Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 8735 |
|---|---|
| ensemblid | ENSG00000006788.14 |
| hgncid | 7571 |
| symbol | MYH13 |
| name | myosin heavy chain 13 |
| refseq_nuc | NM_003802.3 |
| refseq_prot | NP_003793.2 |
| ensembl_nuc | ENST00000252172.9 |
| ensembl_prot | ENSP00000252172.4 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 10300865 |
| end | 10373006 |
| strand | - |
| ver | v1.2 |
| region | chr17:10300865-10373006 |
| region5000 | chr17:10295865-10378006 |
| regionname0 | MYH13_chr17_10300865_10373006 |
| regionname5000 | MYH13_chr17_10295865_10378006 |
| 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 | 0/0 | 1938 | 129 | 39 | 33 | 42 | 7 | 8 | 33 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0002 | 0/0 | 1938 | 55 | 6 | 9 | 36 | 0 | 4 | 31 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0003 | 1/0 | 1938 | 54 | 11 | 12 | 20 | 3 | 7 | 16 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0004 | 0/1 | 1938 | 44 | 2 | 12 | 25 | 1 | 3 | 22 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0005 | 0/0 | 1938 | 23 | 6 | 3 | 12 | 0 | 2 | 11 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0006 | 0/0 | 1938 | 14 | 4 | 2 | 8 | 0 | 0 | 6 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0007 | 0/0 | 1938 | 8 | 4 | 1 | 1 | 0 | 2 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0008 | 0/0 | 1938 | 5 | 0 | 0 | 0 | 0 | 5 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0009 | 0/0 | 1938 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0010 | 0/0 | 1938 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0011 | 0/0 | 1938 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0012 | 0/0 | 1938 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0013 | 0/0 | 1938 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0014 | 0/0 | 1938 | 2 | 0 | 1 | 1 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0015 | 0/0 | 1938 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0016 | 0/0 | 1938 | 2 | 0 | 0 | 0 | 1 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0017 | 0/0 | 1938 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0018 | 0/0 | 1938 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0019 | 0/0 | 1938 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0020 | 0/0 | 1938 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0021 | 0/0 | 1938 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0022 | 0/0 | 1938 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0023 | 0/0 | 1938 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0024 | 0/0 | 1938 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0025 | 0/0 | 1938 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0026 | 0/0 | 1938 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0027 | 0/0 | 1938 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0028 | 0/0 | 1938 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0029 | 0/0 | 1938 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0030 | 0/0 | 1938 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0031 | 0/0 | 1938 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0032 | 0/0 | 1938 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0033 | 0/0 | 1938 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0034 | 0/0 | 1938 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0035 | 0/0 | 1938 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0036 | 0/0 | 1938 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0037 | 0/0 | 1938 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0038 | 0/0 | 1938 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0039 | 0/0 | 1938 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0040 | 0/0 | 1938 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0041 | 0/0 | 1938 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0042 | 0/0 | 1938 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| 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 | 0/0 | 5817 | 25 | 0 | 5 | 17 | 0 | 3 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0002 | 0/1 | 5817 | 24 | 0 | 5 | 18 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0003 | 0/0 | 5817 | 24 | 4 | 12 | 8 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0004 | 0/0 | 5817 | 18 | 3 | 2 | 11 | 2 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0005 | 1/0 | 5817 | 17 | 4 | 6 | 2 | 0 | 4 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0006 | 0/0 | 5817 | 11 | 3 | 3 | 1 | 2 | 2 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0007 | 0/0 | 5817 | 11 | 2 | 1 | 7 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0008 | 0/0 | 5817 | 11 | 1 | 5 | 3 | 2 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0009 | 0/0 | 5817 | 10 | 2 | 0 | 7 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0010 | 0/0 | 5817 | 9 | 0 | 2 | 6 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0011 | 0/0 | 5817 | 9 | 3 | 3 | 2 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0012 | 0/0 | 5817 | 8 | 2 | 0 | 4 | 0 | 2 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0013 | 0/0 | 5817 | 7 | 1 | 0 | 6 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0014 | 0/0 | 5817 | 7 | 4 | 2 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0015 | 0/0 | 5817 | 7 | 5 | 0 | 2 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0016 | 0/0 | 5817 | 7 | 1 | 0 | 4 | 0 | 2 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0017 | 0/0 | 5817 | 6 | 1 | 1 | 2 | 0 | 2 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0018 | 0/0 | 5817 | 6 | 0 | 0 | 6 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0019 | 0/0 | 5817 | 6 | 0 | 0 | 6 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0020 | 0/0 | 5817 | 4 | 2 | 1 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0021 | 0/0 | 5817 | 4 | 1 | 2 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0022 | 0/0 | 5817 | 4 | 4 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0023 | 0/0 | 5817 | 4 | 0 | 0 | 4 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0024 | 0/0 | 5817 | 4 | 1 | 0 | 3 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0025 | 0/0 | 5817 | 4 | 0 | 1 | 0 | 1 | 2 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0026 | 0/0 | 5817 | 4 | 1 | 2 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0027 | 0/0 | 5817 | 4 | 0 | 3 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0028 | 0/0 | 5817 | 3 | 3 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0029 | 0/0 | 5817 | 3 | 0 | 0 | 3 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0030 | 0/0 | 5817 | 3 | 1 | 0 | 2 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0031 | 0/0 | 5817 | 3 | 0 | 3 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0032 | 0/0 | 5817 | 3 | 3 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0033 | 0/0 | 5817 | 3 | 1 | 0 | 2 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0034 | 0/0 | 5817 | 3 | 0 | 2 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0035 | 0/0 | 5817 | 2 | 2 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0036 | 0/0 | 5817 | 2 | 2 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0037 | 0/0 | 5817 | 2 | 2 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0038 | 0/0 | 5817 | 2 | 1 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0039 | 0/0 | 5817 | 2 | 0 | 0 | 2 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0040 | 0/0 | 5817 | 2 | 1 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0041 | 0/0 | 5817 | 2 | 2 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0042 | 0/0 | 5817 | 2 | 2 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0043 | 0/0 | 5817 | 2 | 0 | 0 | 2 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0044 | 0/0 | 5817 | 2 | 0 | 0 | 0 | 0 | 2 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0045 | 0/0 | 5817 | 2 | 0 | 0 | 2 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0046 | 0/0 | 5817 | 2 | 1 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0047 | 0/0 | 5817 | 2 | 0 | 2 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0048 | 0/0 | 5817 | 2 | 0 | 0 | 1 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0049 | 0/0 | 5817 | 2 | 2 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0050 | 0/0 | 5817 | 2 | 0 | 1 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0051 | 0/0 | 5817 | 2 | 0 | 0 | 2 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0052 | 0/0 | 5817 | 2 | 0 | 2 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0053 | 0/0 | 5817 | 2 | 0 | 1 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0054 | 0/0 | 5817 | 2 | 0 | 1 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0055 | 0/0 | 5817 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0056 | 0/0 | 5817 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0057 | 0/0 | 5817 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0058 | 0/0 | 5817 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0059 | 0/0 | 5817 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0060 | 0/0 | 5817 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0061 | 0/0 | 5817 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0062 | 0/0 | 5817 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0063 | 0/0 | 5817 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0064 | 0/0 | 5817 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0065 | 0/0 | 5817 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0066 | 0/0 | 5817 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0067 | 0/0 | 5817 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0068 | 0/0 | 5817 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0069 | 0/0 | 5817 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0070 | 0/0 | 5817 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0071 | 0/0 | 5817 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0072 | 0/0 | 5817 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0073 | 0/0 | 5817 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0074 | 0/0 | 5817 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0075 | 0/0 | 5817 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0076 | 0/0 | 5817 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0077 | 0/0 | 5817 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0078 | 0/0 | 5817 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0079 | 0/0 | 5817 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0080 | 0/0 | 5817 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0081 | 0/0 | 5817 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0082 | 0/0 | 5817 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0083 | 0/0 | 5817 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0084 | 0/0 | 5817 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0085 | 0/0 | 5817 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0086 | 0/0 | 5817 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0087 | 0/0 | 5817 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0088 | 0/0 | 5817 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0089 | 0/0 | 5817 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0090 | 0/0 | 5817 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0091 | 0/0 | 5817 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0092 | 0/0 | 5817 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0093 | 0/0 | 5817 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0094 | 0/0 | 5817 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0095 | 0/0 | 5817 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0096 | 0/0 | 5817 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0097 | 0/0 | 5817 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0098 | 0/0 | 5817 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0099 | 0/0 | 5817 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0100 | 0/0 | 5817 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0101 | 0/0 | 5817 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0102 | 0/0 | 5817 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0103 | 0/0 | 5817 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0104 | 0/0 | 5817 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0105 | 0/0 | 5817 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0106 | 0/0 | 5817 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0107 | 0/0 | 5817 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0108 | 0/0 | 5817 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0109 | 0/0 | 5817 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0110 | 0/0 | 5817 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0111 | 0/0 | 5817 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0112 | 0/0 | 5817 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0113 | 0/0 | 5817 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0114 | 0/0 | 5817 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0115 | 0/0 | 5817 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0116 | 0/0 | 5817 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0117 | 0/0 | 5817 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0118 | 0/0 | 5817 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0119 | 0/0 | 5817 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| c0120 | 0/0 | 5817 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| 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 | 178 | 381 | 88 | 80 | 158 | 16 | 37 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| t0002 | 0/0 | 178 