Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 100820829 |
| ensemblid | ENSG00000263155.6 |
| hgncid | 43444 |
| symbol | MYZAP |
| name | myocardial zonula adherens protein |
| refseq_nuc | NM_001018100.5 |
| refseq_prot | NP_001018110.1 |
| ensembl_nuc | ENST00000267853.10 |
| ensembl_prot | ENSP00000267853.5 |
| mane_status | MANE Select |
| chr | chr15 |
| start | 57591904 |
| end | 57685364 |
| strand | + |
| ver | v1.2 |
| region | chr15:57591904-57685364 |
| region5000 | chr15:57586904-57690364 |
| regionname0 | MYZAP_chr15_57591904_57685364 |
| regionname5000 | MYZAP_chr15_57586904_57690364 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 466 | 254 | 70 | 62 | 84 | 14 | 22 | 59 | MYZAP_chr15_57586904_57690364 | MYZAP | MLRST others(461): Show |
chr15 | 57586904 | 57690364 |
| a0002 | 0/0 | 466 | 91 | 20 | 5 | 59 | 0 | 7 | 44 | MYZAP_chr15_57586904_57690364 | MYZAP | MLRST others(461): Show |
chr15 | 57586904 | 57690364 |
| a0003 | 0/0 | 466 | 3 | 2 | 0 | 0 | 0 | 1 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | MLRST others(461): Show |
chr15 | 57586904 | 57690364 |
| a0004 | 0/0 | 466 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | MLRST others(461): Show |
chr15 | 57586904 | 57690364 |
| a0005 | 0/0 | 466 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | MLRST others(461): Show |
chr15 | 57586904 | 57690364 |
| a0006 | 0/0 | 466 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | MLRST others(461): Show |
chr15 | 57586904 | 57690364 |
| a0007 | 0/0 | 466 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | MLRST others(461): Show |
chr15 | 57586904 | 57690364 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1398 | 175 | 47 | 38 | 69 | 5 | 15 | MYZAP_chr15_57586904_57690364 | MYZAP | ATGCT others(1393): Show |
chr15 | 57586904 | 57690364 | ||
| a0001c0003 | 1/0 | 1398 | 78 | 23 | 24 | 15 | 9 | 6 | MYZAP_chr15_57586904_57690364 | MYZAP | ATGCT others(1393): Show |
chr15 | 57586904 | 57690364 | ||
| a0001c0007 | 0/0 | 1398 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | ATGCT others(1393): Show |
chr15 | 57586904 | 57690364 | ||
| a0002c0002 | 0/0 | 1398 | 82 | 19 | 5 | 52 | 0 | 6 | MYZAP_chr15_57586904_57690364 | MYZAP | ATGCT others(1393): Show |
chr15 | 57586904 | 57690364 | ||
| a0002c0004 | 0/0 | 1398 | 8 | 1 | 0 | 6 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | ATGCT others(1393): Show |
chr15 | 57586904 | 57690364 | ||
| a0002c0009 | 0/0 | 1398 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | ATGCT others(1393): Show |
chr15 | 57586904 | 57690364 | ||
| a0003c0005 | 0/0 | 1398 | 3 | 2 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | ATGCT others(1393): Show |
chr15 | 57586904 | 57690364 | ||
| a0004c0008 | 0/0 | 1398 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | ATGCT others(1393): Show |
chr15 | 57586904 | 57690364 | ||
| a0005c0011 | 0/0 | 1398 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | ATGCT others(1393): Show |
chr15 | 57586904 | 57690364 | ||
| a0006c0006 | 0/0 | 1398 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | ATGCT others(1393): Show |
chr15 | 57586904 | 57690364 | ||
| a0007c0010 | 0/0 | 1398 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | ATGCT others(1393): Show |
chr15 | 57586904 | 57690364 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2398 | 129 | 18 | 30 | 68 | 3 | 9 | MYZAP_chr15_57586904_57690364 | MYZAP | CTTCG others(2393): Show |
chr15 | 57586904 | 57690364 |
| a0001c0001t0002 | 0/0 | 2398 | 18 | 3 | 7 | 0 | 2 | 6 | MYZAP_chr15_57586904_57690364 | MYZAP | CTTCG others(2393): Show |
chr15 | 57586904 | 57690364 |
| a0001c0001t0003 | 0/0 | 2398 | 4 | 3 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | CTTCG others(2393): Show |
chr15 | 57586904 | 57690364 |
| a0001c0001t0004 | 0/0 | 2397 | 9 | 8 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | CTTCG others(2392): Show |
chr15 | 57586904 | 57690364 |
| a0001c0001t0005 | 0/0 | 2397 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | CTTCG others(2392): Show |
chr15 | 57586904 | 57690364 |
| a0001c0001t0006 | 0/0 | 2398 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | CTTCG others(2393): Show |
chr15 | 57586904 | 57690364 |
| a0001c0001t0007 | 0/0 | 2398 | 4 | 4 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | CTTCG others(2393): Show |
chr15 | 57586904 | 57690364 |
| a0001c0001t0008 | 0/0 | 2392 | 3 | 3 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | CTTCG others(2387): Show |
chr15 | 57586904 | 57690364 |
| a0001c0001t0009 | 0/0 | 2398 | 2 | 2 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | CTTCG others(2393): Show |
chr15 | 57586904 | 57690364 |
| a0001c0001t0013 | 0/0 | 2398 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | CTTCG others(2393): Show |
chr15 | 57586904 | 57690364 |
| a0001c0001t0015 | 0/0 | 2398 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | CTTCG others(2393): Show |
chr15 | 57586904 | 57690364 |
| a0001c0001t0019 | 0/0 | 2397 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | CTTCG others(2392): Show |
chr15 | 57586904 | 57690364 |
| a0001c0001t0020 | 0/0 | 2398 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | CTTCG others(2393): Show |
chr15 | 57586904 | 57690364 |
| a0001c0003t0001 | 0/0 | 2398 | 4 | 2 | 1 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | CTTCG others(2393): Show |
chr15 | 57586904 | 57690364 |
| a0001c0003t0002 | 0/0 | 2398 | 33 | 6 | 10 | 10 | 5 | 2 | MYZAP_chr15_57586904_57690364 | MYZAP | CTTCG others(2393): Show |
chr15 | 57586904 | 57690364 |
| a0001c0003t0003 | 0/0 | 2398 | 30 | 7 | 11 | 4 | 4 | 4 | MYZAP_chr15_57586904_57690364 | MYZAP | CTTCG others(2393): Show |
chr15 | 57586904 | 57690364 |
| a0001c0003t0004 | 0/0 | 2397 | 4 | 4 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | CTTCG others(2392): Show |
chr15 | 57586904 | 57690364 |
| a0001c0003t0005 | 0/0 | 2397 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | CTTCG others(2392): Show |
chr15 | 57586904 | 57690364 |
| a0001c0003t0006 | 0/0 | 2398 | 3 | 2 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | CTTCG others(2393): Show |
chr15 | 57586904 | 57690364 |
| a0001c0003t0014 | 0/0 | 2398 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | CTTCG others(2393): Show |
chr15 | 57586904 | 57690364 |
| a0001c0003t0016 | 1/0 | 2398 | 1 | 0 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | CTTCG others(2393): Show |
chr15 | 57586904 | 57690364 |
| a0001c0003t0017 | 0/0 | 2392 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | CTTCG others(2387): Show |
chr15 | 57586904 | 57690364 |
| a0001c0007t0003 | 0/0 | 2398 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | CTTCG others(2393): Show |
chr15 | 57586904 | 57690364 |
| a0002c0002t0001 | 0/0 | 2398 | 2 | 2 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | CTTCG others(2393): Show |
chr15 | 57586904 | 57690364 |
| a0002c0002t0002 | 0/0 | 2398 | 69 | 13 | 5 | 46 | 0 | 5 | MYZAP_chr15_57586904_57690364 | MYZAP | CTTCG others(2393): Show |
chr15 | 57586904 | 57690364 |
| a0002c0002t0003 | 0/0 | 2398 | 2 | 2 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | CTTCG others(2393): Show |
chr15 | 57586904 | 57690364 |
| a0002c0002t0004 | 0/0 | 2397 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | CTTCG others(2392): Show |
chr15 | 57586904 | 57690364 |
| a0002c0002t0005 | 0/0 | 2397 | 5 | 0 | 0 | 4 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | CTTCG others(2392): Show |
chr15 | 57586904 | 57690364 |
| a0002c0002t0011 | 0/0 | 2398 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | CTTCG others(2393): Show |
chr15 | 57586904 | 57690364 |
| a0002c0002t0012 | 0/0 | 2397 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | CTTCG others(2392): Show |
chr15 | 57586904 | 57690364 |
| a0002c0002t0018 | 0/0 | 2397 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | CTTCG others(2392): Show |
chr15 | 57586904 | 57690364 |
| a0002c0004t0001 | 0/0 | 2398 | 6 | 0 | 0 | 6 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | CTTCG others(2393): Show |
chr15 | 57586904 | 57690364 |
| a0002c0004t0002 | 0/0 | 2398 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | CTTCG others(2393): Show |
chr15 | 57586904 | 57690364 |
| a0002c0004t0005 | 0/0 | 2397 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | CTTCG others(2392): Show |
chr15 | 57586904 | 57690364 |
| a0002c0009t0002 | 0/0 | 2398 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | CTTCG others(2393): Show |
chr15 | 57586904 | 57690364 |
| a0003c0005t0004 | 0/0 | 2397 | 2 | 2 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | CTTCG others(2392): Show |
chr15 | 57586904 | 57690364 |
| a0003c0005t0010 | 0/0 | 2398 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | CTTCG others(2393): Show |
chr15 | 57586904 | 57690364 |
| a0004c0008t0003 | 0/0 | 2398 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | CTTCG others(2393): Show |
chr15 | 57586904 | 57690364 |
| a0005c0011t0002 | 0/0 | 2398 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | CTTCG others(2393): Show |
chr15 | 57586904 | 57690364 |
| a0006c0006t0002 | 0/0 | 2398 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | CTTCG others(2393): Show |
chr15 | 57586904 | 57690364 |
| a0007c0010t0001 | 0/0 | 2398 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | CTTCG others(2393): Show |
chr15 | 57586904 | 57690364 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0194 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0002g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0003g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0003g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0003g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0003g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0004g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0004g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0004g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0004g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0004g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0004g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0004g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0005g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0006g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0007g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0007g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0007g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0007g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0008g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0008g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0008g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0009g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0009g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0013g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0015g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0019g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0020g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0002g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0003g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0003g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0003g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0003g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0003g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0003g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0003g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0003g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0003g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0003g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0003g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0003g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0003g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0003g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0003g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0003g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0003g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0005g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0006g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0006g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0006g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0014g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0016g0144 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0017g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0007t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0005g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0005g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0005g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0005g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0005g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0011g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0012g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0018g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0004t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0004t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0004t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0004t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0004t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0004t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0004t0002g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0004t0005g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0009t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0003c0005t0004g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0003c0005t0004g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0003c0005t0010g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0004c0008t0003g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0005c0011t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0006c0006t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0007c0010t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0002 | g0029 | EUR | GBR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0306 | EUR | GBR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG00140 | hp1 | a0001 | c0003 | t0003 | g0147 | EUR | GBR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG00140 | hp2 | a0001 | c0003 | t0002 | g0021 | EUR | GBR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG00323 | hp1 | a0001 | c0003 | t0003 | g0145 | EUR | FIN | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG00323 | hp2 | a0001 | c0003 | t0002 | g0018 | EUR | FIN | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG00423 | hp2 | a0002 | c0002 | t0002 | g0086 | EAS | CHS | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG00438 | hp1 | a0002 | c0002 | t0002 | g0073 | EAS | CHS | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG00438 | hp2 | a0002 | c0002 | t0002 | g0091 | EAS | CHS | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG00544 | hp1 | a0001 | c0003 | t0002 | g0078 | EAS | CHS | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG00558 | hp1 | a0002 | c0002 | t0005 | g0089 | EAS | CHS | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | CHS | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG00597 | hp1 | a0002 | c0002 | t0002 | g0012 | EAS | CHS | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | CHS | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG00609 | hp2 | a0001 | c0003 | t0003 | g0137 | EAS | CHS | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG00621 | hp1 | a0001 | c0003 | t0001 | g0227 | EAS | CHS | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0069 | EAS | CHS | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0317 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG00673 | hp1 | a0002 | c0002 | t0002 | g0101 | EAS | CHS | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG00738 | hp1 | a0001 | c0003 | t0005 | g0090 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG00738 | hp2 | a0001 | c0003 | t0003 | g0150 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0034 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01069 | hp2 | a0001 | c0003 | t0003 | g0154 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01070 | hp2 | a0001 | c0003 | t0003 | g0130 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01071 | hp2 | a0001 | c0003 | t0003 | g0155 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01074 | hp2 | a0001 | c0003 | t0001 | g0171 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0313 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01081 | hp2 | a0001 | c0003 | t0003 | g0129 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01099 | hp1 | a0001 | c0003 | t0002 | g0003 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01106 | hp1 | a0001 | c0003 | t0002 | g0048 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01106 | hp2 | a0001 | c0003 | t0002 | g0031 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01109 | hp2 | a0001 | c0003 | t0006 | g0115 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01167 | hp2 | a0001 | c0003 | t0002 | g0003 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01168 | hp1 | a0001 | c0003 | t0002 | g0030 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01175 | hp2 | a0004 | c0008 | t0003 | g0133 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01192 | hp1 | a0001 | c0003 | t0003 | g0156 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0311 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01243 | hp2 | a0001 | c0003 | t0003 | g0134 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01255 | hp1 | a0002 | c0002 | t0002 | g0127 | AMR | CLM | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01255 | hp2 | a0001 | c0003 | t0002 | g0023 | AMR | CLM | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01256 | hp1 | a0001 | c0003 | t0002 | g0019 | AMR | CLM | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01257 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01258 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01346 | hp1 | a0001 | c0003 | t0002 | g0075 | AMR | CLM | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | CLM | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01358 | hp1 | a0001 | c0003 | t0003 | g0131 | AMR | CLM | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01358 | hp2 | a0001 | c0003 | t0002 | g0033 | AMR | CLM | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01361 | hp1 | a0002 | c0002 | t0002 | g0079 | AMR | CLM | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01496 | hp2 | a0001 | c0003 | t0003 | g0142 | AMR | CLM | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01515 | hp1 | a0001 | c0003 | t0003 | g0146 | EUR | IBS | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0197 | EUR | IBS | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01516 | hp1 | a0001 | c0003 | t0003 | g0141 | EUR | IBS | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01516 | hp2 | a0001 | c0003 | t0002 | g0032 | EUR | IBS | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01884 | hp1 | a0001 | c0001 | t0008 | g0328 | AFR | ACB | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01884 | hp2 | a0001 | c0003 | t0002 | g0035 | AFR | ACB | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01891 | hp1 | a0001 | c0003 | t0004 | g0114 | AFR | ACB | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01891 | hp2 | a0001 | c0003 | t0002 | g0024 | AFR | ACB | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PEL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0322 | AMR | PEL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01934 | hp1 | a0001 | c0003 | t0003 | g0151 | AMR | PEL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PEL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PEL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PEL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0321 | AMR | PEL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0323 | AMR | PEL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | KHV | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02015 | hp2 | a0002 | c0002 | t0004 | g0219 | EAS | KHV | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | KHV | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | KHV | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02055 | hp1 | a0001 | c0003 | t0002 | g0025 | AFR | ACB | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02055 | hp2 | a0001 | c0001 | t0019 | g0326 | AFR | ACB | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | KHV | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02056 | hp2 | a0002 | c0002 | t0005 | g0062 | EAS | KHV | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | KHV | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02080 | hp2 | a0002 | c0002 | t0002 | g0074 | EAS | KHV | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | KHV | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | KHV | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02132 | hp1 | a0002 | c0002 | t0002 | g0066 | EAS | KHV | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02132 | hp2 | a0001 | c0003 | t0003 | g0136 | EAS | KHV | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02135 | hp1 | a0002 | c0002 | t0002 | g0052 | EAS | KHV | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | KHV | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0241 | AFR | ACB | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0336 | AFR | ACB | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02257 | hp2 | a0001 | c0003 | t0003 | g0143 | AFR | ACB | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0294 | AFR | ACB | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | ACB | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0308 | AMR | PEL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02280 | hp1 | a0001 | c0003 | t0014 | g0110 | AFR | ACB | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02280 | hp2 | a0001 | c0003 | t0004 | g0109 | AFR | ACB | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02300 | hp1 | a0002 | c0002 | t0002 | g0097 | AMR | PEL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PEL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02451 | hp1 | a0001 | c0001 | t0015 | g0159 | AFR | ACB | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02523 | hp1 | a0001 | c0001 | t0004 | g0275 | EAS | KHV | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02523 | hp2 | a0001 | c0003 | t0002 | g0061 | EAS | KHV | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02572 | hp1 | a0001 | c0001 | t0009 | g0201 | AFR | GWD | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0177 | AFR | GWD | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02602 | hp1 | a0001 | c0003 | t0003 | g0149 | SAS | PJL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02602 | hp2 | a0002 | c0002 | t0002 | g0022 | SAS | PJL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02615 | hp1 | a0002 | c0002 | t0002 | g0057 | AFR | GWD | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02615 | hp2 | a0001 | c0003 | t0006 | g0119 | AFR | GWD | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0153 | AFR | GWD | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02622 | hp2 | a0002 | c0002 | t0002 | g0054 | AFR | GWD | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0335 | AFR | GWD | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02683 | hp1 | a0002 | c0002 | t0002 | g0067 | SAS | PJL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02698 | hp1 | a0001 | c0003 | t0003 | g0148 | SAS | PJL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02717 | hp1 | a0001 | c0001 | t0008 | g0331 | AFR | GWD | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | GWD | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02723 | hp1 | a0002 | c0002 | t0002 | g0083 | AFR | GWD | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02735 | hp1 | a0001 | c0003 | t0003 | g0140 | SAS | PJL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0318 | SAS | PJL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02738 | hp1 | a0001 | c0003 | t0003 | g0132 | SAS | PJL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02809 | hp1 | a0002 | c0002 | t0002 | g0084 | AFR | GWD | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02809 | hp2 | a0001 | c0003 | t0006 | g0116 | AFR | GWD | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02818 | hp1 | a0002 | c0002 | t0002 | g0059 | AFR | GWD | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02818 | hp2 | a0003 | c0005 | t0004 | g0334 | AFR | GWD | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02886 | hp1 | a0001 | c0003 | t0002 | g0055 | AFR | GWD | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0233 | AFR | GWD | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02895 | hp1 | a0001 | c0001 | t0009 | g0214 | AFR | GWD | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02895 | hp2 | a0001 | c0001 | t0007 | g0327 | AFR | GWD | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02896 | hp2 | a0001 | c0003 | t0003 | g0340 | AFR | GWD | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02897 | hp1 | a0001 | c0001 | t0007 | g0325 | AFR | GWD | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02897 | hp2 | a0001 | c0003 | t0003 | g0339 | AFR | GWD | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02922 | hp1 | a0001 | c0001 | t0013 | g0266 | AFR | ESN | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ESN | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02970 | hp1 | a0002 | c0002 | t0011 | g0072 | AFR | ESN | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02976 | hp1 | a0002 | c0002 | t0003 | g0123 | AFR | ESN | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02976 | hp2 | a0001 | c0001 | t0008 | g0329 | AFR | ESN | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03017 | hp1 | a0002 | c0002 | t0005 | g0060 | SAS | PJL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03041 | hp2 | a0001 | c0001 | t0006 | g0152 | AFR | GWD | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03098 | hp1 | a0002 | c0002 | t0002 | g0017 | AFR | MSL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | MSL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ESN | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03139 | hp2 | a0001 | c0003 | t0002 | g0126 | AFR | ESN | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03195 | hp1 | a0001 | c0003 | t0017 | g0122 | AFR | ESN | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03195 | hp2 | a0002 | c0002 | t0003 | g0124 | AFR | ESN | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0121 | AFR | MSL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03209 | hp2 | a0001 | c0003 | t0001 | g0237 | AFR | MSL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03225 | hp1 | a0002 | c0004 | t0005 | g0305 | AFR | MSL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03225 | hp2 | a0002 | c0002 | t0002 | g0056 | AFR | MSL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03239 | hp1 | a0001 | c0003 | t0002 | g0065 | SAS | PJL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0320 | SAS | PJL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03453 | hp1 | a0001 | c0003 | t0003 | g0296 | AFR | MSL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03453 | hp2 | a0002 | c0002 | t0002 | g0053 | AFR | MSL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0245 | AFR | MSL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03486 | hp2 | a0001 | c0003 | t0003 | g0295 | AFR | MSL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0300 | SAS | PJL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03490 | hp2 | a0002 | c0004 | t0002 | g0330 | SAS | PJL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0291 | SAS | PJL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ESN | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03516 | hp2 | a0001 | c0003 | t0001 | g0113 | AFR | ESN | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03540 | hp1 | a0001 | c0003 | t0004 | g0112 | AFR | GWD | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03540 | hp2 | a0003 | c0005 | t0004 | g0333 | AFR | GWD | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | MSL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0312 | AFR | MSL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0324 | SAS | PJL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03654 | hp2 | a0002 | c0002 | t0002 | g0050 | SAS | PJL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | PJL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03704 | hp2 | a0001 | c0007 | t0003 | g0128 | SAS | PJL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0316 | SAS | PJL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03710 | hp2 | a0002 | c0002 | t0002 | g0026 | SAS | PJL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0315 | SAS | BEB | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0302 | SAS | BEB | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG04199 | hp1 | a0002 | c0002 | t0002 | g0027 | SAS | STU | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG04199 | hp2 | a0003 | c0005 | t0010 | g0310 | SAS | STU | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0342 | AFR | YRI | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18522 | hp2 | a0001 | c0003 | t0003 | g0125 | AFR | YRI | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18612 | hp1 | a0002 | c0004 | t0001 | g0222 | EAS | CHB | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18612 | hp2 | a0002 | c0002 | t0002 | g0103 | EAS | CHB | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | CHB | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | CHB | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0244 | AFR | YRI | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18906 | hp2 | a0001 | c0001 | t0020 | g0309 | AFR | YRI | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18939 | hp2 | a0002 | c0002 | t0002 | g0343 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18941 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18942 | hp2 | a0001 | c0003 | t0002 | g0087 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18944 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18944 | hp2 | a0001 | c0003 | t0002 | g0046 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18945 | hp2 | a0001 | c0003 | t0002 | g0085 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18946 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18947 | hp2 | a0002 | c0002 | t0002 | g0077 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18948 | hp1 | a0002 | c0004 | t0001 | g0205 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18951 | hp2 | a0001 | c0003 | t0003 | g0138 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18952 | hp1 | a0002 | c0002 | t0002 | g0049 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18953 | hp1 | a0002 | c0002 | t0002 | g0064 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18956 | hp1 | a0002 | c0002 | t0005 | g0063 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18964 | hp2 | a0001 | c0003 | t0002 | g0038 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18965 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18975 | hp1 | a0002 | c0002 | t0005 | g0070 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18975 | hp2 | a0002 | c0002 | t0002 | g0105 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18978 | hp2 | a0002 | c0004 | t0001 | g0204 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18979 | hp1 | a0002 | c0002 | t0002 | g0044 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18980 | hp2 | a0002 | c0002 | t0002 | g0096 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18981 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18983 | hp1 | a0001 | c0003 | t0002 | g0041 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18984 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18988 | hp2 | a0001 | c0003 | t0002 | g0042 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18993 | hp1 | a0002 | c0002 | t0002 | g0071 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18995 | hp1 | a0002 | c0002 | t0002 | g0106 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18995 | hp2 | a0002 | c0002 | t0002 | g0102 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18998 | hp1 | a0002 | c0002 | t0002 | g0104 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18998 | hp2 | a0002 | c0002 | t0002 | g0093 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18999 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19003 | hp1 | a0002 | c0009 | t0002 | g0037 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19004 | hp2 | a0002 | c0002 | t0002 | g0045 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19005 | hp2 | a0002 | c0002 | t0002 | g0068 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19007 | hp2 | a0002 | c0002 | t0002 | g0051 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19009 | hp1 | a0002 | c0002 | t0012 | g0088 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0307 | AFR | LWK | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19030 | hp2 | a0006 | c0006 | t0002 | g0120 | AFR | LWK | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0293 | AFR | LWK | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0242 | AFR | LWK | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19056 | hp1 | a0002 | c0002 | t0002 | g0040 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19056 | hp2 | a0002 | c0002 | t0002 | g0099 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19057 | hp1 | a0002 | c0002 | t0002 | g0076 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19063 | hp1 | a0001 | c0003 | t0003 | g0139 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19063 | hp2 | a0002 | c0002 | t0002 | g0080 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19064 | hp1 | a0002 | c0004 | t0001 | g0301 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19064 | hp2 | a0002 | c0002 | t0002 | g0047 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19068 | hp1 | a0007 | c0010 | t0001 | g0158 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19068 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19070 | hp1 | a0002 | c0002 | t0002 | g0039 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19074 | hp1 | a0002 | c0002 | t0002 | g0098 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19076 | hp1 | a0001 | c0003 | t0002 | g0011 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19077 | hp2 | a0002 | c0004 | t0001 | g0297 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19079 | hp2 | a0002 | c0004 | t0001 | g0163 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19080 | hp2 | a0002 | c0002 | t0002 | g0107 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19083 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19087 | hp1 | a0002 | c0002 | t0002 | g0108 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19087 | hp2 | a0001 | c0003 | t0002 | g0043 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19088 | hp1 | a0002 | c0002 | t0002 | g0100 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0341 | AFR | YRI | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | YRI | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA20129 | hp1 | a0002 | c0002 | t0002 | g0092 | AFR | ASW | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA20129 | hp2 | a0001 | c0001 | t0007 | g0243 | AFR | ASW | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0238 | EUR | TSI | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0319 | EUR | TSI | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA20805 | hp1 | a0001 | c0003 | t0002 | g0020 | EUR | TSI | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0178 | EUR | TSI | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA20905 | hp1 | a0001 | c0003 | t0002 | g0028 | SAS | GIH | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0304 | SAS | GIH | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01123 | hp1 | a0001 | c0003 | t0002 | g0036 | AMR | CLM | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01123 | hp2 | a0001 | c0003 | t0003 | g0135 | AMR | CLM | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02109 | hp1 | a0001 | c0001 | t0007 | g0332 | AFR | ACB | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02109 | hp2 | a0002 | c0002 | t0002 | g0095 | AFR | ACB | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02486 | hp1 | a0002 | c0002 | t0002 | g0094 | AFR | ACB | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0314 | AFR | ACB | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02559 | hp1 | a0005 | c0011 | t0002 | g0117 | AFR | ACB | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02559 | hp2 | a0001 | c0003 | t0002 | g0058 | AFR | ACB | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | MSL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | MSL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | USA | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG06807 | hp2 | a0002 | c0002 | t0002 | g0082 | AFR | USA | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18955 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA20300 | hp1 | a0002 | c0002 | t0018 | g0016 | AFR | USA | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA20300 | hp2 | a0001 | c0003 | t0004 | g0111 | AFR | USA | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA21309 | hp1 | a0002 | c0002 | t0002 | g0081 | AFR | LWK | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA21309 | hp2 | a0001 | c0003 | t0003 | g0118 | AFR | LWK | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0194 | REF | REF | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| homoSapiens | grch38p0 | a0001 | c0003 | t0016 | g0144 | REF | REF | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:57592098 | C | T | 1 | a0005 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.64C>T | p.Pro22Ser | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/13 | 195/2398 | 64/1401 | 22/466 | chr15 | 57592098 | |||
| chr15:57618043 | T | C | 1 | a0003 | 3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
missense_variant | MODERATE | c.173T>C | p.Leu58Pro | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/13 | 304/2398 | 173/1401 | 58/466 | chr15 | 57618043 | |||
| chr15:57633638 | C | T | 1 | a0002 | 91 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(88): Show |
missense_variant | MODERATE | c.830C>T | p.Ala277Val | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/13 | 961/2398 | 830/1401 | 277/466 | chr15 | 57633638 | |||
| chr15:57633675 | G | C | 1 | a0006 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.867G>C | p.Glu289Asp | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/13 | 998/2398 | 867/1401 | 289/466 | chr15 | 57633675 | |||
| chr15:57637729 | A | G | 1 | a0004 | 1 | HG01175.hp2 | missense_variant | MODERATE | c.968A>G | p.His323Arg | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 9/13 | 1099/2398 | 968/1401 | 323/466 | chr15 | 57637729 | |||
| chr15:57661450 | A | T | 1 | a0007 | 1 | NA19068.hp1 | missense_variant&splice_region_variant | MODERATE | c.1120A>T | p.Ile374Phe | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/13 | 1251/2398 | 1120/1401 | 374/466 | chr15 | 57661450 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:57625871 | A | G | 5 | a0001c0001 a0002c0004 a0003c0005 others(2): Show |
187 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(184): Show |
synonymous_variant | LOW | c.504A>G | p.Ala168Ala | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/13 | 635/2398 | 504/1401 | 168/466 | chr15 | 57625871 | |||
| chr15:57633684 | A | G | 1 | a0002c0009 | 1 | NA19003.hp1 | synonymous_variant | LOW | c.876A>G | p.Leu292Leu | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/13 | 1007/2398 | 876/1401 | 292/466 | chr15 | 57633684 | |||
| chr15:57633726 | T | C | 1 | a0001c0007 | 1 | HG03704.hp2 | synonymous_variant | LOW | c.918T>C | p.Ile306Ile | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/13 | 1049/2398 | 918/1401 | 306/466 | chr15 | 57633726 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:57591983 | T | C | 29 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(26): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(298): Show |
5_prime_UTR_variant | MODIFIER | c.-52T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/13 | 52 | chr15 | 57591983 | ||||||
| chr15:57591999 | G | A | 1 | a0001c0001t0009 | 2 | HG02572.hp1 HG02895.hp1 |
5_prime_UTR_variant | MODIFIER | c.-36G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/13 | 36 | chr15 | 57591999 | ||||||
| chr15:57592018 | C | G | 4 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0019 others(1): Show |
9 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-17C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/13 | 17 | chr15 | 57592018 | ||||||
| chr15:57592021 | A | G | 13 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0009 others(10): Show |
162 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(159): Show |
5_prime_UTR_variant | MODIFIER | c.-14A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/13 | 14 | chr15 | 57592021 | ||||||
| chr15:57684598 | G | T | 1 | a0001c0001t0020 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*100G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 13/13 | 100 | chr15 | 57684598 | ||||||
| chr15:57684614 | G | A | 5 | a0001c0001t0006 a0001c0001t0013 a0001c0001t0020 others(2): Show |
7 | HG01109.hp2 HG02615.hp2 HG02809.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*116G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 13/13 | 116 | chr15 | 57684614 | ||||||
| chr15:57684724 | C | T | 4 | a0001c0001t0006 a0001c0001t0013 a0001c0001t0020 others(1): Show |
6 | HG01109.hp2 HG02615.hp2 HG02809.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*226C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 13/13 | 226 | chr15 | 57684724 | ||||||
| chr15:57684921 | C | T | 1 | a0002c0002t0012 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*423C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 13/13 | 423 | chr15 | 57684921 | ||||||
| chr15:57684940 | G | A | 1 | a0001c0003t0014 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*442G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 13/13 | 442 | chr15 | 57684940 | ||||||
| chr15:57684991 | AG | A | 11 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0019 others(8): Show |
27 | HG00558.hp1 HG00738.hp1 HG01891.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*496delG | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 13/13 | 496 | INFO_REALIGN_3_PRIME | chr15 | 57684991 | |||||
| chr15:57685172 | A | T | 29 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(26): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
3_prime_UTR_variant | MODIFIER | c.*674A>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 13/13 | 674 | chr15 | 57685172 | ||||||
| chr15:57685192 | CACTTTA | C | 2 | a0001c0001t0008 a0001c0003t0017 |
4 | HG01884.hp1 HG02717.hp1 HG02976.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*699_*704delTAACTT | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 13/13 | 699 | INFO_REALIGN_3_PRIME | chr15 | 57685192 | |||||
| chr15:57685274 | C | T | 1 | a0002c0002t0011 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*776C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 13/13 | 776 | chr15 | 57685274 | ||||||
| chr15:57685281 | A | G | 1 | a0001c0001t0015 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*783A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 13/13 | 783 | chr15 | 57685281 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:57592139 | TCCCGTTC others(18): Show |
T | 1 | a0002c0002t0002g0343 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.75+32_75+56delCCGT others(21): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57592139 | ||||||
| chr15:57592297 | C | T | 2 | a0001c0001t0001g0341 a0001c0001t0001g0342 |
2 | NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.75+188C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57592297 | |||||||
| chr15:57592319 | G | A | 4 | a0001c0003t0002g0011 a0002c0002t0002g0009 a0002c0002t0002g0010 others(1): Show |
4 | HG00597.hp1 NA18965.hp1 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+210G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57592319 | |||||||
| chr15:57592357 | T | C | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01167.hp1 HG01169.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+248T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57592357 | |||||||
| chr15:57592604 | C | T | 2 | a0001c0003t0003g0339 a0001c0003t0003g0340 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.75+495C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57592604 | |||||||
| chr15:57592973 | G | A | 1 | a0002c0002t0018g0016 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.75+864G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57592973 | |||||||
| chr15:57593093 | A | G | 2 | a0001c0001t0001g0337 a0001c0001t0001g0338 |
2 | HG02083.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.75+984A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57593093 | |||||||
| chr15:57593139 | GGT | G | 103 | a0001c0001t0002g0034 a0001c0003t0002g0003 a0001c0003t0002g0011 others(100): Show |
110 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.75+1040_75+1041del others(2): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593139 | ||||||
| chr15:57593170 | T | C | 1 | a0002c0002t0002g0017 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.75+1061T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57593170 | |||||||
| chr15:57593188 | G | GCA | 83 | a0001c0001t0002g0034 a0001c0001t0005g0121 a0001c0003t0002g0003 others(80): Show |
88 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.75+1105_75+1106dup others(2): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCACA | 14 | a0001c0003t0002g0018 a0001c0003t0002g0019 a0001c0003t0002g0020 others(11): Show |
15 | HG00140.hp2 HG00323.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.75+1103_75+1106dup others(4): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCACACA | 3 | a0001c0003t0001g0113 a0001c0003t0004g0112 a0001c0003t0004g0114 |
3 | HG01891.hp1 HG03516.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.75+1101_75+1106dup others(6): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCACACAC others(3): Show |
2 | a0001c0003t0004g0111 a0001c0003t0014g0110 |
2 | HG02280.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.75+1097_75+1106dup others(10): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCACACAC others(5): Show |
