Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 4648 |
|---|---|
| ensemblid | ENSG00000169994.20 |
| hgncid | 7607 |
| symbol | MYO7B |
| name | myosin VIIB |
| refseq_nuc | NM_001393586.1 |
| refseq_prot | NP_001380515.1 |
| ensembl_nuc | ENST00000409816.8 |
| ensembl_prot | ENSP00000386461.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 127535683 |
| end | 127637726 |
| strand | + |
| ver | v1.2 |
| region | chr2:127535683-127637726 |
| region5000 | chr2:127530683-127642726 |
| regionname0 | MYO7B_chr2_127535683_127637726 |
| regionname5000 | MYO7B_chr2_127530683_127642726 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 2142 | 91 | 40 | 17 | 25 | 0 | 8 | 21 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0002 | 0/1 | 2142 | 61 | 3 | 19 | 24 | 5 | 9 | 17 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0003 | 0/0 | 2142 | 33 | 3 | 7 | 15 | 2 | 6 | 11 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0004 | 0/0 | 2142 | 15 | 2 | 9 | 1 | 2 | 1 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0005 | 0/0 | 2142 | 9 | 6 | 1 | 1 | 0 | 1 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0006 | 0/0 | 2142 | 8 | 0 | 2 | 0 | 2 | 4 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0007 | 0/0 | 2142 | 7 | 4 | 0 | 1 | 1 | 1 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0008 | 0/0 | 2142 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0009 | 0/0 | 2142 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0010 | 0/0 | 2142 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0011 | 0/0 | 2142 | 3 | 0 | 1 | 0 | 0 | 2 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0012 | 0/0 | 2142 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0013 | 0/0 | 2142 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0014 | 0/0 | 2142 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0015 | 0/0 | 2142 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0016 | 0/0 | 2142 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0017 | 0/0 | 2142 | 2 | 0 | 1 | 1 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0018 | 0/0 | 2142 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0019 | 0/0 | 2142 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0020 | 0/0 | 2142 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0021 | 0/0 | 2142 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0022 | 0/0 | 2142 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0023 | 0/0 | 2142 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0024 | 0/0 | 2142 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0025 | 0/0 | 2142 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0026 | 0/0 | 2142 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0027 | 0/0 | 2142 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0028 | 0/0 | 2142 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0029 | 0/0 | 2142 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0030 | 0/0 | 2142 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0031 | 0/0 | 2142 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0032 | 0/0 | 2142 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0033 | 0/0 | 2142 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0034 | 0/0 | 2142 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0035 | 0/0 | 2142 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0036 | 0/0 | 2142 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0037 | 0/0 | 2142 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0038 | 0/0 | 2142 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0039 | 0/0 | 2142 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0040 | 0/0 | 2142 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0041 | 0/0 | 2142 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0042 | 0/0 | 2142 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0043 | 0/0 | 2142 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0044 | 0/0 | 2142 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0045 | 0/0 | 2142 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0046 | 0/0 | 2142 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0047 | 0/0 | 2142 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| 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 | 6429 | 38 | 1 | 13 | 16 | 1 | 6 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0002 | 0/0 | 6429 | 36 | 19 | 8 | 8 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0003 | 0/0 | 6429 | 30 | 3 | 7 | 12 | 2 | 6 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0004 | 1/0 | 6429 | 18 | 0 | 3 | 9 | 0 | 5 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0005 | 0/0 | 6429 | 15 | 2 | 4 | 7 | 0 | 2 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0006 | 0/0 | 6429 | 13 | 1 | 6 | 1 | 4 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0007 | 0/0 | 6429 | 12 | 2 | 6 | 1 | 2 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0008 | 0/0 | 6429 | 9 | 6 | 1 | 1 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0009 | 0/0 | 6429 | 8 | 0 | 2 | 0 | 2 | 4 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0010 | 0/0 | 6429 | 6 | 5 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0011 | 0/0 | 6429 | 5 | 1 | 0 | 2 | 0 | 2 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0012 | 0/0 | 6429 | 5 | 0 | 0 | 5 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0013 | 0/0 | 6429 | 5 | 4 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0014 | 0/0 | 6429 | 4 | 4 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0015 | 0/0 | 6429 | 4 | 3 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0016 | 0/0 | 6429 | 3 | 3 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0017 | 0/0 | 6429 | 3 | 3 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0018 | 0/0 | 6429 | 3 | 3 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0019 | 0/0 | 6429 | 2 | 0 | 2 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0020 | 0/0 | 6429 | 2 | 0 | 0 | 0 | 0 | 2 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0021 | 0/0 | 6429 | 2 | 0 | 2 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0022 | 0/0 | 6429 | 2 | 0 | 2 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0023 | 0/0 | 6429 | 2 | 2 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0024 | 0/0 | 6429 | 2 | 2 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0025 | 0/0 | 6429 | 2 | 0 | 0 | 0 | 1 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0026 | 0/0 | 6429 | 2 | 0 | 0 | 2 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0027 | 0/0 | 6429 | 2 | 1 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0028 | 0/0 | 6429 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0029 | 0/0 | 6429 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0030 | 0/0 | 6429 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0031 | 0/0 | 6429 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0032 | 0/0 | 6429 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0033 | 0/0 | 6429 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0034 | 0/0 | 6429 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0035 | 0/0 | 6429 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0036 | 0/0 | 6429 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0037 | 0/0 | 6429 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0038 | 0/0 | 6429 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0039 | 0/0 | 6429 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0040 | 0/0 | 6429 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0041 | 0/0 | 6429 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0042 | 0/0 | 6429 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0043 | 0/0 | 6429 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0044 | 0/0 | 6429 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0045 | 0/0 | 6429 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0046 | 0/0 | 6429 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0047 | 0/0 | 6429 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0048 | 0/0 | 6429 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0049 | 0/0 | 6429 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0050 | 0/0 | 6429 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0051 | 0/0 | 6429 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0052 | 0/0 | 6429 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0053 | 0/0 | 6429 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0054 | 0/0 | 6429 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0055 | 0/0 | 6429 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0056 | 0/0 | 6429 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0057 | 0/0 | 6429 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0058 | 0/0 | 6429 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0059 | 0/0 | 6429 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0060 | 0/0 | 6429 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0061 | 0/0 | 6429 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0062 | 0/0 | 6429 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0063 | 0/0 | 6429 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0064 | 0/0 | 6429 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0065 | 0/0 | 6429 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0066 | 0/0 | 6429 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0067 | 0/0 | 6429 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0068 | 0/0 | 6429 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0069 | 0/0 | 6429 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0070 | 0/0 | 6429 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0071 | 0/0 | 6429 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0072 | 0/0 | 6429 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0073 | 0/0 | 6429 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| c0074 | 0/0 | 6429 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 482 | 242 | 71 | 59 | 68 | 9 | 33 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| t0002 | 0/0 | 482 | 20 | 4 | 4 | 9 | 0 | 3 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| t0003 | 0/0 | 482 | 12 | 4 | 3 | 1 | 2 | 2 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| t0004 | 0/0 | 482 | 4 | 4 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| t0005 | 0/0 | 482 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| t0006 | 0/0 | 482 | 1 | 0 | 0 | 0 | 1 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| t0007 | 0/0 | 482 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| t0008 | 0/0 | 482 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| 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 | 2 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0070 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0218 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/0 | 6429 | 36 | 19 | 8 | 8 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0001c0004 | 1/0 | 6429 | 18 | 0 | 3 | 9 | 0 | 5 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0001c0005 | 0/0 | 6429 | 15 | 2 | 4 | 7 | 0 | 2 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0001c0010 | 0/0 | 6429 | 6 | 5 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0001c0013 | 0/0 | 6429 | 5 | 4 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0001c0017 | 0/0 | 6429 | 3 | 3 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0001c0018 | 0/0 | 6429 | 3 | 3 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0001c0044 | 0/0 | 6429 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0001c0045 | 0/0 | 6429 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0001c0058 | 0/0 | 6429 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0001c0061 | 0/0 | 6429 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0001c0068 | 0/0 | 6429 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0002c0001 | 0/1 | 6429 | 38 | 1 | 13 | 16 | 1 | 6 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0002c0006 | 0/0 | 6429 | 13 | 1 | 6 | 1 | 4 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0002c0011 | 0/0 | 6429 | 5 | 1 | 0 | 2 | 0 | 2 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0002c0012 | 0/0 | 6429 | 5 | 0 | 0 | 5 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0003c0003 | 0/0 | 6429 | 30 | 3 | 7 | 12 | 2 | 6 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0003c0026 | 0/0 | 6429 | 2 | 0 | 0 | 2 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0003c0069 | 0/0 | 6429 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0004c0007 | 0/0 | 6429 | 12 | 2 | 6 | 1 | 2 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0004c0021 | 0/0 | 6429 | 2 | 0 | 2 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0004c0054 | 0/0 | 6429 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0005c0008 | 0/0 | 6429 | 9 | 6 | 1 | 1 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0006c0009 | 0/0 | 6429 | 8 | 0 | 2 | 0 | 2 | 4 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0007c0023 | 0/0 | 6429 | 2 | 2 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0007c0024 | 0/0 | 6429 | 2 | 2 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0007c0025 | 0/0 | 6429 | 2 | 0 | 0 | 0 | 1 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0007c0062 | 0/0 | 6429 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0008c0015 | 0/0 | 6429 | 4 | 3 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0008c0042 | 0/0 | 6429 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0008c0063 | 0/0 | 6429 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0009c0014 | 0/0 | 6429 | 4 | 4 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0010c0016 | 0/0 | 6429 | 3 | 3 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0011c0020 | 0/0 | 6429 | 2 | 0 | 0 | 0 | 0 | 2 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0011c0036 | 0/0 | 6429 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0012c0027 | 0/0 | 6429 | 2 | 1 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0013c0022 | 0/0 | 6429 | 2 | 0 | 2 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0014c0053 | 0/0 | 6429 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0014c0072 | 0/0 | 6429 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0015c0066 | 0/0 | 6429 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0015c0071 | 0/0 | 6429 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0016c0019 | 0/0 | 6429 | 2 | 0 | 2 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0017c0031 | 0/0 | 6429 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0017c0040 | 0/0 | 6429 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0018c0041 | 0/0 | 6429 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0019c0070 | 0/0 | 6429 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0020c0046 | 0/0 | 6429 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0021c0047 | 0/0 | 6429 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0022c0064 | 0/0 | 6429 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0023c0048 | 0/0 | 6429 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0024c0073 | 0/0 | 6429 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0025c0056 | 0/0 | 6429 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0026c0049 | 0/0 | 6429 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0027c0052 | 0/0 | 6429 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0028c0051 | 0/0 | 6429 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0029c0050 | 0/0 | 6429 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0030c0060 | 0/0 | 6429 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0031c0057 | 0/0 | 6429 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0032c0065 | 0/0 | 6429 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0033c0059 | 0/0 | 6429 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0034c0055 | 0/0 | 6429 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0035c0067 | 0/0 | 6429 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0036c0043 | 0/0 | 6429 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0037c0074 | 0/0 | 6429 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0038c0039 | 0/0 | 6429 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0039c0038 | 0/0 | 6429 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0040c0035 | 0/0 | 6429 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0041c0030 | 0/0 | 6429 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0042c0033 | 0/0 | 6429 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0043c0032 | 0/0 | 6429 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0044c0034 | 0/0 | 6429 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0045c0037 | 0/0 | 6429 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0046c0029 | 0/0 | 6429 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0047c0028 | 0/0 | 6429 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001 | 0/0 | 6910 | 34 | 17 | 8 | 8 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0001c0002t0003 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0001c0002t0005 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0001c0004t0001 | 1/0 | 6910 | 18 | 0 | 3 | 9 | 0 | 5 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0001c0005t0001 | 0/0 | 6910 | 2 | 0 | 0 | 1 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0001c0005t0002 | 0/0 | 6910 | 12 | 2 | 4 | 6 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0001c0005t0003 | 0/0 | 6910 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0001c0010t0001 | 0/0 | 6910 | 6 | 5 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0001c0013t0001 | 0/0 | 6910 | 5 | 4 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0001c0017t0004 | 0/0 | 6910 | 3 | 3 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0001c0018t0001 | 0/0 | 6910 | 3 | 3 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0001c0044t0003 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0001c0045t0001 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0001c0058t0002 | 0/0 | 6910 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0001c0061t0001 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0001c0068t0001 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0002c0001t0001 | 0/1 | 6910 | 36 | 1 | 13 | 15 | 0 | 6 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0002c0001t0006 | 0/0 | 6910 | 1 | 0 | 0 | 0 | 1 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0002c0001t0008 | 0/0 | 6910 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0002c0006t0001 | 0/0 | 6910 | 12 | 1 | 6 | 0 | 4 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0002c0006t0007 | 0/0 | 6910 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0002c0011t0002 | 0/0 | 6910 | 5 | 1 | 0 | 2 | 0 | 2 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0002c0012t0001 | 0/0 | 6910 | 5 | 0 | 0 | 5 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0003c0003t0001 | 0/0 | 6910 | 30 | 3 | 7 | 12 | 2 | 6 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0003c0026t0001 | 0/0 | 6910 | 2 | 0 | 0 | 2 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0003c0069t0001 | 0/0 | 6910 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0004c0007t0001 | 0/0 | 6910 | 6 | 1 | 5 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0004c0007t0003 | 0/0 | 6910 | 6 | 1 | 1 | 1 | 2 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0004c0021t0003 | 0/0 | 6910 | 2 | 0 | 2 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0004c0054t0001 | 0/0 | 6910 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0005c0008t0001 | 0/0 | 6910 | 9 | 6 | 1 | 1 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0006c0009t0001 | 0/0 | 6910 | 8 | 0 | 2 | 0 | 2 | 4 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0007c0023t0001 | 0/0 | 6910 | 2 | 2 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0007c0024t0001 | 0/0 | 6910 | 2 | 2 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0007c0025t0001 | 0/0 | 6910 | 2 | 0 | 0 | 0 | 1 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0007c0062t0001 | 0/0 | 6910 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0008c0015t0001 | 0/0 | 6910 | 4 | 3 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0008c0042t0001 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0008c0063t0001 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0009c0014t0001 | 0/0 | 6910 | 4 | 4 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0010c0016t0001 | 0/0 | 6910 | 3 | 3 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0011c0020t0001 | 0/0 | 6910 | 2 | 0 | 0 | 0 | 0 | 2 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0011c0036t0001 | 0/0 | 6910 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0012c0027t0001 | 0/0 | 6910 | 2 | 1 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0013c0022t0001 | 0/0 | 6910 | 2 | 0 | 2 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0014c0053t0001 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0014c0072t0001 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0015c0066t0001 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0015c0071t0001 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0016c0019t0001 | 0/0 | 6910 | 2 | 0 | 2 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0017c0031t0001 | 0/0 | 6910 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0017c0040t0001 | 0/0 | 6910 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0018c0041t0004 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0019c0070t0001 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0020c0046t0003 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0021c0047t0001 | 0/0 | 6910 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0022c0064t0002 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0023c0048t0001 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0024c0073t0001 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0025c0056t0001 | 0/0 | 6910 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0026c0049t0001 | 0/0 | 6910 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0027c0052t0001 | 0/0 | 6910 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0028c0051t0001 | 0/0 | 6910 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0029c0050t0001 | 0/0 | 6910 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0030c0060t0001 | 0/0 | 6910 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0031c0057t0001 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0032c0065t0001 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0033c0059t0001 | 0/0 | 6910 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0034c0055t0001 | 0/0 | 6910 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0035c0067t0001 | 0/0 | 6910 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0036c0043t0001 | 0/0 | 6910 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0037c0074t0001 | 0/0 | 6910 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0038c0039t0001 | 0/0 | 6910 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0039c0038t0002 | 0/0 | 6910 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0040c0035t0001 | 0/0 | 6910 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0041c0030t0001 | 0/0 | 6910 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0042c0033t0001 | 0/0 | 6910 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0043c0032t0001 | 0/0 | 6910 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0044c0034t0001 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0045c0037t0001 | 0/0 | 6910 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0046c0029t0001 | 0/0 | 6910 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| a0047c0028t0001 | 0/0 | 6910 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | copy fasta | chr2 | 127530683 | 127642726 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0002t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0002t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0002t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0002t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0002t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0002t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0002t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0002t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0002t0005g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0004t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0004t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0004t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0004t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0004t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0004t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0004t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0004t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0004t0001g0070 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0004t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0004t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0004t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0004t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0004t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0004t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0004t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0004t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0004t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0005t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0005t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0005t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0005t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0005t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0005t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0005t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0005t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0005t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0005t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0005t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0005t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0005t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0005t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0005t0003g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0010t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0010t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0010t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0010t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0010t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0010t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0013t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0013t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0013t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0013t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0017t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0017t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0017t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0018t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0018t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0018t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0044t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0045t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0058t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0061t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0001c0068t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0001t0001g0218 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0001t0006g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0001t0008g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0006t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0006t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0006t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0006t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0006t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0006t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0006t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0006t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0006t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0006t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0006t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0006t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0006t0007g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0011t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0011t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0011t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0011t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0011t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0012t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0012t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0012t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0012t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0002c0012t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0003c0003t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0003c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0003c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0003c0003t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0003c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0003c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0003c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0003c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0003c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0003c0003t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0003c0003t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0003c0003t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0003c0003t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0003c0003t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0003c0003t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0003c0003t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0003c0003t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0003c0003t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0003c0003t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0003c0003t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0003c0003t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0003c0003t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0003c0003t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0003c0003t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0003c0003t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0003c0003t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0003c0003t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0003c0003t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0003c0003t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0003c0003t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0003c0026t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0003c0026t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0003c0069t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0004c0007t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0004c0007t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0004c0007t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0004c0007t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0004c0007t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0004c0007t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0004c0007t0003g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0004c0007t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0004c0007t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0004c0007t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0004c0007t0003g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0004c0007t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0004c0021t0003g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0004c0021t0003g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0004c0054t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0005c0008t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0005c0008t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0005c0008t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0005c0008t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0005c0008t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0005c0008t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0005c0008t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0005c0008t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0006c0009t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0006c0009t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0006c0009t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0006c0009t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0006c0009t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0006c0009t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0006c0009t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0006c0009t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0007c0023t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0007c0023t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0007c0024t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0007c0024t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0007c0025t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0007c0025t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0007c0062t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0008c0015t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0008c0015t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0008c0015t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0008c0015t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0008c0042t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0008c0063t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0009c0014t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0009c0014t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0009c0014t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0009c0014t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0010c0016t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0010c0016t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0011c0020t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0011c0020t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0011c0036t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0012c0027t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0012c0027t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0013c0022t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0013c0022t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0014c0053t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0014c0072t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0015c0066t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0015c0071t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0016c0019t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0016c0019t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0017c0031t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0017c0040t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0018c0041t0004g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0019c0070t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0020c0046t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0021c0047t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0022c0064t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0023c0048t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0024c0073t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0025c0056t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0026c0049t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0027c0052t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0028c0051t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0029c0050t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0030c0060t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0031c0057t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0032c0065t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0033c0059t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0034c0055t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0035c0067t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0036c0043t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0037c0074t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0038c0039t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0039c0038t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0040c0035t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0041c0030t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0042c0033t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0043c0032t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0044c0034t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0045c0037t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0046c0029t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| a0047c0028t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0006 | t0001 | g0015 | EUR | GBR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG00099 | hp2 | a0002 | c0001 | t0006 | g0180 | EUR | GBR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG00280 | hp1 | a0003 | c0003 | t0001 | g0248 | EUR | FIN | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG00280 | hp2 | a0004 | c0007 | t0003 | g0250 | EUR | FIN | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG00323 | hp1 | a0003 | c0003 | t0001 | g0234 | EUR | FIN | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG00323 | hp2 | a0006 | c0009 | t0001 | g0088 | EUR | FIN | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG00621 | hp1 | a0021 | c0047 | t0001 | g0124 | EAS | CHS | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG00621 | hp2 | a0003 | c0003 | t0001 | g0030 | EAS | CHS | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0097 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG00642 | hp2 | a0004 | c0007 | t0003 | g0125 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG00733 | hp1 | a0003 | c0003 | t0001 | g0230 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG00733 | hp2 | a0006 | c0009 | t0001 | g0059 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG00735 | hp1 | a0002 | c0001 | t0001 | g0004 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG00735 | hp2 | a0004 | c0007 | t0001 | g0158 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG00738 | hp1 | a0002 | c0006 | t0001 | g0156 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG00738 | hp2 | a0002 | c0001 | t0001 | g0191 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG00741 | hp1 | a0002 | c0006 | t0001 | g0012 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG00741 | hp2 | a0002 | c0006 | t0001 | g0155 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01069 | hp1 | a0013 | c0022 | t0001 | g0212 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0259 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01070 | hp1 | a0001 | c0005 | t0002 | g0211 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01070 | hp2 | a0002 | c0006 | t0001 | g0152 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01071 | hp1 | a0013 | c0022 | t0001 | g0115 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01071 | hp2 | a0002 | c0006 | t0001 | g0154 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01081 | hp1 | a0002 | c0001 | t0001 | g0193 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01081 | hp2 | a0038 | c0039 | t0001 | g0014 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0024 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01099 | hp2 | a0002 | c0001 | t0001 | g0004 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01106 | hp1 | a0006 | c0009 | t0001 | g0056 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01106 | hp2 | a0004 | c0007 | t0001 | g0267 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01109 | hp1 | a0003 | c0003 | t0001 | g0116 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01109 | hp2 | a0002 | c0001 | t0001 | g0113 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01168 | hp1 | a0004 | c0021 | t0003 | g0251 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01168 | hp2 | a0002 | c0001 | t0001 | g0184 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01169 | hp1 | a0016 | c0019 | t0001 | g0177 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01169 | hp2 | a0004 | c0021 | t0003 | g0253 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0142 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01175 | hp2 | a0004 | c0054 | t0001 | g0160 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01192 | hp1 | a0011 | c0036 | t0001 | g0151 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01192 | hp2 | a0001 | c0004 | t0001 | g0219 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01243 | hp1 | a0001 | c0013 | t0001 | g0163 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01243 | hp2 | a0008 | c0015 | t0001 | g0044 | AMR | PUR | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01255 | hp1 | a0004 | c0007 | t0001 | g0265 | AMR | CLM | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01255 | hp2 | a0003 | c0003 | t0001 | g0232 | AMR | CLM | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01256 | hp1 | a0001 | c0005 | t0002 | g0091 | AMR | CLM | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01256 | hp2 | a0005 | c0008 | t0001 | g0213 | AMR | CLM | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01257 | hp1 | a0002 | c0001 | t0001 | g0182 | AMR | CLM | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01257 | hp2 | a0004 | c0007 | t0001 | g0254 | AMR | CLM | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01258 | hp1 | a0004 | c0007 | t0001 | g0256 | AMR | CLM | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01258 | hp2 | a0001 | c0005 | t0002 | g0049 | AMR | CLM | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01346 | hp1 | a0001 | c0010 | t0001 | g0159 | AMR | CLM | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01346 | hp2 | a0001 | c0005 | t0002 | g0047 | AMR | CLM | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01358 | hp1 | a0017 | c0031 | t0001 | g0195 | AMR | CLM | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01358 | hp2 | a0034 | c0055 | t0001 | g0266 | AMR | CLM | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01361 | hp1 | a0002 | c0006 | t0001 | g0153 | AMR | CLM | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01361 | hp2 | a0002 | c0001 | t0001 | g0181 | AMR | CLM | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01433 | hp1 | a0003 | c0003 | t0001 | g0242 | AMR | CLM | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01433 | hp2 | a0003 | c0003 | t0001 | g0214 | AMR | CLM | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01515 | hp1 | a0002 | c0006 | t0001 | g0011 | EUR | IBS | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01515 | hp2 | a0002 | c0006 | t0001 | g0150 | EUR | IBS | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01516 | hp1 | a0007 | c0025 | t0001 | g0215 | EUR | IBS | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01516 | hp2 | a0002 | c0006 | t0001 | g0016 | EUR | IBS | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01884 | hp1 | a0015 | c0066 | t0001 | g0064 | AFR | ACB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0149 | AFR | ACB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01891 | hp1 | a0012 | c0027 | t0001 | g0260 | AFR | ACB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01891 | hp2 | a0020 | c0046 | t0003 | g0075 | AFR | ACB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0079 | AMR | PEL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01943 | hp2 | a0001 | c0004 | t0001 | g0018 | AMR | PEL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01952 | hp1 | a0002 | c0001 | t0001 | g0003 | AMR | PEL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0081 | AMR | PEL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01975 | hp1 | a0012 | c0027 | t0001 | g0080 | AMR | PEL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01975 | hp2 | a0003 | c0003 | t0001 | g0236 | AMR | PEL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01981 | hp1 | a0002 | c0001 | t0001 | g0171 | AMR | PEL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01981 | hp2 | a0026 | c0049 | t0001 | g0243 | AMR | PEL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02027 | hp1 | a0001 | c0004 | t0001 | g0055 | EAS | KHV | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02027 | hp2 | a0002 | c0011 | t0002 | g0196 | EAS | KHV | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02055 | hp1 | a0001 | c0013 | t0001 | g0086 | AFR | ACB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0103 | AFR | ACB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02071 | hp1 | a0002 | c0001 | t0001 | g0114 | EAS | KHV | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02071 | hp2 | a0003 | c0003 | t0001 | g0106 | EAS | KHV | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02074 | hp1 | a0001 | c0005 | t0002 | g0051 | EAS | KHV | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02074 | hp2 | a0003 | c0003 | t0001 | g0119 | EAS | KHV | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02132 | hp1 | a0004 | c0007 | t0003 | g0249 | EAS | KHV | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02132 | hp2 | a0002 | c0001 | t0001 | g0202 | EAS | KHV | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02135 | hp1 | a0003 | c0003 | t0001 | g0231 | EAS | KHV | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02135 | hp2 | a0002 | c0001 | t0008 | g0186 | EAS | KHV | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02145 | hp1 | a0008 | c0015 | t0001 | g0104 | AFR | ACB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0085 | AFR | ACB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0038 | AMR | PEL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02148 | hp2 | a0002 | c0001 | t0001 | g0198 | AMR | PEL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02165 | hp1 | a0045 | c0037 | t0001 | g0216 | EAS | CDX | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02165 | hp2 | a0001 | c0005 | t0002 | g0090 | EAS | CDX | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0141 | AFR | ACB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02257 | hp2 | a0019 | c0070 | t0001 | g0025 | AFR | ACB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02258 | hp1 | a0004 | c0007 | t0001 | g0161 | AFR | ACB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02258 | hp2 | a0018 | c0041 | t0004 | g0073 | AFR | ACB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02280 | hp1 | a0008 | c0015 | t0001 | g0164 | AFR | ACB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02280 | hp2 | a0001 | c0005 | t0002 | g0128 | AFR | ACB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02293 | hp1 | a0001 | c0004 | t0001 | g0252 | AMR | PEL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0031 | AMR | PEL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02300 | hp1 | a0002 | c0001 | t0001 | g0110 | AMR | PEL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02300 | hp2 | a0016 | c0019 | t0001 | g0176 | AMR | PEL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02451 | hp1 | a0001 | c0010 | t0001 | g0271 | AFR | ACB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0087 | AFR | ACB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02523 | hp1 | a0002 | c0001 | t0001 | g0107 | EAS | KHV | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02523 | hp2 | a0040 | c0035 | t0001 | g0111 | EAS | KHV | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02572 | hp1 | a0014 | c0053 | t0001 | g0277 | AFR | GWD | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02572 | hp2 | a0009 | c0014 | t0001 | g0101 | AFR | GWD | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02602 | hp1 | a0005 | c0008 | t0001 | g0157 | SAS | PJL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02602 | hp2 | a0003 | c0003 | t0001 | g0123 | SAS | PJL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02622 | hp1 | a0001 | c0018 | t0001 | g0272 | AFR | GWD | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02622 | hp2 | a0007 | c0023 | t0001 | g0126 | AFR | GWD | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02630 | hp1 | a0010 | c0016 | t0001 | g0005 | AFR | GWD | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02630 | hp2 | a0001 | c0017 | t0004 | g0022 | AFR | GWD | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0275 | AFR | GWD | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0043 | AFR | GWD | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02683 | hp1 | a0003 | c0003 | t0001 | g0237 | SAS | PJL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02683 | hp2 | a0001 | c0005 | t0001 | g0095 | SAS | PJL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02698 | hp1 | a0001 | c0004 | t0001 | g0240 | SAS | PJL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02698 | hp2 | a0002 | c0001 | t0001 | g0179 | SAS | PJL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02717 | hp1 | a0005 | c0008 | t0001 | g0001 | AFR | GWD | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02717 | hp2 | a0001 | c0002 | t0003 | g0042 | AFR | GWD | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02723 | hp1 | a0003 | c0003 | t0001 | g0239 | AFR | GWD | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02723 | hp2 | a0031 | c0057 | t0001 | g0076 | AFR | GWD | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02809 | hp1 | a0001 | c0013 | t0001 | g0162 | AFR | GWD | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02809 | hp2 | a0001 | c0044 | t0003 | g0077 | AFR | GWD | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02818 | hp1 | a0001 | c0061 | t0001 | g0096 | AFR | GWD | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02818 | hp2 | a0009 | c0014 | t0001 | g0220 | AFR | GWD | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02886 | hp1 | a0002 | c0001 | t0001 | g0185 | AFR | GWD | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0268 | AFR | GWD | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02895 | hp1 | a0001 | c0045 | t0001 | g0139 | AFR | GWD | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02895 | hp2 | a0001 | c0018 | t0001 | g0274 | AFR | GWD | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02896 | hp1 | a0005 | c0008 | t0001 | g0148 | AFR | GWD | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0094 | AFR | GWD | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02897 | hp1 | a0005 | c0008 | t0001 | g0147 | AFR | GWD | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02897 | hp2 | a0001 | c0018 | t0001 | g0273 | AFR | GWD | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02922 | hp1 | a0005 | c0008 | t0001 | g0166 | AFR | ESN | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02922 | hp2 | a0014 | c0072 | t0001 | g0009 | AFR | ESN | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0052 | AFR | ESN | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02965 | hp2 | a0002 | c0011 | t0002 | g0276 | AFR | ESN | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0130 | AFR | ESN | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02970 | hp2 | a0009 | c0014 | t0001 | g0133 | AFR | ESN | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG03017 | hp1 | a0002 | c0001 | t0001 | g0172 | SAS | PJL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG03017 | hp2 | a0002 | c0011 | t0002 | g0200 | SAS | PJL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG03041 | hp1 | a0010 | c0016 | t0001 | g0005 | AFR | GWD | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG03041 | hp2 | a0001 | c0017 | t0004 | g0021 | AFR | GWD | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG03130 | hp1 | a0001 | c0010 | t0001 | g0270 | AFR | ESN | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG03130 | hp2 | a0001 | c0013 | t0001 | g0002 | AFR | ESN | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG03139 | hp1 | a0005 | c0008 | t0001 | g0001 | AFR | ESN | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG03139 | hp2 | a0001 | c0068 | t0001 | g0089 | AFR | ESN | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG03195 | hp1 | a0001 | c0010 | t0001 | g0262 | AFR | ESN | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG03195 | hp2 | a0007 | c0024 | t0001 | g0083 | AFR | ESN | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG03209 | hp1 | a0022 | c0064 | t0002 | g0140 | AFR | MSL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG03209 | hp2 | a0008 | c0042 | t0001 | g0061 | AFR | MSL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0132 | AFR | MSL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG03225 | hp2 | a0023 | c0048 | t0001 | g0129 | AFR | MSL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG03239 | hp1 | a0006 | c0009 | t0001 | g0057 | SAS | PJL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG03239 | hp2 | a0002 | c0006 | t0001 | g0013 | SAS | PJL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG03453 | hp1 | a0015 | c0071 | t0001 | g0127 | AFR | MSL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG03453 | hp2 | a0001 | c0005 | t0002 | g0062 | AFR | MSL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG03490 | hp1 | a0001 | c0004 | t0001 | g0247 | SAS | PJL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG03490 | hp2 | a0002 | c0001 | t0001 | g0183 | SAS | PJL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG03492 | hp1 | a0002 | c0001 | t0001 | g0178 | SAS | PJL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG03492 | hp2 | a0027 | c0052 | t0001 | g0084 | SAS | PJL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG03516 | hp1 | a0010 | c0016 | t0001 | g0138 | AFR | ESN | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG03516 | hp2 | a0001 | c0002 | t0005 | g0072 | AFR | ESN | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG03654 | hp1 | a0037 | c0074 | t0001 | g0023 | SAS | PJL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG03654 | hp2 | a0001 | c0004 | t0001 | g0255 | SAS | PJL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG03669 | hp1 | a0003 | c0003 | t0001 | g0122 | SAS | PJL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG03669 | hp2 | a0001 | c0004 | t0001 | g0019 | SAS | PJL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG03688 | hp1 | a0004 | c0007 | t0003 | g0007 | SAS | STU | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG03688 | hp2 | a0006 | c0009 | t0001 | g0017 | SAS | STU | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG03710 | hp1 | a0007 | c0025 | t0001 | g0039 | SAS | PJL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG03710 | hp2 | a0011 | c0020 | t0001 | g0145 | SAS | PJL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG03831 | hp1 | a0001 | c0004 | t0001 | g0020 | SAS | BEB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG03831 | hp2 | a0001 | c0005 | t0003 | g0046 | SAS | BEB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG03927 | hp1 | a0006 | c0009 | t0001 | g0034 | SAS | BEB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0058 | SAS | BEB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG03942 | hp1 | a0039 | c0038 | t0002 | g0102 | SAS | BEB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG03942 | hp2 | a0002 | c0001 | t0001 | g0109 | SAS | BEB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG04115 | hp1 | a0003 | c0003 | t0001 | g0120 | SAS | STU | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG04115 | hp2 | a0046 | c0029 | t0001 | g0204 | SAS | STU | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG04184 | hp1 | a0003 | c0003 | t0001 | g0121 | SAS | BEB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG04184 | hp2 | a0002 | c0011 | t0002 | g0105 | SAS | BEB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG04199 | hp1 | a0003 | c0003 | t0001 | g0241 | SAS | STU | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG04199 | hp2 | a0006 | c0009 | t0001 | g0054 | SAS | STU | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG04204 | hp1 | a0011 | c0020 | t0001 | g0144 | SAS | STU | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG04204 | hp2 | a0002 | c0001 | t0001 | g0108 | SAS | STU | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG04228 | hp1 | a0033 | c0059 | t0001 | g0028 | SAS | STU | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG04228 | hp2 | a0035 | c0067 | t0001 | g0117 | SAS | STU | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA18522 | hp1 | a0001 | c0017 | t0004 | g0071 | AFR | YRI | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0093 | AFR | YRI | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA18612 | hp1 | a0002 | c0006 | t0007 | g0175 | EAS | CHB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA18612 | hp2 | a0001 | c0004 | t0001 | g0118 | EAS | CHB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA18747 | hp1 | a0002 | c0001 | t0001 | g0192 | EAS | CHB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA18747 | hp2 | a0029 | c0050 | t0001 | g0224 | EAS | CHB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0098 | AFR | YRI | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA18906 | hp2 | a0008 | c0063 | t0001 | g0263 | AFR | YRI | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA18941 | hp1 | a0002 | c0012 | t0001 | g0167 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA18941 | hp2 | a0003 | c0003 | t0001 | g0269 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA18942 | hp2 | a0001 | c0004 | t0001 | g0225 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA18947 | hp1 | a0002 | c0001 | t0001 | g0207 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA18947 | hp2 | a0003 | c0003 | t0001 | g0238 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA18949 | hp1 | a0002 | c0001 | t0001 | g0189 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA18949 | hp2 | a0036 | c0043 | t0001 | g0027 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA18950 | hp1 | a0002 | c0001 | t0001 | g0208 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA18950 | hp2 | a0003 | c0003 | t0001 | g0223 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA18957 | hp1 | a0001 | c0058 | t0002 | g0100 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA18957 | hp2 | a0002 | c0012 | t0001 | g0209 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA18959 | hp1 | a0017 | c0040 | t0001 | g0190 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA18959 | hp2 | a0003 | c0003 | t0001 | g0222 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA18962 | hp1 | a0042 | c0033 | t0001 | g0066 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA18962 | hp2 | a0001 | c0004 | t0001 | g0040 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA18964 | hp1 | a0002 | c0001 | t0001 | g0188 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA18966 | hp1 | a0002 | c0001 | t0001 | g0187 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA18966 | hp2 | a0003 | c0003 | t0001 | g0226 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA18967 | hp2 | a0002 | c0001 | t0001 | g0174 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA18968 | hp1 | a0001 | c0004 | t0001 | g0199 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA18968 | hp2 | a0001 | c0005 | t0002 | g0041 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA18972 | hp1 | a0003 | c0026 | t0001 | g0143 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA18972 | hp2 | a0001 | c0004 | t0001 | g0235 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA18975 | hp1 | a0028 | c0051 | t0001 | g0227 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA18975 | hp2 | a0001 | c0005 | t0001 | g0045 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA18980 | hp1 | a0030 | c0060 | t0001 | g0053 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA18980 | hp2 | a0001 | c0004 | t0001 | g0008 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA18981 | hp1 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA18981 | hp2 | a0047 | c0028 | t0001 | g0197 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA18983 | hp1 | a0003 | c0003 | t0001 | g0078 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA18984 | hp1 | a0041 | c0030 | t0001 | g0205 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA18984 | hp2 | a0001 | c0005 | t0002 | g0092 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA18985 | hp1 | a0002 | c0001 | t0001 | g0068 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA18985 | hp2 | a0003 | c0003 | t0001 | g0233 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA18986 | hp1 | a0001 | c0005 | t0002 | g0060 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA18986 | hp2 | a0002 | c0001 | t0001 | g0201 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA18995 | hp1 | a0025 | c0056 | t0001 | g0264 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA18995 | hp2 | a0002 | c0001 | t0001 | g0173 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA19000 | hp1 | a0007 | c0062 | t0001 | g0026 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA19000 | hp2 | a0002 | c0012 | t0001 | g0112 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA19007 | hp1 | a0002 | c0001 | t0001 | g0206 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA19007 | hp2 | a0001 | c0005 | t0002 | g0099 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA19010 | hp1 | a0001 | c0004 | t0001 | g0006 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA19010 | hp2 | a0002 | c0001 | t0001 | g0203 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA19030 | hp1 | a0044 | c0034 | t0001 | g0067 | AFR | LWK | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0074 | AFR | LWK | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA19043 | hp1 | a0032 | c0065 | t0001 | g0137 | AFR | LWK | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA19043 | hp2 | a0024 | c0073 | t0001 | g0065 | AFR | LWK | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA19056 | hp1 | a0002 | c0012 | t0001 | g0169 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA19060 | hp1 | a0003 | c0026 | t0001 | g0246 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0050 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA19063 | hp2 | a0002 | c0011 | t0002 | g0210 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA19070 | hp1 | a0001 | c0004 | t0001 | g0063 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA19070 | hp2 | a0005 | c0008 | t0001 | g0217 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA19074 | hp1 | a0043 | c0032 | t0001 | g0168 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA19074 | hp2 | a0003 | c0003 | t0001 | g0228 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA19079 | hp1 | a0002 | c0012 | t0001 | g0194 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA19079 | hp2 | a0003 | c0069 | t0001 | g0245 | EAS | JPT | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0131 | AFR | ASW | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA20129 | hp2 | a0001 | c0010 | t0001 | g0135 | AFR | ASW | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA20752 | hp1 | a0004 | c0007 | t0003 | g0069 | EUR | TSI | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA20752 | hp2 | a0006 | c0009 | t0001 | g0048 | EUR | TSI | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01123 | hp1 | a0002 | c0001 | t0001 | g0003 | AMR | CLM | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG01123 | hp2 | a0003 | c0003 | t0001 | g0258 | AMR | CLM | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02109 | hp1 | a0007 | c0023 | t0001 | g0221 | AFR | ACB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02109 | hp2 | a0001 | c0010 | t0001 | g0136 | AFR | ACB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02486 | hp1 | a0003 | c0003 | t0001 | g0229 | AFR | ACB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02486 | hp2 | a0009 | c0014 | t0001 | g0170 | AFR | ACB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02559 | hp1 | a0003 | c0003 | t0001 | g0244 | AFR | ACB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG02559 | hp2 | a0008 | c0015 | t0001 | g0165 | AFR | ACB | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG03471 | hp1 | a0002 | c0006 | t0001 | g0010 | AFR | MSL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG03471 | hp2 | a0005 | c0008 | t0001 | g0146 | AFR | MSL | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG06807 | hp1 | a0001 | c0013 | t0001 | g0002 | AFR | USA | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| HG06807 | hp2 | a0007 | c0024 | t0001 | g0261 | AFR | USA | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0134 | AFR | LWK | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| NA21309 | hp2 | a0004 | c0007 | t0003 | g0257 | AFR | LWK | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0001 | t0001 | g0218 | REF | REF | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| homoSapiens_grch38 | hp1 | a0001 | c0004 | t0001 | g0070 | REF | REF | MYO7B_chr2_127530683_127642726 | MYO7B | chr2 | 127530683 | 127642726 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:127564195
|
G | A | 15 | a0002a0005a0011others(12): Show | 87 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(84): Show |
missense_variant | MODERATE | c.61G>A | p.Gly21Ser | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 3/48 | 233/6910 | 61/6429 | 21/2142 | chr2 | 127564195 | ||
| chr2:127564211
|
G | A | 1 | a0018 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.77G>A | p.Gly26Asp | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 3/48 | 249/6910 | 77/6429 | 26/2142 | chr2 | 127564211 | ||
| chr2:127569812
|
C | T | 1 | a0038 | 1 | HG01081.hp2 | missense_variant | MODERATE | c.494C>T | p.Thr165Met | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/48 | 666/6910 | 494/6429 | 165/2142 | chr2 | 127569812 | ||
| chr2:127573931
|
G | T | 1 | a0037 | 1 | HG03654.hp1 | missense_variant | MODERATE | c.604G>T | p.Ala202Ser | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/48 | 776/6910 | 604/6429 | 202/2142 | chr2 | 127573931 | ||
| chr2:127574003
|
G | T | 1 | a0039 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.676G>T | p.Val226Leu | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/48 | 848/6910 | 676/6429 | 226/2142 | chr2 | 127574003 | ||
| chr2:127574018
|
C | T | 1 | a0012 | 2 | HG01891.hp1 HG01975.hp1 |
missense_variant | MODERATE | c.691C>T | p.Arg231Cys | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/48 | 863/6910 | 691/6429 | 231/2142 | chr2 | 127574018 | ||
| chr2:127578178
|
G | C | 1 | a0036 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.895G>C | p.Ala299Pro | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/48 | 1067/6910 | 895/6429 | 299/2142 | chr2 | 127578178 | ||
| chr2:127590134
|
T | G | 1 | a0047 | 1 | NA18981.hp2 | missense_variant | MODERATE | c.1897T>G | p.Phe633Val | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 16/48 | 2069/6910 | 1897/6429 | 633/2142 | chr2 | 127590134 | ||
| chr2:127590183
|
C | G | 1 | a0035 | 1 | HG04228.hp2 | missense_variant | MODERATE | c.1946C>G | p.Pro649Arg | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 16/48 | 2118/6910 | 1946/6429 | 649/2142 | chr2 | 127590183 | ||
| chr2:127593588
|
G | A | 1 | a0019 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.2188G>A | p.Val730Met | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 18/48 | 2360/6910 | 2188/6429 | 730/2142 | chr2 | 127593588 | ||
| chr2:127593608
|
A | C | 1 | a0015 | 2 | HG01884.hp1 HG03453.hp1 |
missense_variant | MODERATE | c.2208A>C | p.Lys736Asn | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 18/48 | 2380/6910 | 2208/6429 | 736/2142 | chr2 | 127593608 | ||
| chr2:127607225
|
G | A | 1 | a0020 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.2444G>A | p.Arg815His | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 21/48 | 2616/6910 | 2444/6429 | 815/2142 | chr2 | 127607225 | ||
| chr2:127607399
|
G | A | 1 | a0021 | 1 | HG00621.hp1 | missense_variant | MODERATE | c.2618G>A | p.Arg873His | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 21/48 | 2790/6910 | 2618/6429 | 873/2142 | chr2 | 127607399 | ||
| chr2:127609573
|
C | T | 1 | a0022 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.2882C>T | p.Pro961Leu | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 23/48 | 3054/6910 | 2882/6429 | 961/2142 | chr2 | 127609573 | ||
| chr2:127609858
|
G | A | 2 | a0010a0023 | 4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
missense_variant | MODERATE | c.3034G>A | p.Val1012Ile | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 24/48 | 3206/6910 | 3034/6429 | 1012/2142 | chr2 | 127609858 | ||
| chr2:127609981
|
G | A | 1 | a0010 | 3 | HG02630.hp1 HG03041.hp1 HG03516.hp1 |
missense_variant | MODERATE | c.3157G>A | p.Gly1053Ser | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 24/48 | 3329/6910 | 3157/6429 | 1053/2142 | chr2 | 127609981 | ||
| chr2:127612590
|
C | T | 1 | a0020 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.3385C>T | p.Arg1129Trp | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/48 | 3557/6910 | 3385/6429 | 1129/2142 | chr2 | 127612590 | ||
| chr2:127620434
|
G | A | 1 | a0010 | 3 | HG02630.hp1 HG03041.hp1 HG03516.hp1 |
missense_variant | MODERATE | c.3493G>A | p.Gly1165Ser | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/48 | 3665/6910 | 3493/6429 | 1165/2142 | chr2 | 127620434 | ||
| chr2:127621988
|
C | G | 4 | a0004a0034a0037others(1): Show | 18 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(15): Show |
missense_variant | MODERATE | c.3532C>G | p.Leu1178Val | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 28/48 | 3704/6910 | 3532/6429 | 1178/2142 | chr2 | 127621988 | ||
| chr2:127622034
|
C | T | 1 | a0009 | 4 | HG02486.hp2 HG02572.hp2 HG02818.hp2 others(1): Show |
missense_variant | MODERATE | c.3578C>T | p.Ala1193Val | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 28/48 | 3750/6910 | 3578/6429 | 1193/2142 | chr2 | 127622034 | ||
| chr2:127622040
|
G | A | 1 | a0013 | 2 | HG01069.hp1 HG01071.hp1 |
missense_variant | MODERATE | c.3584G>A | p.Arg1195His | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 28/48 | 3756/6910 | 3584/6429 | 1195/2142 | chr2 | 127622040 | ||
| chr2:127624142
|
G | A | 3 | a0010a0019a0023 | 5 | HG02257.hp2 HG02630.hp1 HG03041.hp1 others(2): Show |
missense_variant | MODERATE | c.3869G>A | p.Arg1290Gln | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 30/48 | 4041/6910 | 3869/6429 | 1290/2142 | chr2 | 127624142 | ||
| chr2:127624156
|
G | A | 1 | a0033 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.3883G>A | p.Ala1295Thr | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 30/48 | 4055/6910 | 3883/6429 | 1295/2142 | chr2 | 127624156 | ||
| chr2:127624198
|
A | G | 1 | a0008 | 6 | HG01243.hp2 HG02145.hp1 HG02280.hp1 others(3): Show |
missense_variant | MODERATE | c.3925A>G | p.Ile1309Val | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 30/48 | 4097/6910 | 3925/6429 | 1309/2142 | chr2 | 127624198 | ||
| chr2:127624286
|
G | A | 2 | a0010a0023 | 4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
missense_variant | MODERATE | c.4013G>A | p.Arg1338Gln | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 30/48 | 4185/6910 | 4013/6429 | 1338/2142 | chr2 | 127624286 | ||
| chr2:127627015
|
G | A | 1 | a0018 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.4256G>A | p.Arg1419Gln | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 32/48 | 4428/6910 | 4256/6429 | 1419/2142 | chr2 | 127627015 | ||
| chr2:127627038
|
C | T | 1 | a0040 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.4279C>T | p.Arg1427Cys | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 32/48 | 4451/6910 | 4279/6429 | 1427/2142 | chr2 | 127627038 | ||
| chr2:127628407
|
C | T | 2 | a0014a0024 | 3 | HG02572.hp1 HG02922.hp2 NA19043.hp2 |
missense_variant | MODERATE | c.4496C>T | p.Thr1499Met | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 34/48 | 4668/6910 | 4496/6429 | 1499/2142 | chr2 | 127628407 | ||
| chr2:127629686
|
G | A | 2 | a0016a0025 | 3 | HG01169.hp1 HG02300.hp2 NA18995.hp1 |
missense_variant | MODERATE | c.4666G>A | p.Val1556Ile | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 35/48 | 4838/6910 | 4666/6429 | 1556/2142 | chr2 | 127629686 | ||
| chr2:127630832
|
T | C | 1 | a0036 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.4861T>C | p.Phe1621Leu | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 36/48 | 5033/6910 | 4861/6429 | 1621/2142 | chr2 | 127630832 | ||
| chr2:127630862
|
A | C | 3 | a0006a0011a0045 | 12 | HG00323.hp2 HG00733.hp2 HG01106.hp1 others(9): Show |
missense_variant | MODERATE | c.4891A>C | p.Lys1631Gln | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 36/48 | 5063/6910 | 4891/6429 | 1631/2142 | chr2 | 127630862 | ||
| chr2:127631219
|
G | A | 1 | a0032 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.4951G>A | p.Asp1651Asn | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 37/48 | 5123/6910 | 4951/6429 | 1651/2142 | chr2 | 127631219 | ||
| chr2:127631237
|
G | A | 1 | a0010 | 3 | HG02630.hp1 HG03041.hp1 HG03516.hp1 |
missense_variant | MODERATE | c.4969G>A | p.Val1657Met | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 37/48 | 5141/6910 | 4969/6429 | 1657/2142 | chr2 | 127631237 | ||
| chr2:127631287
|
G | C | 7 | a0003a0005a0026others(4): Show | 47 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(44): Show |
missense_variant | MODERATE | c.5019G>C | p.Glu1673Asp | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 37/48 | 5191/6910 | 5019/6429 | 1673/2142 | chr2 | 127631287 | ||
| chr2:127632259
|
C | T | 1 | a0044 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.5263C>T | p.Arg1755Trp | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 39/48 | 5435/6910 | 5263/6429 | 1755/2142 | chr2 | 127632259 | ||
| chr2:127632260
|
G | A | 1 | a0026 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.5264G>A | p.Arg1755Gln | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 39/48 | 5436/6910 | 5264/6429 | 1755/2142 | chr2 | 127632260 | ||
| chr2:127634620
|
T | G | 1 | a0041 | 1 | NA18984.hp1 | missense_variant | MODERATE | c.5650T>G | p.Phe1884Val | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 42/48 | 5822/6910 | 5650/6429 | 1884/2142 | chr2 | 127634620 | ||
| chr2:127634621
|
T | A | 1 | a0041 | 1 | NA18984.hp1 | missense_variant | MODERATE | c.5651T>A | p.Phe1884Tyr | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 42/48 | 5823/6910 | 5651/6429 | 1884/2142 | chr2 | 127634621 | ||
| chr2:127634639
|
G | T | 1 | a0042 | 1 | NA18962.hp1 | missense_variant | MODERATE | c.5669G>T | p.Arg1890Met | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 42/48 | 5841/6910 | 5669/6429 | 1890/2142 | chr2 | 127634639 | ||
| chr2:127635123
|
C | T | 1 | a0040 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.5717C>T | p.Ala1906Val | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 43/48 | 5889/6910 | 5717/6429 | 1906/2142 | chr2 | 127635123 | ||
| chr2:127635740
|
C | T | 1 | a0027 | 1 | HG03492.hp2 | missense_variant | MODERATE | c.5839C>T | p.Arg1947Cys | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 44/48 | 6011/6910 | 5839/6429 | 1947/2142 | chr2 | 127635740 | ||
| chr2:127635818
|
C | T | 1 | a0031 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.5917C>T | p.Arg1973Trp | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 44/48 | 6089/6910 | 5917/6429 | 1973/2142 | chr2 | 127635818 | ||
| chr2:127635872
|
C | T | 1 | a0034 | 1 | HG01358.hp2 | missense_variant | MODERATE | c.5971C>T | p.Leu1991Phe | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 44/48 | 6143/6910 | 5971/6429 | 1991/2142 | chr2 | 127635872 | ||
| chr2:127635878
|
C | T | 1 | a0028 | 1 | NA18975.hp1 | missense_variant | MODERATE | c.5977C>T | p.Arg1993Cys | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 44/48 | 6149/6910 | 5977/6429 | 1993/2142 | chr2 | 127635878 | ||
| chr2:127636287
|
G | A | 1 | a0033 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.6086G>A | p.Arg2029Gln | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 45/48 | 6258/6910 | 6086/6429 | 2029/2142 | chr2 | 127636287 | ||
| chr2:127636560
|
T | G | 1 | a0030 | 1 | NA18980.hp1 | missense_variant | MODERATE | c.6139T>G | p.Ser2047Ala | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 46/48 | 6311/6910 | 6139/6429 | 2047/2142 | chr2 | 127636560 | ||
| chr2:127637332
|
A | G | 1 | a0043 | 1 | NA19074.hp1 | missense_variant | MODERATE | c.6344A>G | p.Asp2115Gly | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 48/48 | 6516/6910 | 6344/6429 | 2115/2142 | chr2 | 127637332 | ||
| chr2:127637380
|
A | G | 13 | a0003a0005a0007others(10): Show | 61 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(58): Show |
missense_variant | MODERATE | c.6392A>G | p.Gln2131Arg | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 48/48 | 6564/6910 | 6392/6429 | 2131/2142 | chr2 | 127637380 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:127566753
|
G | A | 1 | a0008c0042 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.396G>A | p.Pro132Pro | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/48 | 568/6910 | 396/6429 | 132/2142 | chr2 | 127566753 | ||
| chr2:127566783
|
C | T | 2 | a0002c0012a0017c0040 | 6 | NA18941.hp1 NA18957.hp2 NA18959.hp1 others(3): Show |
synonymous_variant | LOW | c.426C>T | p.Tyr142Tyr | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/48 | 598/6910 | 426/6429 | 142/2142 | chr2 | 127566783 | ||
| chr2:127574029
|
A | G | 2 | a0014c0072a0024c0073 | 2 | HG02922.hp2 NA19043.hp2 |
synonymous_variant | LOW | c.702A>G | p.Gln234Gln | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/48 | 874/6910 | 702/6429 | 234/2142 | chr2 | 127574029 | ||
| chr2:127580768
|
C | T | 2 | a0015c0071a0019c0070 | 2 | HG02257.hp2 HG03453.hp1 |
synonymous_variant | LOW | c.1026C>T | p.Asp342Asp | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 10/48 | 1198/6910 | 1026/6429 | 342/2142 | chr2 | 127580768 | ||
| chr2:127584215
|
G | A | 1 | a0004c0021 | 2 | HG01168.hp1 HG01169.hp2 |
synonymous_variant | LOW | c.1437G>A | p.Ser479Ser | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 13/48 | 1609/6910 | 1437/6429 | 479/2142 | chr2 | 127584215 | ||
| chr2:127584227
|
C | T | 1 | a0003c0069 | 1 | NA19079.hp2 | synonymous_variant | LOW | c.1449C>T | p.Ser483Ser | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 13/48 | 1621/6910 | 1449/6429 | 483/2142 | chr2 | 127584227 | ||
| chr2:127584308
|
G | A | 1 | a0001c0044 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.1530G>A | p.Leu510Leu | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 13/48 | 1702/6910 | 1530/6429 | 510/2142 | chr2 | 127584308 | ||
| chr2:127584329
|
G | A | 2 | a0001c0045a0010c0016 | 4 | HG02630.hp1 HG02895.hp1 HG03041.hp1 others(1): Show |
synonymous_variant | LOW | c.1551G>A | p.Pro517Pro | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 13/48 | 1723/6910 | 1551/6429 | 517/2142 | chr2 | 127584329 | ||
| chr2:127584801
|
A | G | 1 | a0001c0068 | 1 | HG03139.hp2 | synonymous_variant | LOW | c.1578A>G | p.Gln526Gln | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/48 | 1750/6910 | 1578/6429 | 526/2142 | chr2 | 127584801 | ||
| chr2:127592889
|
G | T | 1 | a0001c0018 | 3 | HG02622.hp1 HG02895.hp2 HG02897.hp2 |
synonymous_variant | LOW | c.2088G>T | p.Thr696Thr | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 17/48 | 2260/6910 | 2088/6429 | 696/2142 | chr2 | 127592889 | ||
| chr2:127607305
|
C | T | 2 | a0003c0026a0003c0069 | 3 | NA18972.hp1 NA19060.hp1 NA19079.hp2 |
synonymous_variant | LOW | c.2524C>T | p.Leu842Leu | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 21/48 | 2696/6910 | 2524/6429 | 842/2142 | chr2 | 127607305 | ||
| chr2:127608788
|
C | T | 1 | a0032c0065 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.2724C>T | p.Thr908Thr | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 22/48 | 2896/6910 | 2724/6429 | 908/2142 | chr2 | 127608788 | ||
| chr2:127609517
|
G | A | 32 | a0001c0010a0001c0017a0001c0018others(29): Show | 98 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(95): Show |
synonymous_variant | LOW | c.2826G>A | p.Ser942Ser | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 23/48 | 2998/6910 | 2826/6429 | 942/2142 | chr2 | 127609517 | ||
| chr2:127612321
|
A | G | 58 | a0001c0002a0001c0005a0001c0010others(55): Show | 207 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(204): Show |
synonymous_variant | LOW | c.3264A>G | p.Thr1088Thr | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 25/48 | 3436/6910 | 3264/6429 | 1088/2142 | chr2 | 127612321 | ||
| chr2:127622035
|
C | T | 1 | a0008c0063 | 1 | NA18906.hp2 | synonymous_variant | LOW | c.3579C>T | p.Ala1193Ala | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 28/48 | 3751/6910 | 3579/6429 | 1193/2142 | chr2 | 127622035 | ||
| chr2:127623204
|
T | G | 1 | a0011c0036 | 1 | HG01192.hp1 | splice_region_variant&synonymous_variant | LOW | c.3648T>G | p.Ala1216Ala | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 29/48 | 3820/6910 | 3648/6429 | 1216/2142 | chr2 | 127623204 | ||
| chr2:127624233
|
C | T | 13 | a0001c0005a0001c0058a0002c0011others(10): Show | 44 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(41): Show |
synonymous_variant | LOW | c.3960C>T | p.His1320His | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 30/48 | 4132/6910 | 3960/6429 | 1320/2142 | chr2 | 127624233 | ||
| chr2:127624314
|
C | T | 1 | a0023c0048 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.4041C>T | p.Phe1347Phe | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 30/48 | 4213/6910 | 4041/6429 | 1347/2142 | chr2 | 127624314 | ||
| chr2:127631215
|
G | A | 9 | a0003c0003a0003c0026a0003c0069others(6): Show | 47 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(44): Show |
synonymous_variant | LOW | c.4947G>A | p.Glu1649Glu | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 37/48 | 5119/6910 | 4947/6429 | 1649/2142 | chr2 | 127631215 | ||
| chr2:127633261
|
G | A | 1 | a0019c0070 | 1 | HG02257.hp2 | synonymous_variant | LOW | c.5409G>A | p.Thr1803Thr | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 40/48 | 5581/6910 | 5409/6429 | 1803/2142 | chr2 | 127633261 | ||
| chr2:127634598
|
C | T | 2 | a0001c0017a0018c0041 | 4 | HG02258.hp2 HG02630.hp2 HG03041.hp2 others(1): Show |
splice_region_variant&synonymous_variant | LOW | c.5628C>T | p.Val1876Val | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 42/48 | 5800/6910 | 5628/6429 | 1876/2142 | chr2 | 127634598 | ||
| chr2:127635784
|
G | A | 1 | a0032c0065 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.5883G>A | p.Ala1961Ala | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 44/48 | 6055/6910 | 5883/6429 | 1961/2142 | chr2 | 127635784 | ||
| chr2:127636225
|
T | C | 20 | a0001c0013a0003c0003a0003c0026others(17): Show | 65 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(62): Show |
synonymous_variant | LOW | c.6024T>C | p.Tyr2008Tyr | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 45/48 | 6196/6910 | 6024/6429 | 2008/2142 | chr2 | 127636225 | ||
| chr2:127636306
|
C | T | 1 | a0001c0061 | 1 | HG02818.hp1 | synonymous_variant | LOW | c.6105C>T | p.Ser2035Ser | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 45/48 | 6277/6910 | 6105/6429 | 2035/2142 | chr2 | 127636306 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:127535770
|
G | A | 3 | a0001c0002t0005a0001c0017t0004a0018c0041t0004 | 5 | HG02258.hp2 HG02630.hp2 HG03041.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-85G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/48 | 23953 | chr2 | 127535770 | |||||
| chr2:127637469
|
C | T | 1 | a0002c0001t0008 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*52C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 48/48 | 52 | chr2 | 127637469 | |||||
| chr2:127637563
|
G | A | 5 | a0001c0005t0002a0001c0058t0002a0002c0011t0002others(2): Show | 20 | HG01070.hp1 HG01256.hp1 HG01258.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*146G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 48/48 | 146 | chr2 | 127637563 | |||||
| chr2:127637620
|
T | G | 1 | a0002c0001t0006 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*203T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 48/48 | 203 | chr2 | 127637620 | |||||
| chr2:127637622
|
G | A | 8 | a0001c0002t0003a0001c0005t0003a0001c0017t0004others(5): Show | 16 | HG00280.hp2 HG00642.hp2 HG01168.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*205G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 48/48 | 205 | chr2 | 127637622 | |||||
| chr2:127637717
|
T | A | 1 | a0002c0006t0007 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*300T>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 48/48 | 300 | chr2 | 127637717 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:127535896
|
G | A | 3 | a0001c0004t0001g0006a0001c0004t0001g0008a0004c0007t0003g0007 | 3 | HG03688.hp1 NA18980.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.-24+65G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127535896 | ||||||
| chr2:127535973
|
C | G | 8 | a0001c0002t0001g0275a0001c0010t0001g0270a0001c0010t0001g0271others(5): Show | 8 | HG02451.hp1 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-24+142C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127535973 | ||||||
| chr2:127535989
|
C | T | 1 | a0003c0003t0001g0269 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-24+158C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127535989 | ||||||
| chr2:127536139
|
G | A | 1 | a0014c0072t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-24+308G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127536139 | ||||||
| chr2:127536206
|
T | A | 7 | a0002c0006t0001g0010a0002c0006t0001g0011a0002c0006t0001g0012others(4): Show | 7 | HG00099.hp1 HG00741.hp1 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.-24+375T>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127536206 | ||||||
| chr2:127536287
|
A | C | 1 | a0001c0002t0001g0268 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-24+456A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127536287 | ||||||
| chr2:127536379
|
G | A | 5 | a0001c0010t0001g0270a0001c0010t0001g0271a0001c0018t0001g0272others(2): Show | 5 | HG02451.hp1 HG02622.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24+548G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127536379 | ||||||
| chr2:127536442
|
G | A | 1 | a0006c0009t0001g0017 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-24+611G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127536442 | ||||||
| chr2:127536467
|
T | TG | 45 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(42): Show | 45 | HG00621.hp2 HG00733.hp2 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.-24+647dupG | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127536467 | |||||
| chr2:127536467
|
TG | T | 37 | a0001c0002t0001g0103a0001c0002t0001g0130a0001c0002t0001g0131others(34): Show | 37 | HG00621.hp1 HG00642.hp2 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.-24+647delG | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127536467 | |||||
| chr2:127536467
|
TGG | T | 152 | a0001c0002t0001g0132a0001c0002t0001g0134a0001c0002t0001g0141others(149): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.-24+646_-24+647del others(2): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127536467 | |||||
| chr2:127536476
|
G | T | 3 | a0004c0007t0001g0265a0004c0007t0001g0267a0034c0055t0001g0266 | 3 | HG01106.hp2 HG01255.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.-24+645G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127536476 | ||||||
| chr2:127536588
|
C | T | 78 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(75): Show | 78 | HG00323.hp2 HG00621.hp2 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.-24+757C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127536588 | ||||||
| chr2:127536677
|
C | T | 2 | a0010c0016t0001g0005a0023c0048t0001g0129 | 3 | HG02630.hp1 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-24+846C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127536677 | ||||||
| chr2:127536820
|
A | G | 1 | a0025c0056t0001g0264 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-24+989A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127536820 | ||||||
| chr2:127536854
|
G | A | 3 | a0001c0002t0001g0132a0001c0005t0002g0062a0009c0014t0001g0133 | 3 | HG02970.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-24+1023G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127536854 | ||||||
| chr2:127536861
|
G | A | 5 | a0001c0002t0005g0072a0001c0017t0004g0021a0001c0017t0004g0022others(2): Show | 5 | HG02258.hp2 HG02630.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24+1030G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127536861 | ||||||
| chr2:127536868
|
C | A | 89 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(86): Show | 90 | HG00323.hp2 HG00621.hp2 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.-24+1037C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127536868 | ||||||
| chr2:127536958
|
C | A | 2 | a0001c0004t0001g0063a0003c0026t0001g0143 | 2 | NA18972.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.-24+1127C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127536958 | ||||||
| chr2:127537479
|
C | A | 215 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(212): Show | 220 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.-24+1648C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127537479 | ||||||
| chr2:127537709
|
G | A | 252 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(249): Show | 257 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.-24+1878G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127537709 | ||||||
| chr2:127537743
|
A | C | 71 | a0001c0004t0001g0199a0001c0004t0001g0219a0001c0005t0002g0211others(68): Show | 73 | HG00099.hp2 HG00735.hp1 HG00738.hp2 others(70): Show |
intron_variant | MODIFIER | c.-24+1912A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127537743 | ||||||
| chr2:127537747
|
T | G | 1 | a0002c0012t0001g0167 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-24+1916T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127537747 | ||||||
| chr2:127537860
|
A | G | 256 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(253): Show | 261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.-24+2029A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127537860 | ||||||
| chr2:127537931
|
G | A | 1 | a0037c0074t0001g0023 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-24+2100G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127537931 | ||||||
| chr2:127537985
|
C | T | 2 | a0001c0005t0002g0128a0008c0063t0001g0263 | 2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-24+2154C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127537985 | ||||||
| chr2:127538053
|
G | A | 3 | a0001c0002t0001g0024a0001c0002t0001g0134a0003c0003t0001g0222 | 3 | HG01099.hp1 NA18959.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-24+2222G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127538053 | ||||||
| chr2:127538119
|
A | T | 1 | a0002c0006t0001g0010 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-24+2288A>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127538119 | ||||||
| chr2:127538209
|
A | C | 1 | a0004c0007t0003g0249 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-24+2378A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127538209 | ||||||
| chr2:127538262
|
C | CGGT | 16 | a0001c0002t0001g0074a0001c0002t0001g0132a0001c0002t0001g0275others(13): Show | 16 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.-24+2432_-24+2434d others(5): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127538262 | |||||
| chr2:127538296
|
G | A | 7 | a0001c0004t0001g0252a0002c0011t0002g0105a0004c0007t0003g0069others(4): Show | 7 | HG00280.hp2 HG00642.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.-24+2465G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127538296 | ||||||
| chr2:127538346
|
A | T | 1 | a0005c0008t0001g0166 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-24+2515A>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127538346 | ||||||
| chr2:127538436
|
C | T | 3 | a0014c0072t0001g0009a0015c0066t0001g0064a0024c0073t0001g0065 | 3 | HG01884.hp1 HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-24+2605C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127538436 | ||||||
| chr2:127538477
|
A | G | 1 | a0001c0044t0003g0077 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-24+2646A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127538477 | ||||||
| chr2:127538485
|
T | C | 2 | a0001c0010t0001g0135a0009c0014t0001g0101 | 2 | HG02572.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-24+2654T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127538485 | ||||||