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0075 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0216 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0344 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0346 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0003 | 0/0 | 5817 | 24 | 4 | 12 | 8 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0004 | 0/0 | 5817 | 18 | 3 | 2 | 11 | 2 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0006 | 0/0 | 5817 | 11 | 3 | 3 | 1 | 2 | 2 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0007 | 0/0 | 5817 | 11 | 2 | 1 | 7 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0012 | 0/0 | 5817 | 8 | 2 | 0 | 4 | 0 | 2 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0014 | 0/0 | 5817 | 7 | 4 | 2 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0015 | 0/0 | 5817 | 7 | 5 | 0 | 2 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0017 | 0/0 | 5817 | 6 | 1 | 1 | 2 | 0 | 2 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0022 | 0/0 | 5817 | 4 | 4 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0027 | 0/0 | 5817 | 4 | 0 | 3 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0034 | 0/0 | 5817 | 3 | 0 | 2 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0039 | 0/0 | 5817 | 2 | 0 | 0 | 2 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0040 | 0/0 | 5817 | 2 | 1 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0042 | 0/0 | 5817 | 2 | 2 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0046 | 0/0 | 5817 | 2 | 1 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0050 | 0/0 | 5817 | 2 | 0 | 1 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0051 | 0/0 | 5817 | 2 | 0 | 0 | 2 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0062 | 0/0 | 5817 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0072 | 0/0 | 5817 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0075 | 0/0 | 5817 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0089 | 0/0 | 5817 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0090 | 0/0 | 5817 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0103 | 0/0 | 5817 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0105 | 0/0 | 5817 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0108 | 0/0 | 5817 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0110 | 0/0 | 5817 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0111 | 0/0 | 5817 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0113 | 0/0 | 5817 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0118 | 0/0 | 5817 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0119 | 0/0 | 5817 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0120 | 0/0 | 5817 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0002c0001 | 0/0 | 5817 | 25 | 0 | 5 | 17 | 0 | 3 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0002c0011 | 0/0 | 5817 | 9 | 3 | 3 | 2 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0002c0019 | 0/0 | 5817 | 6 | 0 | 0 | 6 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0002c0030 | 0/0 | 5817 | 3 | 1 | 0 | 2 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0002c0038 | 0/0 | 5817 | 2 | 1 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0002c0043 | 0/0 | 5817 | 2 | 0 | 0 | 2 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0002c0045 | 0/0 | 5817 | 2 | 0 | 0 | 2 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0002c0064 | 0/0 | 5817 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0002c0065 | 0/0 | 5817 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0002c0070 | 0/0 | 5817 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0002c0078 | 0/0 | 5817 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0002c0081 | 0/0 | 5817 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0002c0094 | 0/0 | 5817 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0003c0005 | 1/0 | 5817 | 17 | 4 | 6 | 2 | 0 | 4 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0003c0008 | 0/0 | 5817 | 11 | 1 | 5 | 3 | 2 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0003c0009 | 0/0 | 5817 | 10 | 2 | 0 | 7 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0003c0013 | 0/0 | 5817 | 7 | 1 | 0 | 6 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0003c0025 | 0/0 | 5817 | 4 | 0 | 1 | 0 | 1 | 2 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0003c0041 | 0/0 | 5817 | 2 | 2 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0003c0061 | 0/0 | 5817 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0003c0071 | 0/0 | 5817 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0003c0091 | 0/0 | 5817 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0004c0002 | 0/1 | 5817 | 24 | 0 | 5 | 18 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0004c0010 | 0/0 | 5817 | 9 | 0 | 2 | 6 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0004c0021 | 0/0 | 5817 | 4 | 1 | 2 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0004c0026 | 0/0 | 5817 | 4 | 1 | 2 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0004c0048 | 0/0 | 5817 | 2 | 0 | 0 | 1 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0004c0106 | 0/0 | 5817 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0005c0016 | 0/0 | 5817 | 7 | 1 | 0 | 4 | 0 | 2 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0005c0018 | 0/0 | 5817 | 6 | 0 | 0 | 6 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0005c0028 | 0/0 | 5817 | 3 | 3 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0005c0037 | 0/0 | 5817 | 2 | 2 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0005c0047 | 0/0 | 5817 | 2 | 0 | 2 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0005c0079 | 0/0 | 5817 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0005c0087 | 0/0 | 5817 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0005c0095 | 0/0 | 5817 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0006c0024 | 0/0 | 5817 | 4 | 1 | 0 | 3 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0006c0029 | 0/0 | 5817 | 3 | 0 | 0 | 3 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0006c0033 | 0/0 | 5817 | 3 | 1 | 0 | 2 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0006c0052 | 0/0 | 5817 | 2 | 0 | 2 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0006c0068 | 0/0 | 5817 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0006c0099 | 0/0 | 5817 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0007c0020 | 0/0 | 5817 | 4 | 2 | 1 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0007c0083 | 0/0 | 5817 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0007c0096 | 0/0 | 5817 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0007c0097 | 0/0 | 5817 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0007c0107 | 0/0 | 5817 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0008c0044 | 0/0 | 5817 | 2 | 0 | 0 | 0 | 0 | 2 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0008c0063 | 0/0 | 5817 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0008c0093 | 0/0 | 5817 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0008c0104 | 0/0 | 5817 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0009c0032 | 0/0 | 5817 | 3 | 3 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0009c0049 | 0/0 | 5817 | 2 | 2 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0010c0023 | 0/0 | 5817 | 4 | 0 | 0 | 4 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0011c0031 | 0/0 | 5817 | 3 | 0 | 3 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0012c0035 | 0/0 | 5817 | 2 | 2 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0012c0058 | 0/0 | 5817 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0013c0116 | 0/0 | 5817 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0013c0117 | 0/0 | 5817 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0014c0054 | 0/0 | 5817 | 2 | 0 | 1 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0015c0053 | 0/0 | 5817 | 2 | 0 | 1 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0016c0059 | 0/0 | 5817 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0016c0060 | 0/0 | 5817 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0017c0036 | 0/0 | 5817 | 2 | 2 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0018c0114 | 0/0 | 5817 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0019c0115 | 0/0 | 5817 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0020c0112 | 0/0 | 5817 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0021c0055 | 0/0 | 5817 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0022c0056 | 0/0 | 5817 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0023c0109 | 0/0 | 5817 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0024c0073 | 0/0 | 5817 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0025c0074 | 0/0 | 5817 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0026c0092 | 0/0 | 5817 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0027c0088 | 0/0 | 5817 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0028c0098 | 0/0 | 5817 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0029c0066 | 0/0 | 5817 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0030c0084 | 0/0 | 5817 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0031c0080 | 0/0 | 5817 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0032c0082 | 0/0 | 5817 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0033c0077 | 0/0 | 5817 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0034c0085 | 0/0 | 5817 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0035c0086 | 0/0 | 5817 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0036c0067 | 0/0 | 5817 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0037c0100 | 0/0 | 5817 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0038c0102 | 0/0 | 5817 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0039c0101 | 0/0 | 5817 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0040c0076 | 0/0 | 5817 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0041c0069 | 0/0 | 5817 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0042c0057 | 0/0 | 5817 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0003t0001 | 0/0 | 5994 | 24 | 4 | 12 | 8 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0004t0001 | 0/0 | 5994 | 18 | 3 | 2 | 11 | 2 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0006t0001 | 0/0 | 5994 | 11 | 3 | 3 | 1 | 2 | 2 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0007t0001 | 0/0 | 5994 | 11 | 2 | 1 | 7 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0012t0001 | 0/0 | 5994 | 8 | 2 | 0 | 4 | 0 | 2 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0014t0001 | 0/0 | 5994 | 7 | 4 | 2 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0015t0001 | 0/0 | 5994 | 7 | 5 | 0 | 2 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0017t0001 | 0/0 | 5994 | 6 | 1 | 1 | 2 | 0 | 2 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0022t0001 | 0/0 | 5994 | 4 | 4 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0027t0001 | 0/0 | 5994 | 4 | 0 | 3 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0034t0001 | 0/0 | 5994 | 3 | 0 | 2 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0039t0001 | 0/0 | 5994 | 2 | 0 | 0 | 2 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0040t0001 | 0/0 | 5994 | 2 | 1 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0042t0001 | 0/0 | 5994 | 2 | 2 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0046t0001 | 0/0 | 5994 | 2 | 1 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0050t0001 | 0/0 | 5994 | 2 | 0 | 1 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0051t0001 | 0/0 | 5994 | 2 | 0 | 0 | 2 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0062t0001 | 0/0 | 5994 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0072t0001 | 0/0 | 5994 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0075t0001 | 0/0 | 5994 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0089t0001 | 0/0 | 5994 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0090t0001 | 0/0 | 5994 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0103t0001 | 0/0 | 5994 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0105t0001 | 0/0 | 5994 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0108t0001 | 0/0 | 5994 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0110t0001 | 0/0 | 5994 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0111t0001 | 0/0 | 5994 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0113t0001 | 0/0 | 5994 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0118t0001 | 0/0 | 5994 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0119t0001 | 0/0 | 5994 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0001c0120t0001 | 0/0 | 5994 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0002c0001t0001 | 0/0 | 5994 | 25 | 0 | 5 | 17 | 0 | 3 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0002c0011t0001 | 0/0 | 5994 | 9 | 3 | 3 | 2 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0002c0019t0001 | 0/0 | 5994 | 6 | 0 | 0 | 6 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0002c0030t0001 | 0/0 | 5994 | 3 | 1 | 0 | 2 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0002c0038t0001 | 0/0 | 5994 | 2 | 1 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0002c0043t0001 | 0/0 | 5994 | 2 | 0 | 0 | 2 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0002c0045t0001 | 0/0 | 5994 | 2 | 0 | 0 | 2 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0002c0064t0001 | 0/0 | 5994 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0002c0065t0001 | 0/0 | 5994 