1 | a0001c0003t0004g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.75+1095_75+1106dup others(12): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(35): Show |
1 | a0001c0001t0001g0157 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.75+1081_75+1082ins others(42): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(19): Show |
1 | a0001c0001t0015g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.75+1081_75+1082ins others(26): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(21): Show |
1 | a0007c0010t0001g0158 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.75+1081_75+1082ins others(28): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(19): Show |
1 | a0001c0001t0001g0181 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.75+1081_75+1082ins others(26): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(21): Show |
3 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0180 |
3 | HG02922.hp2 HG02970.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.75+1081_75+1082ins others(28): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(23): Show |
3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 |
3 | HG00735.hp1 HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.75+1081_75+1082ins others(30): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(25): Show |
6 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(3): Show |
6 | HG01074.hp1 HG01175.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+1081_75+1082ins others(32): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(27): Show |
2 | a0001c0001t0001g0167 a0001c0003t0001g0171 |
2 | HG01074.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.75+1081_75+1082ins others(34): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(29): Show |
3 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 |
3 | HG00423.hp1 HG00609.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.75+1081_75+1082ins others(36): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(31): Show |
1 | a0001c0001t0001g0161 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.75+1081_75+1082ins others(38): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(33): Show |
2 | a0001c0001t0001g0162 a0002c0004t0001g0163 |
2 | HG02027.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.75+1081_75+1082ins others(40): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(35): Show |
1 | a0001c0001t0001g0160 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.75+1081_75+1082ins others(42): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(17): Show |
1 | a0001c0001t0007g0243 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.75+1081_75+1082ins others(24): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(19): Show |
1 | a0001c0001t0001g0239 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.75+1081_75+1082ins others(26): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(21): Show |
5 | a0001c0001t0001g0236 a0001c0001t0004g0007 a0001c0001t0004g0244 others(2): Show |
6 | HG02717.hp2 HG03209.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.75+1081_75+1082ins others(28): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(23): Show |
9 | a0001c0001t0001g0226 a0001c0001t0001g0228 a0001c0001t0001g0229 others(6): Show |
9 | HG00621.hp1 HG02004.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.75+1081_75+1082ins others(30): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(25): Show |
17 | a0001c0001t0001g0213 a0001c0001t0001g0215 a0001c0001t0001g0216 others(14): Show |
17 | HG00673.hp2 HG00741.hp2 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.75+1081_75+1082ins others(32): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(27): Show |
12 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0206 others(9): Show |
12 | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.75+1081_75+1082ins others(34): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(29): Show |
7 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0202 others(4): Show |
7 | HG02572.hp1 NA18747.hp2 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+1081_75+1082ins others(36): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(31): Show |
3 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0198 |
3 | HG01258.hp1 HG01515.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.75+1081_75+1082ins others(38): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(33): Show |
5 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(2): Show |
5 | HG00544.hp2 HG01109.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+1081_75+1082ins others(40): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(35): Show |
5 | a0001c0001t0001g0013 a0001c0001t0001g0184 a0001c0001t0001g0188 others(2): Show |
5 | HG02071.hp1 HG02451.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.75+1081_75+1082ins others(42): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(37): Show |
3 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 |
3 | HG02273.hp1 NA18957.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.75+1081_75+1082ins others(44): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(39): Show |
2 | a0001c0001t0001g0182 a0001c0001t0001g0183 |
2 | HG01257.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.75+1081_75+1082ins others(46): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(27): Show |
2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | HG02698.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.75+1081_75+1082ins others(34): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(29): Show |
1 | a0001c0001t0001g0250 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.75+1081_75+1082ins others(36): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(33): Show |
3 | a0001c0001t0001g0008 a0001c0001t0001g0248 a0001c0001t0001g0249 |
4 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+1081_75+1082ins others(40): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(21): Show |
4 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0001g0276 others(1): Show |
4 | HG02015.hp1 HG02523.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+1081_75+1082ins others(28): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(23): Show |
1 | a0001c0001t0001g0272 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.75+1081_75+1082ins others(30): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(25): Show |
2 | a0001c0001t0001g0270 a0001c0001t0001g0271 |
2 | NA18943.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.75+1081_75+1082ins others(32): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(27): Show |
1 | a0001c0001t0001g0269 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.75+1081_75+1082ins others(34): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(29): Show |
4 | a0001c0001t0001g0265 a0001c0001t0001g0267 a0001c0001t0001g0268 others(1): Show |
4 | HG00642.hp2 HG01978.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+1081_75+1082ins others(36): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(31): Show |
3 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 |
3 | HG01952.hp1 NA18941.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.75+1081_75+1082ins others(38): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(33): Show |
3 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0260 |
3 | HG01934.hp2 NA18957.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.75+1081_75+1082ins others(40): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(35): Show |
3 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0261 |
3 | NA18947.hp1 NA18983.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.75+1081_75+1082ins others(42): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(37): Show |
1 | a0001c0001t0001g0257 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.75+1081_75+1082ins others(44): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(39): Show |
1 | a0001c0001t0001g0254 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.75+1081_75+1082ins others(46): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(43): Show |
1 | a0001c0001t0001g0253 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.75+1081_75+1082ins others(50): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(51): Show |
1 | a0001c0001t0001g0252 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.75+1081_75+1082ins others(58): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(67): Show |
1 | a0001c0001t0001g0251 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.75+1081_75+1082ins others(74): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(21): Show |
2 | a0001c0001t0001g0298 a0002c0004t0001g0297 |
2 | HG01099.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.75+1081_75+1082ins others(28): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(25): Show |
4 | a0001c0001t0003g0293 a0001c0001t0003g0294 a0001c0003t0003g0295 others(1): Show |
4 | HG02258.hp1 HG03453.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+1081_75+1082ins others(32): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(31): Show |
4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG00597.hp2 NA18948.hp2 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+1081_75+1082ins others(38): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(33): Show |
4 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0291 others(1): Show |
4 | HG02040.hp1 HG02896.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+1081_75+1082ins others(40): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(35): Show |
2 | a0001c0001t0001g0287 a0001c0003t0003g0339 |
2 | HG02135.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.75+1081_75+1082ins others(42): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(37): Show |
3 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 |
3 | HG02056.hp1 NA18988.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.75+1081_75+1082ins others(44): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(41): Show |
2 | a0001c0001t0001g0280 a0001c0001t0001g0281 |
2 | NA18984.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.75+1081_75+1082ins others(48): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(45): Show |
2 | a0001c0001t0001g0278 a0001c0001t0001g0279 |
2 | HG02040.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.75+1081_75+1082ins others(52): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(55): Show |
1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.75+1081_75+1082ins others(62): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(21): Show |
1 | a0001c0001t0002g0304 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.75+1081_75+1082ins others(28): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(23): Show |
1 | a0001c0001t0001g0303 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.75+1081_75+1082ins others(30): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(27): Show |
1 | a0001c0001t0001g0302 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.75+1081_75+1082ins others(34): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(31): Show |
2 | a0001c0001t0001g0338 a0002c0004t0001g0301 |
2 | HG02083.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.75+1081_75+1082ins others(38): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(35): Show |
1 | a0001c0001t0001g0300 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.75+1081_75+1082ins others(42): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(41): Show |
1 | a0001c0001t0001g0299 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.75+1081_75+1082ins others(48): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(23): Show |
2 | a0001c0001t0002g0307 a0001c0001t0002g0308 |
2 | HG02273.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.75+1081_75+1082ins others(30): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(25): Show |
1 | a0001c0001t0002g0306 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.75+1081_75+1082ins others(32): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(27): Show |
1 | a0002c0004t0005g0305 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.75+1081_75+1082ins others(34): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(25): Show |
7 | a0001c0001t0002g0318 a0001c0001t0002g0319 a0001c0001t0002g0320 others(4): Show |
7 | HG01928.hp2 HG01978.hp2 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+1081_75+1082ins others(32): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(27): Show |
5 | a0001c0001t0002g0313 a0001c0001t0002g0314 a0001c0001t0002g0315 others(2): Show |
5 | HG00642.hp1 HG01081.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+1081_75+1082ins others(34): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(29): Show |
1 | a0001c0001t0003g0312 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.75+1081_75+1082ins others(36): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(31): Show |
1 | a0001c0001t0003g0311 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.75+1081_75+1082ins others(38): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(35): Show |
1 | a0001c0001t0020g0309 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.75+1081_75+1082ins others(42): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(41): Show |
1 | a0003c0005t0010g0310 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.75+1081_75+1082ins others(48): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(25): Show |
1 | a0003c0005t0004g0334 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.75+1081_75+1082ins others(32): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(29): Show |
1 | a0003c0005t0004g0333 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.75+1081_75+1082ins others(36): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(31): Show |
2 | a0001c0001t0007g0332 a0001c0001t0008g0331 |
2 | HG02109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.75+1081_75+1082ins others(38): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(33): Show |
2 | a0001c0001t0008g0329 a0002c0004t0002g0330 |
2 | HG02976.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.75+1081_75+1082ins others(40): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(35): Show |
1 | a0001c0001t0008g0328 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.75+1081_75+1082ins others(42): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(37): Show |
1 | a0001c0001t0007g0327 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.75+1081_75+1082ins others(44): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCATGCGC others(39): Show |
2 | a0001c0001t0007g0325 a0001c0001t0019g0326 |
2 | HG02055.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.75+1081_75+1082ins others(46): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | G | GCGCGCAC others(5): Show |
2 | a0002c0002t0001g0335 a0002c0002t0001g0336 |
2 | HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.75+1080_75+1081ins others(12): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | GCA | G | 15 | a0002c0002t0002g0006 a0002c0002t0002g0096 a0002c0002t0002g0097 others(12): Show |
16 | HG00673.hp1 HG02083.hp1 HG02300.hp1 others(13): Show |
intron_variant | MODIFIER | c.75+1105_75+1106del others(2): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593188 | GCACA | G | 3 | a0001c0003t0003g0154 a0001c0003t0003g0155 a0001c0003t0003g0156 |
3 | HG01069.hp2 HG01071.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.75+1103_75+1106del others(4): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593188 | ||||||
| chr15:57593208 | A | T | 1 | a0003c0005t0010g0310 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.75+1099A>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57593208 | |||||||
| chr15:57593212 | A | C | 8 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0240 others(5): Show |
9 | HG02145.hp1 HG02145.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.75+1103A>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57593212 | |||||||
| chr15:57593212 | A | T | 1 | a0003c0005t0010g0310 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.75+1103A>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57593212 | |||||||
| chr15:57593214 | A | ACCCCCCC others(4): Show |
1 | a0001c0003t0003g0339 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.75+1109_75+1110ins others(11): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593214 | ||||||
| chr15:57593214 | A | ACCCCCCC others(5): Show |
1 | a0001c0003t0003g0340 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.75+1109_75+1110ins others(12): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593214 | ||||||
| chr15:57593214 | A | C | 44 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0175 others(41): Show |
45 | HG00099.hp2 HG00642.hp1 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.75+1105A>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57593214 | |||||||
| chr15:57593215 | C | CA | 4 | a0001c0001t0001g0161 a0001c0001t0001g0184 a0001c0001t0001g0277 others(1): Show |
4 | HG01192.hp2 HG02071.hp1 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+1106_75+1107ins others(1): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57593215 | |||||||
| chr15:57593216 | C | CCCCCCCC others(6): Show |
2 | a0001c0001t0003g0311 a0001c0001t0003g0312 |
2 | HG01243.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.75+1109_75+1110ins others(13): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57593216 | ||||||
| chr15:57593504 | A | C | 1 | a0005c0011t0002g0117 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.75+1395A>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57593504 | |||||||
| chr15:57593667 | A | G | 4 | a0001c0001t0003g0293 a0001c0001t0003g0294 a0001c0003t0003g0295 others(1): Show |
4 | HG02258.hp1 HG03453.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+1558A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57593667 | |||||||
| chr15:57593905 | G | A | 2 | a0001c0001t0003g0311 a0001c0001t0003g0312 |
2 | HG01243.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.75+1796G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57593905 | |||||||
| chr15:57593982 | A | T | 2 | a0001c0003t0003g0339 a0001c0003t0003g0340 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.75+1873A>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57593982 | |||||||
| chr15:57594178 | C | T | 12 | a0001c0003t0001g0113 a0001c0003t0004g0109 a0001c0003t0004g0111 others(9): Show |
12 | HG01255.hp1 HG01891.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.75+2069C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57594178 | |||||||
| chr15:57594184 | C | T | 1 | a0002c0002t0002g0091 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.75+2075C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57594184 | |||||||
| chr15:57594240 | C | T | 1 | a0005c0011t0002g0117 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.75+2131C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57594240 | |||||||
| chr15:57594304 | C | T | 1 | a0002c0002t0002g0127 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.75+2195C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57594304 | |||||||
| chr15:57594357 | A | C | 202 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(199): Show |
204 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(201): Show |
intron_variant | MODIFIER | c.75+2248A>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57594357 | |||||||
| chr15:57594469 | T | A | 10 | a0001c0001t0002g0034 a0001c0003t0002g0003 a0001c0003t0002g0028 others(7): Show |
11 | HG00099.hp1 HG00741.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.75+2360T>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57594469 | |||||||
| chr15:57594488 | G | C | 9 | a0001c0003t0001g0113 a0001c0003t0004g0109 a0001c0003t0004g0111 others(6): Show |
9 | HG01255.hp1 HG01891.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+2379G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57594488 | |||||||
| chr15:57594556 | T | C | 163 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(160): Show |
165 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(162): Show |
intron_variant | MODIFIER | c.75+2447T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57594556 | |||||||
| chr15:57594582 | C | T | 1 | a0001c0003t0005g0090 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.75+2473C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57594582 | |||||||
| chr15:57594688 | C | A | 1 | a0002c0002t0002g0127 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.75+2579C>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57594688 | |||||||
| chr15:57594808 | C | T | 1 | a0001c0001t0001g0230 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.75+2699C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57594808 | |||||||
| chr15:57594824 | T | C | 1 | a0001c0007t0003g0128 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.75+2715T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57594824 | |||||||
| chr15:57594829 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.75+2720T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57594829 | |||||||
| chr15:57594892 | T | A | 1 | a0003c0005t0010g0310 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.75+2783T>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57594892 | |||||||
| chr15:57595403 | T | C | 1 | a0001c0001t0001g0188 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.75+3294T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57595403 | |||||||
| chr15:57595435 | G | C | 2 | a0001c0001t0001g0337 a0001c0001t0001g0338 |
2 | HG02083.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.75+3326G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57595435 | |||||||
| chr15:57595602 | C | T | 1 | a0005c0011t0002g0117 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.75+3493C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57595602 | |||||||
| chr15:57595651 | G | C | 1 | a0007c0010t0001g0158 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.75+3542G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57595651 | |||||||
| chr15:57595716 | C | G | 4 | a0001c0003t0003g0125 a0001c0003t0017g0122 a0002c0002t0003g0123 others(1): Show |
4 | HG02976.hp1 HG03195.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+3607C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57595716 | |||||||
| chr15:57595747 | G | A | 2 | a0001c0003t0004g0109 a0001c0003t0014g0110 |
2 | HG02280.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.75+3638G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57595747 | |||||||
| chr15:57595801 | T | C | 9 | a0001c0003t0002g0038 a0001c0003t0002g0041 a0001c0003t0002g0042 others(6): Show |
9 | NA18964.hp2 NA18979.hp1 NA18983.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+3692T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57595801 | |||||||
| chr15:57595886 | C | G | 1 | a0001c0001t0007g0243 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.75+3777C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57595886 | |||||||
| chr15:57595983 | G | C | 13 | a0001c0001t0001g0161 a0001c0001t0001g0172 a0001c0001t0001g0175 others(10): Show |
13 | HG00735.hp1 HG00741.hp2 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.75+3874G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57595983 | |||||||
| chr15:57596264 | T | C | 1 | a0001c0003t0002g0126 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.75+4155T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57596264 | |||||||
| chr15:57596391 | A | G | 21 | a0001c0001t0002g0153 a0001c0001t0002g0304 a0001c0001t0002g0306 others(18): Show |
21 | HG00099.hp2 HG00642.hp1 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.75+4282A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57596391 | |||||||
| chr15:57596598 | A | G | 2 | a0001c0001t0001g0187 a0001c0001t0001g0252 |
2 | NA18965.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.75+4489A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57596598 | |||||||
| chr15:57596624 | C | T | 1 | a0001c0001t0001g0292 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.75+4515C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57596624 | |||||||
| chr15:57596710 | C | T | 4 | a0001c0001t0003g0293 a0001c0001t0003g0294 a0001c0003t0003g0295 others(1): Show |
4 | HG02258.hp1 HG03453.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+4601C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57596710 | |||||||
| chr15:57596788 | C | T | 3 | a0001c0003t0002g0003 a0001c0003t0002g0035 a0001c0003t0002g0036 |
4 | HG01099.hp1 HG01123.hp1 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+4679C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57596788 | |||||||
| chr15:57596981 | G | A | 1 | a0002c0002t0002g0096 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.75+4872G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57596981 | |||||||
| chr15:57597028 | G | T | 1 | a0001c0001t0002g0308 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.75+4919G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57597028 | |||||||
| chr15:57597149 | C | T | 5 | a0001c0003t0001g0113 a0001c0003t0004g0109 a0001c0003t0004g0111 others(2): Show |
5 | HG01891.hp1 HG02280.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+5040C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57597149 | |||||||
| chr15:57597162 | G | T | 200 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(197): Show |
202 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(199): Show |
intron_variant | MODIFIER | c.75+5053G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57597162 | |||||||
| chr15:57597531 | A | C | 18 | a0001c0001t0002g0304 a0001c0001t0002g0306 a0001c0001t0002g0307 others(15): Show |
18 | HG00099.hp2 HG00642.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.75+5422A>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57597531 | |||||||
| chr15:57597611 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.75+5502G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57597611 | |||||||
| chr15:57597839 | C | T | 18 | a0001c0001t0002g0304 a0001c0001t0002g0306 a0001c0001t0002g0307 others(15): Show |
18 | HG00099.hp2 HG00642.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.75+5730C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57597839 | |||||||
| chr15:57597840 | G | A | 1 | a0005c0011t0002g0117 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.75+5731G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57597840 | |||||||
| chr15:57597904 | T | C | 1 | a0001c0001t0001g0240 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.75+5795T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57597904 | |||||||
| chr15:57598074 | T | A | 1 | a0001c0003t0017g0122 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.75+5965T>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57598074 | |||||||
| chr15:57598085 | A | T | 2 | a0001c0001t0005g0121 a0006c0006t0002g0120 |
2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.75+5976A>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57598085 | |||||||
| chr15:57598086 | C | G | 8 | a0001c0001t0003g0293 a0001c0001t0003g0294 a0001c0001t0003g0311 others(5): Show |
8 | HG01243.hp1 HG02258.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.75+5977C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57598086 | |||||||
| chr15:57598141 | G | C | 1 | a0001c0003t0014g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.75+6032G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57598141 | |||||||
| chr15:57598173 | T | G | 18 | a0001c0001t0002g0304 a0001c0001t0002g0306 a0001c0001t0002g0307 others(15): Show |
18 | HG00099.hp2 HG00642.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.75+6064T>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57598173 | |||||||
| chr15:57598182 | G | A | 18 | a0001c0001t0002g0304 a0001c0001t0002g0306 a0001c0001t0002g0307 others(15): Show |
18 | HG00099.hp2 HG00642.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.75+6073G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57598182 | |||||||
| chr15:57598242 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.76-6027G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57598242 | |||||||
| chr15:57598383 | G | A | 3 | a0001c0001t0001g0231 a0001c0001t0001g0238 a0001c0001t0001g0302 |
3 | HG00741.hp2 HG03942.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.76-5886G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57598383 | |||||||
| chr15:57598477 | T | A | 2 | a0001c0001t0002g0153 a0001c0001t0006g0152 |
2 | HG02622.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.76-5792T>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57598477 | |||||||
| chr15:57598494 | A | T | 4 | a0001c0001t0003g0311 a0001c0001t0003g0312 a0001c0003t0003g0339 others(1): Show |
4 | HG01243.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-5775A>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57598494 | |||||||
| chr15:57598504 | G | A | 1 | a0001c0001t0001g0206 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.76-5765G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57598504 | |||||||
| chr15:57598551 | C | T | 4 | a0001c0003t0002g0087 a0002c0002t0002g0091 a0002c0002t0005g0089 others(1): Show |
4 | HG00438.hp2 HG00558.hp1 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-5718C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57598551 | |||||||
| chr15:57598660 | A | G | 28 | a0001c0001t0001g0232 a0001c0001t0002g0304 a0001c0001t0002g0306 others(25): Show |
28 | HG00099.hp2 HG00642.hp1 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.76-5609A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57598660 | |||||||
| chr15:57598696 | C | G | 5 | a0001c0003t0003g0147 a0001c0003t0003g0148 a0001c0003t0003g0149 others(2): Show |
5 | HG00140.hp1 HG00738.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.76-5573C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57598696 | |||||||
| chr15:57598703 | G | A | 1 | a0001c0001t0002g0313 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.76-5566G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57598703 | |||||||
| chr15:57598705 | A | T | 1 | a0005c0011t0002g0117 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.76-5564A>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57598705 | |||||||
| chr15:57598743 | A | G | 2 | a0002c0002t0002g0044 a0002c0002t0002g0045 |
2 | NA18979.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.76-5526A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57598743 | |||||||
| chr15:57598751 | G | A | 1 | a0001c0003t0002g0046 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.76-5518G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57598751 | |||||||
| chr15:57599043 | G | A | 4 | a0001c0003t0002g0087 a0002c0002t0002g0091 a0002c0002t0005g0089 others(1): Show |
4 | HG00438.hp2 HG00558.hp1 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-5226G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57599043 | |||||||
| chr15:57599352 | A | AT | 26 | a0001c0001t0001g0166 a0001c0001t0001g0212 a0001c0001t0001g0268 others(23): Show |
26 | HG00609.hp1 HG01891.hp1 HG01978.hp1 others(23): Show |
intron_variant | MODIFIER | c.76-4902dupT | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57599352 | ||||||
| chr15:57599352 | A | ATT | 103 | a0001c0001t0001g0264 a0001c0001t0002g0034 a0001c0001t0005g0121 others(100): Show |
110 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.76-4903_76-4902dup others(2): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57599352 | ||||||
| chr15:57599352 | A | ATTT | 6 | a0001c0003t0002g0085 a0001c0003t0006g0115 a0001c0003t0006g0116 others(3): Show |
6 | HG00423.hp2 HG01109.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.76-4904_76-4902dup others(3): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57599352 | ||||||
| chr15:57599352 | AT | A | 8 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(5): Show |
8 | HG01081.hp1 HG02451.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.76-4902delT | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57599352 | ||||||
| chr15:57599429 | G | A | 1 | a0001c0001t0008g0328 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.76-4840G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57599429 | |||||||
| chr15:57599647 | G | A | 1 | a0001c0001t0003g0312 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.76-4622G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57599647 | |||||||
| chr15:57599660 | A | T | 18 | a0001c0001t0002g0304 a0001c0001t0002g0306 a0001c0001t0002g0307 others(15): Show |
18 | HG00099.hp2 HG00642.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.76-4609A>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57599660 | |||||||
| chr15:57599757 | C | A | 8 | a0001c0001t0007g0243 a0001c0001t0007g0325 a0001c0001t0007g0327 others(5): Show |
8 | HG01884.hp1 HG02055.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.76-4512C>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57599757 | |||||||
| chr15:57599958 | A | T | 1 | a0001c0001t0001g0240 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.76-4311A>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57599958 | |||||||
| chr15:57599961 | C | A | 1 | a0001c0001t0001g0250 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.76-4308C>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57599961 | |||||||
| chr15:57600002 | C | A | 18 | a0001c0001t0002g0304 a0001c0001t0002g0306 a0001c0001t0002g0307 others(15): Show |
18 | HG00099.hp2 HG00642.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.76-4267C>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57600002 | |||||||
| chr15:57600032 | C | T | 2 | a0001c0001t0002g0153 a0001c0001t0006g0152 |
2 | HG02622.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.76-4237C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57600032 | |||||||
| chr15:57600331 | G | A | 8 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(5): Show |
8 | HG02258.hp1 HG02451.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.76-3938G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57600331 | |||||||
| chr15:57600768 | A | T | 19 | a0001c0001t0002g0304 a0001c0001t0002g0306 a0001c0001t0002g0307 others(16): Show |
19 | HG00099.hp2 HG00642.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.76-3501A>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57600768 | |||||||
| chr15:57600976 | C | G | 19 | a0001c0001t0002g0304 a0001c0001t0002g0306 a0001c0001t0002g0307 others(16): Show |
19 | HG00099.hp2 HG00642.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.76-3293C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57600976 | |||||||
| chr15:57601032 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.76-3237C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57601032 | |||||||
| chr15:57601054 | C | T | 16 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(13): Show |
16 | HG01243.hp1 HG02258.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.76-3215C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57601054 | |||||||
| chr15:57601059 | G | C | 8 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(5): Show |
8 | HG02258.hp1 HG02451.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.76-3210G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57601059 | |||||||
| chr15:57601136 | T | C | 1 | a0001c0001t0003g0293 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.76-3133T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57601136 | |||||||
| chr15:57601274 | T | TTG | 240 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(237): Show |
248 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(245): Show |
intron_variant | MODIFIER | c.76-2970_76-2969dup others(2): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57601274 | ||||||
| chr15:57601274 | T | TTGTG | 13 | a0001c0001t0001g0260 a0001c0001t0001g0277 a0001c0001t0001g0279 others(10): Show |
13 | HG02135.hp2 HG02257.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.76-2972_76-2969dup others(4): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57601274 | ||||||
| chr15:57601274 | T | TTGTGTG | 6 | a0001c0001t0007g0325 a0001c0001t0007g0327 a0001c0001t0008g0328 others(3): Show |
6 | HG01884.hp1 HG02055.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.76-2974_76-2969dup others(6): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57601274 | ||||||
| chr15:57601274 | T | TTGTGTGT others(1): Show |
16 | a0001c0001t0002g0304 a0001c0001t0002g0307 a0001c0001t0002g0308 others(13): Show |
16 | HG00642.hp1 HG01928.hp2 HG01978.hp2 others(13): Show |
intron_variant | MODIFIER | c.76-2976_76-2969dup others(8): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57601274 | ||||||
| chr15:57601274 | T | TTGTGTGT others(3): Show |
10 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(7): Show |
10 | HG00099.hp2 HG01081.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-2978_76-2969dup others(10): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57601274 | ||||||
| chr15:57601274 | TTG | T | 7 | a0001c0001t0001g0008 a0001c0001t0001g0161 a0001c0001t0001g0248 others(4): Show |
8 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.76-2970_76-2969del others(2): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57601274 | ||||||
| chr15:57601309 | C | G | 1 | a0001c0003t0003g0146 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.76-2960C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57601309 | |||||||
| chr15:57601678 | G | A | 2 | a0003c0005t0004g0333 a0003c0005t0004g0334 |
2 | HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.76-2591G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57601678 | |||||||
| chr15:57601685 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.76-2584C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57601685 | |||||||
| chr15:57601773 | G | A | 2 | a0001c0001t0002g0153 a0001c0001t0006g0152 |
2 | HG02622.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.76-2496G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57601773 | |||||||
| chr15:57602015 | G | A | 1 | a0002c0002t0002g0083 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.76-2254G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57602015 | |||||||
| chr15:57602038 | T | C | 317 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(314): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(323): Show |
intron_variant | MODIFIER | c.76-2231T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57602038 | |||||||
| chr15:57602191 | G | A | 1 | a0002c0002t0018g0016 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.76-2078G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57602191 | |||||||
| chr15:57602245 | T | G | 35 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(32): Show |
35 | HG00099.hp2 HG00642.hp1 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.76-2024T>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57602245 | |||||||
| chr15:57602357 | C | T | 146 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(143): Show |
148 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(145): Show |
intron_variant | MODIFIER | c.76-1912C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57602357 | |||||||
| chr15:57602387 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.76-1882G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57602387 | |||||||
| chr15:57602422 | T | G | 8 | a0001c0003t0001g0113 a0001c0003t0004g0109 a0001c0003t0004g0111 others(5): Show |
8 | HG01891.hp1 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.76-1847T>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57602422 | |||||||
| chr15:57602450 | A | G | 1 | a0001c0001t0001g0267 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.76-1819A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57602450 | |||||||
| chr15:57602595 | A | C | 1 | a0001c0001t0001g0172 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.76-1674A>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57602595 | |||||||
| chr15:57602597 | G | A | 5 | a0001c0001t0003g0311 a0001c0001t0003g0312 a0001c0003t0001g0237 others(2): Show |
5 | HG01243.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.76-1672G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57602597 | |||||||
| chr15:57602611 | A | G | 2 | a0003c0005t0004g0333 a0003c0005t0004g0334 |
2 | HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.76-1658A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57602611 | |||||||
| chr15:57602793 | G | A | 2 | a0002c0002t0002g0009 a0002c0002t0002g0010 |
2 | NA18965.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.76-1476G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57602793 | |||||||
| chr15:57602804 | G | C | 76 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(73): Show |
76 | HG00544.hp2 HG00558.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.76-1465G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57602804 | |||||||
| chr15:57602900 | A | G | 6 | a0001c0001t0007g0325 a0001c0001t0007g0327 a0001c0001t0008g0328 others(3): Show |
6 | HG01884.hp1 HG02055.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.76-1369A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57602900 | |||||||
| chr15:57602967 | A | G | 1 | a0001c0003t0004g0114 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.76-1302A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57602967 | |||||||
| chr15:57603048 | C | T | 3 | a0001c0001t0002g0153 a0003c0005t0004g0333 a0003c0005t0004g0334 |
3 | HG02622.hp1 HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.76-1221C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57603048 | |||||||
| chr15:57603113 | G | A | 1 | a0003c0005t0010g0310 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.76-1156G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57603113 | |||||||
| chr15:57603155 | G | A | 98 | a0001c0001t0001g0270 a0001c0001t0002g0034 a0001c0003t0001g0227 others(95): Show |
104 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.76-1114G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57603155 | |||||||
| chr15:57603268 | C | T | 1 | a0001c0003t0003g0145 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.76-1001C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57603268 | |||||||
| chr15:57603310 | G | A | 3 | a0001c0001t0002g0153 a0003c0005t0004g0333 a0003c0005t0004g0334 |
3 | HG02622.hp1 HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.76-959G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57603310 | |||||||
| chr15:57603311 | C | CT | 106 | a0001c0001t0001g0015 a0001c0001t0001g0270 a0001c0001t0002g0034 others(103): Show |
113 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.76-948dupT | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 57603311 | ||||||
| chr15:57603312 | T | C | 1 | a0001c0001t0004g0177 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.76-957T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57603312 | |||||||
| chr15:57603318 | T | G | 1 | a0005c0011t0002g0117 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.76-951T>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57603318 | |||||||
| chr15:57603341 | G | A | 3 | a0001c0001t0001g0160 a0001c0001t0001g0206 a0001c0001t0001g0213 |
3 | HG00673.hp2 HG02080.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.76-928G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57603341 | |||||||
| chr15:57603367 | T | G | 2 | a0001c0003t0003g0339 a0001c0003t0003g0340 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.76-902T>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57603367 | |||||||
| chr15:57603582 | G | A | 1 | a0002c0002t0002g0097 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.76-687G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57603582 | |||||||
| chr15:57603677 | A | G | 1 | a0003c0005t0010g0310 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.76-592A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57603677 | |||||||
| chr15:57603793 | A | G | 194 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(191): Show |
196 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(193): Show |
intron_variant | MODIFIER | c.76-476A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57603793 | |||||||
| chr15:57603836 | G | A | 1 | a0001c0001t0002g0314 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.76-433G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57603836 | |||||||
| chr15:57603936 | G | C | 177 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(174): Show |
179 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(176): Show |
intron_variant | MODIFIER | c.76-333G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57603936 | |||||||
| chr15:57603970 | A | C | 164 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(161): Show |
166 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(163): Show |
intron_variant | MODIFIER | c.76-299A>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57603970 | |||||||
| chr15:57604001 | G | A | 2 | a0001c0001t0006g0152 a0006c0006t0002g0120 |
2 | HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.76-268G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57604001 | |||||||
| chr15:57604113 | T | G | 139 | a0001c0001t0001g0270 a0001c0001t0002g0034 a0001c0001t0006g0152 others(136): Show |
146 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.76-156T>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57604113 | |||||||
| chr15:57604168 | A | T | 177 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(174): Show |
179 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(176): Show |
intron_variant | MODIFIER | c.76-101A>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57604168 | |||||||
| chr15:57604257 | C | T | 1 | a0002c0002t0002g0081 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.76-12C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57604257 | |||||||
| chr15:57604460 | C | A | 173 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(170): Show |
175 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(172): Show |
intron_variant | MODIFIER | c.162+105C>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57604460 | |||||||
| chr15:57604478 | C | T | 8 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(5): Show |
8 | HG02258.hp1 HG02451.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.162+123C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57604478 | |||||||
| chr15:57604506 | G | A | 1 | a0001c0003t0002g0018 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.162+151G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57604506 | |||||||