| chr2:127538527
|
C | T | 108 | a0001c0002t0001g0103a0001c0002t0001g0149a0001c0004t0001g0199others(105): Show | 112 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(109): Show |
intron_variant | MODIFIER | c.-24+2696C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127538527 | ||||||
| chr2:127538690
|
C | T | 3 | a0001c0002t0001g0132a0001c0005t0002g0062a0009c0014t0001g0133 | 3 | HG02970.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-24+2859C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127538690 | ||||||
| chr2:127539007
|
C | A | 3 | a0014c0072t0001g0009a0015c0066t0001g0064a0024c0073t0001g0065 | 3 | HG01884.hp1 HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-24+3176C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127539007 | ||||||
| chr2:127539054
|
G | C | 12 | a0001c0002t0001g0134a0001c0002t0001g0141a0001c0002t0001g0142others(9): Show | 13 | HG01175.hp1 HG02109.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.-24+3223G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127539054 | ||||||
| chr2:127539119
|
A | G | 3 | a0001c0002t0001g0132a0001c0005t0002g0062a0009c0014t0001g0133 | 3 | HG02970.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-24+3288A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127539119 | ||||||
| chr2:127539255
|
A | G | 4 | a0001c0004t0001g0219a0002c0001t0001g0218a0005c0008t0001g0217others(1): Show | 4 | HG01192.hp2 HG02165.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.-24+3424A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127539255 | ||||||
| chr2:127539597
|
CA | C | 8 | a0001c0005t0002g0211a0003c0003t0001g0116a0003c0003t0001g0214others(5): Show | 8 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.-24+3767delA | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127539597 | ||||||
| chr2:127539657
|
G | A | 3 | a0001c0010t0001g0135a0001c0010t0001g0136a0009c0014t0001g0101 | 3 | HG02109.hp2 HG02572.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-24+3826G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127539657 | ||||||
| chr2:127539682
|
TA | T | 96 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(93): Show | 97 | HG00323.hp2 HG00621.hp2 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.-24+3862delA | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127539682 | |||||
| chr2:127539697
|
C | A | 136 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(133): Show | 137 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.-24+3866C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127539697 | ||||||
| chr2:127540151
|
T | G | 256 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(253): Show | 261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.-24+4320T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127540151 | ||||||
| chr2:127540164
|
G | GT | 3 | a0001c0002t0001g0132a0001c0005t0002g0062a0009c0014t0001g0133 | 3 | HG02970.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-24+4337dupT | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127540164 | |||||
| chr2:127540168
|
T | A | 1 | a0002c0012t0001g0167 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-24+4337T>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127540168 | ||||||
| chr2:127540169
|
A | AT | 71 | a0001c0002t0005g0072a0001c0004t0001g0199a0001c0004t0001g0219others(68): Show | 73 | HG00099.hp2 HG00735.hp1 HG00738.hp2 others(70): Show |
intron_variant | MODIFIER | c.-24+4350dupT | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127540169 | |||||
| chr2:127540169
|
A | ATT | 66 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(63): Show | 66 | HG00323.hp2 HG00621.hp2 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.-24+4349_-24+4350d others(4): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127540169 | |||||
| chr2:127540169
|
A | T | 4 | a0001c0002t0001g0132a0001c0005t0002g0062a0002c0012t0001g0167others(1): Show | 4 | HG02970.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-24+4338A>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127540169 | ||||||
| chr2:127540383
|
C | T | 40 | a0001c0004t0001g0063a0001c0004t0001g0118a0001c0004t0001g0225others(37): Show | 40 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.-24+4552C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127540383 | ||||||
| chr2:127540454
|
G | A | 1 | a0033c0059t0001g0028 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-24+4623G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127540454 | ||||||
| chr2:127540664
|
A | G | 1 | a0003c0003t0001g0248 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-24+4833A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127540664 | ||||||
| chr2:127540762
|
G | C | 17 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(14): Show | 17 | HG00621.hp2 HG01099.hp1 HG01943.hp1 others(14): Show |
intron_variant | MODIFIER | c.-24+4931G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127540762 | ||||||
| chr2:127540863
|
G | C | 38 | a0001c0002t0001g0103a0001c0002t0001g0149a0001c0010t0001g0159others(35): Show | 40 | HG00099.hp1 HG00735.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.-24+5032G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127540863 | ||||||
| chr2:127540948
|
A | C | 2 | a0001c0018t0001g0273a0001c0018t0001g0274 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-24+5117A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127540948 | ||||||
| chr2:127540994
|
T | C | 3 | a0001c0002t0001g0132a0001c0005t0002g0062a0009c0014t0001g0133 | 3 | HG02970.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-24+5163T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127540994 | ||||||
| chr2:127541057
|
A | T | 1 | a0001c0002t0001g0275 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-24+5226A>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127541057 | ||||||
| chr2:127541068
|
A | T | 40 | a0001c0004t0001g0063a0001c0004t0001g0118a0001c0004t0001g0225others(37): Show | 40 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.-24+5237A>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127541068 | ||||||
| chr2:127541079
|
G | A | 1 | a0001c0010t0001g0136 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-24+5248G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127541079 | ||||||
| chr2:127541090
|
ATCTGCTG others(25): Show |
A | 3 | a0001c0005t0002g0060a0001c0005t0002g0099a0001c0058t0002g0100 | 3 | NA18957.hp1 NA18986.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.-24+5291_-24+5322d others(34): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127541090 | |||||
| chr2:127541121
|
C | T | 8 | a0001c0002t0001g0074a0001c0002t0001g0275a0001c0044t0003g0077others(5): Show | 8 | HG01891.hp2 HG02257.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-24+5290C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127541121 | ||||||
| chr2:127541353
|
C | T | 5 | a0001c0010t0001g0270a0001c0010t0001g0271a0001c0018t0001g0272others(2): Show | 5 | HG02451.hp1 HG02622.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24+5522C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127541353 | ||||||
| chr2:127541436
|
C | T | 118 | a0001c0002t0001g0103a0001c0002t0001g0149a0001c0004t0001g0006others(115): Show | 122 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(119): Show |
intron_variant | MODIFIER | c.-24+5605C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127541436 | ||||||
| chr2:127541441
|
C | T | 261 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(258): Show | 266 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.-24+5610C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127541441 | ||||||
| chr2:127541476
|
G | C | 1 | a0002c0012t0001g0169 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-24+5645G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127541476 | ||||||
| chr2:127541503
|
A | G | 253 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(250): Show | 258 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.-24+5672A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127541503 | ||||||
| chr2:127541537
|
G | C | 5 | a0001c0002t0001g0259a0001c0010t0001g0262a0007c0024t0001g0261others(2): Show | 5 | HG01069.hp2 HG01891.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-24+5706G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127541537 | ||||||
| chr2:127541602
|
C | T | 1 | a0006c0009t0001g0059 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-24+5771C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127541602 | ||||||
| chr2:127541625
|
C | CT | 3 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0001g0268 | 3 | HG00642.hp1 HG02886.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-24+5795dupT | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127541625 | |||||
| chr2:127541828
|
A | T | 40 | a0001c0004t0001g0063a0001c0004t0001g0118a0001c0004t0001g0225others(37): Show | 40 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.-24+5997A>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127541828 | ||||||
| chr2:127541843
|
G | T | 107 | a0001c0002t0001g0103a0001c0002t0001g0149a0001c0004t0001g0199others(104): Show | 111 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(108): Show |
intron_variant | MODIFIER | c.-24+6012G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127541843 | ||||||
| chr2:127541852
|
G | A | 3 | a0014c0072t0001g0009a0015c0066t0001g0064a0024c0073t0001g0065 | 3 | HG01884.hp1 HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-24+6021G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127541852 | ||||||
| chr2:127541951
|
C | A | 258 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(255): Show | 263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.-24+6120C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127541951 | ||||||
| chr2:127542005
|
T | C | 2 | a0011c0020t0001g0144a0011c0020t0001g0145 | 2 | HG03710.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-24+6174T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127542005 | ||||||
| chr2:127542085
|
C | T | 80 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(77): Show | 81 | HG00323.hp2 HG00621.hp2 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.-24+6254C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127542085 | ||||||
| chr2:127542124
|
A | G | 3 | a0008c0015t0001g0104a0008c0015t0001g0164a0008c0015t0001g0165 | 3 | HG02145.hp1 HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-24+6293A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127542124 | ||||||
| chr2:127542237
|
C | T | 1 | a0001c0002t0001g0134 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-24+6406C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127542237 | ||||||
| chr2:127542344
|
C | A | 3 | a0001c0004t0001g0006a0001c0004t0001g0008a0004c0007t0003g0007 | 3 | HG03688.hp1 NA18980.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.-24+6513C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127542344 | ||||||
| chr2:127542429
|
G | A | 9 | a0001c0002t0001g0134a0001c0002t0001g0141a0001c0002t0001g0142others(6): Show | 10 | HG01175.hp1 HG02257.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-24+6598G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127542429 | ||||||
| chr2:127542538
|
A | T | 1 | a0002c0001t0001g0113 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-24+6707A>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127542538 | ||||||
| chr2:127542565
|
T | C | 71 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(68): Show | 71 | HG00323.hp2 HG00621.hp2 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.-24+6734T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127542565 | ||||||
| chr2:127542615
|
C | T | 3 | a0001c0002t0001g0058a0006c0009t0001g0056a0006c0009t0001g0057 | 3 | HG01106.hp1 HG03239.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.-24+6784C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127542615 | ||||||
| chr2:127542616
|
G | A | 1 | a0002c0001t0001g0114 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-24+6785G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127542616 | ||||||
| chr2:127542664
|
T | G | 40 | a0001c0004t0001g0063a0001c0004t0001g0118a0001c0004t0001g0225others(37): Show | 40 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.-24+6833T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127542664 | ||||||
| chr2:127542694
|
C | T | 2 | a0001c0004t0001g0219a0002c0001t0001g0218 | 2 | HG01192.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-24+6863C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127542694 | ||||||
| chr2:127542780
|
A | G | 142 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(139): Show | 143 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.-24+6949A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127542780 | ||||||
| chr2:127542827
|
A | G | 1 | a0004c0007t0003g0069 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-24+6996A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127542827 | ||||||
| chr2:127542874
|
A | C | 1 | a0001c0002t0001g0134 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-24+7043A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127542874 | ||||||
| chr2:127542880
|
A | G | 1 | a0001c0004t0001g0247 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-24+7049A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127542880 | ||||||
| chr2:127543145
|
T | C | 3 | a0001c0002t0001g0132a0001c0005t0002g0062a0009c0014t0001g0133 | 3 | HG02970.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-24+7314T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127543145 | ||||||
| chr2:127543186
|
A | G | 3 | a0001c0002t0001g0275a0002c0011t0002g0276a0014c0053t0001g0277 | 3 | HG02572.hp1 HG02647.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-24+7355A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127543186 | ||||||
| chr2:127543193
|
G | A | 9 | a0001c0002t0001g0134a0001c0002t0001g0141a0001c0002t0001g0142others(6): Show | 10 | HG01175.hp1 HG02257.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-24+7362G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127543193 | ||||||
| chr2:127543473
|
A | G | 3 | a0001c0004t0001g0006a0001c0004t0001g0008a0004c0007t0003g0007 | 3 | HG03688.hp1 NA18980.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.-24+7642A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127543473 | ||||||
| chr2:127543643
|
G | A | 2 | a0001c0002t0001g0074a0001c0044t0003g0077 | 2 | HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-24+7812G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127543643 | ||||||
| chr2:127543739
|
C | CAT | 66 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(63): Show | 66 | HG00323.hp2 HG00621.hp2 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.-24+7921_-24+7922d others(4): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127543739 | |||||
| chr2:127543752
|
A | T | 5 | a0002c0001t0001g0068a0002c0001t0001g0206a0002c0001t0001g0207others(2): Show | 5 | NA18947.hp1 NA18950.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.-24+7921A>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127543752 | ||||||
| chr2:127543754
|
T | A | 109 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(106): Show | 110 | HG00323.hp2 HG00621.hp2 HG00642.hp1 others(107): Show |
intron_variant | MODIFIER | c.-24+7923T>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127543754 | ||||||
| chr2:127543756
|
T | A | 82 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(79): Show | 83 | HG00323.hp2 HG00621.hp2 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.-24+7925T>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127543756 | ||||||
| chr2:127543784
|
A | G | 256 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(253): Show | 261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.-24+7953A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127543784 | ||||||
| chr2:127543822
|
G | A | 1 | a0002c0001t0001g0172 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-24+7991G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127543822 | ||||||
| chr2:127543828
|
T | A | 107 | a0001c0002t0001g0103a0001c0002t0001g0149a0001c0004t0001g0199others(104): Show | 111 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(108): Show |
intron_variant | MODIFIER | c.-24+7997T>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127543828 | ||||||
| chr2:127543831
|
C | G | 256 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(253): Show | 261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.-24+8000C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127543831 | ||||||
| chr2:127543835
|
G | C | 256 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(253): Show | 261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.-24+8004G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127543835 | ||||||
| chr2:127543882
|
C | A | 3 | a0014c0072t0001g0009a0015c0066t0001g0064a0024c0073t0001g0065 | 3 | HG01884.hp1 HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-24+8051C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127543882 | ||||||
| chr2:127543938
|
G | T | 3 | a0001c0004t0001g0006a0001c0004t0001g0008a0004c0007t0003g0007 | 3 | HG03688.hp1 NA18980.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.-24+8107G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127543938 | ||||||
| chr2:127543946
|
C | T | 1 | a0007c0025t0001g0215 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-24+8115C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127543946 | ||||||
| chr2:127543981
|
G | C | 3 | a0014c0072t0001g0009a0015c0066t0001g0064a0024c0073t0001g0065 | 3 | HG01884.hp1 HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-24+8150G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127543981 | ||||||
| chr2:127543997
|
T | C | 3 | a0008c0015t0001g0104a0008c0015t0001g0164a0008c0015t0001g0165 | 3 | HG02145.hp1 HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-24+8166T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127543997 | ||||||
| chr2:127544107
|
T | C | 3 | a0001c0002t0001g0132a0001c0005t0002g0062a0009c0014t0001g0133 | 3 | HG02970.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-24+8276T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127544107 | ||||||
| chr2:127544289
|
T | C | 5 | a0001c0002t0005g0072a0001c0017t0004g0021a0001c0017t0004g0022others(2): Show | 5 | HG02258.hp2 HG02630.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24+8458T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127544289 | ||||||
| chr2:127544462
|
G | A | 5 | a0005c0008t0001g0001a0005c0008t0001g0146a0005c0008t0001g0147others(2): Show | 6 | HG02717.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-24+8631G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127544462 | ||||||
| chr2:127544565
|
C | T | 38 | a0001c0002t0001g0103a0001c0002t0001g0149a0001c0010t0001g0159others(35): Show | 40 | HG00099.hp1 HG00735.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.-24+8734C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127544565 | ||||||
| chr2:127544571
|
G | C | 38 | a0001c0002t0001g0103a0001c0002t0001g0149a0001c0010t0001g0159others(35): Show | 40 | HG00099.hp1 HG00735.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.-24+8740G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127544571 | ||||||
| chr2:127544575
|
A | AT | 155 | a0001c0002t0001g0024a0001c0002t0001g0031a0001c0002t0001g0032others(152): Show | 157 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.-24+8767dupT | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127544575 | |||||
| chr2:127544575
|
A | ATT | 17 | a0001c0002t0001g0038a0001c0002t0001g0082a0001c0002t0001g0098others(14): Show | 17 | HG00621.hp1 HG01106.hp2 HG02027.hp1 others(14): Show |
intron_variant | MODIFIER | c.-24+8766_-24+8767d others(4): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127544575 | |||||
| chr2:127544575
|
AT | A | 6 | a0001c0002t0001g0259a0001c0004t0001g0006a0001c0004t0001g0008others(3): Show | 6 | HG01069.hp2 NA18950.hp2 NA18980.hp2 others(3): Show |
intron_variant | MODIFIER | c.-24+8767delT | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127544575 | |||||
| chr2:127544575
|
ATTTTTTT others(5): Show |
A | 9 | a0001c0002t0001g0134a0001c0002t0001g0141a0001c0002t0001g0142others(6): Show | 10 | HG01175.hp1 HG02257.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-24+8756_-24+8767d others(14): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127544575 | |||||
| chr2:127544641
|
C | T | 1 | a0003c0026t0001g0246 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-24+8810C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127544641 | ||||||
| chr2:127544647
|
C | T | 69 | a0001c0004t0001g0199a0001c0004t0001g0219a0001c0005t0002g0211others(66): Show | 71 | HG00099.hp2 HG00735.hp1 HG00738.hp2 others(68): Show |
intron_variant | MODIFIER | c.-24+8816C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127544647 | ||||||
| chr2:127544870
|
G | A | 1 | a0032c0065t0001g0137 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-24+9039G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127544870 | ||||||
| chr2:127544891
|
A | AT | 9 | a0001c0002t0001g0134a0001c0002t0001g0141a0001c0002t0001g0142others(6): Show | 10 | HG01175.hp1 HG02257.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-24+9067dupT | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127544891 | |||||
| chr2:127544961
|
A | G | 38 | a0001c0002t0001g0103a0001c0002t0001g0149a0001c0010t0001g0159others(35): Show | 40 | HG00099.hp1 HG00735.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.-24+9130A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127544961 | ||||||
| chr2:127545006
|
T | C | 9 | a0001c0002t0001g0134a0001c0002t0001g0141a0001c0002t0001g0142others(6): Show | 10 | HG01175.hp1 HG02257.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-24+9175T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127545006 | ||||||
| chr2:127545014
|
C | T | 1 | a0030c0060t0001g0053 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-24+9183C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127545014 | ||||||
| chr2:127545017
|
A | G | 3 | a0001c0002t0001g0132a0001c0005t0002g0062a0009c0014t0001g0133 | 3 | HG02970.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-24+9186A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127545017 | ||||||
| chr2:127545352
|
C | T | 107 | a0001c0002t0001g0103a0001c0002t0001g0149a0001c0004t0001g0199others(104): Show | 111 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(108): Show |
intron_variant | MODIFIER | c.-24+9521C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127545352 | ||||||
| chr2:127545428
|
G | A | 107 | a0001c0002t0001g0103a0001c0002t0001g0149a0001c0004t0001g0199others(104): Show | 111 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(108): Show |
intron_variant | MODIFIER | c.-24+9597G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127545428 | ||||||
| chr2:127545509
|
G | C | 2 | a0001c0010t0001g0135a0009c0014t0001g0101 | 2 | HG02572.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-24+9678G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127545509 | ||||||
| chr2:127545614
|
G | T | 1 | a0004c0007t0003g0249 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-24+9783G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127545614 | ||||||
| chr2:127545647
|
G | C | 3 | a0001c0002t0001g0132a0001c0005t0002g0062a0009c0014t0001g0133 | 3 | HG02970.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-24+9816G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127545647 | ||||||
| chr2:127545789
|
G | A | 71 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(68): Show | 71 | HG00323.hp2 HG00621.hp2 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.-24+9958G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127545789 | ||||||
| chr2:127545957
|
G | A | 1 | a0007c0024t0001g0083 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-24+10126G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127545957 | ||||||
| chr2:127546029
|
C | T | 1 | a0030c0060t0001g0053 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-24+10198C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127546029 | ||||||
| chr2:127546106
|
T | A | 3 | a0001c0002t0001g0132a0001c0005t0002g0062a0009c0014t0001g0133 | 3 | HG02970.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-24+10275T>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127546106 | ||||||
| chr2:127546238
|
C | T | 3 | a0001c0002t0001g0132a0001c0005t0002g0062a0009c0014t0001g0133 | 3 | HG02970.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-24+10407C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127546238 | ||||||
| chr2:127546283
|
T | C | 1 | a0032c0065t0001g0137 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-24+10452T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127546283 | ||||||
| chr2:127546327
|
G | A | 1 | a0007c0025t0001g0039 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-24+10496G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127546327 | ||||||
| chr2:127546762
|
G | GTCCA | 86 | a0001c0002t0001g0043a0001c0002t0001g0050a0001c0002t0001g0052others(83): Show | 88 | HG00323.hp1 HG00323.hp2 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.-24+10970_-24+1097 others(8): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127546762 | |||||
| chr2:127546762
|
G | GTCCATCC others(1): Show |
6 | a0001c0002t0001g0141a0001c0002t0001g0142a0001c0005t0001g0095others(3): Show | 6 | HG01175.hp1 HG02257.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.-24+10966_-24+1097 others(12): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127546762 | |||||
| chr2:127546762
|
GTCCA | G | 17 | a0001c0004t0001g0006a0001c0004t0001g0008a0001c0005t0002g0211others(14): Show | 17 | HG00621.hp2 HG01069.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.-24+10970_-24+1097 others(8): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127546762 | |||||
| chr2:127546762
|
GTCCATCC others(13): Show |
G | 1 | a0002c0001t0001g0068 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-24+10954_-24+1097 others(24): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127546762 | |||||
| chr2:127546779
|
T | TCCAC | 3 | a0019c0070t0001g0025a0020c0046t0003g0075a0031c0057t0001g0076 | 3 | HG01891.hp2 HG02257.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.-24+10951_-24+1095 others(8): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127546779 | |||||
| chr2:127546816
|
CTGTTTGT others(3): Show |
C | 1 | a0002c0006t0001g0016 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-24+10987_-24+1099 others(14): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127546816 | |||||
| chr2:127546915
|
C | T | 40 | a0001c0004t0001g0063a0001c0004t0001g0118a0001c0004t0001g0225others(37): Show | 40 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.-24+11084C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127546915 | ||||||
| chr2:127546944
|
C | T | 1 | a0018c0041t0004g0073 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-24+11113C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127546944 | ||||||
| chr2:127547243
|
G | A | 1 | a0003c0003t0001g0233 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-24+11412G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127547243 | ||||||
| chr2:127547533
|
G | A | 3 | a0001c0002t0001g0132a0001c0005t0002g0062a0009c0014t0001g0133 | 3 | HG02970.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-24+11702G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127547533 | ||||||
| chr2:127547621
|
T | C | 256 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(253): Show | 261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.-24+11790T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127547621 | ||||||
| chr2:127547699
|
C | T | 3 | a0001c0002t0001g0132a0001c0005t0002g0062a0009c0014t0001g0133 | 3 | HG02970.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-24+11868C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127547699 | ||||||
| chr2:127547884
|
A | G | 1 | a0001c0002t0001g0098 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-23-11816A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127547884 | ||||||
| chr2:127547987
|
C | T | 9 | a0001c0002t0001g0134a0001c0002t0001g0141a0001c0002t0001g0142others(6): Show | 10 | HG01175.hp1 HG02257.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-23-11713C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127547987 | ||||||
| chr2:127548168
|
C | T | 9 | a0001c0002t0001g0134a0001c0002t0001g0141a0001c0002t0001g0142others(6): Show | 10 | HG01175.hp1 HG02257.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-23-11532C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127548168 | ||||||
| chr2:127548419
|
C | CT | 24 | a0001c0002t0001g0074a0001c0002t0001g0103a0001c0002t0001g0134others(21): Show | 25 | HG01175.hp1 HG01891.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.-23-11266dupT | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127548419 | |||||
| chr2:127548478
|
G | A | 90 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(87): Show | 90 | HG00323.hp2 HG00621.hp2 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.-23-11222G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127548478 | ||||||
| chr2:127548492
|
T | C | 3 | a0001c0002t0001g0132a0001c0005t0002g0062a0009c0014t0001g0133 | 3 | HG02970.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-23-11208T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127548492 | ||||||
| chr2:127548562
|
C | T | 3 | a0014c0072t0001g0009a0015c0066t0001g0064a0024c0073t0001g0065 | 3 | HG01884.hp1 HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-23-11138C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127548562 | ||||||
| chr2:127548563
|
G | A | 5 | a0001c0002t0005g0072a0001c0017t0004g0021a0001c0017t0004g0022others(2): Show | 5 | HG02258.hp2 HG02630.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-23-11137G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127548563 | ||||||
| chr2:127548659
|
C | T | 3 | a0001c0002t0001g0132a0001c0005t0002g0062a0009c0014t0001g0133 | 3 | HG02970.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-23-11041C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127548659 | ||||||
| chr2:127548668
|
C | A | 3 | a0001c0002t0001g0132a0001c0005t0002g0062a0009c0014t0001g0133 | 3 | HG02970.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-23-11032C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127548668 | ||||||
| chr2:127548710
|
G | C | 4 | a0001c0002t0001g0103a0001c0013t0001g0002a0001c0013t0001g0162others(1): Show | 5 | HG01243.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23-10990G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127548710 | ||||||
| chr2:127548927
|
T | TGG | 9 | a0001c0002t0001g0134a0001c0002t0001g0141a0001c0002t0001g0142others(6): Show | 10 | HG01175.hp1 HG02257.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-23-10773_-23-1077 others(6): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127548927 | ||||||
| chr2:127548931
|
TCC | T | 9 | a0001c0002t0001g0134a0001c0002t0001g0141a0001c0002t0001g0142others(6): Show | 10 | HG01175.hp1 HG02257.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-23-10768_-23-1076 others(6): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127548931 | ||||||
| chr2:127549127
|
TTCTC | T | 3 | a0001c0002t0001g0275a0002c0011t0002g0276a0014c0053t0001g0277 | 3 | HG02572.hp1 HG02647.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-23-10569_-23-1056 others(8): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127549127 | |||||
| chr2:127549133
|
CTT | C | 3 | a0001c0002t0001g0132a0001c0005t0002g0062a0009c0014t0001g0133 | 3 | HG02970.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-23-10565_-23-1056 others(6): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127549133 | |||||
| chr2:127549155
|
CCTTCCTT others(5): Show |
C | 3 | a0001c0002t0001g0132a0001c0005t0002g0062a0009c0014t0001g0133 | 3 | HG02970.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-23-10541_-23-1053 others(16): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127549155 | |||||
| chr2:127549159
|
CCTTCCTT others(1): Show |
C | 107 | a0001c0002t0001g0103a0001c0002t0001g0149a0001c0004t0001g0199others(104): Show | 111 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(108): Show |
intron_variant | MODIFIER | c.-23-10537_-23-1053 others(12): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127549159 | |||||
| chr2:127549159
|
CCTTCCTT others(5): Show |
C | 1 | a0002c0011t0002g0200 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-23-10537_-23-1052 others(16): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127549159 | |||||
| chr2:127549163
|
CCTTT | C | 56 | a0001c0002t0001g0259a0001c0004t0001g0006a0001c0004t0001g0008others(53): Show | 56 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.-23-10518_-23-1051 others(8): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127549163 | |||||
| chr2:127549163
|
CCTTTCTT others(1): Show |
C | 5 | a0001c0010t0001g0270a0001c0010t0001g0271a0001c0018t0001g0272others(2): Show | 5 | HG02451.hp1 HG02622.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-23-10522_-23-1051 others(12): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127549163 | |||||
| chr2:127549167
|
T | C | 1 | a0006c0009t0001g0088 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-23-10533T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127549167 | ||||||
| chr2:127549174
|
TTCTTTCT others(5): Show |
T | 2 | a0009c0014t0001g0170a0030c0060t0001g0053 | 2 | HG02486.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.-23-10514_-23-1050 others(16): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127549174 | |||||
| chr2:127549178
|
TTCTTTCT others(1): Show |
T | 83 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(80): Show | 84 | HG00323.hp2 HG00621.hp2 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.-23-10514_-23-1050 others(12): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127549178 | |||||
| chr2:127549182
|
TTCTC | T | 5 | a0001c0002t0001g0052a0001c0002t0001g0087a0001c0002t0001g0093others(2): Show | 5 | HG02451.hp2 HG02896.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23-10514_-23-1051 others(8): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127549182 | |||||
| chr2:127549186
|
C | T | 2 | a0001c0010t0001g0136a0002c0011t0002g0200 | 2 | HG02109.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.-23-10514C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127549186 | ||||||
| chr2:127549213
|
T | A | 2 | a0001c0004t0001g0040a0001c0005t0002g0041 | 2 | NA18962.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.-23-10487T>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127549213 | ||||||
| chr2:127549334
|
G | T | 3 | a0001c0010t0001g0159a0004c0007t0001g0161a0004c0054t0001g0160 | 3 | HG01175.hp2 HG01346.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.-23-10366G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127549334 | ||||||
| chr2:127550012
|
C | T | 5 | a0001c0002t0001g0259a0001c0010t0001g0262a0007c0024t0001g0261others(2): Show | 5 | HG01069.hp2 HG01891.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23-9688C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127550012 | ||||||
| chr2:127550016
|
G | T | 40 | a0001c0004t0001g0063a0001c0004t0001g0118a0001c0004t0001g0225others(37): Show | 40 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.-23-9684G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127550016 | ||||||
| chr2:127550131
|
C | T | 1 | a0001c0005t0002g0128 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-23-9569C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127550131 | ||||||
| chr2:127550200
|
T | C | 3 | a0001c0002t0001g0132a0001c0005t0002g0062a0009c0014t0001g0133 | 3 | HG02970.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-23-9500T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127550200 | ||||||
| chr2:127550289
|
G | A | 2 | a0001c0002t0001g0259a0015c0071t0001g0127 | 2 | HG01069.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-23-9411G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127550289 | ||||||
| chr2:127550343
|
C | A | 253 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(250): Show | 258 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.-23-9357C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127550343 | ||||||
| chr2:127550558
|
CA | C | 251 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(248): Show | 256 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.-23-9129delA | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127550558 | |||||
| chr2:127550592
|
G | T | 151 | a0001c0002t0001g0103a0001c0002t0001g0149a0001c0004t0001g0006others(148): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-23-9108G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127550592 | ||||||
| chr2:127550618
|
A | C | 1 | a0001c0002t0001g0142 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-23-9082A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127550618 | ||||||
| chr2:127550840
|
C | T | 6 | a0001c0010t0001g0159a0004c0007t0001g0161a0004c0007t0001g0265others(3): Show | 6 | HG01106.hp2 HG01175.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.-23-8860C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127550840 | ||||||
| chr2:127550867
|
T | A | 2 | a0016c0019t0001g0176a0016c0019t0001g0177 | 2 | HG01169.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.-23-8833T>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127550867 | ||||||
| chr2:127550869
|
A | AG | 258 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(255): Show | 263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.-23-8828dupG | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127550869 | |||||
| chr2:127551110
|
T | C | 5 | a0001c0002t0005g0072a0001c0017t0004g0021a0001c0017t0004g0022others(2): Show | 5 | HG02258.hp2 HG02630.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-23-8590T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127551110 | ||||||
| chr2:127551271
|
T | C | 47 | a0001c0004t0001g0006a0001c0004t0001g0008a0001c0004t0001g0063others(44): Show | 47 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.-23-8429T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127551271 | ||||||
| chr2:127551302
|
T | C | 3 | a0010c0016t0001g0005a0010c0016t0001g0138a0023c0048t0001g0129 | 4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-23-8398T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127551302 | ||||||
| chr2:127551443
|
C | A | 5 | a0001c0002t0001g0259a0001c0010t0001g0262a0007c0024t0001g0261others(2): Show | 5 | HG01069.hp2 HG01891.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23-8257C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127551443 | ||||||
| chr2:127551689
|
G | A | 7 | a0001c0004t0001g0006a0001c0004t0001g0008a0001c0005t0002g0128others(4): Show | 7 | HG02109.hp1 HG02280.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-23-8011G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127551689 | ||||||
| chr2:127551894
|
G | C | 104 | a0001c0002t0001g0103a0001c0002t0001g0149a0001c0004t0001g0199others(101): Show | 108 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(105): Show |
intron_variant | MODIFIER | c.-23-7806G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127551894 | ||||||
| chr2:127552056
|
G | A | 71 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(68): Show | 71 | HG00323.hp2 HG00621.hp2 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.-23-7644G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127552056 | ||||||
| chr2:127552162
|
C | G | 1 | a0001c0061t0001g0096 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-23-7538C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127552162 | ||||||
| chr2:127552408
|
C | T | 5 | a0001c0004t0001g0006a0001c0004t0001g0008a0004c0007t0003g0007others(2): Show | 5 | HG02109.hp1 HG02818.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23-7292C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127552408 | ||||||
| chr2:127552422
|
C | G | 2 | a0001c0002t0001g0036a0001c0002t0001g0037 | 2 | NA18967.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.-23-7278C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127552422 | ||||||
| chr2:127552446
|
A | G | 258 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(255): Show | 263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.-23-7254A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127552446 | ||||||
| chr2:127552463
|
C | A | 40 | a0001c0004t0001g0063a0001c0004t0001g0118a0001c0004t0001g0225others(37): Show | 40 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.-23-7237C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127552463 | ||||||
| chr2:127552468
|
G | C | 3 | a0014c0072t0001g0009a0015c0066t0001g0064a0024c0073t0001g0065 | 3 | HG01884.hp1 HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-23-7232G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127552468 | ||||||
| chr2:127552473
|
T | A | 1 | a0001c0002t0001g0134 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-23-7227T>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127552473 | ||||||
| chr2:127552527
|
C | T | 1 | a0006c0009t0001g0088 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-23-7173C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127552527 | ||||||
| chr2:127552529
|
C | T | 1 | a0016c0019t0001g0177 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-23-7171C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127552529 | ||||||
| chr2:127552571
|
A | G | 1 | a0007c0023t0001g0126 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-23-7129A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127552571 | ||||||
| chr2:127552770
|
G | A | 9 | a0001c0002t0001g0134a0001c0002t0001g0141a0001c0002t0001g0142others(6): Show | 10 | HG01175.hp1 HG02257.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-23-6930G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127552770 | ||||||
| chr2:127552805
|
C | G | 83 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(80): Show | 83 | HG00323.hp2 HG00621.hp2 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.-23-6895C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127552805 | ||||||
| chr2:127552806
|
C | A | 40 | a0001c0004t0001g0063a0001c0004t0001g0118a0001c0004t0001g0225others(37): Show | 40 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.-23-6894C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127552806 | ||||||
| chr2:127552977
|
GTCTCAGC others(3): Show |
G | 7 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0001g0268others(4): Show | 7 | HG00099.hp1 HG00642.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.-23-6706_-23-6697d others(12): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127552977 | |||||
| chr2:127553055
|
C | T | 3 | a0001c0004t0001g0006a0001c0004t0001g0008a0004c0007t0003g0007 | 3 | HG03688.hp1 NA18980.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.-23-6645C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127553055 | ||||||
| chr2:127553106
|
C | T | 3 | a0001c0002t0001g0275a0002c0011t0002g0276a0014c0053t0001g0277 | 3 | HG02572.hp1 HG02647.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-23-6594C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127553106 | ||||||
| chr2:127553145
|
T | C | 1 | a0032c0065t0001g0137 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-23-6555T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127553145 | ||||||
| chr2:127553170
|
G | C | 1 | a0045c0037t0001g0216 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-23-6530G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127553170 | ||||||
| chr2:127553243
|
A | C | 3 | a0001c0002t0001g0132a0001c0005t0002g0062a0009c0014t0001g0133 | 3 | HG02970.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-23-6457A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127553243 | ||||||
| chr2:127553355
|
G | A | 1 | a0001c0013t0001g0162 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-23-6345G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127553355 | ||||||
| chr2:127553487
|
T | G | 93 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(90): Show | 94 | HG00323.hp2 HG00621.hp2 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.-23-6213T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127553487 | ||||||
| chr2:127553491
|
T | C | 253 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(250): Show | 258 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.-23-6209T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127553491 | ||||||
| chr2:127553593
|
G | C | 3 | a0001c0002t0001g0132a0001c0005t0002g0062a0009c0014t0001g0133 | 3 | HG02970.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-23-6107G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127553593 | ||||||
| chr2:127553615
|
G | A | 2 | a0004c0007t0001g0265a0004c0007t0001g0267 | 2 | HG01106.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.-23-6085G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127553615 | ||||||
| chr2:127553731
|
G | A | 3 | a0001c0004t0001g0006a0001c0004t0001g0008a0004c0007t0003g0007 | 3 | HG03688.hp1 NA18980.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.-23-5969G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127553731 | ||||||
| chr2:127553886
|
C | T | 79 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(76): Show | 79 | HG00323.hp2 HG00621.hp2 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.-23-5814C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127553886 | ||||||
| chr2:127553922
|
G | C | 1 | a0001c0002t0001g0134 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-23-5778G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127553922 | ||||||
| chr2:127553979
|
T | C | 2 | a0001c0002t0001g0074a0001c0044t0003g0077 | 2 | HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-23-5721T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127553979 | ||||||
| chr2:127553991
|
C | T | 3 | a0014c0072t0001g0009a0015c0066t0001g0064a0024c0073t0001g0065 | 3 | HG01884.hp1 HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-23-5709C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127553991 | ||||||
