t0050g0330 a0002c0015t0009g0228 |
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 | a0001c0001t0025g0322 a0001c0001t0029g0240 a0001c0001t0029g0319 others(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 | a0001c0001t0001g0241 a0001c0001t0009g0268 a0001c0001t0010g0007 others(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 | a0001c0001t0001g0302 a0001c0001t0002g0062 |
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 | a0001c0001t0049g0235 | 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 | a0001c0001t0001g0188 a0001c0001t0001g0238 a0001c0001t0001g0271 others(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 | 102 | a0001c0001t0001g0167 a0001c0001t0001g0175 a0001c0001t0001g0212 others(99): Show |
102 | HG00280.hp2 HG00323.hp1 HG00544.hp2 others(99): 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 | a0001c0002t0018g0157 a0001c0011t0050g0330 a0002c0015t0009g0228 |
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 | a0001c0001t0009g0268 a0001c0001t0012g0159 a0001c0001t0012g0259 others(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 | a0001c0001t0001g0167 a0001c0001t0001g0175 a0001c0001t0001g0214 others(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 | a0001c0001t0001g0241 a0001c0001t0018g0327 a0001c0001t0048g0326 others(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 | 60 | a0001c0001t0001g0212 a0001c0001t0001g0241 a0001c0001t0002g0102 others(57): Show |
60 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.299-6205T>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45937574 | |||||||
| chr22:45937586 | T | TG | 39 | a0001c0001t0001g0212 a0001c0001t0001g0241 a0001c0001t0002g0102 others(36): Show |
39 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(36): 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 | a0001c0001t0012g0159 a0001c0001t0012g0259 a0001c0001t0012g0329 |
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 | a0001c0001t0003g0065 a0001c0001t0003g0111 a0001c0001t0003g0139 others(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 | 44 | a0001c0001t0001g0212 a0001c0001t0002g0102 a0001c0001t0002g0108 others(41): Show |
44 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(41): 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 | a0001c0001t0019g0290 a0001c0001t0019g0332 |
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 | a0001c0003t0021g0229 a0001c0003t0021g0311 a0001c0003t0040g0046 others(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 | a0001c0002t0018g0157 a0001c0011t0050g0330 a0002c0015t0009g0228 |
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 | a0001c0001t0001g0167 a0001c0001t0001g0175 a0001c0001t0001g0188 others(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 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
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 | a0001c0001t0013g0286 a0001c0003t0021g0311 |
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 | 203 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0167 others(200): Show |
204 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(201): 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 | a0001c0001t0025g0160 a0001c0001t0025g0322 |
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 | a0001c0001t0009g0268 a0001c0001t0019g0244 a0001c0001t0019g0290 others(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 | a0001c0001t0009g0268 a0001c0001t0014g0324 a0001c0001t0019g0244 others(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 | a0001c0001t0009g0268 a0001c0001t0014g0324 a0001c0001t0019g0244 others(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 | a0001c0001t0019g0244 a0001c0001t0019g0290 a0001c0001t0019g0332 |
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 | a0001c0001t0018g0327 a0001c0001t0048g0326 a0001c0014t0018g0260 |
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 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0284 others(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 | 151 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0167 others(148): Show |
151 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.299-7218T>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 2/3 | chr22 | 45938587 | |||||||
| chr22:45938603 | A | T | 151 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0167 others(148): Show |
151 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(148): 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 | a0001c0001t0001g0341 a0001c0001t0012g0259 a0001c0002t0001g0163 others(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 | 163 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0167 others(160): Show |
163 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(160): 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 | a0001c0001t0014g0324 a0001c0001t0024g0099 a0001c0002t0014g0274 others(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 | a0001c0001t0001g0296 | 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 | a0001c0004t0007g0342 a0001c0004t0034g0011 |
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 | a0001c0001t0019g0244 a0001c0001t0019g0290 a0001c0001t0019g0332 others(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 | a0001c0001t0014g0324 a0001c0001t0024g0099 a0001c0002t0014g0274 others(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 | a0001c0001t0001g0308 a0001c0001t0001g0309 |
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 | a0001c0001t0009g0268 a0001c0001t0031g0004 a0001c0001t0038g0009 others(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 | a0001c0001t0001g0167 a0001c0001t0001g0175 a0001c0001t0001g0214 others(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 | a0001c0001t0001g0208 a0001c0001t0002g0137 |
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 | a0001c0001t0001g0150 a0001c0001t0001g0152 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0192 a0001c0001t0004g0221 a0001c0001t0004g0222 others(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 | a0001c0001t0001g0175 a0001c0001t0001g0213 a0001c0001t0001g0275 others(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 | a0001c0001t0001g0184 a0001c0001t0001g0238 a0001c0001t0001g0284 others(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 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0174 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0219 a0001c0001t0001g0266 others(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 | a0001c0001t0001g0202 a0001c0001t0001g0223 a0001c0001t0001g0272 others(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 | a0001c0001t0009g0250 a0001c0001t0063g0344 |
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 | a0001c0001t0019g0290 a0001c0001t0019g0332 |
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 | a0001c0001t0001g0263 a0001c0001t0012g0159 a0001c0001t0012g0329 others(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 | a0001c0001t0029g0240 a0001c0001t0029g0319 a0001c0001t0059g0156 |
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 | a0001c0001t0001g0253 a0001c0001t0002g0031 a0001c0001t0003g0006 others(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 | 16 | a0001c0001t0002g0084 a0001c0001t0005g0249 a0001c0001t0005g0288 others(13): Show |
16 | HG01358.hp2 HG02109.hp1 HG02145.hp2 others(13): 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 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0167 others(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 | a0001c0001t0005g0149 a0001c0001t0006g0121 |
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 | a0001c0001t0001g0231 a0001c0001t0002g0051 a0001c0001t0009g0268 |
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 | a0001c0001t0029g0240 a0001c0001t0029g0319 a0001c0001t0059g0156 |
