Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| 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 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 466 | 254 | 70 | 62 | 84 | 14 | 22 | 59 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0002 | 0/0 | 466 | 91 | 20 | 5 | 59 | 0 | 7 | 44 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0003 | 0/0 | 466 | 3 | 2 | 0 | 0 | 0 | 1 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0004 | 0/0 | 466 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0005 | 0/0 | 466 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0006 | 0/0 | 466 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0007 | 0/0 | 466 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 1401 | 175 | 47 | 38 | 69 | 5 | 15 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| c0002 | 0/0 | 1401 | 82 | 19 | 5 | 52 | 0 | 6 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| c0003 | 1/0 | 1401 | 78 | 23 | 24 | 15 | 9 | 6 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| c0004 | 0/0 | 1401 | 8 | 1 | 0 | 6 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| c0005 | 0/0 | 1401 | 3 | 2 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| c0006 | 0/0 | 1401 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| c0007 | 0/0 | 1401 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| c0008 | 0/0 | 1401 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| c0009 | 0/0 | 1401 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| c0010 | 0/0 | 1401 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| c0011 | 0/0 | 1401 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 998 | 142 | 22 | 31 | 76 | 3 | 9 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| t0002 | 0/0 | 998 | 124 | 24 | 22 | 57 | 7 | 14 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| t0003 | 0/0 | 998 | 38 | 12 | 13 | 4 | 4 | 5 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| t0004 | 0/0 | 997 | 16 | 14 | 0 | 2 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| t0005 | 0/0 | 997 | 8 | 2 | 1 | 4 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| t0006 | 0/0 | 998 | 4 | 3 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| t0007 | 0/0 | 998 | 4 | 4 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| t0008 | 0/0 | 992 | 3 | 3 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| t0009 | 0/0 | 998 | 2 | 2 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| t0010 | 0/0 | 998 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| t0011 | 0/0 | 998 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| t0012 | 0/0 | 997 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| t0013 | 0/0 | 998 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| t0014 | 0/0 | 998 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| t0015 | 0/0 | 998 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| t0016 | 1/0 | 998 | 1 | 0 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| t0017 | 0/0 | 992 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| t0018 | 0/0 | 997 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| t0019 | 0/0 | 997 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| t0020 | 0/0 | 998 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0145 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0195 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1401 | 175 | 47 | 38 | 69 | 5 | 15 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0001c0003 | 1/0 | 1401 | 78 | 23 | 24 | 15 | 9 | 6 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0001c0007 | 0/0 | 1401 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0002c0002 | 0/0 | 1401 | 82 | 19 | 5 | 52 | 0 | 6 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0002c0004 | 0/0 | 1401 | 8 | 1 | 0 | 6 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0002c0009 | 0/0 | 1401 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0003c0005 | 0/0 | 1401 | 3 | 2 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0004c0006 | 0/0 | 1401 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0005c0010 | 0/0 | 1401 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0006c0008 | 0/0 | 1401 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0007c0011 | 0/0 | 1401 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | 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 | copy fasta | chr15 | 57586904 | 57690364 |
| a0001c0001t0002 | 0/0 | 2398 | 18 | 3 | 7 | 0 | 2 | 6 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0001c0001t0003 | 0/0 | 2398 | 4 | 3 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0001c0001t0004 | 0/0 | 2397 | 9 | 8 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0001c0001t0005 | 0/0 | 2397 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0001c0001t0006 | 0/0 | 2398 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0001c0001t0007 | 0/0 | 2398 | 4 | 4 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0001c0001t0008 | 0/0 | 2392 | 3 | 3 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0001c0001t0009 | 0/0 | 2398 | 2 | 2 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0001c0001t0013 | 0/0 | 2398 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0001c0001t0015 | 0/0 | 2398 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0001c0001t0019 | 0/0 | 2397 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0001c0001t0020 | 0/0 | 2398 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0001c0003t0001 | 0/0 | 2398 | 4 | 2 | 1 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0001c0003t0002 | 0/0 | 2398 | 33 | 6 | 10 | 10 | 5 | 2 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0001c0003t0003 | 0/0 | 2398 | 30 | 7 | 11 | 4 | 4 | 4 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0001c0003t0004 | 0/0 | 2397 | 4 | 4 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0001c0003t0005 | 0/0 | 2397 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0001c0003t0006 | 0/0 | 2398 | 3 | 2 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0001c0003t0014 | 0/0 | 2398 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0001c0003t0016 | 1/0 | 2398 | 1 | 0 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0001c0003t0017 | 0/0 | 2392 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0001c0007t0003 | 0/0 | 2398 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0002c0002t0001 | 0/0 | 2398 | 2 | 2 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0002c0002t0002 | 0/0 | 2398 | 69 | 13 | 5 | 46 | 0 | 5 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0002c0002t0003 | 0/0 | 2398 | 2 | 2 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0002c0002t0004 | 0/0 | 2397 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0002c0002t0005 | 0/0 | 2397 | 5 | 0 | 0 | 4 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0002c0002t0011 | 0/0 | 2398 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0002c0002t0012 | 0/0 | 2397 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0002c0002t0018 | 0/0 | 2397 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0002c0004t0001 | 0/0 | 2398 | 6 | 0 | 0 | 6 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0002c0004t0002 | 0/0 | 2398 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0002c0004t0005 | 0/0 | 2397 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0002c0009t0002 | 0/0 | 2398 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0003c0005t0004 | 0/0 | 2397 | 2 | 2 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0003c0005t0010 | 0/0 | 2398 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0004c0006t0002 | 0/0 | 2398 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0005c0010t0001 | 0/0 | 2398 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0006c0008t0003 | 0/0 | 2398 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| a0007c0011t0002 | 0/0 | 2398 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | copy fasta | chr15 | 57586904 | 57690364 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0163 | 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 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 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 | 0 | 1 | 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 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0195 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0201 | 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 |
| a0001c0001t0001g0204 | 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 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0219 | 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 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 0 | 1 | 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 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0275 | 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 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0001g0304 | 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 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0343 | 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 |
| a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0003g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0003g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0003g0313 | 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 |
| a0001c0001t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0004g0234 | 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 |
| a0001c0001t0004g0243 | 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 |
| a0001c0001t0004g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0005g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0006g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0007g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0007g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0007g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0007g0333 | 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 |
| a0001c0001t0008g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0008g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0009g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0009g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0013g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0015g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0019g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0001t0020g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0002g0002 | 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 |
| a0001c0003t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0003g0126 | 0/0 | 1 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0003g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0003g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0003g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0003g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 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 | 1 | 0 | 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 | 0 | 0 | 0 | 1 | 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 |
| a0001c0003t0003g0152 | 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 |
| a0001c0003t0003g0157 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0003t0003g0297 | 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 |
| a0001c0003t0003g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0004g0110 | 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 |
| a0001c0003t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0005g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0006g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0006g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0006g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0014g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0016g0145 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0003t0017g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0001c0007t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0002c0002t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 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 |
| a0002c0002t0002g0072 | 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 |
| a0002c0002t0002g0075 | 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 |
| a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0002c0002t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0002c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0002g0344 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0002c0002t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0004g0220 | 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 |
| a0002c0002t0005g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0011g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0002t0012g0089 | 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 |
| a0002c0004t0001g0164 | 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 |
| a0002c0004t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0004t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0004t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0004t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0004t0002g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0002c0004t0005g0306 | 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 |
| a0003c0005t0004g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0003c0005t0004g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0003c0005t0010g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0004c0006t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0005c0010t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0006c0008t0003g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| a0007c0011t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 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 | g0307 | EUR | GBR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG00140 | hp1 | a0001 | c0003 | t0003 | g0148 | 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 | g0146 | 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 | g0165 | EAS | CHS | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG00423 | hp2 | a0002 | c0002 | t0002 | g0087 | EAS | CHS | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG00438 | hp1 | a0002 | c0002 | t0002 | g0074 | EAS | CHS | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG00438 | hp2 | a0002 | c0002 | t0002 | g0092 | EAS | CHS | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG00544 | hp1 | a0001 | c0003 | t0002 | g0079 | EAS | CHS | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG00558 | hp1 | a0002 | c0002 | t0005 | g0090 | EAS | CHS | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0209 | 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 | g0290 | EAS | CHS | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG00609 | hp2 | a0001 | c0003 | t0003 | g0138 | EAS | CHS | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG00621 | hp1 | a0001 | c0003 | t0001 | g0228 | 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 | g0318 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG00673 | hp1 | a0002 | c0002 | t0002 | g0102 | EAS | CHS | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG00738 | hp1 | a0001 | c0003 | t0005 | g0091 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG00738 | hp2 | a0001 | c0003 | t0003 | g0151 | 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 | g0232 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01069 | hp2 | a0001 | c0003 | t0003 | g0155 | 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 | g0131 | 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 | g0156 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01074 | hp2 | a0001 | c0003 | t0001 | g0172 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0314 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01081 | hp2 | a0001 | c0003 | t0003 | g0130 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01099 | hp1 | a0001 | c0003 | t0002 | g0002 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0299 | 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 | g0194 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01109 | hp2 | a0001 | c0003 | t0006 | g0116 | 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 | g0002 | 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 | g0175 | 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 | g0174 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01175 | hp2 | a0006 | c0008 | t0003 | g0134 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01192 | hp1 | a0001 | c0003 | t0003 | g0157 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0312 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01243 | hp2 | a0001 | c0003 | t0003 | g0135 | AMR | PUR | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01255 | hp1 | a0002 | c0002 | t0002 | g0128 | 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 | g0196 | AMR | CLM | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01257 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01258 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01346 | hp1 | a0001 | c0003 | t0002 | g0076 | AMR | CLM | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01358 | hp1 | a0001 | c0003 | t0003 | g0132 | 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 | g0080 | AMR | CLM | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | CLM | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | CLM | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01496 | hp2 | a0001 | c0003 | t0003 | g0143 | AMR | CLM | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01515 | hp1 | a0001 | c0003 | t0003 | g0147 | EUR | IBS | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0198 | EUR | IBS | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01516 | hp1 | a0001 | c0003 | t0003 | g0142 | 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 | g0329 | 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 | g0115 | 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 | g0255 | AMR | PEL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0323 | AMR | PEL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01934 | hp1 | a0001 | c0003 | t0003 | g0152 | AMR | PEL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PEL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PEL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0322 | AMR | PEL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0324 | AMR | PEL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | KHV | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02015 | hp2 | a0002 | c0002 | t0004 | g0220 | EAS | KHV | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | KHV | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0279 | 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 | g0327 | AFR | ACB | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0285 | 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 | g0185 | EAS | KHV | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | KHV | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02080 | hp2 | a0002 | c0002 | t0002 | g0075 | 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 | g0339 | 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 | g0137 | 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 | g0288 | EAS | KHV | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0242 | AFR | ACB | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0337 | AFR | ACB | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02257 | hp2 | a0001 | c0003 | t0003 | g0144 | AFR | ACB | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0295 | AFR | ACB | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | ACB | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0309 | AMR | PEL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02280 | hp1 | a0001 | c0003 | t0014 | g0111 | AFR | ACB | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02280 | hp2 | a0001 | c0003 | t0004 | g0110 | AFR | ACB | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02300 | hp1 | a0002 | c0002 | t0002 | g0098 | AMR | PEL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02451 | hp1 | a0001 | c0001 | t0015 | g0160 | 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 | g0276 | 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 | g0202 | AFR | GWD | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0178 | AFR | GWD | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02602 | hp1 | a0001 | c0003 | t0003 | g0150 | 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 | g0120 | AFR | GWD | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0154 | 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 | g0336 | AFR | GWD | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0241 | 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 | g0212 | SAS | PJL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02698 | hp1 | a0001 | c0003 | t0003 | g0149 | SAS | PJL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02717 | hp1 | a0001 | c0001 | t0008 | g0332 | 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 | g0084 | AFR | GWD | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02735 | hp1 | a0001 | c0003 | t0003 | g0141 | SAS | PJL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0319 | SAS | PJL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02738 | hp1 | a0001 | c0003 | t0003 | g0133 | SAS | PJL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02809 | hp1 | a0002 | c0002 | t0002 | g0085 | AFR | GWD | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02809 | hp2 | a0001 | c0003 | t0006 | g0117 | 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 | g0335 | 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 | g0234 | AFR | GWD | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02895 | hp1 | a0001 | c0001 | t0009 | g0215 | AFR | GWD | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02895 | hp2 | a0001 | c0001 | t0007 | g0328 | AFR | GWD | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02896 | hp2 | a0001 | c0003 | t0003 | g0341 | AFR | GWD | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02897 | hp1 | a0001 | c0001 | t0007 | g0326 | AFR | GWD | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02897 | hp2 | a0001 | c0003 | t0003 | g0340 | AFR | GWD | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02922 | hp1 | a0001 | c0001 | t0013 | g0267 | AFR | ESN | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02970 | hp1 | a0002 | c0002 | t0011 | g0073 | AFR | ESN | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ESN | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02976 | hp1 | a0002 | c0002 | t0003 | g0124 | AFR | ESN | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02976 | hp2 | a0001 | c0001 | t0008 | g0330 | 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 | g0247 | SAS | PJL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03041 | hp2 | a0001 | c0001 | t0006 | g0153 | 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 | g0217 | AFR | MSL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ESN | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03139 | hp2 | a0001 | c0003 | t0002 | g0127 | AFR | ESN | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03195 | hp1 | a0001 | c0003 | t0017 | g0123 | AFR | ESN | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03195 | hp2 | a0002 | c0002 | t0003 | g0125 | AFR | ESN | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0122 | AFR | MSL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03209 | hp2 | a0001 | c0003 | t0001 | g0238 | AFR | MSL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03225 | hp1 | a0002 | c0004 | t0005 | g0306 | 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 | g0321 | SAS | PJL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03453 | hp1 | a0001 | c0003 | t0003 | g0297 | 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 | g0246 | AFR | MSL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03486 | hp2 | a0001 | c0003 | t0003 | g0296 | AFR | MSL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0301 | SAS | PJL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03490 | hp2 | a0002 | c0004 | t0002 | g0331 | SAS | PJL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0292 | SAS | PJL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | ESN | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03516 | hp2 | a0001 | c0003 | t0001 | g0114 | AFR | ESN | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03540 | hp1 | a0001 | c0003 | t0004 | g0113 | AFR | GWD | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03540 | hp2 | a0003 | c0005 | t0004 | g0334 | AFR | GWD | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | MSL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0313 | AFR | MSL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0325 | 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 | g0268 | SAS | PJL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03704 | hp2 | a0001 | c0007 | t0003 | g0129 | SAS | PJL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0317 | 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 | g0316 | SAS | BEB | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0303 | 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 | g0311 | SAS | STU | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0343 | AFR | YRI | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18522 | hp2 | a0001 | c0003 | t0003 | g0126 | AFR | YRI | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18612 | hp1 | a0002 | c0004 | t0001 | g0223 | EAS | CHB | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18612 | hp2 | a0002 | c0002 | t0002 | g0104 | EAS | CHB | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | CHB | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | CHB | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0245 | AFR | YRI | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18906 | hp2 | a0001 | c0001 | t0020 | g0310 | AFR | YRI | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18939 | hp2 | a0002 | c0002 | t0002 | g0344 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18941 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18942 | hp2 | a0001 | c0003 | t0002 | g0088 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18944 | hp1 | a0002 | c0002 | t0002 | g0003 | 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 | g0272 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18945 | hp2 | a0001 | c0003 | t0002 | g0086 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18946 | hp2 | a0002 | c0002 | t0002 | g0072 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18947 | hp2 | a0002 | c0002 | t0002 | g0078 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18948 | hp1 | a0002 | c0004 | t0001 | g0206 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18951 | hp2 | a0001 | c0003 | t0003 | g0139 | 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 | g0158 | 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 | g0208 | 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 | g0166 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0210 | 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 | g0253 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0275 | 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 | g0106 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18978 | hp2 | a0002 | c0004 | t0001 | g0205 | 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 | g0300 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18980 | hp2 | a0002 | c0002 | t0002 | g0097 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0278 | 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 | g0257 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18984 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0284 | 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 | g0283 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18995 | hp1 | a0002 | c0002 | t0002 | g0107 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18995 | hp2 | a0002 | c0002 | t0002 | g0103 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18998 | hp1 | a0002 | c0002 | t0002 | g0105 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18998 | hp2 | a0002 | c0002 | t0002 | g0094 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA18999 | hp2 | a0002 | c0002 | t0002 | g0004 | 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 | g0262 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0168 | 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 | g0183 | 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 | g0252 | 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 | g0089 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0308 | AFR | LWK | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19030 | hp2 | a0004 | c0006 | t0002 | g0121 | AFR | LWK | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0294 | AFR | LWK | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0243 | 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 | g0100 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19057 | hp1 | a0002 | c0002 | t0002 | g0077 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19063 | hp1 | a0001 | c0003 | t0003 | g0140 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19063 | hp2 | a0002 | c0002 | t0002 | g0081 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19064 | hp1 | a0002 | c0004 | t0001 | g0302 | 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 | a0005 | c0010 | t0001 | g0159 | 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 | g0222 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19074 | hp1 | a0002 | c0002 | t0002 | g0099 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0274 | 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 | g0280 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19077 | hp2 | a0002 | c0004 | t0001 | g0298 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19079 | hp2 | a0002 | c0004 | t0001 | g0164 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19080 | hp2 | a0002 | c0002 | t0002 | g0108 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0207 | 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 | g0219 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19087 | hp1 | a0002 | c0002 | t0002 | g0109 | 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 | g0101 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0342 | AFR | YRI | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | YRI | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA20129 | hp1 | a0002 | c0002 | t0002 | g0093 | AFR | ASW | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA20129 | hp2 | a0001 | c0001 | t0007 | g0244 | AFR | ASW | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0239 | EUR | TSI | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0320 | 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 | g0179 | 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 | g0305 | 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 | g0136 | AMR | CLM | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02109 | hp1 | a0001 | c0001 | t0007 | g0333 | AFR | ACB | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02109 | hp2 | a0002 | c0002 | t0002 | g0096 | AFR | ACB | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02486 | hp1 | a0002 | c0002 | t0002 | g0095 | AFR | ACB | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0315 | AFR | ACB | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG02559 | hp1 | a0007 | c0011 | t0002 | g0118 | 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 | g0169 | AFR | MSL | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | USA | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| HG06807 | hp2 | a0002 | c0002 | t0002 | g0083 | 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 | g0338 | 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 | g0112 | AFR | USA | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA21309 | hp1 | a0002 | c0002 | t0002 | g0082 | AFR | LWK | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| NA21309 | hp2 | a0001 | c0003 | t0003 | g0119 | AFR | LWK | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0195 | REF | REF | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| homoSapiens_grch38 | hp1 | a0001 | c0003 | t0016 | g0145 | REF | REF | MYZAP_chr15_57586904_57690364 | MYZAP | chr15 | 57586904 | 57690364 |
| 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 | a0007 | 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 | a0004 | 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 | a0006 | 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 | a0005 | 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 |
| 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 | a0001c0001a0002c0004a0003c0005others(2): Show | 188 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(185): 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 |
| 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 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(26): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(299): 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 | a0001c0001t0007a0001c0001t0008a0001c0001t0019others(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 | a0001c0001t0001a0001c0001t0004a0001c0001t0009others(10): Show | 163 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(160): 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 | a0001c0001t0006a0001c0001t0013a0001c0001t0020others(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 | a0001c0001t0006a0001c0001t0013a0001c0001t0020others(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 | a0001c0001t0004a0001c0001t0005a0001c0001t0019others(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 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(26): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): 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 | a0001c0001t0008a0001c0003t0017 | 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 |
| 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 | a0002c0002t0002g0344 | 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 | a0001c0001t0001g0342a0001c0001t0001g0343 | 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 | a0001c0003t0002g0011a0002c0002t0002g0009a0002c0002t0002g0010others(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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0003t0003g0340a0001c0003t0003g0341 | 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 | a0001c0001t0001g0338a0001c0001t0001g0339 | 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 | 104 | a0001c0001t0002g0034a0001c0003t0002g0002a0001c0003t0002g0011others(101): 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 | 84 | a0001c0001t0002g0034a0001c0001t0005g0122a0001c0003t0002g0002others(81): 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 | a0001c0003t0002g0018a0001c0003t0002g0019a0001c0003t0002g0020others(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 | a0001c0003t0001g0114a0001c0003t0004g0113a0001c0003t0004g0115 | 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 | a0001c0003t0004g0112a0001c0003t0014g0111 | 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 | a0001c0003t0004g0110 | 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 | a0001c0001t0001g0158 | 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 | a0001c0001t0015g0160 | 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 | a0005c0010t0001g0159 | 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 | a0001c0001t0001g0182 | 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 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181 | 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 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0175 | 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 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(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 | a0001c0001t0001g0168a0001c0003t0001g0172 | 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 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167 | 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 | a0001c0001t0001g0162 | 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 | a0001c0001t0001g0163a0002c0004t0001g0164 | 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 | a0001c0001t0001g0161 | 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 | a0001c0001t0007g0244 | 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 | a0001c0001t0001g0240 | 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 | a0001c0001t0001g0237a0001c0001t0004g0007a0001c0001t0004g0245others(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 | a0001c0001t0001g0227a0001c0001t0001g0229a0001c0001t0001g0230others(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 | a0001c0001t0001g0214a0001c0001t0001g0216a0001c0001t0001g0217others(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 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0207others(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 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0203others(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 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 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 |
6 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0194others(3): Show | 6 | HG00544.hp2 HG01109.hp1 HG01256.hp2 others(3): 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 | a0001c0001t0001g0013a0001c0001t0001g0185a0001c0001t0001g0189others(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 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188 | 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 | a0001c0001t0001g0183a0001c0001t0001g0184 | 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 | a0001c0001t0001g0247a0001c0001t0001g0248 | 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 | a0001c0001t0001g0251 | 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 | a0001c0001t0001g0008a0001c0001t0001g0249a0001c0001t0001g0250 | 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 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0001g0277others(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 | a0001c0001t0001g0273 | 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 | a0001c0001t0001g0271a0001c0001t0001g0272 | 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 | a0001c0001t0001g0270 | 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 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(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 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0001t0001g0265 | 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 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261 | 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 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0262 | 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 | a0001c0001t0001g0258 | 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 | a0001c0001t0001g0255 | 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 | a0001c0001t0001g0254 | 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 | a0001c0001t0001g0253 | 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 | a0001c0001t0001g0252 | 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 | a0001c0001t0001g0299a0002c0004t0001g0298 | 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 | a0001c0001t0003g0294a0001c0001t0003g0295a0001c0003t0003g0296others(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 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291others(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 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0292others(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 | a0001c0001t0001g0288a0001c0003t0003g0340 | 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 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0285 | 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 | a0001c0001t0001g0281a0001c0001t0001g0282 | 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 | a0001c0001t0001g0279a0001c0001t0001g0280 | 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 | a0001c0001t0001g0278 | 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 | a0001c0001t0002g0305 | 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 | a0001c0001t0001g0304 | 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 | a0001c0001t0001g0303 | 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 | a0001c0001t0001g0339a0002c0004t0001g0302 | 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 | a0001c0001t0001g0301 | 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 | a0001c0001t0001g0300 | 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 | a0001c0001t0002g0308a0001c0001t0002g0309 | 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 | a0001c0001t0002g0307 | 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 | a0002c0004t0005g0306 | 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 | a0001c0001t0002g0319a0001c0001t0002g0320a0001c0001t0002g0321others(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 | a0001c0001t0002g0314a0001c0001t0002g0315a0001c0001t0002g0316others(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 | a0001c0001t0003g0313 | 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 | a0001c0001t0003g0312 | 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 | a0001c0001t0020g0310 | 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 | a0003c0005t0010g0311 | 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 | a0003c0005t0004g0335 | 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 | a0003c0005t0004g0334 | 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 | a0001c0001t0007g0333a0001c0001t0008g0332 | 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 | a0001c0001t0008g0330a0002c0004t0002g0331 | 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 | a0001c0001t0008g0329 | 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 | a0001c0001t0007g0328 | 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 | a0001c0001t0007g0326a0001c0001t0019g0327 | 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 | a0002c0002t0001g0336a0002c0002t0001g0337 | 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 | a0002c0002t0002g0006a0002c0002t0002g0097a0002c0002t0002g0098others(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 | a0001c0003t0003g0155a0001c0003t0003g0156a0001c0003t0003g0157 | 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 | a0003c0005t0010g0311 | 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 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0241others(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 | a0003c0005t0010g0311 | 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 | a0001c0003t0003g0340 | 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 | a0001c0003t0003g0341 | 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 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0176others(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 | a0001c0001t0001g0162a0001c0001t0001g0185a0001c0001t0001g0278others(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 | a0001c0001t0003g0312a0001c0001t0003g0313 | 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 | a0007c0011t0002g0118 | 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 | a0001c0001t0003g0294a0001c0001t0003g0295a0001c0003t0003g0296others(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 | a0001c0001t0003g0312a0001c0001t0003g0313 | 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 | a0001c0003t0003g0340a0001c0003t0003g0341 | 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 | a0001c0003t0001g0114a0001c0003t0004g0110a0001c0003t0004g0112others(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 | a0002c0002t0002g0092 | 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 | a0007c0011t0002g0118 | 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 | a0002c0002t0002g0128 | 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 | 203 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(200): Show | 205 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(202): 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 | a0001c0001t0002g0034a0001c0003t0002g0002a0001c0003t0002g0028others(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 | a0001c0003t0001g0114a0001c0003t0004g0110a0001c0003t0004g0112others(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 | 164 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(161): Show | 166 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(163): 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 | a0001c0003t0005g0091 | 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 | a0002c0002t0002g0128 | 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 | a0001c0001t0001g0231 | 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 | a0001c0007t0003g0129 | 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 | a0001c0001t0001g0163 | 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 | a0003c0005t0010g0311 | 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 | a0001c0001t0001g0189 | 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 | a0001c0001t0001g0338a0001c0001t0001g0339 | 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 | a0007c0011t0002g0118 | 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 | a0005c0010t0001g0159 | 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 | a0001c0003t0003g0126a0001c0003t0017g0123a0002c0002t0003g0124others(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 | a0001c0003t0004g0110a0001c0003t0014g0111 | 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 | a0001c0003t0002g0038a0001c0003t0002g0041a0001c0003t0002g0042others(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 | a0001c0001t0007g0244 | 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 | a0001c0001t0001g0162a0001c0001t0001g0173a0001c0001t0001g0176others(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 | a0001c0003t0002g0127 | 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 | a0001c0001t0002g0154a0001c0001t0002g0305a0001c0001t0002g0307others(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 | a0001c0001t0001g0188a0001c0001t0001g0253 | 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 | a0001c0001t0001g0293 | 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 | a0001c0001t0003g0294a0001c0001t0003g0295a0001c0003t0003g0296others(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 | a0001c0003t0002g0002a0001c0003t0002g0035a0001c0003t0002g0036 | 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 | a0002c0002t0002g0097 | 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 | a0001c0001t0002g0309 | 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 | a0001c0003t0001g0114a0001c0003t0004g0110a0001c0003t0004g0112others(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 | 201 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(198): Show | 203 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(200): 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 | a0001c0001t0002g0305a0001c0001t0002g0307a0001c0001t0002g0308others(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 | a0001c0001t0001g0266 | 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 | a0001c0001t0002g0305a0001c0001t0002g0307a0001c0001t0002g0308others(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 | a0007c0011t0002g0118 | 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 | a0001c0001t0001g0241 | 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 | a0001c0003t0017g0123 | 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 | a0001c0001t0005g0122a0004c0006t0002g0121 | 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 | a0001c0001t0003g0294a0001c0001t0003g0295a0001c0001t0003g0312others(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 | a0001c0003t0014g0111 | 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 | a0001c0001t0002g0305a0001c0001t0002g0307a0001c0001t0002g0308others(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 | a0001c0001t0002g0305a0001c0001t0002g0307a0001c0001t0002g0308others(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 | a0001c0001t0001g0227 | 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 | a0001c0001t0001g0232a0001c0001t0001g0239a0001c0001t0001g0303 | 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 | a0001c0001t0002g0154a0001c0001t0006g0153 | 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 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0003t0003g0340others(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 | a0001c0001t0001g0207 | 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 | a0001c0003t0002g0088a0002c0002t0002g0092a0002c0002t0005g0090others(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 | a0001c0001t0001g0233a0001c0001t0002g0305a0001c0001t0002g0307others(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 | a0001c0003t0003g0148a0001c0003t0003g0149a0001c0003t0003g0150others(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 | a0001c0001t0002g0314 | 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 | a0007c0011t0002g0118 | 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 | a0002c0002t0002g0044a0002c0002t0002g0045 | 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 | a0001c0003t0002g0088a0002c0002t0002g0092a0002c0002t0005g0090others(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 | a0001c0001t0001g0167a0001c0001t0001g0213a0001c0001t0001g0269others(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 | 104 | a0001c0001t0001g0265a0001c0001t0002g0034a0001c0001t0005g0122others(101): 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 | a0001c0003t0002g0086a0001c0003t0006g0116a0001c0003t0006g0117others(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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0001c0001t0008g0329 | 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 | a0001c0001t0003g0313 | 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 | a0001c0001t0002g0305a0001c0001t0002g0307a0001c0001t0002g0308others(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 | a0001c0001t0007g0244a0001c0001t0007g0326a0001c0001t0007g0328others(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 | a0001c0001t0001g0241 | 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 | a0001c0001t0001g0251 | 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 | a0001c0001t0002g0305a0001c0001t0002g0307a0001c0001t0002g0308others(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 | a0001c0001t0002g0154a0001c0001t0006g0153 | 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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0001c0001t0002g0305a0001c0001t0002g0307a0001c0001t0002g0308others(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 | a0001c0001t0002g0305a0001c0001t0002g0307a0001c0001t0002g0308others(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 | a0001c0001t0001g0268 | 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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0001c0001t0003g0294 | 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 | 242 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(239): Show | 249 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(246): 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 | a0001c0001t0001g0261a0001c0001t0001g0278a0001c0001t0001g0280others(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 | a0001c0001t0007g0326a0001c0001t0007g0328a0001c0001t0008g0329others(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 | a0001c0001t0002g0305a0001c0001t0002g0308a0001c0001t0002g0309others(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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0001c0001t0001g0008a0001c0001t0001g0162a0001c0001t0001g0249others(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 | a0001c0003t0003g0147 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335 | 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 | a0001c0001t0001g0269 | 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 | a0001c0001t0002g0154a0001c0001t0006g0153 | 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 | a0002c0002t0002g0084 | 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 | 319 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(316): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(324): 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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | 147 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(144): Show | 149 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(146): 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 | a0001c0001t0001g0180 | 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 | a0001c0003t0001g0114a0001c0003t0004g0110a0001c0003t0004g0112others(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 | a0001c0001t0001g0268 | 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 | a0001c0001t0001g0173 | 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 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0003t0001g0238others(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 | a0003c0005t0004g0334a0003c0005t0004g0335 | 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 | a0002c0002t0002g0009a0002c0002t0002g0010 | 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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0001t0007g0326a0001c0001t0007g0328a0001c0001t0008g0329others(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 | a0001c0003t0004g0115 | 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 | a0001c0001t0002g0154a0003c0005t0004g0334a0003c0005t0004g0335 | 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 | a0003c0005t0010g0311 | 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 | 99 | a0001c0001t0001g0271a0001c0001t0002g0034a0001c0003t0001g0228others(96): 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 | a0001c0003t0003g0146 | 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 | a0001c0001t0002g0154a0003c0005t0004g0334a0003c0005t0004g0335 | 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 | 107 | a0001c0001t0001g0015a0001c0001t0001g0271a0001c0001t0002g0034others(104): 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 | a0001c0001t0004g0178 | 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 | a0007c0011t0002g0118 | 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 | a0001c0001t0001g0161a0001c0001t0001g0207a0001c0001t0001g0214 | 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 | a0001c0003t0003g0340a0001c0003t0003g0341 | 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 | a0002c0002t0002g0098 | 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 | a0003c0005t0010g0311 | 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 | 195 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(192): Show | 197 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(194): 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 | a0001c0001t0002g0315 | 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 | 178 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(175): Show | 180 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(177): Show |
intron_variant | MODIFIER | c.76-333G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 1/12 | chr15 | 57603936 | ||||||
| chr15:57603970
|
A | C | 165 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(162): Show | 167 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(164): 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 | a0001c0001t0006g0153a0004c0006t0002g0121 | 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 | 140 | a0001c0001t0001g0271a0001c0001t0002g0034a0001c0001t0006g0153others(137): 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 | 178 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(175): Show | 180 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(177): 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 | a0002c0002t0002g0082 | 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 | 174 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(171): Show | 176 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(173): 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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0001c0003t0003g0148 | 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 | a0001c0001t0001g0170 | 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 | a0002c0002t0002g0081 | 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 | 178 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(175): Show | 180 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(177): Show |
intron_variant | MODIFIER | c.162+470G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57604825 | ||||||
| chr15:57604831
|
G | A | 98 | a0001c0001t0001g0271a0001c0001t0002g0034a0001c0003t0002g0002others(95): 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 | 314 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(311): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(319): 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 | a0003c0005t0004g0334a0003c0005t0004g0335 | 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 | a0002c0002t0002g0087 | 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 | a0001c0001t0001g0219a0002c0004t0001g0205 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335 | 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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0001c0003t0003g0133 | 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 | a0006c0008t0003g0134 | 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 | a0001c0001t0007g0244 | 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 | a0001c0001t0006g0153 | 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 | a0001c0001t0007g0244a0001c0001t0020g0310a0003c0005t0010g0311 | 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 | a0007c0011t0002g0118 | 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 | a0001c0001t0001g0192a0001c0001t0001g0200a0001c0001t0001g0201others(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 | a0002c0004t0001g0302 | 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 | a0002c0004t0001g0302 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335 | 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 | a0001c0001t0002g0034a0001c0003t0002g0002a0001c0003t0002g0028others(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 | a0001c0001t0007g0326a0001c0001t0007g0328a0001c0001t0008g0329others(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 | 142 | a0001c0001t0001g0271a0001c0001t0002g0034a0001c0001t0006g0153others(139): 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 | a0002c0002t0002g0080 | 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 | a0004c0006t0002g0121 | 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 | a0001c0001t0007g0326a0001c0001t0007g0328a0001c0001t0008g0329others(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 | a0001c0003t0001g0238 | 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 | a0004c0006t0002g0121 | 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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | 159 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(156): Show | 161 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(158): 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 | 312 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(309): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(317): 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 | a0001c0001t0001g0343 | 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 | a0001c0003t0001g0114a0001c0003t0004g0110a0001c0003t0004g0112others(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 | a0003c0005t0004g0334a0003c0005t0004g0335 | 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 | a0002c0002t0003g0124a0002c0002t0003g0125 | 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 | a0001c0001t0001g0211 | 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 | 314 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(311): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(319): 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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0001c0001t0003g0294 | 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 | a0007c0011t0002g0118 | 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 | a0001c0001t0001g0274 | 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 | a0001c0001t0007g0244a0001c0001t0020g0310 | 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 | a0006c0008t0003g0134 | 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 | 142 | a0001c0001t0001g0271a0001c0001t0002g0034a0001c0003t0001g0172others(139): 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 | 147 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(144): Show | 149 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(146): 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 | a0001c0003t0001g0114a0001c0003t0004g0110a0001c0003t0004g0112others(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 | 144 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(141): Show | 146 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(143): Show |
intron_variant | MODIFIER | c.162+3737G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57608092 | ||||||
| chr15:57608172
|
G | A | 113 | a0001c0001t0001g0271a0001c0001t0002g0034a0001c0003t0001g0172others(110): 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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0001c0001t0001g0173 | 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 | a0001c0001t0006g0153a0001c0001t0007g0244a0001c0001t0020g0310 | 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 | a0001c0001t0007g0244a0001c0001t0020g0310 | 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 | a0001c0001t0004g0243 | 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 | a0007c0011t0002g0118 | 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 | 108 | a0001c0001t0001g0271a0001c0001t0002g0034a0001c0003t0001g0172others(105): 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 | a0001c0007t0003g0129 | 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 | a0007c0011t0002g0118 | 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 | a0001c0001t0001g0233a0001c0001t0002g0305a0001c0001t0002g0307others(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 | a0001c0001t0001g0233a0001c0001t0002g0305a0001c0001t0002g0307others(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 | 109 | a0001c0001t0001g0271a0001c0001t0002g0034a0001c0003t0001g0172others(106): 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 | a0001c0003t0003g0144 | 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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0001c0003t0001g0114a0001c0003t0004g0110a0001c0003t0004g0112others(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 | a0001c0001t0008g0329a0001c0001t0008g0332 | 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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0002c0002t0002g0103 | 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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0002c0004t0002g0331 | 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 | a0001c0001t0007g0244a0001c0001t0020g0310a0003c0005t0010g0311 | 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 | a0001c0001t0001g0188 | 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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0001c0001t0007g0326a0001c0001t0007g0328a0001c0001t0008g0329others(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 | 171 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(168): Show | 173 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(170): 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 | a0001c0001t0001g0189 | 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 | a0001c0001t0004g0007a0001c0001t0004g0242a0001c0001t0004g0243others(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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0004g0234others(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 | a0001c0003t0003g0297 | 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 | a0001c0001t0001g0247a0001c0001t0001g0248 | 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 | a0001c0003t0003g0340a0001c0003t0003g0341 | 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 | a0001c0001t0001g0187 | 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 | a0001c0001t0001g0184 | 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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0002c0002t0002g0095 | 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 | 177 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(174): Show | 179 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(176): 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 | a0001c0003t0002g0079 | 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 | a0001c0001t0001g0187 | 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 | a0001c0001t0007g0326a0001c0001t0007g0328a0001c0001t0008g0329others(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 | a0002c0002t0002g0099a0002c0002t0002g0100a0002c0002t0002g0101 | 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 | 83 | a0001c0001t0001g0271a0001c0001t0002g0034a0001c0003t0001g0172others(80): 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 | a0001c0001t0007g0326a0001c0001t0007g0328a0001c0001t0008g0329others(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 | a0001c0001t0007g0244a0001c0001t0020g0310 | 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 | a0007c0011t0002g0118 | 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 | a0001c0003t0001g0172a0001c0003t0002g0002a0001c0003t0002g0035others(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 | a0001c0003t0003g0146 | 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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0001c0003t0003g0133 | 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 | a0001c0001t0002g0305a0001c0001t0002g0307a0001c0001t0002g0308others(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 | a0003c0005t0010g0311 | 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 | a0001c0003t0001g0114a0001c0003t0004g0110a0001c0003t0004g0112others(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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0001c0001t0001g0176 | 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 | a0004c0006t0002g0121 | 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 | a0001c0001t0002g0305a0001c0001t0002g0307a0001c0001t0002g0308others(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 | a0001c0003t0003g0119a0001c0003t0003g0126a0001c0003t0003g0130others(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 | 145 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(142): Show | 147 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(144): 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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0007c0011t0002g0118 | 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 | a0001c0001t0002g0305a0001c0001t0002g0307a0001c0001t0002g0308others(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 | a0003c0005t0004g0334a0003c0005t0004g0335 | 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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0001c0001t0002g0305a0001c0001t0002g0307a0001c0001t0002g0308others(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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | 145 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(142): Show | 147 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(144): 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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0001c0001t0006g0153 | 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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0001c0003t0003g0155a0001c0003t0003g0156a0001c0003t0003g0157 | 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 | a0001c0001t0001g0290 | 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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0001c0001t0001g0212 | 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 | a0001c0001t0002g0305a0001c0001t0002g0307a0001c0001t0002g0308others(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 | 188 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(185): Show | 190 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(187): 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 | a0001c0001t0001g0169a0001c0001t0001g0190a0001c0001t0001g0216others(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 | 146 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(143): Show | 148 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(145): Show |