| chr2:127554040
|
A | G | 2 | a0001c0002t0001g0029a0001c0002t0001g0035 | 2 | NA18942.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.-23-5660A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127554040 | ||||||
| chr2:127554056
|
A | C | 1 | a0003c0003t0001g0232 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-23-5644A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127554056 | ||||||
| chr2:127554096
|
C | T | 1 | a0007c0024t0001g0083 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-23-5604C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127554096 | ||||||
| chr2:127554275
|
T | A | 1 | a0023c0048t0001g0129 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-23-5425T>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127554275 | ||||||
| chr2:127554511
|
A | G | 2 | a0011c0020t0001g0144a0011c0020t0001g0145 | 2 | HG03710.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-23-5189A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127554511 | ||||||
| chr2:127554519
|
C | G | 1 | a0042c0033t0001g0066 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-23-5181C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127554519 | ||||||
| chr2:127554656
|
G | C | 5 | a0001c0002t0005g0072a0001c0017t0004g0021a0001c0017t0004g0022others(2): Show | 5 | HG02258.hp2 HG02630.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-23-5044G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127554656 | ||||||
| chr2:127554949
|
A | AT | 7 | a0001c0002t0001g0103a0001c0002t0001g0134a0001c0004t0001g0020others(4): Show | 7 | HG02055.hp2 HG02895.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-23-4735dupT | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | INFO_REALIGN_3_PRIME | chr2 | 127554949 | |||||
| chr2:127555196
|
C | T | 40 | a0001c0004t0001g0063a0001c0004t0001g0118a0001c0004t0001g0225others(37): Show | 40 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.-23-4504C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127555196 | ||||||
| chr2:127555252
|
A | G | 3 | a0014c0072t0001g0009a0015c0066t0001g0064a0024c0073t0001g0065 | 3 | HG01884.hp1 HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-23-4448A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127555252 | ||||||
| chr2:127555367
|
T | A | 40 | a0001c0004t0001g0063a0001c0004t0001g0118a0001c0004t0001g0225others(37): Show | 40 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.-23-4333T>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127555367 | ||||||
| chr2:127555534
|
G | A | 5 | a0001c0010t0001g0270a0001c0010t0001g0271a0001c0018t0001g0272others(2): Show | 5 | HG02451.hp1 HG02622.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-23-4166G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127555534 | ||||||
| chr2:127555653
|
C | T | 3 | a0001c0002t0001g0085a0001c0002t0001g0130a0001c0013t0001g0086 | 3 | HG02055.hp1 HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-23-4047C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127555653 | ||||||
| chr2:127555719
|
T | C | 2 | a0003c0003t0001g0030a0003c0003t0001g0078 | 2 | HG00621.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.-23-3981T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127555719 | ||||||
| chr2:127555721
|
G | A | 9 | a0001c0002t0001g0134a0001c0002t0001g0141a0001c0002t0001g0142others(6): Show | 10 | HG01175.hp1 HG02257.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-23-3979G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127555721 | ||||||
| chr2:127555793
|
T | C | 3 | a0019c0070t0001g0025a0020c0046t0003g0075a0031c0057t0001g0076 | 3 | HG01891.hp2 HG02257.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.-23-3907T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127555793 | ||||||
| chr2:127555978
|
A | G | 2 | a0007c0023t0001g0221a0009c0014t0001g0220 | 2 | HG02109.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-23-3722A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127555978 | ||||||
| chr2:127556229
|
T | A | 3 | a0014c0072t0001g0009a0015c0066t0001g0064a0024c0073t0001g0065 | 3 | HG01884.hp1 HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-23-3471T>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127556229 | ||||||
| chr2:127556325
|
G | T | 1 | a0009c0014t0001g0133 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-23-3375G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127556325 | ||||||
| chr2:127556736
|
A | G | 1 | a0002c0011t0002g0276 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-23-2964A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127556736 | ||||||
| chr2:127556909
|
T | C | 45 | a0001c0004t0001g0006a0001c0004t0001g0008a0001c0004t0001g0063others(42): Show | 45 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.-23-2791T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127556909 | ||||||
| chr2:127556927
|
A | T | 5 | a0001c0002t0001g0132a0001c0005t0002g0062a0001c0005t0002g0128others(2): Show | 5 | HG02280.hp2 HG02970.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23-2773A>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127556927 | ||||||
| chr2:127557044
|
A | G | 5 | a0003c0003t0001g0119a0003c0003t0001g0223a0003c0003t0001g0226others(2): Show | 5 | HG02074.hp2 HG02135.hp1 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.-23-2656A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127557044 | ||||||
| chr2:127557213
|
G | T | 40 | a0001c0004t0001g0063a0001c0004t0001g0118a0001c0004t0001g0225others(37): Show | 40 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.-23-2487G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127557213 | ||||||
| chr2:127557255
|
G | A | 5 | a0001c0002t0001g0259a0001c0010t0001g0262a0007c0024t0001g0261others(2): Show | 5 | HG01069.hp2 HG01891.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23-2445G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127557255 | ||||||
| chr2:127557341
|
C | T | 1 | a0030c0060t0001g0053 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-23-2359C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127557341 | ||||||
| chr2:127557414
|
C | A | 5 | a0001c0002t0001g0259a0001c0010t0001g0262a0007c0024t0001g0261others(2): Show | 5 | HG01069.hp2 HG01891.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23-2286C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127557414 | ||||||
| chr2:127557654
|
C | T | 71 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(68): Show | 71 | HG00323.hp2 HG00621.hp2 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.-23-2046C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127557654 | ||||||
| chr2:127557891
|
C | A | 2 | a0003c0003t0001g0122a0003c0003t0001g0234 | 2 | HG00323.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.-23-1809C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127557891 | ||||||
| chr2:127557992
|
G | C | 4 | a0001c0045t0001g0139a0010c0016t0001g0005a0010c0016t0001g0138others(1): Show | 5 | HG02630.hp1 HG02895.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23-1708G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127557992 | ||||||
| chr2:127558004
|
T | C | 104 | a0001c0002t0001g0103a0001c0002t0001g0149a0001c0004t0001g0199others(101): Show | 108 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(105): Show |
intron_variant | MODIFIER | c.-23-1696T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127558004 | ||||||
| chr2:127558433
|
T | C | 7 | a0001c0004t0001g0006a0001c0004t0001g0008a0001c0005t0002g0128others(4): Show | 7 | HG02109.hp1 HG02280.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-23-1267T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127558433 | ||||||
| chr2:127558451
|
A | G | 4 | a0001c0002t0001g0074a0001c0010t0001g0135a0001c0044t0003g0077others(1): Show | 4 | HG02572.hp2 HG02809.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.-23-1249A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127558451 | ||||||
| chr2:127558545
|
C | T | 2 | a0001c0005t0002g0128a0008c0063t0001g0263 | 2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-23-1155C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127558545 | ||||||
| chr2:127558598
|
A | C | 18 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(15): Show | 18 | HG00621.hp2 HG01099.hp1 HG01943.hp1 others(15): Show |
intron_variant | MODIFIER | c.-23-1102A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127558598 | ||||||
| chr2:127558652
|
T | C | 2 | a0001c0010t0001g0135a0009c0014t0001g0101 | 2 | HG02572.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-23-1048T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127558652 | ||||||
| chr2:127558741
|
G | A | 1 | a0007c0023t0001g0126 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-23-959G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127558741 | ||||||
| chr2:127558759
|
T | G | 255 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(252): Show | 260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.-23-941T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127558759 | ||||||
| chr2:127558856
|
G | A | 5 | a0001c0002t0005g0072a0001c0017t0004g0021a0001c0017t0004g0022others(2): Show | 5 | HG02258.hp2 HG02630.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-23-844G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127558856 | ||||||
| chr2:127558915
|
T | C | 3 | a0001c0004t0001g0006a0001c0004t0001g0008a0004c0007t0003g0007 | 3 | HG03688.hp1 NA18980.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.-23-785T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127558915 | ||||||
| chr2:127558983
|
C | T | 2 | a0007c0023t0001g0221a0009c0014t0001g0220 | 2 | HG02109.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-23-717C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127558983 | ||||||
| chr2:127559315
|
G | T | 1 | a0001c0002t0001g0275 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-23-385G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127559315 | ||||||
| chr2:127559325
|
G | A | 40 | a0001c0004t0001g0063a0001c0004t0001g0118a0001c0004t0001g0225others(37): Show | 40 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.-23-375G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127559325 | ||||||
| chr2:127559438
|
C | A | 2 | a0007c0023t0001g0221a0009c0014t0001g0220 | 2 | HG02109.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-23-262C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127559438 | ||||||
| chr2:127559511
|
G | A | 1 | a0001c0002t0001g0085 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-23-189G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127559511 | ||||||
| chr2:127559533
|
G | A | 1 | a0001c0002t0001g0134 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-23-167G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127559533 | ||||||
| chr2:127559619
|
A | C | 8 | a0001c0002t0001g0074a0001c0002t0001g0275a0001c0010t0001g0135others(5): Show | 8 | HG02109.hp2 HG02572.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.-23-81A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 1/47 | chr2 | 127559619 | ||||||
| chr2:127559841
|
T | C | 3 | a0001c0002t0001g0141a0001c0002t0001g0142a0022c0064t0002g0140 | 3 | HG01175.hp1 HG02257.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.18+101T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127559841 | ||||||
| chr2:127560006
|
ATTTCTTT others(3): Show |
A | 1 | a0002c0011t0002g0276 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.18+285_18+294delCT others(8): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr2 | 127560006 | |||||
| chr2:127560030
|
C | CT | 15 | a0001c0002t0001g0134a0001c0002t0001g0141a0001c0002t0001g0142others(12): Show | 16 | HG01175.hp1 HG02257.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.18+304dupT | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr2 | 127560030 | |||||
| chr2:127560030
|
CT | C | 116 | a0001c0002t0001g0103a0001c0002t0001g0149a0001c0002t0005g0072others(113): Show | 120 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.18+304delT | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr2 | 127560030 | |||||
| chr2:127560102
|
C | T | 2 | a0001c0005t0002g0128a0008c0063t0001g0263 | 2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.18+362C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127560102 | ||||||
| chr2:127560349
|
G | A | 3 | a0001c0005t0002g0099a0001c0010t0001g0136a0001c0058t0002g0100 | 3 | HG02109.hp2 NA18957.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.18+609G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127560349 | ||||||
| chr2:127560451
|
C | T | 5 | a0001c0002t0001g0259a0001c0010t0001g0262a0007c0024t0001g0261others(2): Show | 5 | HG01069.hp2 HG01891.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.18+711C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127560451 | ||||||
| chr2:127560546
|
A | G | 96 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(93): Show | 97 | HG00323.hp2 HG00621.hp2 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.18+806A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127560546 | ||||||
| chr2:127560560
|
T | C | 1 | a0003c0003t0001g0234 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.18+820T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127560560 | ||||||
| chr2:127560584
|
G | T | 1 | a0001c0005t0002g0041 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.18+844G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127560584 | ||||||
| chr2:127560873
|
C | A | 3 | a0019c0070t0001g0025a0020c0046t0003g0075a0031c0057t0001g0076 | 3 | HG01891.hp2 HG02257.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.18+1133C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127560873 | ||||||
| chr2:127560889
|
C | A | 3 | a0019c0070t0001g0025a0020c0046t0003g0075a0031c0057t0001g0076 | 3 | HG01891.hp2 HG02257.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.18+1149C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127560889 | ||||||
| chr2:127561023
|
G | A | 14 | a0001c0002t0001g0134a0001c0002t0001g0141a0001c0002t0001g0142others(11): Show | 15 | HG01175.hp1 HG02257.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.18+1283G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127561023 | ||||||
| chr2:127561320
|
G | A | 1 | a0027c0052t0001g0084 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.18+1580G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127561320 | ||||||
| chr2:127561327
|
C | T | 14 | a0001c0002t0001g0134a0001c0002t0001g0141a0001c0002t0001g0142others(11): Show | 15 | HG01175.hp1 HG02257.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.18+1587C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127561327 | ||||||
| chr2:127561343
|
C | T | 1 | a0001c0002t0001g0134 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.18+1603C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127561343 | ||||||
| chr2:127561354
|
G | T | 7 | a0001c0010t0001g0159a0004c0007t0001g0158a0004c0007t0001g0161others(4): Show | 7 | HG00735.hp2 HG01106.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.18+1614G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127561354 | ||||||
| chr2:127561360
|
G | A | 71 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(68): Show | 71 | HG00323.hp2 HG00621.hp2 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.18+1620G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127561360 | ||||||
| chr2:127561373
|
C | T | 4 | a0003c0003t0001g0229a0003c0003t0001g0230a0003c0003t0001g0232others(1): Show | 4 | HG00280.hp1 HG00733.hp1 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.18+1633C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127561373 | ||||||
| chr2:127561541
|
G | C | 79 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(76): Show | 79 | HG00323.hp2 HG00621.hp2 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.18+1801G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127561541 | ||||||
| chr2:127561620
|
G | A | 79 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(76): Show | 79 | HG00323.hp2 HG00621.hp2 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.18+1880G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127561620 | ||||||
| chr2:127561637
|
G | A | 2 | a0001c0005t0002g0128a0008c0063t0001g0263 | 2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.18+1897G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127561637 | ||||||
| chr2:127561729
|
G | A | 4 | a0001c0002t0001g0149a0008c0015t0001g0104a0008c0015t0001g0164others(1): Show | 4 | HG01884.hp2 HG02145.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+1989G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127561729 | ||||||
| chr2:127561849
|
G | A | 12 | a0002c0001t0001g0108a0002c0001t0001g0113a0002c0001t0001g0172others(9): Show | 12 | HG00099.hp2 HG01109.hp2 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.18+2109G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127561849 | ||||||
| chr2:127561878
|
A | G | 5 | a0001c0010t0001g0270a0001c0010t0001g0271a0001c0018t0001g0272others(2): Show | 5 | HG02451.hp1 HG02622.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+2138A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127561878 | ||||||
| chr2:127561981
|
T | G | 252 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(249): Show | 257 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.19-2172T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127561981 | ||||||
| chr2:127562028
|
G | GGA | 47 | a0001c0004t0001g0006a0001c0004t0001g0008a0001c0004t0001g0063others(44): Show | 47 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.19-2113_19-2112dup others(2): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr2 | 127562028 | |||||
| chr2:127562072
|
C | T | 2 | a0001c0004t0001g0040a0001c0005t0002g0041 | 2 | NA18962.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.19-2081C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127562072 | ||||||
| chr2:127562220
|
A | C | 78 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(75): Show | 78 | HG00323.hp2 HG00621.hp2 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.19-1933A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127562220 | ||||||
| chr2:127562266
|
C | T | 1 | a0008c0063t0001g0263 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.19-1887C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127562266 | ||||||
| chr2:127562359
|
C | A | 1 | a0023c0048t0001g0129 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.19-1794C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127562359 | ||||||
| chr2:127562430
|
G | A | 4 | a0001c0002t0001g0074a0001c0010t0001g0135a0001c0044t0003g0077others(1): Show | 4 | HG02572.hp2 HG02809.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-1723G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127562430 | ||||||
| chr2:127562441
|
C | T | 1 | a0001c0002t0001g0131 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.19-1712C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127562441 | ||||||
| chr2:127562482
|
G | GTTT | 27 | a0001c0004t0001g0225a0001c0004t0001g0240a0001c0004t0001g0247others(24): Show | 27 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.19-1649_19-1647dup others(3): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr2 | 127562482 | |||||
| chr2:127562482
|
G | GTTTT | 8 | a0003c0003t0001g0120a0003c0003t0001g0121a0003c0003t0001g0122others(5): Show | 8 | HG01433.hp1 HG01981.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.19-1650_19-1647dup others(4): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr2 | 127562482 | |||||
| chr2:127562482
|
GT | G | 149 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(146): Show | 154 | HG00099.hp1 HG00099.hp2 HG00621.hp2 others(151): Show |
intron_variant | MODIFIER | c.19-1647delT | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr2 | 127562482 | |||||
| chr2:127562484
|
T | G | 1 | a0001c0002t0001g0142 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.19-1669T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127562484 | ||||||
| chr2:127562485
|
T | G | 13 | a0001c0002t0001g0134a0001c0002t0001g0141a0001c0010t0001g0270others(10): Show | 14 | HG02257.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.19-1668T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127562485 | ||||||
| chr2:127562558
|
G | A | 1 | a0001c0005t0001g0045 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.19-1595G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127562558 | ||||||
| chr2:127562602
|
G | C | 14 | a0001c0002t0001g0134a0001c0002t0001g0141a0001c0002t0001g0142others(11): Show | 15 | HG01175.hp1 HG02257.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.19-1551G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127562602 | ||||||
| chr2:127562635
|
T | G | 252 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(249): Show | 257 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.19-1518T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127562635 | ||||||
| chr2:127562733
|
G | A | 2 | a0001c0004t0001g0247a0001c0010t0001g0136 | 2 | HG02109.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.19-1420G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127562733 | ||||||
| chr2:127562900
|
C | T | 3 | a0019c0070t0001g0025a0020c0046t0003g0075a0031c0057t0001g0076 | 3 | HG01891.hp2 HG02257.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.19-1253C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127562900 | ||||||
| chr2:127562914
|
T | C | 7 | a0001c0004t0001g0006a0001c0004t0001g0008a0001c0005t0002g0128others(4): Show | 7 | HG02109.hp1 HG02280.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-1239T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127562914 | ||||||
| chr2:127563087
|
C | T | 1 | a0002c0006t0001g0010 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.19-1066C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127563087 | ||||||
| chr2:127563091
|
T | G | 2 | a0001c0010t0001g0135a0009c0014t0001g0101 | 2 | HG02572.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.19-1062T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127563091 | ||||||
| chr2:127563133
|
G | C | 2 | a0002c0006t0001g0012a0002c0006t0001g0013 | 2 | HG00741.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.19-1020G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127563133 | ||||||
| chr2:127563411
|
T | C | 1 | a0002c0001t0001g0201 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.19-742T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127563411 | ||||||
| chr2:127563503
|
TCCTGCAA others(10): Show |
T | 1 | a0031c0057t0001g0076 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.19-636_19-620delAA others(15): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | INFO_REALIGN_3_PRIME | chr2 | 127563503 | |||||
| chr2:127563592
|
C | T | 1 | a0001c0002t0001g0098 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.19-561C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127563592 | ||||||
| chr2:127563715
|
G | A | 3 | a0014c0072t0001g0009a0015c0066t0001g0064a0024c0073t0001g0065 | 3 | HG01884.hp1 HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.19-438G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127563715 | ||||||
| chr2:127563792
|
C | T | 3 | a0019c0070t0001g0025a0020c0046t0003g0075a0031c0057t0001g0076 | 3 | HG01891.hp2 HG02257.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.19-361C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127563792 | ||||||
| chr2:127563838
|
A | G | 1 | a0001c0005t0002g0051 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.19-315A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127563838 | ||||||
| chr2:127564002
|
A | G | 2 | a0001c0002t0001g0132a0009c0014t0001g0133 | 2 | HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.19-151A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127564002 | ||||||
| chr2:127564106
|
G | T | 1 | a0002c0001t0001g0208 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.19-47G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127564106 | ||||||
| chr2:127564108
|
A | G | 4 | a0002c0001t0001g0068a0002c0001t0001g0206a0002c0001t0001g0207others(1): Show | 4 | NA18947.hp1 NA18950.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.19-45A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 2/47 | chr2 | 127564108 | ||||||
| chr2:127564274
|
T | C | 2 | a0007c0023t0001g0221a0009c0014t0001g0220 | 2 | HG02109.hp1 HG02818.hp2 |
splice_region_variant&intron_variant | LOW | c.132+8T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 3/47 | chr2 | 127564274 | ||||||
| chr2:127564300
|
C | T | 1 | a0001c0005t0002g0211 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.132+34C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 3/47 | chr2 | 127564300 | ||||||
| chr2:127564578
|
G | A | 1 | a0001c0002t0001g0134 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.132+312G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 3/47 | chr2 | 127564578 | ||||||
| chr2:127564752
|
GGCTTAGC others(6): Show |
G | 2 | a0001c0002t0001g0074a0001c0044t0003g0077 | 2 | HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.133-479_133-467del others(13): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 3/47 | INFO_REALIGN_3_PRIME | chr2 | 127564752 | |||||
| chr2:127564925
|
C | T | 1 | a0001c0005t0002g0051 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.133-308C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 3/47 | chr2 | 127564925 | ||||||
| chr2:127565088
|
G | T | 3 | a0007c0024t0001g0261a0014c0072t0001g0009a0024c0073t0001g0065 | 3 | HG02922.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.133-145G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 3/47 | chr2 | 127565088 | ||||||
| chr2:127565613
|
G | T | 6 | a0001c0004t0001g0006a0001c0004t0001g0008a0004c0007t0003g0007others(3): Show | 6 | HG02922.hp2 HG03688.hp1 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.285+228G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 4/47 | chr2 | 127565613 | ||||||
| chr2:127565760
|
C | A | 11 | a0001c0002t0001g0134a0001c0002t0001g0141a0001c0002t0001g0142others(8): Show | 12 | HG01175.hp1 HG02257.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.285+375C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 4/47 | chr2 | 127565760 | ||||||
| chr2:127565782
|
C | G | 1 | a0001c0010t0001g0136 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.285+397C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 4/47 | chr2 | 127565782 | ||||||
| chr2:127565921
|
G | A | 8 | a0001c0010t0001g0262a0001c0010t0001g0270a0001c0010t0001g0271others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.285+536G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 4/47 | chr2 | 127565921 | ||||||
| chr2:127566142
|
T | C | 6 | a0001c0010t0001g0136a0002c0001t0001g0173a0002c0001t0001g0187others(3): Show | 6 | HG02109.hp2 HG02135.hp2 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.286-501T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 4/47 | chr2 | 127566142 | ||||||
| chr2:127566230
|
C | T | 1 | a0004c0007t0003g0257 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.286-413C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 4/47 | chr2 | 127566230 | ||||||
| chr2:127566354
|
C | T | 1 | a0008c0042t0001g0061 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.286-289C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 4/47 | chr2 | 127566354 | ||||||
| chr2:127566363
|
T | C | 3 | a0001c0002t0001g0093a0001c0002t0001g0094a0001c0002t0001g0259 | 3 | HG01069.hp2 HG02896.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.286-280T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 4/47 | chr2 | 127566363 | ||||||
| chr2:127566431
|
C | T | 1 | a0047c0028t0001g0197 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.286-212C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 4/47 | chr2 | 127566431 | ||||||
| chr2:127566457
|
C | T | 1 | a0003c0003t0001g0236 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.286-186C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 4/47 | chr2 | 127566457 | ||||||
| chr2:127566475
|
G | A | 5 | a0001c0002t0005g0072a0001c0017t0004g0021a0001c0017t0004g0022others(2): Show | 5 | HG02258.hp2 HG02630.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.286-168G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 4/47 | chr2 | 127566475 | ||||||
| chr2:127566550
|
C | CT | 253 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(250): Show | 258 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.286-93_286-92insT | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 4/47 | chr2 | 127566550 | ||||||
| chr2:127566936
|
C | T | 2 | a0001c0002t0001g0132a0009c0014t0001g0133 | 2 | HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.470+109C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | chr2 | 127566936 | ||||||
| chr2:127566991
|
C | T | 1 | a0008c0042t0001g0061 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.470+164C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | chr2 | 127566991 | ||||||
| chr2:127567306
|
G | A | 1 | a0002c0001t0001g0109 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.470+479G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | chr2 | 127567306 | ||||||
| chr2:127567319
|
C | CA | 67 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(64): Show | 67 | HG00323.hp2 HG00621.hp2 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.470+501dupA | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | INFO_REALIGN_3_PRIME | chr2 | 127567319 | |||||
| chr2:127567330
|
A | T | 256 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(253): Show | 261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.470+503A>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | chr2 | 127567330 | ||||||
| chr2:127567345
|
G | A | 2 | a0001c0002t0001g0132a0009c0014t0001g0133 | 2 | HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.470+518G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | chr2 | 127567345 | ||||||
| chr2:127567561
|
C | A | 3 | a0001c0010t0001g0262a0012c0027t0001g0260a0015c0071t0001g0127 | 3 | HG01891.hp1 HG03195.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.470+734C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | chr2 | 127567561 | ||||||
| chr2:127567598
|
T | C | 1 | a0002c0001t0001g0202 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.470+771T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | chr2 | 127567598 | ||||||
| chr2:127567662
|
GATTC | G | 3 | a0010c0016t0001g0005a0010c0016t0001g0138a0023c0048t0001g0129 | 4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.470+861_470+864del others(4): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | INFO_REALIGN_3_PRIME | chr2 | 127567662 | |||||
| chr2:127567832
|
G | A | 1 | a0001c0010t0001g0136 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.470+1005G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | chr2 | 127567832 | ||||||
| chr2:127567835
|
C | T | 35 | a0001c0004t0001g0240a0001c0004t0001g0247a0003c0003t0001g0106others(32): Show | 35 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.470+1008C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | chr2 | 127567835 | ||||||
| chr2:127567899
|
C | T | 4 | a0001c0002t0001g0103a0001c0013t0001g0002a0001c0013t0001g0162others(1): Show | 5 | HG01243.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.470+1072C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | chr2 | 127567899 | ||||||
| chr2:127568574
|
G | C | 1 | a0006c0009t0001g0057 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.471-1215G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | chr2 | 127568574 | ||||||
| chr2:127568624
|
C | T | 3 | a0001c0002t0001g0141a0001c0002t0001g0142a0022c0064t0002g0140 | 3 | HG01175.hp1 HG02257.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.471-1165C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | chr2 | 127568624 | ||||||
| chr2:127568725
|
C | T | 3 | a0001c0002t0001g0058a0006c0009t0001g0056a0006c0009t0001g0057 | 3 | HG01106.hp1 HG03239.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.471-1064C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | chr2 | 127568725 | ||||||
| chr2:127568795
|
G | A | 75 | a0001c0002t0001g0074a0001c0002t0001g0275a0001c0004t0001g0063others(72): Show | 77 | HG00099.hp2 HG00735.hp1 HG00738.hp2 others(74): Show |
intron_variant | MODIFIER | c.471-994G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | chr2 | 127568795 | ||||||
| chr2:127568814
|
T | A | 5 | a0001c0010t0001g0270a0001c0010t0001g0271a0001c0018t0001g0272others(2): Show | 5 | HG02451.hp1 HG02622.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.471-975T>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | chr2 | 127568814 | ||||||
| chr2:127568861
|
G | T | 5 | a0001c0010t0001g0270a0001c0010t0001g0271a0001c0018t0001g0272others(2): Show | 5 | HG02451.hp1 HG02622.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.471-928G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | chr2 | 127568861 | ||||||
| chr2:127568862
|
C | T | 5 | a0001c0010t0001g0270a0001c0010t0001g0271a0001c0018t0001g0272others(2): Show | 5 | HG02451.hp1 HG02622.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.471-927C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | chr2 | 127568862 | ||||||
| chr2:127568866
|
C | G | 5 | a0001c0010t0001g0270a0001c0010t0001g0271a0001c0018t0001g0272others(2): Show | 5 | HG02451.hp1 HG02622.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.471-923C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | chr2 | 127568866 | ||||||
| chr2:127568959
|
G | A | 2 | a0014c0072t0001g0009a0024c0073t0001g0065 | 2 | HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.471-830G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | chr2 | 127568959 | ||||||
| chr2:127568973
|
C | T | 1 | a0001c0002t0001g0085 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.471-816C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | chr2 | 127568973 | ||||||
| chr2:127569144
|
G | A | 1 | a0001c0002t0001g0085 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.471-645G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | chr2 | 127569144 | ||||||
| chr2:127569207
|
C | CA | 160 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0032others(157): Show | 163 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.471-562dupA | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | INFO_REALIGN_3_PRIME | chr2 | 127569207 | |||||
| chr2:127569207
|
C | CAA | 13 | a0001c0002t0001g0031a0001c0002t0001g0098a0001c0004t0001g0235others(10): Show | 13 | HG00741.hp1 HG02293.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.471-563_471-562dup others(2): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | INFO_REALIGN_3_PRIME | chr2 | 127569207 | |||||
| chr2:127569207
|
CA | C | 7 | a0001c0010t0001g0262a0002c0001t0001g0183a0002c0001t0001g0184others(4): Show | 7 | HG01168.hp2 HG01169.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.471-562delA | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | INFO_REALIGN_3_PRIME | chr2 | 127569207 | |||||
| chr2:127569282
|
C | T | 1 | a0008c0042t0001g0061 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.471-507C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | chr2 | 127569282 | ||||||
| chr2:127569431
|
C | T | 1 | a0009c0014t0001g0170 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.471-358C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | chr2 | 127569431 | ||||||
| chr2:127569504
|
G | A | 1 | a0001c0002t0001g0134 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.471-285G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | chr2 | 127569504 | ||||||
| chr2:127569522
|
C | T | 3 | a0002c0006t0001g0010a0007c0023t0001g0221a0009c0014t0001g0220 | 3 | HG02109.hp1 HG02818.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.471-267C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 5/47 | chr2 | 127569522 | ||||||
| chr2:127569917
|
A | C | 1 | a0001c0004t0001g0019 | 1 | HG03669.hp2 | splice_region_variant&intron_variant | LOW | c.592+7A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127569917 | ||||||
| chr2:127569923
|
C | G | 1 | a0002c0001t0001g0172 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.592+13C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127569923 | ||||||
| chr2:127569934
|
C | A | 1 | a0007c0024t0001g0261 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.592+24C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127569934 | ||||||
| chr2:127569994
|
T | G | 6 | a0001c0004t0001g0252a0004c0007t0003g0069a0004c0007t0003g0125others(3): Show | 6 | HG00280.hp2 HG00642.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.592+84T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127569994 | ||||||
| chr2:127570091
|
G | A | 1 | a0008c0063t0001g0263 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.592+181G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127570091 | ||||||
| chr2:127570154
|
T | C | 11 | a0001c0002t0001g0141a0001c0002t0001g0142a0001c0005t0002g0062others(8): Show | 12 | HG01175.hp1 HG02257.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.592+244T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127570154 | ||||||
| chr2:127570367
|
G | A | 1 | a0011c0020t0001g0144 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.592+457G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127570367 | ||||||
| chr2:127570527
|
A | G | 1 | a0006c0009t0001g0017 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.592+617A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127570527 | ||||||
| chr2:127570583
|
C | T | 1 | a0001c0018t0001g0272 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.592+673C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127570583 | ||||||
| chr2:127570743
|
C | T | 1 | a0001c0004t0001g0247 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.592+833C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127570743 | ||||||
| chr2:127570783
|
C | T | 7 | a0001c0002t0001g0074a0001c0044t0003g0077a0002c0006t0001g0010others(4): Show | 7 | HG02109.hp1 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.592+873C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127570783 | ||||||
| chr2:127570800
|
C | T | 78 | a0001c0002t0001g0050a0001c0002t0001g0275a0001c0004t0001g0006others(75): Show | 80 | HG00099.hp2 HG00735.hp1 HG00738.hp2 others(77): Show |
intron_variant | MODIFIER | c.592+890C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127570800 | ||||||
| chr2:127570866
|
T | G | 3 | a0001c0005t0002g0128a0001c0010t0001g0136a0008c0063t0001g0263 | 3 | HG02109.hp2 HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.592+956T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127570866 | ||||||
| chr2:127570882
|
T | C | 9 | a0001c0002t0001g0141a0001c0002t0001g0142a0001c0005t0002g0062others(6): Show | 10 | HG01175.hp1 HG02257.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.592+972T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127570882 | ||||||
| chr2:127570970
|
C | T | 1 | a0002c0001t0001g0218 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.592+1060C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127570970 | ||||||
| chr2:127571011
|
C | T | 1 | a0033c0059t0001g0028 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.592+1101C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127571011 | ||||||
| chr2:127571029
|
G | T | 3 | a0001c0005t0002g0128a0001c0010t0001g0136a0008c0063t0001g0263 | 3 | HG02109.hp2 HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.592+1119G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127571029 | ||||||
| chr2:127571190
|
C | T | 5 | a0004c0007t0001g0161a0004c0007t0001g0265a0004c0007t0001g0267others(2): Show | 5 | HG01106.hp2 HG01175.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.592+1280C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127571190 | ||||||
| chr2:127571199
|
C | T | 1 | a0007c0024t0001g0261 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.592+1289C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127571199 | ||||||
| chr2:127571247
|
G | A | 3 | a0001c0005t0002g0128a0001c0010t0001g0136a0008c0063t0001g0263 | 3 | HG02109.hp2 HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.592+1337G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127571247 | ||||||
| chr2:127571261
|
C | A | 256 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(253): Show | 261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.592+1351C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127571261 | ||||||
| chr2:127571410
|
A | G | 5 | a0002c0006t0001g0152a0002c0006t0001g0153a0002c0006t0001g0154others(2): Show | 5 | HG00738.hp1 HG00741.hp2 HG01070.hp2 others(2): Show |
intron_variant | MODIFIER | c.592+1500A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127571410 | ||||||
| chr2:127571442
|
G | GTTTTTT | 12 | a0003c0003t0001g0119a0003c0003t0001g0122a0003c0003t0001g0223others(9): Show | 13 | HG00323.hp1 HG01433.hp1 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.592+1544_592+1549d others(8): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127571442 | |||||
| chr2:127571442
|
G | GTTTTTTT others(3): Show |
20 | a0001c0002t0001g0024a0001c0002t0001g0031a0001c0002t0001g0052others(17): Show | 20 | HG00621.hp2 HG00642.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.592+1540_592+1549d others(12): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127571442 | |||||
| chr2:127571442
|
G | GTTTTTTT others(11): Show |
5 | a0001c0010t0001g0159a0005c0008t0001g0213a0013c0022t0001g0115others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.592+1542_592+1543i others(20): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127571442 | |||||
| chr2:127571442
|
G | GTTTTTTT others(12): Show |
22 | a0001c0013t0001g0002a0001c0013t0001g0162a0001c0013t0001g0163others(19): Show | 23 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.592+1542_592+1543i others(21): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127571442 | |||||
| chr2:127571442
|
G | GTTTTTTT others(13): Show |
13 | a0001c0002t0001g0103a0001c0002t0001g0149a0001c0017t0004g0021others(10): Show | 13 | HG00735.hp2 HG00738.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.592+1542_592+1543i others(22): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127571442 | |||||
| chr2:127571442
|
G | GTTTTTTT others(4): Show |
35 | a0001c0002t0001g0029a0001c0002t0001g0033a0001c0002t0001g0035others(32): Show | 35 | HG01175.hp1 HG01255.hp2 HG01952.hp2 others(32): Show |
intron_variant | MODIFIER | c.592+1539_592+1549d others(13): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127571442 | |||||
| chr2:127571442
|
G | GTTTTTTT others(13): Show |
1 | a0011c0020t0001g0144 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.592+1543_592+1544i others(22): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127571442 | |||||
| chr2:127571442
|
G | GTTTTTTT others(14): Show |
1 | a0011c0020t0001g0145 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.592+1543_592+1544i others(23): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127571442 | |||||
| chr2:127571442
|
G | GTTTTTTT others(5): Show |
7 | a0001c0002t0001g0037a0001c0002t0001g0131a0003c0003t0001g0230others(4): Show | 7 | HG00280.hp1 HG00621.hp1 HG00733.hp1 others(4): Show |
intron_variant | MODIFIER | c.592+1538_592+1549d others(14): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127571442 | |||||
| chr2:127571442
|
G | GTTTTTTT others(6): Show |
2 | a0001c0002t0001g0141a0009c0014t0001g0220 | 2 | HG02257.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.592+1537_592+1549d others(15): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127571442 | |||||
| chr2:127571442
|
G | GTTTTTTT others(9): Show |
2 | a0002c0001t0001g0201a0002c0012t0001g0167 | 2 | NA18941.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.592+1534_592+1549d others(18): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127571442 | |||||
| chr2:127571442
|
G | GTTTTTTT others(10): Show |
2 | a0001c0004t0001g0219a0002c0012t0001g0169 | 2 | HG01192.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.592+1533_592+1549d others(19): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127571442 | |||||
| chr2:127571442
|
G | GTTTTTTT others(11): Show |
16 | a0001c0002t0001g0050a0001c0004t0001g0118a0001c0004t0001g0199others(13): Show | 17 | HG00099.hp2 HG01109.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.592+1549_592+1550i others(20): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127571442 | |||||
| chr2:127571442
|
G | GTTTTTTT others(12): Show |
27 | a0001c0004t0001g0006a0001c0004t0001g0008a0001c0004t0001g0063others(24): Show | 28 | HG00735.hp1 HG00738.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.592+1549_592+1550i others(21): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127571442 | |||||
| chr2:127571442
|
G | GTTTTTTT others(13): Show |
11 | a0002c0001t0001g0068a0002c0001t0001g0109a0002c0001t0001g0185others(8): Show | 11 | HG01358.hp1 HG02132.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.592+1549_592+1550i others(22): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127571442 | |||||
| chr2:127571442
|
G | GTTTTTTT others(14): Show |
6 | a0001c0004t0001g0055a0001c0004t0001g0235a0002c0001t0001g0198others(3): Show | 6 | HG02027.hp1 HG02027.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.592+1549_592+1550i others(23): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127571442 | |||||
| chr2:127571442
|
G | GTTTTTTT others(15): Show |
1 | a0002c0001t0001g0114 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.592+1549_592+1550i others(24): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127571442 | |||||
| chr2:127571442
|
G | GTTTTTTT others(21): Show |
1 | a0047c0028t0001g0197 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.592+1549_592+1550i others(30): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127571442 | |||||
| chr2:127571513
|
T | C | 2 | a0001c0002t0001g0052a0001c0002t0001g0087 | 2 | HG02451.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.592+1603T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127571513 | ||||||
| chr2:127571573
|
T | C | 3 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0001g0268 | 3 | HG00642.hp1 HG02886.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.592+1663T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127571573 | ||||||
| chr2:127571584