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0002c0070t0001 | 0/0 | 5994 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0002c0078t0001 | 0/0 | 5994 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0002c0081t0001 | 0/0 | 5994 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0002c0094t0001 | 0/0 | 5994 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0003c0005t0001 | 1/0 | 5994 | 17 | 4 | 6 | 2 | 0 | 4 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0003c0008t0001 | 0/0 | 5994 | 11 | 1 | 5 | 3 | 2 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0003c0009t0001 | 0/0 | 5994 | 9 | 2 | 0 | 7 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0003c0009t0002 | 0/0 | 5994 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0003c0013t0001 | 0/0 | 5994 | 7 | 1 | 0 | 6 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0003c0025t0001 | 0/0 | 5994 | 4 | 0 | 1 | 0 | 1 | 2 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0003c0041t0001 | 0/0 | 5994 | 2 | 2 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0003c0061t0001 | 0/0 | 5994 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0003c0071t0001 | 0/0 | 5994 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0003c0091t0001 | 0/0 | 5994 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0004c0002t0001 | 0/1 | 5994 | 24 | 0 | 5 | 18 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0004c0010t0001 | 0/0 | 5994 | 9 | 0 | 2 | 6 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0004c0021t0001 | 0/0 | 5994 | 4 | 1 | 2 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0004c0026t0001 | 0/0 | 5994 | 4 | 1 | 2 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0004c0048t0001 | 0/0 | 5994 | 2 | 0 | 0 | 1 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0004c0106t0001 | 0/0 | 5994 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0005c0016t0001 | 0/0 | 5994 | 7 | 1 | 0 | 4 | 0 | 2 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0005c0018t0001 | 0/0 | 5994 | 6 | 0 | 0 | 6 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0005c0028t0001 | 0/0 | 5994 | 3 | 3 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0005c0037t0001 | 0/0 | 5994 | 2 | 2 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0005c0047t0001 | 0/0 | 5994 | 2 | 0 | 2 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0005c0079t0001 | 0/0 | 5994 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0005c0087t0001 | 0/0 | 5994 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0005c0095t0001 | 0/0 | 5994 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0006c0024t0001 | 0/0 | 5994 | 4 | 1 | 0 | 3 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0006c0029t0001 | 0/0 | 5994 | 3 | 0 | 0 | 3 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0006c0033t0001 | 0/0 | 5994 | 3 | 1 | 0 | 2 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0006c0052t0001 | 0/0 | 5994 | 2 | 0 | 2 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0006c0068t0001 | 0/0 | 5994 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0006c0099t0001 | 0/0 | 5994 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0007c0020t0001 | 0/0 | 5994 | 4 | 2 | 1 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0007c0083t0001 | 0/0 | 5994 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0007c0096t0001 | 0/0 | 5994 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0007c0097t0001 | 0/0 | 5994 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0007c0107t0001 | 0/0 | 5994 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0008c0044t0001 | 0/0 | 5994 | 2 | 0 | 0 | 0 | 0 | 2 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0008c0063t0001 | 0/0 | 5994 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0008c0093t0001 | 0/0 | 5994 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0008c0104t0001 | 0/0 | 5994 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0009c0032t0001 | 0/0 | 5994 | 3 | 3 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0009c0049t0001 | 0/0 | 5994 | 2 | 2 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0010c0023t0001 | 0/0 | 5994 | 4 | 0 | 0 | 4 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0011c0031t0001 | 0/0 | 5994 | 3 | 0 | 3 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0012c0035t0001 | 0/0 | 5994 | 2 | 2 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0012c0058t0001 | 0/0 | 5994 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0013c0116t0001 | 0/0 | 5994 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0013c0117t0001 | 0/0 | 5994 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0014c0054t0001 | 0/0 | 5994 | 2 | 0 | 1 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0015c0053t0001 | 0/0 | 5994 | 2 | 0 | 1 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0016c0059t0001 | 0/0 | 5994 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0016c0060t0001 | 0/0 | 5994 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0017c0036t0001 | 0/0 | 5994 | 2 | 2 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0018c0114t0001 | 0/0 | 5994 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0019c0115t0001 | 0/0 | 5994 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0020c0112t0001 | 0/0 | 5994 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0021c0055t0001 | 0/0 | 5994 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0022c0056t0001 | 0/0 | 5994 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0023c0109t0001 | 0/0 | 5994 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0024c0073t0001 | 0/0 | 5994 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0025c0074t0001 | 0/0 | 5994 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0026c0092t0001 | 0/0 | 5994 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0027c0088t0001 | 0/0 | 5994 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0028c0098t0001 | 0/0 | 5994 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0029c0066t0001 | 0/0 | 5994 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0030c0084t0001 | 0/0 | 5994 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0031c0080t0001 | 0/0 | 5994 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0032c0082t0001 | 0/0 | 5994 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0033c0077t0001 | 0/0 | 5994 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0034c0085t0001 | 0/0 | 5994 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0035c0086t0001 | 0/0 | 5994 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0036c0067t0001 | 0/0 | 5994 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0037c0100t0001 | 0/0 | 5994 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0038c0102t0001 | 0/0 | 5994 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0039c0101t0001 | 0/0 | 5994 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0040c0076t0001 | 0/0 | 5994 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0041c0069t0001 | 0/0 | 5994 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| a0042c0057t0001 | 0/0 | 5994 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | copy fasta | chr17 | 10295865 | 10378006 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0003t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0003t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0003t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0003t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0003t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0003t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0003t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0003t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0003t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0003t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0003t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0003t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0003t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0003t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0003t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0003t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0003t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0003t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0003t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0003t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0003t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0004t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0004t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0004t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0004t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0004t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0004t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0004t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0004t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0004t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0004t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0004t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0004t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0004t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0004t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0004t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0004t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0004t0001g0346 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0004t0001g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0006t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0006t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0006t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0006t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0006t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0006t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0006t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0006t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0006t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0006t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0007t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0007t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0007t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0007t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0007t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0007t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0007t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0007t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0007t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0007t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0007t0001g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0012t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0012t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0012t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0012t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0012t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0012t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0012t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0012t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0014t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0014t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0014t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0014t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0014t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0014t0001g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0014t0001g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0015t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0015t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0015t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0015t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0015t0001g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0015t0001g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0015t0001g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0017t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0017t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0017t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0017t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0017t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0017t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0022t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0022t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0022t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0022t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0027t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0027t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0027t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0027t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0034t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0034t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0034t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0039t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0039t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0040t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0040t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0042t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0042t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0046t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0046t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0050t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0