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 | a0001c0001t0014g0313 a0001c0001t0063g0344 |
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 | a0001c0001t0001g0284 a0001c0001t0014g0254 a0001c0001t0019g0244 others(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 | 38 | a0001c0001t0001g0212 a0001c0001t0001g0261 a0001c0001t0001g0262 others(35): Show |
38 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(35): 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 | 94 | a0001c0001t0001g0167 a0001c0001t0001g0175 a0001c0001t0001g0212 others(91): Show |
94 | HG00544.hp2 HG00639.hp1 HG00642.hp2 others(91): 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 | a0001c0001t0001g0167 a0001c0001t0001g0175 a0001c0001t0001g0214 others(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 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0284 others(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 | a0001c0002t0037g0015 a0001c0003t0021g0229 a0001c0003t0021g0311 others(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 | a0001c0001t0018g0327 a0001c0001t0020g0225 a0001c0001t0065g0347 others(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 | a0001c0001t0014g0313 a0001c0001t0063g0344 |
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 | a0001c0001t0009g0268 a0001c0003t0053g0310 |
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 | a0001c0001t0001g0148 a0001c0001t0001g0154 a0001c0001t0001g0174 others(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 | a0001c0001t0001g0197 a0001c0001t0001g0284 a0001c0001t0068g0348 |
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 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0172 others(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 | a0001c0001t0031g0004 a0001c0001t0038g0009 a0001c0002t0052g0338 others(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 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0320 others(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 | a0001c0001t0001g0241 a0001c0001t0001g0323 a0001c0001t0002g0012 |
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 | a0001c0001t0001g0194 a0001c0001t0001g0196 a0001c0001t0001g0213 others(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 | a0001c0001t0001g0271 a0001c0001t0005g0283 a0001c0001t0007g0161 others(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 | a0001c0001t0001g0152 a0001c0001t0001g0216 a0001c0001t0001g0261 others(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 | a0001c0001t0012g0159 a0001c0001t0012g0329 a0001c0001t0017g0257 others(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 | a0001c0001t0014g0324 a0001c0001t0024g0099 a0001c0001t0031g0004 others(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 | a0001c0002t0014g0274 a0001c0002t0020g0336 a0001c0014t0018g0260 |
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 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0174 others(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 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0325 others(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 | a0001c0001t0068g0348 a0001c0002t0018g0157 a0001c0003t0053g0310 |
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 | 268 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0152 others(265): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): 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 | a0001c0001t0001g0246 a0001c0001t0001g0253 |
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 | a0001c0001t0009g0268 a0001c0002t0007g0230 a0001c0002t0052g0338 |
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 | a0001c0001t0001g0241 a0001c0001t0001g0245 a0001c0001t0001g0278 others(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 | a0001c0001t0059g0156 a0001c0003t0053g0310 a0001c0007t0054g0334 |
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 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0174 others(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 | a0001c0001t0001g0320 a0001c0001t0007g0252 a0001c0001t0009g0250 others(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 | a0001c0001t0001g0170 a0001c0001t0001g0172 a0001c0001t0001g0177 others(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 | a0001c0001t0001g0241 a0001c0001t0001g0323 a0001c0001t0002g0012 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0174 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0174 others(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 | a0001c0001t0008g0039 a0001c0001t0008g0142 |
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 | 91 | a0001c0001t0001g0150 a0001c0001t0001g0152 a0001c0001t0001g0153 others(88): Show |
92 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(89): 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 | a0001c0001t0029g0240 a0001c0002t0018g0157 a0001c0007t0054g0334 |
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 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0174 others(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 | 299 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0152 others(296): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): 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 | a0001c0001t0001g0195 a0001c0001t0002g0095 a0001c0001t0013g0317 others(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 | a0001c0001t0001g0241 a0001c0001t0001g0323 a0001c0001t0002g0012 others(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 | a0001c0001t0029g0240 a0001c0002t0018g0157 a0001c0007t0054g0334 |
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 | a0001c0001t0009g0282 a0001c0001t0012g0331 |
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 | a0001c0001t0001g0148 a0001c0001t0001g0234 a0001c0001t0002g0061 |
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 | a0001c0001t0014g0254 a0001c0001t0017g0257 |
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 | a0001c0001t0001g0148 a0001c0001t0001g0153 a0001c0001t0001g0166 others(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 | a0001c0001t0001g0184 a0001c0001t0002g0069 a0001c0001t0002g0112 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0174 others(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 | a0001c0001t0001g0292 a0001c0001t0005g0288 a0001c0001t0006g0120 |
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 | a0001c0001t0012g0159 a0001c0001t0012g0329 a0001c0001t0014g0313 others(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 | a0001c0001t0001g0241 a0001c0001t0001g0323 a0001c0001t0002g0012 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0174 others(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 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0320 others(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 | a0001c0001t0001g0170 a0001c0001t0001g0172 a0001c0001t0001g0177 others(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 | a0001c0002t0007g0230 a0001c0002t0030g0003 a0001c0002t0037g0015 others(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 | a0001c0001t0001g0284 a0001c0001t0001g0341 a0001c0001t0012g0259 others(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 | a0001c0002t0014g0274 a0001c0002t0020g0336 a0001c0014t0018g0260 |
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 | a0001c0002t0001g0163 a0001c0002t0001g0224 a0001c0002t0007g0230 others(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 | a0001c0001t0017g0257 a0001c0002t0001g0163 a0001c0002t0001g0224 others(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 | a0001c0002t0001g0163 a0001c0002t0001g0224 a0001c0002t0007g0230 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0170 others(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 | a0001c0001t0001g0153 a0001c0001t0002g0113 |