| chr15:57604601 | T | A | 1 | a0001c0003t0003g0147 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.162+246T>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57604601 | |||||||
| chr15:57604649 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.162+294C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57604649 | |||||||
| chr15:57604710 | C | T | 1 | a0002c0002t0002g0080 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.162+355C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57604710 | |||||||
| chr15:57604825 | G | A | 177 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(174): Show |
179 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(176): Show |
intron_variant | MODIFIER | c.162+470G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57604825 | |||||||
| chr15:57604831 | G | A | 97 | a0001c0001t0001g0270 a0001c0001t0002g0034 a0001c0003t0002g0003 others(94): Show |
103 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.162+476G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57604831 | |||||||
| chr15:57604856 | A | C | 312 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(309): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(318): Show |
intron_variant | MODIFIER | c.162+501A>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57604856 | |||||||
| chr15:57604949 | T | C | 2 | a0003c0005t0004g0333 a0003c0005t0004g0334 |
2 | HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.162+594T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57604949 | |||||||
| chr15:57604967 | A | G | 1 | a0002c0002t0002g0086 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.162+612A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57604967 | |||||||
| chr15:57604992 | C | G | 2 | a0001c0001t0001g0218 a0002c0004t0001g0204 |
2 | NA18978.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.162+637C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57604992 | |||||||
| chr15:57605020 | G | C | 2 | a0003c0005t0004g0333 a0003c0005t0004g0334 |
2 | HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.162+665G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57605020 | |||||||
| chr15:57605092 | G | A | 1 | a0002c0002t0002g0049 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.162+737G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57605092 | |||||||
| chr15:57605203 | A | G | 19 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(16): Show |
19 | HG01243.hp1 HG02258.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.162+848A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57605203 | |||||||
| chr15:57605291 | T | G | 1 | a0001c0003t0003g0132 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.162+936T>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57605291 | |||||||
| chr15:57605364 | T | A | 1 | a0004c0008t0003g0133 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.162+1009T>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57605364 | |||||||
| chr15:57605428 | C | T | 1 | a0001c0001t0007g0243 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.162+1073C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57605428 | |||||||
| chr15:57605501 | T | C | 1 | a0001c0001t0006g0152 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.162+1146T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57605501 | |||||||
| chr15:57605551 | C | G | 3 | a0001c0001t0007g0243 a0001c0001t0020g0309 a0003c0005t0010g0310 |
3 | HG04199.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.162+1196C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57605551 | |||||||
| chr15:57605558 | C | T | 1 | a0005c0011t0002g0117 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.162+1203C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57605558 | |||||||
| chr15:57605623 | G | A | 7 | a0001c0001t0001g0191 a0001c0001t0001g0199 a0001c0001t0001g0200 others(4): Show |
7 | HG00544.hp2 HG00558.hp2 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.162+1268G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57605623 | |||||||
| chr15:57605645 | C | G | 1 | a0002c0004t0001g0301 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.162+1290C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57605645 | |||||||
| chr15:57605669 | G | T | 1 | a0002c0004t0001g0301 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.162+1314G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57605669 | |||||||
| chr15:57605717 | A | G | 2 | a0003c0005t0004g0333 a0003c0005t0004g0334 |
2 | HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.162+1362A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57605717 | |||||||
| chr15:57605830 | A | G | 10 | a0001c0001t0002g0034 a0001c0003t0002g0003 a0001c0003t0002g0028 others(7): Show |
11 | HG00099.hp1 HG00741.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.162+1475A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57605830 | |||||||
| chr15:57605934 | T | TA | 6 | a0001c0001t0007g0325 a0001c0001t0007g0327 a0001c0001t0008g0328 others(3): Show |
6 | HG01884.hp1 HG02055.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.162+1587dupA | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 57605934 | ||||||
| chr15:57605994 | G | C | 141 | a0001c0001t0001g0270 a0001c0001t0002g0034 a0001c0001t0006g0152 others(138): Show |
148 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.162+1639G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57605994 | |||||||
| chr15:57606149 | C | T | 1 | a0002c0002t0002g0079 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.162+1794C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57606149 | |||||||
| chr15:57606213 | C | A | 1 | a0006c0006t0002g0120 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.162+1858C>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57606213 | |||||||
| chr15:57606294 | A | G | 6 | a0001c0001t0007g0325 a0001c0001t0007g0327 a0001c0001t0008g0328 others(3): Show |
6 | HG01884.hp1 HG02055.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.162+1939A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57606294 | |||||||
| chr15:57606377 | T | C | 1 | a0002c0002t0002g0050 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.162+2022T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57606377 | |||||||
| chr15:57606435 | G | C | 1 | a0001c0003t0001g0237 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.162+2080G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57606435 | |||||||
| chr15:57606639 | T | C | 1 | a0006c0006t0002g0120 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.162+2284T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57606639 | |||||||
| chr15:57606695 | T | C | 25 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(22): Show |
25 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.162+2340T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57606695 | |||||||
| chr15:57606723 | T | TATA | 158 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(155): Show |
160 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(157): Show |
intron_variant | MODIFIER | c.162+2379_162+2381d others(5): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 57606723 | ||||||
| chr15:57606872 | G | C | 310 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(307): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.162+2517G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57606872 | |||||||
| chr15:57607038 | G | A | 1 | a0001c0001t0001g0342 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.162+2683G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57607038 | |||||||
| chr15:57607140 | C | G | 8 | a0001c0003t0001g0113 a0001c0003t0004g0109 a0001c0003t0004g0111 others(5): Show |
8 | HG01891.hp1 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.162+2785C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57607140 | |||||||
| chr15:57607340 | G | A | 2 | a0003c0005t0004g0333 a0003c0005t0004g0334 |
2 | HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.162+2985G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57607340 | |||||||
| chr15:57607347 | C | A | 2 | a0002c0002t0003g0123 a0002c0002t0003g0124 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.162+2992C>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57607347 | |||||||
| chr15:57607358 | C | A | 1 | a0001c0001t0001g0210 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.162+3003C>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57607358 | |||||||
| chr15:57607379 | A | G | 312 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(309): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(318): Show |
intron_variant | MODIFIER | c.162+3024A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57607379 | |||||||
| chr15:57607462 | T | TA | 9 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(6): Show |
9 | HG02258.hp1 HG02451.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.162+3116dupA | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 57607462 | ||||||
| chr15:57607525 | G | A | 1 | a0002c0002t0002g0051 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.162+3170G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57607525 | |||||||
| chr15:57607556 | C | A | 1 | a0001c0001t0003g0293 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.162+3201C>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57607556 | |||||||
| chr15:57607646 | C | T | 1 | a0005c0011t0002g0117 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.162+3291C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57607646 | |||||||
| chr15:57607771 | G | C | 1 | a0001c0001t0001g0273 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.162+3416G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57607771 | |||||||
| chr15:57607772 | A | G | 2 | a0001c0001t0007g0243 a0001c0001t0020g0309 |
2 | NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.162+3417A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57607772 | |||||||
| chr15:57607796 | C | G | 1 | a0004c0008t0003g0133 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.162+3441C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57607796 | |||||||
| chr15:57607861 | G | C | 141 | a0001c0001t0001g0270 a0001c0001t0002g0034 a0001c0003t0001g0171 others(138): Show |
148 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.162+3506G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57607861 | |||||||
| chr15:57607938 | G | A | 146 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(143): Show |
148 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(145): Show |
intron_variant | MODIFIER | c.162+3583G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57607938 | |||||||
| chr15:57608015 | G | A | 6 | a0001c0003t0001g0113 a0001c0003t0004g0109 a0001c0003t0004g0111 others(3): Show |
6 | HG01891.hp1 HG02280.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.162+3660G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57608015 | |||||||
| chr15:57608092 | G | T | 143 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(140): Show |
145 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(142): Show |
intron_variant | MODIFIER | c.162+3737G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57608092 | |||||||
| chr15:57608172 | G | A | 112 | a0001c0001t0001g0270 a0001c0001t0002g0034 a0001c0003t0001g0171 others(109): Show |
119 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.162+3817G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57608172 | |||||||
| chr15:57608233 | C | T | 8 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(5): Show |
8 | HG02258.hp1 HG02451.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.162+3878C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57608233 | |||||||
| chr15:57608301 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.162+3946C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57608301 | |||||||
| chr15:57608373 | C | T | 3 | a0001c0001t0006g0152 a0001c0001t0007g0243 a0001c0001t0020g0309 |
3 | HG03041.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.162+4018C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57608373 | |||||||
| chr15:57608461 | G | A | 2 | a0001c0001t0007g0243 a0001c0001t0020g0309 |
2 | NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.162+4106G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57608461 | |||||||
| chr15:57608482 | C | G | 1 | a0001c0001t0004g0242 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.162+4127C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57608482 | |||||||
| chr15:57608504 | C | G | 1 | a0005c0011t0002g0117 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.162+4149C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57608504 | |||||||
| chr15:57608541 | C | T | 107 | a0001c0001t0001g0270 a0001c0001t0002g0034 a0001c0003t0001g0171 others(104): Show |
114 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.162+4186C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57608541 | |||||||
| chr15:57608608 | A | G | 1 | a0001c0007t0003g0128 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.162+4253A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57608608 | |||||||
| chr15:57608766 | C | G | 1 | a0005c0011t0002g0117 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.162+4411C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57608766 | |||||||
| chr15:57608785 | A | G | 19 | a0001c0001t0001g0232 a0001c0001t0002g0304 a0001c0001t0002g0306 others(16): Show |
19 | HG00099.hp2 HG00642.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.162+4430A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57608785 | |||||||
| chr15:57608975 | T | C | 19 | a0001c0001t0001g0232 a0001c0001t0002g0304 a0001c0001t0002g0306 others(16): Show |
19 | HG00099.hp2 HG00642.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.162+4620T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57608975 | |||||||
| chr15:57608976 | A | G | 108 | a0001c0001t0001g0270 a0001c0001t0002g0034 a0001c0003t0001g0171 others(105): Show |
115 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.162+4621A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57608976 | |||||||
| chr15:57609109 | A | G | 1 | a0001c0003t0003g0143 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.162+4754A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57609109 | |||||||
| chr15:57609111 | G | A | 20 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(17): Show |
20 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.162+4756G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57609111 | |||||||
| chr15:57609284 | G | A | 8 | a0001c0003t0001g0113 a0001c0003t0004g0109 a0001c0003t0004g0111 others(5): Show |
8 | HG01891.hp1 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.162+4929G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57609284 | |||||||
| chr15:57609332 | T | C | 2 | a0001c0001t0008g0328 a0001c0001t0008g0331 |
2 | HG01884.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.162+4977T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57609332 | |||||||
| chr15:57609362 | T | C | 25 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(22): Show |
25 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.162+5007T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57609362 | |||||||
| chr15:57609447 | C | T | 1 | a0002c0002t0002g0102 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.162+5092C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57609447 | |||||||
| chr15:57609616 | C | A | 20 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(17): Show |
20 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.162+5261C>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57609616 | |||||||
| chr15:57609670 | C | G | 1 | a0002c0004t0002g0330 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.162+5315C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57609670 | |||||||
| chr15:57609729 | T | C | 3 | a0001c0001t0007g0243 a0001c0001t0020g0309 a0003c0005t0010g0310 |
3 | HG04199.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.162+5374T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57609729 | |||||||
| chr15:57609901 | C | G | 1 | a0001c0001t0001g0187 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.162+5546C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57609901 | |||||||
| chr15:57609902 | T | G | 1 | a0002c0002t0002g0052 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.162+5547T>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57609902 | |||||||
| chr15:57609958 | C | G | 19 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(16): Show |
19 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.162+5603C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57609958 | |||||||
| chr15:57609963 | A | G | 6 | a0001c0001t0007g0325 a0001c0001t0007g0327 a0001c0001t0008g0328 others(3): Show |
6 | HG01884.hp1 HG02055.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.162+5608A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57609963 | |||||||
| chr15:57610033 | C | A | 170 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(167): Show |
172 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(169): Show |
intron_variant | MODIFIER | c.162+5678C>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57610033 | |||||||
| chr15:57610064 | G | T | 1 | a0001c0001t0001g0188 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.162+5709G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57610064 | |||||||
| chr15:57610277 | T | C | 5 | a0001c0001t0004g0007 a0001c0001t0004g0241 a0001c0001t0004g0242 others(2): Show |
6 | HG02145.hp2 HG02717.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.162+5922T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57610277 | |||||||
| chr15:57610284 | G | C | 20 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(17): Show |
20 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.162+5929G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57610284 | |||||||
| chr15:57610400 | G | A | 4 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0004g0233 others(1): Show |
4 | HG02145.hp1 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+6045G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57610400 | |||||||
| chr15:57610448 | C | T | 1 | a0001c0003t0003g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.162+6093C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57610448 | |||||||
| chr15:57610449 | G | A | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | HG02698.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.162+6094G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57610449 | |||||||
| chr15:57610451 | G | A | 2 | a0001c0003t0003g0339 a0001c0003t0003g0340 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.162+6096G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57610451 | |||||||
| chr15:57610651 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.162+6296A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57610651 | |||||||
| chr15:57610669 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.162+6314G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57610669 | |||||||
| chr15:57610677 | A | T | 19 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(16): Show |
19 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.162+6322A>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57610677 | |||||||
| chr15:57610755 | C | T | 1 | a0002c0002t0002g0094 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.162+6400C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57610755 | |||||||
| chr15:57610766 | C | A | 176 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(173): Show |
178 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(175): Show |
intron_variant | MODIFIER | c.162+6411C>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57610766 | |||||||
| chr15:57610791 | C | G | 1 | a0001c0003t0002g0078 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.162+6436C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57610791 | |||||||
| chr15:57610845 | C | A | 1 | a0001c0001t0001g0186 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.162+6490C>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57610845 | |||||||
| chr15:57610899 | G | A | 6 | a0001c0001t0007g0325 a0001c0001t0007g0327 a0001c0001t0008g0328 others(3): Show |
6 | HG01884.hp1 HG02055.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.162+6544G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57610899 | |||||||
| chr15:57610993 | G | A | 3 | a0002c0002t0002g0098 a0002c0002t0002g0099 a0002c0002t0002g0100 |
3 | NA19056.hp2 NA19074.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.162+6638G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57610993 | |||||||
| chr15:57611006 | C | T | 82 | a0001c0001t0001g0270 a0001c0001t0002g0034 a0001c0003t0001g0171 others(79): Show |
89 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.162+6651C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57611006 | |||||||
| chr15:57611190 | T | C | 6 | a0001c0001t0007g0325 a0001c0001t0007g0327 a0001c0001t0008g0328 others(3): Show |
6 | HG01884.hp1 HG02055.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.162+6835T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57611190 | |||||||
| chr15:57611292 | C | A | 2 | a0001c0001t0007g0243 a0001c0001t0020g0309 |
2 | NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.163-6741C>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57611292 | |||||||
| chr15:57611356 | G | A | 1 | a0005c0011t0002g0117 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.163-6677G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57611356 | |||||||
| chr15:57611378 | A | G | 4 | a0001c0003t0001g0171 a0001c0003t0002g0003 a0001c0003t0002g0035 others(1): Show |
5 | HG01074.hp2 HG01099.hp1 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-6655A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57611378 | |||||||
| chr15:57611386 | G | A | 1 | a0001c0003t0003g0145 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.163-6647G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57611386 | |||||||
| chr15:57611468 | G | C | 20 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(17): Show |
20 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.163-6565G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57611468 | |||||||
| chr15:57611480 | C | G | 8 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(5): Show |
8 | HG02258.hp1 HG02451.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.163-6553C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57611480 | |||||||
| chr15:57611518 | T | A | 1 | a0001c0003t0003g0132 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.163-6515T>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57611518 | |||||||
| chr15:57611551 | C | T | 17 | a0001c0001t0002g0304 a0001c0001t0002g0306 a0001c0001t0002g0307 others(14): Show |
17 | HG00099.hp2 HG00642.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.163-6482C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57611551 | |||||||
| chr15:57611595 | A | G | 1 | a0003c0005t0010g0310 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.163-6438A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57611595 | |||||||
| chr15:57611807 | A | G | 6 | a0001c0003t0001g0113 a0001c0003t0004g0109 a0001c0003t0004g0111 others(3): Show |
6 | HG01891.hp1 HG02280.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.163-6226A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57611807 | |||||||
| chr15:57611923 | G | A | 24 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(21): Show |
24 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.163-6110G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57611923 | |||||||
| chr15:57611944 | A | G | 1 | a0001c0001t0001g0175 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.163-6089A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57611944 | |||||||
| chr15:57611947 | T | C | 1 | a0006c0006t0002g0120 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.163-6086T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57611947 | |||||||
| chr15:57612049 | A | G | 18 | a0001c0001t0002g0304 a0001c0001t0002g0306 a0001c0001t0002g0307 others(15): Show |
18 | HG00099.hp2 HG00642.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.163-5984A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57612049 | |||||||
| chr15:57612097 | C | G | 32 | a0001c0003t0003g0118 a0001c0003t0003g0125 a0001c0003t0003g0129 others(29): Show |
32 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.163-5936C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57612097 | |||||||
| chr15:57612139 | A | C | 144 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(141): Show |
146 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(143): Show |
intron_variant | MODIFIER | c.163-5894A>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57612139 | |||||||
| chr15:57612153 | C | T | 24 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(21): Show |
24 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.163-5880C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57612153 | |||||||
| chr15:57612264 | C | A | 1 | a0005c0011t0002g0117 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.163-5769C>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57612264 | |||||||
| chr15:57612325 | C | T | 18 | a0001c0001t0002g0304 a0001c0001t0002g0306 a0001c0001t0002g0307 others(15): Show |
18 | HG00099.hp2 HG00642.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.163-5708C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57612325 | |||||||
| chr15:57612383 | C | G | 2 | a0003c0005t0004g0333 a0003c0005t0004g0334 |
2 | HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.163-5650C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57612383 | |||||||
| chr15:57612572 | T | C | 25 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(22): Show |
25 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.163-5461T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57612572 | |||||||
| chr15:57612628 | T | C | 17 | a0001c0001t0002g0304 a0001c0001t0002g0306 a0001c0001t0002g0307 others(14): Show |
17 | HG00099.hp2 HG00642.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.163-5405T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57612628 | |||||||
| chr15:57612654 | G | C | 25 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(22): Show |
25 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.163-5379G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57612654 | |||||||
| chr15:57612722 | C | T | 144 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(141): Show |
146 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(143): Show |
intron_variant | MODIFIER | c.163-5311C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57612722 | |||||||
| chr15:57612797 | A | T | 25 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(22): Show |
25 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.163-5236A>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57612797 | |||||||
| chr15:57612801 | A | G | 1 | a0001c0001t0006g0152 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.163-5232A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57612801 | |||||||
| chr15:57612802 | T | A | 25 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(22): Show |
25 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.163-5231T>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57612802 | |||||||
| chr15:57612804 | C | G | 3 | a0001c0003t0003g0154 a0001c0003t0003g0155 a0001c0003t0003g0156 |
3 | HG01069.hp2 HG01071.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.163-5229C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57612804 | |||||||
| chr15:57612840 | T | C | 1 | a0001c0001t0001g0289 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.163-5193T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57612840 | |||||||
| chr15:57612879 | T | C | 25 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(22): Show |
25 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.163-5154T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57612879 | |||||||
| chr15:57612880 | A | T | 1 | a0001c0001t0001g0211 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.163-5153A>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57612880 | |||||||
| chr15:57612933 | A | C | 17 | a0001c0001t0002g0304 a0001c0001t0002g0306 a0001c0001t0002g0307 others(14): Show |
17 | HG00099.hp2 HG00642.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.163-5100A>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57612933 | |||||||
| chr15:57612948 | C | T | 187 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(184): Show |
189 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(186): Show |
intron_variant | MODIFIER | c.163-5085C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57612948 | |||||||
| chr15:57612963 | G | A | 12 | a0001c0001t0001g0168 a0001c0001t0001g0189 a0001c0001t0001g0215 others(9): Show |
12 | HG02258.hp2 HG02572.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.163-5070G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57612963 | |||||||
| chr15:57612995 | G | A | 145 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(142): Show |
147 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(144): Show |
intron_variant | MODIFIER | c.163-5038G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57612995 | |||||||
| chr15:57613077 | G | A | 144 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(141): Show |
146 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(143): Show |
intron_variant | MODIFIER | c.163-4956G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57613077 | |||||||
| chr15:57613080 | T | C | 309 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(306): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.163-4953T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57613080 | |||||||
| chr15:57613081 | G | A | 24 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(21): Show |
24 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.163-4952G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57613081 | |||||||
| chr15:57613113 | T | C | 7 | a0001c0001t0001g0164 a0001c0001t0001g0166 a0001c0001t0001g0167 others(4): Show |
7 | HG00423.hp1 HG00609.hp1 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.163-4920T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57613113 | |||||||
| chr15:57613115 | T | G | 25 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(22): Show |
25 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.163-4918T>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57613115 | |||||||
| chr15:57613134 | G | A | 14 | a0001c0003t0002g0055 a0001c0003t0002g0058 a0002c0002t0002g0017 others(11): Show |
14 | HG01255.hp1 HG02109.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.163-4899G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57613134 | |||||||
| chr15:57613165 | C | A | 4 | a0001c0003t0003g0118 a0001c0003t0003g0130 a0001c0003t0003g0131 others(1): Show |
4 | HG01070.hp2 HG01358.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.163-4868C>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57613165 | |||||||
| chr15:57613177 | C | G | 25 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(22): Show |
25 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.163-4856C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57613177 | |||||||
| chr15:57613415 | G | C | 25 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(22): Show |
25 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.163-4618G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57613415 | |||||||
| chr15:57613479 | T | C | 13 | a0001c0003t0002g0018 a0001c0003t0002g0019 a0001c0003t0002g0020 others(10): Show |
14 | HG00140.hp2 HG00323.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.163-4554T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57613479 | |||||||
| chr15:57613567 | T | C | 309 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(306): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.163-4466T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57613567 | |||||||
| chr15:57613582 | G | T | 4 | a0001c0003t0001g0113 a0001c0003t0004g0111 a0001c0003t0004g0112 others(1): Show |
4 | HG01891.hp1 HG03516.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.163-4451G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57613582 | |||||||
| chr15:57613749 | A | G | 309 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(306): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.163-4284A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57613749 | |||||||
| chr15:57613754 | C | T | 25 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(22): Show |
25 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.163-4279C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57613754 | |||||||
| chr15:57613828 | A | G | 25 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(22): Show |
25 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.163-4205A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57613828 | |||||||
| chr15:57613908 | CAA | C | 25 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(22): Show |
25 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.163-4124_163-4123d others(4): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57613908 | |||||||
| chr15:57613945 | A | G | 1 | a0001c0001t0001g0217 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.163-4088A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57613945 | |||||||
| chr15:57614039 | T | C | 25 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(22): Show |
25 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.163-3994T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57614039 | |||||||
| chr15:57614106 | G | C | 76 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(73): Show |
76 | HG00544.hp2 HG00558.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.163-3927G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57614106 | |||||||
| chr15:57614236 | G | A | 309 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(306): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.163-3797G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57614236 | |||||||
| chr15:57614258 | C | G | 1 | a0003c0005t0010g0310 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.163-3775C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57614258 | |||||||
| chr15:57614261 | G | A | 144 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(141): Show |
146 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(143): Show |
intron_variant | MODIFIER | c.163-3772G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57614261 | |||||||
| chr15:57614438 | A | G | 309 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(306): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.163-3595A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57614438 | |||||||
| chr15:57614441 | C | T | 2 | a0001c0001t0001g0188 a0001c0001t0001g0196 |
2 | NA18946.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.163-3592C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57614441 | |||||||
| chr15:57614455 | G | A | 57 | a0001c0003t0001g0227 a0001c0003t0002g0011 a0001c0003t0002g0038 others(54): Show |
62 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.163-3578G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57614455 | |||||||
| chr15:57614472 | A | G | 309 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(306): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.163-3561A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57614472 | |||||||
| chr15:57614624 | A | C | 1 | a0003c0005t0004g0333 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.163-3409A>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57614624 | |||||||
| chr15:57614707 | C | T | 4 | a0001c0003t0001g0113 a0001c0003t0004g0111 a0001c0003t0004g0112 others(1): Show |
4 | HG01891.hp1 HG03516.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.163-3326C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57614707 | |||||||
| chr15:57614807 | G | A | 18 | a0001c0001t0002g0304 a0001c0001t0002g0306 a0001c0001t0002g0307 others(15): Show |
18 | HG00099.hp2 HG00642.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.163-3226G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57614807 | |||||||
| chr15:57614813 | C | T | 1 | a0001c0003t0002g0078 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.163-3220C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57614813 | |||||||
| chr15:57614815 | C | T | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | HG02698.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.163-3218C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57614815 | |||||||
| chr15:57615021 | G | T | 2 | a0003c0005t0004g0333 a0003c0005t0004g0334 |
2 | HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.163-3012G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57615021 | |||||||
| chr15:57615024 | C | T | 1 | a0002c0002t0002g0084 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.163-3009C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57615024 | |||||||
| chr15:57615099 | G | A | 23 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(20): Show |
23 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.163-2934G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57615099 | |||||||
| chr15:57615102 | G | A | 22 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(19): Show |
22 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.163-2931G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57615102 | |||||||
| chr15:57615130 | A | G | 171 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(168): Show |
173 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(170): Show |
intron_variant | MODIFIER | c.163-2903A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57615130 | |||||||
| chr15:57615319 | T | C | 1 | a0003c0005t0010g0310 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.163-2714T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57615319 | |||||||
| chr15:57615355 | C | A | 1 | a0001c0001t0001g0207 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.163-2678C>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57615355 | |||||||
| chr15:57615376 | C | T | 189 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(186): Show |
191 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(188): Show |
intron_variant | MODIFIER | c.163-2657C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57615376 | |||||||
| chr15:57615442 | G | A | 3 | a0001c0003t0003g0132 a0001c0003t0003g0134 a0001c0003t0003g0143 |
3 | HG01243.hp2 HG02257.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.163-2591G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57615442 | |||||||
| chr15:57615442 | G | C | 1 | a0003c0005t0010g0310 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.163-2591G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57615442 | |||||||
| chr15:57615491 | C | T | 26 | a0001c0001t0002g0304 a0001c0001t0002g0306 a0001c0001t0002g0307 others(23): Show |
26 | HG00099.hp2 HG00642.hp1 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.163-2542C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57615491 | |||||||
| chr15:57615573 | T | G | 175 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(172): Show |
177 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(174): Show |
intron_variant | MODIFIER | c.163-2460T>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57615573 | |||||||
| chr15:57615577 | A | G | 1 | a0003c0005t0004g0333 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.163-2456A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57615577 | |||||||
| chr15:57615782 | G | A | 2 | a0001c0001t0007g0243 a0001c0001t0020g0309 |
2 | NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.163-2251G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57615782 | |||||||
| chr15:57615861 | T | C | 176 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(173): Show |
178 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(175): Show |
intron_variant | MODIFIER | c.163-2172T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57615861 | |||||||
| chr15:57615893 | G | C | 6 | a0001c0001t0007g0325 a0001c0001t0007g0327 a0001c0001t0008g0328 others(3): Show |
6 | HG01884.hp1 HG02055.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-2140G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57615893 | |||||||
| chr15:57615912 | T | C | 1 | a0001c0003t0003g0125 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.163-2121T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57615912 | |||||||
| chr15:57615945 | A | G | 1 | a0001c0003t0002g0126 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.163-2088A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57615945 | |||||||
| chr15:57615956 | G | GCAAAA | 186 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(183): Show |
188 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(185): Show |
intron_variant | MODIFIER | c.163-2066_163-2062d others(7): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 57615956 | ||||||
| chr15:57616000 | C | A | 265 | a0001c0001t0001g0008 a0001c0001t0001g0161 a0001c0001t0001g0164 others(262): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.163-2033C>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57616000 | |||||||
| chr15:57616014 | C | T | 183 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(180): Show |
185 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(182): Show |
intron_variant | MODIFIER | c.163-2019C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57616014 | |||||||
| chr15:57616118 | C | G | 12 | a0001c0001t0001g0168 a0001c0001t0001g0189 a0001c0001t0001g0215 others(9): Show |
12 | HG02258.hp2 HG02572.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.163-1915C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57616118 | |||||||
| chr15:57616257 | G | A | 8 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(5): Show |
8 | HG02258.hp1 HG02451.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.163-1776G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57616257 | |||||||
| chr15:57616305 | A | T | 2 | a0001c0003t0003g0339 a0001c0003t0003g0340 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.163-1728A>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57616305 | |||||||
| chr15:57616354 | A | C | 3 | a0001c0003t0001g0237 a0001c0003t0003g0339 a0001c0003t0003g0340 |
3 | HG02896.hp2 HG02897.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.163-1679A>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57616354 | |||||||
| chr15:57616361 | T | C | 310 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(307): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.163-1672T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57616361 | |||||||
| chr15:57616457 | A | G | 150 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(147): Show |
152 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(149): Show |
intron_variant | MODIFIER | c.163-1576A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57616457 | |||||||
| chr15:57616498 | C | T | 2 | a0003c0005t0004g0333 a0003c0005t0004g0334 |
2 | HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.163-1535C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57616498 | |||||||
| chr15:57616599 | G | T | 147 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(144): Show |
149 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(146): Show |
intron_variant | MODIFIER | c.163-1434G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57616599 | |||||||
| chr15:57616601 | T | A | 340 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(337): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.163-1432T>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57616601 | |||||||
| chr15:57616754 | G | A | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.163-1279G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57616754 | |||||||
| chr15:57616761 | G | A | 1 | a0001c0003t0002g0046 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.163-1272G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57616761 | |||||||
| chr15:57616767 | G | A | 26 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(23): Show |
26 | HG00099.hp2 HG00642.hp1 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.163-1266G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57616767 | |||||||
| chr15:57616822 | C | CT | 77 | a0001c0001t0001g0176 a0001c0001t0001g0185 a0001c0001t0001g0192 others(74): Show |
79 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.163-1186dupT | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 57616822 | ||||||
| chr15:57616822 | C | CTT | 12 | a0001c0001t0001g0157 a0001c0001t0001g0179 a0001c0001t0001g0180 others(9): Show |
13 | HG00597.hp2 HG01891.hp1 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.163-1187_163-1186d others(4): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 57616822 | ||||||
| chr15:57616822 | C | CTTT | 13 | a0001c0001t0001g0251 a0001c0001t0001g0256 a0001c0001t0001g0285 others(10): Show |
13 | HG01884.hp1 HG02258.hp1 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.163-1188_163-1186d others(5): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 57616822 | ||||||
| chr15:57616822 | C | CTTTT | 17 | a0001c0001t0001g0184 a0001c0001t0001g0202 a0001c0001t0001g0203 others(14): Show |
18 | HG02055.hp2 HG02071.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.163-1189_163-1186d others(6): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 57616822 | ||||||
| chr15:57616822 | C | CTTTTTTT others(3): Show |
3 | a0001c0001t0001g0269 a0001c0001t0001g0283 a0002c0004t0002g0330 |
3 | HG02071.hp2 HG03490.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.163-1195_163-1186d others(12): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 57616822 | ||||||
| chr15:57616822 | C | CTTTTTTT others(4): Show |
2 | a0001c0001t0001g0260 a0001c0001t0001g0299 |
2 | NA18979.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.163-1196_163-1186d others(13): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 57616822 | ||||||
| chr15:57616822 | C | CTTTTTTT others(5): Show |
2 | a0001c0001t0002g0304 a0001c0001t0002g0319 |