intron_variant | MODIFIER | c.163-5038G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57612995 | ||||||
| chr15:57613077
|
G | A | 145 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(142): Show | 147 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(144): Show |
intron_variant | MODIFIER | c.163-4956G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57613077 | ||||||
| chr15:57613080
|
T | C | 311 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(308): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(316): 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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0001c0001t0001g0165a0001c0001t0001g0167a0001c0001t0001g0168others(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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0001c0003t0002g0055a0001c0003t0002g0058a0002c0002t0002g0017others(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 | a0001c0003t0003g0119a0001c0003t0003g0131a0001c0003t0003g0132others(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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0001c0003t0002g0018a0001c0003t0002g0019a0001c0003t0002g0020others(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 | 311 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(308): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(316): 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 | a0001c0003t0001g0114a0001c0003t0004g0112a0001c0003t0004g0113others(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 | 311 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(308): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(316): 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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0001c0001t0001g0218 | 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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | 311 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(308): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(316): 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 | a0003c0005t0010g0311 | 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 | 145 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(142): Show | 147 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(144): Show |
intron_variant | MODIFIER | c.163-3772G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57614261 | ||||||
| chr15:57614438
|
A | G | 311 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(308): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(316): 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 | a0001c0001t0001g0189a0001c0001t0001g0197 | 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 | 58 | a0001c0003t0001g0228a0001c0003t0002g0011a0001c0003t0002g0038others(55): 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 | 311 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(308): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(316): 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 | a0003c0005t0004g0334 | 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 | a0001c0003t0001g0114a0001c0003t0004g0112a0001c0003t0004g0113others(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 | a0001c0001t0002g0305a0001c0001t0002g0307a0001c0001t0002g0308others(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 | a0001c0003t0002g0079 | 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 | a0001c0001t0001g0247a0001c0001t0001g0248 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335 | 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 | a0002c0002t0002g0085 | 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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | 172 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(169): Show | 174 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(171): 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 | a0003c0005t0010g0311 | 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 | a0001c0001t0001g0208 | 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 | 190 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(187): Show | 192 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(189): 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 | a0001c0003t0003g0133a0001c0003t0003g0135a0001c0003t0003g0144 | 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 | a0003c0005t0010g0311 | 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 | a0001c0001t0002g0305a0001c0001t0002g0307a0001c0001t0002g0308others(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 | 176 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(173): Show | 178 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(175): 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 | a0003c0005t0004g0334 | 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 | a0001c0001t0007g0244a0001c0001t0020g0310 | 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 | 177 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(174): Show | 179 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(176): 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 | a0001c0001t0007g0326a0001c0001t0007g0328a0001c0001t0008g0329others(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 | a0001c0003t0003g0126 | 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 | a0001c0003t0002g0127 | 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 | 187 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(184): Show | 189 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(186): 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 | 267 | a0001c0001t0001g0008a0001c0001t0001g0162a0001c0001t0001g0165others(264): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.163-2033C>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57616000 | ||||||
| chr15:57616014
|
C | T | 184 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(181): Show | 186 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(183): 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 | a0001c0001t0001g0169a0001c0001t0001g0190a0001c0001t0001g0216others(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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0001c0003t0003g0340a0001c0003t0003g0341 | 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 | a0001c0003t0001g0238a0001c0003t0003g0340a0001c0003t0003g0341 | 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 | 312 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(309): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.163-1672T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57616361 | ||||||
| chr15:57616457
|
A | G | 151 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(148): Show | 153 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(150): 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 | a0003c0005t0004g0334a0003c0005t0004g0335 | 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 | 148 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(145): Show | 150 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(147): Show |
intron_variant | MODIFIER | c.163-1434G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57616599 | ||||||
| chr15:57616601
|
T | A | 342 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(339): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): 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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | 78 | a0001c0001t0001g0177a0001c0001t0001g0186a0001c0001t0001g0193others(75): 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 | a0001c0001t0001g0158a0001c0001t0001g0180a0001c0001t0001g0181others(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 | a0001c0001t0001g0252a0001c0001t0001g0257a0001c0001t0001g0286others(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 | a0001c0001t0001g0185a0001c0001t0001g0203a0001c0001t0001g0204others(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 | a0001c0001t0001g0270a0001c0001t0001g0284a0002c0004t0002g0331 | 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 | a0001c0001t0001g0261a0001c0001t0001g0300 | 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 | a0001c0001t0002g0305a0001c0001t0002g0320 | 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 | a0001c0001t0001g0268a0001c0001t0002g0307a0001c0001t0002g0309others(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 | a0001c0001t0001g0235a0001c0001t0002g0308a0001c0001t0002g0323others(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 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0291others(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 | a0001c0001t0001g0014a0001c0001t0001g0169a0001c0001t0001g0188others(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 | a0001c0001t0001g0170a0001c0001t0001g0179a0001c0001t0001g0183others(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 | a0001c0001t0001g0192a0001c0001t0001g0266a0001c0001t0001g0277others(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 | a0001c0001t0001g0173a0001c0001t0001g0222a0001c0001t0001g0233others(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 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0174others(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 |
5 | a0001c0001t0001g0165a0001c0001t0001g0171a0001c0001t0001g0195others(2): Show | 5 | HG00423.hp1 HG01099.hp2 NA18943.hp2 others(2): 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 | a0001c0001t0001g0176a0001c0001t0001g0221a0001c0001t0001g0236others(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 | a0001c0001t0001g0196a0001c0001t0001g0208a0001c0001t0001g0225others(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 | a0001c0001t0001g0199a0001c0001t0001g0231 | 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 | a0001c0001t0001g0211a0001c0001t0001g0226a0001c0001t0001g0240others(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 | a0001c0001t0001g0008a0001c0001t0001g0241a0001c0001t0001g0281others(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 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0285 | 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 | a0001c0001t0001g0265 | 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 | a0001c0001t0007g0244a0001c0001t0020g0310 | 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 | a0002c0002t0003g0124a0002c0002t0003g0125 | 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 | a0001c0003t0001g0238a0001c0003t0003g0341 | 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 | a0001c0003t0003g0340 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | 190 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(187): Show | 192 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(189): 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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | a0001c0001t0006g0153 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | a0002c0002t0002g0097 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | a0001c0001t0007g0326a0001c0001t0007g0328a0001c0001t0008g0329others(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 | a0003c0005t0010g0311 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335 | 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 | 147 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(144): Show | 149 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(146): 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 | a0001c0003t0003g0133a0001c0003t0003g0135a0001c0003t0003g0144 | 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 | a0001c0003t0003g0141 | 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 | a0001c0001t0001g0271 | 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 | a0001c0003t0001g0172 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | 190 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(187): Show | 192 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(189): 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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | a0001c0001t0001g0221 | 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 | 190 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(187): Show | 192 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(189): Show |
intron_variant | MODIFIER | c.163-67G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 2/12 | chr15 | 57617966 | ||||||
| chr15:57618246
|
A | G | 337 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(334): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): 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 | a0001c0003t0003g0340a0001c0003t0003g0341 | 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 | a0001c0001t0001g0187 | 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 | a0001c0003t0003g0119a0001c0003t0003g0126a0001c0003t0003g0130others(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 | a0001c0003t0006g0116a0001c0003t0006g0117a0001c0003t0006g0120 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | a0001c0003t0002g0086 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | a0001c0001t0001g0300 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0003t0001g0172 | 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 | a0003c0005t0010g0311 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | a0002c0002t0002g0128 | 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 | a0002c0002t0002g0082 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | 191 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(188): Show | 193 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(190): Show |
intron_variant | MODIFIER | c.318+1342G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 3/12 | chr15 | 57619530 | ||||||
| chr15:57619701
|
G | A | 316 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(313): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(321): 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 | a0001c0003t0001g0172 | 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 | a0001c0003t0003g0131a0001c0003t0003g0132 | 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 | 309 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(306): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(314): 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 | a0001c0003t0002g0061a0001c0003t0002g0079a0001c0003t0002g0088others(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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | a0001c0001t0007g0326a0001c0001t0007g0328a0001c0001t0008g0329others(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 | 309 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(306): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(314): 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 | a0001c0001t0006g0153a0001c0001t0007g0326a0001c0001t0007g0328others(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 | a0001c0001t0007g0244a0001c0001t0020g0310 | 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 | a0001c0001t0001g0008a0001c0001t0001g0249a0001c0001t0001g0250others(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 | 191 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(188): Show | 193 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(190): 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 | a0001c0003t0017g0123 | 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 | 152 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(149): Show | 154 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(151): 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 | a0001c0003t0003g0136 | 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 | a0001c0001t0001g0265 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | a0001c0001t0007g0244a0001c0001t0020g0310 | 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 | a0001c0001t0001g0169a0001c0001t0001g0190a0001c0001t0001g0218others(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 | 153 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(150): Show | 155 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(152): 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 | a0003c0005t0010g0311 | 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 | a0002c0002t0001g0336 | 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 | a0002c0002t0001g0337 | 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 | a0001c0001t0007g0326a0001c0001t0007g0328a0001c0001t0008g0329others(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 | a0001c0003t0001g0238a0001c0003t0003g0340a0001c0003t0003g0341others(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 | 191 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(188): Show | 193 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(190): 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 | a0001c0001t0001g0177a0001c0001t0001g0235a0001c0001t0001g0236others(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 | 97 | a0001c0001t0002g0034a0001c0001t0007g0328a0001c0003t0001g0172others(94): 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 | a0001c0001t0006g0153a0001c0001t0007g0326a0001c0001t0008g0329others(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 | a0001c0001t0001g0249a0001c0001t0001g0301a0001c0001t0002g0305others(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 | 191 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(188): Show | 193 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(190): 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 | a0007c0011t0002g0118 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | a0002c0002t0002g0006a0002c0002t0002g0105a0002c0002t0002g0106others(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 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0004g0234others(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 | a0001c0001t0007g0326a0001c0001t0007g0328a0001c0001t0008g0329others(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 | a0001c0001t0001g0289 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | a0007c0011t0002g0118 | 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 | 312 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(309): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.411+196G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 4/12 | chr15 | 57621896 | ||||||
| chr15:57621971
|