|
G | A | 1 | a0007c0024t0001g0261 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.592+1674G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127571584 | ||||||
| chr2:127571606
|
G | A | 3 | a0001c0002t0001g0024a0016c0019t0001g0176a0016c0019t0001g0177 | 3 | HG01099.hp1 HG01169.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.592+1696G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127571606 | ||||||
| chr2:127571668
|
C | T | 1 | a0001c0002t0001g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.592+1758C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127571668 | ||||||
| chr2:127571708
|
G | A | 1 | a0030c0060t0001g0053 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.592+1798G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127571708 | ||||||
| chr2:127571726
|
C | T | 1 | a0007c0024t0001g0261 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.592+1816C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127571726 | ||||||
| chr2:127571727
|
G | A | 28 | a0001c0002t0001g0058a0001c0004t0001g0040a0001c0005t0001g0045others(25): Show | 28 | HG00323.hp2 HG00733.hp2 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.592+1817G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127571727 | ||||||
| chr2:127571760
|
G | A | 3 | a0019c0070t0001g0025a0020c0046t0003g0075a0031c0057t0001g0076 | 3 | HG01891.hp2 HG02257.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.592+1850G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127571760 | ||||||
| chr2:127571887
|
T | C | 2 | a0001c0002t0001g0074a0001c0044t0003g0077 | 2 | HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.592+1977T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127571887 | ||||||
| chr2:127571962
|
T | C | 1 | a0001c0005t0002g0047 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.593-1958T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127571962 | ||||||
| chr2:127571995
|
C | A | 1 | a0006c0009t0001g0088 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.593-1925C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127571995 | ||||||
| chr2:127572021
|
A | G | 1 | a0002c0001t0001g0218 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.593-1899A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127572021 | ||||||
| chr2:127572089
|
G | A | 2 | a0001c0002t0001g0074a0001c0044t0003g0077 | 2 | HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.593-1831G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127572089 | ||||||
| chr2:127572277
|
A | G | 1 | a0018c0041t0004g0073 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.593-1643A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127572277 | ||||||
| chr2:127572349
|
G | A | 1 | a0002c0001t0001g0171 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.593-1571G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127572349 | ||||||
| chr2:127572367
|
C | T | 4 | a0001c0045t0001g0139a0010c0016t0001g0005a0010c0016t0001g0138others(1): Show | 5 | HG02630.hp1 HG02895.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.593-1553C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127572367 | ||||||
| chr2:127572368
|
G | A | 1 | a0007c0023t0001g0126 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.593-1552G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127572368 | ||||||
| chr2:127572416
|
C | CA | 130 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(127): Show | 132 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.593-1489dupA | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127572416 | |||||
| chr2:127572416
|
C | CAA | 10 | a0001c0004t0001g0235a0001c0005t0002g0128a0001c0010t0001g0136others(7): Show | 10 | HG01243.hp1 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.593-1490_593-1489d others(4): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127572416 | |||||
| chr2:127572416
|
C | CAAA | 100 | a0001c0002t0001g0050a0001c0002t0001g0149a0001c0004t0001g0006others(97): Show | 103 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(100): Show |
intron_variant | MODIFIER | c.593-1491_593-1489d others(5): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127572416 | |||||
| chr2:127572468
|
C | CTTTTCTC others(14): Show |
5 | a0003c0003t0001g0121a0003c0003t0001g0123a0004c0007t0003g0007others(2): Show | 5 | HG02132.hp1 HG02602.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.593-1335_593-1315d others(23): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127572468 | |||||
| chr2:127572468
|
C | CTTTTCTC others(56): Show |
1 | a0047c0028t0001g0197 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.593-1377_593-1315d others(65): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127572468 | |||||
| chr2:127572468
|
CTTTTCTC others(14): Show |
C | 10 | a0001c0002t0001g0043a0001c0002t0001g0093a0001c0002t0001g0094others(7): Show | 10 | HG01243.hp2 HG01884.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.593-1335_593-1315d others(23): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127572468 | |||||
| chr2:127572468
|
CTTTTCTC others(35): Show |
C | 6 | a0001c0005t0002g0128a0001c0010t0001g0136a0001c0010t0001g0262others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.593-1356_593-1315d others(44): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127572468 | |||||
| chr2:127572722
|
A | G | 2 | a0014c0072t0001g0009a0024c0073t0001g0065 | 2 | HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.593-1198A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127572722 | ||||||
| chr2:127572750
|
T | TTATC | 2 | a0001c0002t0001g0141a0022c0064t0002g0140 | 2 | HG02257.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.593-1168_593-1165d others(6): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127572750 | |||||
| chr2:127572757
|
C | A | 5 | a0003c0003t0001g0121a0003c0003t0001g0123a0004c0007t0003g0007others(2): Show | 5 | HG02132.hp1 HG02602.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.593-1163C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127572757 | ||||||
| chr2:127572883
|
A | C | 245 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(242): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.593-1037A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127572883 | ||||||
| chr2:127572935
|
C | CA | 81 | a0001c0002t0001g0058a0001c0002t0001g0074a0001c0002t0001g0141others(78): Show | 81 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.593-972dupA | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | INFO_REALIGN_3_PRIME | chr2 | 127572935 | |||||
| chr2:127573300
|
A | G | 1 | a0002c0011t0002g0276 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.593-620A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127573300 | ||||||
| chr2:127573530
|
C | T | 1 | a0001c0002t0001g0141 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.593-390C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127573530 | ||||||
| chr2:127573596
|
C | T | 1 | a0014c0072t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.593-324C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127573596 | ||||||
| chr2:127573752
|
G | T | 1 | a0001c0002t0001g0050 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.593-168G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127573752 | ||||||
| chr2:127573903
|
C | T | 1 | a0002c0006t0001g0011 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.593-17C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127573903 | ||||||
| chr2:127573904
|
G | A | 1 | a0001c0004t0001g0219 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.593-16G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 6/47 | chr2 | 127573904 | ||||||
| chr2:127574069
|
C | G | 1 | a0001c0004t0001g0055 | 1 | HG02027.hp1 | splice_region_variant&intron_variant | LOW | c.735+7C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/47 | chr2 | 127574069 | ||||||
| chr2:127574070
|
C | A | 30 | a0001c0002t0001g0058a0001c0004t0001g0040a0001c0005t0001g0045others(27): Show | 30 | HG00323.hp2 HG00733.hp2 HG01070.hp1 others(27): Show |
splice_region_variant&intron_variant | LOW | c.735+8C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/47 | chr2 | 127574070 | ||||||
| chr2:127574205
|
C | T | 1 | a0011c0036t0001g0151 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.735+143C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/47 | chr2 | 127574205 | ||||||
| chr2:127574405
|
T | C | 1 | a0001c0002t0001g0134 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.735+343T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/47 | chr2 | 127574405 | ||||||
| chr2:127574459
|
G | A | 1 | a0004c0007t0003g0257 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.735+397G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/47 | chr2 | 127574459 | ||||||
| chr2:127574738
|
T | C | 40 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(37): Show | 40 | HG00621.hp2 HG00642.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.735+676T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/47 | chr2 | 127574738 | ||||||
| chr2:127574869
|
C | G | 1 | a0008c0063t0001g0263 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.735+807C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/47 | chr2 | 127574869 | ||||||
| chr2:127574988
|
A | G | 2 | a0001c0005t0003g0046a0007c0025t0001g0039 | 2 | HG03710.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.735+926A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/47 | chr2 | 127574988 | ||||||
| chr2:127574999
|
C | T | 7 | a0001c0017t0004g0021a0001c0017t0004g0022a0001c0017t0004g0071others(4): Show | 7 | HG01891.hp2 HG02257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.735+937C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/47 | chr2 | 127574999 | ||||||
| chr2:127575079
|
G | A | 40 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(37): Show | 40 | HG00621.hp2 HG00642.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.735+1017G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/47 | chr2 | 127575079 | ||||||
| chr2:127575160
|
A | G | 1 | a0008c0042t0001g0061 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.735+1098A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/47 | chr2 | 127575160 | ||||||
| chr2:127575240
|
T | C | 2 | a0001c0002t0001g0074a0001c0044t0003g0077 | 2 | HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.735+1178T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/47 | chr2 | 127575240 | ||||||
| chr2:127575335
|
A | AGT | 3 | a0001c0010t0001g0262a0012c0027t0001g0260a0015c0071t0001g0127 | 3 | HG01891.hp1 HG03195.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.736-1258_736-1257d others(4): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/47 | INFO_REALIGN_3_PRIME | chr2 | 127575335 | |||||
| chr2:127575398
|
C | T | 1 | a0002c0011t0002g0210 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.736-1197C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/47 | chr2 | 127575398 | ||||||
| chr2:127575489
|
T | C | 4 | a0002c0006t0001g0015a0002c0006t0001g0016a0002c0006t0001g0150others(1): Show | 4 | HG00099.hp1 HG01081.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.736-1106T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/47 | chr2 | 127575489 | ||||||
| chr2:127575549
|
C | A | 1 | a0008c0063t0001g0263 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.736-1046C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/47 | chr2 | 127575549 | ||||||
| chr2:127575618
|
A | G | 4 | a0001c0002t0001g0024a0001c0002t0001g0031a0001c0002t0001g0038others(1): Show | 4 | HG01099.hp1 HG01943.hp1 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.736-977A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/47 | chr2 | 127575618 | ||||||
| chr2:127575635
|
T | A | 1 | a0007c0023t0001g0221 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.736-960T>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/47 | chr2 | 127575635 | ||||||
| chr2:127575663
|
G | T | 1 | a0001c0004t0001g0055 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.736-932G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/47 | chr2 | 127575663 | ||||||
| chr2:127575948
|
G | T | 2 | a0009c0014t0001g0170a0009c0014t0001g0220 | 2 | HG02486.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.736-647G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/47 | chr2 | 127575948 | ||||||
| chr2:127576056
|
G | A | 4 | a0002c0001t0001g0198a0004c0007t0003g0007a0004c0007t0003g0249others(1): Show | 4 | HG02132.hp1 HG02148.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.736-539G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/47 | chr2 | 127576056 | ||||||
| chr2:127576107
|
G | A | 33 | a0001c0004t0001g0240a0001c0004t0001g0247a0003c0003t0001g0106others(30): Show | 33 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.736-488G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/47 | chr2 | 127576107 | ||||||
| chr2:127576413
|
G | A | 1 | a0001c0005t0002g0128 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.736-182G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/47 | chr2 | 127576413 | ||||||
| chr2:127576413
|
G | T | 6 | a0004c0007t0001g0158a0004c0007t0001g0161a0004c0007t0001g0265others(3): Show | 6 | HG00735.hp2 HG01106.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.736-182G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 7/47 | chr2 | 127576413 | ||||||
| chr2:127576727
|
G | A | 1 | a0003c0003t0001g0237 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.849+19G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 8/47 | chr2 | 127576727 | ||||||
| chr2:127576770
|
G | T | 1 | a0007c0023t0001g0126 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.849+62G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 8/47 | chr2 | 127576770 | ||||||
| chr2:127576780
|
C | T | 5 | a0004c0007t0001g0161a0004c0007t0001g0265a0004c0007t0001g0267others(2): Show | 5 | HG01106.hp2 HG01175.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.849+72C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 8/47 | chr2 | 127576780 | ||||||
| chr2:127576817
|
C | T | 1 | a0001c0068t0001g0089 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.849+109C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 8/47 | chr2 | 127576817 | ||||||
| chr2:127576838
|
C | T | 40 | a0001c0004t0001g0240a0001c0005t0003g0046a0003c0003t0001g0030others(37): Show | 41 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.849+130C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 8/47 | chr2 | 127576838 | ||||||
| chr2:127576851
|
C | T | 5 | a0002c0001t0001g0114a0002c0001t0001g0192a0002c0001t0001g0193others(2): Show | 5 | HG01081.hp1 HG01358.hp1 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.849+143C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 8/47 | chr2 | 127576851 | ||||||
| chr2:127576866
|
G | C | 1 | a0028c0051t0001g0227 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.849+158G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 8/47 | chr2 | 127576866 | ||||||
| chr2:127576887
|
G | A | 1 | a0001c0002t0001g0058 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.849+179G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 8/47 | chr2 | 127576887 | ||||||
| chr2:127576895
|
C | T | 62 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(59): Show | 63 | HG00099.hp1 HG00642.hp1 HG00738.hp1 others(60): Show |
intron_variant | MODIFIER | c.849+187C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 8/47 | chr2 | 127576895 | ||||||
| chr2:127576922
|
C | T | 1 | a0002c0006t0007g0175 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.849+214C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 8/47 | chr2 | 127576922 | ||||||
| chr2:127576951
|
A | G | 76 | a0001c0002t0001g0141a0001c0004t0001g0006a0001c0004t0001g0008others(73): Show | 78 | HG00099.hp2 HG00735.hp1 HG00738.hp2 others(75): Show |
intron_variant | MODIFIER | c.849+243A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 8/47 | chr2 | 127576951 | ||||||
| chr2:127576991
|
G | C | 1 | a0001c0005t0002g0062 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.849+283G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 8/47 | chr2 | 127576991 | ||||||
| chr2:127577148
|
C | A | 1 | a0003c0026t0001g0143 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.849+440C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 8/47 | chr2 | 127577148 | ||||||
| chr2:127577164
|
G | A | 3 | a0001c0002t0001g0093a0001c0002t0001g0094a0001c0061t0001g0096 | 3 | HG02818.hp1 HG02896.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.849+456G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 8/47 | chr2 | 127577164 | ||||||
| chr2:127577271
|
C | T | 1 | a0001c0005t0002g0062 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.849+563C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 8/47 | chr2 | 127577271 | ||||||
| chr2:127577302
|
C | T | 2 | a0014c0072t0001g0009a0024c0073t0001g0065 | 2 | HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.849+594C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 8/47 | chr2 | 127577302 | ||||||
| chr2:127577338
|
G | A | 1 | a0001c0002t0001g0134 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.849+630G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 8/47 | chr2 | 127577338 | ||||||
| chr2:127577388
|
C | T | 3 | a0007c0023t0001g0221a0007c0024t0001g0261a0014c0053t0001g0277 | 3 | HG02109.hp1 HG02572.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.849+680C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 8/47 | chr2 | 127577388 | ||||||
| chr2:127577554
|
C | T | 1 | a0002c0001t0001g0184 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.850-579C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 8/47 | chr2 | 127577554 | ||||||
| chr2:127577633
|
C | T | 1 | a0007c0023t0001g0126 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.850-500C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 8/47 | chr2 | 127577633 | ||||||
| chr2:127577696
|
C | T | 3 | a0003c0003t0001g0116a0003c0003t0001g0214a0035c0067t0001g0117 | 3 | HG01109.hp1 HG01433.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.850-437C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 8/47 | chr2 | 127577696 | ||||||
| chr2:127577697
|
G | A | 9 | a0001c0010t0001g0135a0001c0010t0001g0136a0001c0010t0001g0270others(6): Show | 9 | HG02109.hp2 HG02451.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.850-436G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 8/47 | chr2 | 127577697 | ||||||
| chr2:127577806
|
T | C | 83 | a0001c0002t0001g0058a0001c0004t0001g0040a0001c0004t0001g0240others(80): Show | 84 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.850-327T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 8/47 | chr2 | 127577806 | ||||||
| chr2:127577875
|
C | T | 1 | a0001c0005t0002g0051 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.850-258C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 8/47 | chr2 | 127577875 | ||||||
| chr2:127577896
|
GAGA | G | 5 | a0001c0002t0001g0141a0001c0005t0002g0062a0007c0023t0001g0221others(2): Show | 5 | HG02109.hp1 HG02257.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.850-231_850-229del others(3): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 8/47 | INFO_REALIGN_3_PRIME | chr2 | 127577896 | |||||
| chr2:127578304
|
C | G | 1 | a0001c0005t0002g0062 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1003+18C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127578304 | ||||||
| chr2:127578444
|
TC | T | 9 | a0001c0010t0001g0135a0001c0010t0001g0136a0001c0010t0001g0270others(6): Show | 9 | HG02109.hp2 HG02451.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1003+159delC | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127578444 | ||||||
| chr2:127578483
|
C | A | 1 | a0007c0023t0001g0126 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1003+197C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127578483 | ||||||
| chr2:127578509
|
C | T | 1 | a0006c0009t0001g0054 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1003+223C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127578509 | ||||||
| chr2:127578569
|
A | T | 1 | a0036c0043t0001g0027 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1003+283A>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127578569 | ||||||
| chr2:127578614
|
T | C | 264 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(261): Show | 269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.1003+328T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127578614 | ||||||
| chr2:127578652
|
C | G | 9 | a0001c0002t0001g0043a0001c0002t0001g0093a0001c0002t0001g0094others(6): Show | 9 | HG00642.hp1 HG02647.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1003+366C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127578652 | ||||||
| chr2:127578653
|
C | A | 1 | a0036c0043t0001g0027 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1003+367C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127578653 | ||||||
| chr2:127578692
|
A | G | 255 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(252): Show | 259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.1003+406A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127578692 | ||||||
| chr2:127578766
|
G | C | 1 | a0007c0023t0001g0126 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1003+480G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127578766 | ||||||
| chr2:127578975
|
C | T | 1 | a0001c0002t0001g0134 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1003+689C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127578975 | ||||||
| chr2:127578976
|
A | G | 259 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(256): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.1003+690A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127578976 | ||||||
| chr2:127579013
|
A | T | 9 | a0001c0010t0001g0135a0001c0010t0001g0136a0001c0010t0001g0270others(6): Show | 9 | HG02109.hp2 HG02451.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1003+727A>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127579013 | ||||||
| chr2:127579022
|
A | C | 4 | a0001c0017t0004g0021a0001c0017t0004g0022a0001c0017t0004g0071others(1): Show | 4 | HG02258.hp2 HG02630.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1003+736A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127579022 | ||||||
| chr2:127579113
|
T | G | 83 | a0001c0002t0001g0058a0001c0004t0001g0040a0001c0004t0001g0240others(80): Show | 84 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.1003+827T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127579113 | ||||||
| chr2:127579231
|
G | C | 184 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(181): Show | 186 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.1003+945G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127579231 | ||||||
| chr2:127579346
|
T | C | 1 | a0001c0044t0003g0077 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1003+1060T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127579346 | ||||||
| chr2:127579381
|
C | T | 7 | a0001c0002t0001g0149a0002c0011t0002g0276a0008c0015t0001g0044others(4): Show | 7 | HG01243.hp2 HG01884.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1003+1095C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127579381 | ||||||
| chr2:127579382
|
A | G | 259 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(256): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.1003+1096A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127579382 | ||||||
| chr2:127579491
|
C | T | 1 | a0001c0005t0002g0062 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1003+1205C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127579491 | ||||||
| chr2:127579574
|
A | ATTTG | 160 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(157): Show | 162 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.1004-1148_1004-114 others(8): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | INFO_REALIGN_3_PRIME | chr2 | 127579574 | |||||
| chr2:127579574
|
A | ATTTGTTT others(1): Show |
3 | a0001c0002t0001g0134a0015c0066t0001g0064a0020c0046t0003g0075 | 3 | HG01884.hp1 HG01891.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1004-1152_1004-114 others(12): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | INFO_REALIGN_3_PRIME | chr2 | 127579574 | |||||
| chr2:127579574
|
A | ATTTGTTT others(5): Show |
1 | a0001c0005t0002g0128 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1004-1156_1004-114 others(16): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | INFO_REALIGN_3_PRIME | chr2 | 127579574 | |||||
| chr2:127579574
|
ATTTG | A | 10 | a0001c0002t0001g0141a0001c0005t0002g0062a0001c0045t0001g0139others(7): Show | 11 | HG02109.hp1 HG02257.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1004-1148_1004-114 others(8): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | INFO_REALIGN_3_PRIME | chr2 | 127579574 | |||||
| chr2:127579700
|
C | G | 1 | a0001c0002t0001g0050 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1004-1046C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127579700 | ||||||
| chr2:127579841
|
C | T | 1 | a0002c0006t0001g0010 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1004-905C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127579841 | ||||||
| chr2:127579931
|
G | A | 1 | a0001c0058t0002g0100 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1004-815G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127579931 | ||||||
| chr2:127579937
|
A | G | 153 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(150): Show | 155 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.1004-809A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127579937 | ||||||
| chr2:127579970
|
C | T | 16 | a0001c0002t0001g0134a0001c0002t0001g0141a0001c0002t0001g0149others(13): Show | 16 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1004-776C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127579970 | ||||||
| chr2:127580046
|
A | C | 1 | a0007c0023t0001g0126 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1004-700A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127580046 | ||||||
| chr2:127580122
|
C | G | 1 | a0015c0066t0001g0064 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1004-624C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127580122 | ||||||
| chr2:127580170
|
A | C | 1 | a0009c0014t0001g0133 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1004-576A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127580170 | ||||||
| chr2:127580204
|
G | A | 2 | a0002c0001t0001g0114a0002c0011t0002g0210 | 2 | HG02071.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1004-542G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127580204 | ||||||
| chr2:127580206
|
C | A | 9 | a0001c0010t0001g0135a0001c0010t0001g0136a0001c0010t0001g0270others(6): Show | 9 | HG02109.hp2 HG02451.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1004-540C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127580206 | ||||||
| chr2:127580583
|
G | A | 2 | a0001c0002t0001g0085a0045c0037t0001g0216 | 2 | HG02145.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.1004-163G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127580583 | ||||||
| chr2:127580627
|
C | T | 2 | a0003c0003t0001g0121a0003c0003t0001g0123 | 2 | HG02602.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1004-119C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127580627 | ||||||
| chr2:127580628
|
G | A | 11 | a0001c0010t0001g0135a0001c0010t0001g0136a0001c0010t0001g0270others(8): Show | 11 | HG02109.hp2 HG02257.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1004-118G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 9/47 | chr2 | 127580628 | ||||||
| chr2:127580923
|
C | T | 3 | a0001c0002t0001g0141a0022c0064t0002g0140a0023c0048t0001g0129 | 3 | HG02257.hp1 HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1080+101C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 10/47 | chr2 | 127580923 | ||||||
| chr2:127580924
|
C | CA | 9 | a0001c0002t0001g0043a0001c0002t0001g0093a0001c0002t0001g0094others(6): Show | 9 | HG00642.hp1 HG02647.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1080+103dupA | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 10/47 | INFO_REALIGN_3_PRIME | chr2 | 127580924 | |||||
| chr2:127580944
|
T | G | 75 | a0001c0004t0001g0006a0001c0004t0001g0008a0001c0004t0001g0055others(72): Show | 78 | HG00099.hp2 HG00621.hp1 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.1080+122T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 10/47 | chr2 | 127580944 | ||||||
| chr2:127580959
|
C | G | 3 | a0005c0008t0001g0001a0005c0008t0001g0147a0005c0008t0001g0148 | 4 | HG02717.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1080+137C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 10/47 | chr2 | 127580959 | ||||||
| chr2:127581138
|
C | T | 7 | a0001c0002t0001g0149a0002c0011t0002g0276a0008c0015t0001g0044others(4): Show | 7 | HG01243.hp2 HG01884.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1080+316C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 10/47 | chr2 | 127581138 | ||||||
| chr2:127581139
|
A | G | 105 | a0001c0002t0001g0134a0001c0002t0001g0141a0001c0002t0001g0149others(102): Show | 108 | HG00099.hp2 HG00621.hp1 HG00735.hp1 others(105): Show |
intron_variant | MODIFIER | c.1080+317A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 10/47 | chr2 | 127581139 | ||||||
| chr2:127581166
|
T | C | 78 | a0001c0004t0001g0006a0001c0004t0001g0008a0001c0004t0001g0055others(75): Show | 81 | HG00099.hp2 HG00621.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.1080+344T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 10/47 | chr2 | 127581166 | ||||||
| chr2:127581203
|
C | T | 1 | a0019c0070t0001g0025 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1080+381C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 10/47 | chr2 | 127581203 | ||||||
| chr2:127581222
|
G | T | 3 | a0005c0008t0001g0001a0005c0008t0001g0147a0005c0008t0001g0148 | 4 | HG02717.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1080+400G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 10/47 | chr2 | 127581222 | ||||||
| chr2:127581307
|
A | C | 1 | a0001c0002t0001g0131 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1080+485A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 10/47 | chr2 | 127581307 | ||||||
| chr2:127581486
|
G | A | 3 | a0007c0023t0001g0221a0007c0024t0001g0261a0014c0053t0001g0277 | 3 | HG02109.hp1 HG02572.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1081-405G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 10/47 | chr2 | 127581486 | ||||||
| chr2:127581590
|
G | T | 1 | a0002c0006t0001g0150 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1081-301G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 10/47 | chr2 | 127581590 | ||||||
| chr2:127581636
|
A | G | 272 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(269): Show | 277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.1081-255A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 10/47 | chr2 | 127581636 | ||||||
| chr2:127581651
|
G | C | 78 | a0001c0004t0001g0006a0001c0004t0001g0008a0001c0004t0001g0055others(75): Show | 81 | HG00099.hp2 HG00621.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.1081-240G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 10/47 | chr2 | 127581651 | ||||||
| chr2:127581710
|
G | A | 7 | a0001c0002t0001g0149a0002c0011t0002g0276a0008c0015t0001g0044others(4): Show | 7 | HG01243.hp2 HG01884.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1081-181G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 10/47 | chr2 | 127581710 | ||||||
| chr2:127581800
|
C | T | 4 | a0001c0044t0003g0077a0001c0045t0001g0139a0010c0016t0001g0005others(1): Show | 5 | HG02630.hp1 HG02809.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1081-91C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 10/47 | chr2 | 127581800 | ||||||
| chr2:127581864
|
C | T | 4 | a0001c0002t0001g0141a0001c0005t0002g0128a0022c0064t0002g0140others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1081-27C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 10/47 | chr2 | 127581864 | ||||||
| chr2:127581881
|
G | T | 70 | a0001c0004t0001g0006a0001c0004t0001g0008a0001c0004t0001g0055others(67): Show | 72 | HG00099.hp2 HG00621.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.1081-10G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 10/47 | chr2 | 127581881 | ||||||
| chr2:127582183
|
C | G | 154 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(151): Show | 156 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.1201-121C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 11/47 | chr2 | 127582183 | ||||||
| chr2:127582211
|
G | A | 1 | a0001c0005t0002g0051 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1201-93G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 11/47 | chr2 | 127582211 | ||||||
| chr2:127582256
|
C | T | 2 | a0001c0004t0001g0006a0001c0004t0001g0008 | 2 | NA18980.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1201-48C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 11/47 | chr2 | 127582256 | ||||||
| chr2:127582468
|
G | A | 10 | a0001c0005t0002g0060a0001c0005t0002g0090a0001c0005t0002g0092others(7): Show | 10 | HG01070.hp1 HG01516.hp1 HG02165.hp2 others(7): Show |
intron_variant | MODIFIER | c.1343+22G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 12/47 | chr2 | 127582468 | ||||||
| chr2:127582535
|
G | A | 1 | a0041c0030t0001g0205 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1343+89G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 12/47 | chr2 | 127582535 | ||||||
| chr2:127582551
|
G | A | 1 | a0009c0014t0001g0133 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1343+105G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 12/47 | chr2 | 127582551 | ||||||
| chr2:127582678
|
T | C | 259 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(256): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.1343+232T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 12/47 | chr2 | 127582678 | ||||||
| chr2:127582702
|
T | C | 1 | a0003c0003t0001g0229 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1343+256T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 12/47 | chr2 | 127582702 | ||||||
| chr2:127582741
|
CAG | C | 154 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(151): Show | 156 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.1343+297_1343+298d others(4): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 12/47 | INFO_REALIGN_3_PRIME | chr2 | 127582741 | |||||
| chr2:127582975
|
G | T | 154 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(151): Show | 156 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.1343+529G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 12/47 | chr2 | 127582975 | ||||||
| chr2:127582996
|
G | T | 1 | a0002c0001t0001g0181 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1343+550G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 12/47 | chr2 | 127582996 | ||||||
| chr2:127583033
|
T | G | 3 | a0007c0023t0001g0221a0007c0024t0001g0261a0014c0053t0001g0277 | 3 | HG02109.hp1 HG02572.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1343+587T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 12/47 | chr2 | 127583033 | ||||||
| chr2:127583076
|
G | A | 1 | a0012c0027t0001g0080 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1343+630G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 12/47 | chr2 | 127583076 | ||||||
| chr2:127583146
|
T | A | 8 | a0002c0001t0001g0178a0002c0001t0001g0179a0002c0001t0001g0181others(5): Show | 8 | HG01168.hp2 HG01257.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.1343+700T>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 12/47 | chr2 | 127583146 | ||||||
| chr2:127583157
|
G | C | 2 | a0007c0024t0001g0261a0014c0053t0001g0277 | 2 | HG02572.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1343+711G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 12/47 | chr2 | 127583157 | ||||||
| chr2:127583191
|
C | T | 1 | a0007c0023t0001g0126 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1343+745C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 12/47 | chr2 | 127583191 | ||||||
| chr2:127583224
|
C | T | 1 | a0002c0006t0001g0010 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1343+778C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 12/47 | chr2 | 127583224 | ||||||
| chr2:127583280
|
G | A | 59 | a0001c0002t0001g0043a0001c0002t0001g0052a0001c0002t0001g0058others(56): Show | 60 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.1343+834G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 12/47 | chr2 | 127583280 | ||||||
| chr2:127583286
|
C | A | 1 | a0007c0023t0001g0126 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1344-836C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 12/47 | chr2 | 127583286 | ||||||
| chr2:127583326
|
C | T | 75 | a0001c0004t0001g0006a0001c0004t0001g0008a0001c0004t0001g0055others(72): Show | 78 | HG00099.hp2 HG00621.hp1 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.1344-796C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 12/47 | chr2 | 127583326 | ||||||
| chr2:127583327
|
G | A | 1 | a0002c0006t0001g0011 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1344-795G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 12/47 | chr2 | 127583327 | ||||||
| chr2:127583347
|
G | A | 2 | a0014c0072t0001g0009a0024c0073t0001g0065 | 2 | HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1344-775G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 12/47 | chr2 | 127583347 | ||||||
| chr2:127583415
|
G | A | 1 | a0004c0007t0003g0249 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1344-707G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 12/47 | chr2 | 127583415 | ||||||
| chr2:127583436
|
G | A | 1 | a0004c0054t0001g0160 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1344-686G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 12/47 | chr2 | 127583436 | ||||||
| chr2:127583567
|
C | G | 70 | a0001c0004t0001g0006a0001c0004t0001g0008a0001c0004t0001g0055others(67): Show | 72 | HG00099.hp2 HG00621.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.1344-555C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 12/47 | chr2 | 127583567 | ||||||
| chr2:127583910
|
G | T | 16 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(13): Show | 16 | HG01099.hp1 HG01943.hp1 HG01952.hp2 others(13): Show |
intron_variant | MODIFIER | c.1344-212G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 12/47 | chr2 | 127583910 | ||||||
| chr2:127583956
|
AGT | A | 75 | a0001c0004t0001g0006a0001c0004t0001g0008a0001c0004t0001g0055others(72): Show | 78 | HG00099.hp2 HG00621.hp1 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.1344-162_1344-161d others(4): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 12/47 | INFO_REALIGN_3_PRIME | chr2 | 127583956 | |||||
| chr2:127584028
|
T | G | 75 | a0001c0004t0001g0006a0001c0004t0001g0008a0001c0004t0001g0055others(72): Show | 78 | HG00099.hp2 HG00621.hp1 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.1344-94T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 12/47 | chr2 | 127584028 | ||||||
| chr2:127584446
|
T | C | 1 | a0001c0002t0001g0134 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1554+114T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 13/47 | chr2 | 127584446 | ||||||
| chr2:127584650
|
T | C | 7 | a0001c0002t0001g0149a0002c0011t0002g0276a0008c0015t0001g0044others(4): Show | 7 | HG01243.hp2 HG01884.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1555-128T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 13/47 | chr2 | 127584650 | ||||||
| chr2:127584972
|
G | A | 259 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(256): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.1690+59G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127584972 | ||||||
| chr2:127585100
|
A | G | 76 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(73): Show | 77 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.1690+187A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127585100 | ||||||
| chr2:127585160
|
T | C | 70 | a0001c0004t0001g0006a0001c0004t0001g0008a0001c0004t0001g0055others(67): Show | 72 | HG00099.hp2 HG00621.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.1690+247T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127585160 | ||||||
| chr2:127585232
|
C | T | 30 | a0001c0004t0001g0040a0001c0005t0001g0045a0001c0005t0001g0095others(27): Show | 30 | HG01070.hp1 HG01256.hp1 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.1690+319C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127585232 | ||||||
| chr2:127585290
|
C | G | 1 | a0031c0057t0001g0076 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1690+377C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127585290 | ||||||
| chr2:127585343
|
T | C | 1 | a0002c0001t0001g0174 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1690+430T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127585343 | ||||||
| chr2:127585452
|
T | C | 3 | a0001c0010t0001g0159a0013c0022t0001g0115a0013c0022t0001g0212 | 3 | HG01069.hp1 HG01071.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.1690+539T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127585452 | ||||||
| chr2:127585732
|
C | T | 1 | a0001c0002t0001g0134 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1690+819C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127585732 | ||||||
| chr2:127585790
|
C | T | 1 | a0006c0009t0001g0048 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1690+877C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127585790 | ||||||
| chr2:127585969
|
A | G | 1 | a0002c0011t0002g0196 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1690+1056A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127585969 | ||||||
| chr2:127585990
|
A | C | 2 | a0002c0001t0001g0207a0002c0001t0001g0208 | 2 | NA18947.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.1690+1077A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127585990 | ||||||
| chr2:127585991
|
A | T | 16 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(13): Show | 16 | HG01099.hp1 HG01943.hp1 HG01952.hp2 others(13): Show |
intron_variant | MODIFIER | c.1690+1078A>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127585991 | ||||||
| chr2:127586194
|
G | A | 10 | a0001c0002t0001g0103a0001c0013t0001g0002a0001c0013t0001g0162others(7): Show | 11 | HG00735.hp2 HG01106.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.1690+1281G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127586194 | ||||||
| chr2:127586234
|
T | C | 1 | a0007c0024t0001g0083 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1690+1321T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127586234 | ||||||
| chr2:127586487
|
T | A | 7 | a0001c0002t0001g0149a0002c0011t0002g0276a0008c0015t0001g0044others(4): Show | 7 | HG01243.hp2 HG01884.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1690+1574T>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127586487 | ||||||
| chr2:127586784
|
C | T | 1 | a0007c0023t0001g0126 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1691-1608C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127586784 | ||||||
| chr2:127586785
|
T | C | 1 | a0007c0023t0001g0126 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1691-1607T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127586785 | ||||||
| chr2:127586814
|
G | T | 10 | a0001c0010t0001g0135a0001c0010t0001g0136a0001c0010t0001g0270others(7): Show | 10 | HG02109.hp2 HG02257.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1691-1578G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127586814 | ||||||
| chr2:127586854
|
C | A | 1 | a0007c0025t0001g0039 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1691-1538C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127586854 | ||||||
| chr2:127586907
|
T | C | 70 | a0001c0004t0001g0006a0001c0004t0001g0008a0001c0004t0001g0055others(67): Show | 72 | HG00099.hp2 HG00621.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.1691-1485T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127586907 | ||||||
| chr2:127587265
|
G | A | 3 | a0001c0002t0001g0058a0006c0009t0001g0056a0006c0009t0001g0057 | 3 | HG01106.hp1 HG03239.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1691-1127G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127587265 | ||||||
| chr2:127587293
|
G | A | 2 | a0001c0002t0001g0149a0002c0011t0002g0276 | 2 | HG01884.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1691-1099G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127587293 | ||||||
| chr2:127587523
|
T | C | 259 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(256): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.1691-869T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127587523 | ||||||
| chr2:127587545
|
C | A | 1 | a0007c0025t0001g0039 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1691-847C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127587545 | ||||||
| chr2:127587568
|
C | CT | 26 | a0001c0002t0001g0036a0001c0002t0001g0038a0001c0002t0001g0058others(23): Show | 27 | HG01175.hp2 HG01884.hp2 HG01981.hp2 others(24): Show |
intron_variant | MODIFIER | c.1691-806dupT | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | INFO_REALIGN_3_PRIME | chr2 | 127587568 | |||||
| chr2:127587568
|
CT | C | 72 | a0001c0004t0001g0006a0001c0004t0001g0008a0001c0004t0001g0055others(69): Show | 74 | HG00099.hp2 HG00621.hp1 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.1691-806delT | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | INFO_REALIGN_3_PRIME | chr2 | 127587568 | |||||
| chr2:127587572
|
T | C | 1 | a0001c0013t0001g0086 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1691-820T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127587572 | ||||||
| chr2:127587625
|
A | G | 2 | a0002c0012t0001g0112a0002c0012t0001g0194 | 2 | NA19000.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1691-767A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127587625 | ||||||
| chr2:127587694
|
G | A | 4 | a0001c0044t0003g0077a0001c0045t0001g0139a0010c0016t0001g0005others(1): Show | 5 | HG02630.hp1 HG02809.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1691-698G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127587694 | ||||||
| chr2:127587881
|