2 | NA20752.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.163-1197_163-1186d others(14): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 57616822 | ||||||
| chr15:57616822 | C | CTTTTTTT others(6): Show |
12 | a0001c0001t0001g0267 a0001c0001t0002g0306 a0001c0001t0002g0308 others(9): Show |
12 | HG00099.hp2 HG00642.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.163-1198_163-1186d others(15): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 57616822 | ||||||
| chr15:57616822 | C | CTTTTTTT others(7): Show |
6 | a0001c0001t0001g0234 a0001c0001t0002g0307 a0001c0001t0002g0322 others(3): Show |
6 | HG01928.hp2 HG02004.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-1199_163-1186d others(16): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 57616822 | ||||||
| chr15:57616822 | C | CTTTTTTT others(9): Show |
6 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0290 others(3): Show |
6 | HG01169.hp1 HG02451.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-1201_163-1186d others(18): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 57616822 | ||||||
| chr15:57616822 | C | CTTTTTTT others(10): Show |
15 | a0001c0001t0001g0014 a0001c0001t0001g0168 a0001c0001t0001g0187 others(12): Show |
15 | HG01167.hp1 HG02109.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.163-1202_163-1186d others(19): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 57616822 | ||||||
| chr15:57616822 | C | CTTTTTTT others(11): Show |
11 | a0001c0001t0001g0169 a0001c0001t0001g0178 a0001c0001t0001g0182 others(8): Show |
11 | HG00558.hp2 HG01074.hp1 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.163-1203_163-1186d others(20): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 57616822 | ||||||
| chr15:57616822 | C | CTTTTTTT others(12): Show |
5 | a0001c0001t0001g0191 a0001c0001t0001g0265 a0001c0001t0001g0276 others(2): Show |
5 | HG00544.hp2 HG00642.hp2 HG02015.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-1204_163-1186d others(21): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 57616822 | ||||||
| chr15:57616822 | C | CTTTTTTT others(13): Show |
8 | a0001c0001t0001g0172 a0001c0001t0001g0221 a0001c0001t0001g0232 others(5): Show |
8 | HG00735.hp1 HG01361.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.163-1205_163-1186d others(22): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 57616822 | ||||||
| chr15:57616822 | C | CTTTTTTT others(14): Show |
9 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0173 others(6): Show |
9 | HG00609.hp1 HG01168.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.163-1206_163-1186d others(23): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 57616822 | ||||||
| chr15:57616822 | C | CTTTTTTT others(15): Show |
4 | a0001c0001t0001g0164 a0001c0001t0001g0170 a0001c0001t0001g0270 others(1): Show |
4 | HG00423.hp1 HG01099.hp2 NA18943.hp2 others(1): Show |
intron_variant | MODIFIER | c.163-1207_163-1186d others(24): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 57616822 | ||||||
| chr15:57616822 | C | CTTTTTTT others(16): Show |
5 | a0001c0001t0001g0175 a0001c0001t0001g0220 a0001c0001t0001g0235 others(2): Show |
5 | HG01175.hp1 HG02027.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.163-1208_163-1186d others(25): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 57616822 | ||||||
| chr15:57616822 | C | CTTTTTTT others(17): Show |
6 | a0001c0001t0001g0195 a0001c0001t0001g0207 a0001c0001t0001g0224 others(3): Show |
6 | HG00741.hp2 HG01256.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-1209_163-1186d others(26): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 57616822 | ||||||
| chr15:57616822 | C | CTTTTTTT others(18): Show |
2 | a0001c0001t0001g0198 a0001c0001t0001g0230 |
2 | HG01258.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.163-1210_163-1186d others(27): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 57616822 | ||||||
| chr15:57616822 | C | CTTTTTTT others(19): Show |
5 | a0001c0001t0001g0210 a0001c0001t0001g0225 a0001c0001t0001g0239 others(2): Show |
5 | HG01069.hp1 HG02738.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-1186_163-1185i others(28): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 57616822 | ||||||
| chr15:57616822 | C | CTTTTTTT others(20): Show |
4 | a0001c0001t0001g0008 a0001c0001t0001g0240 a0001c0001t0001g0280 others(1): Show |
5 | HG01070.hp1 HG01071.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-1186_163-1185i others(29): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 57616822 | ||||||
| chr15:57616822 | C | CTTTTTTT others(21): Show |
3 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0284 |
3 | HG01346.hp2 HG02056.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.163-1186_163-1185i others(30): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 57616822 | ||||||
| chr15:57616822 | C | CTTTTTTT others(23): Show |
1 | a0001c0001t0001g0264 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163-1186_163-1185i others(32): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 57616822 | ||||||
| chr15:57616822 | CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0007g0243 a0001c0001t0020g0309 |
2 | NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.163-1195_163-1186d others(12): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 57616822 | ||||||
| chr15:57616822 | CTTTTTTT others(6): Show |
C | 2 | a0002c0002t0003g0123 a0002c0002t0003g0124 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.163-1198_163-1186d others(15): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 57616822 | ||||||
| chr15:57616839 | T | TTTTTTTT others(4): Show |
2 | a0001c0003t0001g0237 a0001c0003t0003g0340 |
2 | HG02896.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.163-1186_163-1185i others(13): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 57616839 | ||||||
| chr15:57616839 | T | TTTTTTTT others(5): Show |
1 | a0001c0003t0003g0339 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.163-1186_163-1185i others(14): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 57616839 | ||||||
| chr15:57616968 | T | C | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.163-1065T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57616968 | |||||||
| chr15:57616988 | T | C | 189 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(186): Show |
191 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(188): Show |
intron_variant | MODIFIER | c.163-1045T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57616988 | |||||||
| chr15:57617060 | A | C | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.163-973A>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57617060 | |||||||
| chr15:57617087 | A | G | 1 | a0001c0001t0006g0152 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.163-946A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57617087 | |||||||
| chr15:57617179 | G | C | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.163-854G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57617179 | |||||||
| chr15:57617286 | C | A | 1 | a0002c0002t0002g0096 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.163-747C>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57617286 | |||||||
| chr15:57617298 | T | G | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.163-735T>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57617298 | |||||||
| chr15:57617299 | T | C | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.163-734T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57617299 | |||||||
| chr15:57617318 | C | T | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.163-715C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57617318 | |||||||
| chr15:57617319 | C | A | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.163-714C>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57617319 | |||||||
| chr15:57617341 | T | A | 6 | a0001c0001t0007g0325 a0001c0001t0007g0327 a0001c0001t0008g0328 others(3): Show |
6 | HG01884.hp1 HG02055.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-692T>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57617341 | |||||||
| chr15:57617350 | A | G | 1 | a0003c0005t0010g0310 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.163-683A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57617350 | |||||||
| chr15:57617470 | G | C | 2 | a0003c0005t0004g0333 a0003c0005t0004g0334 |
2 | HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.163-563G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57617470 | |||||||
| chr15:57617487 | C | T | 146 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(143): Show |
148 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(145): Show |
intron_variant | MODIFIER | c.163-546C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57617487 | |||||||
| chr15:57617551 | C | G | 3 | a0001c0003t0003g0132 a0001c0003t0003g0134 a0001c0003t0003g0143 |
3 | HG01243.hp2 HG02257.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.163-482C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57617551 | |||||||
| chr15:57617551 | C | T | 1 | a0001c0003t0003g0140 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.163-482C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57617551 | |||||||
| chr15:57617587 | C | T | 1 | a0001c0001t0001g0270 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.163-446C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57617587 | |||||||
| chr15:57617674 | G | C | 1 | a0001c0003t0001g0171 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.163-359G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57617674 | |||||||
| chr15:57617795 | A | G | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.163-238A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57617795 | |||||||
| chr15:57617806 | T | C | 189 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(186): Show |
191 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(188): Show |
intron_variant | MODIFIER | c.163-227T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57617806 | |||||||
| chr15:57617818 | C | G | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.163-215C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57617818 | |||||||
| chr15:57617900 | C | G | 1 | a0002c0002t0002g0057 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.163-133C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57617900 | |||||||
| chr15:57617912 | A | T | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.163-121A>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57617912 | |||||||
| chr15:57617945 | A | G | 1 | a0001c0001t0001g0220 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.163-88A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57617945 | |||||||
| chr15:57617966 | G | A | 189 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(186): Show |
191 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(188): Show |
intron_variant | MODIFIER | c.163-67G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57617966 | |||||||
| chr15:57618246 | A | G | 335 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(332): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.318+58A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57618246 | |||||||
| chr15:57618281 | G | C | 2 | a0001c0003t0003g0339 a0001c0003t0003g0340 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.318+93G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57618281 | |||||||
| chr15:57618452 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.318+264G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57618452 | |||||||
| chr15:57618543 | G | C | 34 | a0001c0003t0003g0118 a0001c0003t0003g0125 a0001c0003t0003g0129 others(31): Show |
34 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.318+355G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57618543 | |||||||
| chr15:57618555 | A | C | 3 | a0001c0003t0006g0115 a0001c0003t0006g0116 a0001c0003t0006g0119 |
3 | HG01109.hp2 HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.318+367A>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57618555 | |||||||
| chr15:57618657 | T | A | 2 | a0003c0005t0004g0333 a0003c0005t0004g0334 |
2 | HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.318+469T>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57618657 | |||||||
| chr15:57618665 | G | A | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.318+477G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57618665 | |||||||
| chr15:57618672 | G | A | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.318+484G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57618672 | |||||||
| chr15:57618747 | T | A | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.318+559T>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57618747 | |||||||
| chr15:57618748 | C | A | 1 | a0001c0003t0002g0085 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.318+560C>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57618748 | |||||||
| chr15:57618820 | G | A | 2 | a0003c0005t0004g0333 a0003c0005t0004g0334 |
2 | HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.318+632G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57618820 | |||||||
| chr15:57618833 | G | C | 1 | a0002c0002t0018g0016 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.318+645G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57618833 | |||||||
| chr15:57618882 | T | C | 2 | a0003c0005t0004g0333 a0003c0005t0004g0334 |
2 | HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.318+694T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57618882 | |||||||
| chr15:57619117 | T | C | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.318+929T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57619117 | |||||||
| chr15:57619119 | G | C | 1 | a0001c0001t0001g0299 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.318+931G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57619119 | |||||||
| chr15:57619149 | G | T | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.318+961G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57619149 | |||||||
| chr15:57619166 | T | C | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.318+978T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57619166 | |||||||
| chr15:57619188 | G | A | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.318+1000G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57619188 | |||||||
| chr15:57619213 | G | C | 76 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(73): Show |
76 | HG00544.hp2 HG00558.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.318+1025G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57619213 | |||||||
| chr15:57619270 | G | C | 1 | a0001c0003t0001g0171 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.318+1082G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57619270 | |||||||
| chr15:57619274 | G | A | 1 | a0003c0005t0010g0310 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.318+1086G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57619274 | |||||||
| chr15:57619292 | T | C | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.318+1104T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57619292 | |||||||
| chr15:57619308 | T | C | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.318+1120T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57619308 | |||||||
| chr15:57619370 | C | T | 1 | a0002c0002t0002g0127 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.318+1182C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57619370 | |||||||
| chr15:57619379 | G | A | 1 | a0002c0002t0002g0081 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.318+1191G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57619379 | |||||||
| chr15:57619441 | A | G | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.318+1253A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57619441 | |||||||
| chr15:57619502 | C | G | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.318+1314C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57619502 | |||||||
| chr15:57619530 | G | A | 190 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(187): Show |
192 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(189): Show |
intron_variant | MODIFIER | c.318+1342G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57619530 | |||||||
| chr15:57619701 | G | A | 314 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(311): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.318+1513G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57619701 | |||||||
| chr15:57619716 | G | C | 1 | a0001c0003t0001g0171 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.318+1528G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57619716 | |||||||
| chr15:57619717 | A | T | 2 | a0001c0003t0003g0130 a0001c0003t0003g0131 |
2 | HG01070.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.318+1529A>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57619717 | |||||||
| chr15:57619733 | G | C | 307 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(304): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(313): Show |
intron_variant | MODIFIER | c.318+1545G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57619733 | |||||||
| chr15:57619786 | G | T | 9 | a0001c0003t0002g0061 a0001c0003t0002g0078 a0001c0003t0002g0087 others(6): Show |
9 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(6): Show |
intron_variant | MODIFIER | c.318+1598G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57619786 | |||||||
| chr15:57619893 | A | G | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.318+1705A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57619893 | |||||||
| chr15:57619903 | T | C | 7 | a0001c0001t0007g0325 a0001c0001t0007g0327 a0001c0001t0008g0328 others(4): Show |
7 | HG01884.hp1 HG02055.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.319-1705T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57619903 | |||||||
| chr15:57619936 | G | A | 307 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(304): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(313): Show |
intron_variant | MODIFIER | c.319-1672G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57619936 | |||||||
| chr15:57619942 | C | T | 8 | a0001c0001t0006g0152 a0001c0001t0007g0325 a0001c0001t0007g0327 others(5): Show |
8 | HG01884.hp1 HG02055.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.319-1666C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57619942 | |||||||
| chr15:57620039 | G | GCAGCTCA others(14): Show |
2 | a0001c0001t0007g0243 a0001c0001t0020g0309 |
2 | NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.319-1566_319-1546d others(23): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr15 | 57620039 | ||||||
| chr15:57620061 | C | T | 7 | a0001c0001t0001g0008 a0001c0001t0001g0248 a0001c0001t0001g0249 others(4): Show |
8 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.319-1547C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57620061 | |||||||
| chr15:57620140 | C | T | 190 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(187): Show |
192 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(189): Show |
intron_variant | MODIFIER | c.319-1468C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57620140 | |||||||
| chr15:57620146 | C | A | 1 | a0001c0003t0017g0122 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.319-1462C>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57620146 | |||||||
| chr15:57620371 | A | G | 151 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(148): Show |
153 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(150): Show |
intron_variant | MODIFIER | c.319-1237A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57620371 | |||||||
| chr15:57620407 | G | A | 1 | a0001c0003t0003g0135 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.319-1201G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57620407 | |||||||
| chr15:57620478 | G | C | 1 | a0001c0001t0001g0264 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.319-1130G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57620478 | |||||||
| chr15:57620645 | C | T | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.319-963C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57620645 | |||||||
| chr15:57620757 | G | A | 2 | a0001c0001t0007g0243 a0001c0001t0020g0309 |
2 | NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.319-851G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57620757 | |||||||
| chr15:57620907 | A | G | 9 | a0001c0001t0001g0168 a0001c0001t0001g0189 a0001c0001t0001g0217 others(6): Show |
9 | HG02258.hp2 HG02572.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.319-701A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57620907 | |||||||
| chr15:57620936 | C | G | 152 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(149): Show |
154 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(151): Show |
intron_variant | MODIFIER | c.319-672C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57620936 | |||||||
| chr15:57620957 | A | G | 1 | a0003c0005t0010g0310 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.319-651A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57620957 | |||||||
| chr15:57620966 | T | TAATTATA others(146): Show |
1 | a0002c0002t0001g0335 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.319-626_319-625ins others(153): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr15 | 57620966 | ||||||
| chr15:57620966 | T | TAATTATA others(151): Show |
1 | a0002c0002t0001g0336 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.319-626_319-625ins others(158): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr15 | 57620966 | ||||||
| chr15:57620971 | A | G | 7 | a0001c0001t0007g0325 a0001c0001t0007g0327 a0001c0001t0008g0328 others(4): Show |
7 | HG01884.hp1 HG02055.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.319-637A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57620971 | |||||||
| chr15:57621012 | G | A | 6 | a0001c0003t0001g0237 a0001c0003t0003g0339 a0001c0003t0003g0340 others(3): Show |
6 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.319-596G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57621012 | |||||||
| chr15:57621173 | T | A | 190 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(187): Show |
192 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(189): Show |
intron_variant | MODIFIER | c.319-435T>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57621173 | |||||||
| chr15:57621205 | C | CT | 24 | a0001c0001t0001g0176 a0001c0001t0001g0234 a0001c0001t0001g0235 others(21): Show |
24 | HG01255.hp1 HG02109.hp2 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.319-387dupT | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr15 | 57621205 | ||||||
| chr15:57621205 | C | CTT | 96 | a0001c0001t0002g0034 a0001c0001t0007g0327 a0001c0003t0001g0171 others(93): Show |
103 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.319-388_319-387dup others(2): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr15 | 57621205 | ||||||
| chr15:57621205 | C | CTTT | 10 | a0001c0001t0006g0152 a0001c0001t0007g0325 a0001c0001t0008g0328 others(7): Show |
10 | HG01884.hp1 HG02055.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.319-389_319-387dup others(3): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr15 | 57621205 | ||||||
| chr15:57621205 | CT | C | 18 | a0001c0001t0001g0248 a0001c0001t0001g0300 a0001c0001t0002g0304 others(15): Show |
18 | HG00099.hp2 HG01069.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.319-387delT | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr15 | 57621205 | ||||||
| chr15:57621250 | A | G | 190 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(187): Show |
192 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(189): Show |
intron_variant | MODIFIER | c.319-358A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57621250 | |||||||
| chr15:57621252 | C | T | 1 | a0005c0011t0002g0117 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.319-356C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57621252 | |||||||
| chr15:57621277 | C | G | 2 | a0003c0005t0004g0333 a0003c0005t0004g0334 |
2 | HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.319-331C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57621277 | |||||||
| chr15:57621296 | C | T | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.319-312C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57621296 | |||||||
| chr15:57621303 | C | T | 6 | a0002c0002t0002g0006 a0002c0002t0002g0104 a0002c0002t0002g0105 others(3): Show |
7 | HG02083.hp1 NA18955.hp1 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.319-305C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57621303 | |||||||
| chr15:57621336 | G | A | 4 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0004g0233 others(1): Show |
4 | HG02145.hp1 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.319-272G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57621336 | |||||||
| chr15:57621511 | C | T | 7 | a0001c0001t0007g0325 a0001c0001t0007g0327 a0001c0001t0008g0328 others(4): Show |
7 | HG01884.hp1 HG02055.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.319-97C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57621511 | |||||||
| chr15:57621515 | G | T | 1 | a0001c0001t0001g0288 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.319-93G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57621515 | |||||||
| chr15:57621522 | T | G | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.319-86T>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57621522 | |||||||
| chr15:57621602 | C | A | 1 | a0005c0011t0002g0117 | 1 | HG02559.hp1 | splice_region_variant&intron_variant | LOW | c.319-6C>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57621602 | |||||||
| chr15:57621896 | G | T | 310 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(307): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.411+196G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57621896 | |||||||
| chr15:57621971 | A | G | 113 | a0001c0001t0002g0034 a0001c0001t0006g0152 a0001c0003t0001g0171 others(110): Show |
120 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.411+271A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57621971 | |||||||
| chr15:57621988 | G | A | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.411+288G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57621988 | |||||||
| chr15:57621991 | C | G | 13 | a0001c0001t0002g0304 a0001c0001t0002g0306 a0001c0001t0002g0307 others(10): Show |
13 | HG00099.hp2 HG01081.hp1 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.411+291C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57621991 | |||||||
| chr15:57622113 | A | G | 23 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(20): Show |
23 | HG00099.hp2 HG01081.hp1 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.411+413A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57622113 | |||||||
| chr15:57622206 | A | G | 1 | a0001c0001t0001g0188 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.411+506A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57622206 | |||||||
| chr15:57622260 | TA | T | 13 | a0001c0001t0001g0162 a0001c0001t0001g0182 a0001c0001t0001g0185 others(10): Show |
13 | HG00735.hp2 HG01952.hp2 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.411+561delA | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57622260 | |||||||
| chr15:57622284 | T | C | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.411+584T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57622284 | |||||||
| chr15:57622417 | T | G | 3 | a0001c0003t0001g0237 a0001c0003t0003g0339 a0001c0003t0003g0340 |
3 | HG02896.hp2 HG02897.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.411+717T>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57622417 | |||||||
| chr15:57622447 | G | T | 8 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(5): Show |
8 | HG02258.hp1 HG02451.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.411+747G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57622447 | |||||||
| chr15:57622524 | C | G | 1 | a0002c0002t0002g0077 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.411+824C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57622524 | |||||||
| chr15:57622547 | T | C | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.411+847T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57622547 | |||||||
| chr15:57622599 | G | A | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.411+899G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57622599 | |||||||
| chr15:57622638 | T | C | 8 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(5): Show |
8 | HG02258.hp1 HG02451.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.411+938T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57622638 | |||||||
| chr15:57622643 | T | G | 1 | a0003c0005t0010g0310 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.411+943T>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57622643 | |||||||
| chr15:57622812 | T | C | 3 | a0001c0003t0001g0237 a0001c0003t0003g0339 a0001c0003t0003g0340 |
3 | HG02896.hp2 HG02897.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.411+1112T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57622812 | |||||||
| chr15:57622953 | C | G | 28 | a0001c0003t0003g0118 a0001c0003t0003g0125 a0001c0003t0003g0129 others(25): Show |
28 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.411+1253C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57622953 | |||||||
| chr15:57623119 | C | T | 2 | a0001c0001t0007g0243 a0001c0001t0020g0309 |
2 | NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.411+1419C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57623119 | |||||||
| chr15:57623271 | A | G | 1 | a0003c0005t0010g0310 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.411+1571A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57623271 | |||||||
| chr15:57623395 | T | C | 4 | a0001c0003t0002g0126 a0001c0003t0006g0115 a0001c0003t0006g0116 others(1): Show |
4 | HG01109.hp2 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.411+1695T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57623395 | |||||||
| chr15:57623453 | A | C | 6 | a0001c0003t0001g0237 a0001c0003t0003g0339 a0001c0003t0003g0340 others(3): Show |
6 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.411+1753A>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57623453 | |||||||
| chr15:57623487 | T | C | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.411+1787T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57623487 | |||||||
| chr15:57623502 | G | A | 1 | a0001c0003t0003g0147 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.411+1802G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57623502 | |||||||
| chr15:57623531 | G | A | 1 | a0001c0001t0003g0293 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.411+1831G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57623531 | |||||||
| chr15:57623561 | T | A | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.411+1861T>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57623561 | |||||||
| chr15:57623626 | C | A | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.411+1926C>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57623626 | |||||||
| chr15:57623644 | A | G | 6 | a0001c0003t0001g0113 a0001c0003t0004g0109 a0001c0003t0004g0111 others(3): Show |
6 | HG01891.hp1 HG02280.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.411+1944A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57623644 | |||||||
| chr15:57623667 | A | G | 2 | a0001c0001t0007g0243 a0001c0001t0020g0309 |
2 | NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.411+1967A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57623667 | |||||||
| chr15:57623668 | G | A | 1 | a0001c0003t0003g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.411+1968G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57623668 | |||||||
| chr15:57623732 | C | CA | 117 | a0001c0001t0001g0170 a0001c0001t0007g0243 a0001c0001t0020g0309 others(114): Show |
124 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.412-2035dupA | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr15 | 57623732 | ||||||
| chr15:57623745 | T | A | 1 | a0001c0001t0003g0293 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.412-2034T>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57623745 | |||||||
| chr15:57623777 | C | T | 28 | a0001c0003t0003g0118 a0001c0003t0003g0125 a0001c0003t0003g0129 others(25): Show |
28 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.412-2002C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57623777 | |||||||
| chr15:57623802 | TA | T | 89 | a0001c0001t0001g0195 a0001c0001t0001g0197 a0001c0003t0001g0171 others(86): Show |
96 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.412-1963delA | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr15 | 57623802 | ||||||
| chr15:57623839 | A | C | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.412-1940A>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57623839 | |||||||
| chr15:57623863 | C | T | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.412-1916C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57623863 | |||||||
| chr15:57623943 | A | G | 1 | a0001c0001t0001g0273 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.412-1836A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57623943 | |||||||
| chr15:57624009 | C | G | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.412-1770C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57624009 | |||||||
| chr15:57624025 | G | A | 1 | a0001c0003t0002g0058 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.412-1754G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57624025 | |||||||
| chr15:57624065 | A | T | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.412-1714A>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57624065 | |||||||
| chr15:57624077 | A | G | 1 | a0003c0005t0010g0310 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.412-1702A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57624077 | |||||||
| chr15:57624104 | A | G | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.412-1675A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57624104 | |||||||
| chr15:57624124 | G | C | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.412-1655G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57624124 | |||||||
| chr15:57624148 | C | T | 3 | a0001c0001t0003g0294 a0001c0003t0003g0295 a0001c0003t0003g0296 |
3 | HG02258.hp1 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.412-1631C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57624148 | |||||||
| chr15:57624176 | A | G | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.412-1603A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57624176 | |||||||
| chr15:57624369 | G | A | 2 | a0001c0001t0007g0243 a0001c0001t0020g0309 |
2 | NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.412-1410G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57624369 | |||||||
| chr15:57624391 | CCCCATTT others(41): Show |
C | 1 | a0002c0002t0005g0070 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.412-1384_412-1337d others(50): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr15 | 57624391 | ||||||
| chr15:57624398 | T | C | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.412-1381T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57624398 | |||||||
| chr15:57624444 | T | G | 1 | a0005c0011t0002g0117 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.412-1335T>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57624444 | |||||||
| chr15:57624460 | A | G | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.412-1319A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57624460 | |||||||
| chr15:57624470 | A | G | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.412-1309A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57624470 | |||||||
| chr15:57624499 | T | G | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.412-1280T>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57624499 | |||||||
| chr15:57624558 | G | C | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.412-1221G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57624558 | |||||||
| chr15:57624608 | A | G | 50 | a0001c0001t0001g0008 a0001c0001t0001g0164 a0001c0001t0001g0165 others(47): Show |
51 | HG00423.hp1 HG00609.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.412-1171A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57624608 | |||||||
| chr15:57624719 | T | TCCTCCTT others(29): Show |
1 | a0001c0003t0003g0139 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.412-1059_412-1024d others(38): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr15 | 57624719 | ||||||
| chr15:57624823 | C | A | 2 | a0003c0005t0004g0333 a0003c0005t0004g0334 |
2 | HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.412-956C>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57624823 | |||||||
| chr15:57624852 | C | T | 1 | a0001c0001t0001g0252 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.412-927C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57624852 | |||||||
| chr15:57624866 | C | T | 28 | a0001c0003t0003g0118 a0001c0003t0003g0125 a0001c0003t0003g0129 others(25): Show |
28 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.412-913C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57624866 | |||||||
| chr15:57624899 | C | T | 1 | a0001c0001t0001g0278 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.412-880C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57624899 | |||||||
| chr15:57624946 | G | A | 1 | a0002c0002t0001g0336 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.412-833G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57624946 | |||||||
| chr15:57625055 | C | CT | 16 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(13): Show |
16 | HG01891.hp1 HG02257.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.412-709dupT | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr15 | 57625055 | ||||||
| chr15:57625091 | G | A | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.412-688G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57625091 | |||||||
| chr15:57625118 | C | T | 11 | a0002c0002t0002g0006 a0002c0002t0002g0096 a0002c0002t0002g0097 others(8): Show |
12 | HG00673.hp1 HG02083.hp1 HG02300.hp1 others(9): Show |
intron_variant | MODIFIER | c.412-661C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57625118 | |||||||
| chr15:57625122 | A | G | 6 | a0001c0001t0007g0325 a0001c0001t0007g0327 a0001c0001t0008g0328 others(3): Show |
6 | HG01884.hp1 HG02055.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.412-657A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57625122 | |||||||
| chr15:57625142 | T | TGGCTCAC others(9): Show |
1 | a0001c0001t0003g0293 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.412-636_412-621dup others(16): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr15 | 57625142 | ||||||
| chr15:57625165 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.412-614C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57625165 | |||||||
| chr15:57625166 | G | C | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.412-613G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57625166 | |||||||
| chr15:57625223 | G | A | 1 | a0001c0001t0001g0188 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.412-556G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57625223 | |||||||
| chr15:57625276 | G | A | 1 | a0001c0003t0006g0119 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.412-503G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57625276 | |||||||
| chr15:57625317 | G | A | 1 | a0001c0001t0001g0259 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.412-462G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57625317 | |||||||
| chr15:57625325 | C | T | 6 | a0001c0001t0001g0220 a0001c0001t0001g0230 a0001c0001t0001g0271 others(3): Show |
6 | HG02027.hp2 HG02818.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.412-454C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57625325 | |||||||
| chr15:57625391 | C | T | 2 | a0003c0005t0004g0333 a0003c0005t0004g0334 |
2 | HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.412-388C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57625391 | |||||||
| chr15:57625423 | C | T | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.412-356C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57625423 | |||||||
| chr15:57625436 | A | T | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.412-343A>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57625436 | |||||||
| chr15:57625458 | C | T | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.412-321C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57625458 | |||||||
| chr15:57625623 | C | T | 150 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(147): Show |
152 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(149): Show |
intron_variant | MODIFIER | c.412-156C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57625623 | |||||||
| chr15:57625723 | A | G | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.412-56A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57625723 | |||||||
| chr15:57625746 | G | C | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.412-33G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57625746 | |||||||
| chr15:57625767 | C | T | 2 | a0001c0001t0007g0243 a0001c0001t0020g0309 |
2 | NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.412-12C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57625767 | |||||||
| chr15:57625966 | A | G | 2 | a0002c0002t0001g0335 a0002c0002t0001g0336 |
2 | HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.525+74A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57625966 | |||||||
| chr15:57626059 | G | T | 7 | a0001c0001t0001g0008 a0001c0001t0001g0248 a0001c0001t0001g0249 others(4): Show |
8 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.525+167G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57626059 | |||||||
| chr15:57626165 | C | T | 153 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(150): Show |
155 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(152): Show |
intron_variant | MODIFIER | c.525+273C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57626165 | |||||||
| chr15:57626186 | G | C | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.525+294G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57626186 | |||||||
| chr15:57626200 | G | A | 335 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(332): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.525+308G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57626200 | |||||||
| chr15:57626376 | C | T | 33 | a0001c0003t0003g0118 a0001c0003t0003g0125 a0001c0003t0003g0129 others(30): Show |
33 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.525+484C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57626376 | |||||||
| chr15:57626417 | C | G | 4 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(1): Show |
4 | HG02451.hp1 HG02922.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.525+525C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57626417 | |||||||
| chr15:57626458 | C | G | 159 | a0001c0003t0001g0113 a0001c0003t0001g0171 a0001c0003t0001g0227 others(156): Show |
166 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.525+566C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57626458 | |||||||
| chr15:57626573 | T | C | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0003c0005t0010g0310 |
3 | HG02818.hp2 HG03540.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.525+681T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57626573 | |||||||
| chr15:57626695 | C | G | 6 | a0001c0001t0007g0243 a0001c0001t0020g0309 a0003c0005t0004g0333 others(3): Show |
6 | HG02818.hp2 HG03540.hp2 HG04199.hp2 others(3): Show |
intron_variant | MODIFIER | c.525+803C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57626695 | |||||||
| chr15:57626729 | A | C | 1 | a0001c0001t0001g0223 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.525+837A>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57626729 | |||||||
| chr15:57626937 | G | A | 1 | a0006c0006t0002g0120 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.525+1045G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57626937 | |||||||
| chr15:57627014 | C | CA | 35 | a0001c0001t0001g0161 a0001c0001t0001g0173 a0001c0001t0001g0174 others(32): Show |
36 | HG00642.hp2 HG00741.hp2 HG01168.hp2 others(33): Show |
intron_variant | MODIFIER | c.525+1122_525+1123i others(3): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57627014 | |||||||
| chr15:57627015 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.525+1123G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57627015 | |||||||
| chr15:57627020 | G | T | 1 | a0001c0001t0006g0152 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.525+1128G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57627020 | |||||||
| chr15:57627161 | AT | A | 6 | a0001c0001t0006g0152 a0001c0003t0001g0113 a0001c0003t0004g0109 others(3): Show |
6 | HG01891.hp1 HG02280.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.525+1272delT | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr15 | 57627161 | ||||||
| chr15:57627313 | C | T | 1 | a0001c0007t0003g0128 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.525+1421C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57627313 | |||||||
| chr15:57627330 | C | G | 6 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(3): Show |
6 | HG02258.hp1 HG02451.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.525+1438C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57627330 | |||||||
| chr15:57627336 | C | T | 1 | a0002c0002t0002g0084 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.525+1444C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57627336 | |||||||
| chr15:57627349 | C | G | 28 | a0001c0001t0002g0304 a0001c0001t0002g0306 a0001c0001t0002g0308 others(25): Show |
28 | HG00099.hp2 HG01081.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.525+1457C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57627349 | |||||||
| chr15:57627362 | A | G | 1 | a0005c0011t0002g0117 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.525+1470A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57627362 | |||||||
| chr15:57627378 | AGGGAGG | A | 33 | a0001c0003t0003g0118 a0001c0003t0003g0125 a0001c0003t0003g0129 others(30): Show |