A | G | 114 | a0001c0001t0002g0034a0001c0001t0006g0153a0001c0003t0001g0172others(111): 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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | a0001c0001t0002g0305a0001c0001t0002g0307a0001c0001t0002g0308others(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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0001c0001t0001g0189 | 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 | a0001c0001t0001g0163a0001c0001t0001g0183a0001c0001t0001g0186others(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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | a0001c0003t0001g0238a0001c0003t0003g0340a0001c0003t0003g0341 | 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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0002c0002t0002g0078 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0003c0005t0010g0311 | 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 | a0001c0003t0001g0238a0001c0003t0003g0340a0001c0003t0003g0341 | 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 | a0001c0003t0003g0119a0001c0003t0003g0126a0001c0003t0003g0130others(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 | a0001c0001t0007g0244a0001c0001t0020g0310 | 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 | a0003c0005t0010g0311 | 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 | a0001c0003t0002g0127a0001c0003t0006g0116a0001c0003t0006g0117others(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 | a0001c0003t0001g0238a0001c0003t0003g0340a0001c0003t0003g0341others(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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | a0001c0003t0003g0148 | 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 | a0001c0001t0003g0294 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | a0001c0003t0001g0114a0001c0003t0004g0110a0001c0003t0004g0112others(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 | a0001c0001t0007g0244a0001c0001t0020g0310 | 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 | a0001c0003t0003g0119 | 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 | 118 | a0001c0001t0001g0171a0001c0001t0007g0244a0001c0001t0020g0310others(115): 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 | a0001c0001t0003g0294 | 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 | a0001c0003t0003g0119a0001c0003t0003g0126a0001c0003t0003g0130others(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 | 90 | a0001c0001t0001g0196a0001c0001t0001g0198a0001c0003t0001g0172others(87): 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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | a0001c0001t0001g0274 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | a0003c0005t0010g0311 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | a0001c0001t0003g0295a0001c0003t0003g0296a0001c0003t0003g0297 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | a0001c0001t0007g0244a0001c0001t0020g0310 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | a0007c0011t0002g0118 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | 51 | a0001c0001t0001g0008a0001c0001t0001g0165a0001c0001t0001g0166others(48): Show | 52 | HG00423.hp1 HG00609.hp1 HG00642.hp1 others(49): 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 | a0001c0003t0003g0140 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335 | 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 | a0001c0001t0001g0253 | 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 | a0001c0003t0003g0119a0001c0003t0003g0126a0001c0003t0003g0130others(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 | a0001c0001t0001g0279 | 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 | a0002c0002t0001g0337 | 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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | a0002c0002t0002g0006a0002c0002t0002g0097a0002c0002t0002g0098others(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 | a0001c0001t0007g0326a0001c0001t0007g0328a0001c0001t0008g0329others(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 | a0001c0001t0003g0294 | 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 | a0001c0001t0001g0193 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | a0001c0001t0001g0189 | 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 | a0001c0003t0006g0120 | 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 | a0001c0001t0001g0260 | 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 | a0001c0001t0001g0221a0001c0001t0001g0231a0001c0001t0001g0272others(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 | a0003c0005t0004g0334a0003c0005t0004g0335 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | 151 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(148): Show | 153 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(150): 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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | a0001c0001t0007g0244a0001c0001t0020g0310 | 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 | a0002c0002t0001g0336a0002c0002t0001g0337 | 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 | a0001c0001t0001g0008a0001c0001t0001g0249a0001c0001t0001g0250others(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 | 154 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(151): Show | 156 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(153): 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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | 337 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(334): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): 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 | a0001c0003t0003g0119a0001c0003t0003g0126a0001c0003t0003g0130others(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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | 160 | a0001c0003t0001g0114a0001c0003t0001g0172a0001c0003t0001g0228others(157): 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 | a0003c0005t0004g0334a0003c0005t0004g0335a0003c0005t0010g0311 | 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 | a0001c0001t0007g0244a0001c0001t0020g0310a0003c0005t0004g0334others(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 | a0001c0001t0001g0224 | 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 | a0004c0006t0002g0121 | 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 | a0001c0001t0001g0162a0001c0001t0001g0174a0001c0001t0001g0175others(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 | a0001c0001t0001g0173 | 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 | a0001c0001t0006g0153 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.525+1128G>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57627020 | ||||||
| chr15:57627113
|
C | T | 343 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(340): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.525+1221C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 5/12 | chr15 | 57627113 | ||||||
| chr15:57627161
|
AT | A | 6 | a0001c0001t0006g0153a0001c0003t0001g0114a0001c0003t0004g0110others(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 | a0001c0007t0003g0129 | 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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0002c0002t0002g0085 | 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 | a0001c0001t0002g0305a0001c0001t0002g0307a0001c0001t0002g0309others(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 | a0007c0011t0002g0118 | 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 | a0001c0003t0003g0119a0001c0003t0003g0126a0001c0003t0003g0130others(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 | a0001c0001t0006g0153 | 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 | a0001c0001t0008g0330a0001c0001t0019g0327 | 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 | a0003c0005t0010g0311 | 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 | a0001c0001t0002g0305a0001c0001t0002g0307a0001c0001t0002g0309others(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 | a0001c0001t0002g0305a0001c0001t0002g0307a0001c0001t0002g0309others(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 | a0001c0001t0007g0244a0001c0001t0020g0310 | 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 | 154 | a0001c0001t0002g0308a0001c0001t0006g0153a0001c0001t0007g0326others(151): 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 | 182 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(179): 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 | a0001c0001t0001g0169a0001c0001t0001g0190a0001c0001t0001g0218others(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 | 168 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(165): 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 | 176 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(173): Show | 178 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(175): 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 | a0001c0003t0003g0119 | 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 | 168 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(165): 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 | a0001c0003t0003g0119a0001c0003t0003g0130a0001c0003t0003g0131others(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 | a0001c0001t0001g0227 | 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 | a0002c0002t0002g0075 | 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 | a0001c0003t0001g0114a0001c0003t0004g0110a0001c0003t0004g0112others(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 | a0001c0001t0006g0153 | 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 | a0002c0002t0002g0084 | 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 | a0004c0006t0002g0121 | 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 | 136 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(133): 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 | 76 | a0001c0001t0001g0008a0001c0001t0001g0162a0001c0001t0001g0165others(73): Show | 78 | HG00423.hp1 HG00609.hp1 HG00642.hp1 others(75): 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 | a0001c0001t0001g0163a0001c0001t0001g0177a0001c0001t0001g0192others(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 | 94 | a0001c0001t0001g0253a0001c0001t0002g0308a0001c0001t0007g0244others(91): 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 | a0001c0001t0006g0153a0001c0003t0002g0055a0001c0003t0002g0058others(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 | a0004c0006t0002g0121 | 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 | a0003c0005t0010g0311 | 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 | a0001c0001t0001g0287a0001c0003t0001g0114a0001c0003t0004g0110others(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 | a0001c0001t0002g0323 | 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 | a0001c0001t0001g0252a0001c0001t0001g0257a0001c0003t0002g0086 | 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 | 168 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(165): 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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0001c0003t0001g0114a0001c0003t0004g0110a0001c0003t0004g0112others(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 | a0001c0001t0007g0244a0001c0001t0020g0310 | 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 | a0007c0011t0002g0118 | 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 | a0001c0001t0003g0295 | 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 | a0001c0001t0007g0244a0001c0001t0020g0310 | 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 | a0001c0001t0001g0166a0001c0001t0001g0233a0001c0001t0001g0240others(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 | a0001c0001t0001g0241a0001c0001t0007g0326a0001c0001t0008g0329others(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 | a0001c0001t0006g0153a0001c0001t0007g0244a0001c0001t0019g0327others(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 |
79 | a0001c0003t0001g0172a0001c0003t0001g0228a0001c0003t0002g0002others(76): 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 | a0001c0001t0002g0308a0001c0003t0002g0018a0001c0003t0002g0033others(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 | a0001c0003t0001g0114a0001c0003t0004g0115 | 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 | a0001c0001t0003g0294 | 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 | a0001c0001t0003g0295 | 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 | a0003c0005t0010g0311 | 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 | a0001c0003t0002g0127a0001c0003t0014g0111a0007c0011t0002g0118 | 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 | a0001c0001t0001g0292a0001c0001t0001g0301 | 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 | a0001c0001t0007g0326a0001c0001t0007g0328a0001c0001t0008g0329others(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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0001c0001t0001g0290 | 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 | a0001c0001t0007g0326a0001c0001t0007g0328a0001c0001t0008g0329others(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 | a0001c0003t0006g0116a0001c0003t0006g0117a0001c0003t0006g0120others(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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0001c0001t0001g0212a0001c0001t0001g0269 | 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 | a0001c0001t0008g0330 | 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 | a0001c0001t0007g0244 | 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 | a0001c0001t0001g0198 | 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 | a0001c0001t0007g0244a0001c0001t0020g0310a0001c0003t0002g0127 | 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 | 150 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(147): Show | 156 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(153): 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 | a0001c0001t0001g0233a0001c0001t0002g0307a0001c0001t0002g0314others(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 | a0001c0001t0001g0233a0001c0001t0002g0307a0001c0001t0002g0314others(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 | a0001c0001t0001g0162a0001c0001t0001g0170a0001c0001t0001g0173others(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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | 145 | a0001c0001t0001g0008a0001c0001t0001g0177a0001c0001t0001g0180others(142): 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 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0001t0001g0158a0001c0001t0001g0188a0001c0001t0001g0221others(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 | 338 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(335): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): 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 | a0001c0003t0001g0238 | 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 | a0001c0001t0001g0289 | 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 | a0001c0001t0001g0226 | 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 | 191 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0015others(188): Show | 198 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(195): 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 | a0001c0003t0005g0091 | 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 | a0002c0002t0002g0128 | 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 | a0001c0001t0007g0326a0001c0001t0007g0328a0001c0001t0008g0329others(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 | a0001c0001t0001g0282 | 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 | a0002c0002t0002g0039a0002c0002t0002g0044a0002c0002t0002g0045others(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 | a0001c0003t0006g0116a0001c0003t0006g0117a0001c0003t0006g0120 | 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 | a0001c0001t0001g0013a0001c0001t0001g0158a0001c0001t0001g0161others(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 | a0001c0001t0001g0177a0001c0001t0001g0235a0001c0001t0001g0236others(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 | a0001c0001t0007g0326a0001c0001t0007g0328a0001c0001t0008g0329others(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 | a0001c0003t0003g0340a0001c0003t0003g0341 | 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 | a0001c0001t0006g0153a0001c0001t0013g0267 | 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 | a0001c0001t0006g0153a0001c0001t0013g0267 | 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 | a0001c0001t0001g0187a0001c0001t0001g0189a0001c0001t0001g0196others(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 | a0001c0001t0001g0255a0001c0001t0001g0264 | 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 | a0001c0001t0007g0326a0001c0001t0007g0328a0001c0001t0008g0329others(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 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0003t0002g0127others(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 | a0001c0001t0001g0254 | 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 | 335 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(332): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.804+434C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 7/12 | chr15 | 57632993 | ||||||
| chr15:57633135
|
A | G | 194 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0015others(191): Show | 201 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(198): 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 | a0002c0004t0001g0223 | 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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0001c0001t0006g0153a0001c0001t0013g0267 | 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 | 94 | a0001c0001t0001g0261a0001c0003t0002g0011a0001c0003t0002g0030others(91): 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 | a0001c0003t0006g0116a0001c0003t0006g0117a0001c0003t0006g0120 | 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 | a0001c0003t0001g0172 | 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 | a0001c0001t0001g0222 | 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 | a0001c0001t0001g0233 | 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 | 104 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0260others(101): 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 | a0001c0001t0002g0315 | 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 | a0001c0001t0001g0282 | 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 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0007g0333others(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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | 257 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(254): 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 | a0001c0003t0003g0297 | 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 | a0001c0001t0001g0233a0001c0001t0001g0260a0001c0001t0002g0307others(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 | 213 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0015others(210): Show | 221 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(218): 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 | a0002c0002t0005g0090 | 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 | a0001c0001t0003g0295a0001c0003t0002g0058a0001c0003t0003g0296others(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 | 178 | a0001c0001t0001g0008a0001c0001t0001g0161a0001c0001t0001g0180others(175): Show | 185 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(182): 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 | a0002c0002t0011g0073 | 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 | a0001c0001t0001g0235a0001c0001t0001g0236 | 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 | a0007c0011t0002g0118 | 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 | a0001c0003t0006g0116a0001c0003t0006g0117a0001c0003t0006g0120 | 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 | 143 | a0001c0001t0001g0161a0001c0001t0001g0184a0001c0001t0001g0185others(140): Show | 148 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(145): 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 | a0007c0011t0002g0118 | 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 | 48 | a0001c0001t0001g0161a0001c0001t0001g0185a0001c0001t0001g0193others(45): Show | 49 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(46): 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 | a0002c0002t0002g0040a0002c0002t0012g0089a0002c0009t0002g0037 | 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 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0007g0333others(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 | a0001c0003t0001g0238 | 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 | a0001c0003t0001g0238 | 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 | 190 | a0001c0001t0001g0008a0001c0001t0001g0161a0001c0001t0001g0177others(187): Show | 197 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(194): 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 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0007g0333others(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 | a0003c0005t0010g0311 | 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 | a0001c0001t0002g0318 | 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 | a0001c0001t0001g0177a0001c0001t0001g0235a0001c0001t0001g0236others(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 | a0001c0003t0003g0146 | 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 | a0001c0003t0005g0091 | 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 | 129 | a0001c0001t0001g0008a0001c0001t0001g0177a0001c0001t0001g0180others(126): 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 | 205 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0015others(202): Show | 212 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.934-1967G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 8/12 | chr15 | 57635728 | ||||||
| chr15:57635908
|
A | T | 81 | a0001c0003t0002g0011a0001c0003t0002g0030a0001c0003t0002g0033others(78): 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 | a0003c0005t0010g0311 | 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 | a0003c0005t0010g0311 | 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 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0233others(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 | a0001c0001t0001g0235a0001c0001t0001g0236 | 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 | 89 | a0001c0001t0001g0233a0001c0001t0001g0260a0001c0001t0002g0034others(86): 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 | a0001c0001t0007g0244 | 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 | 282 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(279): 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 | a0001c0001t0001g0184 | 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 | 281 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(278): 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 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0229 | 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 | a0001c0001t0001g0204 | 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 | 135 | a0001c0001t0001g0008a0001c0001t0001g0177a0001c0001t0001g0180others(132): 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 | a0002c0002t0002g0082 | 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 | a0001c0001t0001g0204 | 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 | a0002c0002t0002g0082 | 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 | a0001c0003t0004g0112 | 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 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0007g0333others(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 | a0001c0001t0001g0008a0001c0001t0001g0180a0001c0001t0001g0181others(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 | a0001c0001t0001g0240 | 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 | a0001c0001t0001g0235 | 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 | 84 | a0001c0001t0001g0260a0001c0001t0002g0307a0001c0001t0002g0314others(81): 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 | 81 | a0001c0001t0002g0034a0001c0003t0002g0011a0001c0003t0002g0030others(78): 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 | 83 | a0001c0001t0002g0034a0001c0003t0002g0011a0001c0003t0002g0030others(80): 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 | a0001c0001t0007g0333 | 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 | a0001c0001t0001g0008a0001c0001t0001g0180a0001c0001t0001g0181others(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 | a0001c0003t0006g0116a0001c0003t0006g0117a0001c0003t0006g0120 | 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 | 100 | a0001c0001t0001g0177a0001c0001t0001g0226a0001c0001t0001g0235others(97): 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 | a0001c0001t0001g0211 | 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 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0260others(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 | a0001c0001t0001g0162a0001c0001t0001g0180a0001c0001t0001g0181others(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 | a0001c0001t0002g0307a0001c0001t0002g0314 | 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 | a0001c0001t0003g0294a0001c0001t0007g0244a0001c0003t0001g0238others(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 | a0001c0001t0001g0008a0001c0001t0001g0180a0001c0001t0001g0181others(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 | a0001c0001t0001g0008a0001c0001t0001g0180a0001c0001t0001g0181others(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 | a0002c0002t0002g0084 | 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 | a0001c0001t0001g0268 | 