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 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0170 others(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 | a0001c0001t0014g0254 a0001c0001t0017g0257 |
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 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0325 others(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 | a0001c0001t0014g0324 a0001c0001t0024g0099 a0001c0001t0029g0240 others(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 | a0001c0001t0014g0324 a0001c0001t0024g0099 a0001c0001t0029g0240 others(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 | a0001c0002t0001g0163 a0001c0002t0001g0224 a0001c0002t0007g0230 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0170 others(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 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0284 others(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 | a0001c0001t0031g0004 a0001c0001t0047g0251 a0001c0001t0065g0347 |
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 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0320 others(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 | a0001c0001t0024g0099 a0001c0001t0029g0240 a0001c0007t0054g0334 |
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 | a0001c0001t0019g0290 a0001c0001t0019g0332 a0001c0001t0020g0225 |
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 | a0001c0001t0014g0254 a0001c0001t0017g0257 a0001c0001t0019g0244 others(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 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0325 others(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 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0284 others(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 | a0001c0002t0014g0274 a0001c0002t0020g0336 a0001c0014t0018g0260 |
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 | a0001c0001t0001g0308 a0001c0001t0001g0309 |
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 | a0001c0002t0014g0274 a0001c0002t0020g0336 a0001c0014t0018g0260 |
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 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0167 others(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 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0284 others(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 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0284 others(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 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0284 others(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 | a0001c0001t0019g0290 a0001c0001t0019g0332 a0001c0001t0020g0225 |
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 | a0001c0001t0014g0324 a0001c0001t0024g0099 a0001c0001t0029g0240 others(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 | a0001c0001t0031g0004 a0001c0001t0047g0251 a0001c0001t0065g0347 |
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 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0174 others(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 | a0001c0001t0001g0196 a0001c0001t0002g0081 a0001c0001t0002g0101 others(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 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0284 others(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 | a0001c0001t0014g0324 a0001c0001t0024g0099 a0001c0011t0050g0330 |
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 | a0001c0002t0001g0163 a0001c0002t0001g0224 a0001c0002t0007g0230 others(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 | a0001c0001t0019g0244 a0001c0001t0038g0009 a0001c0004t0007g0342 |
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 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0174 others(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 | a0001c0001t0001g0170 a0001c0001t0001g0172 a0001c0001t0001g0177 others(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 | a0001c0002t0001g0163 a0001c0002t0001g0224 a0001c0002t0007g0230 others(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 | a0001c0001t0001g0167 a0001c0001t0001g0175 |
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 | a0001c0001t0019g0244 a0001c0001t0038g0009 a0001c0002t0014g0274 others(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 | a0001c0001t0019g0290 a0001c0001t0019g0332 a0001c0001t0020g0225 others(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 | a0001c0001t0001g0184 a0001c0001t0001g0287 a0001c0001t0003g0111 others(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 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0325 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0174 others(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 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0284 others(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 | a0001c0001t0002g0061 a0001c0001t0002g0123 |
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 | a0001c0001t0001g0263 a0001c0001t0005g0283 a0001c0001t0005g0333 others(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 | a0001c0001t0014g0324 a0001c0001t0017g0257 a0001c0001t0024g0099 others(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 | a0001c0001t0031g0004 a0001c0001t0047g0251 a0001c0001t0065g0347 |
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 | a0001c0001t0001g0303 a0001c0001t0001g0306 a0001c0001t0002g0077 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0170 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0170 others(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 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0320 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0170 others(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 | a0001c0001t0002g0086 a0001c0001t0002g0087 |
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 | a0001c0001t0001g0241 a0001c0001t0001g0269 a0001c0001t0001g0270 others(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 | a0001c0001t0001g0284 a0001c0001t0001g0341 a0001c0001t0063g0344 |
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 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0320 others(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 | a0001c0001t0002g0127 a0001c0001t0003g0050 a0001c0001t0003g0096 others(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 | a0001c0001t0001g0241 a0001c0001t0001g0269 a0001c0001t0001g0270 others(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 | a0001c0001t0001g0284 a0001c0001t0001g0341 a0001c0001t0027g0256 others(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 | a0001c0001t0001g0241 a0001c0001t0001g0269 a0001c0001t0001g0270 others(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 | a0001c0001t0014g0324 a0001c0001t0024g0099 a0001c0011t0050g0330 |
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 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0320 others(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 | a0001c0001t0031g0004 a0001c0001t0047g0251 a0001c0001t0065g0347 |
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 | a0001c0001t0002g0082 a0001c0001t0010g0029 |
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 | a0001c0002t0001g0163 a0001c0002t0001g0224 a0001c0002t0007g0230 others(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 | a0001c0001t0001g0284 a0001c0001t0001g0341 a0001c0001t0012g0259 others(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 | a0001c0001t0002g0086 a0001c0001t0002g0087 |