33 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.525+1507_525+1512d others(8): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr15 | 57627378 | ||||||
| chr15:57627391 | G | A | 1 | a0001c0001t0006g0152 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.525+1499G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57627391 | |||||||
| chr15:57627393 | GAGGGGGA others(10): Show |
G | 2 | a0001c0001t0008g0329 a0001c0001t0019g0326 |
2 | HG02055.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.525+1511_525+1527d others(19): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr15 | 57627393 | ||||||
| chr15:57627413 | G | A | 1 | a0003c0005t0010g0310 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.525+1521G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57627413 | |||||||
| chr15:57627414 | GGGA | G | 19 | a0001c0001t0002g0304 a0001c0001t0002g0306 a0001c0001t0002g0308 others(16): Show |
19 | HG00099.hp2 HG01081.hp1 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.525+1539_525+1541d others(5): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr15 | 57627414 | ||||||
| chr15:57627530 | A | G | 21 | a0001c0001t0002g0304 a0001c0001t0002g0306 a0001c0001t0002g0308 others(18): Show |
21 | HG00099.hp2 HG01081.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.525+1638A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57627530 | |||||||
| chr15:57627544 | C | A | 2 | a0001c0001t0007g0243 a0001c0001t0020g0309 |
2 | NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.525+1652C>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57627544 | |||||||
| chr15:57627776 | G | A | 153 | a0001c0001t0002g0307 a0001c0001t0006g0152 a0001c0001t0007g0325 others(150): Show |
160 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.525+1884G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57627776 | |||||||
| chr15:57627932 | A | G | 181 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(178): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.526-1770A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57627932 | |||||||
| chr15:57628026 | A | T | 9 | a0001c0001t0001g0168 a0001c0001t0001g0189 a0001c0001t0001g0217 others(6): Show |
9 | HG02258.hp2 HG02572.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.526-1676A>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57628026 | |||||||
| chr15:57628178 | C | T | 1 | a0002c0002t0018g0016 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.526-1524C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57628178 | |||||||
| chr15:57628239 | C | T | 1 | a0002c0002t0002g0056 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.526-1463C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57628239 | |||||||
| chr15:57628445 | T | A | 1 | a0001c0003t0002g0023 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.526-1257T>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57628445 | |||||||
| chr15:57628460 | C | T | 167 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(164): Show |
174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.526-1242C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57628460 | |||||||
| chr15:57628505 | A | G | 175 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(172): Show |
177 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(174): Show |
intron_variant | MODIFIER | c.526-1197A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57628505 | |||||||
| chr15:57628523 | G | A | 1 | a0001c0003t0003g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.526-1179G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57628523 | |||||||
| chr15:57628603 | T | C | 167 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(164): Show |
174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.526-1099T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57628603 | |||||||
| chr15:57628612 | G | A | 28 | a0001c0003t0003g0118 a0001c0003t0003g0129 a0001c0003t0003g0130 others(25): Show |
28 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.526-1090G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57628612 | |||||||
| chr15:57628636 | T | A | 1 | a0001c0001t0001g0226 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.526-1066T>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57628636 | |||||||
| chr15:57628639 | A | G | 1 | a0002c0002t0002g0074 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.526-1063A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57628639 | |||||||
| chr15:57628770 | G | A | 5 | a0001c0003t0001g0113 a0001c0003t0004g0109 a0001c0003t0004g0111 others(2): Show |
5 | HG01891.hp1 HG02280.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.526-932G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57628770 | |||||||
| chr15:57628823 | G | A | 1 | a0001c0001t0006g0152 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.526-879G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57628823 | |||||||
| chr15:57628851 | G | C | 1 | a0002c0002t0002g0083 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.526-851G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57628851 | |||||||
| chr15:57628955 | C | A | 1 | a0006c0006t0002g0120 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.526-747C>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57628955 | |||||||
| chr15:57628997 | C | T | 135 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(132): Show |
142 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.526-705C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57628997 | |||||||
| chr15:57629031 | C | T | 75 | a0001c0001t0001g0008 a0001c0001t0001g0161 a0001c0001t0001g0164 others(72): Show |
77 | HG00423.hp1 HG00609.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.526-671C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57629031 | |||||||
| chr15:57629088 | C | CA | 7 | a0001c0001t0001g0162 a0001c0001t0001g0176 a0001c0001t0001g0191 others(4): Show |
7 | HG00544.hp2 HG02027.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.526-595dupA | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr15 | 57629088 | ||||||
| chr15:57629088 | CA | C | 93 | a0001c0001t0001g0252 a0001c0001t0002g0307 a0001c0001t0007g0243 others(90): Show |
100 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.526-595delA | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr15 | 57629088 | ||||||
| chr15:57629088 | CAA | C | 59 | a0001c0001t0006g0152 a0001c0003t0002g0055 a0001c0003t0002g0058 others(56): Show |
59 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.526-596_526-595del others(2): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr15 | 57629088 | ||||||
| chr15:57629088 | CAAAAAAA others(3): Show |
C | 1 | a0006c0006t0002g0120 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.526-604_526-595del others(10): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr15 | 57629088 | ||||||
| chr15:57629119 | A | G | 1 | a0003c0005t0010g0310 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.526-583A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57629119 | |||||||
| chr15:57629150 | G | A | 6 | a0001c0001t0001g0286 a0001c0003t0001g0113 a0001c0003t0004g0109 others(3): Show |
6 | HG01891.hp1 HG02040.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.526-552G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57629150 | |||||||
| chr15:57629168 | T | C | 1 | a0001c0001t0002g0322 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.526-534T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57629168 | |||||||
| chr15:57629170 | A | T | 3 | a0001c0001t0001g0251 a0001c0001t0001g0256 a0001c0003t0002g0085 |
3 | NA18945.hp2 NA18983.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.526-532A>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57629170 | |||||||
| chr15:57629218 | C | T | 167 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(164): Show |
174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.526-484C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57629218 | |||||||
| chr15:57629340 | A | G | 6 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(3): Show |
6 | HG02258.hp1 HG02451.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.526-362A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57629340 | |||||||
| chr15:57629437 | A | G | 21 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(18): Show |
21 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.526-265A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57629437 | |||||||
| chr15:57629637 | T | C | 5 | a0001c0003t0001g0113 a0001c0003t0004g0109 a0001c0003t0004g0111 others(2): Show |
5 | HG01891.hp1 HG02280.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.526-65T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57629637 | |||||||
| chr15:57629638 | G | A | 2 | a0001c0001t0007g0243 a0001c0001t0020g0309 |
2 | NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.526-64G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57629638 | |||||||
| chr15:57629661 | C | T | 1 | a0005c0011t0002g0117 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.526-41C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57629661 | |||||||
| chr15:57629667 | C | T | 1 | a0001c0001t0003g0294 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.526-35C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57629667 | |||||||
| chr15:57629889 | A | G | 2 | a0001c0001t0007g0243 a0001c0001t0020g0309 |
2 | NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.678+35A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 6/12 | chr15 | 57629889 | |||||||
| chr15:57629971 | A | AT | 18 | a0001c0001t0001g0165 a0001c0001t0001g0232 a0001c0001t0001g0239 others(15): Show |
18 | HG00099.hp2 HG01081.hp1 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.678+132dupT | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr15 | 57629971 | ||||||
| chr15:57629971 | A | ATTTTTTT others(4): Show |
1 | a0001c0003t0002g0023 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.678+124_678+125ins others(11): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr15 | 57629971 | ||||||
| chr15:57629971 | A | ATTTTTTT others(2): Show |
6 | a0001c0001t0001g0240 a0001c0001t0007g0325 a0001c0001t0008g0328 others(3): Show |
6 | HG01884.hp1 HG02280.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.678+124_678+132dup others(9): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr15 | 57629971 | ||||||
| chr15:57629971 | A | ATTTTTTT others(3): Show |
5 | a0001c0001t0006g0152 a0001c0001t0007g0243 a0001c0001t0019g0326 others(2): Show |
5 | HG02055.hp2 HG03041.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.678+123_678+132dup others(10): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr15 | 57629971 | ||||||
| chr15:57629971 | A | ATTTTTTT others(4): Show |
78 | a0001c0003t0001g0171 a0001c0003t0001g0227 a0001c0003t0002g0003 others(75): Show |
85 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.678+122_678+132dup others(11): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr15 | 57629971 | ||||||
| chr15:57629971 | A | ATTTTTTT others(5): Show |
33 | a0001c0001t0002g0307 a0001c0003t0002g0018 a0001c0003t0002g0033 others(30): Show |
33 | HG00323.hp2 HG00597.hp1 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.678+121_678+132dup others(12): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr15 | 57629971 | ||||||
| chr15:57629971 | A | ATTTTTTT others(6): Show |
2 | a0001c0003t0001g0113 a0001c0003t0004g0114 |
2 | HG01891.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.678+120_678+132dup others(13): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr15 | 57629971 | ||||||
| chr15:57629971 | A | ATTTTTTT others(7): Show |
1 | a0001c0001t0003g0293 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.678+119_678+132dup others(14): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr15 | 57629971 | ||||||
| chr15:57629971 | A | ATTTTTTT others(9): Show |
1 | a0001c0001t0003g0294 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.678+132_678+133ins others(16): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr15 | 57629971 | ||||||
| chr15:57630121 | A | C | 1 | a0003c0005t0010g0310 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.678+267A>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 6/12 | chr15 | 57630121 | |||||||
| chr15:57630211 | G | A | 3 | a0001c0003t0002g0126 a0001c0003t0014g0110 a0005c0011t0002g0117 |
3 | HG02280.hp1 HG02559.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.678+357G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 6/12 | chr15 | 57630211 | |||||||
| chr15:57630278 | C | T | 2 | a0001c0001t0001g0291 a0001c0001t0001g0300 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.678+424C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 6/12 | chr15 | 57630278 | |||||||
| chr15:57630312 | CTT | C | 9 | a0001c0001t0007g0325 a0001c0001t0007g0327 a0001c0001t0008g0328 others(6): Show |
9 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.678+459_678+460del others(2): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 6/12 | chr15 | 57630312 | |||||||
| chr15:57630403 | T | A | 5 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(2): Show |
5 | HG02258.hp1 HG02451.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.678+549T>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 6/12 | chr15 | 57630403 | |||||||
| chr15:57630408 | C | T | 1 | a0001c0001t0001g0289 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.678+554C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 6/12 | chr15 | 57630408 | |||||||
| chr15:57630497 | G | T | 14 | a0001c0001t0007g0325 a0001c0001t0007g0327 a0001c0001t0008g0328 others(11): Show |
14 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.678+643G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 6/12 | chr15 | 57630497 | |||||||
| chr15:57630690 | T | C | 4 | a0001c0003t0006g0115 a0001c0003t0006g0116 a0001c0003t0006g0119 others(1): Show |
4 | HG01109.hp2 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.678+836T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 6/12 | chr15 | 57630690 | |||||||
| chr15:57630866 | G | C | 6 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(3): Show |
6 | HG02258.hp1 HG02451.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.678+1012G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 6/12 | chr15 | 57630866 | |||||||
| chr15:57630888 | G | T | 2 | a0001c0001t0001g0211 a0001c0001t0001g0268 |
2 | HG01978.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.678+1034G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 6/12 | chr15 | 57630888 | |||||||
| chr15:57630889 | G | T | 1 | a0001c0001t0008g0329 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.678+1035G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 6/12 | chr15 | 57630889 | |||||||
| chr15:57630966 | G | A | 1 | a0001c0001t0007g0243 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.678+1112G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 6/12 | chr15 | 57630966 | |||||||
| chr15:57631038 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.678+1184G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 6/12 | chr15 | 57631038 | |||||||
| chr15:57631092 | G | A | 3 | a0001c0001t0007g0243 a0001c0001t0020g0309 a0001c0003t0002g0126 |
3 | HG03139.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.678+1238G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 6/12 | chr15 | 57631092 | |||||||
| chr15:57631180 | A | AT | 148 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(145): Show |
155 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.679-1247dupT | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr15 | 57631180 | ||||||
| chr15:57631180 | AT | A | 5 | a0001c0001t0001g0232 a0001c0001t0002g0306 a0001c0001t0002g0313 others(2): Show |
5 | HG00099.hp2 HG01081.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.679-1247delT | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr15 | 57631180 | ||||||
| chr15:57631182 | T | C | 5 | a0001c0001t0001g0232 a0001c0001t0002g0306 a0001c0001t0002g0313 others(2): Show |
5 | HG00099.hp2 HG01081.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.679-1252T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 6/12 | chr15 | 57631182 | |||||||
| chr15:57631259 | G | C | 22 | a0001c0001t0001g0161 a0001c0001t0001g0169 a0001c0001t0001g0172 others(19): Show |
22 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.679-1175G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 6/12 | chr15 | 57631259 | |||||||
| chr15:57631264 | G | T | 5 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(2): Show |
5 | HG02451.hp1 HG02886.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.679-1170G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 6/12 | chr15 | 57631264 | |||||||
| chr15:57631464 | G | GA | 144 | a0001c0001t0001g0008 a0001c0001t0001g0176 a0001c0001t0001g0179 others(141): Show |
152 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.679-970_679-969ins others(1): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 6/12 | chr15 | 57631464 | |||||||
| chr15:57631464 | G | GAA | 140 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(137): Show |
141 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.679-970_679-969ins others(2): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 6/12 | chr15 | 57631464 | |||||||
| chr15:57631464 | G | GAAA | 13 | a0001c0001t0001g0157 a0001c0001t0001g0187 a0001c0001t0001g0220 others(10): Show |
13 | HG00597.hp2 HG01243.hp1 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.679-970_679-969ins others(3): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 6/12 | chr15 | 57631464 | |||||||
| chr15:57631465 | G | A | 336 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(333): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.679-969G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 6/12 | chr15 | 57631465 | |||||||
| chr15:57631509 | C | T | 1 | a0001c0003t0001g0237 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.679-925C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 6/12 | chr15 | 57631509 | |||||||
| chr15:57631775 | A | G | 1 | a0001c0001t0001g0288 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.679-659A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 6/12 | chr15 | 57631775 | |||||||
| chr15:57631822 | G | A | 1 | a0001c0001t0001g0225 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.679-612G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 6/12 | chr15 | 57631822 | |||||||
| chr15:57631840 | C | T | 189 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0015 others(186): Show |
197 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.679-594C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 6/12 | chr15 | 57631840 | |||||||
| chr15:57631885 | G | A | 1 | a0001c0003t0005g0090 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.679-549G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 6/12 | chr15 | 57631885 | |||||||
| chr15:57631947 | A | T | 1 | a0002c0002t0002g0127 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.679-487A>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 6/12 | chr15 | 57631947 | |||||||
| chr15:57631960 | C | T | 8 | a0001c0001t0007g0325 a0001c0001t0007g0327 a0001c0001t0008g0328 others(5): Show |
8 | HG01884.hp1 HG02717.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.679-474C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 6/12 | chr15 | 57631960 | |||||||
| chr15:57632036 | A | C | 1 | a0001c0001t0001g0281 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.679-398A>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 6/12 | chr15 | 57632036 | |||||||
| chr15:57632131 | A | G | 5 | a0002c0002t0002g0039 a0002c0002t0002g0044 a0002c0002t0002g0045 others(2): Show |
5 | HG00423.hp2 HG00438.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.679-303A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 6/12 | chr15 | 57632131 | |||||||
| chr15:57632276 | C | G | 3 | a0001c0003t0006g0115 a0001c0003t0006g0116 a0001c0003t0006g0119 |
3 | HG01109.hp2 HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.679-158C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 6/12 | chr15 | 57632276 | |||||||
| chr15:57632388 | T | A | 142 | a0001c0001t0001g0013 a0001c0001t0001g0157 a0001c0001t0001g0160 others(139): Show |
143 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.679-46T>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 6/12 | chr15 | 57632388 | |||||||
| chr15:57632409 | C | T | 13 | a0001c0001t0001g0176 a0001c0001t0001g0234 a0001c0001t0001g0235 others(10): Show |
13 | HG00738.hp1 HG01891.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.679-25C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 6/12 | chr15 | 57632409 | |||||||
| chr15:57632427 | G | A | 8 | a0001c0001t0007g0325 a0001c0001t0007g0327 a0001c0001t0008g0328 others(5): Show |
8 | HG01884.hp1 HG02717.hp1 HG02818.hp2 others(5): Show |
splice_region_variant&intron_variant | LOW | c.679-7G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 6/12 | chr15 | 57632427 | |||||||
| chr15:57632579 | C | T | 2 | a0001c0003t0003g0339 a0001c0003t0003g0340 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.804+20C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 7/12 | chr15 | 57632579 | |||||||
| chr15:57632590 | T | C | 2 | a0001c0001t0006g0152 a0001c0001t0013g0266 |
2 | HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.804+31T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 7/12 | chr15 | 57632590 | |||||||
| chr15:57632748 | C | T | 2 | a0001c0001t0006g0152 a0001c0001t0013g0266 |
2 | HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.804+189C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 7/12 | chr15 | 57632748 | |||||||
| chr15:57632751 | C | T | 6 | a0001c0001t0001g0186 a0001c0001t0001g0188 a0001c0001t0001g0195 others(3): Show |
6 | HG00741.hp1 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.804+192C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 7/12 | chr15 | 57632751 | |||||||
| chr15:57632755 | A | T | 2 | a0001c0001t0001g0254 a0001c0001t0001g0263 |
2 | HG01928.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.804+196A>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 7/12 | chr15 | 57632755 | |||||||
| chr15:57632853 | G | A | 8 | a0001c0001t0007g0325 a0001c0001t0007g0327 a0001c0001t0008g0328 others(5): Show |
8 | HG01884.hp1 HG02717.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.804+294G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 7/12 | chr15 | 57632853 | |||||||
| chr15:57632864 | C | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0003t0002g0126 others(1): Show |
4 | HG01167.hp1 HG01169.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.804+305C>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 7/12 | chr15 | 57632864 | |||||||
| chr15:57632959 | A | G | 1 | a0001c0001t0001g0253 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.804+400A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 7/12 | chr15 | 57632959 | |||||||
| chr15:57632993 | C | G | 333 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(330): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.804+434C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 7/12 | chr15 | 57632993 | |||||||
| chr15:57633135 | A | G | 192 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0015 others(189): Show |
200 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.805-478A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 7/12 | chr15 | 57633135 | |||||||
| chr15:57633156 | G | A | 1 | a0002c0004t0001g0222 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.805-457G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 7/12 | chr15 | 57633156 | |||||||
| chr15:57633436 | A | C | 5 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(2): Show |
5 | HG02451.hp1 HG02886.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.805-177A>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 7/12 | chr15 | 57633436 | |||||||
| chr15:57633783 | T | G | 2 | a0001c0001t0006g0152 a0001c0001t0013g0266 |
2 | HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.933+42T>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57633783 | |||||||
| chr15:57633792 | A | G | 93 | a0001c0001t0001g0260 a0001c0003t0002g0011 a0001c0003t0002g0030 others(90): Show |
99 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.933+51A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57633792 | |||||||
| chr15:57633860 | A | G | 3 | a0001c0003t0006g0115 a0001c0003t0006g0116 a0001c0003t0006g0119 |
3 | HG01109.hp2 HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.933+119A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57633860 | |||||||
| chr15:57633876 | T | A | 1 | a0001c0003t0001g0171 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.933+135T>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57633876 | |||||||
| chr15:57633920 | A | C | 1 | a0001c0001t0001g0221 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.933+179A>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57633920 | |||||||
| chr15:57634006 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.933+265G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57634006 | |||||||
| chr15:57634075 | G | A | 103 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0259 others(100): Show |
109 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.933+334G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57634075 | |||||||
| chr15:57634194 | G | T | 1 | a0001c0001t0002g0314 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.933+453G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57634194 | |||||||
| chr15:57634212 | C | T | 1 | a0001c0001t0001g0281 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.933+471C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57634212 | |||||||
| chr15:57634227 | G | A | 5 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0007g0332 others(2): Show |
5 | HG01167.hp1 HG01169.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.933+486G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57634227 | |||||||
| chr15:57634296 | G | A | 27 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(24): Show |
28 | HG00642.hp2 HG01074.hp2 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.933+555G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57634296 | |||||||
| chr15:57634413 | G | C | 256 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(253): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.933+672G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57634413 | |||||||
| chr15:57634549 | G | T | 1 | a0001c0003t0003g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.933+808G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57634549 | |||||||
| chr15:57634597 | G | C | 7 | a0001c0001t0001g0232 a0001c0001t0001g0259 a0001c0001t0002g0306 others(4): Show |
7 | HG00099.hp2 HG01081.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.933+856G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57634597 | |||||||
| chr15:57634609 | A | C | 211 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0015 others(208): Show |
220 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.933+868A>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57634609 | |||||||
| chr15:57634663 | C | G | 1 | a0002c0002t0005g0089 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.933+922C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57634663 | |||||||
| chr15:57634664 | C | T | 4 | a0001c0001t0003g0294 a0001c0003t0002g0058 a0001c0003t0003g0295 others(1): Show |
4 | HG02258.hp1 HG02559.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.933+923C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57634664 | |||||||
| chr15:57634694 | G | C | 176 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0001g0179 others(173): Show |
184 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.933+953G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57634694 | |||||||
| chr15:57634776 | A | G | 1 | a0002c0002t0011g0072 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.933+1035A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57634776 | |||||||
| chr15:57634798 | C | G | 2 | a0001c0001t0001g0234 a0001c0001t0001g0235 |
2 | HG02145.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.933+1057C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57634798 | |||||||
| chr15:57634984 | T | G | 1 | a0005c0011t0002g0117 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.933+1243T>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57634984 | |||||||
| chr15:57635027 | C | G | 3 | a0001c0003t0006g0115 a0001c0003t0006g0116 a0001c0003t0006g0119 |
3 | HG01109.hp2 HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.933+1286C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57635027 | |||||||
| chr15:57635084 | A | T | 141 | a0001c0001t0001g0160 a0001c0001t0001g0183 a0001c0001t0001g0184 others(138): Show |
147 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.933+1343A>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57635084 | |||||||
| chr15:57635094 | G | C | 1 | a0005c0011t0002g0117 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.933+1353G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57635094 | |||||||
| chr15:57635191 | G | A | 47 | a0001c0001t0001g0160 a0001c0001t0001g0184 a0001c0001t0001g0192 others(44): Show |
48 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.933+1450G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57635191 | |||||||
| chr15:57635253 | A | G | 3 | a0002c0002t0002g0040 a0002c0002t0012g0088 a0002c0009t0002g0037 |
3 | NA19003.hp1 NA19009.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.933+1512A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57635253 | |||||||
| chr15:57635265 | T | C | 5 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0007g0332 others(2): Show |
5 | HG01167.hp1 HG01169.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.933+1524T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57635265 | |||||||
| chr15:57635279 | T | A | 1 | a0001c0003t0001g0237 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.933+1538T>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57635279 | |||||||
| chr15:57635281 | A | G | 1 | a0001c0003t0001g0237 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.933+1540A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57635281 | |||||||
| chr15:57635307 | G | T | 188 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0001g0176 others(185): Show |
196 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(193): Show |
intron_variant | MODIFIER | c.933+1566G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57635307 | |||||||
| chr15:57635310 | C | T | 5 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0007g0332 others(2): Show |
5 | HG01167.hp1 HG01169.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.933+1569C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57635310 | |||||||
| chr15:57635447 | T | C | 1 | a0003c0005t0010g0310 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.933+1706T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57635447 | |||||||
| chr15:57635464 | A | G | 1 | a0001c0001t0002g0317 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.933+1723A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57635464 | |||||||
| chr15:57635479 | G | A | 12 | a0001c0001t0001g0176 a0001c0001t0001g0234 a0001c0001t0001g0235 others(9): Show |
12 | HG00738.hp1 HG01891.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.933+1738G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57635479 | |||||||
| chr15:57635636 | A | G | 1 | a0001c0003t0003g0145 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.933+1895A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57635636 | |||||||
| chr15:57635664 | T | C | 1 | a0001c0003t0005g0090 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.933+1923T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57635664 | |||||||
| chr15:57635708 | A | C | 128 | a0001c0001t0001g0008 a0001c0001t0001g0176 a0001c0001t0001g0179 others(125): Show |
135 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.933+1967A>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57635708 | |||||||
| chr15:57635728 | G | C | 203 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0015 others(200): Show |
211 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.934-1967G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57635728 | |||||||
| chr15:57635908 | A | T | 80 | a0001c0003t0002g0011 a0001c0003t0002g0030 a0001c0003t0002g0033 others(77): Show |
85 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.934-1787A>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57635908 | |||||||
| chr15:57635966 | A | C | 1 | a0003c0005t0010g0310 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.934-1729A>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57635966 | |||||||
| chr15:57636135 | T | A | 1 | a0002c0002t0002g0067 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.934-1560T>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57636135 | |||||||
| chr15:57636557 | A | G | 1 | a0003c0005t0010g0310 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.934-1138A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57636557 | |||||||
| chr15:57636624 | G | C | 16 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0232 others(13): Show |
16 | HG00099.hp2 HG01081.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.934-1071G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57636624 | |||||||
| chr15:57636739 | C | T | 2 | a0001c0001t0001g0234 a0001c0001t0001g0235 |
2 | HG02145.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.934-956C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57636739 | |||||||
| chr15:57636780 | T | C | 88 | a0001c0001t0001g0232 a0001c0001t0001g0259 a0001c0001t0002g0034 others(85): Show |
93 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.934-915T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57636780 | |||||||
| chr15:57636845 | C | G | 1 | a0001c0001t0007g0243 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.934-850C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57636845 | |||||||
| chr15:57636859 | G | T | 1 | a0002c0002t0002g0052 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.934-836G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57636859 | |||||||
| chr15:57636967 | T | C | 281 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(278): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.934-728T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57636967 | |||||||
| chr15:57637084 | C | A | 1 | a0001c0001t0001g0183 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.934-611C>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57637084 | |||||||
| chr15:57637149 | T | C | 280 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(277): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.934-546T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57637149 | |||||||
| chr15:57637151 | T | C | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0228 |
3 | HG03098.hp2 HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.934-544T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57637151 | |||||||
| chr15:57637197 | C | T | 1 | a0001c0001t0001g0203 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.934-498C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57637197 | |||||||
| chr15:57637463 | A | G | 134 | a0001c0001t0001g0008 a0001c0001t0001g0176 a0001c0001t0001g0179 others(131): Show |
142 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.934-232A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57637463 | |||||||
| chr15:57637538 | G | A | 1 | a0002c0002t0002g0081 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.934-157G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57637538 | |||||||
| chr15:57637574 | G | A | 1 | a0001c0001t0001g0203 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.934-121G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57637574 | |||||||
| chr15:57637781 | C | T | 1 | a0002c0002t0002g0054 | 1 | HG02622.hp2 | splice_region_variant&intron_variant | LOW | c.1013+7C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 9/12 | chr15 | 57637781 | |||||||
| chr15:57637834 | A | G | 1 | a0002c0002t0002g0081 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1013+60A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 9/12 | chr15 | 57637834 | |||||||
| chr15:57638195 | A | G | 1 | a0001c0003t0004g0111 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1013+421A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 9/12 | chr15 | 57638195 | |||||||
| chr15:57638316 | T | G | 5 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0007g0332 others(2): Show |
5 | HG01167.hp1 HG01169.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1013+542T>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 9/12 | chr15 | 57638316 | |||||||
| chr15:57638394 | C | T | 39 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0180 others(36): Show |
41 | HG00099.hp2 HG01069.hp1 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.1013+620C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 9/12 | chr15 | 57638394 | |||||||
| chr15:57638469 | C | T | 1 | a0001c0001t0001g0239 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1013+695C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 9/12 | chr15 | 57638469 | |||||||
| chr15:57638470 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1013+696G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 9/12 | chr15 | 57638470 | |||||||
| chr15:57638577 | C | T | 83 | a0001c0001t0001g0259 a0001c0001t0002g0306 a0001c0001t0002g0313 others(80): Show |
88 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.1013+803C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 9/12 | chr15 | 57638577 | |||||||
| chr15:57638695 | G | A | 80 | a0001c0001t0002g0034 a0001c0003t0002g0011 a0001c0003t0002g0030 others(77): Show |
85 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.1014-745G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 9/12 | chr15 | 57638695 | |||||||
| chr15:57638819 | T | C | 82 | a0001c0001t0002g0034 a0001c0003t0002g0011 a0001c0003t0002g0030 others(79): Show |
87 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1014-621T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 9/12 | chr15 | 57638819 | |||||||
| chr15:57638858 | C | T | 1 | a0001c0001t0007g0332 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1014-582C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 9/12 | chr15 | 57638858 | |||||||
| chr15:57638872 | A | G | 35 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0180 others(32): Show |
37 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.1014-568A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 9/12 | chr15 | 57638872 | |||||||
| chr15:57639087 | G | C | 3 | a0001c0003t0006g0115 a0001c0003t0006g0116 a0001c0003t0006g0119 |
3 | HG01109.hp2 HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1014-353G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 9/12 | chr15 | 57639087 | |||||||
| chr15:57639096 | A | G | 1 | a0001c0003t0002g0029 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1014-344A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 9/12 | chr15 | 57639096 | |||||||
| chr15:57639214 | A | AT | 99 | a0001c0001t0001g0176 a0001c0001t0001g0225 a0001c0001t0001g0234 others(96): Show |
105 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.1014-214dupT | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr15 | 57639214 | ||||||
| chr15:57639214 | A | T | 1 | a0001c0001t0001g0210 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1014-226A>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 9/12 | chr15 | 57639214 | |||||||
| chr15:57639214 | AT | A | 11 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0259 others(8): Show |
11 | HG00099.hp2 HG00609.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.1014-214delT | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr15 | 57639214 | ||||||
| chr15:57639218 | T | A | 15 | a0001c0001t0001g0161 a0001c0001t0001g0179 a0001c0001t0001g0180 others(12): Show |
15 | HG01192.hp2 HG02451.hp1 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.1014-222T>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 9/12 | chr15 | 57639218 | |||||||
| chr15:57639219 | T | A | 2 | a0001c0001t0002g0306 a0001c0001t0002g0313 |
2 | HG00099.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.1014-221T>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 9/12 | chr15 | 57639219 | |||||||
| chr15:57639222 | T | A | 5 | a0001c0001t0003g0293 a0001c0001t0007g0243 a0001c0003t0001g0237 others(2): Show |
5 | HG02896.hp2 HG02897.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1014-218T>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 9/12 | chr15 | 57639222 | |||||||
| chr15:57639334 | G | A | 31 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0180 others(28): Show |
33 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.1014-106G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 9/12 | chr15 | 57639334 | |||||||
| chr15:57639346 | G | C | 39 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0180 others(36): Show |
41 | HG00099.hp2 HG01069.hp1 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.1014-94G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 9/12 | chr15 | 57639346 | |||||||
| chr15:57639579 | T | A | 1 | a0002c0002t0002g0083 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1119+34T>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57639579 | |||||||
| chr15:57639642 | T | C | 1 | a0001c0001t0001g0267 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1119+97T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57639642 | |||||||
| chr15:57639645 | C | T | 5 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0007g0332 others(2): Show |
5 | HG01167.hp1 HG01169.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1119+100C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57639645 | |||||||
| chr15:57639708 | A | G | 1 | a0001c0001t0003g0312 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1119+163A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57639708 | |||||||
| chr15:57639803 | C | T | 1 | a0002c0002t0002g0053 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1119+258C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57639803 | |||||||
| chr15:57639862 | G | T | 2 | a0001c0001t0001g0240 a0001c0003t0003g0125 |
2 | HG02647.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1119+317G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57639862 | |||||||
| chr15:57639920 | G | GTC | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0005c0011t0002g0117 |
3 | HG02559.hp1 HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1119+392_1119+393d others(4): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr15 | 57639920 | ||||||
| chr15:57639924 | C | G | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0007c0010t0001g0158 |
3 | HG03098.hp2 HG06807.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1119+379C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57639924 | |||||||
| chr15:57640024 | C | T | 38 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0180 others(35): Show |
40 | HG00099.hp2 HG01069.hp1 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.1119+479C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57640024 | |||||||
| chr15:57640461 | T | C | 30 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0180 others(27): Show |
32 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.1119+916T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57640461 | |||||||
| chr15:57640480 | T | C | 5 | a0001c0003t0001g0113 a0001c0003t0004g0109 a0001c0003t0004g0111 others(2): Show |
5 | HG01891.hp1 HG02280.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1119+935T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57640480 | |||||||
| chr15:57640496 | A | G | 1 | a0003c0005t0010g0310 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1119+951A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57640496 | |||||||
| chr15:57640530 | A | G | 7 | a0001c0001t0007g0243 a0001c0001t0007g0325 a0001c0001t0007g0327 others(4): Show |
7 | HG01884.hp1 HG02717.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1119+985A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57640530 | |||||||
| chr15:57640551 | A | G | 1 | a0005c0011t0002g0117 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1119+1006A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57640551 | |||||||
| chr15:57640597 | A | C | 1 | a0001c0001t0001g0169 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1119+1052A>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57640597 | |||||||
| chr15:57640650 | G | C | 1 | a0002c0004t0001g0205 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1119+1105G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57640650 | |||||||
| chr15:57640695 | A | C | 6 | a0001c0001t0001g0259 a0001c0001t0001g0302 a0001c0001t0002g0306 others(3): Show |
6 | HG00099.hp2 HG01081.hp1 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.1119+1150A>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57640695 | |||||||
| chr15:57640738 | G | T | 2 | a0001c0001t0001g0014 a0001c0001t0001g0015 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1119+1193G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57640738 | |||||||
| chr15:57640772 | A | G | 1 | a0007c0010t0001g0158 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1119+1227A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57640772 | |||||||
| chr15:57640812 | G | A | 3 | a0001c0003t0006g0115 a0001c0003t0006g0116 a0001c0003t0006g0119 |
3 | HG01109.hp2 HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1119+1267G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57640812 | |||||||
| chr15:57640826 | G | A | 1 | a0005c0011t0002g0117 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1119+1281G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57640826 | |||||||
| chr15:57640876 | G | A | 1 | a0005c0011t0002g0117 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1119+1331G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57640876 | |||||||
| chr15:57640949 | T | A | 1 | a0001c0001t0001g0226 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1119+1404T>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57640949 | |||||||
| chr15:57641002 | C | T | 1 | a0005c0011t0002g0117 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1119+1457C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57641002 | |||||||