050t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0051t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0051t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0062t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0072t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0075t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0089t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0090t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0103t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0105t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0108t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0110t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0111t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0113t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0118t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0119t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0001c0120t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0001t0001g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0011t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0011t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0011t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0011t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0011t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0011t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0011t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0011t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0011t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0019t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0019t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0019t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0019t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0019t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0019t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0030t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0030t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0030t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0038t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0038t0001g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0043t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0043t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0045t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0045t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0064t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0065t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0070t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0078t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0081t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0002c0094t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0005t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0005t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0005t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0005t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0005t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0005t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0005t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0005t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0005t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0005t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0005t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0005t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0005t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0005t0001g0216 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0005t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0005t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0005t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0008t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0008t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0008t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0008t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0008t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0008t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0008t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0008t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0008t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0008t0001g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0008t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0009t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0009t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0009t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0009t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0009t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0009t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0009t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0009t0001g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0009t0001g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0009t0002g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0013t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0013t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0013t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0013t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0013t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0013t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0013t0001g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0025t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0025t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0025t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0025t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0041t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0041t0001g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0061t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0071t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0003c0091t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0004c0002t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0004c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0004c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0004c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0004c0002t0001g0075 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0004c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0004c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0004c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0004c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0004c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0004c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0004c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0004c0002t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0004c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0004c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0004c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0004c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0004c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0004c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0004c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0004c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0004c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0004c0002t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0004c0010t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0004c0010t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0004c0010t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0004c0010t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0004c0010t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0004c0010t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0004c0010t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0004c0010t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0004c0010t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0004c0021t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0004c0021t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0004c0021t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0004c0021t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0004c0026t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0004c0026t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0004c0026t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0004c0026t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0004c0048t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0004c0048t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0004c0106t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0005c0016t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0005c0016t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0005c0016t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0005c0016t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0005c0016t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0005c0016t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0005c0016t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0005c0018t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0005c0018t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0005c0018t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0005c0018t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0005c0018t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0005c0018t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0005c0028t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0005c0028t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0005c0028t0001g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0005c0037t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0005c0037t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0005c0047t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0005c0047t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0005c0079t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0005c0087t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0005c0095t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0006c0024t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0006c0024t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0006c0024t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0006c0024t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0006c0029t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0006c0029t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0006c0029t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0006c0033t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0006c0033t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0006c0033t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0006c0052t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0006c0052t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0006c0068t0001g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0006c0099t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0007c0020t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0007c0020t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0007c0020t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0007c0020t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0007c0083t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0007c0096t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0007c0097t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0007c0107t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0008c0044t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0008c0044t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0008c0063t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0008c0093t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0008c0104t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0009c0032t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0009c0032t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0009c0032t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0009c0049t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0009c0049t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0010c0023t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0010c0023t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0010c0023t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0010c0023t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0011c0031t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0011c0031t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0011c0031t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0012c0035t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0012c0035t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0012c0058t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0013c0116t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0013c0117t0001g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0014c0054t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0014c0054t0001g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0015c0053t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0015c0053t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0016c0059t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0016c0060t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0017c0036t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0017c0036t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0018c0114t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0019c0115t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0020c0112t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0021c0055t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0022c0056t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0023c0109t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0024c0073t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0025c0074t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0026c0092t0001g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0027c0088t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0028c0098t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0029c0066t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0030c0084t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0031c0080t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0032c0082t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0033c0077t0001g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0034c0085t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0035c0086t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0036c0067t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0037c0100t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0038c0102t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0039c0101t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0040c0076t0001g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0041c0069t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| a0042c0057t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0008 | t0001 | g0058 | EUR | GBR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG00099 | hp2 | a0015 | c0053 | t0001 | g0055 | EUR | GBR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG00140 | hp1 | a0003 | c0025 | t0001 | g0166 | EUR | GBR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG00140 | hp2 | a0016 | c0059 | t0001 | g0037 | EUR | GBR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG00323 | hp1 | a0001 | c0050 | t0001 | g0065 | EUR | FIN | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG00323 | hp2 | a0001 | c0034 | t0001 | g0168 | EUR | FIN | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG00408 | hp1 | a0004 | c0010 | t0001 | g0179 | EAS | CHS | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG00408 | hp2 | a0001 | c0007 | t0001 | g0007 | EAS | CHS | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG00423 | hp1 | a0037 | c0100 | t0001 | g0064 | EAS | CHS | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG00423 | hp2 | a0001 | c0015 | t0001 | g0014 | EAS | CHS | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG00438 | hp1 | a0004 | c0002 | t0001 | g0212 | EAS | CHS | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG00438 | hp2 | a0006 | c0024 | t0001 | g0340 | EAS | CHS | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG00544 | hp1 | a0003 | c0013 | t0001 | g0017 | EAS | CHS | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG00544 | hp2 | a0004 | c0010 | t0001 | g0073 | EAS | CHS | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG00621 | hp1 | a0002 | c0001 | t0001 | g0004 | EAS | CHS | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG00621 | hp2 | a0001 | c0004 | t0001 | g0062 | EAS | CHS | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG00639 | hp1 | a0001 | c0003 | t0001 | g0045 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG00639 | hp2 | a0001 | c0006 | t0001 | g0218 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG00733 | hp1 | a0040 | c0076 | t0001 | g0343 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG00733 | hp2 | a0004 | c0026 | t0001 | g0167 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG00735 | hp1 | a0001 | c0004 | t0001 | g0345 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG00735 | hp2 | a0003 | c0025 | t0001 | g0157 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG00738 | hp1 | a0001 | c0034 | t0001 | g0288 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG00738 | hp2 | a0003 | c0008 | t0001 | g0036 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG00741 | hp1 | a0001 | c0046 | t0001 | g0271 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG00741 | hp2 | a0005 | c0087 | t0001 | g0290 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01069 | hp1 | a0004 | c0021 | t0001 | g0094 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01069 | hp2 | a0001 | c0003 | t0001 | g0227 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01070 | hp1 | a0003 | c0005 | t0001 | g0125 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01070 | hp2 | a0001 | c0108 | t0001 | g0156 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01071 | hp1 | a0003 | c0005 | t0001 | g0124 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01071 | hp2 | a0001 | c0003 | t0001 | g0228 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01074 | hp1 | a0004 | c0021 | t0001 | g0093 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01074 | hp2 | a0001 | c0003 | t0001 | g0232 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01081 | hp1 | a0002 | c0011 | t0001 | g0202 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01081 | hp2 | a0001 | c0003 | t0001 | g0043 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01099 | hp1 | a0001 | c0027 | t0001 | g0161 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01099 | hp2 | a0026 | c0092 | t0001 | g0368 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01106 | hp1 | a0001 | c0027 | t0001 | g0266 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01106 | hp2 | a0001 | c0007 | t0001 | g0260 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01109 | hp1 | a0001 | c0111 | t0001 | g0078 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01109 | hp2 | a0001 | c0034 | t0001 | g0152 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01167 | hp1 | a0005 | c0047 | t0001 | g0099 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01167 | hp2 | a0001 | c0072 | t0001 | g0160 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01169 | hp1 | a0005 | c0047 | t0001 | g0103 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01169 | hp2 | a0003 | c0008 | t0001 | g0038 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01175 | hp1 | a0001 | c0027 | t0001 | g0009 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01175 | hp2 | a0001 | c0006 | t0001 | g0140 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01192 | hp1 | a0001 | c0003 | t0001 | g0049 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01192 | hp2 | a0001 | c0120 | t0001 | g0178 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01243 | hp1 | a0001 | c0014 | t0001 | g0219 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01243 | hp2 | a0007 | c0020 | t0001 | g0291 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01255 | hp1 | a0001 | c0014 | t0001 | g0136 | AMR | CLM | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01255 | hp2 | a0004 | c0106 | t0001 | g0176 | AMR | CLM | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01256 | hp1 | a0003 | c0008 | t0001 | g0230 | AMR | CLM | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01256 | hp2 | a0004 | c0026 | t0001 | g0165 | AMR | CLM | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01257 | hp1 | a0004 | c0002 | t0001 | g0002 | AMR | CLM | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01257 | hp2 | a0015 | c0053 | t0001 | g0047 | AMR | CLM | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01258 | hp1 | a0003 | c0008 | t0001 | g0229 | AMR | CLM | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01258 | hp2 | a0004 | c0002 | t0001 | g0002 | AMR | CLM | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01261 | hp1 | a0003 | c0005 | t0001 | g0147 | AMR | CLM | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01261 | hp2 | a0003 | c0008 | t0001 | g0354 | AMR | CLM | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01346 | hp1 | a0001 | c0006 | t0001 | g0105 | AMR | CLM | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01346 | hp2 | a0002 | c0001 | t0001 | g0321 | AMR | CLM | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01358 | hp1 | a0001 | c0017 | t0001 | g0141 | AMR | CLM | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01358 | hp2 | a0011 | c0031 | t0001 | g0061 | AMR | CLM | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01361 | hp1 | a0003 | c0005 | t0001 | g0130 | AMR | CLM | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01361 | hp2 | a0011 | c0031 | t0001 | g0041 | AMR | CLM | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01433 | hp1 | a0002 | c0001 | t0001 | g0335 | AMR | CLM | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01433 | hp2 | a0011 | c0031 | t0001 | g0056 | AMR | CLM | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01496 | hp1 | a0001 | c0003 | t0001 | g0044 | AMR | CLM | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01496 | hp2 | a0001 | c0050 | t0001 | g0042 | AMR | CLM | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01515 | hp1 | a0003 | c0008 | t0001 | g0053 | EUR | IBS | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01515 | hp2 | a0001 | c0004 | t0001 | g0346 | EUR | IBS | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01516 | hp1 | a0022 | c0056 | t0001 | g0209 | EUR | IBS | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01516 | hp2 | a0001 | c0006 | t0001 | g0001 | EUR | IBS | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01517 | hp1 | a0001 | c0004 | t0001 | g0344 | EUR | IBS | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01517 | hp2 | a0001 | c0006 | t0001 | g0001 | EUR | IBS | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01884 | hp1 | a0001 | c0003 | t0001 | g0269 | AFR | ACB | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01884 | hp2 | a0001 | c0006 | t0001 | g0268 | AFR | ACB | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01891 | hp1 | a0001 | c0042 | t0001 | g0120 | AFR | ACB | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01891 | hp2 | a0004 | c0026 | t0001 | g0153 | AFR | ACB | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01928 | hp1 | a0001 | c0003 | t0001 | g0246 | AMR | PEL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01928 | hp2 | a0004 | c0010 | t0001 | g0324 | AMR | PEL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01934 | hp1 | a0002 | c0070 | t0001 | g0106 | AMR | PEL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01934 | hp2 | a0001 | c0003 | t0001 | g0243 | AMR | PEL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01943 | hp1 | a0001 | c0003 | t0001 | g0204 | AMR | PEL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01943 | hp2 | a0006 | c0052 | t0001 | g0242 | AMR | PEL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01952 | hp1 | a0014 | c0054 | t0001 | g0150 | AMR | PEL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01952 | hp2 | a0003 | c0005 | t0001 | g0114 | AMR | PEL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01975 | hp1 | a0004 | c0002 | t0001 | g0070 | AMR | PEL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01975 | hp2 | a0002 | c0011 | t0001 | g0247 | AMR | PEL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01978 | hp1 | a0002 | c0001 | t0001 | g0359 | AMR | PEL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01978 | hp2 | a0039 | c0101 | t0001 | g0074 | AMR | PEL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01981 | hp1 | a0002 | c0001 | t0001 | g0258 | AMR | PEL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01981 | hp2 | a0001 | c0004 | t0001 | g0236 | AMR | PEL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02004 | hp1 | a0002 | c0011 | t0001 | g0313 | AMR | PEL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02004 | hp2 | a0001 | c0003 | t0001 | g0205 | AMR | PEL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02027 | hp1 | a0003 | c0008 | t0001 | g0338 | EAS | KHV | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02027 | hp2 | a0001 | c0075 | t0001 | g0358 | EAS | KHV | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02055 | hp1 | a0005 | c0016 | t0001 | g0091 | AFR | ACB | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02055 | hp2 | a0001 | c0113 | t0001 | g0102 | AFR | ACB | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02074 | hp1 | a0002 | c0094 | t0001 | g0226 | EAS | KHV | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02074 | hp2 | a0013 | c0116 | t0001 | g0087 | EAS | KHV | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02080 | hp1 | a0002 | c0001 | t0001 | g0349 | EAS | KHV | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02080 | hp2 | a0003 | c0009 | t0001 | g0362 | EAS | KHV | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02083 | hp1 | a0001 | c0007 | t0001 | g0285 | EAS | KHV | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02083 | hp2 | a0005 | c0018 | t0001 | g0282 | EAS | KHV | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02135 | hp1 | a0006 | c0029 | t0001 | g0259 | EAS | KHV | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02135 | hp2 | a0001 | c0051 | t0001 | g0245 | EAS | KHV | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02145 | hp1 | a0005 | c0037 | t0001 | g0195 | AFR | ACB | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02145 | hp2 | a0003 | c0013 | t0001 | g0370 | AFR | ACB | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02148 | hp1 | a0006 | c0052 | t0001 | g0201 | AMR | PEL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02148 | hp2 | a0001 | c0040 | t0001 | g0117 | AMR | PEL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02155 | hp1 | a0003 | c0009 | t0001 | g0319 | EAS | CDX | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02155 | hp2 | a0001 | c0051 | t0001 | g0052 | EAS | CDX | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02165 | hp1 | a0002 | c0001 | t0001 | g0280 | EAS | CDX | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02165 | hp2 | a0001 | c0110 | t0001 | g0108 | EAS | CDX | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02257 | hp1 | a0001 | c0040 | t0001 | g0137 | AFR | ACB | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02257 | hp2 | a0001 | c0119 | t0001 | g0274 | AFR | ACB | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02258 | hp1 | a0001 | c0046 | t0001 | g0265 | AFR | ACB | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02258 | hp2 | a0025 | c0074 | t0001 | g0076 | AFR | ACB | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02280 | hp1 | a0007 | c0020 | t0001 | g0121 | AFR | ACB | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02280 | hp2 | a0001 | c0090 | t0001 | g0364 | AFR | ACB | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02293 | hp1 | a0004 | c0010 | t0001 | g0322 | AMR | PEL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02293 | hp2 | a0004 | c0002 | t0001 | g0072 | AMR | PEL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02300 | hp1 | a0001 | c0003 | t0001 | g0203 | AMR | PEL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02300 | hp2 | a0002 | c0001 | t0001 | g0316 | AMR | PEL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02451 | hp1 | a0001 | c0022 | t0001 | g0292 | AFR | ACB | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02451 | hp2 | a0001 | c0015 | t0001 | g0092 | AFR | ACB | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02523 | hp1 | a0001 | c0004 | t0001 | g0077 | EAS | KHV | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02523 | hp2 | a0002 | c0011 | t0001 | g0217 | EAS | KHV | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02602 | hp1 | a0002 | c0011 | t0001 | g0081 | SAS | PJL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02602 | hp2 | a0004 | c0048 | t0001 | g0301 | SAS | PJL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02622 | hp1 | a0001 | c0007 | t0001 | g0107 | AFR | GWD | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02622 | hp2 | a0007 | c0083 | t0001 | g0096 | AFR | GWD | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02630 | hp1 | a0009 | c0032 | t0001 | g0171 | AFR | GWD | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02630 | hp2 | a0005 | c0028 | t0001 | g0082 | AFR | GWD | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02647 | hp1 | a0006 | c0033 | t0001 | g0185 | AFR | GWD | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02647 | hp2 | a0002 | c0038 | t0001 | g0369 | AFR | GWD | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02698 | hp1 | a0003 | c0005 | t0001 | g0299 | SAS | PJL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02698 | hp2 | a0001 | c0007 | t0001 | g0336 | SAS | PJL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02717 | hp1 | a0002 | c0011 | t0001 | g0186 | AFR | GWD | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02717 | hp2 | a0001 | c0014 | t0001 | g0374 | AFR | GWD | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02723 | hp1 | a0001 | c0015 | t0001 | g0098 | AFR | GWD | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02723 | hp2 | a0002 | c0011 | t0001 | g0234 | AFR | GWD | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02735 | hp1 | a0001 | c0012 | t0001 | g0310 | SAS | PJL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02735 | hp2 | a0019 | c0115 | t0001 | g0304 | SAS | PJL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02809 | hp1 | a0001 | c0015 | t0001 | g0372 | AFR | GWD | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02809 | hp2 | a0017 | c0036 | t0001 | g0146 | AFR | GWD | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02886 | hp1 | a0001 | c0022 | t0001 | g0293 | AFR | GWD | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02886 | hp2 | a0001 | c0118 | t0001 | g0273 | AFR | GWD | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02895 | hp1 | a0001 | c0012 | t0001 | g0272 | AFR | GWD | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02895 | hp2 | a0009 | c0032 | t0001 | g0172 | AFR | GWD | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02897 | hp1 | a0001 | c0012 | t0001 | g0267 | AFR | GWD | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02897 | hp2 | a0009 | c0032 | t0001 | g0175 | AFR | GWD | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02922 | hp1 | a0005 | c0037 | t0001 | g0148 | AFR | ESN | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02922 | hp2 | a0003 | c0005 | t0001 | g0215 | AFR | ESN | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02965 | hp1 | a0003 | c0009 | t0001 | g0377 | AFR | ESN | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02965 | hp2 | a0001 | c0062 | t0001 | g0262 | AFR | ESN | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02970 | hp1 | a0003 | c0091 | t0001 | g0101 | AFR | ESN | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02970 | hp2 | a0001 | c0015 | t0001 | g0378 | AFR | ESN | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02976 | hp1 | a0001 | c0042 | t0001 | g0199 | AFR | ESN | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02976 | hp2 | a0002 | c0011 | t0001 | g0235 | AFR | ESN | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG03041 | hp1 | a0002 | c0030 | t0001 | g0097 | AFR | GWD | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG03041 | hp2 | a0009 | c0049 | t0001 | g0151 | AFR | GWD | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG03098 | hp1 | a0003 | c0008 | t0001 | g0238 | AFR | MSL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG03098 | hp2 | a0003 | c0005 | t0001 | g0122 | AFR | MSL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG03130 | hp1 | a0003 | c0005 | t0001 | g0294 | AFR | ESN | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG03130 | hp2 | a0001 | c0004 | t0001 | g0194 | AFR | ESN | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG03139 | hp1 | a0006 | c0099 | t0001 | g0270 | AFR | ESN | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG03139 | hp2 | a0001 | c0014 | t0001 | g0100 | AFR | ESN | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG03209 | hp1 | a0001 | c0014 | t0001 | g0110 | AFR | MSL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG03209 | hp2 | a0001 | c0103 | t0001 | g0174 | AFR | MSL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG03225 | hp1 | a0001 | c0007 | t0001 | g0376 | AFR | MSL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG03225 | hp2 | a0017 | c0036 | t0001 | g0144 | AFR | MSL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG03239 | hp1 | a0004 | c0010 | t0001 | g0329 | SAS | PJL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG03239 | hp2 | a0003 | c0025 | t0001 | g0155 | SAS | PJL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG03453 | hp1 | a0001 | c0006 | t0001 | g0198 | AFR | MSL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG03453 | hp2 | a0006 | c0024 | t0001 | g0095 | AFR | MSL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG03486 | hp1 | a0001 | c0022 | t0001 | g0149 | AFR | MSL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG03486 | hp2 | a0041 | c0069 | t0001 | g0200 | AFR | MSL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG03491 | hp1 | a0002 | c0001 | t0001 | g0306 | SAS | PJL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG03491 | hp2 | a0008 | c0044 | t0001 | g0138 | SAS | PJL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG03492 | hp1 | a0008 | c0044 | t0001 | g0139 | SAS | PJL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG03492 | hp2 | a0005 | c0016 | t0001 | g0060 | SAS | PJL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG03516 | hp1 | a0001 | c0014 | t0001 | g0375 | AFR | ESN | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG03516 | hp2 | a0029 | c0066 | t0001 | g0240 | AFR | ESN | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG03540 | hp1 | a0012 | c0035 | t0001 | g0143 | AFR | GWD | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG03540 | hp2 | a0001 | c0003 | t0001 | g0233 | AFR | GWD | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG03579 | hp1 | a0009 | c0049 | t0001 | g0248 | AFR | MSL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG03579 | hp2 | a0003 | c0041 | t0001 | g0365 | AFR | MSL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG03654 | hp1 | a0001 | c0006 | t0001 | g0126 | SAS | PJL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG03654 | hp2 | a0028 | c0098 | t0001 | g0024 | SAS | PJL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG03669 | hp1 | a0007 | c0107 | t0001 | g0162 | SAS | PJL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG03669 | hp2 | a0033 | c0077 | t0001 | g0355 | SAS | PJL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG03688 | hp1 | a0002 | c0001 | t0001 | g0331 | SAS | STU | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG03688 | hp2 | a0002 | c0001 | t0001 | g0250 | SAS | STU | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG03704 | hp1 | a0005 | c0016 | t0001 | g0210 | SAS | PJL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG03704 | hp2 | a0035 | c0086 | t0001 | g0300 | SAS | PJL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG03710 | hp1 | a0018 | c0114 | t0001 | g0339 | SAS | PJL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG03710 | hp2 | a0001 | c0006 | t0001 | g0085 | SAS | PJL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG03834 | hp1 | a0001 | c0017 | t0001 | g0129 | SAS | BEB | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG03834 | hp2 | a0008 | c0093 | t0001 | g0257 | SAS | BEB | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG03927 | hp1 | a0008 | c0063 | t0001 | g0298 | SAS | BEB | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG03927 | hp2 | a0007 | c0020 | t0001 | g0342 | SAS | BEB | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG03942 | hp1 | a0001 | c0017 | t0001 | g0131 | SAS | BEB | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG03942 | hp2 | a0008 | c0104 | t0001 | g0164 | SAS | BEB | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG04115 | hp1 | a0001 | c0105 | t0001 | g0163 | SAS | STU | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG04115 | hp2 | a0003 | c0005 | t0001 | g0123 | SAS | STU | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG04199 | hp1 | a0038 | c0102 | t0001 | g0066 | SAS | STU | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG04199 | hp2 | a0003 | c0005 | t0001 | g0046 | SAS | STU | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG04204 | hp1 | a0016 | c0060 | t0001 | g0111 | SAS | STU | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG04204 | hp2 | a0003 | c0009 | t0002 | g0003 | SAS | STU | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG04228 | hp1 | a0003 | c0005 | t0001 | g0112 | SAS | STU | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG04228 | hp2 | a0001 | c0012 | t0001 | g0314 | SAS | STU | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18522 | hp1 | a0001 | c0003 | t0001 | g0237 | AFR | YRI | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18522 | hp2 | a0006 | c0068 | t0001 | g0366 | AFR | YRI | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18906 | hp1 | a0001 | c0017 | t0001 | g0090 | AFR | YRI | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18906 | hp2 | a0003 | c0009 | t0001 | g0373 | AFR | YRI | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18939 | hp1 | a0020 | c0112 | t0001 | g0067 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18939 | hp2 | a0002 | c0019 | t0001 | g0188 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18941 | hp1 | a0002 | c0001 | t0001 | g0303 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18941 | hp2 | a0002 | c0019 | t0001 | g0054 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18942 | hp1 | a0004 | c0002 | t0001 | g0225 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18942 | hp2 | a0002 | c0045 | t0001 | g0337 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18943 | hp1 | a0001 | c0003 | t0001 | g0063 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18943 | hp2 | a0002 | c0001 | t0001 | g0327 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18944 | hp1 | a0004 | c0002 | t0001 | g0223 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18944 | hp2 | a0002 | c0030 | t0001 | g0020 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18946 | hp1 | a0002 | c0019 | t0001 | g0193 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18946 | hp2 | a0002 | c0001 | t0001 | g0283 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18947 | hp1 | a0002 | c0011 | t0001 | g0239 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18947 | hp2 | a0001 | c0003 | t0001 | g0244 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18948 | hp1 | a0006 | c0029 | t0001 | g0309 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18948 | hp2 | a0002 | c0045 | t0001 | g0033 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18950 | hp1 | a0001 | c0007 | t0001 | g0312 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18950 | hp2 | a0001 | c0004 | t0001 | g0025 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18951 | hp1 | a0003 | c0061 | t0001 | g0119 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18951 | hp2 | a0001 | c0012 | t0001 | g0279 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18952 | hp1 | a0001 | c0003 | t0001 | g0356 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18952 | hp2 | a0003 | c0005 | t0001 | g0088 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18953 | hp1 | a0002 | c0030 | t0001 | g0022 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18953 | hp2 | a0003 | c0005 | t0001 | g0089 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18954 | hp1 | a0004 | c0002 | t0001 | g0208 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18954 | hp2 | a0005 | c0018 | t0001 | g0015 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18959 | hp1 | a0002 | c0001 | t0001 | g0048 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18959 | hp2 | a0002 | c0078 | t0001 | g0308 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18961 | hp1 | a0004 | c0002 | t0001 | g0211 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18961 | hp2 | a0001 | c0004 | t0001 | g0028 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18962 | hp1 | a0003 | c0008 | t0001 | g0255 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18962 | hp2 | a0002 | c0043 | t0001 | g0251 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18964 | hp1 | a0001 | c0014 | t0001 | g0010 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18964 | hp2 | a0001 | c0003 | t0001 | g0032 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18965 | hp1 | a0004 | c0002 | t0001 | g0278 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18965 | hp2 | a0003 | c0071 | t0001 | g0118 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18967 | hp1 | a0010 | c0023 | t0001 | g0350 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18967 | hp2 | a0002 | c0001 | t0001 | g0275 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18968 | hp1 | a0004 | c0002 | t0001 | g0221 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18968 | hp2 | a0001 | c0003 | t0001 | g0241 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18969 | hp1 | a0003 | c0009 | t0001 | g0039 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18969 | hp2 | a0002 | c0038 | t0001 | g0133 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18972 | hp1 | a0004 | c0002 | t0001 | g0231 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18972 | hp2 | a0001 | c0003 | t0001 | g0069 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18973 | hp1 | a0002 | c0019 | t0001 | g0189 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18973 | hp2 | a0004 | c0002 | t0001 | g0276 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18974 | hp1 | a0005 | c0018 | t0001 | g0206 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18974 | hp2 | a0034 | c0085 | t0001 | g0315 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18975 | hp1 | a0004 | c0010 | t0001 | g0320 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18975 | hp2 | a0001 | c0004 | t0001 | g0341 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18978 | hp1 | a0005 | c0095 | t0001 | g0059 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18978 | hp2 | a0005 | c0018 | t0001 | g0264 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18979 | hp1 | a0002 | c0065 | t0001 | g0079 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18979 | hp2 | a0004 | c0010 | t0001 | g0302 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18980 | hp1 | a0002 | c0001 | t0001 | g0317 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18980 | hp2 | a0005 | c0079 | t0001 | g0013 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18983 | hp1 | a0004 | c0002 | t0001 | g0277 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18983 | hp2 | a0002 | c0001 | t0001 | g0348 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18984 | hp1 | a0001 | c0004 | t0001 | g0328 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18984 | hp2 | a0004 | c0002 | t0001 | g0224 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18985 | hp1 | a0007 | c0096 | t0001 | g0034 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18985 | hp2 | a0005 | c0018 | t0001 | g0281 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18988 | hp1 | a0001 | c0003 | t0001 | g0051 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18988 | hp2 | a0001 | c0007 | t0001 | g0307 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18990 | hp1 | a0014 | c0054 | t0001 | g0379 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18990 | hp2 | a0002 | c0001 | t0001 | g0040 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18991 | hp1 | a0024 | c0073 | t0001 | g0050 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18991 | hp2 | a0001 | c0007 | t0001 | g0289 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18992 | hp1 | a0001 | c0039 | t0001 | g0113 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18992 | hp2 | a0004 | c0002 | t0001 | g0192 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18993 | hp1 | a0002 | c0001 | t0001 | g0352 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18993 | hp2 | a0004 | c0002 | t0001 | g0222 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18995 | hp1 | a0006 | c0024 | t0001 | g0182 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18995 | hp2 | a0003 | c0013 | t0001 | g0016 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18998 | hp1 | a0010 | c0023 | t0001 | g0311 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18998 | hp2 | a0002 | c0001 | t0001 | g0253 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18999 | hp1 | a0001 | c0012 | t0001 | g0286 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18999 | hp2 | a0023 | c0109 | t0001 | g0287 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19000 | hp1 | a0004 | c0002 | t0001 | g0026 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19000 | hp2 | a0003 | c0009 | t0001 | g0330 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19003 | hp1 | a0004 | c0048 | t0001 | g0207 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19003 | hp2 | a0005 | c0016 | t0001 | g0080 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19004 | hp1 | a0001 | c0017 | t0001 | g0086 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19004 | hp2 | a0001 | c0012 | t0001 | g0353 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19007 | hp1 | a0001 | c0015 | t0001 | g0011 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19007 | hp2 | a0001 | c0007 | t0001 | g0284 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19010 | hp1 | a0003 | c0013 | t0001 | g0023 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19010 | hp2 | a0006 | c0033 | t0001 | g0213 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19043 | hp1 | a0001 | c0006 | t0001 | g0132 | AFR | LWK | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19043 | hp2 | a0002 | c0064 | t0001 | g0196 | AFR | LWK | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19055 | hp1 | a0004 | c0010 | t0001 | g0326 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19055 | hp2 | a0001 | c0004 | t0001 | g0071 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19056 | hp1 | a0001 | c0039 | t0001 | g0115 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19056 | hp2 | a0003 | c0013 | t0001 | g0021 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19060 | hp1 | a0001 | c0003 | t0001 | g0249 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19060 | hp2 | a0001 | c0004 | t0001 | g0030 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19062 | hp1 | a0006 | c0033 | t0001 | g0029 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19062 | hp2 | a0006 | c0024 | t0001 | g0183 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19063 | hp1 | a0002 | c0001 | t0001 | g0357 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19063 | hp2 | a0030 | c0084 | t0001 | g0254 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19064 | hp1 | a0001 | c0006 | t0001 | g0084 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19064 | hp2 | a0001 | c0004 | t0001 | g0031 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19065 | hp1 | a0001 | c0007 | t0001 | g0006 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19065 | hp2 | a0003 | c0009 | t0001 | g0332 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19066 | hp1 | a0004 | c0002 | t0001 | g0360 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19066 | hp2 | a0006 | c0029 | t0001 | g0325 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19067 | hp1 | a0032 | c0082 | t0001 | g0180 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19067 | hp2 | a0005 | c0016 | t0001 | g0068 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19068 | hp1 | a0005 | c0018 | t0001 | g0018 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19068 | hp2 | a0004 | c0002 | t0001 | g0187 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19070 | hp1 | a0010 | c0023 | t0001 | g0347 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19070 | hp2 | a0002 | c0019 | t0001 | g0190 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19072 | hp1 | a0004 | c0002 | t0001 | g0134 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19072 | hp2 | a0002 | c0019 | t0001 | g0191 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19074 | hp1 | a0003 | c0008 | t0001 | g0361 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19074 | hp2 | a0002 | c0001 | t0001 | g0323 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19078 | hp1 | a0003 | c0013 | t0001 | g0012 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19078 | hp2 | a0013 | c0117 | t0001 | g0380 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19079 | hp1 | a0002 | c0081 | t0001 | g0005 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19079 | hp2 | a0005 | c0016 | t0001 | g0057 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19083 | hp1 | a0001 | c0017 | t0001 | g0128 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19083 | hp2 | a0010 | c0023 | t0001 | g0351 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19084 | hp1 | a0003 | c0009 | t0001 | g0305 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19084 | hp2 | a0004 | c0002 | t0001 | g0135 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19085 | hp1 | a0003 | c0013 | t0001 | g0019 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19085 | hp2 | a0001 | c0004 | t0001 | g0367 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19087 | hp1 | a0004 | c0010 | t0001 | g0296 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19087 | hp2 | a0005 | c0016 | t0001 | g0035 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19088 | hp1 | a0002 | c0001 | t0001 | g0334 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19088 | hp2 | a0003 | c0009 | t0001 | g0318 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19091 | hp1 | a0001 | c0004 | t0001 | g0027 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19091 | hp2 | a0001 | c0012 | t0001 | g0297 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19240 | hp1 | a0004 | c0021 | t0001 | g0109 | AFR | YRI | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA19240 | hp2 | a0005 | c0028 | t0001 | g0363 | AFR | YRI | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA20129 | hp1 | a0031 | c0080 | t0001 | g0220 | AFR | ASW | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA20129 | hp2 | a0001 | c0004 | t0001 | g0170 | AFR | ASW | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA20752 | hp1 | a0004 | c0026 | t0001 | g0177 | EUR | TSI | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA20752 | hp2 | a0001 | c0027 | t0001 | g0154 | EUR | TSI | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA20805 | hp1 | a0036 | c0067 | t0001 | g0104 | EUR | TSI | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA20805 | hp2 | a0042 | c0057 | t0001 | g0159 | EUR | TSI | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA20905 | hp1 | a0003 | c0025 | t0001 | g0158 | SAS | GIH | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA20905 | hp2 | a0004 | c0021 | t0001 | g0127 | SAS | GIH | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01123 | hp1 | a0004 | c0002 | t0001 | g0214 | AMR | CLM | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG01123 | hp2 | a0003 | c0005 | t0001 | g0116 | AMR | CLM | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02109 | hp1 | a0007 | c0097 | t0001 | g0173 | AFR | ACB | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02109 | hp2 | a0005 | c0028 | t0001 | g0083 | AFR | ACB | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02486 | hp1 | a0001 | c0089 | t0001 | g0184 | AFR | ACB | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02486 | hp2 | a0027 | c0088 | t0001 | g0256 | AFR | ACB | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02559 | hp1 | a0001 | c0004 | t0001 | g0169 | AFR | ACB | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG02559 | hp2 | a0001 | c0022 | t0001 | g0181 | AFR | ACB | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG03471 | hp1 | a0021 | c0055 | t0001 | g0263 | AFR | MSL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG03471 | hp2 | a0003 | c0005 | t0001 | g0295 | AFR | MSL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG06807 | hp1 | a0012 | c0035 | t0001 | g0145 | AFR | USA | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| HG06807 | hp2 | a0012 | c0058 | t0001 | g0142 | AFR | USA | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18955 | hp1 | a0002 | c0043 | t0001 | g0333 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA18955 | hp2 | a0002 | c0001 | t0001 | g0252 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA20300 | hp1 | a0007 | c0020 | t0001 | g0261 | AFR | USA | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA20300 | hp2 | a0001 | c0003 | t0001 | g0008 | AFR | USA | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA21309 | hp1 | a0001 | c0015 | t0001 | g0371 | AFR | LWK | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| NA21309 | hp2 | a0003 | c0041 | t0001 | g0197 | AFR | LWK | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| homoSapiens_chm13v2 | hp1 | a0004 | c0002 | t0001 | g0075 | REF | REF | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| homoSapiens_grch38 | hp1 | a0003 | c0005 | t0001 | g0216 | REF | REF | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:10303278