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 | a0001c0001t0001g0284 a0001c0001t0001g0341 a0001c0001t0012g0259 others(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 | a0001c0001t0001g0241 a0001c0001t0001g0269 a0001c0001t0001g0270 others(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 | a0001c0001t0012g0259 a0001c0001t0014g0254 a0001c0001t0038g0009 others(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 | a0001c0001t0001g0154 a0001c0001t0001g0170 a0001c0001t0001g0177 others(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 | a0001c0001t0001g0185 a0001c0001t0001g0191 a0001c0001t0009g0268 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0218 others(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 | a0001c0001t0001g0174 a0001c0001t0001g0182 a0001c0001t0001g0193 others(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 | a0001c0001t0001g0184 a0001c0001t0001g0265 a0001c0001t0001g0271 others(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 | a0001c0001t0001g0341 a0001c0001t0012g0259 a0001c0001t0014g0254 others(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 | a0001c0001t0019g0290 a0001c0001t0019g0332 a0001c0001t0020g0225 |
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 | a0001c0001t0011g0189 a0001c0001t0013g0286 |
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 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0325 others(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 | a0001c0001t0001g0263 a0001c0001t0005g0283 a0001c0001t0005g0333 others(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 | a0001c0001t0014g0324 a0001c0001t0024g0099 a0001c0011t0050g0330 |
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 | a0001c0001t0001g0341 a0001c0001t0012g0259 a0001c0001t0014g0254 others(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 | a0001c0001t0001g0284 a0001c0001t0001g0341 a0001c0001t0012g0259 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0174 others(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 | 1 | a0001c0001t0006g0073 | 1 | HG02109.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 | a0001c0001t0001g0284 a0001c0001t0001g0341 a0001c0001t0012g0259 others(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 | a0001c0001t0001g0241 a0001c0001t0001g0323 a0001c0001t0002g0012 others(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 | a0001c0001t0025g0160 a0001c0001t0025g0322 |
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 | a0001c0001t0001g0284 a0001c0001t0001g0341 a0001c0001t0012g0259 others(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 | a0001c0001t0029g0240 a0001c0007t0054g0334 |
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 | a0001c0001t0038g0009 a0001c0004t0007g0342 |
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 | a0001c0001t0031g0004 a0001c0001t0047g0251 a0001c0001t0065g0347 |
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 | a0001c0001t0001g0284 a0001c0001t0012g0259 a0001c0001t0014g0254 others(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 | a0001c0001t0005g0333 a0001c0003t0021g0311 |
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 | a0001c0001t0001g0263 a0001c0001t0005g0283 a0001c0001t0005g0333 others(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 | a0001c0001t0001g0263 a0001c0001t0005g0283 a0001c0001t0005g0333 others(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 | a0001c0001t0001g0241 a0001c0001t0001g0269 a0001c0001t0001g0270 others(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 | a0001c0001t0001g0284 a0001c0001t0001g0341 a0001c0001t0027g0256 others(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 | a0001c0001t0001g0278 a0001c0001t0001g0292 a0001c0001t0005g0249 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0174 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0174 others(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 | a0001c0001t0012g0259 a0001c0001t0014g0254 a0001c0001t0038g0009 others(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 | a0001c0001t0014g0254 a0001c0001t0031g0004 a0001c0001t0047g0251 others(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 | a0001c0001t0001g0241 a0001c0001t0001g0261 a0001c0001t0001g0262 others(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 | a0001c0001t0001g0241 a0001c0001t0001g0261 a0001c0001t0001g0262 others(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 | a0001c0001t0001g0263 a0001c0001t0005g0283 a0001c0001t0005g0333 others(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 | a0001c0001t0001g0241 a0001c0001t0001g0261 a0001c0001t0001g0262 others(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 | a0001c0001t0001g0300 a0001c0001t0001g0302 a0001c0001t0002g0062 |
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 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0320 others(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 | a0001c0001t0001g0263 a0001c0001t0005g0283 a0001c0001t0005g0333 others(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 | a0001c0001t0001g0241 a0001c0001t0001g0323 a0001c0001t0002g0012 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0170 others(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 | a0001c0001t0001g0192 a0001c0001t0002g0028 a0001c0001t0002g0031 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0170 others(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 | a0001c0001t0031g0004 a0001c0001t0047g0251 a0001c0001t0065g0347 |
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 | a0001c0001t0014g0324 a0001c0001t0024g0099 a0001c0011t0050g0330 |
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 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0170 others(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 | a0001c0001t0001g0263 a0001c0001t0005g0283 a0001c0001t0005g0333 others(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 | a0001c0001t0001g0278 a0001c0001t0001g0292 a0001c0001t0005g0249 others(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 | a0001c0001t0014g0324 a0001c0001t0024g0099 a0001c0011t0050g0330 |
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 | a0001c0001t0001g0278 a0001c0001t0001g0292 a0001c0001t0005g0249 others(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 | a0001c0001t0001g0241 a0001c0001t0001g0323 a0001c0001t0002g0012 others(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 | a0001c0001t0001g0184 a0001c0001t0001g0213 a0001c0001t0002g0069 others(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 | a0001c0002t0014g0274 a0001c0014t0018g0260 |
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 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0320 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0170 others(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 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0325 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0170 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0170 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0170 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0170 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0170 others(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 | a0001c0001t0001g0278 a0001c0001t0001g0292 a0001c0001t0005g0249 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0170 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0170 others(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 | a0001c0001t0012g0259 a0001c0001t0014g0254 a0001c0001t0038g0009 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0170 others(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 | a0001c0001t0001g0210 a0001c0001t0002g0058 |
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 | a0001c0001t0001g0194 a0001c0001t0001g0196 a0001c0001t0001g0234 others(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 | a0001c0001t0001g0241 a0001c0001t0001g0269 a0001c0001t0001g0270 others(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 | a0001c0001t0001g0241 a0001c0001t0001g0278 a0001c0001t0001g0292 others(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 | a0001c0001t0009g0268 a0001c0001t0014g0324 a0001c0001t0024g0099 others(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 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0320 |