T | C | 3 | a0001c0010t0001g0135a0001c0010t0001g0136a0009c0014t0001g0101 | 3 | HG02109.hp2 HG02572.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1691-511T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127587881 | ||||||
| chr2:127587939
|
A | T | 2 | a0002c0006t0001g0015a0002c0006t0001g0016 | 2 | HG00099.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.1691-453A>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127587939 | ||||||
| chr2:127588146
|
A | G | 2 | a0002c0001t0001g0173a0025c0056t0001g0264 | 2 | NA18995.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1691-246A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127588146 | ||||||
| chr2:127588191
|
T | C | 1 | a0007c0023t0001g0126 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1691-201T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127588191 | ||||||
| chr2:127588385
|
T | C | 87 | a0001c0002t0001g0134a0001c0002t0001g0141a0001c0002t0001g0149others(84): Show | 90 | HG00099.hp2 HG00621.hp1 HG00735.hp1 others(87): Show |
splice_region_variant&intron_variant | LOW | c.1691-7T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 14/47 | chr2 | 127588385 | ||||||
| chr2:127588588
|
C | A | 1 | a0001c0004t0001g0240 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1854+33C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 15/47 | chr2 | 127588588 | ||||||
| chr2:127588653
|
A | C | 259 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(256): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.1854+98A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 15/47 | chr2 | 127588653 | ||||||
| chr2:127588791
|
G | T | 3 | a0009c0014t0001g0170a0009c0014t0001g0220a0032c0065t0001g0137 | 3 | HG02486.hp2 HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1854+236G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 15/47 | chr2 | 127588791 | ||||||
| chr2:127588877
|
T | C | 1 | a0019c0070t0001g0025 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1854+322T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 15/47 | chr2 | 127588877 | ||||||
| chr2:127588889
|
ATGGATGG others(9): Show |
A | 4 | a0001c0002t0001g0141a0001c0005t0002g0128a0022c0064t0002g0140others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1854+346_1854+361d others(18): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 15/47 | INFO_REALIGN_3_PRIME | chr2 | 127588889 | |||||
| chr2:127589031
|
A | G | 3 | a0002c0012t0001g0167a0002c0012t0001g0169a0017c0040t0001g0190 | 3 | NA18941.hp1 NA18959.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1854+476A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 15/47 | chr2 | 127589031 | ||||||
| chr2:127589086
|
G | C | 7 | a0001c0002t0001g0093a0001c0002t0001g0094a0001c0002t0001g0097others(4): Show | 7 | HG00642.hp1 HG02717.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1854+531G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 15/47 | chr2 | 127589086 | ||||||
| chr2:127589139
|
G | A | 3 | a0007c0023t0001g0221a0007c0024t0001g0261a0014c0053t0001g0277 | 3 | HG02109.hp1 HG02572.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1854+584G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 15/47 | chr2 | 127589139 | ||||||
| chr2:127589267
|
A | ATGGATGG others(5): Show |
1 | a0001c0002t0001g0134 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1854+728_1854+739d others(14): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 15/47 | INFO_REALIGN_3_PRIME | chr2 | 127589267 | |||||
| chr2:127589429
|
A | G | 1 | a0044c0034t0001g0067 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1855-663A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 15/47 | chr2 | 127589429 | ||||||
| chr2:127589462
|
G | A | 4 | a0002c0006t0001g0015a0002c0006t0001g0016a0002c0006t0001g0150others(1): Show | 4 | HG00099.hp1 HG01081.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.1855-630G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 15/47 | chr2 | 127589462 | ||||||
| chr2:127589788
|
G | A | 1 | a0001c0002t0001g0098 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1855-304G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 15/47 | chr2 | 127589788 | ||||||
| chr2:127589796
|
G | A | 3 | a0001c0010t0001g0159a0013c0022t0001g0115a0013c0022t0001g0212 | 3 | HG01069.hp1 HG01071.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.1855-296G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 15/47 | chr2 | 127589796 | ||||||
| chr2:127589851
|
G | A | 24 | a0001c0004t0001g0040a0001c0005t0001g0045a0001c0005t0001g0095others(21): Show | 24 | HG01070.hp1 HG01256.hp1 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.1855-241G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 15/47 | chr2 | 127589851 | ||||||
| chr2:127589876
|
G | A | 3 | a0001c0045t0001g0139a0010c0016t0001g0005a0010c0016t0001g0138 | 4 | HG02630.hp1 HG02895.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1855-216G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 15/47 | chr2 | 127589876 | ||||||
| chr2:127590010
|
G | A | 1 | a0002c0011t0002g0200 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1855-82G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 15/47 | chr2 | 127590010 | ||||||
| chr2:127590272
|
G | A | 6 | a0003c0003t0001g0228a0003c0003t0001g0269a0003c0026t0001g0143others(3): Show | 6 | NA18941.hp2 NA18972.hp1 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1992+43G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 16/47 | chr2 | 127590272 | ||||||
| chr2:127590399
|
G | T | 4 | a0009c0014t0001g0170a0009c0014t0001g0220a0020c0046t0003g0075others(1): Show | 4 | HG01891.hp2 HG02486.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1992+170G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 16/47 | chr2 | 127590399 | ||||||
| chr2:127590470
|
G | A | 4 | a0001c0044t0003g0077a0001c0045t0001g0139a0010c0016t0001g0005others(1): Show | 5 | HG02630.hp1 HG02809.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1992+241G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 16/47 | chr2 | 127590470 | ||||||
| chr2:127590616
|
A | C | 275 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(272): Show | 280 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.1992+387A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 16/47 | chr2 | 127590616 | ||||||
| chr2:127590673
|
G | A | 1 | a0044c0034t0001g0067 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1992+444G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 16/47 | chr2 | 127590673 | ||||||
| chr2:127590755
|
G | A | 1 | a0007c0023t0001g0126 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1992+526G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 16/47 | chr2 | 127590755 | ||||||
| chr2:127590905
|
G | A | 3 | a0001c0045t0001g0139a0010c0016t0001g0005a0010c0016t0001g0138 | 4 | HG02630.hp1 HG02895.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1992+676G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 16/47 | chr2 | 127590905 | ||||||
| chr2:127591060
|
G | A | 8 | a0007c0023t0001g0221a0007c0024t0001g0261a0008c0015t0001g0044others(5): Show | 8 | HG01243.hp2 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1992+831G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 16/47 | chr2 | 127591060 | ||||||
| chr2:127591203
|
A | G | 259 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(256): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.1992+974A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 16/47 | chr2 | 127591203 | ||||||
| chr2:127591369
|
C | T | 24 | a0001c0004t0001g0040a0001c0005t0001g0045a0001c0005t0001g0095others(21): Show | 24 | HG01070.hp1 HG01256.hp1 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.1992+1140C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 16/47 | chr2 | 127591369 | ||||||
| chr2:127591403
|
A | G | 3 | a0007c0023t0001g0221a0007c0024t0001g0261a0014c0053t0001g0277 | 3 | HG02109.hp1 HG02572.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1992+1174A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 16/47 | chr2 | 127591403 | ||||||
| chr2:127591608
|
C | T | 1 | a0027c0052t0001g0084 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1993-1186C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 16/47 | chr2 | 127591608 | ||||||
| chr2:127592070
|
C | T | 1 | a0001c0002t0001g0098 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1993-724C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 16/47 | chr2 | 127592070 | ||||||
| chr2:127592237
|
A | C | 1 | a0007c0023t0001g0126 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1993-557A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 16/47 | chr2 | 127592237 | ||||||
| chr2:127592423
|
A | T | 6 | a0004c0007t0001g0158a0004c0007t0001g0161a0004c0007t0001g0265others(3): Show | 6 | HG00735.hp2 HG01106.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.1993-371A>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 16/47 | chr2 | 127592423 | ||||||
| chr2:127592431
|
A | T | 3 | a0001c0010t0001g0135a0001c0010t0001g0136a0009c0014t0001g0101 | 3 | HG02109.hp2 HG02572.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1993-363A>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 16/47 | chr2 | 127592431 | ||||||
| chr2:127592572
|
C | T | 1 | a0001c0002t0001g0024 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1993-222C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 16/47 | chr2 | 127592572 | ||||||
| chr2:127592775
|
G | A | 5 | a0008c0015t0001g0044a0008c0015t0001g0104a0008c0015t0001g0164others(2): Show | 5 | HG01243.hp2 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1993-19G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 16/47 | chr2 | 127592775 | ||||||
| chr2:127592976
|
G | A | 153 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(150): Show | 155 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.2145+30G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 17/47 | chr2 | 127592976 | ||||||
| chr2:127593003
|
T | TG | 273 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(270): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.2145+59dupG | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 17/47 | INFO_REALIGN_3_PRIME | chr2 | 127593003 | |||||
| chr2:127593034
|
C | G | 2 | a0001c0002t0001g0149a0002c0011t0002g0276 | 2 | HG01884.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2145+88C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 17/47 | chr2 | 127593034 | ||||||
| chr2:127593054
|
C | G | 1 | a0002c0001t0001g0203 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2145+108C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 17/47 | chr2 | 127593054 | ||||||
| chr2:127593119
|
C | G | 1 | a0003c0003t0001g0222 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2145+173C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 17/47 | chr2 | 127593119 | ||||||
| chr2:127593169
|
C | A | 185 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(182): Show | 187 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.2145+223C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 17/47 | chr2 | 127593169 | ||||||
| chr2:127593233
|
C | T | 201 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(198): Show | 204 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.2145+287C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 17/47 | chr2 | 127593233 | ||||||
| chr2:127593279
|
T | C | 2 | a0001c0002t0001g0149a0002c0011t0002g0276 | 2 | HG01884.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2146-267T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 17/47 | chr2 | 127593279 | ||||||
| chr2:127593371
|
T | TC | 5 | a0008c0015t0001g0044a0008c0015t0001g0104a0008c0015t0001g0164others(2): Show | 5 | HG01243.hp2 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.2146-172dupC | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 17/47 | INFO_REALIGN_3_PRIME | chr2 | 127593371 | |||||
| chr2:127593375
|
T | A | 3 | a0001c0045t0001g0139a0010c0016t0001g0005a0010c0016t0001g0138 | 4 | HG02630.hp1 HG02895.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2146-171T>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 17/47 | chr2 | 127593375 | ||||||
| chr2:127593390
|
C | T | 194 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(191): Show | 196 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.2146-156C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 17/47 | chr2 | 127593390 | ||||||
| chr2:127593404
|
C | T | 1 | a0001c0002t0001g0275 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2146-142C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 17/47 | chr2 | 127593404 | ||||||
| chr2:127593457
|
G | C | 1 | a0001c0004t0001g0055 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2146-89G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 17/47 | chr2 | 127593457 | ||||||
| chr2:127593771
|
T | C | 201 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(198): Show | 204 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.2244+127T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 18/47 | chr2 | 127593771 | ||||||
| chr2:127593808
|
C | T | 2 | a0001c0002t0001g0134a0009c0014t0001g0133 | 2 | HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2244+164C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 18/47 | chr2 | 127593808 | ||||||
| chr2:127593868
|
T | C | 1 | a0001c0044t0003g0077 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2244+224T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 18/47 | chr2 | 127593868 | ||||||
| chr2:127593882
|
G | T | 1 | a0001c0005t0002g0062 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2244+238G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 18/47 | chr2 | 127593882 | ||||||
| chr2:127593929
|
C | T | 4 | a0001c0002t0001g0141a0001c0005t0002g0128a0022c0064t0002g0140others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2244+285C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 18/47 | chr2 | 127593929 | ||||||
| chr2:127594209
|
C | T | 5 | a0008c0015t0001g0044a0008c0015t0001g0104a0008c0015t0001g0164others(2): Show | 5 | HG01243.hp2 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.2244+565C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 18/47 | chr2 | 127594209 | ||||||
| chr2:127594280
|
A | C | 2 | a0001c0002t0001g0149a0002c0011t0002g0276 | 2 | HG01884.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2244+636A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 18/47 | chr2 | 127594280 | ||||||
| chr2:127594529
|
C | T | 1 | a0014c0053t0001g0277 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2244+885C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 18/47 | chr2 | 127594529 | ||||||
| chr2:127594901
|
C | T | 1 | a0001c0002t0001g0134 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2244+1257C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 18/47 | chr2 | 127594901 | ||||||
| chr2:127595020
|
A | G | 2 | a0001c0018t0001g0273a0001c0018t0001g0274 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2244+1376A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 18/47 | chr2 | 127595020 | ||||||
| chr2:127595045
|
A | T | 1 | a0001c0002t0001g0032 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2244+1401A>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 18/47 | chr2 | 127595045 | ||||||
| chr2:127595157
|
G | T | 5 | a0008c0015t0001g0044a0008c0015t0001g0104a0008c0015t0001g0164others(2): Show | 5 | HG01243.hp2 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.2245-1305G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 18/47 | chr2 | 127595157 | ||||||
| chr2:127595288
|
T | G | 194 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(191): Show | 196 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.2245-1174T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 18/47 | chr2 | 127595288 | ||||||
| chr2:127595435
|
A | G | 5 | a0005c0008t0001g0001a0005c0008t0001g0146a0005c0008t0001g0147others(2): Show | 6 | HG02717.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2245-1027A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 18/47 | chr2 | 127595435 | ||||||
| chr2:127595454
|
G | A | 1 | a0001c0002t0001g0275 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2245-1008G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 18/47 | chr2 | 127595454 | ||||||
| chr2:127595540
|
A | C | 1 | a0002c0001t0001g0109 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2245-922A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 18/47 | chr2 | 127595540 | ||||||
| chr2:127595661
|
A | G | 2 | a0001c0002t0001g0149a0002c0011t0002g0276 | 2 | HG01884.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2245-801A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 18/47 | chr2 | 127595661 | ||||||
| chr2:127595701
|
G | T | 1 | a0001c0044t0003g0077 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2245-761G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 18/47 | chr2 | 127595701 | ||||||
| chr2:127595908
|
T | C | 1 | a0007c0023t0001g0126 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2245-554T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 18/47 | chr2 | 127595908 | ||||||
| chr2:127596074
|
A | G | 34 | a0001c0004t0001g0040a0001c0005t0001g0045a0001c0005t0001g0095others(31): Show | 34 | HG01070.hp1 HG01256.hp1 HG01258.hp2 others(31): Show |
intron_variant | MODIFIER | c.2245-388A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 18/47 | chr2 | 127596074 | ||||||
| chr2:127596130
|
A | T | 188 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(185): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.2245-332A>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 18/47 | chr2 | 127596130 | ||||||
| chr2:127596235
|
A | G | 1 | a0047c0028t0001g0197 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2245-227A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 18/47 | chr2 | 127596235 | ||||||
| chr2:127596338
|
T | A | 1 | a0001c0002t0001g0134 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2245-124T>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 18/47 | chr2 | 127596338 | ||||||
| chr2:127596449
|
T | C | 1 | a0003c0003t0001g0229 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2245-13T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 18/47 | chr2 | 127596449 | ||||||
| chr2:127596560
|
C | T | 1 | a0032c0065t0001g0137 | 1 | NA19043.hp1 | splice_region_variant&intron_variant | LOW | c.2339+4C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127596560 | ||||||
| chr2:127596804
|
G | A | 1 | a0005c0008t0001g0213 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2339+248G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127596804 | ||||||
| chr2:127596979
|
G | A | 1 | a0001c0044t0003g0077 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2339+423G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127596979 | ||||||
| chr2:127597074
|
G | A | 2 | a0001c0002t0001g0033a0001c0002t0001g0082 | 2 | NA18964.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.2339+518G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127597074 | ||||||
| chr2:127597092
|
C | T | 67 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(64): Show | 68 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.2339+536C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127597092 | ||||||
| chr2:127597135
|
A | G | 1 | a0032c0065t0001g0137 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2339+579A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127597135 | ||||||
| chr2:127597160
|
C | T | 1 | a0001c0004t0001g0020 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2339+604C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127597160 | ||||||
| chr2:127597248
|
G | C | 48 | a0001c0004t0001g0240a0001c0005t0002g0062a0003c0003t0001g0030others(45): Show | 49 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.2339+692G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127597248 | ||||||
| chr2:127597277
|
A | G | 74 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(71): Show | 75 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.2339+721A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127597277 | ||||||
| chr2:127597356
|
A | C | 6 | a0001c0002t0001g0052a0001c0002t0001g0087a0001c0002t0001g0149others(3): Show | 6 | HG01884.hp1 HG01884.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2339+800A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127597356 | ||||||
| chr2:127597384
|
G | A | 6 | a0001c0002t0001g0052a0001c0002t0001g0087a0001c0002t0001g0149others(3): Show | 7 | HG01884.hp2 HG02451.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2339+828G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127597384 | ||||||
| chr2:127597611
|
A | ATATT | 69 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(66): Show | 70 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.2339+1093_2339+109 others(8): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | INFO_REALIGN_3_PRIME | chr2 | 127597611 | |||||
| chr2:127597611
|
A | ATATTTAT others(1): Show |
19 | a0001c0002t0001g0074a0001c0002t0001g0081a0001c0002t0001g0131others(16): Show | 20 | HG01069.hp1 HG01071.hp1 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.2339+1089_2339+109 others(12): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | INFO_REALIGN_3_PRIME | chr2 | 127597611 | |||||
| chr2:127597611
|
A | ATATTTAT others(5): Show |
2 | a0001c0005t0002g0128a0007c0024t0001g0261 | 2 | HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2339+1085_2339+109 others(16): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | INFO_REALIGN_3_PRIME | chr2 | 127597611 | |||||
| chr2:127597611
|
ATATT | A | 51 | a0001c0017t0004g0021a0001c0017t0004g0022a0001c0017t0004g0071others(48): Show | 51 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.2339+1093_2339+109 others(8): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | INFO_REALIGN_3_PRIME | chr2 | 127597611 | |||||
| chr2:127597611
|
ATATTTAT others(1): Show |
A | 26 | a0001c0004t0001g0040a0001c0005t0001g0045a0001c0005t0001g0095others(23): Show | 26 | HG01070.hp1 HG01256.hp1 HG01258.hp2 others(23): Show |
intron_variant | MODIFIER | c.2339+1089_2339+109 others(12): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | INFO_REALIGN_3_PRIME | chr2 | 127597611 | |||||
| chr2:127597655
|
A | G | 1 | a0001c0044t0003g0077 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2339+1099A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127597655 | ||||||
| chr2:127597822
|
G | A | 22 | a0001c0002t0001g0134a0001c0005t0002g0128a0001c0010t0001g0135others(19): Show | 22 | HG02109.hp1 HG02109.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.2339+1266G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127597822 | ||||||
| chr2:127597880
|
C | T | 7 | a0001c0002t0001g0259a0002c0006t0001g0012a0002c0006t0001g0013others(4): Show | 7 | HG00099.hp1 HG00741.hp1 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.2339+1324C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127597880 | ||||||
| chr2:127597962
|
C | T | 4 | a0001c0017t0004g0021a0001c0017t0004g0022a0001c0017t0004g0071others(1): Show | 4 | HG02258.hp2 HG02630.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2339+1406C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127597962 | ||||||
| chr2:127598005
|
A | G | 6 | a0001c0005t0002g0062a0001c0045t0001g0139a0007c0024t0001g0261others(3): Show | 7 | HG02572.hp1 HG02630.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.2339+1449A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127598005 | ||||||
| chr2:127598025
|
C | T | 1 | a0001c0005t0002g0051 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2339+1469C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127598025 | ||||||
| chr2:127598186
|
A | C | 1 | a0014c0053t0001g0277 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2339+1630A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127598186 | ||||||
| chr2:127598207
|
C | T | 105 | a0001c0004t0001g0040a0001c0004t0001g0240a0001c0004t0001g0252others(102): Show | 107 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.2339+1651C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127598207 | ||||||
| chr2:127598307
|
G | A | 4 | a0001c0010t0001g0159a0013c0022t0001g0115a0013c0022t0001g0212others(1): Show | 4 | HG01069.hp1 HG01071.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.2339+1751G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127598307 | ||||||
| chr2:127598759
|
C | T | 8 | a0002c0001t0001g0178a0002c0001t0001g0179a0002c0001t0001g0181others(5): Show | 8 | HG01168.hp2 HG01257.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.2339+2203C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127598759 | ||||||
| chr2:127599066
|
C | T | 1 | a0002c0012t0001g0169 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2339+2510C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127599066 | ||||||
| chr2:127599392
|
A | T | 2 | a0007c0023t0001g0126a0007c0023t0001g0221 | 2 | HG02109.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.2339+2836A>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127599392 | ||||||
| chr2:127599422
|
C | T | 183 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(180): Show | 186 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.2339+2866C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127599422 | ||||||
| chr2:127599453
|
G | T | 1 | a0001c0004t0001g0055 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2339+2897G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127599453 | ||||||
| chr2:127599811
|
C | T | 1 | a0042c0033t0001g0066 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2339+3255C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127599811 | ||||||
| chr2:127599812
|
G | A | 1 | a0020c0046t0003g0075 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2339+3256G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127599812 | ||||||
| chr2:127599952
|
G | A | 2 | a0003c0003t0001g0030a0003c0003t0001g0078 | 2 | HG00621.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.2339+3396G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127599952 | ||||||
| chr2:127599980
|
T | G | 2 | a0002c0001t0001g0110a0016c0019t0001g0176 | 2 | HG02300.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.2339+3424T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127599980 | ||||||
| chr2:127600072
|
C | T | 199 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(196): Show | 202 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.2339+3516C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127600072 | ||||||
| chr2:127600073
|
G | A | 1 | a0002c0001t0001g0172 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2339+3517G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127600073 | ||||||
| chr2:127600121
|
G | A | 46 | a0001c0004t0001g0240a0003c0003t0001g0030a0003c0003t0001g0078others(43): Show | 47 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.2339+3565G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127600121 | ||||||
| chr2:127600191
|
T | C | 7 | a0008c0015t0001g0044a0008c0015t0001g0104a0008c0015t0001g0164others(4): Show | 7 | HG01243.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.2339+3635T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127600191 | ||||||
| chr2:127600207
|
T | G | 2 | a0007c0023t0001g0126a0007c0023t0001g0221 | 2 | HG02109.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.2339+3651T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127600207 | ||||||
| chr2:127600211
|
C | T | 1 | a0019c0070t0001g0025 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2339+3655C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127600211 | ||||||
| chr2:127600270
|
G | A | 19 | a0001c0004t0001g0252a0004c0007t0001g0158a0004c0007t0001g0161others(16): Show | 19 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.2339+3714G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127600270 | ||||||
| chr2:127600289
|
C | G | 23 | a0001c0004t0001g0040a0001c0005t0001g0045a0001c0005t0001g0095others(20): Show | 23 | HG01070.hp1 HG01256.hp1 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.2339+3733C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127600289 | ||||||
| chr2:127600433
|
G | A | 1 | a0001c0044t0003g0077 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2339+3877G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127600433 | ||||||
| chr2:127600475
|
C | T | 5 | a0001c0045t0001g0139a0007c0024t0001g0261a0010c0016t0001g0005others(2): Show | 6 | HG02572.hp1 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2339+3919C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127600475 | ||||||
| chr2:127600538
|
C | A | 19 | a0001c0004t0001g0252a0004c0007t0001g0158a0004c0007t0001g0161others(16): Show | 19 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.2339+3982C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127600538 | ||||||
| chr2:127600937
|
A | G | 1 | a0004c0007t0001g0267 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2339+4381A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127600937 | ||||||
| chr2:127601013
|
T | G | 1 | a0002c0012t0001g0167 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2339+4457T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127601013 | ||||||
| chr2:127601373
|
T | C | 1 | a0033c0059t0001g0028 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2340-4471T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127601373 | ||||||
| chr2:127601518
|
T | C | 46 | a0001c0004t0001g0240a0003c0003t0001g0030a0003c0003t0001g0078others(43): Show | 47 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.2340-4326T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127601518 | ||||||
| chr2:127601846
|
G | A | 3 | a0009c0014t0001g0170a0009c0014t0001g0220a0032c0065t0001g0137 | 3 | HG02486.hp2 HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2340-3998G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127601846 | ||||||
| chr2:127601910
|
A | G | 1 | a0003c0003t0001g0120 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2340-3934A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127601910 | ||||||
| chr2:127601927
|
G | A | 1 | a0020c0046t0003g0075 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2340-3917G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127601927 | ||||||
| chr2:127602076
|
T | C | 23 | a0001c0004t0001g0040a0001c0005t0001g0045a0001c0005t0001g0095others(20): Show | 23 | HG01070.hp1 HG01256.hp1 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.2340-3768T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127602076 | ||||||
| chr2:127602098
|
C | G | 2 | a0001c0005t0002g0128a0002c0011t0002g0276 | 2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2340-3746C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127602098 | ||||||
| chr2:127602241
|
T | C | 1 | a0001c0004t0001g0006 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2340-3603T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127602241 | ||||||
| chr2:127602626
|
A | G | 183 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(180): Show | 186 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.2340-3218A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127602626 | ||||||
| chr2:127602651
|
AAAAAAGA others(4): Show |
A | 6 | a0008c0015t0001g0044a0008c0015t0001g0104a0008c0015t0001g0164others(3): Show | 6 | HG01243.hp2 HG02145.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.2340-3189_2340-317 others(15): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | INFO_REALIGN_3_PRIME | chr2 | 127602651 | |||||
| chr2:127603176
|
T | A | 23 | a0001c0004t0001g0040a0001c0005t0001g0045a0001c0005t0001g0095others(20): Show | 23 | HG01070.hp1 HG01256.hp1 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.2340-2668T>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127603176 | ||||||
| chr2:127603216
|
C | G | 1 | a0020c0046t0003g0075 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2340-2628C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127603216 | ||||||
| chr2:127603221
|
C | T | 1 | a0020c0046t0003g0075 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2340-2623C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127603221 | ||||||
| chr2:127603232
|
A | G | 74 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(71): Show | 75 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.2340-2612A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127603232 | ||||||
| chr2:127603781
|
T | C | 1 | a0040c0035t0001g0111 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2340-2063T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127603781 | ||||||
| chr2:127603805
|
C | T | 45 | a0003c0003t0001g0030a0003c0003t0001g0078a0003c0003t0001g0106others(42): Show | 46 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.2340-2039C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127603805 | ||||||
| chr2:127603861
|
T | C | 4 | a0003c0026t0001g0143a0003c0026t0001g0246a0003c0069t0001g0245others(1): Show | 4 | HG01192.hp1 NA18972.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.2340-1983T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127603861 | ||||||
| chr2:127603871
|
T | C | 1 | a0019c0070t0001g0025 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2340-1973T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127603871 | ||||||
| chr2:127603937
|
G | T | 2 | a0003c0003t0001g0223a0003c0003t0001g0226 | 2 | NA18950.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.2340-1907G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127603937 | ||||||
| chr2:127603942
|
G | A | 1 | a0009c0014t0001g0220 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2340-1902G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127603942 | ||||||
| chr2:127603956
|
AC | A | 19 | a0003c0003t0001g0229a0004c0007t0001g0158a0004c0007t0001g0161others(16): Show | 19 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.2340-1884delC | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | INFO_REALIGN_3_PRIME | chr2 | 127603956 | |||||
| chr2:127603990
|
G | A | 73 | a0001c0005t0001g0095a0001c0005t0002g0062a0003c0003t0001g0030others(70): Show | 74 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.2340-1854G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127603990 | ||||||
| chr2:127604023
|
C | T | 1 | a0001c0002t0001g0094 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2340-1821C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127604023 | ||||||
| chr2:127604048
|
G | A | 2 | a0001c0005t0002g0128a0002c0011t0002g0276 | 2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2340-1796G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127604048 | ||||||
| chr2:127604074
|
A | G | 2 | a0001c0002t0001g0093a0001c0002t0001g0094 | 2 | HG02896.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2340-1770A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127604074 | ||||||
| chr2:127604132
|
C | A | 75 | a0001c0005t0002g0062a0001c0045t0001g0139a0003c0003t0001g0030others(72): Show | 77 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.2340-1712C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127604132 | ||||||
| chr2:127604209
|
G | A | 22 | a0001c0004t0001g0040a0001c0005t0001g0045a0001c0005t0001g0095others(19): Show | 22 | HG01070.hp1 HG01256.hp1 HG01258.hp2 others(19): Show |
intron_variant | MODIFIER | c.2340-1635G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127604209 | ||||||
| chr2:127604223
|
A | G | 18 | a0004c0007t0001g0158a0004c0007t0001g0161a0004c0007t0001g0254others(15): Show | 18 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.2340-1621A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127604223 | ||||||
| chr2:127604253
|
T | G | 1 | a0014c0053t0001g0277 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2340-1591T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127604253 | ||||||
| chr2:127604539
|
G | A | 1 | a0009c0014t0001g0101 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2340-1305G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127604539 | ||||||
| chr2:127604725
|
C | T | 1 | a0003c0003t0001g0122 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2340-1119C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127604725 | ||||||
| chr2:127604726
|
G | A | 1 | a0001c0002t0001g0134 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2340-1118G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127604726 | ||||||
| chr2:127604789
|
G | A | 1 | a0008c0063t0001g0263 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2340-1055G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127604789 | ||||||
| chr2:127604947
|
C | T | 1 | a0033c0059t0001g0028 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2340-897C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127604947 | ||||||
| chr2:127604985
|
A | G | 18 | a0001c0010t0001g0135a0001c0010t0001g0136a0001c0010t0001g0159others(15): Show | 18 | HG01069.hp1 HG01071.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.2340-859A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127604985 | ||||||
| chr2:127605129
|
G | A | 1 | a0001c0044t0003g0077 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2340-715G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127605129 | ||||||
| chr2:127605145
|
C | T | 1 | a0020c0046t0003g0075 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2340-699C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127605145 | ||||||
| chr2:127605412
|
G | A | 94 | a0001c0010t0001g0135a0001c0010t0001g0136a0001c0010t0001g0159others(91): Show | 96 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.2340-432G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127605412 | ||||||
| chr2:127605426
|
T | C | 2 | a0010c0016t0001g0005a0010c0016t0001g0138 | 3 | HG02630.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2340-418T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127605426 | ||||||
| chr2:127605551
|
C | T | 79 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(76): Show | 80 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.2340-293C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 19/47 | chr2 | 127605551 | ||||||
| chr2:127605955
|
G | GC | 276 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(273): Show | 281 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.2424+29dupC | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 20/47 | INFO_REALIGN_3_PRIME | chr2 | 127605955 | |||||
| chr2:127606033
|
G | A | 46 | a0003c0003t0001g0030a0003c0003t0001g0078a0003c0003t0001g0106others(43): Show | 47 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.2424+105G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 20/47 | chr2 | 127606033 | ||||||
| chr2:127606034
|
G | A | 1 | a0001c0004t0001g0247 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2424+106G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 20/47 | chr2 | 127606034 | ||||||
| chr2:127606073
|
A | T | 26 | a0001c0005t0001g0045a0001c0005t0001g0095a0001c0005t0002g0041others(23): Show | 26 | HG01070.hp1 HG01256.hp1 HG01258.hp2 others(23): Show |
intron_variant | MODIFIER | c.2424+145A>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 20/47 | chr2 | 127606073 | ||||||
| chr2:127606356
|
T | C | 1 | a0001c0004t0001g0225 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2424+428T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 20/47 | chr2 | 127606356 | ||||||
| chr2:127606416
|
G | A | 1 | a0001c0010t0001g0135 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2424+488G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 20/47 | chr2 | 127606416 | ||||||
| chr2:127606557
|
C | G | 23 | a0001c0010t0001g0135a0001c0010t0001g0136a0001c0010t0001g0159others(20): Show | 23 | HG01069.hp1 HG01071.hp1 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.2424+629C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 20/47 | chr2 | 127606557 | ||||||
| chr2:127606648
|
G | A | 1 | a0009c0014t0001g0101 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2425-558G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 20/47 | chr2 | 127606648 | ||||||
| chr2:127606679
|
G | A | 1 | a0032c0065t0001g0137 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2425-527G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 20/47 | chr2 | 127606679 | ||||||
| chr2:127606696
|
G | A | 2 | a0015c0066t0001g0064a0015c0071t0001g0127 | 2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2425-510G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 20/47 | chr2 | 127606696 | ||||||
| chr2:127607082
|
C | T | 2 | a0001c0002t0001g0029a0001c0002t0001g0035 | 2 | NA18942.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.2425-124C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 20/47 | chr2 | 127607082 | ||||||
| chr2:127607109
|
G | A | 45 | a0003c0003t0001g0030a0003c0003t0001g0078a0003c0003t0001g0106others(42): Show | 46 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.2425-97G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 20/47 | chr2 | 127607109 | ||||||
| chr2:127607133
|
T | C | 1 | a0001c0005t0002g0041 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2425-73T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 20/47 | chr2 | 127607133 | ||||||
| chr2:127607147
|
C | T | 2 | a0003c0003t0001g0214a0014c0053t0001g0277 | 2 | HG01433.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.2425-59C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 20/47 | chr2 | 127607147 | ||||||
| chr2:127607588
|
A | G | 2 | a0003c0003t0001g0222a0003c0003t0001g0233 | 2 | NA18959.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.2643+164A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 21/47 | chr2 | 127607588 | ||||||
| chr2:127607592
|
C | T | 1 | a0009c0014t0001g0101 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2643+168C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 21/47 | chr2 | 127607592 | ||||||
| chr2:127607727
|
G | A | 2 | a0010c0016t0001g0005a0010c0016t0001g0138 | 3 | HG02630.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2643+303G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 21/47 | chr2 | 127607727 | ||||||
| chr2:127607809
|
G | T | 1 | a0009c0014t0001g0101 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2643+385G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 21/47 | chr2 | 127607809 | ||||||
| chr2:127607893
|
G | A | 1 | a0006c0009t0001g0059 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2643+469G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 21/47 | chr2 | 127607893 | ||||||
| chr2:127607925
|
A | G | 2 | a0014c0072t0001g0009a0024c0073t0001g0065 | 2 | HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2643+501A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 21/47 | chr2 | 127607925 | ||||||
| chr2:127607945
|
C | T | 1 | a0004c0007t0003g0257 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2643+521C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 21/47 | chr2 | 127607945 | ||||||
| chr2:127608089
|
G | A | 1 | a0001c0044t0003g0077 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2644-619G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 21/47 | chr2 | 127608089 | ||||||
| chr2:127608182
|
G | T | 1 | a0009c0014t0001g0133 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2644-526G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 21/47 | chr2 | 127608182 | ||||||
| chr2:127608339
|
G | A | 22 | a0001c0010t0001g0135a0001c0010t0001g0136a0001c0010t0001g0159others(19): Show | 22 | HG01069.hp1 HG01071.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.2644-369G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 21/47 | chr2 | 127608339 | ||||||
| chr2:127608376
|
G | C | 1 | a0001c0002t0001g0134 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2644-332G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 21/47 | chr2 | 127608376 | ||||||
| chr2:127608466
|
C | A | 1 | a0032c0065t0001g0137 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2644-242C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 21/47 | chr2 | 127608466 | ||||||
| chr2:127608483
|
C | T | 2 | a0010c0016t0001g0005a0010c0016t0001g0138 | 3 | HG02630.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2644-225C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 21/47 | chr2 | 127608483 | ||||||
| chr2:127608526
|
T | C | 1 | a0032c0065t0001g0137 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2644-182T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 21/47 | chr2 | 127608526 | ||||||
| chr2:127608582
|
T | G | 1 | a0023c0048t0001g0129 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2644-126T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 21/47 | chr2 | 127608582 | ||||||
| chr2:127608697
|
G | A | 24 | a0004c0007t0001g0158a0004c0007t0001g0161a0004c0007t0001g0254others(21): Show | 25 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.2644-11G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 21/47 | chr2 | 127608697 | ||||||
| chr2:127609061
|
G | C | 96 | a0001c0010t0001g0135a0001c0010t0001g0136a0001c0010t0001g0159others(93): Show | 98 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.2814+183G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 22/47 | chr2 | 127609061 | ||||||
| chr2:127609192
|
G | A | 1 | a0002c0011t0002g0210 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2814+314G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 22/47 | chr2 | 127609192 | ||||||
| chr2:127609204
|
T | C | 23 | a0001c0005t0001g0045a0001c0005t0001g0095a0001c0005t0002g0041others(20): Show | 23 | HG01070.hp1 HG01256.hp1 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.2815-302T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 22/47 | chr2 | 127609204 | ||||||
| chr2:127609784
|
G | A | 22 | a0004c0007t0001g0158a0004c0007t0001g0161a0004c0007t0001g0254others(19): Show | 22 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.3025-65G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 23/47 | chr2 | 127609784 | ||||||
| chr2:127610102
|
C | T | 1 | a0002c0001t0001g0188 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.3192+86C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 24/47 | chr2 | 127610102 | ||||||
| chr2:127610318
|
A | G | 2 | a0009c0014t0001g0170a0009c0014t0001g0220 | 2 | HG02486.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.3192+302A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 24/47 | chr2 | 127610318 | ||||||
| chr2:127610475
|