| chr15:57641003 | G | A | 2 | a0001c0003t0003g0148 a0001c0003t0003g0149 |
2 | HG02602.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.1119+1458G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57641003 | |||||||
| chr15:57641219 | T | C | 1 | a0001c0003t0002g0075 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1119+1674T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57641219 | |||||||
| chr15:57641517 | A | C | 1 | a0002c0002t0005g0060 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1119+1972A>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57641517 | |||||||
| chr15:57641593 | G | C | 1 | a0002c0002t0003g0123 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1119+2048G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57641593 | |||||||
| chr15:57641732 | G | A | 30 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0180 others(27): Show |
32 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.1119+2187G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57641732 | |||||||
| chr15:57641840 | A | C | 1 | a0003c0005t0010g0310 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1119+2295A>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57641840 | |||||||
| chr15:57642027 | A | T | 30 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0180 others(27): Show |
32 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.1119+2482A>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57642027 | |||||||
| chr15:57642065 | A | G | 2 | a0003c0005t0004g0333 a0003c0005t0004g0334 |
2 | HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1119+2520A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57642065 | |||||||
| chr15:57642111 | C | G | 30 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0180 others(27): Show |
32 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.1119+2566C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57642111 | |||||||
| chr15:57642139 | A | G | 2 | a0001c0001t0001g0209 a0001c0001t0001g0274 |
2 | NA18964.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.1119+2594A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57642139 | |||||||
| chr15:57642303 | T | A | 1 | a0001c0001t0001g0228 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1119+2758T>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57642303 | |||||||
| chr15:57642390 | G | A | 1 | a0005c0011t0002g0117 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1119+2845G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57642390 | |||||||
| chr15:57642503 | G | A | 58 | a0001c0001t0001g0160 a0001c0001t0001g0184 a0001c0001t0001g0192 others(55): Show |
59 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.1119+2958G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57642503 | |||||||
| chr15:57642512 | G | A | 1 | a0001c0003t0003g0135 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1119+2967G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57642512 | |||||||
| chr15:57642549 | G | A | 1 | a0001c0001t0001g0200 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1119+3004G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57642549 | |||||||
| chr15:57642779 | T | TAAATAAT others(8): Show |
37 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0180 others(34): Show |
39 | HG00099.hp2 HG01069.hp1 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.1119+3245_1119+324 others(19): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr15 | 57642779 | ||||||
| chr15:57642813 | A | T | 1 | a0007c0010t0001g0158 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1119+3268A>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57642813 | |||||||
| chr15:57643024 | T | C | 1 | a0003c0005t0010g0310 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1119+3479T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57643024 | |||||||
| chr15:57643052 | G | A | 59 | a0001c0001t0001g0013 a0001c0001t0001g0161 a0001c0001t0001g0164 others(56): Show |
59 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.1119+3507G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57643052 | |||||||
| chr15:57643094 | G | A | 1 | a0002c0002t0018g0016 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1119+3549G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57643094 | |||||||
| chr15:57643206 | T | C | 1 | a0001c0003t0003g0140 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1119+3661T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57643206 | |||||||
| chr15:57643221 | A | C | 57 | a0001c0001t0001g0160 a0001c0001t0001g0184 a0001c0001t0001g0192 others(54): Show |
58 | HG00140.hp1 HG00323.hp1 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.1119+3676A>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57643221 | |||||||
| chr15:57643249 | C | T | 281 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(278): Show |
289 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(286): Show |
intron_variant | MODIFIER | c.1119+3704C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57643249 | |||||||
| chr15:57643278 | G | A | 3 | a0001c0003t0006g0115 a0001c0003t0006g0116 a0001c0003t0006g0119 |
3 | HG01109.hp2 HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1119+3733G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57643278 | |||||||
| chr15:57643282 | A | T | 93 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0001g0179 others(90): Show |
96 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.1119+3737A>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57643282 | |||||||
| chr15:57643311 | T | A | 46 | a0001c0001t0001g0160 a0001c0001t0001g0184 a0001c0001t0001g0192 others(43): Show |
47 | HG00140.hp1 HG00323.hp1 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.1119+3766T>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57643311 | |||||||
| chr15:57643593 | A | G | 5 | a0001c0001t0001g0256 a0001c0001t0001g0277 a0001c0001t0001g0279 others(2): Show |
5 | NA18981.hp1 NA18983.hp2 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.1119+4048A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57643593 | |||||||
| chr15:57643616 | G | T | 5 | a0001c0003t0001g0227 a0001c0003t0002g0038 a0001c0003t0002g0041 others(2): Show |
5 | HG00621.hp1 NA18964.hp2 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.1119+4071G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57643616 | |||||||
| chr15:57643641 | C | G | 3 | a0001c0003t0001g0237 a0001c0003t0003g0339 a0001c0003t0003g0340 |
3 | HG02896.hp2 HG02897.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1119+4096C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57643641 | |||||||
| chr15:57643667 | G | A | 42 | a0001c0003t0002g0011 a0001c0003t0003g0137 a0001c0003t0003g0138 others(39): Show |
46 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.1119+4122G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57643667 | |||||||
| chr15:57643741 | G | GT | 15 | a0001c0001t0001g0176 a0001c0003t0001g0113 a0001c0003t0004g0109 others(12): Show |
15 | HG00738.hp1 HG01109.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.1119+4210dupT | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr15 | 57643741 | ||||||
| chr15:57643741 | GT | G | 37 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0180 others(34): Show |
39 | HG00099.hp2 HG01069.hp1 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.1119+4210delT | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr15 | 57643741 | ||||||
| chr15:57643742 | T | G | 1 | a0005c0011t0002g0117 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1119+4197T>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57643742 | |||||||
| chr15:57643797 | G | A | 37 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0180 others(34): Show |
39 | HG00099.hp2 HG01069.hp1 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.1119+4252G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57643797 | |||||||
| chr15:57643834 | A | G | 1 | a0001c0003t0002g0011 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1119+4289A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57643834 | |||||||
| chr15:57643859 | G | A | 1 | a0001c0001t0001g0221 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1119+4314G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57643859 | |||||||
| chr15:57643887 | AGAG | A | 4 | a0001c0001t0001g0259 a0001c0001t0002g0306 a0001c0001t0002g0313 others(1): Show |
4 | HG00099.hp2 HG01081.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.1119+4347_1119+434 others(7): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr15 | 57643887 | ||||||
| chr15:57643931 | A | G | 251 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0157 others(248): Show |
258 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(255): Show |
intron_variant | MODIFIER | c.1119+4386A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57643931 | |||||||
| chr15:57644039 | G | A | 1 | a0001c0003t0003g0138 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1119+4494G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57644039 | |||||||
| chr15:57644246 | G | A | 3 | a0001c0003t0006g0115 a0001c0003t0006g0116 a0001c0003t0006g0119 |
3 | HG01109.hp2 HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1119+4701G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57644246 | |||||||
| chr15:57644323 | A | T | 1 | a0005c0011t0002g0117 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1119+4778A>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57644323 | |||||||
| chr15:57644591 | C | T | 2 | a0001c0001t0001g0240 a0001c0003t0003g0125 |
2 | HG02647.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1119+5046C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57644591 | |||||||
| chr15:57644622 | ACT | A | 4 | a0001c0001t0001g0259 a0001c0001t0002g0306 a0001c0001t0002g0313 others(1): Show |
4 | HG00099.hp2 HG01081.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.1119+5078_1119+507 others(6): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57644622 | |||||||
| chr15:57644705 | A | G | 21 | a0001c0001t0001g0176 a0001c0001t0001g0234 a0001c0001t0001g0235 others(18): Show |
22 | HG00738.hp1 HG01891.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.1119+5160A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57644705 | |||||||
| chr15:57644729 | G | A | 2 | a0001c0001t0006g0152 a0001c0001t0013g0266 |
2 | HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1119+5184G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57644729 | |||||||
| chr15:57645006 | C | G | 1 | a0001c0003t0003g0150 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1119+5461C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57645006 | |||||||
| chr15:57645019 | C | T | 29 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0180 others(26): Show |
31 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.1119+5474C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57645019 | |||||||
| chr15:57645029 | T | C | 1 | a0001c0003t0003g0150 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1119+5484T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57645029 | |||||||
| chr15:57645309 | G | T | 36 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0176 others(33): Show |
37 | HG00099.hp2 HG00738.hp1 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.1119+5764G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57645309 | |||||||
| chr15:57645408 | G | A | 22 | a0001c0001t0001g0008 a0001c0001t0001g0196 a0001c0001t0001g0206 others(19): Show |
24 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.1119+5863G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57645408 | |||||||
| chr15:57645425 | G | A | 5 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(2): Show |
5 | HG02451.hp1 HG02886.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1119+5880G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57645425 | |||||||
| chr15:57645527 | G | T | 1 | a0001c0003t0003g0149 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1119+5982G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57645527 | |||||||
| chr15:57645546 | C | G | 1 | a0005c0011t0002g0117 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1119+6001C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57645546 | |||||||
| chr15:57645578 | A | G | 1 | a0002c0002t0002g0069 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1119+6033A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57645578 | |||||||
| chr15:57645790 | G | A | 22 | a0001c0001t0001g0008 a0001c0001t0001g0196 a0001c0001t0001g0206 others(19): Show |
24 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.1119+6245G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57645790 | |||||||
| chr15:57646198 | G | A | 1 | a0001c0003t0003g0143 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1119+6653G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57646198 | |||||||
| chr15:57646243 | A | G | 4 | a0001c0003t0005g0090 a0002c0002t0018g0016 a0003c0005t0004g0333 others(1): Show |
4 | HG00738.hp1 HG02818.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1119+6698A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57646243 | |||||||
| chr15:57646467 | T | C | 1 | a0001c0001t0001g0228 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1119+6922T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57646467 | |||||||
| chr15:57646720 | G | T | 1 | a0002c0002t0001g0336 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1119+7175G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57646720 | |||||||
| chr15:57647088 | G | A | 40 | a0001c0003t0003g0137 a0001c0003t0003g0138 a0002c0002t0002g0001 others(37): Show |
44 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.1119+7543G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57647088 | |||||||
| chr15:57647118 | T | C | 10 | a0001c0001t0001g0175 a0001c0001t0001g0259 a0001c0001t0002g0306 others(7): Show |
10 | HG00099.hp2 HG00642.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.1119+7573T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57647118 | |||||||
| chr15:57647349 | G | T | 243 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0157 others(240): Show |
250 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(247): Show |
intron_variant | MODIFIER | c.1119+7804G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57647349 | |||||||
| chr15:57647448 | A | G | 21 | a0001c0001t0001g0176 a0001c0001t0001g0234 a0001c0001t0001g0235 others(18): Show |
22 | HG00738.hp1 HG01891.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.1119+7903A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57647448 | |||||||
| chr15:57647624 | C | T | 213 | a0001c0001t0001g0013 a0001c0001t0001g0157 a0001c0001t0001g0161 others(210): Show |
218 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(215): Show |
intron_variant | MODIFIER | c.1119+8079C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57647624 | |||||||
| chr15:57647657 | G | A | 6 | a0001c0001t0007g0325 a0001c0001t0007g0327 a0001c0001t0008g0328 others(3): Show |
6 | HG01884.hp1 HG02717.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1119+8112G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57647657 | |||||||
| chr15:57647871 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1119+8326T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57647871 | |||||||
| chr15:57647946 | T | A | 57 | a0001c0001t0001g0160 a0001c0001t0001g0184 a0001c0001t0001g0192 others(54): Show |
58 | HG00140.hp1 HG00323.hp1 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.1119+8401T>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57647946 | |||||||
| chr15:57647951 | T | C | 1 | a0001c0003t0002g0065 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1119+8406T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57647951 | |||||||
| chr15:57647970 | G | C | 1 | a0001c0003t0001g0171 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1119+8425G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57647970 | |||||||
| chr15:57648019 | C | T | 18 | a0001c0001t0001g0008 a0001c0001t0001g0196 a0001c0001t0001g0206 others(15): Show |
20 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.1119+8474C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57648019 | |||||||
| chr15:57648064 | T | C | 334 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(331): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.1119+8519T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57648064 | |||||||
| chr15:57648101 | T | A | 1 | a0001c0001t0002g0308 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1119+8556T>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57648101 | |||||||
| chr15:57648104 | C | T | 4 | a0001c0001t0001g0183 a0001c0001t0001g0195 a0001c0001t0001g0198 others(1): Show |
4 | HG01256.hp2 HG01257.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1119+8559C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57648104 | |||||||
| chr15:57648116 | C | CA | 334 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(331): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.1119+8571_1119+857 others(5): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57648116 | |||||||
| chr15:57648399 | A | G | 1 | a0002c0002t0001g0335 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1119+8854A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57648399 | |||||||
| chr15:57648527 | G | A | 1 | a0001c0001t0007g0243 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1119+8982G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57648527 | |||||||
| chr15:57648784 | GT | G | 83 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0160 others(80): Show |
85 | HG00140.hp1 HG00323.hp1 HG00673.hp2 others(82): Show |
intron_variant | MODIFIER | c.1119+9256delT | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr15 | 57648784 | ||||||
| chr15:57648839 | C | G | 3 | a0001c0003t0006g0115 a0001c0003t0006g0116 a0001c0003t0006g0119 |
3 | HG01109.hp2 HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1119+9294C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57648839 | |||||||
| chr15:57648954 | A | T | 214 | a0001c0001t0001g0013 a0001c0001t0001g0157 a0001c0001t0001g0161 others(211): Show |
219 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.1119+9409A>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57648954 | |||||||
| chr15:57648992 | G | A | 5 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0007g0332 others(2): Show |
5 | HG01167.hp1 HG01169.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1119+9447G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57648992 | |||||||
| chr15:57649034 | A | C | 2 | a0001c0001t0007g0325 a0001c0001t0007g0327 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1119+9489A>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57649034 | |||||||
| chr15:57649144 | A | G | 1 | a0001c0003t0002g0021 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1119+9599A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57649144 | |||||||
| chr15:57649191 | T | C | 1 | a0001c0003t0001g0171 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1119+9646T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57649191 | |||||||
| chr15:57649211 | G | A | 1 | a0005c0011t0002g0117 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1119+9666G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57649211 | |||||||
| chr15:57649218 | T | C | 30 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0176 others(27): Show |
31 | HG00738.hp1 HG01109.hp2 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.1119+9673T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57649218 | |||||||
| chr15:57649273 | A | G | 2 | a0001c0001t0001g0240 a0001c0003t0003g0125 |
2 | HG02647.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1119+9728A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57649273 | |||||||
| chr15:57649283 | A | G | 10 | a0001c0001t0001g0175 a0001c0001t0001g0259 a0001c0001t0002g0306 others(7): Show |
10 | HG00099.hp2 HG00642.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.1119+9738A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57649283 | |||||||
| chr15:57649592 | A | G | 3 | a0001c0003t0003g0132 a0001c0003t0003g0134 a0001c0003t0003g0143 |
3 | HG01243.hp2 HG02257.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1119+10047A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57649592 | |||||||
| chr15:57649731 | G | A | 1 | a0001c0001t0003g0293 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1119+10186G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57649731 | |||||||
| chr15:57649805 | C | T | 1 | a0001c0001t0003g0293 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1119+10260C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57649805 | |||||||
| chr15:57649854 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1119+10309C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57649854 | |||||||
| chr15:57650025 | T | C | 17 | a0001c0001t0001g0176 a0001c0001t0001g0234 a0001c0001t0001g0235 others(14): Show |
17 | HG00738.hp1 HG01891.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1119+10480T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57650025 | |||||||
| chr15:57650115 | T | G | 1 | a0001c0001t0003g0293 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1119+10570T>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57650115 | |||||||
| chr15:57650153 | G | A | 1 | a0002c0002t0002g0051 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1119+10608G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57650153 | |||||||
| chr15:57650422 | A | C | 1 | a0002c0002t0002g0002 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1119+10877A>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57650422 | |||||||
| chr15:57650536 | C | T | 1 | a0001c0001t0001g0230 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1120-10914C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57650536 | |||||||
| chr15:57650615 | G | A | 14 | a0001c0001t0001g0008 a0001c0001t0001g0196 a0001c0001t0001g0206 others(11): Show |
15 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.1120-10835G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57650615 | |||||||
| chr15:57650916 | G | T | 17 | a0001c0001t0001g0176 a0001c0001t0001g0234 a0001c0001t0001g0235 others(14): Show |
18 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.1120-10534G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57650916 | |||||||
| chr15:57650927 | A | G | 5 | a0002c0002t0002g0049 a0002c0002t0002g0064 a0002c0002t0002g0073 others(2): Show |
5 | HG00438.hp1 NA18952.hp1 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.1120-10523A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57650927 | |||||||
| chr15:57651043 | C | G | 23 | a0001c0001t0001g0008 a0001c0001t0001g0196 a0001c0001t0001g0206 others(20): Show |
25 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.1120-10407C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57651043 | |||||||
| chr15:57651181 | C | T | 7 | a0001c0001t0007g0243 a0001c0001t0007g0325 a0001c0001t0007g0327 others(4): Show |
7 | HG01884.hp1 HG02717.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1120-10269C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57651181 | |||||||
| chr15:57651364 | C | T | 2 | a0001c0001t0004g0233 a0001c0001t0005g0121 |
2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1120-10086C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57651364 | |||||||
| chr15:57651692 | A | C | 1 | a0001c0001t0001g0253 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1120-9758A>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57651692 | |||||||
| chr15:57652171 | C | T | 56 | a0001c0001t0001g0013 a0001c0001t0001g0161 a0001c0001t0001g0164 others(53): Show |
56 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.1120-9279C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57652171 | |||||||
| chr15:57652267 | C | G | 30 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0180 others(27): Show |
32 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.1120-9183C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57652267 | |||||||
| chr15:57652267 | C | T | 1 | a0002c0002t0002g0095 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1120-9183C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57652267 | |||||||
| chr15:57652705 | A | C | 1 | a0001c0003t0003g0140 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1120-8745A>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57652705 | |||||||
| chr15:57653158 | C | T | 2 | a0001c0001t0001g0226 a0002c0002t0002g0080 |
2 | HG02004.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1120-8292C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57653158 | |||||||
| chr15:57653232 | A | G | 2 | a0002c0002t0001g0335 a0002c0002t0001g0336 |
2 | HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1120-8218A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57653232 | |||||||
| chr15:57653312 | A | T | 5 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(2): Show |
5 | HG02451.hp1 HG02886.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1120-8138A>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57653312 | |||||||
| chr15:57653327 | C | T | 329 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0157 others(326): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.1120-8123C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57653327 | |||||||
| chr15:57653375 | G | A | 1 | a0001c0001t0003g0293 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1120-8075G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57653375 | |||||||
| chr15:57653485 | T | A | 1 | a0001c0001t0001g0249 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1120-7965T>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57653485 | |||||||
| chr15:57653511 | A | G | 30 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0180 others(27): Show |
32 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.1120-7939A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57653511 | |||||||
| chr15:57653832 | C | G | 2 | a0001c0001t0006g0152 a0001c0001t0013g0266 |
2 | HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1120-7618C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57653832 | |||||||
| chr15:57653966 | C | T | 1 | a0001c0003t0003g0141 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1120-7484C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57653966 | |||||||
| chr15:57653996 | C | T | 1 | a0002c0002t0002g0081 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1120-7454C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57653996 | |||||||
| chr15:57654002 | C | CA | 70 | a0001c0001t0001g0157 a0001c0001t0001g0161 a0001c0001t0001g0168 others(67): Show |
71 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.1120-7418dupA | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr15 | 57654002 | ||||||
| chr15:57654002 | C | CAA | 43 | a0001c0001t0001g0013 a0001c0001t0001g0162 a0001c0001t0001g0183 others(40): Show |
44 | HG00597.hp2 HG00741.hp1 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.1120-7419_1120-741 others(6): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr15 | 57654002 | ||||||
| chr15:57654002 | C | CAAA | 29 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0001c0001t0001g0170 others(26): Show |
29 | HG00621.hp1 HG00741.hp2 HG01168.hp2 others(26): Show |
intron_variant | MODIFIER | c.1120-7420_1120-741 others(7): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr15 | 57654002 | ||||||
| chr15:57654002 | C | CAAAA | 24 | a0001c0001t0001g0166 a0001c0001t0001g0173 a0001c0001t0001g0182 others(21): Show |
24 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(21): Show |
intron_variant | MODIFIER | c.1120-7421_1120-741 others(8): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr15 | 57654002 | ||||||
| chr15:57654002 | C | CAAAAA | 19 | a0001c0001t0001g0225 a0001c0003t0002g0019 a0001c0003t0002g0058 others(16): Show |
23 | HG00438.hp1 HG00673.hp1 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.1120-7422_1120-741 others(9): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr15 | 57654002 | ||||||
| chr15:57654002 | C | CAAAAAA | 13 | a0001c0001t0001g0240 a0001c0003t0003g0296 a0002c0002t0002g0045 others(10): Show |
13 | HG00423.hp2 HG00438.hp2 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.1120-7423_1120-741 others(10): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr15 | 57654002 | ||||||
| chr15:57654002 | C | CAAAAAAA | 20 | a0001c0001t0001g0008 a0001c0001t0001g0196 a0001c0001t0001g0206 others(17): Show |
21 | HG00544.hp1 HG00609.hp2 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.1120-7424_1120-741 others(11): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr15 | 57654002 | ||||||
| chr15:57654002 | C | CAAAAAAA others(1): Show |
6 | a0001c0001t0001g0283 a0001c0001t0001g0299 a0001c0001t0003g0294 others(3): Show |
7 | HG01074.hp2 HG01099.hp1 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.1120-7425_1120-741 others(12): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr15 | 57654002 | ||||||
| chr15:57654002 | C | CAAAAAAA others(2): Show |
7 | a0001c0001t0001g0179 a0001c0001t0001g0181 a0001c0001t0001g0265 others(4): Show |
7 | HG00642.hp2 HG01884.hp2 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.1120-7426_1120-741 others(13): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr15 | 57654002 | ||||||
| chr15:57654002 | C | CAAAAAAA others(3): Show |
3 | a0001c0001t0001g0180 a0001c0003t0002g0055 a0002c0002t0002g0039 |
3 | HG02886.hp1 HG02970.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1120-7427_1120-741 others(14): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr15 | 57654002 | ||||||
| chr15:57654002 | CA | C | 44 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0213 others(41): Show |
45 | HG00140.hp1 HG00323.hp1 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.1120-7418delA | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr15 | 57654002 | ||||||
| chr15:57654002 | CAA | C | 19 | a0001c0001t0001g0176 a0001c0001t0001g0209 a0001c0001t0001g0234 others(16): Show |
19 | HG01884.hp1 HG01891.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.1120-7419_1120-741 others(6): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr15 | 57654002 | ||||||
| chr15:57654002 | CAAAAAA | C | 12 | a0001c0001t0001g0175 a0001c0001t0001g0259 a0001c0001t0002g0306 others(9): Show |
12 | HG00099.hp2 HG00642.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.1120-7423_1120-741 others(10): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr15 | 57654002 | ||||||
| chr15:57654040 | TTTAGAGG | T | 330 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(327): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.1120-7398_1120-739 others(11): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr15 | 57654040 | ||||||
| chr15:57654086 | A | G | 2 | a0001c0001t0001g0240 a0001c0003t0003g0125 |
2 | HG02647.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1120-7364A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57654086 | |||||||
| chr15:57654111 | A | G | 2 | a0001c0001t0007g0332 a0006c0006t0002g0120 |
2 | HG02109.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1120-7339A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57654111 | |||||||
| chr15:57654176 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1120-7274T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57654176 | |||||||
| chr15:57654189 | A | G | 1 | a0001c0003t0003g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1120-7261A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57654189 | |||||||
| chr15:57654364 | A | T | 3 | a0003c0005t0004g0333 a0003c0005t0004g0334 a0005c0011t0002g0117 |
3 | HG02559.hp1 HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1120-7086A>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57654364 | |||||||
| chr15:57654374 | G | A | 1 | a0001c0003t0014g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1120-7076G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57654374 | |||||||
| chr15:57654642 | A | G | 3 | a0001c0001t0007g0332 a0001c0003t0002g0126 a0006c0006t0002g0120 |
3 | HG02109.hp1 HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1120-6808A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57654642 | |||||||
| chr15:57654867 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1120-6583A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57654867 | |||||||
| chr15:57654905 | C | T | 2 | a0001c0001t0001g0284 a0001c0001t0001g0286 |
2 | HG02040.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.1120-6545C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57654905 | |||||||
| chr15:57654915 | C | A | 3 | a0001c0001t0007g0332 a0001c0003t0002g0126 a0006c0006t0002g0120 |
3 | HG02109.hp1 HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1120-6535C>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57654915 | |||||||
| chr15:57654988 | A | G | 66 | a0001c0001t0004g0275 a0001c0003t0003g0137 a0001c0003t0003g0138 others(63): Show |
70 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.1120-6462A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57654988 | |||||||
| chr15:57655037 | A | C | 1 | a0001c0001t0007g0243 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1120-6413A>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57655037 | |||||||
| chr15:57655093 | G | T | 1 | a0002c0002t0002g0096 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1120-6357G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57655093 | |||||||
| chr15:57655115 | A | G | 6 | a0001c0001t0004g0007 a0001c0001t0004g0241 a0001c0001t0004g0242 others(3): Show |
7 | HG02055.hp2 HG02145.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1120-6335A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57655115 | |||||||
| chr15:57655134 | G | A | 3 | a0001c0001t0004g0275 a0002c0002t0004g0219 a0002c0002t0005g0062 |
3 | HG02015.hp2 HG02056.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.1120-6316G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57655134 | |||||||
| chr15:57655156 | C | T | 1 | a0001c0003t0017g0122 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1120-6294C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57655156 | |||||||
| chr15:57655285 | A | G | 2 | a0001c0001t0006g0152 a0001c0001t0013g0266 |
2 | HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1120-6165A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57655285 | |||||||
| chr15:57655355 | G | A | 1 | a0001c0003t0002g0024 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1120-6095G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57655355 | |||||||
| chr15:57655401 | C | T | 1 | a0001c0001t0001g0279 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1120-6049C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57655401 | |||||||
| chr15:57655434 | C | T | 210 | a0001c0001t0001g0013 a0001c0001t0001g0157 a0001c0001t0001g0161 others(207): Show |
215 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.1120-6016C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57655434 | |||||||
| chr15:57655528 | G | A | 2 | a0001c0001t0001g0240 a0001c0003t0003g0125 |
2 | HG02647.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1120-5922G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57655528 | |||||||
| chr15:57655536 | A | G | 1 | a0001c0003t0003g0148 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1120-5914A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57655536 | |||||||
| chr15:57655598 | G | GA | 10 | a0001c0001t0001g0175 a0001c0001t0001g0259 a0001c0001t0002g0306 others(7): Show |
10 | HG00099.hp2 HG00642.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.1120-5842dupA | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr15 | 57655598 | ||||||
| chr15:57655609 | G | T | 1 | a0001c0003t0002g0025 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1120-5841G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57655609 | |||||||
| chr15:57655881 | T | A | 2 | a0001c0001t0001g0176 a0001c0001t0004g0177 |
2 | HG02572.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1120-5569T>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57655881 | |||||||
| chr15:57656581 | T | C | 1 | a0002c0002t0002g0052 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1120-4869T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57656581 | |||||||
| chr15:57656828 | A | G | 1 | a0001c0003t0014g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1120-4622A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57656828 | |||||||
| chr15:57656898 | C | G | 1 | a0001c0001t0001g0224 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1120-4552C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57656898 | |||||||
| chr15:57656899 | T | G | 1 | a0001c0001t0001g0224 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1120-4551T>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57656899 | |||||||
| chr15:57656907 | C | T | 1 | a0001c0001t0001g0272 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1120-4543C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57656907 | |||||||
| chr15:57657025 | C | T | 1 | a0001c0003t0002g0011 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1120-4425C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57657025 | |||||||
| chr15:57657248 | C | A | 209 | a0001c0001t0001g0013 a0001c0001t0001g0157 a0001c0001t0001g0161 others(206): Show |
214 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(211): Show |
intron_variant | MODIFIER | c.1120-4202C>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57657248 | |||||||
| chr15:57657307 | A | G | 1 | a0002c0002t0002g0091 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1120-4143A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57657307 | |||||||
| chr15:57657309 | C | T | 2 | a0001c0003t0003g0339 a0001c0003t0003g0340 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1120-4141C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57657309 | |||||||
| chr15:57657339 | T | G | 1 | a0001c0003t0002g0126 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1120-4111T>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57657339 | |||||||
| chr15:57657358 | G | C | 1 | a0001c0003t0001g0113 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1120-4092G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57657358 | |||||||
| chr15:57657573 | C | A | 1 | a0001c0001t0003g0293 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1120-3877C>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57657573 | |||||||
| chr15:57657582 | G | T | 1 | a0001c0001t0003g0293 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1120-3868G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57657582 | |||||||
| chr15:57657693 | A | G | 3 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG02922.hp2 HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1120-3757A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57657693 | |||||||
| chr15:57657697 | T | C | 1 | a0003c0005t0010g0310 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1120-3753T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57657697 | |||||||
| chr15:57657907 | G | A | 4 | a0001c0001t0007g0332 a0001c0003t0002g0126 a0002c0002t0002g0050 others(1): Show |
4 | HG02109.hp1 HG03139.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.1120-3543G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57657907 | |||||||
| chr15:57657981 | T | C | 2 | a0001c0003t0003g0130 a0001c0003t0003g0131 |
2 | HG01070.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.1120-3469T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57657981 | |||||||
| chr15:57658222 | C | T | 2 | a0001c0001t0001g0176 a0001c0001t0004g0177 |
2 | HG02572.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1120-3228C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57658222 | |||||||
| chr15:57658280 | T | G | 1 | a0001c0001t0001g0170 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1120-3170T>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57658280 | |||||||
| chr15:57658297 | G | A | 1 | a0001c0001t0001g0292 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1120-3153G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57658297 | |||||||
| chr15:57658422 | T | G | 1 | a0003c0005t0010g0310 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1120-3028T>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57658422 | |||||||
| chr15:57658424 | T | A | 2 | a0001c0001t0009g0201 a0001c0001t0009g0214 |
2 | HG02572.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1120-3026T>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57658424 | |||||||
| chr15:57658424 | T | G | 1 | a0003c0005t0010g0310 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1120-3026T>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57658424 | |||||||
| chr15:57658436 | T | C | 43 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0015 others(40): Show |
45 | HG00099.hp2 HG00642.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.1120-3014T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57658436 | |||||||
| chr15:57658455 | A | G | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | HG02698.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1120-2995A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57658455 | |||||||
| chr15:57658500 | G | A | 17 | a0001c0001t0001g0176 a0001c0001t0001g0234 a0001c0001t0001g0235 others(14): Show |
17 | HG00738.hp1 HG01891.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.1120-2950G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57658500 | |||||||
| chr15:57658503 | T | C | 1 | a0001c0001t0020g0309 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1120-2947T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57658503 | |||||||
| chr15:57658556 | T | C | 1 | a0001c0003t0017g0122 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1120-2894T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57658556 | |||||||
| chr15:57658738 | G | A | 3 | a0002c0002t0002g0098 a0002c0002t0002g0099 a0002c0002t0002g0100 |
3 | NA19056.hp2 NA19074.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1120-2712G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57658738 | |||||||
| chr15:57658760 | A | C | 11 | a0001c0001t0001g0240 a0001c0001t0003g0293 a0001c0001t0007g0325 others(8): Show |
11 | HG01884.hp1 HG02647.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1120-2690A>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57658760 | |||||||
| chr15:57658866 | C | G | 2 | a0001c0001t0006g0152 a0001c0001t0013g0266 |
2 | HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1120-2584C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57658866 | |||||||
| chr15:57658997 | T | C | 9 | a0001c0001t0001g0175 a0001c0001t0001g0259 a0001c0001t0002g0306 others(6): Show |
9 | HG00099.hp2 HG00642.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.1120-2453T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57658997 | |||||||
| chr15:57659341 | G | A | 337 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0157 others(334): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.1120-2109G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57659341 | |||||||
| chr15:57659550 | C | T | 224 | a0001c0001t0001g0013 a0001c0001t0001g0157 a0001c0001t0001g0161 others(221): Show |
229 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(226): Show |
intron_variant | MODIFIER | c.1120-1900C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57659550 | |||||||
| chr15:57659673 | A | G | 2 | a0002c0002t0001g0335 a0002c0002t0001g0336 |
2 | HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1120-1777A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57659673 | |||||||
| chr15:57659673 | A | T | 1 | a0001c0003t0014g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1120-1777A>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57659673 | |||||||
| chr15:57659688 | A | G | 5 | a0001c0001t0001g0175 a0001c0001t0002g0317 a0001c0001t0002g0318 others(2): Show |
5 | HG00642.hp1 HG01175.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.1120-1762A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57659688 | |||||||
| chr15:57659706 | A | C | 1 | a0001c0001t0001g0192 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1120-1744A>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57659706 | |||||||
| chr15:57659877 | C | T | 110 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0015 others(107): Show |
113 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.1120-1573C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57659877 | |||||||
| chr15:57659954 | C | G | 101 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0015 others(98): Show |
104 | HG00140.hp1 HG00323.hp1 HG00673.hp2 others(101): Show |
intron_variant | MODIFIER | c.1120-1496C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57659954 | |||||||
| chr15:57659969 | G | A | 101 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0015 others(98): Show |
104 | HG00140.hp1 HG00323.hp1 HG00673.hp2 others(101): Show |
intron_variant | MODIFIER | c.1120-1481G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57659969 | |||||||
| chr15:57660001 | A | G | 1 | a0002c0002t0011g0072 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1120-1449A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57660001 | |||||||
| chr15:57660005 | C | T | 1 | a0001c0003t0014g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1120-1445C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57660005 | |||||||
| chr15:57660017 | C | G | 1 | a0002c0002t0002g0103 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1120-1433C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57660017 | |||||||
| chr15:57660152 | C | T | 2 | a0002c0002t0001g0335 a0002c0002t0001g0336 |
2 | HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1120-1298C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57660152 | |||||||
| chr15:57660158 | C | T | 1 | a0001c0001t0020g0309 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1120-1292C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57660158 | |||||||
| chr15:57660200 | T | G | 111 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0015 others(108): Show |
114 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.1120-1250T>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57660200 | |||||||