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 | a0001c0001t0001g0261 a0001c0001t0001g0262 |
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 | a0001c0001t0001g0241 a0001c0001t0001g0269 a0001c0001t0001g0270 others(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 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0320 |
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 | a0001c0001t0014g0324 a0001c0001t0024g0099 a0001c0002t0014g0274 others(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 | a0001c0001t0001g0241 a0001c0001t0001g0269 a0001c0001t0001g0270 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0170 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0170 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0174 others(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 | a0001c0001t0019g0290 a0001c0001t0019g0332 a0001c0001t0020g0225 others(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 | a0001c0001t0012g0259 a0001c0001t0038g0009 a0001c0004t0007g0342 |
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 | a0001c0001t0009g0268 a0001c0001t0059g0156 a0001c0002t0014g0274 others(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 | a0001c0001t0001g0263 a0001c0001t0005g0283 a0001c0001t0005g0333 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0170 others(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 | a0001c0001t0001g0241 a0001c0001t0001g0278 a0001c0001t0001g0292 others(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 | a0001c0001t0001g0241 a0001c0001t0001g0278 a0001c0001t0001g0292 others(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 | a0001c0001t0009g0250 a0001c0001t0023g0017 a0001c0001t0056g0226 others(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 | a0001c0001t0014g0324 a0001c0001t0024g0099 a0001c0001t0025g0160 others(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 | a0001c0001t0001g0184 a0001c0001t0001g0213 a0001c0001t0001g0261 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0174 others(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 | a0001c0001t0001g0170 a0001c0001t0001g0172 a0001c0001t0001g0177 others(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 | a0001c0001t0001g0263 a0001c0001t0005g0283 a0001c0001t0005g0333 others(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 | a0001c0001t0001g0263 a0001c0001t0005g0283 a0001c0001t0005g0333 others(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 | a0001c0001t0001g0263 a0001c0001t0005g0283 a0001c0001t0005g0333 others(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 | a0001c0001t0001g0263 a0001c0001t0005g0283 a0001c0001t0005g0333 others(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 | a0001c0001t0001g0263 a0001c0001t0005g0283 a0001c0001t0005g0333 others(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 | a0001c0001t0001g0184 a0001c0001t0001g0213 a0001c0001t0001g0261 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0174 others(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 | a0001c0001t0001g0170 a0001c0001t0001g0172 a0001c0001t0001g0177 others(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 | a0001c0001t0002g0043 a0001c0001t0002g0052 |
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 | a0001c0001t0001g0170 a0001c0001t0001g0172 a0001c0001t0001g0177 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0174 others(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 | a0001c0001t0001g0153 a0001c0001t0001g0241 a0001c0001t0001g0261 others(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 | a0001c0001t0009g0268 a0001c0001t0063g0344 a0001c0002t0014g0274 others(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 | a0001c0001t0012g0259 a0001c0001t0014g0254 a0001c0001t0014g0324 others(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 | a0001c0001t0001g0263 a0001c0001t0005g0283 a0001c0001t0005g0333 others(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 | a0001c0001t0001g0341 a0001c0001t0007g0321 a0001c0001t0062g0339 others(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 | a0001c0001t0001g0241 a0001c0001t0001g0269 a0001c0001t0001g0270 others(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 | a0001c0001t0001g0170 a0001c0001t0001g0172 a0001c0001t0001g0177 others(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 | a0001c0001t0025g0160 a0001c0001t0047g0251 a0001c0001t0065g0347 |
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 | a0001c0001t0001g0170 a0001c0001t0001g0172 a0001c0001t0001g0177 others(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 | a0001c0001t0025g0160 a0001c0001t0047g0251 a0001c0001t0065g0347 |
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 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0170 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0170 others(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 | a0001c0001t0012g0159 a0001c0001t0012g0329 a0001c0001t0014g0313 others(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 | a0001c0001t0001g0170 a0001c0001t0001g0172 a0001c0001t0001g0177 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0174 others(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 | a0001c0001t0002g0146 a0001c0001t0003g0019 a0001c0001t0003g0040 others(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 | a0001c0001t0014g0254 a0001c0001t0038g0009 a0001c0004t0007g0342 |
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 | a0001c0001t0007g0161 a0001c0001t0007g0162 |
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 | a0001c0001t0001g0341 a0001c0001t0007g0321 a0001c0001t0062g0339 others(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 | a0001c0001t0002g0146 a0001c0001t0003g0040 a0001c0001t0003g0145 |
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 | a0001c0001t0001g0300 a0001c0001t0001g0302 a0001c0001t0002g0062 |
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 | a0001c0001t0020g0225 a0001c0002t0020g0336 |
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 | a0001c0001t0014g0254 a0001c0001t0025g0160 a0001c0001t0038g0009 others(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 | a0001c0001t0014g0254 a0001c0001t0025g0160 a0001c0001t0047g0251 others(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 | a0001c0001t0001g0170 a0001c0001t0001g0172 a0001c0001t0001g0177 others(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 | a0001c0001t0001g0170 a0001c0001t0001g0172 a0001c0001t0001g0177 others(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 | a0001c0001t0001g0284 a0001c0001t0007g0252 |
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 | a0001c0001t0001g0238 a0001c0001t0001g0275 a0001c0001t0002g0002 others(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 | a0001c0001t0014g0324 a0001c0001t0017g0257 a0001c0001t0024g0099 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0174 others(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 | a0001c0001t0001g0170 a0001c0001t0001g0172 a0001c0001t0001g0177 others(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 | a0001c0001t0001g0241 a0001c0001t0001g0261 a0001c0001t0001g0262 others(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 | a0001c0001t0001g0302 a0001c0001t0002g0110 a0001c0001t0004g0204 others(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 | a0001c0001t0001g0245 a0001c0001t0001g0269 a0001c0001t0001g0270 others(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 | a0001c0001t0001g0153 a0001c0001t0002g0070 a0001c0001t0002g0071 |