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 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0007g0333others(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 | a0001c0001t0003g0313 | 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 | a0001c0001t0001g0241a0001c0003t0003g0126 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335a0007c0011t0002g0118 | 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 | a0001c0001t0001g0216a0001c0001t0001g0217a0005c0010t0001g0159 | 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 | a0001c0001t0001g0008a0001c0001t0001g0180a0001c0001t0001g0181others(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 | a0001c0001t0001g0008a0001c0001t0001g0180a0001c0001t0001g0181others(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 | a0001c0003t0001g0114a0001c0003t0004g0110a0001c0003t0004g0112others(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 | a0003c0005t0010g0311 | 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 | a0001c0001t0007g0244a0001c0001t0007g0326a0001c0001t0007g0328others(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 | a0007c0011t0002g0118 | 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 | a0001c0001t0001g0170 | 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 | a0002c0004t0001g0206 | 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 | a0001c0001t0001g0260a0001c0001t0001g0303a0001c0001t0002g0307others(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 | a0001c0001t0001g0014a0001c0001t0001g0015 | 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 | a0005c0010t0001g0159 | 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 | a0001c0003t0006g0116a0001c0003t0006g0117a0001c0003t0006g0120 | 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 | a0007c0011t0002g0118 | 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 | a0007c0011t0002g0118 | 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 | a0001c0001t0001g0227 | 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 | a0007c0011t0002g0118 | 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 | a0001c0003t0003g0149a0001c0003t0003g0150 | 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 | a0001c0003t0002g0076 | 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 | a0002c0002t0003g0124 | 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 | a0001c0001t0001g0008a0001c0001t0001g0180a0001c0001t0001g0181others(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 | a0003c0005t0010g0311 | 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 | a0001c0001t0001g0008a0001c0001t0001g0180a0001c0001t0001g0181others(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 | a0003c0005t0004g0334a0003c0005t0004g0335 | 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 | a0001c0001t0001g0008a0001c0001t0001g0180a0001c0001t0001g0181others(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 | a0001c0001t0001g0210a0001c0001t0001g0275 | 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 | a0001c0001t0001g0229 | 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 | a0007c0011t0002g0118 | 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 | 59 | a0001c0001t0001g0161a0001c0001t0001g0185a0001c0001t0001g0193others(56): Show | 60 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(57): 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 | a0001c0003t0003g0136 | 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 | a0001c0001t0001g0201 | 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 | a0001c0001t0001g0008a0001c0001t0001g0180a0001c0001t0001g0181others(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 | a0005c0010t0001g0159 | 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 | a0003c0005t0010g0311 | 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 | a0001c0001t0001g0013a0001c0001t0001g0162a0001c0001t0001g0165others(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 | a0001c0003t0003g0141 | 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 | 58 | a0001c0001t0001g0161a0001c0001t0001g0185a0001c0001t0001g0193others(55): Show | 59 | HG00140.hp1 HG00323.hp1 HG00673.hp2 others(56): Show |
intron_variant | MODIFIER | c.1119+3676A>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57643221 | ||||||
| chr15:57643249
|
C | T | 282 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(279): 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 | a0001c0003t0006g0116a0001c0003t0006g0117a0001c0003t0006g0120 | 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 | 94 | a0001c0001t0001g0008a0001c0001t0001g0161a0001c0001t0001g0180others(91): Show | 97 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.1119+3737A>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57643282 | ||||||
| chr15:57643311
|
T | A | 47 | a0001c0001t0001g0161a0001c0001t0001g0185a0001c0001t0001g0193others(44): Show | 48 | HG00140.hp1 HG00323.hp1 HG00673.hp2 others(45): 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 | a0001c0001t0001g0257a0001c0001t0001g0278a0001c0001t0001g0280others(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 | a0001c0003t0001g0228a0001c0003t0002g0038a0001c0003t0002g0041others(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 | a0001c0003t0001g0238a0001c0003t0003g0340a0001c0003t0003g0341 | 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 | 43 | a0001c0003t0002g0011a0001c0003t0003g0138a0001c0003t0003g0139others(40): 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 | a0001c0001t0001g0177a0001c0003t0001g0114a0001c0003t0004g0110others(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 | a0001c0001t0001g0008a0001c0001t0001g0180a0001c0001t0001g0181others(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 | a0007c0011t0002g0118 | 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 | a0001c0001t0001g0008a0001c0001t0001g0180a0001c0001t0001g0181others(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 | a0001c0001t0001g0222 | 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 | a0001c0001t0001g0260a0001c0001t0002g0307a0001c0001t0002g0314others(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 | 252 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0158others(249): 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 | a0001c0003t0003g0139 | 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 | a0001c0003t0006g0116a0001c0003t0006g0117a0001c0003t0006g0120 | 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 | a0007c0011t0002g0118 | 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 | a0001c0001t0001g0241a0001c0003t0003g0126 | 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 | a0001c0001t0001g0260a0001c0001t0002g0307a0001c0001t0002g0314others(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 | a0001c0001t0001g0177a0001c0001t0001g0235a0001c0001t0001g0236others(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 | a0001c0001t0006g0153a0001c0001t0013g0267 | 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 | a0001c0003t0003g0151 | 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 | a0001c0001t0001g0008a0001c0001t0001g0180a0001c0001t0001g0181others(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 | a0001c0003t0003g0151 | 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 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0177others(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 | a0001c0001t0001g0008a0001c0001t0001g0197a0001c0001t0001g0207others(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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0001c0003t0003g0150 | 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 | a0007c0011t0002g0118 | 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 | a0001c0001t0001g0008a0001c0001t0001g0197a0001c0001t0001g0207others(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 | a0001c0003t0003g0144 | 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 | a0001c0003t0005g0091a0002c0002t0018g0016a0003c0005t0004g0334others(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 | a0001c0001t0001g0229 | 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 | a0002c0002t0001g0337 | 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 | 41 | a0001c0003t0003g0138a0001c0003t0003g0139a0002c0002t0002g0003others(38): 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 | a0001c0001t0001g0176a0001c0001t0001g0260a0001c0001t0002g0307others(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 | 244 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0158others(241): 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 | a0001c0001t0001g0177a0001c0001t0001g0235a0001c0001t0001g0236others(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 | 214 | a0001c0001t0001g0013a0001c0001t0001g0158a0001c0001t0001g0162others(211): 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 | a0001c0001t0007g0326a0001c0001t0007g0328a0001c0001t0008g0329others(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 | a0001c0001t0001g0173 | 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 | 58 | a0001c0001t0001g0161a0001c0001t0001g0185a0001c0001t0001g0193others(55): Show | 59 | HG00140.hp1 HG00323.hp1 HG00673.hp2 others(56): 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 | a0001c0003t0001g0172 | 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 | a0001c0001t0001g0008a0001c0001t0001g0197a0001c0001t0001g0207others(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 | 336 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(333): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): 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 | a0001c0001t0002g0309 | 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 | a0001c0001t0001g0184a0001c0001t0001g0196a0001c0001t0001g0199others(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 | 336 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(333): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): 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 | a0002c0002t0001g0336 | 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 | a0001c0001t0007g0244 | 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 | 84 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0161others(81): Show | 86 | HG00140.hp1 HG00323.hp1 HG00673.hp2 others(83): 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 | a0001c0003t0006g0116a0001c0003t0006g0117a0001c0003t0006g0120 | 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 | 215 | a0001c0001t0001g0013a0001c0001t0001g0158a0001c0001t0001g0162others(212): 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 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0007g0333others(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 | a0001c0001t0007g0326a0001c0001t0007g0328 | 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 | a0001c0003t0001g0172 | 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 | a0007c0011t0002g0118 | 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 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0177others(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 | a0001c0001t0001g0241a0001c0003t0003g0126 | 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 | a0001c0001t0001g0176a0001c0001t0001g0260a0001c0001t0002g0307others(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 | a0001c0003t0003g0133a0001c0003t0003g0135a0001c0003t0003g0144 | 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 | a0001c0001t0003g0294 | 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 | a0001c0001t0003g0294 | 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0177a0001c0001t0001g0235a0001c0001t0001g0236others(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 | a0001c0001t0003g0294 | 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 | a0002c0002t0002g0001 | 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 | a0001c0001t0001g0231 | 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 | a0001c0001t0001g0008a0001c0001t0001g0197a0001c0001t0001g0207others(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 | a0001c0001t0001g0177a0001c0001t0001g0235a0001c0001t0001g0236others(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 | a0002c0002t0002g0049a0002c0002t0002g0064a0002c0002t0002g0074others(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 | a0001c0001t0001g0008a0001c0001t0001g0197a0001c0001t0001g0207others(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 | a0001c0001t0007g0244a0001c0001t0007g0326a0001c0001t0007g0328others(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 | a0001c0001t0004g0234a0001c0001t0005g0122 | 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 | a0001c0001t0001g0254 | 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 | a0001c0001t0001g0013a0001c0001t0001g0162a0001c0001t0001g0165others(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 | a0001c0001t0001g0008a0001c0001t0001g0180a0001c0001t0001g0181others(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 | a0002c0002t0002g0096 | 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 | a0001c0003t0003g0141 | 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 | a0001c0001t0001g0227a0002c0002t0002g0081 | 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 | a0002c0002t0001g0336a0002c0002t0001g0337 | 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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | 331 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0158others(328): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): 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 | a0001c0001t0003g0294 | 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 | a0001c0001t0001g0250 | 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 | a0001c0001t0001g0008a0001c0001t0001g0180a0001c0001t0001g0181others(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 | a0001c0001t0006g0153a0001c0001t0013g0267 | 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 | a0001c0003t0003g0142 | 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 | a0002c0002t0002g0082 | 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 | a0001c0001t0001g0158a0001c0001t0001g0162a0001c0001t0001g0169others(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 | a0001c0001t0001g0013a0001c0001t0001g0163a0001c0001t0001g0184others(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 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0171others(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 | a0001c0001t0001g0167a0001c0001t0001g0174a0001c0001t0001g0183others(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 | 20 | a0001c0001t0001g0226a0001c0003t0002g0019a0001c0003t0002g0058others(17): 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 | a0001c0001t0001g0241a0001c0003t0003g0297a0002c0002t0002g0045others(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 | a0001c0001t0001g0008a0001c0001t0001g0197a0001c0001t0001g0207others(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 | a0001c0001t0001g0284a0001c0001t0001g0300a0001c0001t0003g0295others(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 | a0001c0001t0001g0180a0001c0001t0001g0182a0001c0001t0001g0266others(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 | a0001c0001t0001g0181a0001c0003t0002g0055a0002c0002t0002g0039 | 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 | 45 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(42): Show | 46 | HG00140.hp1 HG00323.hp1 HG00673.hp2 others(43): 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 | a0001c0001t0001g0177a0001c0001t0001g0210a0001c0001t0001g0235others(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 | a0001c0001t0001g0176a0001c0001t0001g0260a0001c0001t0002g0307others(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 | 332 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(329): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): 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 | a0001c0001t0001g0241a0001c0003t0003g0126 | 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 | a0001c0001t0007g0333a0004c0006t0002g0121 | 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 | a0001c0001t0001g0173 | 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 | a0001c0003t0003g0119 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335a0007c0011t0002g0118 | 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 | a0001c0003t0014g0111 | 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 | a0001c0001t0007g0333a0001c0003t0002g0127a0004c0006t0002g0121 | 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 | a0001c0001t0001g0173 | 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 | a0001c0001t0001g0285a0001c0001t0001g0287 | 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 | a0001c0001t0007g0333a0001c0003t0002g0127a0004c0006t0002g0121 | 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 | 67 | a0001c0001t0004g0276a0001c0003t0003g0138a0001c0003t0003g0139others(64): 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 | a0001c0001t0007g0244 | 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 | a0002c0002t0002g0097 | 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 | a0001c0001t0004g0007a0001c0001t0004g0242a0001c0001t0004g0243others(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 | a0001c0001t0004g0276a0002c0002t0004g0220a0002c0002t0005g0062 | 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 | a0001c0003t0017g0123 | 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 | a0001c0001t0006g0153a0001c0001t0013g0267 | 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 | a0001c0001t0001g0280 | 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 | 211 | a0001c0001t0001g0013a0001c0001t0001g0158a0001c0001t0001g0162others(208): 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 | a0001c0001t0001g0241a0001c0003t0003g0126 | 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 | a0001c0003t0003g0149 | 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 | a0001c0001t0001g0176a0001c0001t0001g0260a0001c0001t0002g0307others(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 | a0001c0001t0001g0177a0001c0001t0004g0178 | 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 | a0001c0003t0014g0111 | 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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0273 | 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 | 210 | a0001c0001t0001g0013a0001c0001t0001g0158a0001c0001t0001g0162others(207): 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 | a0002c0002t0002g0092 | 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 | a0001c0003t0003g0340a0001c0003t0003g0341 | 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 | a0001c0003t0002g0127 | 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 | a0001c0003t0001g0114 | 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 | a0001c0001t0003g0294 | 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 | a0001c0001t0003g0294 | 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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182 | 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 | a0003c0005t0010g0311 | 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 | a0001c0001t0007g0333a0001c0003t0002g0127a0002c0002t0002g0050others(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 | a0001c0003t0003g0131a0001c0003t0003g0132 | 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 | a0001c0001t0001g0177a0001c0001t0004g0178 | 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 | a0001c0001t0001g0171 | 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 | a0001c0001t0001g0293 | 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 | a0003c0005t0010g0311 | 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 | a0001c0001t0009g0202a0001c0001t0009g0215 | 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 | a0003c0005t0010g0311 | 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 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0015others(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 | a0001c0001t0001g0247a0001c0001t0001g0248 | 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 | a0001c0001t0001g0177a0001c0001t0001g0235a0001c0001t0001g0236others(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 | a0001c0001t0020g0310 | 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 | a0001c0003t0017g0123 | 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 | a0002c0002t0002g0099a0002c0002t0002g0100a0002c0002t0002g0101 | 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 | a0001c0001t0001g0241a0001c0001t0003g0294a0001c0001t0007g0326others(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 | a0001c0001t0006g0153a0001c0001t0013g0267 | 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 | a0001c0001t0001g0176a0001c0001t0001g0260a0001c0001t0002g0307others(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 | 339 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0158others(336): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.1120-2109G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57659341 | ||||||
| chr15:57659550
|
C | T | 225 | a0001c0001t0001g0013a0001c0001t0001g0158a0001c0001t0001g0162others(222): 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 | a0002c0002t0001g0336a0002c0002t0001g0337 | 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 | a0001c0003t0014g0111 | 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 | a0001c0001t0001g0176a0001c0001t0002g0318a0001c0001t0002g0319others(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 | a0001c0001t0001g0193 | 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 | 111 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0015others(108): Show | 114 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.1120-1573C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57659877 | ||||||
| chr15:57659954
|
C | G | 102 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0015others(99): Show | 105 | HG00140.hp1 HG00323.hp1 HG00673.hp2 others(102): Show |
intron_variant | MODIFIER | c.1120-1496C>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57659954 | ||||||
| chr15:57659969
|
G | A | 102 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0015others(99): Show | 105 | HG00140.hp1 HG00323.hp1 HG00673.hp2 others(102): 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 | a0002c0002t0011g0073 | 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 | a0001c0003t0014g0111 | 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 | a0002c0002t0002g0104 | 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 | a0002c0002t0001g0336a0002c0002t0001g0337 | 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 | a0001c0001t0020g0310 | 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 | 112 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0015others(109): Show | 115 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.1120-1250T>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 10/12 | chr15 | 57660200 | ||||||