| chr15:57660289 | A | G | 319 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(316): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.1120-1161A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57660289 | |||||||
| chr15:57660390 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1120-1060C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57660390 | |||||||
| chr15:57660417 | C | A | 1 | a0001c0003t0003g0142 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1120-1033C>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57660417 | |||||||
| chr15:57660610 | C | T | 26 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0180 others(23): Show |
28 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.1120-840C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57660610 | |||||||
| chr15:57660645 | G | A | 1 | a0001c0001t0015g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1120-805G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57660645 | |||||||
| chr15:57660662 | A | G | 1 | a0002c0002t0002g0105 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1120-788A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57660662 | |||||||
| chr15:57660693 | A | G | 1 | a0001c0001t0003g0293 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1120-757A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57660693 | |||||||
| chr15:57660725 | T | C | 1 | a0002c0002t0002g0067 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1120-725T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57660725 | |||||||
| chr15:57660802 | A | G | 1 | a0001c0003t0002g0065 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1120-648A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57660802 | |||||||
| chr15:57660869 | G | A | 1 | a0001c0003t0002g0025 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1120-581G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57660869 | |||||||
| chr15:57661067 | A | G | 3 | a0001c0003t0006g0115 a0001c0003t0006g0116 a0001c0003t0006g0119 |
3 | HG01109.hp2 HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1120-383A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57661067 | |||||||
| chr15:57661105 | A | G | 9 | a0001c0001t0001g0175 a0001c0001t0001g0259 a0001c0001t0002g0306 others(6): Show |
9 | HG00099.hp2 HG00642.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.1120-345A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57661105 | |||||||
| chr15:57661111 | T | C | 252 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0157 others(249): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.1120-339T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57661111 | |||||||
| chr15:57661135 | C | A | 1 | a0002c0002t0002g0082 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1120-315C>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57661135 | |||||||
| chr15:57661366 | C | T | 246 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0157 others(243): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.1120-84C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57661366 | |||||||
| chr15:57661721 | A | T | 1 | a0002c0002t0002g0103 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1203+188A>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57661721 | |||||||
| chr15:57661788 | C | G | 1 | a0001c0003t0014g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1203+255C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57661788 | |||||||
| chr15:57661814 | T | C | 3 | a0001c0001t0004g0233 a0001c0001t0005g0121 a0002c0004t0005g0305 |
3 | HG02886.hp2 HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1203+281T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57661814 | |||||||
| chr15:57661823 | G | A | 23 | a0001c0001t0001g0176 a0001c0001t0004g0177 a0001c0001t0004g0233 others(20): Show |
23 | HG00558.hp1 HG00738.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.1203+290G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57661823 | |||||||
| chr15:57661907 | G | A | 1 | a0001c0003t0003g0141 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1203+374G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57661907 | |||||||
| chr15:57661928 | A | G | 1 | a0002c0002t0002g0051 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1203+395A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57661928 | |||||||
| chr15:57661982 | T | G | 1 | a0005c0011t0002g0117 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1203+449T>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57661982 | |||||||
| chr15:57662070 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1203+537G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57662070 | |||||||
| chr15:57662152 | T | G | 259 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0157 others(256): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.1203+619T>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57662152 | |||||||
| chr15:57662223 | G | T | 6 | a0001c0001t0001g0291 a0001c0001t0001g0300 a0001c0003t0002g0028 others(3): Show |
6 | HG00099.hp1 HG01106.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1203+690G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57662223 | |||||||
| chr15:57662446 | A | G | 9 | a0001c0001t0004g0275 a0002c0002t0004g0219 a0002c0002t0005g0060 others(6): Show |
9 | HG00558.hp1 HG02015.hp2 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.1203+913A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57662446 | |||||||
| chr15:57662782 | T | C | 1 | a0001c0003t0001g0113 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1203+1249T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57662782 | |||||||
| chr15:57662838 | C | A | 3 | a0001c0003t0006g0115 a0001c0003t0006g0116 a0001c0003t0006g0119 |
3 | HG01109.hp2 HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1203+1305C>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57662838 | |||||||
| chr15:57662846 | G | C | 3 | a0001c0001t0007g0332 a0001c0003t0002g0126 a0006c0006t0002g0120 |
3 | HG02109.hp1 HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1203+1313G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57662846 | |||||||
| chr15:57662930 | T | C | 87 | a0001c0001t0001g0013 a0001c0001t0001g0161 a0001c0001t0001g0164 others(84): Show |
89 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.1203+1397T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57662930 | |||||||
| chr15:57662954 | G | A | 54 | a0001c0001t0001g0160 a0001c0001t0001g0170 a0001c0001t0001g0184 others(51): Show |
55 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.1203+1421G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57662954 | |||||||
| chr15:57663131 | G | T | 84 | a0001c0001t0001g0160 a0001c0001t0001g0170 a0001c0001t0001g0184 others(81): Show |
85 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1203+1598G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57663131 | |||||||
| chr15:57663210 | C | T | 3 | a0001c0001t0001g0218 a0001c0001t0001g0270 a0001c0001t0001g0303 |
3 | NA18943.hp2 NA18978.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1203+1677C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57663210 | |||||||
| chr15:57663211 | A | G | 252 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0157 others(249): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.1203+1678A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57663211 | |||||||
| chr15:57663285 | A | G | 252 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0157 others(249): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.1203+1752A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57663285 | |||||||
| chr15:57663339 | C | T | 1 | a0003c0005t0010g0310 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1203+1806C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57663339 | |||||||
| chr15:57663342 | A | G | 1 | a0001c0003t0014g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1203+1809A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57663342 | |||||||
| chr15:57663371 | C | A | 245 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0157 others(242): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.1203+1838C>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57663371 | |||||||
| chr15:57663396 | T | C | 28 | a0001c0001t0004g0007 a0001c0001t0004g0177 a0001c0001t0004g0233 others(25): Show |
29 | HG00558.hp1 HG00738.hp1 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.1203+1863T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57663396 | |||||||
| chr15:57663475 | G | A | 1 | a0001c0001t0020g0309 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1203+1942G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57663475 | |||||||
| chr15:57664031 | T | C | 42 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0180 others(39): Show |
44 | HG00609.hp2 HG01069.hp1 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.1203+2498T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57664031 | |||||||
| chr15:57664070 | G | GT | 55 | a0001c0001t0001g0160 a0001c0001t0001g0170 a0001c0001t0001g0184 others(52): Show |
56 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.1203+2551dupT | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 57664070 | ||||||
| chr15:57664070 | GT | G | 73 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0179 others(70): Show |
75 | HG00558.hp1 HG00609.hp2 HG00738.hp1 others(72): Show |
intron_variant | MODIFIER | c.1203+2551delT | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 57664070 | ||||||
| chr15:57664136 | A | T | 1 | a0005c0011t0002g0117 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1203+2603A>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57664136 | |||||||
| chr15:57664476 | C | T | 6 | a0001c0001t0007g0325 a0001c0001t0007g0327 a0001c0001t0008g0328 others(3): Show |
6 | HG01884.hp1 HG02717.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1203+2943C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57664476 | |||||||
| chr15:57664503 | A | C | 258 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0157 others(255): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.1203+2970A>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57664503 | |||||||
| chr15:57664625 | TCTTTCTA others(3): Show |
T | 1 | a0001c0003t0003g0146 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1203+3093_1203+310 others(14): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57664625 | |||||||
| chr15:57664711 | G | C | 1 | a0001c0003t0004g0111 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1203+3178G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57664711 | |||||||
| chr15:57665011 | C | G | 258 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0157 others(255): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.1203+3478C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57665011 | |||||||
| chr15:57665029 | A | G | 258 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0157 others(255): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.1203+3496A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57665029 | |||||||
| chr15:57665054 | T | G | 22 | a0001c0001t0004g0177 a0001c0001t0004g0233 a0001c0001t0004g0275 others(19): Show |
22 | HG00558.hp1 HG00738.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.1203+3521T>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57665054 | |||||||
| chr15:57665116 | A | G | 258 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0157 others(255): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.1203+3583A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57665116 | |||||||
| chr15:57665300 | T | C | 1 | a0002c0002t0002g0026 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1203+3767T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57665300 | |||||||
| chr15:57665366 | C | A | 1 | a0002c0002t0002g0039 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1203+3833C>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57665366 | |||||||
| chr15:57665468 | T | C | 2 | a0001c0001t0007g0325 a0001c0001t0007g0327 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1203+3935T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57665468 | |||||||
| chr15:57665626 | C | T | 252 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0157 others(249): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.1203+4093C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57665626 | |||||||
| chr15:57665706 | A | G | 42 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0180 others(39): Show |
44 | HG00609.hp2 HG01069.hp1 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.1203+4173A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57665706 | |||||||
| chr15:57665766 | G | A | 252 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0157 others(249): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.1203+4233G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57665766 | |||||||
| chr15:57665893 | G | A | 1 | a0001c0001t0001g0285 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1203+4360G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57665893 | |||||||
| chr15:57665914 | C | A | 2 | a0001c0001t0001g0223 a0001c0001t0001g0239 |
2 | NA19009.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1203+4381C>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57665914 | |||||||
| chr15:57666029 | T | C | 2 | a0003c0005t0004g0333 a0003c0005t0004g0334 |
2 | HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1203+4496T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57666029 | |||||||
| chr15:57666286 | C | T | 54 | a0001c0001t0001g0160 a0001c0001t0001g0170 a0001c0001t0001g0184 others(51): Show |
55 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.1203+4753C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57666286 | |||||||
| chr15:57666369 | T | C | 336 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0157 others(333): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.1203+4836T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57666369 | |||||||
| chr15:57666523 | A | G | 6 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0003g0293 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1203+4990A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57666523 | |||||||
| chr15:57666631 | C | T | 1 | a0002c0002t0002g0027 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1203+5098C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57666631 | |||||||
| chr15:57666672 | G | A | 23 | a0001c0001t0001g0008 a0001c0001t0001g0196 a0001c0001t0001g0206 others(20): Show |
25 | HG00609.hp2 HG01069.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.1203+5139G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57666672 | |||||||
| chr15:57666710 | A | T | 1 | a0001c0001t0007g0243 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1203+5177A>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57666710 | |||||||
| chr15:57666781 | C | G | 2 | a0001c0001t0001g0169 a0001c0001t0002g0307 |
2 | HG01074.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1203+5248C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57666781 | |||||||
| chr15:57666800 | A | T | 3 | a0001c0001t0007g0325 a0001c0001t0007g0327 a0005c0011t0002g0117 |
3 | HG02559.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1203+5267A>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57666800 | |||||||
| chr15:57666825 | T | G | 300 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0157 others(297): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.1203+5292T>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57666825 | |||||||
| chr15:57666946 | A | G | 1 | a0001c0001t0001g0240 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1203+5413A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57666946 | |||||||
| chr15:57667007 | C | G | 3 | a0001c0003t0003g0154 a0001c0003t0003g0155 a0001c0003t0003g0156 |
3 | HG01069.hp2 HG01071.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1203+5474C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57667007 | |||||||
| chr15:57667037 | C | T | 1 | a0001c0001t0007g0243 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1203+5504C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57667037 | |||||||
| chr15:57667300 | A | C | 3 | a0001c0003t0003g0154 a0001c0003t0003g0155 a0001c0003t0003g0156 |
3 | HG01069.hp2 HG01071.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1203+5767A>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57667300 | |||||||
| chr15:57667311 | G | A | 5 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0176 others(2): Show |
5 | HG01167.hp1 HG01169.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1203+5778G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57667311 | |||||||
| chr15:57667430 | T | C | 197 | a0001c0001t0001g0013 a0001c0001t0001g0157 a0001c0001t0001g0160 others(194): Show |
200 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.1203+5897T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57667430 | |||||||
| chr15:57667433 | A | G | 1 | a0005c0011t0002g0117 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1203+5900A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57667433 | |||||||
| chr15:57667560 | T | G | 2 | a0001c0001t0001g0291 a0001c0001t0001g0300 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1203+6027T>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57667560 | |||||||
| chr15:57667609 | A | G | 1 | a0001c0003t0014g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1203+6076A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57667609 | |||||||
| chr15:57667637 | A | G | 289 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0157 others(286): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.1203+6104A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57667637 | |||||||
| chr15:57667658 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1203+6125C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57667658 | |||||||
| chr15:57667695 | T | C | 1 | a0001c0003t0003g0139 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1203+6162T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57667695 | |||||||
| chr15:57667812 | C | T | 289 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0157 others(286): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.1203+6279C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57667812 | |||||||
| chr15:57667867 | G | T | 10 | a0001c0001t0001g0185 a0001c0001t0001g0187 a0001c0001t0001g0190 others(7): Show |
10 | NA18943.hp2 NA18944.hp2 NA18947.hp1 others(7): Show |
intron_variant | MODIFIER | c.1203+6334G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57667867 | |||||||
| chr15:57667994 | G | A | 336 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0157 others(333): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.1203+6461G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57667994 | |||||||
| chr15:57668002 | A | G | 6 | a0001c0001t0006g0152 a0001c0001t0013g0266 a0001c0001t0020g0309 others(3): Show |
6 | HG01109.hp2 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1203+6469A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57668002 | |||||||
| chr15:57668114 | G | A | 289 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0157 others(286): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.1203+6581G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57668114 | |||||||
| chr15:57668212 | G | C | 289 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0157 others(286): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.1203+6679G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57668212 | |||||||
| chr15:57668216 | T | G | 335 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0157 others(332): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.1203+6683T>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57668216 | |||||||
| chr15:57668432 | C | A | 3 | a0001c0003t0006g0115 a0001c0003t0006g0116 a0001c0003t0006g0119 |
3 | HG01109.hp2 HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1204-6536C>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57668432 | |||||||
| chr15:57668447 | C | T | 1 | a0002c0002t0002g0081 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1204-6521C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57668447 | |||||||
| chr15:57668499 | TAGGTTTT others(11): Show |
T | 1 | a0003c0005t0010g0310 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1204-6466_1204-644 others(22): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 57668499 | ||||||
| chr15:57668643 | C | T | 1 | a0001c0001t0007g0243 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1204-6325C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57668643 | |||||||
| chr15:57668689 | T | A | 9 | a0001c0001t0004g0177 a0001c0001t0004g0233 a0001c0001t0005g0121 others(6): Show |
9 | HG01891.hp1 HG02280.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1204-6279T>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57668689 | |||||||
| chr15:57668717 | G | A | 1 | a0001c0001t0001g0188 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1204-6251G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57668717 | |||||||
| chr15:57668788 | G | A | 1 | a0001c0001t0007g0243 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1204-6180G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57668788 | |||||||
| chr15:57668836 | G | T | 6 | a0001c0001t0006g0152 a0001c0001t0013g0266 a0001c0001t0020g0309 others(3): Show |
6 | HG01109.hp2 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1204-6132G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57668836 | |||||||
| chr15:57668838 | C | G | 1 | a0001c0003t0004g0111 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1204-6130C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57668838 | |||||||
| chr15:57668873 | GAT | G | 25 | a0001c0001t0001g0008 a0001c0001t0001g0196 a0001c0001t0001g0206 others(22): Show |
27 | HG00323.hp2 HG00609.hp2 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.1204-6074_1204-607 others(6): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 57668873 | ||||||
| chr15:57668873 | GATAT | G | 194 | a0001c0001t0001g0013 a0001c0001t0001g0157 a0001c0001t0001g0161 others(191): Show |
200 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.1204-6076_1204-607 others(8): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 57668873 | ||||||
| chr15:57668887 | TATA | T | 4 | a0001c0001t0008g0328 a0001c0001t0008g0329 a0001c0001t0008g0331 others(1): Show |
4 | HG01884.hp1 HG02717.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1204-6080_1204-607 others(7): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57668887 | |||||||
| chr15:57668889 | TATA | T | 4 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(1): Show |
4 | HG02486.hp2 HG02922.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1204-6078_1204-607 others(7): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57668889 | |||||||
| chr15:57668891 | TATA | T | 24 | a0001c0001t0001g0170 a0001c0001t0001g0175 a0001c0001t0001g0217 others(21): Show |
24 | HG00099.hp2 HG00642.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.1204-6076_1204-607 others(7): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57668891 | |||||||
| chr15:57668892 | A | AT | 13 | a0001c0001t0004g0275 a0001c0001t0015g0159 a0002c0002t0004g0219 others(10): Show |
13 | HG00558.hp1 HG02015.hp2 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.1204-6075dupT | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 57668892 | ||||||
| chr15:57668892 | A | T | 7 | a0001c0001t0001g0210 a0001c0001t0008g0328 a0001c0001t0008g0329 others(4): Show |
7 | HG01884.hp1 HG02717.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.1204-6076A>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57668892 | |||||||
| chr15:57668892 | ATAT | A | 23 | a0001c0001t0001g0178 a0001c0001t0001g0191 a0001c0001t0001g0197 others(20): Show |
23 | HG00544.hp2 HG00741.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.1204-6074_1204-607 others(7): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 57668892 | ||||||
| chr15:57668892 | ATATT | A | 13 | a0001c0001t0001g0160 a0001c0001t0001g0173 a0001c0001t0001g0174 others(10): Show |
13 | HG00140.hp1 HG00735.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.1204-6074_1204-607 others(8): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 57668892 | ||||||
| chr15:57668894 | A | AT | 9 | a0001c0001t0004g0177 a0001c0001t0004g0233 a0001c0001t0005g0121 others(6): Show |
9 | HG00738.hp1 HG01891.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1204-6061dupT | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 57668894 | ||||||
| chr15:57668894 | A | ATAT | 6 | a0001c0001t0004g0007 a0001c0001t0004g0241 a0001c0001t0004g0242 others(3): Show |
7 | HG02055.hp2 HG02145.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1204-6073_1204-607 others(7): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 57668894 | ||||||
| chr15:57668894 | A | ATATATAT others(7): Show |
1 | a0001c0003t0006g0116 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1204-6073_1204-607 others(18): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 57668894 | ||||||
| chr15:57668894 | A | ATATATAT others(9): Show |
1 | a0001c0003t0006g0119 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1204-6073_1204-607 others(20): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 57668894 | ||||||
| chr15:57668894 | A | ATATATAT others(7): Show |
1 | a0001c0003t0006g0115 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1204-6073_1204-607 others(18): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 57668894 | ||||||
| chr15:57668894 | A | ATATTTTT others(5): Show |
2 | a0001c0001t0006g0152 a0001c0001t0013g0266 |
2 | HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1204-6073_1204-607 others(16): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 57668894 | ||||||
| chr15:57668894 | A | T | 84 | a0001c0001t0001g0013 a0001c0001t0001g0179 a0001c0001t0001g0180 others(81): Show |
88 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.1204-6074A>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57668894 | |||||||
| chr15:57668896 | T | A | 6 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0003g0293 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1204-6072T>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57668896 | |||||||
| chr15:57668897 | T | A | 1 | a0001c0001t0020g0309 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1204-6071T>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57668897 | |||||||
| chr15:57669081 | G | T | 9 | a0001c0001t0001g0175 a0001c0001t0001g0259 a0001c0001t0002g0306 others(6): Show |
9 | HG00099.hp2 HG00642.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.1204-5887G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57669081 | |||||||
| chr15:57669098 | G | A | 4 | a0001c0001t0001g0191 a0001c0001t0001g0199 a0001c0001t0001g0207 others(1): Show |
4 | HG00544.hp2 HG02071.hp2 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.1204-5870G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57669098 | |||||||
| chr15:57669377 | T | G | 1 | a0001c0003t0003g0146 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1204-5591T>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57669377 | |||||||
| chr15:57669405 | C | T | 1 | a0001c0003t0003g0146 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1204-5563C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57669405 | |||||||
| chr15:57669422 | T | TGGGGGGG others(36): Show |
1 | a0001c0003t0003g0146 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1204-5545_1204-554 others(47): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 57669422 | ||||||
| chr15:57669424 | C | G | 1 | a0001c0003t0003g0146 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1204-5544C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57669424 | |||||||
| chr15:57669425 | C | G | 1 | a0001c0003t0003g0146 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1204-5543C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57669425 | |||||||
| chr15:57669426 | C | G | 1 | a0001c0003t0003g0146 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1204-5542C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57669426 | |||||||
| chr15:57669427 | A | G | 1 | a0001c0003t0003g0146 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1204-5541A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57669427 | |||||||
| chr15:57669429 | T | G | 1 | a0001c0003t0003g0146 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1204-5539T>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57669429 | |||||||
| chr15:57669430 | T | G | 1 | a0001c0003t0003g0146 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1204-5538T>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57669430 | |||||||
| chr15:57669431 | GTTTACTT others(5): Show |
G | 1 | a0001c0003t0003g0146 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1204-5536_1204-552 others(16): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57669431 | |||||||
| chr15:57669445 | T | G | 1 | a0001c0003t0003g0146 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1204-5523T>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57669445 | |||||||
| chr15:57669502 | G | C | 4 | a0001c0001t0008g0328 a0001c0001t0008g0329 a0001c0001t0008g0331 others(1): Show |
4 | HG01884.hp1 HG02717.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1204-5466G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57669502 | |||||||
| chr15:57669550 | T | C | 299 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0157 others(296): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.1204-5418T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57669550 | |||||||
| chr15:57669600 | G | T | 4 | a0001c0001t0008g0328 a0001c0001t0008g0329 a0001c0001t0008g0331 others(1): Show |
4 | HG01884.hp1 HG02717.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1204-5368G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57669600 | |||||||
| chr15:57669617 | T | A | 1 | a0001c0003t0003g0151 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1204-5351T>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57669617 | |||||||
| chr15:57669617 | T | G | 298 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0157 others(295): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.1204-5351T>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57669617 | |||||||
| chr15:57669650 | G | A | 3 | a0001c0001t0007g0332 a0001c0003t0002g0126 a0006c0006t0002g0120 |
3 | HG02109.hp1 HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1204-5318G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57669650 | |||||||
| chr15:57669662 | T | C | 265 | a0001c0001t0001g0013 a0001c0001t0001g0157 a0001c0001t0001g0160 others(262): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.1204-5306T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57669662 | |||||||
| chr15:57669733 | A | G | 1 | a0001c0001t0001g0188 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1204-5235A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57669733 | |||||||
| chr15:57669742 | A | G | 2 | a0001c0001t0001g0211 a0001c0001t0001g0268 |
2 | HG01978.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.1204-5226A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57669742 | |||||||
| chr15:57669831 | C | T | 293 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0157 others(290): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.1204-5137C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57669831 | |||||||
| chr15:57669864 | T | G | 299 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0157 others(296): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.1204-5104T>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57669864 | |||||||
| chr15:57669906 | T | C | 7 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0076 others(4): Show |
10 | NA18941.hp1 NA18946.hp2 NA18947.hp2 others(7): Show |
intron_variant | MODIFIER | c.1204-5062T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57669906 | |||||||
| chr15:57670038 | G | A | 1 | a0001c0001t0009g0214 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1204-4930G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57670038 | |||||||
| chr15:57670061 | A | G | 4 | a0001c0001t0002g0034 a0001c0003t0002g0030 a0001c0003t0002g0033 others(1): Show |
4 | HG00741.hp1 HG01168.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.1204-4907A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57670061 | |||||||
| chr15:57670095 | T | C | 299 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0157 others(296): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.1204-4873T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57670095 | |||||||
| chr15:57670171 | T | TAA | 9 | a0001c0001t0001g0170 a0001c0001t0001g0202 a0002c0002t0002g0074 others(6): Show |
9 | HG00673.hp1 HG02080.hp2 NA18939.hp1 others(6): Show |
intron_variant | MODIFIER | c.1204-4797_1204-479 others(6): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57670171 | |||||||
| chr15:57670223 | G | A | 4 | a0001c0001t0008g0328 a0001c0001t0008g0329 a0001c0001t0008g0331 others(1): Show |
4 | HG01884.hp1 HG02717.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1204-4745G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57670223 | |||||||
| chr15:57670355 | C | T | 293 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0157 others(290): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.1204-4613C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57670355 | |||||||
| chr15:57670384 | A | G | 1 | a0001c0001t0002g0313 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1204-4584A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57670384 | |||||||
| chr15:57670434 | C | A | 293 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0157 others(290): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.1204-4534C>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57670434 | |||||||
| chr15:57670598 | T | G | 9 | a0001c0001t0001g0175 a0001c0001t0001g0259 a0001c0001t0002g0306 others(6): Show |
9 | HG00099.hp2 HG00642.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.1204-4370T>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57670598 | |||||||
| chr15:57670611 | A | G | 1 | a0002c0002t0018g0016 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1204-4357A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57670611 | |||||||
| chr15:57670734 | A | G | 7 | a0002c0002t0002g0006 a0002c0002t0002g0104 a0002c0002t0002g0105 others(4): Show |
8 | HG02083.hp1 NA18939.hp2 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.1204-4234A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57670734 | |||||||
| chr15:57670827 | G | C | 293 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0157 others(290): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.1204-4141G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57670827 | |||||||
| chr15:57670884 | T | C | 293 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0157 others(290): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.1204-4084T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57670884 | |||||||
| chr15:57670887 | G | A | 4 | a0001c0001t0008g0328 a0001c0001t0008g0329 a0001c0001t0008g0331 others(1): Show |
4 | HG01884.hp1 HG02717.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1204-4081G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57670887 | |||||||
| chr15:57670929 | T | C | 1 | a0001c0001t0020g0309 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1204-4039T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57670929 | |||||||
| chr15:57671027 | A | G | 4 | a0001c0001t0008g0328 a0001c0001t0008g0329 a0001c0001t0008g0331 others(1): Show |
4 | HG01884.hp1 HG02717.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1204-3941A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57671027 | |||||||
| chr15:57671139 | C | T | 1 | a0001c0001t0001g0182 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1204-3829C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57671139 | |||||||
| chr15:57671276 | G | A | 326 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0157 others(323): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.1204-3692G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57671276 | |||||||
| chr15:57671401 | T | C | 3 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0261 |
3 | NA18942.hp1 NA18957.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.1204-3567T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57671401 | |||||||
| chr15:57671450 | G | A | 4 | a0001c0001t0008g0328 a0001c0001t0008g0329 a0001c0001t0008g0331 others(1): Show |
4 | HG01884.hp1 HG02717.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1204-3518G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57671450 | |||||||
| chr15:57671462 | T | C | 1 | a0001c0001t0020g0309 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1204-3506T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57671462 | |||||||
| chr15:57671514 | A | G | 242 | a0001c0001t0001g0013 a0001c0001t0001g0157 a0001c0001t0001g0160 others(239): Show |
248 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.1204-3454A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57671514 | |||||||
| chr15:57671629 | T | C | 1 | a0002c0002t0002g0002 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1204-3339T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57671629 | |||||||
| chr15:57671753 | T | C | 2 | a0001c0001t0001g0203 a0001c0001t0001g0220 |
2 | HG02027.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.1204-3215T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57671753 | |||||||
| chr15:57671800 | G | C | 289 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0157 others(286): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.1204-3168G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57671800 | |||||||
| chr15:57671853 | T | G | 293 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0157 others(290): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.1204-3115T>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57671853 | |||||||
| chr15:57671915 | C | T | 293 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0157 others(290): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.1204-3053C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57671915 | |||||||
| chr15:57671923 | T | C | 315 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(312): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.1204-3045T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57671923 | |||||||
| chr15:57672104 | A | G | 1 | a0001c0001t0002g0314 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1204-2864A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57672104 | |||||||
| chr15:57672171 | C | T | 2 | a0001c0003t0003g0339 a0001c0003t0003g0340 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1204-2797C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57672171 | |||||||
| chr15:57672172 | A | T | 2 | a0001c0003t0003g0339 a0001c0003t0003g0340 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1204-2796A>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57672172 | |||||||
| chr15:57672283 | C | G | 293 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0157 others(290): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.1204-2685C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57672283 | |||||||
| chr15:57672352 | C | T | 2 | a0001c0003t0003g0339 a0001c0003t0003g0340 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1204-2616C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57672352 | |||||||
| chr15:57672458 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1204-2510C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57672458 | |||||||
| chr15:57672459 | T | G | 4 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(1): Show |
4 | HG02886.hp1 HG02922.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1204-2509T>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57672459 | |||||||
| chr15:57672522 | C | CT | 294 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0157 others(291): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.1204-2446_1204-244 others(5): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57672522 | |||||||
| chr15:57672675 | A | G | 4 | a0001c0001t0008g0328 a0001c0001t0008g0329 a0001c0001t0008g0331 others(1): Show |
4 | HG01884.hp1 HG02717.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1204-2293A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57672675 | |||||||
| chr15:57672800 | T | C | 293 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0157 others(290): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.1204-2168T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57672800 | |||||||
| chr15:57672818 | T | C | 1 | a0003c0005t0010g0310 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1204-2150T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57672818 | |||||||
| chr15:57672883 | T | G | 1 | a0001c0001t0002g0314 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1204-2085T>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57672883 | |||||||
| chr15:57672890 | T | G | 1 | a0001c0001t0007g0243 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1204-2078T>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57672890 | |||||||
| chr15:57672924 | C | CG | 6 | a0001c0001t0006g0152 a0001c0001t0013g0266 a0001c0001t0020g0309 others(3): Show |
6 | HG01109.hp2 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1204-2043dupG | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 57672924 | ||||||
| chr15:57673057 | T | C | 25 | a0001c0001t0004g0007 a0001c0001t0004g0177 a0001c0001t0004g0233 others(22): Show |
26 | HG00558.hp1 HG00738.hp1 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.1204-1911T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57673057 | |||||||
| chr15:57673072 | A | G | 1 | a0002c0002t0002g0050 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1204-1896A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57673072 | |||||||
| chr15:57673237 | G | A | 3 | a0001c0003t0006g0115 a0001c0003t0006g0116 a0001c0003t0006g0119 |
3 | HG01109.hp2 HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1204-1731G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57673237 | |||||||
| chr15:57673300 | A | T | 1 | a0001c0001t0015g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1204-1668A>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57673300 | |||||||
| chr15:57673444 | G | A | 6 | a0001c0001t0001g0202 a0002c0002t0002g0074 a0002c0002t0002g0098 others(3): Show |
6 | HG02080.hp2 NA18939.hp1 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.1204-1524G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57673444 | |||||||
| chr15:57673452 | A | T | 20 | a0001c0001t0001g0178 a0001c0001t0001g0197 a0001c0001t0001g0231 others(17): Show |
20 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.1204-1516A>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57673452 | |||||||
| chr15:57673455 | CGTGCATG others(3): Show |
C | 1 | a0001c0001t0006g0152 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1204-1509_1204-150 others(14): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 57673455 | ||||||
| chr15:57673456 | G | A | 3 | a0001c0001t0007g0325 a0001c0001t0007g0327 a0005c0011t0002g0117 |
3 | HG02559.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1204-1512G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57673456 | |||||||
| chr15:57673463 | C | CGT | 35 | a0001c0001t0001g0175 a0001c0001t0001g0182 a0001c0001t0001g0188 others(32): Show |
35 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(32): Show |
intron_variant | MODIFIER | c.1204-1451_1204-145 others(6): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 57673463 | ||||||
| chr15:57673463 | C | CGTGT | 12 | a0001c0001t0001g0161 a0001c0001t0001g0187 a0001c0001t0001g0202 others(9): Show |
12 | HG00438.hp2 HG00673.hp2 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.1204-1453_1204-145 others(8): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 57673463 | ||||||
| chr15:57673463 | C | CGTGTGT | 9 | a0001c0001t0001g0184 a0001c0001t0001g0191 a0001c0001t0001g0209 others(6): Show |
9 | HG00544.hp2 HG01109.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.1204-1455_1204-145 others(10): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 57673463 | ||||||
| chr15:57673463 | C | CGTGTGTG others(1): Show |
3 | a0001c0003t0003g0147 a0001c0003t0003g0149 a0002c0002t0005g0089 |
3 | HG00140.hp1 HG00558.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.1204-1457_1204-145 others(12): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 57673463 | ||||||
| chr15:57673463 | C | CGTGTGTG others(3): Show |
1 | a0002c0002t0002g0001 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1204-1459_1204-145 others(14): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 57673463 | ||||||
| chr15:57673463 | CGT | C | 85 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0157 others(82): Show |
87 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.1204-1451_1204-145 others(6): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 57673463 | ||||||
| chr15:57673463 | CGTGT | C | 62 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0160 others(59): Show |
64 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1204-1453_1204-145 others(8): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 57673463 | ||||||
| chr15:57673463 | CGTGTGT | C | 18 | a0001c0001t0001g0257 a0001c0001t0001g0282 a0001c0001t0001g0342 others(15): Show |
18 | HG01074.hp2 HG01123.hp1 HG02015.hp2 others(15): Show |
intron_variant | MODIFIER | c.1204-1455_1204-145 others(10): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 57673463 | ||||||
| chr15:57673463 | CGTGTGTG others(1): Show |
C | 8 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0228 others(5): Show |
8 | HG01243.hp1 HG02109.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1204-1457_1204-145 others(12): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 57673463 | ||||||
| chr15:57673463 | CGTGTGTG others(3): Show |
C | 9 | a0001c0001t0008g0328 a0001c0001t0008g0331 a0001c0003t0001g0113 others(6): Show |
9 | HG01884.hp1 HG01891.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1204-1459_1204-145 others(14): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 57673463 | ||||||
| chr15:57673463 | CGTGTGTG others(5): Show |