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 | a0001c0001t0001g0295 | 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 | a0001c0001t0007g0315 a0001c0001t0007g0328 |
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 | a0001c0001t0001g0246 a0001c0001t0001g0253 |
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 | a0001c0001t0020g0225 a0001c0002t0018g0157 a0001c0007t0054g0334 others(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 | a0001c0001t0001g0271 a0001c0001t0020g0158 a0001c0014t0018g0260 |
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 | a0001c0001t0001g0263 a0001c0001t0001g0278 a0001c0001t0012g0259 others(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 | a0001c0001t0001g0271 a0001c0001t0001g0284 a0001c0001t0005g0283 others(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 | a0001c0001t0001g0165 a0001c0001t0001g0241 a0001c0001t0001g0261 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0152 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0214 a0001c0001t0010g0063 |
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 | a0001c0001t0007g0161 a0001c0001t0007g0162 a0001c0001t0009g0268 others(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 | a0001c0001t0001g0179 a0001c0001t0001g0181 a0001c0001t0001g0187 others(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 | a0001c0001t0001g0165 a0001c0001t0001g0270 a0001c0001t0001g0291 others(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 | a0001c0001t0001g0177 a0001c0001t0001g0312 a0001c0001t0001g0335 others(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 | a0001c0001t0005g0333 a0001c0001t0014g0254 a0001c0001t0014g0324 others(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 | a0001c0001t0001g0195 a0001c0001t0001g0261 a0001c0001t0001g0262 others(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 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0253 others(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 | a0001c0001t0001g0278 a0001c0001t0004g0171 a0001c0001t0018g0327 others(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 | a0001c0001t0001g0341 a0001c0001t0035g0018 a0001c0001t0042g0013 others(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 | 155 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(152): Show |
156 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(153): 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 | a0001c0001t0001g0177 a0001c0001t0001g0195 a0001c0001t0001g0241 others(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 | 146 | a0001c0001t0001g0148 a0001c0001t0001g0152 a0001c0001t0001g0153 others(143): Show |
147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): 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 | a0001c0001t0001g0150 a0001c0001t0001g0165 a0001c0001t0001g0193 others(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 | a0001c0001t0007g0314 a0001c0001t0007g0315 a0001c0001t0007g0328 others(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 | a0001c0001t0001g0241 a0003c0006t0064g0343 |
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 | a0001c0001t0001g0150 a0001c0001t0001g0165 a0001c0001t0001g0170 others(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 | a0001c0001t0001g0166 a0001c0001t0001g0181 a0001c0001t0001g0191 others(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 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0174 others(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 | 55 | a0001c0001t0001g0148 a0001c0001t0001g0152 a0001c0001t0001g0167 others(52): Show |
55 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(52): 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 | a0001c0001t0001g0175 a0001c0001t0001g0214 a0001c0001t0002g0028 others(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 | a0001c0001t0001g0312 a0001c0001t0001g0335 a0001c0001t0004g0173 others(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 | a0001c0001t0001g0253 a0001c0001t0009g0282 a0001c0001t0012g0259 others(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 | a0001c0001t0001g0246 a0001c0001t0001g0261 a0001c0001t0029g0240 |
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 | a0001c0001t0001g0179 a0001c0001t0001g0187 a0001c0001t0001g0188 others(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 | a0001c0001t0001g0150 a0001c0001t0001g0170 a0001c0001t0001g0284 others(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 | a0001c0001t0001g0165 a0001c0001t0001g0193 a0001c0001t0001g0277 others(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 | a0001c0001t0001g0245 a0001c0001t0002g0041 |
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 | a0001c0001t0001g0150 a0001c0001t0001g0170 a0001c0001t0001g0263 others(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 | a0001c0001t0001g0150 a0001c0001t0001g0165 a0001c0001t0001g0170 others(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 | 147 | a0001c0001t0001g0148 a0001c0001t0001g0152 a0001c0001t0001g0153 others(144): Show |
148 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(145): 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 | a0001c0001t0005g0293 a0001c0001t0022g0093 a0001c0001t0026g0340 |
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 | 145 | a0001c0001t0001g0148 a0001c0001t0001g0152 a0001c0001t0001g0153 others(142): Show |
146 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(143): 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 | a0001c0001t0001g0271 a0001c0001t0001g0278 |
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 | a0001c0001t0001g0271 a0001c0001t0001g0278 |
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 | a0001c0001t0005g0333 a0001c0001t0014g0324 a0001c0001t0017g0257 others(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 | 171 | a0001c0001t0001g0148 a0001c0001t0001g0152 a0001c0001t0001g0153 others(168): Show |
172 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(169): 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 | a0001c0001t0001g0179 a0001c0001t0001g0187 a0001c0001t0001g0231 others(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 | a0001c0001t0001g0341 a0001c0001t0014g0254 a0001c0001t0019g0290 others(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 | 306 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0152 others(303): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): 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 | a0001c0001t0005g0333 a0001c0001t0014g0324 a0001c0001t0024g0099 others(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 | a0001c0001t0001g0165 a0001c0001t0001g0291 a0001c0001t0001g0292 others(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 | a0001c0001t0001g0177 a0001c0001t0001g0195 a0001c0001t0001g0241 others(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 | a0001c0001t0001g0150 a0001c0001t0001g0165 a0001c0001t0001g0170 others(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 | a0001c0001t0001g0341 a0001c0001t0035g0018 a0001c0001t0042g0013 others(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 | a0001c0001t0001g0295 a0001c0001t0002g0028 |
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 | 44 | a0001c0001t0001g0166 a0001c0001t0001g0234 a0001c0001t0001g0241 others(41): Show |
44 | HG00099.hp1 HG00735.hp1 HG00741.hp1 others(41): 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 | a0001c0001t0007g0161 a0001c0001t0007g0162 |
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 | a0001c0001t0002g0115 a0001c0001t0003g0096 |
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 | a0001c0001t0012g0329 a0001c0001t0018g0327 |
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 | a0001c0001t0004g0173 a0001c0001t0011g0164 |
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 | a0001c0001t0014g0254 a0001c0001t0027g0256 |