| chr15:57660289
|
A | G | 321 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(318): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): 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 | a0001c0001t0001g0222 | 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 | a0001c0003t0003g0143 | 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 | a0001c0001t0001g0008a0001c0001t0001g0180a0001c0001t0001g0181others(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 | a0001c0001t0015g0160 | 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 | a0002c0002t0002g0106 | 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 | a0001c0001t0003g0294 | 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 | a0001c0003t0006g0116a0001c0003t0006g0117a0001c0003t0006g0120 | 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 | a0001c0001t0001g0176a0001c0001t0001g0260a0001c0001t0002g0307others(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 | 253 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0158others(250): 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 | a0002c0002t0002g0083 | 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 | 247 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0158others(244): 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 | a0002c0002t0002g0104 | 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 | a0001c0003t0014g0111 | 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 | a0001c0001t0004g0234a0001c0001t0005g0122a0002c0004t0005g0306 | 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 | a0001c0001t0001g0177a0001c0001t0004g0178a0001c0001t0004g0234others(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 | a0001c0003t0003g0142 | 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 | a0007c0011t0002g0118 | 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 | a0001c0001t0001g0161 | 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 | 260 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0158others(257): 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 | a0001c0001t0001g0292a0001c0001t0001g0301a0001c0003t0002g0028others(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 | a0001c0001t0004g0276a0002c0002t0004g0220a0002c0002t0005g0060others(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 | a0001c0003t0001g0114 | 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 | a0001c0003t0006g0116a0001c0003t0006g0117a0001c0003t0006g0120 | 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 | a0001c0001t0007g0333a0001c0003t0002g0127a0004c0006t0002g0121 | 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 | a0001c0001t0001g0013a0001c0001t0001g0162a0001c0001t0001g0165others(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 | 55 | a0001c0001t0001g0161a0001c0001t0001g0171a0001c0001t0001g0185others(52): Show | 56 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.1203+1421G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57662954 | ||||||
| chr15:57663131
|
G | T | 85 | a0001c0001t0001g0161a0001c0001t0001g0171a0001c0001t0001g0185others(82): Show | 86 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(83): 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 | a0001c0001t0001g0219a0001c0001t0001g0271a0001c0001t0001g0304 | 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 | 253 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0158others(250): 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 | 253 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0158others(250): 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 | a0003c0005t0010g0311 | 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 | a0001c0003t0014g0111 | 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 | 246 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0158others(243): 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 | a0001c0001t0004g0007a0001c0001t0004g0178a0001c0001t0004g0234others(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 | a0001c0001t0020g0310 | 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 | a0001c0001t0001g0008a0001c0001t0001g0180a0001c0001t0001g0181others(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 | 56 | a0001c0001t0001g0161a0001c0001t0001g0171a0001c0001t0001g0185others(53): Show | 57 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(54): 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 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0180others(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 | a0007c0011t0002g0118 | 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 | a0001c0001t0007g0326a0001c0001t0007g0328a0001c0001t0008g0329others(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 | 259 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0158others(256): 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 | ||||||
| chr15:57664538
|
T | C | 343 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(340): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.1203+3005T>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57664538 | ||||||
| chr15:57664625
|
TCTTTCTA others(3): Show |
T | 1 | a0001c0003t0003g0147 | 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 | a0001c0003t0004g0112 | 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 | 259 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0158others(256): 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 | 259 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0158others(256): 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 | a0001c0001t0004g0178a0001c0001t0004g0234a0001c0001t0004g0276others(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 | 259 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0158others(256): 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 | a0001c0001t0007g0326a0001c0001t0007g0328 | 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 | 253 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0158others(250): 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 | a0001c0001t0001g0008a0001c0001t0001g0180a0001c0001t0001g0181others(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 | 253 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0158others(250): 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 | a0001c0001t0001g0286 | 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 | a0001c0001t0001g0224a0001c0001t0001g0240 | 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 | a0003c0005t0004g0334a0003c0005t0004g0335 | 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 | 55 | a0001c0001t0001g0161a0001c0001t0001g0171a0001c0001t0001g0185others(52): Show | 56 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.1203+4753C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57666286 | ||||||
| chr15:57666369
|
T | C | 338 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0158others(335): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): 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 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0003g0294others(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 | a0001c0001t0001g0008a0001c0001t0001g0197a0001c0001t0001g0207others(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 | a0001c0001t0007g0244 | 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 | a0001c0001t0001g0170a0001c0001t0002g0308 | 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 | a0001c0001t0007g0326a0001c0001t0007g0328a0007c0011t0002g0118 | 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 | 302 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0158others(299): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): 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 | a0001c0001t0001g0241 | 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 | a0001c0003t0003g0155a0001c0003t0003g0156a0001c0003t0003g0157 | 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 | a0001c0001t0007g0244 | 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 | a0001c0003t0003g0155a0001c0003t0003g0156a0001c0003t0003g0157 | 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 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0177others(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 | 198 | a0001c0001t0001g0013a0001c0001t0001g0158a0001c0001t0001g0161others(195): Show | 201 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(198): 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 | a0007c0011t0002g0118 | 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 | a0001c0001t0001g0292a0001c0001t0001g0301 | 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 | a0001c0003t0014g0111 | 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 | 291 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0158others(288): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): 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 | a0001c0001t0001g0177 | 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 | a0001c0003t0003g0140 | 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 | 291 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0158others(288): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): 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 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0001g0191others(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 | 338 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0158others(335): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): 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 | a0001c0001t0006g0153a0001c0001t0013g0267a0001c0001t0020g0310others(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 | 291 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0158others(288): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.1203+6581G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57668114 | ||||||
| chr15:57668212
|
G | C | 291 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0158others(288): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.1203+6679G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57668212 | ||||||
| chr15:57668216
|
T | G | 337 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0158others(334): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): 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 | a0001c0003t0006g0116a0001c0003t0006g0117a0001c0003t0006g0120 | 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 | a0002c0002t0002g0082 | 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 | a0003c0005t0010g0311 | 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 | a0001c0001t0007g0244 | 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 | a0001c0001t0004g0178a0001c0001t0004g0234a0001c0001t0005g0122others(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 | a0001c0001t0001g0189 | 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 | a0001c0001t0007g0244 | 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 | a0001c0001t0006g0153a0001c0001t0013g0267a0001c0001t0020g0310others(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 | a0001c0003t0004g0112 | 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 | a0001c0001t0001g0008a0001c0001t0001g0197a0001c0001t0001g0207others(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 | 195 | a0001c0001t0001g0013a0001c0001t0001g0158a0001c0001t0001g0162others(192): 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 | a0001c0001t0008g0329a0001c0001t0008g0330a0001c0001t0008g0332others(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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0001c0001t0001g0171a0001c0001t0001g0176a0001c0001t0001g0218others(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 | a0001c0001t0004g0276a0001c0001t0015g0160a0002c0002t0004g0220others(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 | a0001c0001t0001g0211a0001c0001t0008g0329a0001c0001t0008g0330others(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 | a0001c0001t0001g0179a0001c0001t0001g0192a0001c0001t0001g0198others(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 | 14 | a0001c0001t0001g0161a0001c0001t0001g0174a0001c0001t0001g0175others(11): Show | 14 | HG00140.hp1 HG00735.hp2 HG00738.hp2 others(11): 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 | a0001c0001t0004g0178a0001c0001t0004g0234a0001c0001t0005g0122others(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 | a0001c0001t0004g0007a0001c0001t0004g0242a0001c0001t0004g0243others(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 | a0001c0003t0006g0117 | 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 | a0001c0003t0006g0120 | 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 | a0001c0003t0006g0116 | 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 | a0001c0001t0006g0153a0001c0001t0013g0267 | 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 | 85 | a0001c0001t0001g0013a0001c0001t0001g0180a0001c0001t0001g0181others(82): 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 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0003g0294others(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 | a0001c0001t0020g0310 | 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 | a0001c0001t0001g0176a0001c0001t0001g0260a0001c0001t0002g0307others(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 | a0001c0001t0001g0192a0001c0001t0001g0200a0001c0001t0001g0208others(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 | a0001c0003t0003g0147 | 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 | a0001c0003t0003g0147 | 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 | a0001c0003t0003g0147 | 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 | a0001c0003t0003g0147 | 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 | a0001c0003t0003g0147 | 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 | a0001c0003t0003g0147 | 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 | a0001c0003t0003g0147 | 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 | a0001c0003t0003g0147 | 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 | a0001c0003t0003g0147 | 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 | a0001c0003t0003g0147 | 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 | a0001c0003t0003g0147 | 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 | a0001c0001t0008g0329a0001c0001t0008g0330a0001c0001t0008g0332others(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 | 301 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0158others(298): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): 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 | a0001c0001t0008g0329a0001c0001t0008g0330a0001c0001t0008g0332others(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 | a0001c0003t0003g0152 | 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 | 300 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0158others(297): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): 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 | a0001c0001t0007g0333a0001c0003t0002g0127a0004c0006t0002g0121 | 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 | 267 | a0001c0001t0001g0013a0001c0001t0001g0158a0001c0001t0001g0161others(264): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): 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 | a0001c0001t0001g0189 | 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 | a0001c0001t0001g0212a0001c0001t0001g0269 | 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 | 295 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0158others(292): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.1204-5137C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57669831 | ||||||
| chr15:57669864
|
T | G | 301 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0158others(298): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.1204-5104T>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57669864 | ||||||
| chr15:57669906
|
T | C | 8 | a0002c0002t0002g0004a0002c0002t0002g0005a0002c0002t0002g0072others(5): 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 | a0001c0001t0009g0215 | 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 | a0001c0001t0002g0034a0001c0003t0002g0030a0001c0003t0002g0033others(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 | 301 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0158others(298): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): 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 | a0001c0001t0001g0171a0001c0001t0001g0203a0002c0002t0002g0075others(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 | a0001c0001t0008g0329a0001c0001t0008g0330a0001c0001t0008g0332others(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 | 295 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0158others(292): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): 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 | a0001c0001t0002g0314 | 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 | 295 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0158others(292): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): 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 | a0001c0001t0001g0176a0001c0001t0001g0260a0001c0001t0002g0307others(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 | a0002c0002t0002g0006a0002c0002t0002g0105a0002c0002t0002g0106others(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 | 295 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0158others(292): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.1204-4141G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57670827 | ||||||
| chr15:57670884
|
T | C | 295 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0158others(292): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): 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 | a0001c0001t0008g0329a0001c0001t0008g0330a0001c0001t0008g0332others(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 | a0001c0001t0020g0310 | 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 | a0001c0001t0008g0329a0001c0001t0008g0330a0001c0001t0008g0332others(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 | a0001c0001t0001g0183 | 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 | 328 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0158others(325): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): 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 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0001g0262 | 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 | a0001c0001t0008g0329a0001c0001t0008g0330a0001c0001t0008g0332others(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 | a0001c0001t0020g0310 | 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 | 244 | a0001c0001t0001g0013a0001c0001t0001g0158a0001c0001t0001g0161others(241): Show | 249 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(246): 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 | a0002c0002t0002g0001 | 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 | a0001c0001t0001g0204a0001c0001t0001g0221 | 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 | 291 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0158others(288): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.1204-3168G>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57671800 | ||||||
| chr15:57671853
|
T | G | 295 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0158others(292): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.1204-3115T>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57671853 | ||||||
| chr15:57671915
|
C | T | 295 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0158others(292): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.1204-3053C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 11/12 | chr15 | 57671915 | ||||||
| chr15:57671923
|