C | 13 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(10): Show |
13 | HG01109.hp1 HG02559.hp1 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.1204-1461_1204-145 others(16): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 57673463 | ||||||
| chr15:57673463 | CGTGTGTG others(7): Show |
C | 1 | a0001c0001t0003g0294 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1204-1463_1204-145 others(18): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 57673463 | ||||||
| chr15:57673463 | CGTGTGTG others(17): Show |
C | 1 | a0001c0001t0003g0293 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1204-1473_1204-145 others(28): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 57673463 | ||||||
| chr15:57673535 | C | T | 23 | a0001c0001t0001g0008 a0001c0001t0001g0196 a0001c0001t0001g0206 others(20): Show |
25 | HG00609.hp2 HG01069.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.1204-1433C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57673535 | |||||||
| chr15:57673743 | C | T | 1 | a0001c0001t0007g0243 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1204-1225C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57673743 | |||||||
| chr15:57673786 | A | G | 6 | a0001c0001t0006g0152 a0001c0001t0013g0266 a0001c0001t0020g0309 others(3): Show |
6 | HG01109.hp2 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1204-1182A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57673786 | |||||||
| chr15:57673808 | A | T | 1 | a0001c0001t0001g0236 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1204-1160A>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57673808 | |||||||
| chr15:57673895 | T | C | 1 | a0001c0001t0001g0225 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1204-1073T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57673895 | |||||||
| chr15:57673918 | C | A | 310 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(307): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.1204-1050C>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57673918 | |||||||
| chr15:57673920 | G | T | 1 | a0001c0001t0001g0225 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1204-1048G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57673920 | |||||||
| chr15:57674071 | G | A | 3 | a0001c0003t0006g0115 a0001c0003t0006g0116 a0001c0003t0006g0119 |
3 | HG01109.hp2 HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1204-897G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57674071 | |||||||
| chr15:57674105 | G | A | 1 | a0001c0001t0001g0182 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1204-863G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57674105 | |||||||
| chr15:57674138 | A | AT | 31 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0180 others(28): Show |
33 | HG00609.hp2 HG01069.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.1204-820dupT | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 57674138 | ||||||
| chr15:57674428 | G | T | 4 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0003t0001g0113 others(1): Show |
4 | HG02145.hp1 HG02257.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1204-540G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57674428 | |||||||
| chr15:57674503 | G | A | 31 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0180 others(28): Show |
33 | HG00609.hp2 HG01069.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.1204-465G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57674503 | |||||||
| chr15:57674548 | G | T | 3 | a0001c0003t0002g0048 a0001c0003t0002g0065 a0001c0003t0003g0118 |
3 | HG01106.hp1 HG03239.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1204-420G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57674548 | |||||||
| chr15:57674743 | A | G | 1 | a0003c0005t0010g0310 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1204-225A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57674743 | |||||||
| chr15:57674782 | G | A | 2 | a0001c0003t0001g0237 a0007c0010t0001g0158 |
2 | HG03209.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1204-186G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57674782 | |||||||
| chr15:57674812 | C | G | 3 | a0001c0003t0003g0154 a0001c0003t0003g0155 a0001c0003t0003g0156 |
3 | HG01069.hp2 HG01071.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1204-156C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57674812 | |||||||
| chr15:57675087 | AT | A | 242 | a0001c0001t0001g0013 a0001c0001t0001g0157 a0001c0001t0001g0160 others(239): Show |
248 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.1304+30delT | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 57675087 | ||||||
| chr15:57675221 | T | G | 4 | a0001c0001t0007g0243 a0001c0001t0007g0332 a0001c0003t0002g0126 others(1): Show |
4 | HG02109.hp1 HG03139.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1304+153T>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57675221 | |||||||
| chr15:57675476 | G | A | 4 | a0001c0001t0008g0328 a0001c0001t0008g0329 a0001c0001t0008g0331 others(1): Show |
4 | HG01884.hp1 HG02717.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1304+408G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57675476 | |||||||
| chr15:57675509 | T | C | 302 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0157 others(299): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.1304+441T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57675509 | |||||||
| chr15:57675544 | T | C | 1 | a0001c0003t0003g0147 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1304+476T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57675544 | |||||||
| chr15:57675546 | A | G | 6 | a0001c0001t0006g0152 a0001c0001t0013g0266 a0001c0001t0020g0309 others(3): Show |
6 | HG01109.hp2 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1304+478A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57675546 | |||||||
| chr15:57675621 | A | G | 1 | a0001c0001t0001g0217 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1304+553A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57675621 | |||||||
| chr15:57675624 | G | A | 2 | a0001c0001t0001g0223 a0001c0001t0001g0239 |
2 | NA19009.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1304+556G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57675624 | |||||||
| chr15:57675808 | C | G | 1 | a0001c0003t0002g0025 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1304+740C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57675808 | |||||||
| chr15:57675957 | A | G | 6 | a0001c0001t0006g0152 a0001c0001t0013g0266 a0001c0001t0020g0309 others(3): Show |
6 | HG01109.hp2 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1304+889A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57675957 | |||||||
| chr15:57676020 | G | T | 1 | a0001c0001t0015g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1304+952G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57676020 | |||||||
| chr15:57676106 | C | T | 2 | a0001c0001t0001g0211 a0001c0001t0001g0268 |
2 | HG01978.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.1304+1038C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57676106 | |||||||
| chr15:57676117 | C | T | 1 | a0001c0001t0001g0196 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1304+1049C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57676117 | |||||||
| chr15:57676190 | A | T | 4 | a0001c0001t0003g0294 a0001c0003t0002g0058 a0001c0003t0003g0295 others(1): Show |
4 | HG02258.hp1 HG02559.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1304+1122A>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57676190 | |||||||
| chr15:57676276 | C | G | 2 | a0001c0001t0001g0223 a0001c0001t0001g0239 |
2 | NA19009.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1304+1208C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57676276 | |||||||
| chr15:57676342 | C | T | 2 | a0001c0001t0001g0240 a0001c0003t0003g0125 |
2 | HG02647.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1304+1274C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57676342 | |||||||
| chr15:57676392 | T | C | 3 | a0001c0001t0007g0332 a0001c0003t0002g0126 a0006c0006t0002g0120 |
3 | HG02109.hp1 HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1304+1324T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57676392 | |||||||
| chr15:57676397 | AAT | A | 3 | a0001c0001t0004g0233 a0001c0001t0005g0121 a0002c0004t0005g0305 |
3 | HG02886.hp2 HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1304+1340_1304+134 others(6): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 57676397 | ||||||
| chr15:57676397 | AATATATA others(19): Show |
A | 262 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0157 others(259): Show |
270 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.1304+1352_1304+137 others(30): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 57676397 | ||||||
| chr15:57676410 | GTATATAT others(7): Show |
G | 1 | a0001c0001t0001g0189 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1304+1352_1304+136 others(18): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 57676410 | ||||||
| chr15:57676410 | GTATATAT others(9): Show |
G | 2 | a0001c0001t0001g0014 a0001c0001t0001g0015 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1304+1354_1304+136 others(20): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 57676410 | ||||||
| chr15:57676412 | ATATATAT others(17): Show |
A | 20 | a0001c0001t0001g0182 a0001c0001t0001g0202 a0001c0001t0001g0223 others(17): Show |
20 | HG00673.hp1 HG02080.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.1304+1352_1304+137 others(28): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 57676412 | ||||||
| chr15:57676414 | ATATATGT others(15): Show |
A | 16 | a0001c0001t0001g0175 a0001c0001t0001g0259 a0001c0001t0002g0306 others(13): Show |
16 | HG00099.hp2 HG00642.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.1304+1352_1304+137 others(26): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 57676414 | ||||||
| chr15:57676416 | ATATGTGT others(13): Show |
A | 10 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0015g0159 others(7): Show |
10 | HG01109.hp2 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1304+1352_1304+137 others(24): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 57676416 | ||||||
| chr15:57676418 | ATGTGTAT others(11): Show |
A | 4 | a0001c0001t0001g0176 a0001c0001t0001g0272 a0001c0001t0003g0293 others(1): Show |
4 | HG02258.hp2 HG02280.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1304+1352_1304+136 others(22): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 57676418 | ||||||
| chr15:57676420 | GTGTA | G | 4 | a0002c0002t0005g0060 a0002c0002t0005g0063 a0002c0002t0005g0070 others(1): Show |
4 | HG00558.hp1 HG03017.hp1 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.1304+1354_1304+135 others(8): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 57676420 | ||||||
| chr15:57676420 | GTGTATA | G | 4 | a0001c0001t0004g0275 a0002c0002t0004g0219 a0002c0002t0005g0062 others(1): Show |
4 | HG02015.hp2 HG02056.hp2 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.1304+1354_1304+135 others(10): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 57676420 | ||||||
| chr15:57676422 | G | A | 18 | a0001c0001t0004g0007 a0001c0001t0004g0177 a0001c0001t0004g0233 others(15): Show |
19 | HG00738.hp1 HG01891.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1304+1354G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57676422 | |||||||
| chr15:57676436 | G | A | 12 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0189 others(9): Show |
12 | HG00558.hp1 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.1304+1368G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57676436 | |||||||
| chr15:57676436 | G | GTA | 7 | a0001c0001t0004g0007 a0001c0001t0004g0241 a0001c0001t0004g0244 others(4): Show |
8 | HG00738.hp1 HG02055.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1304+1389_1304+139 others(6): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 57676436 | ||||||
| chr15:57676438 | A | G | 34 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0180 others(31): Show |
36 | HG00609.hp2 HG01069.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.1304+1370A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57676438 | |||||||
| chr15:57676453 | T | C | 6 | a0001c0001t0006g0152 a0001c0001t0013g0266 a0001c0001t0020g0309 others(3): Show |
6 | HG01109.hp2 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1304+1385T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57676453 | |||||||
| chr15:57676455 | T | C | 310 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0157 others(307): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.1304+1387T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57676455 | |||||||
| chr15:57676457 | T | C | 8 | a0001c0001t0004g0275 a0002c0002t0004g0219 a0002c0002t0005g0060 others(5): Show |
8 | HG00558.hp1 HG02015.hp2 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.1304+1389T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57676457 | |||||||
| chr15:57676459 | C | T | 8 | a0001c0001t0004g0275 a0002c0002t0004g0219 a0002c0002t0005g0060 others(5): Show |
8 | HG00558.hp1 HG02015.hp2 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.1304+1391C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57676459 | |||||||
| chr15:57676460 | A | G | 8 | a0001c0001t0004g0275 a0002c0002t0004g0219 a0002c0002t0005g0060 others(5): Show |
8 | HG00558.hp1 HG02015.hp2 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.1304+1392A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57676460 | |||||||
| chr15:57676484 | C | T | 1 | a0001c0003t0014g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1304+1416C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57676484 | |||||||
| chr15:57676582 | GGCCGTTT others(95): Show |
G | 1 | a0001c0003t0003g0150 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1304+1516_1304+161 others(4): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 57676582 | ||||||
| chr15:57676594 | C | A | 4 | a0001c0001t0008g0328 a0001c0001t0008g0329 a0001c0001t0008g0331 others(1): Show |
4 | HG01884.hp1 HG02717.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1304+1526C>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57676594 | |||||||
| chr15:57676720 | C | T | 61 | a0001c0001t0001g0157 a0001c0001t0001g0162 a0001c0001t0001g0169 others(58): Show |
61 | HG00544.hp2 HG00597.hp2 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.1304+1652C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57676720 | |||||||
| chr15:57676734 | A | G | 1 | a0003c0005t0010g0310 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1304+1666A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57676734 | |||||||
| chr15:57676834 | A | C | 1 | a0001c0003t0002g0048 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1304+1766A>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57676834 | |||||||
| chr15:57677069 | G | C | 296 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0157 others(293): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.1304+2001G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57677069 | |||||||
| chr15:57677101 | C | T | 1 | a0001c0001t0015g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1304+2033C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57677101 | |||||||
| chr15:57677116 | G | A | 336 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0157 others(333): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.1304+2048G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57677116 | |||||||
| chr15:57677132 | G | A | 26 | a0001c0001t0004g0007 a0001c0001t0004g0177 a0001c0001t0004g0233 others(23): Show |
27 | HG00558.hp1 HG00738.hp1 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.1304+2064G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57677132 | |||||||
| chr15:57677494 | A | C | 1 | a0001c0001t0001g0280 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1304+2426A>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57677494 | |||||||
| chr15:57677731 | C | T | 2 | a0001c0001t0007g0325 a0001c0001t0007g0327 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1304+2663C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57677731 | |||||||
| chr15:57677736 | A | G | 9 | a0001c0001t0001g0183 a0001c0001t0001g0186 a0001c0001t0001g0188 others(6): Show |
9 | HG01256.hp2 HG01257.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1304+2668A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57677736 | |||||||
| chr15:57677876 | G | T | 29 | a0001c0001t0001g0008 a0001c0001t0001g0179 a0001c0001t0001g0180 others(26): Show |
31 | HG00609.hp2 HG01069.hp1 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.1304+2808G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57677876 | |||||||
| chr15:57678041 | C | CAAA | 7 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0003g0293 others(4): Show |
7 | HG02145.hp1 HG02257.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1304+2992_1304+299 others(7): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 57678041 | ||||||
| chr15:57678041 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0006g0152 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1304+2984_1304+299 others(15): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 57678041 | ||||||
| chr15:57678041 | C | CAAAAAAA others(5): Show |
3 | a0001c0001t0013g0266 a0001c0001t0020g0309 a0001c0003t0006g0116 |
3 | HG02809.hp2 HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1304+2983_1304+299 others(16): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 57678041 | ||||||
| chr15:57678041 | C | CAAAAAAA others(6): Show |
2 | a0001c0003t0006g0115 a0001c0003t0006g0119 |
2 | HG01109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1304+2982_1304+299 others(17): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 57678041 | ||||||
| chr15:57678041 | CA | C | 44 | a0001c0001t0001g0206 a0001c0001t0001g0249 a0001c0001t0001g0250 others(41): Show |
46 | HG00558.hp1 HG00609.hp2 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.1304+2994delA | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 57678041 | ||||||
| chr15:57678041 | CAA | C | 10 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(7): Show |
10 | HG02559.hp1 HG02886.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.1304+2993_1304+299 others(6): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 57678041 | ||||||
| chr15:57678041 | CAAA | C | 6 | a0001c0001t0001g0168 a0001c0001t0001g0341 a0001c0001t0001g0342 others(3): Show |
6 | HG01175.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1304+2992_1304+299 others(7): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 57678041 | ||||||
| chr15:57678041 | CAAAA | C | 234 | a0001c0001t0001g0013 a0001c0001t0001g0157 a0001c0001t0001g0160 others(231): Show |
240 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.1304+2991_1304+299 others(8): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 57678041 | ||||||
| chr15:57678041 | CAAAAA | C | 19 | a0001c0001t0001g0165 a0001c0001t0001g0175 a0001c0001t0001g0190 others(16): Show |
19 | HG00099.hp2 HG00642.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.1304+2990_1304+299 others(9): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 57678041 | ||||||
| chr15:57678058 | A | G | 1 | a0002c0002t0002g0081 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1304+2990A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57678058 | |||||||
| chr15:57678071 | A | G | 1 | a0001c0001t0008g0328 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1304+3003A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57678071 | |||||||
| chr15:57678081 | G | A | 7 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0003g0293 others(4): Show |
7 | HG02145.hp1 HG02257.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1304+3013G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57678081 | |||||||
| chr15:57678188 | C | G | 2 | a0001c0001t0001g0168 a0001c0001t0001g0341 |
2 | HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1304+3120C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57678188 | |||||||
| chr15:57678618 | T | C | 7 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0003g0293 others(4): Show |
7 | HG02145.hp1 HG02257.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1304+3550T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57678618 | |||||||
| chr15:57678666 | A | AAAACTCT others(95): Show |
1 | a0001c0003t0003g0150 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1304+3633_1304+363 others(106): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 57678666 | ||||||
| chr15:57678727 | C | A | 1 | a0002c0002t0002g0056 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1304+3659C>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57678727 | |||||||
| chr15:57678749 | A | T | 1 | a0002c0002t0002g0049 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1304+3681A>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57678749 | |||||||
| chr15:57678757 | T | C | 315 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(312): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.1304+3689T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57678757 | |||||||
| chr15:57678771 | A | G | 7 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0003g0293 others(4): Show |
7 | HG02145.hp1 HG02257.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1304+3703A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57678771 | |||||||
| chr15:57679091 | A | G | 7 | a0001c0001t0007g0325 a0001c0001t0007g0327 a0001c0001t0008g0328 others(4): Show |
7 | HG01884.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1304+4023A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57679091 | |||||||
| chr15:57679134 | C | G | 1 | a0001c0001t0015g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1304+4066C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57679134 | |||||||
| chr15:57679189 | A | G | 1 | a0002c0002t0018g0016 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1304+4121A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57679189 | |||||||
| chr15:57679237 | A | G | 1 | a0002c0002t0002g0097 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1304+4169A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57679237 | |||||||
| chr15:57679333 | C | T | 301 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0157 others(298): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.1304+4265C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57679333 | |||||||
| chr15:57679336 | C | T | 4 | a0001c0003t0001g0171 a0001c0003t0002g0003 a0001c0003t0002g0035 others(1): Show |
5 | HG01074.hp2 HG01099.hp1 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.1304+4268C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57679336 | |||||||
| chr15:57679340 | T | TTG | 13 | a0001c0001t0001g0223 a0001c0001t0001g0234 a0001c0001t0001g0235 others(10): Show |
13 | HG02109.hp2 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1304+4306_1304+430 others(6): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 57679340 | ||||||
| chr15:57679340 | T | TTGTG | 37 | a0001c0001t0001g0175 a0001c0001t0001g0182 a0001c0001t0001g0196 others(34): Show |
37 | HG00099.hp2 HG00609.hp2 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1304+4304_1304+430 others(8): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 57679340 | ||||||
| chr15:57679340 | T | TTGTGTG | 22 | a0001c0001t0001g0185 a0001c0001t0001g0212 a0001c0001t0001g0225 others(19): Show |
23 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(20): Show |
intron_variant | MODIFIER | c.1304+4302_1304+430 others(10): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 57679340 | ||||||
| chr15:57679340 | T | TTGTGTGT others(1): Show |
94 | a0001c0001t0001g0008 a0001c0001t0001g0162 a0001c0001t0001g0164 others(91): Show |
98 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1304+4300_1304+430 others(12): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 57679340 | ||||||
| chr15:57679340 | T | TTGTGTGT others(3): Show |
75 | a0001c0001t0001g0013 a0001c0001t0001g0157 a0001c0001t0001g0160 others(72): Show |
77 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(74): Show |
intron_variant | MODIFIER | c.1304+4298_1304+430 others(14): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 57679340 | ||||||
| chr15:57679340 | T | TTGTGTGT others(5): Show |
26 | a0001c0001t0001g0161 a0001c0001t0001g0173 a0001c0001t0001g0174 others(23): Show |
26 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.1304+4296_1304+430 others(16): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 57679340 | ||||||
| chr15:57679340 | T | TTGTGTGT others(7): Show |
14 | a0001c0001t0001g0232 a0001c0003t0001g0237 a0001c0003t0003g0125 others(11): Show |
15 | HG01192.hp1 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1304+4294_1304+430 others(18): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 57679340 | ||||||
| chr15:57679340 | T | TTGTGTGT others(9): Show |
3 | a0001c0001t0001g0217 a0001c0001t0002g0153 a0001c0001t0009g0201 |
3 | HG02572.hp1 HG02622.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1304+4292_1304+430 others(20): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 57679340 | ||||||
| chr15:57679340 | T | TTGTGTGT others(11): Show |
1 | a0001c0001t0001g0179 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1304+4290_1304+430 others(22): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 57679340 | ||||||
| chr15:57679370 | GTGTGTT | G | 27 | a0001c0001t0001g0169 a0001c0001t0004g0007 a0001c0001t0004g0177 others(24): Show |
28 | HG00558.hp1 HG00738.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.1304+4304_1304+430 others(10): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 57679370 | ||||||
| chr15:57679372 | GTGTT | G | 4 | a0001c0001t0006g0152 a0001c0001t0013g0266 a0001c0001t0015g0159 others(1): Show |
4 | HG02451.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1304+4306_1304+430 others(8): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 57679372 | ||||||
| chr15:57679372 | GTGTTTCT others(1): Show |
G | 3 | a0001c0003t0006g0115 a0001c0003t0006g0116 a0001c0003t0006g0119 |
3 | HG01109.hp2 HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1304+4306_1304+431 others(12): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 57679372 | ||||||
| chr15:57679375 | T | TGTGTGTG others(4): Show |
2 | a0001c0001t0001g0302 a0001c0001t0009g0214 |
2 | HG02895.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1304+4307_1304+430 others(15): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57679375 | |||||||
| chr15:57679376 | T | G | 290 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0157 others(287): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.1304+4308T>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57679376 | |||||||
| chr15:57679376 | TTC | T | 7 | a0001c0001t0001g0218 a0001c0001t0008g0328 a0001c0001t0008g0329 others(4): Show |
7 | HG01884.hp1 HG02280.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1304+4326_1304+432 others(6): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 57679376 | ||||||
| chr15:57679377 | T | G | 4 | a0001c0001t0001g0167 a0001c0001t0001g0302 a0001c0001t0009g0214 others(1): Show |
4 | HG02895.hp1 HG03942.hp2 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.1304+4309T>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57679377 | |||||||
| chr15:57679378 | C | G | 2 | a0002c0002t0011g0072 a0003c0005t0010g0310 |
2 | HG02970.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1304+4310C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57679378 | |||||||
| chr15:57679378 | C | T | 324 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0157 others(321): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.1304+4310C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57679378 | |||||||
| chr15:57679380 | C | G | 1 | a0002c0002t0011g0072 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1304+4312C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57679380 | |||||||
| chr15:57679382 | C | T | 4 | a0001c0003t0006g0115 a0001c0003t0006g0116 a0001c0003t0006g0119 others(1): Show |
4 | HG01109.hp2 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1304+4314C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57679382 | |||||||
| chr15:57679395 | T | A | 3 | a0001c0001t0007g0332 a0001c0003t0002g0126 a0006c0006t0002g0120 |
3 | HG02109.hp1 HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1304+4327T>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57679395 | |||||||
| chr15:57679536 | T | C | 1 | a0002c0002t0002g0127 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1304+4468T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57679536 | |||||||
| chr15:57679627 | A | G | 13 | a0001c0001t0001g0175 a0001c0001t0001g0259 a0001c0001t0002g0306 others(10): Show |
13 | HG00099.hp2 HG00642.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.1304+4559A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57679627 | |||||||
| chr15:57679755 | A | G | 1 | a0001c0001t0001g0217 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1305-4647A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57679755 | |||||||
| chr15:57679830 | C | T | 4 | a0001c0001t0001g0267 a0001c0003t0003g0154 a0001c0003t0003g0155 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1305-4572C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57679830 | |||||||
| chr15:57679907 | T | C | 13 | a0001c0001t0001g0175 a0001c0001t0001g0259 a0001c0001t0002g0306 others(10): Show |
13 | HG00099.hp2 HG00642.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.1305-4495T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57679907 | |||||||
| chr15:57679937 | G | A | 4 | a0002c0002t0002g0057 a0002c0002t0002g0092 a0002c0002t0002g0094 others(1): Show |
4 | HG01255.hp1 HG02486.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1305-4465G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57679937 | |||||||
| chr15:57679984 | C | T | 1 | a0001c0001t0007g0243 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1305-4418C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57679984 | |||||||
| chr15:57680063 | A | G | 1 | a0001c0001t0001g0288 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1305-4339A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57680063 | |||||||
| chr15:57680159 | C | T | 1 | a0001c0003t0014g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1305-4243C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57680159 | |||||||
| chr15:57680227 | C | T | 3 | a0001c0003t0003g0154 a0001c0003t0003g0155 a0001c0003t0003g0156 |
3 | HG01069.hp2 HG01071.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1305-4175C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57680227 | |||||||
| chr15:57680485 | T | TCA | 16 | a0001c0001t0004g0007 a0001c0001t0004g0241 a0001c0001t0004g0242 others(13): Show |
17 | HG00738.hp1 HG02055.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1305-3886_1305-388 others(6): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 57680485 | ||||||
| chr15:57680485 | TCA | T | 198 | a0001c0001t0001g0013 a0001c0001t0001g0157 a0001c0001t0001g0160 others(195): Show |
203 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.1305-3886_1305-388 others(6): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 57680485 | ||||||
| chr15:57680489 | A | G | 1 | a0003c0005t0010g0310 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1305-3913A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57680489 | |||||||
| chr15:57680493 | A | ACACACAC others(7): Show |
6 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0176 others(3): Show |
6 | HG01167.hp1 HG01169.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1305-3896_1305-389 others(18): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 57680493 | ||||||
| chr15:57680495 | A | ACACACAC others(5): Show |
7 | a0001c0001t0006g0152 a0001c0001t0013g0266 a0001c0001t0020g0309 others(4): Show |
7 | HG01109.hp2 HG02280.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1305-3896_1305-389 others(16): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 57680495 | ||||||
| chr15:57680515 | A | ACACACAC others(9): Show |
1 | a0002c0002t0001g0336 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1305-3885_1305-388 others(20): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 57680515 | ||||||
| chr15:57680515 | A | ACACACAC others(7): Show |
1 | a0002c0002t0001g0335 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1305-3885_1305-388 others(18): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 57680515 | ||||||
| chr15:57680515 | A | ACACACAC others(5): Show |
1 | a0001c0001t0003g0293 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1305-3885_1305-388 others(16): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 57680515 | ||||||
| chr15:57680515 | A | ACACACAC others(3): Show |
8 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(5): Show |
8 | HG02145.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1305-3885_1305-388 others(14): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 57680515 | ||||||
| chr15:57680515 | A | ACACACAC others(1): Show |
3 | a0001c0001t0007g0325 a0001c0001t0007g0327 a0001c0003t0017g0122 |
3 | HG02895.hp2 HG02897.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1305-3885_1305-388 others(12): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 57680515 | ||||||
| chr15:57680515 | A | ACACACG | 4 | a0001c0001t0008g0328 a0001c0001t0008g0329 a0001c0001t0008g0331 others(1): Show |
4 | HG01884.hp1 HG02559.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1305-3885_1305-388 others(10): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 57680515 | ||||||
| chr15:57680515 | A | ACACG | 4 | a0001c0001t0001g0196 a0001c0001t0007g0332 a0001c0003t0002g0126 others(1): Show |
4 | HG02109.hp1 HG03139.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.1305-3885_1305-388 others(8): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 57680515 | ||||||
| chr15:57680515 | A | ACG | 21 | a0001c0001t0001g0008 a0001c0001t0001g0206 a0001c0001t0001g0248 others(18): Show |
23 | HG00609.hp2 HG01069.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.1305-3886_1305-388 others(6): Show |
MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 57680515 | ||||||
| chr15:57680515 | A | G | 272 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(269): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.1305-3887A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57680515 | |||||||
| chr15:57680890 | T | C | 3 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG02922.hp2 HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1305-3512T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57680890 | |||||||
| chr15:57681045 | C | G | 4 | a0001c0001t0001g0183 a0001c0001t0001g0195 a0001c0001t0001g0198 others(1): Show |
4 | HG01256.hp2 HG01257.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1305-3357C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57681045 | |||||||
| chr15:57681065 | G | C | 3 | a0001c0003t0006g0115 a0001c0003t0006g0116 a0001c0003t0006g0119 |
3 | HG01109.hp2 HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1305-3337G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57681065 | |||||||
| chr15:57681076 | G | A | 5 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0176 others(2): Show |
5 | HG01167.hp1 HG01169.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1305-3326G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57681076 | |||||||
| chr15:57681078 | C | T | 14 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0176 others(11): Show |
14 | HG01167.hp1 HG01169.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1305-3324C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57681078 | |||||||
| chr15:57681111 | A | T | 3 | a0001c0003t0003g0154 a0001c0003t0003g0155 a0001c0003t0003g0156 |
3 | HG01069.hp2 HG01071.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1305-3291A>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57681111 | |||||||
| chr15:57681170 | A | G | 335 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0157 others(332): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.1305-3232A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57681170 | |||||||
| chr15:57681200 | C | T | 290 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0157 others(287): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.1305-3202C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57681200 | |||||||
| chr15:57681248 | G | A | 283 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0157 others(280): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.1305-3154G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57681248 | |||||||
| chr15:57681356 | A | G | 15 | a0001c0001t0001g0175 a0001c0001t0001g0240 a0001c0001t0001g0259 others(12): Show |
15 | HG00099.hp2 HG00642.hp1 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.1305-3046A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57681356 | |||||||
| chr15:57681401 | A | G | 1 | a0001c0001t0020g0309 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1305-3001A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57681401 | |||||||
| chr15:57681456 | G | C | 6 | a0001c0001t0006g0152 a0001c0001t0013g0266 a0001c0001t0020g0309 others(3): Show |
6 | HG01109.hp2 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1305-2946G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57681456 | |||||||
| chr15:57681523 | C | T | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | HG02698.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1305-2879C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57681523 | |||||||
| chr15:57681558 | C | T | 1 | a0002c0002t0002g0012 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1305-2844C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57681558 | |||||||
| chr15:57681577 | G | A | 191 | a0001c0001t0001g0013 a0001c0001t0001g0157 a0001c0001t0001g0160 others(188): Show |
196 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.1305-2825G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57681577 | |||||||
| chr15:57681600 | C | A | 308 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(305): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.1305-2802C>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57681600 | |||||||
| chr15:57681613 | G | A | 4 | a0001c0001t0001g0197 a0001c0001t0001g0231 a0001c0001t0001g0238 others(1): Show |
4 | HG00741.hp2 HG01515.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.1305-2789G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57681613 | |||||||
| chr15:57681726 | A | G | 2 | a0001c0001t0001g0240 a0001c0003t0003g0125 |
2 | HG02647.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1305-2676A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57681726 | |||||||
| chr15:57681768 | G | A | 191 | a0001c0001t0001g0013 a0001c0001t0001g0157 a0001c0001t0001g0160 others(188): Show |
196 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.1305-2634G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57681768 | |||||||
| chr15:57681818 | G | A | 7 | a0001c0001t0007g0325 a0001c0001t0007g0327 a0001c0001t0008g0328 others(4): Show |
7 | HG01884.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1305-2584G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57681818 | |||||||
| chr15:57681820 | A | G | 1 | a0001c0001t0001g0168 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1305-2582A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57681820 | |||||||
| chr15:57681983 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1305-2419G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57681983 | |||||||
| chr15:57682093 | T | C | 1 | a0001c0003t0002g0023 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1305-2309T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57682093 | |||||||
| chr15:57682452 | C | T | 1 | a0001c0001t0015g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1305-1950C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57682452 | |||||||
| chr15:57682572 | C | G | 6 | a0001c0001t0006g0152 a0001c0001t0013g0266 a0001c0001t0020g0309 others(3): Show |
6 | HG01109.hp2 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1305-1830C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57682572 | |||||||
| chr15:57682783 | A | C | 1 | a0001c0001t0001g0272 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1305-1619A>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57682783 | |||||||
| chr15:57682816 | C | G | 4 | a0002c0002t0002g0002 a0002c0002t0002g0022 a0002c0002t0002g0026 others(1): Show |
5 | HG01257.hp1 HG01258.hp2 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.1305-1586C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57682816 | |||||||
| chr15:57682826 | C | G | 1 | a0001c0001t0001g0013 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1305-1576C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57682826 | |||||||
| chr15:57682833 | C | T | 13 | a0001c0001t0001g0175 a0001c0001t0001g0259 a0001c0001t0002g0306 others(10): Show |
13 | HG00099.hp2 HG00642.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.1305-1569C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57682833 | |||||||
| chr15:57682855 | G | T | 1 | a0003c0005t0010g0310 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1305-1547G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57682855 | |||||||
| chr15:57682871 | C | G | 3 | a0001c0001t0007g0325 a0001c0001t0007g0327 a0005c0011t0002g0117 |
3 | HG02559.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1305-1531C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57682871 | |||||||
| chr15:57682902 | G | T | 1 | a0001c0003t0003g0131 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1305-1500G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57682902 | |||||||
| chr15:57682904 | G | T | 9 | a0001c0001t0007g0325 a0001c0001t0007g0327 a0001c0001t0008g0328 others(6): Show |
9 | HG01884.hp1 HG02559.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1305-1498G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57682904 | |||||||
| chr15:57682989 | G | C | 6 | a0001c0001t0006g0152 a0001c0001t0013g0266 a0001c0001t0020g0309 others(3): Show |
6 | HG01109.hp2 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1305-1413G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57682989 | |||||||
| chr15:57683081 | G | A | 317 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(314): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.1305-1321G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57683081 | |||||||
| chr15:57683129 | A | T | 24 | a0001c0001t0004g0007 a0001c0001t0004g0177 a0001c0001t0004g0233 others(21): Show |
25 | HG00558.hp1 HG00738.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.1305-1273A>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57683129 | |||||||
| chr15:57683244 | C | T | 315 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(312): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.1305-1158C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57683244 | |||||||
| chr15:57683262 | A | C | 7 | a0001c0003t0002g0038 a0001c0003t0002g0041 a0001c0003t0002g0042 others(4): Show |
7 | NA18964.hp2 NA18983.hp1 NA18988.hp2 others(4): Show |
intron_variant | MODIFIER | c.1305-1140A>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57683262 | |||||||
| chr15:57683306 | CT | C | 4 | a0001c0001t0001g0197 a0001c0001t0001g0231 a0001c0001t0001g0238 others(1): Show |
4 | HG00741.hp2 HG01515.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.1305-1095delT | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57683306 | |||||||
| chr15:57683377 | G | T | 1 | a0001c0003t0003g0134 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1305-1025G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57683377 | |||||||
| chr15:57683465 | A | C | 4 | a0001c0003t0001g0171 a0001c0003t0002g0003 a0001c0003t0002g0035 others(1): Show |
5 | HG01074.hp2 HG01099.hp1 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.1305-937A>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57683465 | |||||||
| chr15:57683682 | C | A | 1 | a0001c0003t0002g0126 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1305-720C>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57683682 | |||||||
| chr15:57683875 | A | T | 1 | a0001c0003t0014g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1305-527A>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57683875 | |||||||
| chr15:57684074 | G | A | 1 | a0003c0005t0010g0310 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1305-328G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57684074 | |||||||
| chr15:57684085 | C | T | 4 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(1): Show |
4 | HG02886.hp1 HG02922.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1305-317C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57684085 | |||||||
| chr15:57684107 | A | G | 1 | a0002c0004t0001g0163 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1305-295A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57684107 | |||||||
| chr15:57684131 | AG | A | 239 | a0001c0001t0001g0013 a0001c0001t0001g0157 a0001c0001t0001g0160 others(236): Show |
245 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.1305-268delG | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 57684131 | ||||||
| chr15:57684192 | A | T | 4 | a0001c0001t0008g0328 a0001c0001t0008g0329 a0001c0001t0008g0331 others(1): Show |
4 | HG01884.hp1 HG02717.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1305-210A>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57684192 | |||||||
| chr15:57684213 | T | C | 1 | a0007c0010t0001g0158 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1305-189T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57684213 | |||||||
| chr15:57684325 | A | G | 289 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0157 others(286): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.1305-77A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57684325 | |||||||
| chr15:57684355 | G | A | 2 | a0001c0003t0001g0227 a0002c0002t0002g0091 |
2 | HG00438.hp2 HG00621.hp1 |
intron_variant | MODIFIER | c.1305-47G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57684355 | |||||||
| chr15:57684385 | A | C | 327 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0157 others(324): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.1305-17A>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57684385 |