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 | a0001c0001t0001g0275 a0001c0001t0004g0276 |
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 | 199 | a0001c0001t0001g0148 a0001c0001t0001g0152 a0001c0001t0001g0153 others(196): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.72-10324delG | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45960469 | |||||||
| chr22:45960554 | T | C | 298 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0152 others(295): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): 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 | a0001c0001t0012g0329 a0001c0001t0018g0327 a0001c0014t0018g0260 |
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 | a0001c0001t0001g0271 a0001c0001t0005g0333 |
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 | 265 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0152 others(262): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): 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 | a0001c0001t0009g0282 a0001c0001t0009g0285 a0001c0001t0012g0159 others(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 | a0001c0001t0009g0282 a0001c0001t0009g0285 a0001c0001t0012g0159 others(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 | a0001c0001t0009g0282 a0001c0001t0009g0285 a0001c0001t0012g0159 others(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 | a0001c0001t0068g0348 a0001c0002t0014g0274 |
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 | a0001c0001t0012g0329 a0001c0001t0018g0327 a0001c0014t0018g0260 |
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 | a0001c0001t0012g0329 a0001c0001t0018g0327 a0001c0014t0018g0260 |
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 | a0001c0001t0016g0032 a0001c0001t0016g0034 a0001c0001t0016g0035 |
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 | a0001c0001t0001g0223 a0001c0001t0004g0221 a0001c0001t0004g0222 |
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 | a0001c0001t0006g0073 a0001c0008t0002g0072 |
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 | 275 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0152 others(272): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): 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 | a0001c0001t0007g0161 a0001c0001t0007g0162 |
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 | a0001c0001t0068g0348 a0001c0002t0014g0274 |
2 | HG01496.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.72-11915C>T | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45962061 | |||||||
| chr22:45962316 | 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 | a0001c0001t0001g0241 a0001c0001t0001g0245 a0001c0001t0001g0246 others(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 | a0001c0001t0012g0329 a0001c0001t0018g0327 a0001c0014t0018g0260 |
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 | a0001c0001t0012g0329 a0001c0001t0018g0327 a0001c0014t0018g0260 |
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 | a0001c0001t0001g0241 a0001c0001t0001g0245 a0001c0001t0001g0246 others(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 | a0001c0001t0009g0282 a0001c0001t0009g0285 a0001c0001t0012g0159 others(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 | 201 | a0001c0001t0001g0148 a0001c0001t0001g0152 a0001c0001t0001g0153 others(198): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): 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 | a0001c0001t0001g0341 a0001c0001t0002g0070 a0001c0001t0002g0071 others(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 | a0001c0001t0001g0278 a0001c0001t0001g0320 |
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 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0325 others(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 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0325 |
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 | a0001c0001t0002g0140 a0001c0001t0008g0141 a0001c0001t0008g0142 |
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 | a0001c0001t0001g0241 a0001c0001t0001g0245 a0001c0001t0001g0246 others(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 | a0001c0001t0002g0012 a0001c0001t0023g0014 a0001c0001t0024g0010 others(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 | a0001c0002t0014g0274 a0001c0002t0018g0157 |
2 | HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.71+12741G>A | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45963943 | |||||||
| chr22:45964203 | G | A | 105 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0174 others(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 | a0001c0001t0009g0250 a0001c0002t0001g0163 |
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 | a0001c0001t0001g0271 a0001c0001t0001g0341 a0001c0001t0012g0259 others(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 | a0001c0001t0001g0150 a0001c0001t0001g0152 a0001c0001t0001g0165 others(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 | a0001c0001t0001g0292 a0001c0001t0001g0320 a0001c0001t0001g0323 others(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 | a0001c0001t0001g0253 a0001c0001t0001g0278 a0001c0001t0001g0284 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0167 others(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 | a0001c0001t0002g0113 a0001c0001t0002g0115 a0001c0001t0002g0116 others(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 | a0001c0001t0001g0172 a0001c0001t0004g0171 a0001c0001t0013g0286 |
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 | a0001c0001t0002g0012 a0001c0001t0023g0014 a0001c0001t0024g0010 others(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 | a0001c0001t0001g0277 a0001c0001t0026g0340 |
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 | a0001c0001t0001g0277 a0001c0001t0001g0291 a0001c0001t0001g0292 others(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 | a0001c0001t0001g0269 a0001c0001t0001g0270 |
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 | a0001c0001t0001g0277 a0001c0001t0026g0340 |
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 | a0001c0001t0003g0125 a0001c0001t0006g0124 |
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 | a0001c0001t0007g0161 a0001c0001t0007g0162 |
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 | 184 | a0001c0001t0001g0150 a0001c0001t0001g0170 a0001c0001t0001g0220 others(181): Show |
186 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(183): 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 | a0001c0001t0065g0347 a0001c0001t0066g0345 a0001c0001t0067g0346 others(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 | a0001c0001t0025g0160 a0003c0006t0064g0343 |
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 | a0001c0001t0005g0333 a0001c0001t0007g0161 a0001c0001t0007g0162 others(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 | a0001c0001t0001g0277 a0001c0001t0026g0340 |
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 | a0001c0001t0065g0347 a0001c0001t0066g0345 a0001c0001t0067g0346 others(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 | 239 | a0001c0001t0001g0150 a0001c0001t0001g0170 a0001c0001t0001g0220 others(236): Show |
241 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(238): 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 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 others(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 | a0001c0001t0001g0261 a0001c0001t0001g0262 |
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 | a0001c0001t0001g0263 a0001c0002t0020g0336 a0001c0002t0052g0338 others(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 | a0001c0001t0012g0329 a0001c0011t0050g0330 |