T | C | 317 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(314): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): 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 | a0001c0001t0002g0315 | 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 | a0001c0003t0003g0340a0001c0003t0003g0341 | 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 | a0001c0003t0003g0340a0001c0003t0003g0341 | 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 | 295 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0158others(292): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): 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 | a0001c0003t0003g0340a0001c0003t0003g0341 | 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 | a0001c0001t0001g0161 | 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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | 296 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0158others(293): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): 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 | a0001c0001t0008g0329a0001c0001t0008g0330a0001c0001t0008g0332others(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 | 295 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0158others(292): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): 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 | a0003c0005t0010g0311 | 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 | a0001c0001t0002g0315 | 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 | a0001c0001t0007g0244 | 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 | a0001c0001t0006g0153a0001c0001t0013g0267a0001c0001t0020g0310others(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 | a0001c0001t0004g0007a0001c0001t0004g0178a0001c0001t0004g0234others(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 | a0001c0003t0006g0116a0001c0003t0006g0117a0001c0003t0006g0120 | 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 | a0001c0001t0015g0160 | 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 | a0001c0001t0001g0203a0002c0002t0002g0075a0002c0002t0002g0099others(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 | a0001c0001t0001g0179a0001c0001t0001g0198a0001c0001t0001g0232others(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 | a0001c0001t0006g0153 | 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 | a0001c0001t0007g0326a0001c0001t0007g0328a0007c0011t0002g0118 | 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 | a0001c0001t0001g0176a0001c0001t0001g0183a0001c0001t0001g0189others(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 | a0001c0001t0001g0162a0001c0001t0001g0188a0001c0001t0001g0203others(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 | a0001c0001t0001g0185a0001c0001t0001g0192a0001c0001t0001g0210others(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 | a0001c0003t0003g0148a0001c0003t0003g0150a0002c0002t0005g0090 | 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 | a0002c0002t0002g0072 | 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 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0158others(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 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0161others(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 | a0001c0001t0001g0258a0001c0001t0001g0283a0001c0001t0001g0343others(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 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0229others(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 | a0001c0001t0008g0329a0001c0001t0008g0332a0001c0003t0001g0114others(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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0001c0001t0003g0295 | 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 | a0001c0001t0003g0294 | 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 | a0001c0001t0001g0008a0001c0001t0001g0197a0001c0001t0001g0207others(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 | a0001c0001t0007g0244 | 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 | a0001c0001t0006g0153a0001c0001t0013g0267a0001c0001t0020g0310others(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 | a0001c0001t0001g0237 | 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 | a0001c0001t0001g0226 | 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 | 312 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(309): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): 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 | a0001c0001t0001g0226 | 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 | a0001c0003t0006g0116a0001c0003t0006g0117a0001c0003t0006g0120 | 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 | a0001c0001t0001g0183 | 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 | a0001c0001t0001g0008a0001c0001t0001g0180a0001c0001t0001g0181others(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 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0003t0001g0114others(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 | a0001c0001t0001g0008a0001c0001t0001g0180a0001c0001t0001g0181others(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 | a0001c0003t0002g0048a0001c0003t0002g0065a0001c0003t0003g0119 | 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 | a0003c0005t0010g0311 | 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 | a0001c0003t0001g0238a0005c0010t0001g0159 | 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 | a0001c0003t0003g0155a0001c0003t0003g0156a0001c0003t0003g0157 | 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 | 244 | a0001c0001t0001g0013a0001c0001t0001g0158a0001c0001t0001g0161others(241): Show | 249 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(246): 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 | a0001c0001t0007g0244a0001c0001t0007g0333a0001c0003t0002g0127others(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 | a0001c0001t0008g0329a0001c0001t0008g0330a0001c0001t0008g0332others(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 | 304 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0158others(301): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): 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 | a0001c0003t0003g0148 | 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 | a0001c0001t0006g0153a0001c0001t0013g0267a0001c0001t0020g0310others(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 | a0001c0001t0001g0218 | 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 | a0001c0001t0001g0224a0001c0001t0001g0240 | 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 | a0001c0001t0006g0153a0001c0001t0013g0267a0001c0001t0020g0310others(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 | a0001c0001t0015g0160 | 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 | a0001c0001t0001g0212a0001c0001t0001g0269 | 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 | a0001c0001t0001g0197 | 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 | a0001c0001t0003g0295a0001c0003t0002g0058a0001c0003t0003g0296others(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 | a0001c0001t0001g0224a0001c0001t0001g0240 | 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 | a0001c0001t0001g0241a0001c0003t0003g0126 | 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 | a0001c0001t0007g0333a0001c0003t0002g0127a0004c0006t0002g0121 | 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 | a0001c0001t0004g0234a0001c0001t0005g0122a0002c0004t0005g0306 | 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 | 264 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0158others(261): Show | 271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): 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 | a0001c0001t0001g0190 | 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 | a0001c0001t0001g0014a0001c0001t0001g0015 | 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 | a0001c0001t0001g0183a0001c0001t0001g0203a0001c0001t0001g0224others(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 | a0001c0001t0001g0176a0001c0001t0001g0260a0001c0001t0002g0307others(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 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0015g0160others(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 | a0001c0001t0001g0177a0001c0001t0001g0273a0001c0001t0003g0294others(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 | a0002c0002t0005g0060a0002c0002t0005g0063a0002c0002t0005g0070others(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 | a0001c0001t0004g0276a0002c0002t0004g0220a0002c0002t0005g0062others(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 | a0001c0001t0004g0007a0001c0001t0004g0178a0001c0001t0004g0234others(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 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0190others(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 | a0001c0001t0004g0007a0001c0001t0004g0242a0001c0001t0004g0245others(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 | a0001c0001t0001g0008a0001c0001t0001g0180a0001c0001t0001g0181others(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 | a0001c0001t0006g0153a0001c0001t0013g0267a0001c0001t0020g0310others(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 | 312 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0158others(309): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): 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 | a0001c0001t0004g0276a0002c0002t0004g0220a0002c0002t0005g0060others(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 | a0001c0001t0004g0276a0002c0002t0004g0220a0002c0002t0005g0060others(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 | a0001c0001t0004g0276a0002c0002t0004g0220a0002c0002t0005g0060others(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 | a0001c0003t0014g0111 | 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 | a0001c0003t0003g0151 | 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 | a0001c0001t0008g0329a0001c0001t0008g0330a0001c0001t0008g0332others(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 | a0001c0001t0001g0158a0001c0001t0001g0163a0001c0001t0001g0170others(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 | a0003c0005t0010g0311 | 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 | 298 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0158others(295): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): 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 | a0001c0001t0015g0160 | 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 | 338 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0158others(335): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): 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 | a0001c0001t0004g0007a0001c0001t0004g0178a0001c0001t0004g0234others(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 | a0001c0001t0001g0281 | 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 | a0001c0001t0007g0326a0001c0001t0007g0328 | 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 | a0001c0001t0001g0184a0001c0001t0001g0187a0001c0001t0001g0189others(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 | a0001c0001t0001g0008a0001c0001t0001g0180a0001c0001t0001g0181others(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 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0003g0294others(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 | a0001c0001t0006g0153 | 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 | a0001c0001t0013g0267a0001c0001t0020g0310a0001c0003t0006g0117 | 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 | a0001c0003t0006g0116a0001c0003t0006g0120 | 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 | a0001c0001t0001g0207a0001c0001t0001g0250a0001c0001t0001g0251others(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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0001c0001t0001g0169a0001c0001t0001g0342a0001c0001t0001g0343others(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 | 236 | a0001c0001t0001g0013a0001c0001t0001g0158a0001c0001t0001g0161others(233): Show | 241 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(238): 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 | a0001c0001t0001g0166a0001c0001t0001g0176a0001c0001t0001g0191others(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 | a0002c0002t0002g0082 | 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 | a0001c0001t0008g0329 | 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 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0003g0294others(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 | a0001c0001t0001g0169a0001c0001t0001g0342 | 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 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0003g0294others(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 | a0001c0003t0003g0151 | 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 | 317 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(314): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): 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 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0003g0294others(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 | a0001c0001t0007g0326a0001c0001t0007g0328a0001c0001t0008g0329others(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 | a0001c0001t0015g0160 | 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 | a0002c0002t0002g0098 | 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 | 303 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0158others(300): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): 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 | a0001c0003t0001g0172a0001c0003t0002g0002a0001c0003t0002g0035others(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 | a0001c0001t0001g0224a0001c0001t0001g0235a0001c0001t0001g0236others(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 | a0001c0001t0001g0176a0001c0001t0001g0183a0001c0001t0001g0197others(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 | a0001c0001t0001g0186a0001c0001t0001g0213a0001c0001t0001g0226others(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 |
95 | a0001c0001t0001g0008a0001c0001t0001g0163a0001c0001t0001g0165others(92): 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 |
76 | a0001c0001t0001g0013a0001c0001t0001g0158a0001c0001t0001g0161others(73): Show | 78 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(75): 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 | a0001c0001t0001g0162a0001c0001t0001g0174a0001c0001t0001g0175others(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 | a0001c0001t0001g0233a0001c0003t0001g0238a0001c0003t0003g0126others(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 | a0001c0001t0001g0218a0001c0001t0002g0154a0001c0001t0009g0202 | 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 | a0001c0001t0001g0180 | 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 | a0001c0001t0001g0170a0001c0001t0004g0007a0001c0001t0004g0178others(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 | a0001c0001t0006g0153a0001c0001t0013g0267a0001c0001t0015g0160others(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 | a0001c0003t0006g0116a0001c0003t0006g0117a0001c0003t0006g0120 | 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 | a0001c0001t0001g0303a0001c0001t0009g0215 | 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 | 292 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0158others(289): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): 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 | a0001c0001t0001g0219a0001c0001t0008g0329a0001c0001t0008g0330others(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 | a0001c0001t0001g0168a0001c0001t0001g0303a0001c0001t0009g0215others(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 | a0002c0002t0011g0073a0003c0005t0010g0311 | 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 | 326 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0158others(323): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): 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 | a0002c0002t0011g0073 | 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 | a0001c0003t0006g0116a0001c0003t0006g0117a0001c0003t0006g0120others(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 | a0001c0001t0007g0333a0001c0003t0002g0127a0004c0006t0002g0121 | 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 | a0002c0002t0002g0128 | 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 | a0001c0001t0001g0176a0001c0001t0001g0260a0001c0001t0002g0307others(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 | a0001c0001t0001g0218 | 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 | a0001c0001t0001g0268a0001c0003t0003g0155a0001c0003t0003g0156others(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 | a0001c0001t0001g0176a0001c0001t0001g0260a0001c0001t0002g0307others(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 | a0002c0002t0002g0057a0002c0002t0002g0093a0002c0002t0002g0095others(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 | a0001c0001t0007g0244 | 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 | a0001c0001t0001g0289 | 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 | a0001c0003t0014g0111 | 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 | a0001c0003t0003g0155a0001c0003t0003g0156a0001c0003t0003g0157 | 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 | a0001c0001t0004g0007a0001c0001t0004g0242a0001c0001t0004g0243others(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 | 200 | a0001c0001t0001g0013a0001c0001t0001g0158a0001c0001t0001g0161others(197): Show | 204 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(201): 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 | a0003c0005t0010g0311 | 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 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0177others(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 | a0001c0001t0006g0153a0001c0001t0013g0267a0001c0001t0020g0310others(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 | a0002c0002t0001g0337 | 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 | a0002c0002t0001g0336 | 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 | a0001c0001t0003g0294 | 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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0001c0001t0007g0326a0001c0001t0007g0328a0001c0003t0017g0123 | 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 | a0001c0001t0008g0329a0001c0001t0008g0330a0001c0001t0008g0332others(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 | a0001c0001t0001g0197a0001c0001t0007g0333a0001c0003t0002g0127others(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 | a0001c0001t0001g0008a0001c0001t0001g0207a0001c0001t0001g0249others(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 | 274 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(271): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): 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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182 | 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 | a0001c0001t0001g0184a0001c0001t0001g0196a0001c0001t0001g0199others(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 | a0001c0003t0006g0116a0001c0003t0006g0117a0001c0003t0006g0120 | 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 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0177others(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 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0177others(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 | a0001c0003t0003g0155a0001c0003t0003g0156a0001c0003t0003g0157 | 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 | 337 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0158others(334): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.1305-3232A>G | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57681170 | ||||||
| chr15:57681200
|
C | T | 292 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0158others(289): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1305-3202C>T | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57681200 | ||||||
| chr15:57681248
|
G | A | 285 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0158others(282): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): 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 | a0001c0001t0001g0176a0001c0001t0001g0241a0001c0001t0001g0260others(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 | a0001c0001t0020g0310 | 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 | a0001c0001t0006g0153a0001c0001t0013g0267a0001c0001t0020g0310others(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 | a0001c0001t0001g0247a0001c0001t0001g0248 | 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 | 193 | a0001c0001t0001g0013a0001c0001t0001g0158a0001c0001t0001g0161others(190): Show | 197 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.1305-2825G>A | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57681577 | ||||||
| chr15:57681600
|
C | A | 310 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(307): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): 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 | a0001c0001t0001g0198a0001c0001t0001g0232a0001c0001t0001g0239others(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 | a0001c0001t0001g0241a0001c0003t0003g0126 | 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 | 193 | a0001c0001t0001g0013a0001c0001t0001g0158a0001c0001t0001g0161others(190): Show | 197 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(194): 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 | a0001c0001t0007g0326a0001c0001t0007g0328a0001c0001t0008g0329others(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 | a0001c0001t0001g0169 | 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 | a0001c0001t0001g0163 | 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 | a0001c0001t0015g0160 | 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 | a0001c0001t0006g0153a0001c0001t0013g0267a0001c0001t0020g0310others(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 | a0001c0001t0001g0273 | 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 | a0002c0002t0002g0001a0002c0002t0002g0022a0002c0002t0002g0026others(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 | a0001c0001t0001g0176a0001c0001t0001g0260a0001c0001t0002g0307others(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 | a0003c0005t0010g0311 | 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 | a0001c0001t0007g0326a0001c0001t0007g0328a0007c0011t0002g0118 | 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 | a0001c0003t0003g0132 | 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 | a0001c0001t0007g0326a0001c0001t0007g0328a0001c0001t0008g0329others(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 | a0001c0001t0006g0153a0001c0001t0013g0267a0001c0001t0020g0310others(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 | 319 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(316): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): 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 | a0001c0001t0004g0007a0001c0001t0004g0178a0001c0001t0004g0234others(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 | 317 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(314): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): 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 | a0001c0003t0002g0038a0001c0003t0002g0041a0001c0003t0002g0042others(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 | a0001c0001t0001g0198a0001c0001t0001g0232a0001c0001t0001g0239others(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 | a0001c0003t0003g0135 | 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 | a0001c0003t0001g0172a0001c0003t0002g0002a0001c0003t0002g0035others(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 | a0001c0003t0002g0127 | 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 | a0001c0003t0014g0111 | 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 | a0003c0005t0010g0311 | 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 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0002c0004t0001g0164 | 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 | 241 | a0001c0001t0001g0013a0001c0001t0001g0158a0001c0001t0001g0161others(238): Show | 246 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(243): 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 | a0001c0001t0008g0329a0001c0001t0008g0330a0001c0001t0008g0332others(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 | a0005c0010t0001g0159 | 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 | 291 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0158others(288): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): 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 | a0001c0003t0001g0228a0002c0002t0002g0092 | 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 | 329 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0158others(326): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.1305-17A>C | MYZAP | ENSG00000263155.6 | transcript | ENST00000267853.10 | protein_coding | 12/12 | chr15 | 57684385 |