G | A | 46 | a0003c0003t0001g0030a0003c0003t0001g0078a0003c0003t0001g0106others(43): Show | 47 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.3192+459G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 24/47 | chr2 | 127610475 | ||||||
| chr2:127610614
|
C | T | 2 | a0001c0005t0002g0049a0001c0005t0002g0091 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.3192+598C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 24/47 | chr2 | 127610614 | ||||||
| chr2:127610660
|
T | C | 96 | a0001c0010t0001g0135a0001c0010t0001g0136a0001c0010t0001g0159others(93): Show | 98 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.3192+644T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 24/47 | chr2 | 127610660 | ||||||
| chr2:127610750
|
G | C | 1 | a0019c0070t0001g0025 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3192+734G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 24/47 | chr2 | 127610750 | ||||||
| chr2:127610805
|
A | G | 18 | a0004c0007t0001g0158a0004c0007t0001g0161a0004c0007t0001g0254others(15): Show | 18 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.3192+789A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 24/47 | chr2 | 127610805 | ||||||
| chr2:127610926
|
A | G | 2 | a0002c0001t0001g0193a0017c0031t0001g0195 | 2 | HG01081.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.3192+910A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 24/47 | chr2 | 127610926 | ||||||
| chr2:127611081
|
G | A | 1 | a0001c0044t0003g0077 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3192+1065G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 24/47 | chr2 | 127611081 | ||||||
| chr2:127611149
|
C | T | 1 | a0004c0007t0003g0125 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3193-1101C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 24/47 | chr2 | 127611149 | ||||||
| chr2:127611203
|
T | G | 2 | a0010c0016t0001g0005a0010c0016t0001g0138 | 3 | HG02630.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3193-1047T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 24/47 | chr2 | 127611203 | ||||||
| chr2:127611300
|
C | T | 2 | a0037c0074t0001g0023a0046c0029t0001g0204 | 2 | HG03654.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.3193-950C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 24/47 | chr2 | 127611300 | ||||||
| chr2:127611792
|
C | T | 1 | a0023c0048t0001g0129 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3193-458C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 24/47 | chr2 | 127611792 | ||||||
| chr2:127611800
|
C | T | 4 | a0009c0014t0001g0101a0009c0014t0001g0133a0009c0014t0001g0170others(1): Show | 4 | HG02486.hp2 HG02572.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.3193-450C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 24/47 | chr2 | 127611800 | ||||||
| chr2:127612177
|
A | G | 46 | a0003c0003t0001g0030a0003c0003t0001g0078a0003c0003t0001g0106others(43): Show | 47 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.3193-73A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 24/47 | chr2 | 127612177 | ||||||
| chr2:127612182
|
G | A | 1 | a0032c0065t0001g0137 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3193-68G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 24/47 | chr2 | 127612182 | ||||||
| chr2:127612228
|
C | T | 2 | a0001c0002t0001g0093a0001c0002t0001g0094 | 2 | HG02896.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.3193-22C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 24/47 | chr2 | 127612228 | ||||||
| chr2:127612342
|
C | T | 46 | a0003c0003t0001g0030a0003c0003t0001g0078a0003c0003t0001g0106others(43): Show | 47 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.3270+15C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 25/47 | chr2 | 127612342 | ||||||
| chr2:127612352
|
G | A | 1 | a0001c0044t0003g0077 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3270+25G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 25/47 | chr2 | 127612352 | ||||||
| chr2:127612625
|
G | A | 48 | a0003c0003t0001g0030a0003c0003t0001g0078a0003c0003t0001g0106others(45): Show | 49 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.3398+22G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127612625 | ||||||
| chr2:127612753
|
C | T | 1 | a0031c0057t0001g0076 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3398+150C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127612753 | ||||||
| chr2:127612891
|
C | T | 46 | a0003c0003t0001g0030a0003c0003t0001g0078a0003c0003t0001g0106others(43): Show | 47 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.3398+288C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127612891 | ||||||
| chr2:127613012
|
T | C | 1 | a0003c0003t0001g0234 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.3398+409T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127613012 | ||||||
| chr2:127613180
|
C | G | 1 | a0022c0064t0002g0140 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3398+577C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127613180 | ||||||
| chr2:127613245
|
T | C | 1 | a0040c0035t0001g0111 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.3398+642T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127613245 | ||||||
| chr2:127613281
|
T | C | 46 | a0003c0003t0001g0030a0003c0003t0001g0078a0003c0003t0001g0106others(43): Show | 47 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.3398+678T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127613281 | ||||||
| chr2:127613583
|
G | T | 2 | a0007c0023t0001g0126a0007c0023t0001g0221 | 2 | HG02109.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.3398+980G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127613583 | ||||||
| chr2:127613678
|
G | C | 1 | a0042c0033t0001g0066 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.3398+1075G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127613678 | ||||||
| chr2:127613890
|
T | C | 1 | a0002c0006t0001g0010 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3398+1287T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127613890 | ||||||
| chr2:127613961
|
T | C | 1 | a0032c0065t0001g0137 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3398+1358T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127613961 | ||||||
| chr2:127614104
|
GCCA | G | 6 | a0001c0010t0001g0262a0001c0010t0001g0270a0001c0010t0001g0271others(3): Show | 6 | HG02451.hp1 HG02622.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.3398+1506_3398+150 others(7): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr2 | 127614104 | |||||
| chr2:127614446
|
T | C | 6 | a0003c0003t0001g0228a0003c0003t0001g0269a0003c0026t0001g0143others(3): Show | 6 | NA18941.hp2 NA18972.hp1 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.3398+1843T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127614446 | ||||||
| chr2:127614504
|
C | G | 22 | a0004c0007t0001g0158a0004c0007t0001g0161a0004c0007t0001g0254others(19): Show | 22 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.3398+1901C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127614504 | ||||||
| chr2:127614533
|
C | T | 4 | a0001c0002t0001g0103a0001c0013t0001g0002a0001c0013t0001g0162others(1): Show | 5 | HG01243.hp1 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.3398+1930C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127614533 | ||||||
| chr2:127614562
|
A | G | 2 | a0001c0058t0002g0100a0002c0001t0001g0068 | 2 | NA18957.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.3398+1959A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127614562 | ||||||
| chr2:127614624
|
C | T | 2 | a0003c0003t0001g0214a0003c0003t0001g0258 | 2 | HG01123.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.3398+2021C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127614624 | ||||||
| chr2:127614735
|
A | G | 1 | a0032c0065t0001g0137 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3398+2132A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127614735 | ||||||
| chr2:127614764
|
G | A | 2 | a0010c0016t0001g0005a0010c0016t0001g0138 | 3 | HG02630.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3398+2161G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127614764 | ||||||
| chr2:127614807
|
A | T | 1 | a0023c0048t0001g0129 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3398+2204A>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127614807 | ||||||
| chr2:127614825
|
A | G | 22 | a0001c0010t0001g0135a0001c0010t0001g0136a0001c0010t0001g0159others(19): Show | 22 | HG01069.hp1 HG01071.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.3398+2222A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127614825 | ||||||
| chr2:127614855
|
C | T | 1 | a0001c0005t0003g0046 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3398+2252C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127614855 | ||||||
| chr2:127614947
|
T | C | 23 | a0001c0010t0001g0135a0001c0010t0001g0136a0001c0010t0001g0159others(20): Show | 23 | HG01069.hp1 HG01071.hp1 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.3398+2344T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127614947 | ||||||
| chr2:127615210
|
G | A | 1 | a0004c0007t0003g0257 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3398+2607G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127615210 | ||||||
| chr2:127615281
|
T | C | 130 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(127): Show | 131 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(128): Show |
intron_variant | MODIFIER | c.3398+2678T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127615281 | ||||||
| chr2:127615386
|
G | A | 2 | a0002c0006t0001g0150a0038c0039t0001g0014 | 2 | HG01081.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.3398+2783G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127615386 | ||||||
| chr2:127615448
|
G | A | 78 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(75): Show | 79 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.3398+2845G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127615448 | ||||||
| chr2:127615464
|
C | T | 1 | a0001c0004t0001g0055 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3398+2861C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127615464 | ||||||
| chr2:127615465
|
G | A | 1 | a0019c0070t0001g0025 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3398+2862G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127615465 | ||||||
| chr2:127615470
|
G | C | 1 | a0019c0070t0001g0025 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3398+2867G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127615470 | ||||||
| chr2:127615744
|
C | T | 1 | a0047c0028t0001g0197 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3398+3141C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127615744 | ||||||
| chr2:127615768
|
A | G | 22 | a0001c0005t0001g0045a0001c0005t0001g0095a0001c0005t0002g0041others(19): Show | 22 | HG01070.hp1 HG01256.hp1 HG01258.hp2 others(19): Show |
intron_variant | MODIFIER | c.3398+3165A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127615768 | ||||||
| chr2:127615783
|
T | C | 1 | a0003c0003t0001g0232 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3398+3180T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127615783 | ||||||
| chr2:127615852
|
C | T | 1 | a0001c0010t0001g0159 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3398+3249C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127615852 | ||||||
| chr2:127615853
|
G | A | 2 | a0002c0001t0001g0173a0003c0003t0001g0233 | 2 | NA18985.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.3398+3250G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127615853 | ||||||
| chr2:127615987
|
G | A | 51 | a0003c0003t0001g0030a0003c0003t0001g0078a0003c0003t0001g0106others(48): Show | 53 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.3398+3384G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127615987 | ||||||
| chr2:127615996
|
C | G | 1 | a0005c0008t0001g0217 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.3398+3393C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127615996 | ||||||
| chr2:127616053
|
G | A | 1 | a0019c0070t0001g0025 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3398+3450G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127616053 | ||||||
| chr2:127616125
|
G | A | 48 | a0001c0005t0001g0045a0001c0005t0001g0095a0001c0005t0002g0041others(45): Show | 48 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.3398+3522G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127616125 | ||||||
| chr2:127616359
|
A | G | 2 | a0009c0014t0001g0101a0009c0014t0001g0133 | 2 | HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.3398+3756A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127616359 | ||||||
| chr2:127616409
|
G | A | 18 | a0004c0007t0001g0158a0004c0007t0001g0161a0004c0007t0001g0254others(15): Show | 18 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.3398+3806G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127616409 | ||||||
| chr2:127616455
|
C | T | 1 | a0001c0002t0001g0134 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3398+3852C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127616455 | ||||||
| chr2:127616533
|
G | A | 44 | a0001c0005t0001g0045a0001c0005t0001g0095a0001c0005t0002g0041others(41): Show | 44 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.3399-3807G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127616533 | ||||||
| chr2:127616605
|
T | A | 47 | a0003c0003t0001g0030a0003c0003t0001g0078a0003c0003t0001g0106others(44): Show | 48 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.3399-3735T>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127616605 | ||||||
| chr2:127616802
|
C | G | 48 | a0001c0005t0001g0045a0001c0005t0001g0095a0001c0005t0002g0041others(45): Show | 48 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.3399-3538C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127616802 | ||||||
| chr2:127616827
|
G | A | 1 | a0007c0024t0001g0261 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3399-3513G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127616827 | ||||||
| chr2:127616862
|
G | A | 2 | a0001c0010t0001g0135a0001c0010t0001g0136 | 2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3399-3478G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127616862 | ||||||
| chr2:127616886
|
A | G | 4 | a0009c0014t0001g0101a0009c0014t0001g0133a0009c0014t0001g0170others(1): Show | 4 | HG02486.hp2 HG02572.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.3399-3454A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127616886 | ||||||
| chr2:127616962
|
C | T | 48 | a0001c0005t0001g0045a0001c0005t0001g0095a0001c0005t0002g0041others(45): Show | 48 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.3399-3378C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127616962 | ||||||
| chr2:127617036
|
T | G | 1 | a0002c0001t0001g0107 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.3399-3304T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617036 | ||||||
| chr2:127617071
|
C | G | 1 | a0001c0002t0001g0130 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3399-3269C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617071 | ||||||
| chr2:127617232
|
G | A | 48 | a0001c0005t0001g0045a0001c0005t0001g0095a0001c0005t0002g0041others(45): Show | 48 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.3399-3108G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617232 | ||||||
| chr2:127617275
|
C | G | 1 | a0020c0046t0003g0075 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3399-3065C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617275 | ||||||
| chr2:127617453
|
A | C | 1 | a0001c0004t0001g0219 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3399-2887A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617453 | ||||||
| chr2:127617475
|
ACTTGTAA others(318): Show |
A | 1 | a0001c0044t0003g0077 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3399-2849_3399-252 others(4): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr2 | 127617475 | |||||
| chr2:127617486
|
G | T | 1 | a0020c0046t0003g0075 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3399-2854G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617486 | ||||||
| chr2:127617487
|
G | GT | 27 | a0001c0002t0001g0032a0001c0002t0001g0043a0001c0002t0001g0085others(24): Show | 27 | HG00738.hp2 HG01081.hp1 HG01981.hp2 others(24): Show |
intron_variant | MODIFIER | c.3399-2827dupT | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr2 | 127617487 | |||||
| chr2:127617487
|
G | GTT | 31 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0033others(28): Show | 32 | HG00099.hp1 HG00735.hp2 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.3399-2828_3399-282 others(6): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr2 | 127617487 | |||||
| chr2:127617487
|
G | GTTT | 56 | a0001c0002t0001g0031a0001c0002t0001g0036a0001c0002t0001g0038others(53): Show | 56 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.3399-2829_3399-282 others(7): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr2 | 127617487 | |||||
| chr2:127617487
|
G | GTTTT | 29 | a0001c0002t0001g0097a0001c0002t0001g0098a0001c0002t0001g0103others(26): Show | 30 | HG00642.hp1 HG00642.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.3399-2830_3399-282 others(8): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr2 | 127617487 | |||||
| chr2:127617487
|
G | GTTTTT | 10 | a0001c0013t0001g0163a0002c0006t0001g0156a0004c0007t0001g0161others(7): Show | 10 | HG00738.hp1 HG01106.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.3399-2831_3399-282 others(9): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr2 | 127617487 | |||||
| chr2:127617487
|
G | GTTTTTTT | 11 | a0001c0005t0002g0041a0001c0005t0002g0047a0001c0005t0002g0090others(8): Show | 11 | HG01070.hp1 HG01256.hp1 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.3399-2833_3399-282 others(11): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr2 | 127617487 | |||||
| chr2:127617487
|
G | GTTTTTTT others(1): Show |
12 | a0001c0005t0001g0045a0001c0005t0001g0095a0001c0005t0002g0049others(9): Show | 12 | HG01258.hp2 HG01516.hp1 HG02027.hp2 others(9): Show |
intron_variant | MODIFIER | c.3399-2834_3399-282 others(12): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr2 | 127617487 | |||||
| chr2:127617487
|
G | T | 1 | a0020c0046t0003g0075 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3399-2853G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617487 | ||||||
| chr2:127617487
|
GT | G | 21 | a0003c0003t0001g0030a0003c0003t0001g0078a0003c0003t0001g0106others(18): Show | 22 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.3399-2827delT | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr2 | 127617487 | |||||
| chr2:127617487
|
GTT | G | 6 | a0001c0002t0001g0275a0003c0003t0001g0119a0003c0003t0001g0223others(3): Show | 6 | HG02074.hp2 HG02647.hp1 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.3399-2828_3399-282 others(6): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr2 | 127617487 | |||||
| chr2:127617487
|
GTTTTTTT others(6): Show |
G | 1 | a0001c0004t0001g0235 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.3399-2839_3399-282 others(17): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr2 | 127617487 | |||||
| chr2:127617487
|
GTTTTTTT others(7): Show |
G | 3 | a0001c0004t0001g0063a0001c0004t0001g0118a0001c0004t0001g0225 | 3 | NA18612.hp2 NA18942.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.3399-2840_3399-282 others(18): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr2 | 127617487 | |||||
| chr2:127617503
|
T | G | 1 | a0007c0025t0001g0039 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3399-2837T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617503 | ||||||
| chr2:127617519
|
G | A | 8 | a0004c0007t0001g0254a0004c0007t0001g0256a0004c0007t0003g0069others(5): Show | 8 | HG00280.hp2 HG00642.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.3399-2821G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617519 | ||||||
| chr2:127617550
|
C | CG | 9 | a0002c0006t0001g0013a0006c0009t0001g0017a0006c0009t0001g0034others(6): Show | 9 | HG00323.hp2 HG00733.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.3399-2788dupG | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr2 | 127617550 | |||||
| chr2:127617566
|
C | A | 99 | a0001c0005t0001g0045a0001c0005t0001g0095a0001c0005t0002g0041others(96): Show | 101 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.3399-2774C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617566 | ||||||
| chr2:127617567
|
A | G | 1 | a0022c0064t0002g0140 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3399-2773A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617567 | ||||||
| chr2:127617591
|
T | C | 1 | a0020c0046t0003g0075 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3399-2749T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617591 | ||||||
| chr2:127617596
|
A | G | 206 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(203): Show | 209 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.3399-2744A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617596 | ||||||
| chr2:127617643
|
C | CT | 2 | a0010c0016t0001g0005a0010c0016t0001g0138 | 3 | HG02630.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3399-2697_3399-269 others(5): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617643 | ||||||
| chr2:127617658
|
G | T | 1 | a0032c0065t0001g0137 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3399-2682G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617658 | ||||||
| chr2:127617659
|
C | T | 6 | a0004c0007t0001g0158a0004c0007t0001g0161a0004c0007t0001g0265others(3): Show | 6 | HG00735.hp2 HG01106.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.3399-2681C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617659 | ||||||
| chr2:127617664
|
G | A | 1 | a0032c0065t0001g0137 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3399-2676G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617664 | ||||||
| chr2:127617692
|
C | T | 51 | a0001c0005t0001g0045a0001c0005t0001g0095a0001c0005t0002g0041others(48): Show | 52 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.3399-2648C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617692 | ||||||
| chr2:127617710
|
G | T | 1 | a0030c0060t0001g0053 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.3399-2630G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617710 | ||||||
| chr2:127617748
|
C | T | 1 | a0020c0046t0003g0075 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3399-2592C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617748 | ||||||
| chr2:127617779
|
G | A | 2 | a0002c0012t0001g0112a0002c0012t0001g0194 | 2 | NA19000.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.3399-2561G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617779 | ||||||
| chr2:127617797
|
C | T | 1 | a0002c0001t0001g0171 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.3399-2543C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617797 | ||||||
| chr2:127617815
|
T | A | 1 | a0001c0044t0003g0077 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3399-2525T>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617815 | ||||||
| chr2:127617855
|
G | GT | 6 | a0002c0001t0001g0188a0003c0003t0001g0237a0005c0008t0001g0213others(3): Show | 6 | HG01256.hp2 HG02486.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.3399-2471dupT | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr2 | 127617855 | |||||
| chr2:127617855
|
G | GTT | 82 | a0001c0002t0001g0032a0001c0005t0001g0045a0001c0005t0001g0095others(79): Show | 82 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.3399-2472_3399-247 others(6): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr2 | 127617855 | |||||
| chr2:127617855
|
G | GTTT | 109 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(106): Show | 111 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(108): Show |
intron_variant | MODIFIER | c.3399-2473_3399-247 others(7): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr2 | 127617855 | |||||
| chr2:127617901
|
A | G | 151 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(148): Show | 152 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.3399-2439A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617901 | ||||||
| chr2:127617967
|
C | T | 48 | a0003c0003t0001g0030a0003c0003t0001g0078a0003c0003t0001g0106others(45): Show | 49 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.3399-2373C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617967 | ||||||
| chr2:127617982
|
C | T | 1 | a0002c0006t0001g0150 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.3399-2358C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617982 | ||||||
| chr2:127617990
|
A | G | 44 | a0001c0005t0001g0045a0001c0005t0001g0095a0001c0005t0002g0041others(41): Show | 44 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.3399-2350A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127617990 | ||||||
| chr2:127618095
|
G | T | 53 | a0001c0005t0001g0045a0001c0005t0001g0095a0001c0005t0002g0041others(50): Show | 54 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.3399-2245G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618095 | ||||||
| chr2:127618096
|
C | G | 1 | a0001c0005t0002g0062 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3399-2244C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618096 | ||||||
| chr2:127618147
|
C | T | 99 | a0001c0005t0001g0045a0001c0005t0001g0095a0001c0005t0002g0041others(96): Show | 101 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.3399-2193C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618147 | ||||||
| chr2:127618157
|
C | A | 1 | a0001c0002t0001g0134 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3399-2183C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618157 | ||||||
| chr2:127618238
|
G | A | 2 | a0014c0072t0001g0009a0024c0073t0001g0065 | 2 | HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3399-2102G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618238 | ||||||
| chr2:127618246
|
G | C | 48 | a0001c0005t0001g0045a0001c0005t0001g0095a0001c0005t0002g0041others(45): Show | 48 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.3399-2094G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618246 | ||||||
| chr2:127618260
|
G | T | 1 | a0037c0074t0001g0023 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3399-2080G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618260 | ||||||
| chr2:127618270
|
G | A | 1 | a0001c0044t0003g0077 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3399-2070G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618270 | ||||||
| chr2:127618271
|
T | C | 1 | a0002c0001t0001g0172 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3399-2069T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618271 | ||||||
| chr2:127618277
|
T | C | 5 | a0003c0003t0001g0121a0003c0003t0001g0123a0003c0003t0001g0214others(2): Show | 5 | HG01123.hp2 HG01433.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.3399-2063T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618277 | ||||||
| chr2:127618279
|
A | G | 2 | a0009c0014t0001g0101a0009c0014t0001g0133 | 2 | HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.3399-2061A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618279 | ||||||
| chr2:127618367
|
C | T | 1 | a0001c0017t0004g0021 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3399-1973C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618367 | ||||||
| chr2:127618368
|
A | G | 203 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(200): Show | 206 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.3399-1972A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618368 | ||||||
| chr2:127618378
|
A | G | 1 | a0032c0065t0001g0137 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3399-1962A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618378 | ||||||
| chr2:127618420
|
G | A | 1 | a0001c0044t0003g0077 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3399-1920G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618420 | ||||||
| chr2:127618424
|
C | T | 51 | a0003c0003t0001g0030a0003c0003t0001g0078a0003c0003t0001g0106others(48): Show | 53 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.3399-1916C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618424 | ||||||
| chr2:127618425
|
G | A | 3 | a0001c0044t0003g0077a0019c0070t0001g0025a0020c0046t0003g0075 | 3 | HG01891.hp2 HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.3399-1915G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618425 | ||||||
| chr2:127618443
|
C | T | 102 | a0001c0005t0001g0045a0001c0005t0001g0095a0001c0005t0002g0041others(99): Show | 104 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.3399-1897C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618443 | ||||||
| chr2:127618460
|
T | G | 47 | a0003c0003t0001g0030a0003c0003t0001g0078a0003c0003t0001g0106others(44): Show | 48 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.3399-1880T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618460 | ||||||
| chr2:127618497
|
T | A | 1 | a0002c0001t0001g0189 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.3399-1843T>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618497 | ||||||
| chr2:127618542
|
C | T | 222 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(219): Show | 225 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.3399-1798C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618542 | ||||||
| chr2:127618600
|
T | C | 54 | a0003c0003t0001g0030a0003c0003t0001g0078a0003c0003t0001g0106others(51): Show | 56 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.3399-1740T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618600 | ||||||
| chr2:127618613
|
C | T | 1 | a0019c0070t0001g0025 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3399-1727C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618613 | ||||||
| chr2:127618632
|
T | C | 1 | a0032c0065t0001g0137 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3399-1708T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618632 | ||||||
| chr2:127618826
|
G | A | 100 | a0001c0005t0001g0045a0001c0005t0001g0095a0001c0005t0002g0041others(97): Show | 102 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.3399-1514G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618826 | ||||||
| chr2:127618885
|
A | C | 3 | a0010c0016t0001g0005a0010c0016t0001g0138a0023c0048t0001g0129 | 4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3399-1455A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618885 | ||||||
| chr2:127618984
|
C | T | 3 | a0010c0016t0001g0005a0010c0016t0001g0138a0023c0048t0001g0129 | 4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3399-1356C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127618984 | ||||||
| chr2:127619038
|
G | GGTGGGCG others(11): Show |
3 | a0010c0016t0001g0005a0010c0016t0001g0138a0023c0048t0001g0129 | 4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3399-1296_3399-127 others(22): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr2 | 127619038 | |||||
| chr2:127619054
|
A | ATTGTGGG others(11): Show |
5 | a0001c0010t0001g0159a0013c0022t0001g0115a0013c0022t0001g0212others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.3399-1250_3399-123 others(22): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr2 | 127619054 | |||||
| chr2:127619056
|
TGTG | T | 47 | a0003c0003t0001g0030a0003c0003t0001g0078a0003c0003t0001g0106others(44): Show | 48 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.3399-1282_3399-128 others(7): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr2 | 127619056 | |||||
| chr2:127619062
|
G | A | 45 | a0001c0005t0001g0045a0001c0005t0001g0095a0001c0005t0002g0041others(42): Show | 45 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.3399-1278G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127619062 | ||||||
| chr2:127619138
|
A | G | 3 | a0010c0016t0001g0005a0010c0016t0001g0138a0023c0048t0001g0129 | 4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3399-1202A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127619138 | ||||||
| chr2:127619149
|
G | C | 5 | a0002c0006t0001g0152a0002c0006t0001g0153a0002c0006t0001g0154others(2): Show | 5 | HG00738.hp1 HG00741.hp2 HG01070.hp2 others(2): Show |
intron_variant | MODIFIER | c.3399-1191G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127619149 | ||||||
| chr2:127619173
|
T | C | 3 | a0010c0016t0001g0005a0010c0016t0001g0138a0023c0048t0001g0129 | 4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3399-1167T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127619173 | ||||||
| chr2:127619226
|
GTGGTTGG others(11): Show |
G | 2 | a0007c0024t0001g0083a0007c0024t0001g0261 | 2 | HG03195.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3399-1099_3399-108 others(22): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr2 | 127619226 | |||||
| chr2:127619230
|
TTGGGTTG others(44): Show |
T | 3 | a0010c0016t0001g0005a0010c0016t0001g0138a0023c0048t0001g0129 | 4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3399-1104_3399-105 others(55): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr2 | 127619230 | |||||
| chr2:127619260
|
C | T | 1 | a0001c0044t0003g0077 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3399-1080C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127619260 | ||||||
| chr2:127619279
|
G | A | 6 | a0004c0007t0001g0158a0004c0007t0001g0161a0004c0007t0001g0265others(3): Show | 6 | HG00735.hp2 HG01106.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.3399-1061G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127619279 | ||||||
| chr2:127619285
|
G | A | 3 | a0010c0016t0001g0005a0010c0016t0001g0138a0023c0048t0001g0129 | 4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3399-1055G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127619285 | ||||||
| chr2:127619294
|
G | T | 3 | a0010c0016t0001g0005a0010c0016t0001g0138a0023c0048t0001g0129 | 4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3399-1046G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127619294 | ||||||
| chr2:127619303
|
G | A | 3 | a0010c0016t0001g0005a0010c0016t0001g0138a0023c0048t0001g0129 | 4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3399-1037G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127619303 | ||||||
| chr2:127619336
|
T | C | 3 | a0010c0016t0001g0005a0010c0016t0001g0138a0023c0048t0001g0129 | 4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3399-1004T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127619336 | ||||||
| chr2:127619349
|
C | T | 3 | a0010c0016t0001g0005a0010c0016t0001g0138a0023c0048t0001g0129 | 4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3399-991C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127619349 | ||||||
| chr2:127619353
|
G | A | 3 | a0010c0016t0001g0005a0010c0016t0001g0138a0023c0048t0001g0129 | 4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3399-987G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127619353 | ||||||
| chr2:127619361
|
C | G | 6 | a0008c0015t0001g0104a0008c0015t0001g0164a0008c0015t0001g0165others(3): Show | 7 | HG02145.hp1 HG02280.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.3399-979C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127619361 | ||||||
| chr2:127619365
|
AGCTGAGT others(11): Show |
A | 3 | a0010c0016t0001g0005a0010c0016t0001g0138a0023c0048t0001g0129 | 4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3399-970_3399-953d others(20): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | INFO_REALIGN_3_PRIME | chr2 | 127619365 | |||||
| chr2:127619383
|
G | A | 1 | a0011c0020t0001g0144 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3399-957G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127619383 | ||||||
| chr2:127619400
|
T | C | 3 | a0010c0016t0001g0005a0010c0016t0001g0138a0023c0048t0001g0129 | 4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3399-940T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127619400 | ||||||
| chr2:127619403
|
A | C | 3 | a0010c0016t0001g0005a0010c0016t0001g0138a0023c0048t0001g0129 | 4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3399-937A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127619403 | ||||||
| chr2:127619407
|
A | G | 3 | a0010c0016t0001g0005a0010c0016t0001g0138a0023c0048t0001g0129 | 4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3399-933A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127619407 | ||||||
| chr2:127619473
|
C | T | 1 | a0001c0004t0001g0240 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3399-867C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127619473 | ||||||
| chr2:127619497
|
C | T | 2 | a0009c0014t0001g0101a0009c0014t0001g0133 | 2 | HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.3399-843C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127619497 | ||||||
| chr2:127619679
|
T | G | 3 | a0010c0016t0001g0005a0010c0016t0001g0138a0023c0048t0001g0129 | 4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3399-661T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127619679 | ||||||
| chr2:127619857
|
C | T | 3 | a0010c0016t0001g0005a0010c0016t0001g0138a0023c0048t0001g0129 | 4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3399-483C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127619857 | ||||||
| chr2:127619983
|
G | A | 1 | a0002c0006t0001g0011 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.3399-357G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127619983 | ||||||
| chr2:127620003
|
G | A | 1 | a0031c0057t0001g0076 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3399-337G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127620003 | ||||||
| chr2:127620126
|
G | A | 1 | a0001c0002t0001g0275 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3399-214G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127620126 | ||||||
| chr2:127620213
|
C | T | 1 | a0001c0002t0001g0032 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.3399-127C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127620213 | ||||||
| chr2:127620216
|
C | T | 3 | a0010c0016t0001g0005a0010c0016t0001g0138a0023c0048t0001g0129 | 4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3399-124C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127620216 | ||||||
| chr2:127620229
|
C | A | 3 | a0010c0016t0001g0005a0010c0016t0001g0138a0023c0048t0001g0129 | 4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3399-111C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127620229 | ||||||
| chr2:127620258
|
C | G | 206 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(203): Show | 209 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.3399-82C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127620258 | ||||||
| chr2:127620267
|
T | C | 18 | a0004c0007t0001g0158a0004c0007t0001g0161a0004c0007t0001g0254others(15): Show | 18 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.3399-73T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 26/47 | chr2 | 127620267 | ||||||
| chr2:127620561
|
A | C | 102 | a0001c0005t0001g0045a0001c0005t0001g0095a0001c0005t0002g0041others(99): Show | 104 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.3525+95A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127620561 | ||||||
| chr2:127620562
|
C | T | 3 | a0001c0044t0003g0077a0008c0015t0001g0044a0008c0063t0001g0263 | 3 | HG01243.hp2 HG02809.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3525+96C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127620562 | ||||||
| chr2:127620619
|
C | T | 1 | a0020c0046t0003g0075 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3525+153C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127620619 | ||||||
| chr2:127620623
|
A | C | 3 | a0010c0016t0001g0005a0010c0016t0001g0138a0023c0048t0001g0129 | 4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3525+157A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127620623 | ||||||
| chr2:127620680
|
G | A | 1 | a0019c0070t0001g0025 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3525+214G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127620680 | ||||||
| chr2:127620685
|
G | T | 1 | a0001c0004t0001g0252 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.3525+219G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127620685 | ||||||
| chr2:127620726
|
T | C | 3 | a0010c0016t0001g0005a0010c0016t0001g0138a0023c0048t0001g0129 | 4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3525+260T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127620726 | ||||||
| chr2:127620760
|
G | A | 1 | a0032c0065t0001g0137 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3525+294G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127620760 | ||||||
| chr2:127620790
|
G | T | 3 | a0001c0005t0002g0049a0001c0005t0002g0091a0033c0059t0001g0028 | 3 | HG01256.hp1 HG01258.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.3525+324G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127620790 | ||||||
| chr2:127620812
|
C | T | 1 | a0008c0042t0001g0061 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3525+346C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127620812 | ||||||
| chr2:127620884
|
C | G | 2 | a0014c0072t0001g0009a0024c0073t0001g0065 | 2 | HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3525+418C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127620884 | ||||||
| chr2:127620965
|
C | T | 2 | a0007c0024t0001g0083a0020c0046t0003g0075 | 2 | HG01891.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.3525+499C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127620965 | ||||||
| chr2:127620988
|
G | A | 102 | a0001c0005t0001g0045a0001c0005t0001g0095a0001c0005t0002g0041others(99): Show | 104 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.3525+522G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127620988 | ||||||
| chr2:127620998
|
C | T | 3 | a0001c0005t0001g0045a0001c0005t0002g0041a0002c0011t0002g0105 | 3 | HG04184.hp2 NA18968.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.3525+532C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127620998 | ||||||
| chr2:127621249
|
T | G | 4 | a0001c0017t0004g0021a0001c0017t0004g0022a0001c0017t0004g0071others(1): Show | 4 | HG02258.hp2 HG02630.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.3526-733T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127621249 | ||||||
| chr2:127621253
|
AT | A | 147 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(144): Show | 149 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.3526-718delT | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | INFO_REALIGN_3_PRIME | chr2 | 127621253 | |||||
| chr2:127621259
|
T | G | 1 | a0001c0044t0003g0077 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3526-723T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127621259 | ||||||
| chr2:127621263
|
T | TG | 4 | a0001c0005t0002g0047a0001c0005t0002g0049a0001c0005t0002g0091others(1): Show | 4 | HG01256.hp1 HG01258.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.3526-719_3526-718i others(3): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127621263 | ||||||
| chr2:127621264
|
T | G | 49 | a0001c0002t0001g0033a0001c0002t0001g0058a0001c0005t0001g0045others(46): Show | 49 | HG00099.hp1 HG00280.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.3526-718T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127621264 | ||||||
| chr2:127621265
|
G | T | 53 | a0001c0002t0001g0033a0001c0002t0001g0058a0001c0005t0001g0045others(50): Show | 53 | HG00099.hp1 HG00280.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.3526-717G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127621265 | ||||||
| chr2:127621266
|
T | G | 1 | a0002c0012t0001g0209 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.3526-716T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127621266 | ||||||
| chr2:127621267
|
T | G | 2 | a0019c0070t0001g0025a0022c0064t0002g0140 | 2 | HG02257.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.3526-715T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127621267 | ||||||
| chr2:127621303
|
G | A | 1 | a0010c0016t0001g0138 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3526-679G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127621303 | ||||||
| chr2:127621460
|
C | T | 1 | a0001c0002t0001g0134 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3526-522C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127621460 | ||||||
| chr2:127621753
|
T | C | 1 | a0001c0044t0003g0077 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3526-229T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127621753 | ||||||
| chr2:127621765
|
A | G | 106 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(103): Show | 107 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(104): Show |
intron_variant | MODIFIER | c.3526-217A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127621765 | ||||||
| chr2:127621863
|
G | T | 4 | a0009c0014t0001g0101a0009c0014t0001g0133a0009c0014t0001g0170others(1): Show | 4 | HG02486.hp2 HG02572.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.3526-119G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127621863 | ||||||
| chr2:127621907
|
G | A | 18 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(15): Show | 18 | HG01099.hp1 HG01943.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.3526-75G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 27/47 | chr2 | 127621907 | ||||||
| chr2:127622144
|
C | T | 3 | a0010c0016t0001g0005a0010c0016t0001g0138a0023c0048t0001g0129 | 4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3645+43C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 28/47 | chr2 | 127622144 | ||||||
| chr2:127622231
|
A | G | 1 | a0032c0065t0001g0137 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3645+130A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 28/47 | chr2 | 127622231 | ||||||
| chr2:127622261
|
T | C | 1 | a0019c0070t0001g0025 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3645+160T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 28/47 | chr2 | 127622261 | ||||||
| chr2:127622274
|
C | T | 1 | a0001c0044t0003g0077 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3645+173C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 28/47 | chr2 | 127622274 | ||||||
| chr2:127622375
|