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 | a0001c0001t0001g0281 a0001c0001t0002g0001 a0001c0001t0002g0002 others(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 | a0001c0001t0001g0281 a0001c0001t0036g0128 |
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 | 230 | a0001c0001t0001g0150 a0001c0001t0001g0220 a0001c0001t0001g0263 others(227): Show |
232 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(229): 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 | a0001c0001t0007g0161 a0001c0001t0007g0162 |
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 | a0001c0001t0001g0150 a0001c0001t0005g0149 a0001c0001t0013g0151 |
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 | a0001c0001t0001g0272 a0001c0001t0001g0275 a0001c0001t0001g0277 others(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 | a0001c0001t0001g0302 a0001c0001t0001g0303 a0001c0001t0001g0305 others(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 | a0001c0002t0020g0336 a0001c0002t0052g0338 a0001c0013t0021g0337 |
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 | a0001c0002t0020g0336 a0001c0002t0052g0338 a0001c0013t0021g0337 |
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 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0008 others(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 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 others(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 | a0001c0001t0001g0253 a0001c0001t0007g0252 a0001c0001t0047g0251 |
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 | a0001c0001t0065g0347 a0001c0001t0066g0345 a0001c0001t0067g0346 others(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 | a0001c0001t0005g0333 a0001c0001t0007g0161 a0001c0001t0007g0162 others(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 | a0001c0001t0001g0263 a0001c0001t0001g0272 a0001c0001t0001g0275 others(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 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0008 others(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 | a0001c0001t0001g0284 a0001c0001t0019g0332 |
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 | a0001c0001t0001g0263 a0001c0001t0001g0272 a0001c0001t0001g0275 others(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 | a0001c0001t0020g0158 a0001c0001t0059g0156 a0001c0002t0018g0157 |
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 | a0001c0001t0001g0281 a0001c0001t0002g0012 a0001c0001t0023g0014 others(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 | 217 | a0001c0001t0001g0150 a0001c0001t0001g0216 a0001c0001t0001g0220 others(214): Show |
219 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.71+6437C>G | WNT7B | ENSG00000188064.10 | transcript | ENST00000339464.9 | protein_coding | 1/3 | chr22 | 45970247 | |||||||
| chr22:45970285 | C | T | 98 | a0001c0001t0001g0150 a0001c0001t0001g0220 a0001c0001t0001g0269 others(95): Show |
98 | HG00621.hp1 HG00639.hp2 HG00733.hp1 others(95): 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 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0219 |
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 | 95 | a0001c0001t0001g0150 a0001c0001t0001g0220 a0001c0001t0001g0269 others(92): Show |
95 | HG00621.hp1 HG00639.hp2 HG00733.hp1 others(92): 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 | a0001c0001t0001g0261 a0001c0001t0001g0262 |
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 | a0001c0001t0023g0017 a0001c0001t0035g0018 |
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 | a0001c0001t0001g0223 a0001c0001t0004g0221 a0001c0001t0004g0222 |
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 | a0001c0001t0001g0269 a0001c0001t0001g0270 |
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 | a0001c0001t0065g0347 a0001c0001t0066g0345 a0001c0001t0067g0346 others(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 | a0001c0001t0002g0135 a0001c0001t0002g0137 a0001c0001t0003g0136 |
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 | a0001c0001t0001g0281 a0001c0001t0005g0283 a0001c0016t0007g0280 |
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 | a0001c0002t0020g0336 a0001c0002t0052g0338 a0001c0013t0021g0337 |
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 | 87 | a0001c0001t0001g0150 a0001c0001t0001g0269 a0001c0001t0001g0270 others(84): Show |
87 | HG00621.hp1 HG00639.hp2 HG00733.hp1 others(84): 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 | a0001c0001t0001g0281 a0001c0016t0007g0280 |
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 | a0001c0002t0020g0336 a0001c0002t0052g0338 a0001c0013t0021g0337 |
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 | a0001c0001t0002g0002 a0001c0001t0003g0132 |
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 | 279 | a0001c0001t0001g0150 a0001c0001t0001g0223 a0001c0001t0001g0231 others(276): Show |
281 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(278): 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 | a0001c0001t0059g0156 a0001c0002t0018g0157 |
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 | a0001c0001t0002g0135 a0001c0001t0002g0137 a0001c0001t0003g0136 |
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 | a0001c0001t0002g0138 a0001c0001t0003g0139 |
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 | a0001c0001t0002g0140 a0001c0001t0008g0141 a0001c0001t0008g0142 |
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 | a0001c0001t0059g0156 a0001c0002t0018g0157 |
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 | a0001c0001t0001g0272 a0001c0001t0001g0275 a0001c0001t0001g0277 others(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 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 others(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 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0266 |
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 | 223 | a0001c0001t0001g0150 a0001c0001t0001g0272 a0001c0001t0001g0275 others(220): Show |
225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): 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 | a0001c0001t0001g0154 a0001c0001t0011g0155 |
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 | 233 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 others(230): Show |
235 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(232): 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 | a0001c0001t0002g0143 a0001c0001t0002g0146 a0001c0001t0003g0144 others(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 | a0001c0002t0020g0336 a0001c0002t0052g0338 a0001c0013t0021g0337 |
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 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 |
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 | 227 | a0001c0001t0001g0150 a0001c0001t0001g0154 a0001c0001t0001g0272 others(224): Show |
229 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(226): 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 | a0001c0001t0020g0158 a0001c0001t0059g0156 a0001c0002t0018g0157 |
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 | a0001c0001t0020g0158 a0001c0001t0059g0156 a0001c0001t0065g0347 others(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 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0002g0001 others(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 | a0001c0001t0002g0012 a0001c0001t0023g0014 a0001c0001t0024g0010 others(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 | a0001c0001t0065g0347 a0001c0001t0066g0345 a0001c0001t0067g0346 others(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 | a0001c0001t0001g0150 a0001c0001t0005g0149 a0001c0001t0013g0151 |
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 | a0001c0001t0001g0150 a0001c0001t0005g0149 |
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 |