G | A | 4 | a0001c0017t0004g0021a0001c0017t0004g0022a0001c0017t0004g0071others(1): Show | 4 | HG02258.hp2 HG02630.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.3645+274G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 28/47 | chr2 | 127622375 | ||||||
| chr2:127622376
|
C | G | 5 | a0001c0010t0001g0159a0013c0022t0001g0115a0013c0022t0001g0212others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.3645+275C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 28/47 | chr2 | 127622376 | ||||||
| chr2:127622416
|
G | C | 46 | a0003c0003t0001g0030a0003c0003t0001g0078a0003c0003t0001g0106others(43): Show | 47 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.3645+315G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 28/47 | chr2 | 127622416 | ||||||
| chr2:127622524
|
G | A | 1 | a0027c0052t0001g0084 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.3645+423G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 28/47 | chr2 | 127622524 | ||||||
| chr2:127622526
|
T | C | 1 | a0031c0057t0001g0076 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3645+425T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 28/47 | chr2 | 127622526 | ||||||
| chr2:127622622
|
C | T | 1 | a0001c0002t0001g0134 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3645+521C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 28/47 | chr2 | 127622622 | ||||||
| chr2:127622646
|
G | A | 2 | a0002c0001t0001g0185a0012c0027t0001g0260 | 2 | HG01891.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.3645+545G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 28/47 | chr2 | 127622646 | ||||||
| chr2:127622712
|
C | G | 2 | a0007c0023t0001g0126a0007c0023t0001g0221 | 2 | HG02109.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.3646-490C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 28/47 | chr2 | 127622712 | ||||||
| chr2:127622737
|
C | T | 1 | a0020c0046t0003g0075 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3646-465C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 28/47 | chr2 | 127622737 | ||||||
| chr2:127622959
|
C | T | 1 | a0002c0001t0006g0180 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3646-243C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 28/47 | chr2 | 127622959 | ||||||
| chr2:127623104
|
C | T | 1 | a0020c0046t0003g0075 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3646-98C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 28/47 | chr2 | 127623104 | ||||||
| chr2:127623397
|
C | T | 8 | a0001c0010t0001g0135a0001c0010t0001g0136a0001c0010t0001g0262others(5): Show | 8 | HG02109.hp2 HG02451.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.3819+22C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 29/47 | chr2 | 127623397 | ||||||
| chr2:127623509
|
C | T | 1 | a0001c0010t0001g0270 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3819+134C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 29/47 | chr2 | 127623509 | ||||||
| chr2:127623579
|
G | A | 98 | a0001c0005t0001g0045a0001c0005t0001g0095a0001c0005t0002g0041others(95): Show | 99 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.3819+204G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 29/47 | chr2 | 127623579 | ||||||
| chr2:127623636
|
A | C | 2 | a0002c0006t0001g0012a0002c0006t0001g0013 | 2 | HG00741.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.3819+261A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 29/47 | chr2 | 127623636 | ||||||
| chr2:127623752
|
A | G | 1 | a0001c0044t0003g0077 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3820-341A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 29/47 | chr2 | 127623752 | ||||||
| chr2:127623753
|
C | A | 1 | a0001c0044t0003g0077 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3820-340C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 29/47 | chr2 | 127623753 | ||||||
| chr2:127623803
|
T | TCAGA | 3 | a0010c0016t0001g0005a0010c0016t0001g0138a0023c0048t0001g0129 | 4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3820-288_3820-287i others(6): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr2 | 127623803 | |||||
| chr2:127623810
|
C | G | 2 | a0007c0023t0001g0126a0007c0023t0001g0221 | 2 | HG02109.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.3820-283C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 29/47 | chr2 | 127623810 | ||||||
| chr2:127623810
|
C | T | 1 | a0001c0005t0002g0128 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3820-283C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 29/47 | chr2 | 127623810 | ||||||
| chr2:127623828
|
C | T | 3 | a0010c0016t0001g0005a0010c0016t0001g0138a0023c0048t0001g0129 | 4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3820-265C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 29/47 | chr2 | 127623828 | ||||||
| chr2:127623969
|
C | T | 3 | a0010c0016t0001g0005a0010c0016t0001g0138a0023c0048t0001g0129 | 4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3820-124C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 29/47 | chr2 | 127623969 | ||||||
| chr2:127624019
|
C | T | 46 | a0003c0003t0001g0030a0003c0003t0001g0078a0003c0003t0001g0106others(43): Show | 47 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.3820-74C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 29/47 | chr2 | 127624019 | ||||||
| chr2:127624020
|
G | A | 4 | a0001c0017t0004g0021a0001c0017t0004g0022a0001c0017t0004g0071others(1): Show | 4 | HG02258.hp2 HG02630.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.3820-73G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 29/47 | chr2 | 127624020 | ||||||
| chr2:127624414
|
A | C | 4 | a0002c0001t0001g0173a0002c0001t0001g0187a0002c0001t0001g0188others(1): Show | 4 | HG02135.hp2 NA18964.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.4047+94A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 30/47 | chr2 | 127624414 | ||||||
| chr2:127624519
|
C | T | 1 | a0004c0007t0001g0158 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.4047+199C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 30/47 | chr2 | 127624519 | ||||||
| chr2:127624569
|
C | T | 3 | a0001c0018t0001g0272a0001c0018t0001g0273a0001c0018t0001g0274 | 3 | HG02622.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.4047+249C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 30/47 | chr2 | 127624569 | ||||||
| chr2:127624607
|
C | T | 3 | a0010c0016t0001g0005a0010c0016t0001g0138a0023c0048t0001g0129 | 4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.4047+287C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 30/47 | chr2 | 127624607 | ||||||
| chr2:127624761
|
G | A | 1 | a0002c0011t0002g0196 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.4047+441G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 30/47 | chr2 | 127624761 | ||||||
| chr2:127624862
|
G | A | 3 | a0010c0016t0001g0005a0010c0016t0001g0138a0023c0048t0001g0129 | 4 | HG02630.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.4048-506G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 30/47 | chr2 | 127624862 | ||||||
| chr2:127624898
|
A | G | 2 | a0007c0023t0001g0126a0007c0023t0001g0221 | 2 | HG02109.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.4048-470A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 30/47 | chr2 | 127624898 | ||||||
| chr2:127624914
|
C | T | 1 | a0009c0014t0001g0220 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.4048-454C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 30/47 | chr2 | 127624914 | ||||||
| chr2:127625079
|
G | A | 1 | a0002c0006t0001g0013 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.4048-289G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 30/47 | chr2 | 127625079 | ||||||
| chr2:127625082
|
G | A | 26 | a0001c0005t0001g0045a0001c0005t0001g0095a0001c0005t0002g0041others(23): Show | 26 | HG01070.hp1 HG01256.hp1 HG01258.hp2 others(23): Show |
intron_variant | MODIFIER | c.4048-286G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 30/47 | chr2 | 127625082 | ||||||
| chr2:127625086
|
C | T | 3 | a0014c0053t0001g0277a0014c0072t0001g0009a0024c0073t0001g0065 | 3 | HG02572.hp1 HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.4048-282C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 30/47 | chr2 | 127625086 | ||||||
| chr2:127625103
|
C | G | 26 | a0001c0005t0001g0045a0001c0005t0001g0095a0001c0005t0002g0041others(23): Show | 26 | HG01070.hp1 HG01256.hp1 HG01258.hp2 others(23): Show |
intron_variant | MODIFIER | c.4048-265C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 30/47 | chr2 | 127625103 | ||||||
| chr2:127625230
|
G | A | 1 | a0001c0002t0001g0134 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4048-138G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 30/47 | chr2 | 127625230 | ||||||
| chr2:127625262
|
T | C | 22 | a0001c0005t0001g0045a0001c0005t0001g0095a0001c0005t0002g0041others(19): Show | 22 | HG01070.hp1 HG01256.hp1 HG01258.hp2 others(19): Show |
intron_variant | MODIFIER | c.4048-106T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 30/47 | chr2 | 127625262 | ||||||
| chr2:127625267
|
T | C | 51 | a0003c0003t0001g0030a0003c0003t0001g0078a0003c0003t0001g0106others(48): Show | 53 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.4048-101T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 30/47 | chr2 | 127625267 | ||||||
| chr2:127625284
|
C | T | 209 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(206): Show | 212 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.4048-84C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 30/47 | chr2 | 127625284 | ||||||
| chr2:127625599
|
T | C | 19 | a0004c0007t0001g0158a0004c0007t0001g0161a0004c0007t0001g0254others(16): Show | 19 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.4215+64T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 31/47 | chr2 | 127625599 | ||||||
| chr2:127625791
|
T | C | 47 | a0001c0002t0001g0268a0001c0005t0001g0045a0001c0005t0001g0095others(44): Show | 47 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.4215+256T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 31/47 | chr2 | 127625791 | ||||||
| chr2:127625795
|
C | T | 1 | a0003c0003t0001g0241 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4215+260C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 31/47 | chr2 | 127625795 | ||||||
| chr2:127625871
|
C | A | 2 | a0001c0005t0002g0128a0002c0011t0002g0276 | 2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.4215+336C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 31/47 | chr2 | 127625871 | ||||||
| chr2:127625936
|
C | T | 2 | a0010c0016t0001g0005a0010c0016t0001g0138 | 3 | HG02630.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.4215+401C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 31/47 | chr2 | 127625936 | ||||||
| chr2:127626004
|
T | C | 2 | a0010c0016t0001g0005a0010c0016t0001g0138 | 3 | HG02630.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.4215+469T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 31/47 | chr2 | 127626004 | ||||||
| chr2:127626069
|
A | T | 5 | a0001c0010t0001g0159a0013c0022t0001g0115a0013c0022t0001g0212others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.4215+534A>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 31/47 | chr2 | 127626069 | ||||||
| chr2:127626243
|
A | G | 2 | a0007c0024t0001g0083a0007c0024t0001g0261 | 2 | HG03195.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.4215+708A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 31/47 | chr2 | 127626243 | ||||||
| chr2:127626280
|
G | A | 2 | a0010c0016t0001g0005a0010c0016t0001g0138 | 3 | HG02630.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.4216-695G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 31/47 | chr2 | 127626280 | ||||||
| chr2:127626305
|
C | T | 1 | a0002c0006t0001g0011 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.4216-670C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 31/47 | chr2 | 127626305 | ||||||
| chr2:127626402
|
GC | G | 4 | a0009c0014t0001g0101a0009c0014t0001g0133a0009c0014t0001g0170others(1): Show | 4 | HG02486.hp2 HG02572.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.4216-569delC | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 31/47 | INFO_REALIGN_3_PRIME | chr2 | 127626402 | |||||
| chr2:127626405
|
C | T | 4 | a0009c0014t0001g0101a0009c0014t0001g0133a0009c0014t0001g0170others(1): Show | 4 | HG02486.hp2 HG02572.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.4216-570C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 31/47 | chr2 | 127626405 | ||||||
| chr2:127626406
|
C | A | 4 | a0009c0014t0001g0101a0009c0014t0001g0133a0009c0014t0001g0170others(1): Show | 4 | HG02486.hp2 HG02572.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.4216-569C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 31/47 | chr2 | 127626406 | ||||||
| chr2:127626440
|
C | T | 2 | a0010c0016t0001g0005a0010c0016t0001g0138 | 3 | HG02630.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.4216-535C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 31/47 | chr2 | 127626440 | ||||||
| chr2:127626574
|
A | C | 1 | a0020c0046t0003g0075 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.4216-401A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 31/47 | chr2 | 127626574 | ||||||
| chr2:127626639
|
C | T | 23 | a0002c0006t0001g0015a0002c0006t0001g0016a0002c0006t0001g0150others(20): Show | 23 | HG00099.hp1 HG00280.hp2 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.4216-336C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 31/47 | chr2 | 127626639 | ||||||
| chr2:127626651
|
C | T | 26 | a0001c0005t0001g0045a0001c0005t0001g0095a0001c0005t0002g0041others(23): Show | 26 | HG01070.hp1 HG01256.hp1 HG01258.hp2 others(23): Show |
intron_variant | MODIFIER | c.4216-324C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 31/47 | chr2 | 127626651 | ||||||
| chr2:127626719
|
C | T | 1 | a0008c0063t0001g0263 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.4216-256C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 31/47 | chr2 | 127626719 | ||||||
| chr2:127626734
|
G | A | 1 | a0002c0006t0001g0153 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.4216-241G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 31/47 | chr2 | 127626734 | ||||||
| chr2:127626765
|
C | T | 1 | a0002c0001t0001g0184 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.4216-210C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 31/47 | chr2 | 127626765 | ||||||
| chr2:127626799
|
A | C | 1 | a0002c0001t0001g0184 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.4216-176A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 31/47 | chr2 | 127626799 | ||||||
| chr2:127627139
|
C | G | 1 | a0003c0003t0001g0030 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.4334-45C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 32/47 | chr2 | 127627139 | ||||||
| chr2:127627169
|
G | A | 22 | a0001c0010t0001g0135a0001c0010t0001g0136a0001c0010t0001g0159others(19): Show | 22 | HG01069.hp1 HG01071.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.4334-15G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 32/47 | chr2 | 127627169 | ||||||
| chr2:127627392
|
G | A | 2 | a0010c0016t0001g0005a0010c0016t0001g0138 | 3 | HG02630.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.4460+82G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 33/47 | chr2 | 127627392 | ||||||
| chr2:127627617
|
C | T | 1 | a0043c0032t0001g0168 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.4460+307C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 33/47 | chr2 | 127627617 | ||||||
| chr2:127627649
|
C | G | 100 | a0001c0005t0001g0045a0001c0005t0001g0095a0001c0005t0002g0041others(97): Show | 101 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.4460+339C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 33/47 | chr2 | 127627649 | ||||||
| chr2:127627653
|
G | A | 1 | a0003c0003t0001g0123 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.4460+343G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 33/47 | chr2 | 127627653 | ||||||
| chr2:127627669
|
T | C | 51 | a0001c0005t0001g0045a0001c0005t0001g0095a0001c0005t0002g0041others(48): Show | 51 | HG00099.hp1 HG00280.hp2 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.4460+359T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 33/47 | chr2 | 127627669 | ||||||
| chr2:127627756
|
C | CCCATGGG others(3): Show |
1 | a0001c0002t0001g0103 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4460+453_4460+462d others(12): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 33/47 | INFO_REALIGN_3_PRIME | chr2 | 127627756 | |||||
| chr2:127627765
|
C | A | 6 | a0001c0004t0001g0247a0002c0001t0001g0178a0002c0001t0001g0179others(3): Show | 6 | HG01168.hp2 HG01257.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.4460+455C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 33/47 | chr2 | 127627765 | ||||||
| chr2:127627811
|
G | A | 1 | a0001c0005t0003g0046 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4460+501G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 33/47 | chr2 | 127627811 | ||||||
| chr2:127627892
|
G | A | 1 | a0041c0030t0001g0205 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.4461-480G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 33/47 | chr2 | 127627892 | ||||||
| chr2:127628024
|
C | T | 2 | a0001c0002t0001g0033a0001c0002t0001g0082 | 2 | NA18964.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.4461-348C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 33/47 | chr2 | 127628024 | ||||||
| chr2:127628177
|
C | T | 2 | a0007c0023t0001g0126a0007c0023t0001g0221 | 2 | HG02109.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.4461-195C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 33/47 | chr2 | 127628177 | ||||||
| chr2:127628247
|
T | C | 2 | a0010c0016t0001g0005a0010c0016t0001g0138 | 3 | HG02630.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.4461-125T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 33/47 | chr2 | 127628247 | ||||||
| chr2:127628358
|
T | C | 2 | a0010c0016t0001g0005a0010c0016t0001g0138 | 3 | HG02630.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.4461-14T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 33/47 | chr2 | 127628358 | ||||||
| chr2:127628545
|
TGGGTG | T | 207 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(204): Show | 210 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.4624+39_4624+43del others(5): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 34/47 | INFO_REALIGN_3_PRIME | chr2 | 127628545 | |||||
| chr2:127628545
|
TGGGTGGG others(3): Show |
T | 2 | a0001c0002t0001g0130a0002c0001t0001g0181 | 2 | HG01361.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.4624+34_4624+43del others(10): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 34/47 | INFO_REALIGN_3_PRIME | chr2 | 127628545 | |||||
| chr2:127628545
|
TGGGTGGG others(13): Show |
T | 1 | a0001c0044t0003g0077 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4624+24_4624+43del others(20): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 34/47 | INFO_REALIGN_3_PRIME | chr2 | 127628545 | |||||
| chr2:127628563
|
G | T | 2 | a0009c0014t0001g0170a0009c0014t0001g0220 | 2 | HG02486.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.4624+28G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 34/47 | chr2 | 127628563 | ||||||
| chr2:127628632
|
G | A | 1 | a0008c0015t0001g0164 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.4624+97G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 34/47 | chr2 | 127628632 | ||||||
| chr2:127628675
|
G | A | 78 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(75): Show | 79 | HG00323.hp2 HG00642.hp1 HG00733.hp2 others(76): Show |
intron_variant | MODIFIER | c.4624+140G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 34/47 | chr2 | 127628675 | ||||||
| chr2:127628711
|
C | T | 1 | a0041c0030t0001g0205 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.4624+176C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 34/47 | chr2 | 127628711 | ||||||
| chr2:127628734
|
G | A | 1 | a0001c0044t0003g0077 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4624+199G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 34/47 | chr2 | 127628734 | ||||||
| chr2:127628789
|
G | T | 21 | a0001c0005t0001g0045a0001c0005t0001g0095a0001c0005t0002g0041others(18): Show | 21 | HG01070.hp1 HG01256.hp1 HG01258.hp2 others(18): Show |
intron_variant | MODIFIER | c.4624+254G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 34/47 | chr2 | 127628789 | ||||||
| chr2:127629045
|
G | A | 2 | a0010c0016t0001g0005a0010c0016t0001g0138 | 3 | HG02630.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.4624+510G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 34/47 | chr2 | 127629045 | ||||||
| chr2:127629069
|
G | C | 124 | a0001c0005t0001g0045a0001c0005t0001g0095a0001c0005t0002g0041others(121): Show | 126 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.4624+534G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 34/47 | chr2 | 127629069 | ||||||
| chr2:127629129
|
G | A | 1 | a0001c0005t0002g0128 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4625-516G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 34/47 | chr2 | 127629129 | ||||||
| chr2:127629235
|
A | C | 1 | a0001c0002t0001g0130 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.4625-410A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 34/47 | chr2 | 127629235 | ||||||
| chr2:127629415
|
G | A | 3 | a0001c0018t0001g0272a0001c0018t0001g0273a0001c0018t0001g0274 | 3 | HG02622.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.4625-230G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 34/47 | chr2 | 127629415 | ||||||
| chr2:127629614
|
C | T | 1 | a0001c0005t0003g0046 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4625-31C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 34/47 | chr2 | 127629614 | ||||||
| chr2:127629864
|
C | T | 1 | a0003c0003t0001g0214 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.4806+38C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 35/47 | chr2 | 127629864 | ||||||
| chr2:127629958
|
C | T | 1 | a0002c0011t0002g0276 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.4806+132C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 35/47 | chr2 | 127629958 | ||||||
| chr2:127630068
|
T | G | 1 | a0004c0007t0003g0007 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.4806+242T>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 35/47 | chr2 | 127630068 | ||||||
| chr2:127630082
|
C | A | 1 | a0002c0001t0001g0109 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.4806+256C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 35/47 | chr2 | 127630082 | ||||||
| chr2:127630105
|
C | G | 2 | a0007c0023t0001g0126a0007c0023t0001g0221 | 2 | HG02109.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.4806+279C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 35/47 | chr2 | 127630105 | ||||||
| chr2:127630144
|
G | A | 22 | a0001c0010t0001g0135a0001c0010t0001g0136a0001c0010t0001g0159others(19): Show | 22 | HG01069.hp1 HG01071.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.4806+318G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 35/47 | chr2 | 127630144 | ||||||
| chr2:127630168
|
A | T | 46 | a0003c0003t0001g0030a0003c0003t0001g0078a0003c0003t0001g0106others(43): Show | 47 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.4806+342A>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 35/47 | chr2 | 127630168 | ||||||
| chr2:127630181
|
C | G | 2 | a0010c0016t0001g0005a0010c0016t0001g0138 | 3 | HG02630.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.4806+355C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 35/47 | chr2 | 127630181 | ||||||
| chr2:127630267
|
TAGC | T | 4 | a0009c0014t0001g0101a0009c0014t0001g0133a0009c0014t0001g0170others(1): Show | 4 | HG02486.hp2 HG02572.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.4806+445_4806+447d others(5): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 35/47 | INFO_REALIGN_3_PRIME | chr2 | 127630267 | |||||
| chr2:127630362
|
G | A | 49 | a0001c0005t0001g0045a0001c0005t0001g0095a0001c0005t0002g0041others(46): Show | 49 | HG00099.hp1 HG00280.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.4807-416G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 35/47 | chr2 | 127630362 | ||||||
| chr2:127630364
|
G | A | 1 | a0003c0003t0001g0238 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.4807-414G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 35/47 | chr2 | 127630364 | ||||||
| chr2:127630395
|
C | T | 4 | a0009c0014t0001g0101a0009c0014t0001g0133a0009c0014t0001g0170others(1): Show | 4 | HG02486.hp2 HG02572.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.4807-383C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 35/47 | chr2 | 127630395 | ||||||
| chr2:127630512
|
C | T | 2 | a0009c0014t0001g0170a0009c0014t0001g0220 | 2 | HG02486.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.4807-266C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 35/47 | chr2 | 127630512 | ||||||
| chr2:127630732
|
C | T | 1 | a0016c0019t0001g0177 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.4807-46C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 35/47 | chr2 | 127630732 | ||||||
| chr2:127630758
|
C | T | 1 | a0001c0005t0002g0128 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4807-20C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 35/47 | chr2 | 127630758 | ||||||
| chr2:127630925
|
C | T | 2 | a0010c0016t0001g0005a0010c0016t0001g0138 | 3 | HG02630.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.4937+17C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 36/47 | chr2 | 127630925 | ||||||
| chr2:127630929
|
G | A | 1 | a0004c0007t0003g0257 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4937+21G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 36/47 | chr2 | 127630929 | ||||||
| chr2:127630940
|
CCCCCACC others(6): Show |
C | 1 | a0002c0006t0001g0011 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.4937+42_4937+54del others(13): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 36/47 | INFO_REALIGN_3_PRIME | chr2 | 127630940 | |||||
| chr2:127631030
|
C | CCA | 5 | a0002c0001t0001g0068a0002c0001t0001g0206a0002c0001t0001g0207others(2): Show | 5 | NA18947.hp1 NA18950.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.4937+124_4937+125d others(4): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 36/47 | INFO_REALIGN_3_PRIME | chr2 | 127631030 | |||||
| chr2:127631091
|
C | T | 1 | a0001c0044t0003g0077 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4938-115C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 36/47 | chr2 | 127631091 | ||||||
| chr2:127631093
|
G | A | 2 | a0010c0016t0001g0005a0010c0016t0001g0138 | 3 | HG02630.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.4938-113G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 36/47 | chr2 | 127631093 | ||||||
| chr2:127631584
|
T | C | 2 | a0002c0006t0001g0015a0002c0006t0001g0016 | 2 | HG00099.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.5096-16T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 37/47 | chr2 | 127631584 | ||||||
| chr2:127631765
|
C | G | 1 | a0002c0001t0001g0191 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.5249+12C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 38/47 | chr2 | 127631765 | ||||||
| chr2:127631766
|
G | C | 1 | a0002c0001t0001g0191 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.5249+13G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 38/47 | chr2 | 127631766 | ||||||
| chr2:127631768
|
C | T | 123 | a0001c0005t0001g0045a0001c0005t0001g0095a0001c0005t0002g0041others(120): Show | 124 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.5249+15C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 38/47 | chr2 | 127631768 | ||||||
| chr2:127631847
|
G | C | 125 | a0001c0005t0001g0045a0001c0005t0001g0095a0001c0005t0002g0041others(122): Show | 127 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.5249+94G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 38/47 | chr2 | 127631847 | ||||||
| chr2:127631853
|
G | A | 6 | a0003c0003t0001g0119a0003c0003t0001g0223a0003c0003t0001g0226others(3): Show | 6 | HG02074.hp2 HG02135.hp1 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.5249+100G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 38/47 | chr2 | 127631853 | ||||||
| chr2:127631902
|
C | G | 4 | a0009c0014t0001g0101a0009c0014t0001g0133a0009c0014t0001g0170others(1): Show | 4 | HG02486.hp2 HG02572.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.5249+149C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 38/47 | chr2 | 127631902 | ||||||
| chr2:127631929
|
G | A | 2 | a0004c0007t0001g0254a0004c0007t0001g0256 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.5249+176G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 38/47 | chr2 | 127631929 | ||||||
| chr2:127631998
|
C | T | 4 | a0009c0014t0001g0101a0009c0014t0001g0133a0009c0014t0001g0170others(1): Show | 4 | HG02486.hp2 HG02572.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.5249+245C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 38/47 | chr2 | 127631998 | ||||||
| chr2:127632003
|
C | T | 77 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(74): Show | 78 | HG00323.hp2 HG00642.hp1 HG00733.hp2 others(75): Show |
intron_variant | MODIFIER | c.5250-243C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 38/47 | chr2 | 127632003 | ||||||
| chr2:127632049
|
G | A | 125 | a0001c0005t0001g0045a0001c0005t0001g0095a0001c0005t0002g0041others(122): Show | 127 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.5250-197G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 38/47 | chr2 | 127632049 | ||||||
| chr2:127632075
|
C | T | 70 | a0001c0010t0001g0135a0001c0010t0001g0136a0001c0010t0001g0159others(67): Show | 71 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.5250-171C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 38/47 | chr2 | 127632075 | ||||||
| chr2:127632135
|
C | T | 1 | a0002c0012t0001g0194 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.5250-111C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 38/47 | chr2 | 127632135 | ||||||
| chr2:127632176
|
C | T | 21 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(18): Show | 21 | HG01081.hp1 HG01099.hp1 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.5250-70C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 38/47 | chr2 | 127632176 | ||||||
| chr2:127632197
|
C | G | 1 | a0002c0001t0001g0184 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.5250-49C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 38/47 | chr2 | 127632197 | ||||||
| chr2:127632223
|
G | A | 1 | a0001c0005t0003g0046 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.5250-23G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 38/47 | chr2 | 127632223 | ||||||
| chr2:127632224
|
G | A | 2 | a0010c0016t0001g0005a0010c0016t0001g0138 | 3 | HG02630.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.5250-22G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 38/47 | chr2 | 127632224 | ||||||
| chr2:127632469
|
G | A | 1 | a0001c0044t0003g0077 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.5405+68G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 39/47 | chr2 | 127632469 | ||||||
| chr2:127632611
|
C | A | 1 | a0004c0007t0003g0257 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.5405+210C>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 39/47 | chr2 | 127632611 | ||||||
| chr2:127632734
|
AGTCCATG others(41): Show |
A | 1 | a0022c0064t0002g0140 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.5405+335_5405+382d others(50): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 39/47 | INFO_REALIGN_3_PRIME | chr2 | 127632734 | |||||
| chr2:127632757
|
G | A | 2 | a0004c0007t0001g0161a0004c0054t0001g0160 | 2 | HG01175.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.5405+356G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 39/47 | chr2 | 127632757 | ||||||
| chr2:127632825
|
G | A | 25 | a0001c0005t0001g0045a0001c0005t0001g0095a0001c0005t0002g0041others(22): Show | 25 | HG01070.hp1 HG01256.hp1 HG01258.hp2 others(22): Show |
intron_variant | MODIFIER | c.5405+424G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 39/47 | chr2 | 127632825 | ||||||
| chr2:127632879
|
A | G | 1 | a0001c0004t0001g0118 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.5406-379A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 39/47 | chr2 | 127632879 | ||||||
| chr2:127632911
|
G | A | 21 | a0001c0005t0001g0045a0001c0005t0001g0095a0001c0005t0002g0041others(18): Show | 21 | HG01070.hp1 HG01256.hp1 HG01258.hp2 others(18): Show |
intron_variant | MODIFIER | c.5406-347G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 39/47 | chr2 | 127632911 | ||||||
| chr2:127632913
|
C | T | 1 | a0003c0003t0001g0241 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.5406-345C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 39/47 | chr2 | 127632913 | ||||||
| chr2:127632939
|
G | A | 1 | a0024c0073t0001g0065 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.5406-319G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 39/47 | chr2 | 127632939 | ||||||
| chr2:127632965
|
C | T | 1 | a0023c0048t0001g0129 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.5406-293C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 39/47 | chr2 | 127632965 | ||||||
| chr2:127633008
|
G | A | 2 | a0014c0053t0001g0277a0014c0072t0001g0009 | 2 | HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.5406-250G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 39/47 | chr2 | 127633008 | ||||||
| chr2:127633013
|
C | T | 82 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(79): Show | 83 | HG00323.hp2 HG00642.hp1 HG00733.hp2 others(80): Show |
intron_variant | MODIFIER | c.5406-245C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 39/47 | chr2 | 127633013 | ||||||
| chr2:127633087
|
C | T | 18 | a0001c0010t0001g0135a0001c0010t0001g0136a0001c0010t0001g0262others(15): Show | 18 | HG02109.hp1 HG02109.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.5406-171C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 39/47 | chr2 | 127633087 | ||||||
| chr2:127633088
|
G | A | 5 | a0004c0007t0003g0007a0004c0007t0003g0249a0007c0025t0001g0039others(2): Show | 5 | HG02132.hp1 HG03654.hp1 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.5406-170G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 39/47 | chr2 | 127633088 | ||||||
| chr2:127633114
|
A | G | 209 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(206): Show | 212 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.5406-144A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 39/47 | chr2 | 127633114 | ||||||
| chr2:127633183
|
G | A | 2 | a0002c0006t0001g0012a0002c0006t0001g0013 | 2 | HG00741.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.5406-75G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 39/47 | chr2 | 127633183 | ||||||
| chr2:127633243
|
C | T | 3 | a0001c0005t0002g0060a0001c0005t0002g0099a0001c0058t0002g0100 | 3 | NA18957.hp1 NA18986.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.5406-15C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 39/47 | chr2 | 127633243 | ||||||
| chr2:127633399
|
G | A | 1 | a0032c0065t0001g0137 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.5511+36G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 40/47 | chr2 | 127633399 | ||||||
| chr2:127633520
|
A | G | 1 | a0002c0001t0001g0201 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.5511+157A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 40/47 | chr2 | 127633520 | ||||||
| chr2:127633636
|
A | G | 2 | a0014c0053t0001g0277a0014c0072t0001g0009 | 2 | HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.5511+273A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 40/47 | chr2 | 127633636 | ||||||
| chr2:127633687
|
G | A | 2 | a0010c0016t0001g0005a0010c0016t0001g0138 | 3 | HG02630.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.5511+324G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 40/47 | chr2 | 127633687 | ||||||
| chr2:127633839
|
AGTGGGCA others(15): Show |
A | 1 | a0001c0005t0002g0051 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.5512-336_5512-315d others(24): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 40/47 | chr2 | 127633839 | ||||||
| chr2:127634066
|
T | C | 1 | a0001c0004t0001g0225 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.5512-110T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 40/47 | chr2 | 127634066 | ||||||
| chr2:127634148
|
G | A | 1 | a0002c0006t0001g0013 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.5512-28G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 40/47 | chr2 | 127634148 | ||||||
| chr2:127634156
|
C | T | 1 | a0002c0006t0001g0153 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.5512-20C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 40/47 | chr2 | 127634156 | ||||||
| chr2:127634322
|
C | T | 2 | a0013c0022t0001g0115a0013c0022t0001g0212 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.5625+33C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 41/47 | chr2 | 127634322 | ||||||
| chr2:127634374
|
C | T | 3 | a0001c0010t0001g0159a0013c0022t0001g0115a0013c0022t0001g0212 | 3 | HG01069.hp1 HG01071.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.5625+85C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 41/47 | chr2 | 127634374 | ||||||
| chr2:127634380
|
G | A | 5 | a0001c0010t0001g0159a0013c0022t0001g0115a0013c0022t0001g0212others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.5625+91G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 41/47 | chr2 | 127634380 | ||||||
| chr2:127634556
|
C | T | 1 | a0001c0005t0002g0211 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.5626-40C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 41/47 | chr2 | 127634556 | ||||||
| chr2:127634569
|
A | G | 1 | a0031c0057t0001g0076 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.5626-27A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 41/47 | chr2 | 127634569 | ||||||
| chr2:127634690
|
AGGCCTCT others(47): Show |
A | 3 | a0008c0015t0001g0104a0008c0015t0001g0164a0008c0015t0001g0165 | 3 | HG02145.hp1 HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.5713+18_5713+71del others(54): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 42/47 | INFO_REALIGN_3_PRIME | chr2 | 127634690 | |||||
| chr2:127634731
|
G | A | 2 | a0001c0005t0002g0041a0002c0001t0001g0179 | 2 | HG02698.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.5713+48G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 42/47 | chr2 | 127634731 | ||||||
| chr2:127634745
|
G | A | 1 | a0014c0072t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5713+62G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 42/47 | chr2 | 127634745 | ||||||
| chr2:127634756
|
G | A | 1 | a0032c0065t0001g0137 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.5713+73G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 42/47 | chr2 | 127634756 | ||||||
| chr2:127634893
|
A | G | 206 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(203): Show | 209 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.5713+210A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 42/47 | chr2 | 127634893 | ||||||
| chr2:127634972
|
A | C | 210 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(207): Show | 213 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.5714-148A>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 42/47 | chr2 | 127634972 | ||||||
| chr2:127635072
|
G | T | 43 | a0001c0005t0002g0041a0001c0005t0002g0047a0001c0005t0002g0049others(40): Show | 44 | HG00735.hp2 HG01069.hp1 HG01071.hp1 others(41): Show |
intron_variant | MODIFIER | c.5714-48G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 42/47 | chr2 | 127635072 | ||||||
| chr2:127635113
|
C | T | 9 | a0001c0002t0003g0042a0001c0044t0003g0077a0004c0007t0003g0007others(6): Show | 9 | HG00280.hp2 HG00642.hp2 HG01168.hp1 others(6): Show |
splice_region_variant&intron_variant | LOW | c.5714-7C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 42/47 | chr2 | 127635113 | ||||||
| chr2:127635307
|
G | A | 1 | a0002c0011t0002g0210 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.5820+81G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 43/47 | chr2 | 127635307 | ||||||
| chr2:127635576
|
C | T | 1 | a0001c0002t0001g0134 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.5821-146C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 43/47 | chr2 | 127635576 | ||||||
| chr2:127635654
|
G | A | 1 | a0001c0005t0003g0046 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.5821-68G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 43/47 | chr2 | 127635654 | ||||||
| chr2:127635686
|
T | C | 210 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(207): Show | 213 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.5821-36T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 43/47 | chr2 | 127635686 | ||||||
| chr2:127635714
|
T | C | 108 | a0001c0005t0002g0041a0001c0005t0002g0047a0001c0005t0002g0049others(105): Show | 110 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(107): Show |
splice_region_variant&intron_variant | LOW | c.5821-8T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 43/47 | chr2 | 127635714 | ||||||
| chr2:127635918
|
G | A | 1 | a0001c0002t0001g0131 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.6006+11G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 44/47 | chr2 | 127635918 | ||||||
| chr2:127635920
|
G | T | 1 | a0003c0026t0001g0246 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.6006+13G>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 44/47 | chr2 | 127635920 | ||||||
| chr2:127635956
|
G | A | 1 | a0001c0004t0001g0040 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.6006+49G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 44/47 | chr2 | 127635956 | ||||||
| chr2:127635979
|
C | T | 2 | a0009c0014t0001g0170a0009c0014t0001g0220 | 2 | HG02486.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.6006+72C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 44/47 | chr2 | 127635979 | ||||||
| chr2:127636044
|
C | G | 1 | a0001c0005t0003g0046 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.6006+137C>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 44/47 | chr2 | 127636044 | ||||||
| chr2:127636333
|
T | C | 5 | a0002c0006t0001g0015a0002c0006t0001g0016a0002c0006t0001g0150others(2): Show | 5 | HG00099.hp1 HG00733.hp1 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.6123+9T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 45/47 | chr2 | 127636333 | ||||||
| chr2:127636368
|
C | T | 1 | a0001c0005t0003g0046 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.6123+44C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 45/47 | chr2 | 127636368 | ||||||
| chr2:127636496
|
A | G | 1 | a0009c0014t0001g0133 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.6124-49A>G | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 45/47 | chr2 | 127636496 | ||||||
| chr2:127636511
|
G | C | 2 | a0007c0023t0001g0126a0007c0023t0001g0221 | 2 | HG02109.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.6124-34G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 45/47 | chr2 | 127636511 | ||||||
| chr2:127636669
|
CCAGGGAC others(5): Show |
C | 1 | a0001c0005t0002g0211 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.6207+46_6207+57del others(12): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 46/47 | INFO_REALIGN_3_PRIME | chr2 | 127636669 | |||||
| chr2:127636682
|
C | T | 1 | a0033c0059t0001g0028 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.6207+54C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 46/47 | chr2 | 127636682 | ||||||
| chr2:127636720
|
T | C | 1 | a0001c0005t0003g0046 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.6208-74T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 46/47 | chr2 | 127636720 | ||||||
| chr2:127636738
|
A | T | 8 | a0006c0009t0001g0017a0006c0009t0001g0034a0006c0009t0001g0048others(5): Show | 8 | HG00323.hp2 HG00733.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.6208-56A>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 46/47 | chr2 | 127636738 | ||||||
| chr2:127636745
|
G | C | 1 | a0039c0038t0002g0102 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.6208-49G>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 46/47 | chr2 | 127636745 | ||||||
| chr2:127636750
|
C | T | 2 | a0014c0053t0001g0277a0014c0072t0001g0009 | 2 | HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.6208-44C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 46/47 | chr2 | 127636750 | ||||||
| chr2:127636767
|
C | T | 1 | a0001c0044t0003g0077 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.6208-27C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 46/47 | chr2 | 127636767 | ||||||
| chr2:127637048
|
G | A | 1 | a0019c0070t0001g0025 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.6327+135G>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 47/47 | chr2 | 127637048 | ||||||
| chr2:127637111
|
T | A | 2 | a0009c0014t0001g0170a0009c0014t0001g0220 | 2 | HG02486.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.6327+198T>A | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 47/47 | chr2 | 127637111 | ||||||
| chr2:127637183
|
T | C | 132 | a0001c0002t0001g0134a0001c0002t0003g0042a0001c0005t0002g0041others(129): Show | 135 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.6328-133T>C | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 47/47 | chr2 | 127637183 | ||||||
| chr2:127637300
|
C | CA | 108 | a0001c0005t0002g0041a0001c0005t0002g0047a0001c0005t0002g0049others(105): Show | 110 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.6328-16_6328-15ins others(1): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 47/47 | chr2 | 127637300 | ||||||
| chr2:127637302
|
C | CT | 99 | a0001c0002t0001g0024a0001c0002t0001g0029a0001c0002t0001g0031others(96): Show | 100 | HG00280.hp2 HG00323.hp2 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.6328-14_6328-13ins others(1): Show |
MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 47/47 | chr2 | 127637302 | ||||||
| chr2:127637302
|
C | T | 108 | a0001c0005t0002g0041a0001c0005t0002g0047a0001c0005t0002g0049others(105): Show | 110 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.6328-14C>T | MYO7B | ENSG00000169994.20 | transcript | ENST00000409816.8 | protein_coding | 47/47 | chr2 | 127637302 |