|
T | C | 12 | a0002a0006a0007others(9): Show | 87 | HG00423.hp1 HG00438.hp2 HG00621.hp1 others(84): Show |
missense_variant | MODERATE | c.5585A>G | p.His1862Arg | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 39/41 | 5676/5994 | 5585/5817 | 1862/1938 | chr17 | 10303278 | ||
| chr17:10303495
|
G | A | 1 | a0030 | 1 | NA19063.hp2 | missense_variant | MODERATE | c.5470C>T | p.Arg1824Trp | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 38/41 | 5561/5994 | 5470/5817 | 1824/1938 | chr17 | 10303495 | ||
| chr17:10306461
|
G | A | 3 | a0015a0036a0038 | 4 | HG00099.hp2 HG01257.hp2 HG04199.hp1 others(1): Show |
missense_variant&splice_region_variant | MODERATE | c.5464C>T | p.Arg1822Trp | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 37/41 | 5555/5994 | 5464/5817 | 1822/1938 | chr17 | 10306461 | ||
| chr17:10306526
|
C | T | 1 | a0037 | 1 | HG00423.hp1 | missense_variant | MODERATE | c.5399G>A | p.Arg1800His | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 37/41 | 5490/5994 | 5399/5817 | 1800/1938 | chr17 | 10306526 | ||
| chr17:10309279
|
C | G | 1 | a0029 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.5124G>C | p.Gln1708His | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 35/41 | 5215/5994 | 5124/5817 | 1708/1938 | chr17 | 10309279 | ||
| chr17:10309647
|
C | G | 1 | a0011 | 3 | HG01358.hp2 HG01361.hp2 HG01433.hp2 |
missense_variant | MODERATE | c.4840G>C | p.Asp1614His | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 34/41 | 4931/5994 | 4840/5817 | 1614/1938 | chr17 | 10309647 | ||
| chr17:10309797
|
G | C | 1 | a0031 | 1 | NA20129.hp1 | missense_variant | MODERATE | c.4690C>G | p.Arg1564Gly | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 34/41 | 4781/5994 | 4690/5817 | 1564/1938 | chr17 | 10309797 | ||
| chr17:10312627
|
G | A | 1 | a0035 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.4312C>T | p.Arg1438Cys | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 31/41 | 4403/5994 | 4312/5817 | 1438/1938 | chr17 | 10312627 | ||
| chr17:10312639
|
G | A | 1 | a0032 | 1 | NA19067.hp1 | missense_variant | MODERATE | c.4300C>T | p.Arg1434Trp | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 31/41 | 4391/5994 | 4300/5817 | 1434/1938 | chr17 | 10312639 | ||
| chr17:10312746
|
G | A | 1 | a0039 | 1 | HG01978.hp2 | missense_variant | MODERATE | c.4193C>T | p.Ala1398Val | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 31/41 | 4284/5994 | 4193/5817 | 1398/1938 | chr17 | 10312746 | ||
| chr17:10315763
|
A | T | 1 | a0009 | 5 | HG02630.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
missense_variant | MODERATE | c.3914T>A | p.Leu1305Gln | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 29/41 | 4005/5994 | 3914/5817 | 1305/1938 | chr17 | 10315763 | ||
| chr17:10315780
|
C | A | 1 | a0028 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.3897G>T | p.Glu1299Asp | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 29/41 | 3988/5994 | 3897/5817 | 1299/1938 | chr17 | 10315780 | ||
| chr17:10315796
|
C | T | 11 | a0004a0008a0010others(8): Show | 61 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(58): Show |
missense_variant | MODERATE | c.3881G>A | p.Arg1294Gln | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 29/41 | 3972/5994 | 3881/5817 | 1294/1938 | chr17 | 10315796 | ||
| chr17:10315927
|
C | T | 2 | a0010a0034 | 5 | NA18967.hp1 NA18974.hp2 NA18998.hp1 others(2): Show |
missense_variant | MODERATE | c.3837G>A | p.Met1279Ile | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 28/41 | 3928/5994 | 3837/5817 | 1279/1938 | chr17 | 10315927 | ||
| chr17:10319161
|
C | T | 1 | a0023 | 1 | NA18999.hp2 | missense_variant | MODERATE | c.3367G>A | p.Glu1123Lys | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 27/41 | 3458/5994 | 3367/5817 | 1123/1938 | chr17 | 10319161 | ||
| chr17:10320233
|
C | G | 1 | a0033 | 1 | HG03669.hp2 | missense_variant | MODERATE | c.3268G>C | p.Glu1090Gln | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 26/41 | 3359/5994 | 3268/5817 | 1090/1938 | chr17 | 10320233 | ||
| chr17:10320380
|
G | T | 11 | a0002a0005a0008others(8): Show | 92 | HG00621.hp1 HG00741.hp2 HG01081.hp1 others(89): Show |
missense_variant | MODERATE | c.3228C>A | p.Asp1076Glu | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 25/41 | 3319/5994 | 3228/5817 | 1076/1938 | chr17 | 10320380 | ||
| chr17:10320397
|
T | C | 20 | a0001a0004a0006others(17): Show | 214 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(211): Show |
missense_variant | MODERATE | c.3211A>G | p.Met1071Val | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 25/41 | 3302/5994 | 3211/5817 | 1071/1938 | chr17 | 10320397 | ||
| chr17:10320465
|
A | G | 1 | a0040 | 1 | HG00733.hp1 | missense_variant | MODERATE | c.3143T>C | p.Leu1048Pro | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 25/41 | 3234/5994 | 3143/5817 | 1048/1938 | chr17 | 10320465 | ||
| chr17:10324150
|
T | C | 1 | a0041 | 1 | HG03486.hp2 | missense_variant | MODERATE | c.2806A>G | p.Met936Val | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/41 | 2897/5994 | 2806/5817 | 936/1938 | chr17 | 10324150 | ||
| chr17:10327951
|
C | T | 1 | a0026 | 1 | HG01099.hp2 | missense_variant | MODERATE | c.2606G>A | p.Arg869Gln | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/41 | 2697/5994 | 2606/5817 | 869/1938 | chr17 | 10327951 | ||
| chr17:10333147
|
C | T | 1 | a0016 | 2 | HG00140.hp2 HG04204.hp1 |
missense_variant | MODERATE | c.2101G>A | p.Gly701Arg | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 19/41 | 2192/5994 | 2101/5817 | 701/1938 | chr17 | 10333147 | ||
| chr17:10333189
|
C | T | 1 | a0025 | 1 | HG02258.hp2 | missense_variant&splice_region_variant | MODERATE | c.2059G>A | p.Val687Met | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 19/41 | 2150/5994 | 2059/5817 | 687/1938 | chr17 | 10333189 | ||
| chr17:10340336
|
C | T | 1 | a0024 | 1 | NA18991.hp1 | missense_variant | MODERATE | c.1960G>A | p.Val654Met | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 17/41 | 2051/5994 | 1960/5817 | 654/1938 | chr17 | 10340336 | ||
| chr17:10343955
|
G | A | 1 | a0023 | 1 | NA18999.hp2 | missense_variant | MODERATE | c.1739C>T | p.Ser580Leu | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/41 | 1830/5994 | 1739/5817 | 580/1938 | chr17 | 10343955 | ||
| chr17:10343992
|
G | T | 2 | a0012a0017 | 5 | HG02809.hp2 HG03225.hp2 HG03540.hp1 others(2): Show |
missense_variant | MODERATE | c.1702C>A | p.Pro568Thr | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/41 | 1793/5994 | 1702/5817 | 568/1938 | chr17 | 10343992 | ||
| chr17:10345362
|
A | G | 1 | a0042 | 1 | NA20805.hp2 | missense_variant | MODERATE | c.1424T>C | p.Leu475Pro | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 15/41 | 1515/5994 | 1424/5817 | 475/1938 | chr17 | 10345362 | ||
| chr17:10350556
|
C | T | 1 | a0022 | 1 | HG01516.hp1 | missense_variant&splice_region_variant | MODERATE | c.1144G>A | p.Val382Met | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 12/41 | 1235/5994 | 1144/5817 | 382/1938 | chr17 | 10350556 | ||
| chr17:10355116
|
G | T | 1 | a0021 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.770C>A | p.Thr257Lys | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 9/41 | 861/5994 | 770/5817 | 257/1938 | chr17 | 10355116 | ||
| chr17:10362168
|
G | A | 1 | a0020 | 1 | NA18939.hp1 | missense_variant | MODERATE | c.455C>T | p.Pro152Leu | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 5/41 | 546/5994 | 455/5817 | 152/1938 | chr17 | 10362168 | ||
| chr17:10362383
|
G | A | 2 | a0018a0019 | 2 | HG02735.hp2 HG03710.hp1 |
missense_variant | MODERATE | c.325C>T | p.Arg109Cys | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 4/41 | 416/5994 | 325/5817 | 109/1938 | chr17 | 10362383 | ||
| chr17:10362397
|
T | C | 2 | a0013a0014 | 4 | HG01952.hp1 HG02074.hp2 NA18990.hp1 others(1): Show |
missense_variant | MODERATE | c.311A>G | p.Tyr104Cys | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 4/41 | 402/5994 | 311/5817 | 104/1938 | chr17 | 10362397 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:10301698
|
C | T | 1 | a0001c0051 | 2 | HG02135.hp2 HG02155.hp2 |
synonymous_variant | LOW | c.5673G>A | p.Glu1891Glu | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 40/41 | 5764/5994 | 5673/5817 | 1891/1938 | chr17 | 10301698 | ||
| chr17:10309681
|
C | T | 1 | a0002c0064 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.4806G>A | p.Gln1602Gln | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 34/41 | 4897/5994 | 4806/5817 | 1602/1938 | chr17 | 10309681 | ||
| chr17:10309701
|
G | T | 1 | a0002c0078 | 1 | NA18959.hp2 | synonymous_variant | LOW | c.4786C>A | p.Arg1596Arg | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 34/41 | 4877/5994 | 4786/5817 | 1596/1938 | chr17 | 10309701 | ||
| chr17:10311118
|
G | A | 1 | a0018c0114 | 1 | HG03710.hp1 | synonymous_variant | LOW | c.4641C>T | p.Ala1547Ala | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 33/41 | 4732/5994 | 4641/5817 | 1547/1938 | chr17 | 10311118 | ||
| chr17:10313193
|
G | A | 33 | a0001c0003a0001c0006a0001c0012others(30): Show | 98 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(95): Show |
synonymous_variant | LOW | c.4146C>T | p.Asp1382Asp | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 30/41 | 4237/5994 | 4146/5817 | 1382/1938 | chr17 | 10313193 | ||
| chr17:10313199
|
C | T | 2 | a0002c0019a0002c0043 | 8 | NA18939.hp2 NA18941.hp2 NA18946.hp1 others(5): Show |
synonymous_variant | LOW | c.4140G>A | p.Glu1380Glu | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 30/41 | 4231/5994 | 4140/5817 | 1380/1938 | chr17 | 10313199 | ||
| chr17:10313220
|
G | A | 1 | a0001c0108 | 1 | HG01070.hp2 | synonymous_variant | LOW | c.4119C>T | p.Ala1373Ala | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 30/41 | 4210/5994 | 4119/5817 | 1373/1938 | chr17 | 10313220 | ||
| chr17:10313232
|
G | A | 1 | a0001c0042 | 2 | HG01891.hp1 HG02976.hp1 |
synonymous_variant | LOW | c.4107C>T | p.Asn1369Asn | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 30/41 | 4198/5994 | 4107/5817 | 1369/1938 | chr17 | 10313232 | ||
| chr17:10313247
|
C | T | 2 | a0002c0019a0002c0043 | 8 | NA18939.hp2 NA18941.hp2 NA18946.hp1 others(5): Show |
synonymous_variant | LOW | c.4092G>A | p.Ala1364Ala | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 30/41 | 4183/5994 | 4092/5817 | 1364/1938 | chr17 | 10313247 | ||
| chr17:10313313
|
G | A | 2 | a0002c0019a0002c0043 | 8 | NA18939.hp2 NA18941.hp2 NA18946.hp1 others(5): Show |
synonymous_variant | LOW | c.4026C>T | p.His1342His | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 30/41 | 4117/5994 | 4026/5817 | 1342/1938 | chr17 | 10313313 | ||
| chr17:10313337
|
C | T | 1 | a0006c0099 | 1 | HG03139.hp1 | synonymous_variant | LOW | c.4002G>A | p.Ala1334Ala | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 30/41 | 4093/5994 | 4002/5817 | 1334/1938 | chr17 | 10313337 | ||
| chr17:10316002
|
C | T | 2 | a0007c0096a0013c0116 | 2 | HG02074.hp2 NA18985.hp1 |
synonymous_variant | LOW | c.3762G>A | p.Arg1254Arg | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 28/41 | 3853/5994 | 3762/5817 | 1254/1938 | chr17 | 10316002 | ||
| chr17:10318814
|
G | A | 2 | a0002c0081a0002c0094 | 2 | HG02074.hp1 NA19079.hp1 |
synonymous_variant | LOW | c.3714C>T | p.Asn1238Asn | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 27/41 | 3805/5994 | 3714/5817 | 1238/1938 | chr17 | 10318814 | ||
| chr17:10318832
|
A | G | 29 | a0001c0089a0002c0001a0002c0011others(26): Show | 82 | HG00621.hp1 HG01081.hp1 HG01167.hp1 others(79): Show |
synonymous_variant | LOW | c.3696T>C | p.Ile1232Ile | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 27/41 | 3787/5994 | 3696/5817 | 1232/1938 | chr17 | 10318832 | ||
| chr17:10318850
|
G | A | 6 | a0001c0022a0001c0046a0001c0062others(3): Show | 10 | HG00741.hp1 HG02055.hp2 HG02258.hp1 others(7): Show |
synonymous_variant | LOW | c.3678C>T | p.Ser1226Ser | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 27/41 | 3769/5994 | 3678/5817 | 1226/1938 | chr17 | 10318850 | ||
| chr17:10318913
|
G | A | 2 | a0002c0019a0002c0043 | 8 | NA18939.hp2 NA18941.hp2 NA18946.hp1 others(5): Show |
synonymous_variant | LOW | c.3615C>T | p.Ala1205Ala | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 27/41 | 3706/5994 | 3615/5817 | 1205/1938 | chr17 | 10318913 | ||
| chr17:10320476
|
C | T | 4 | a0001c0040a0001c0050a0001c0105others(1): Show | 6 | HG00140.hp2 HG00323.hp1 HG01496.hp2 others(3): Show |
synonymous_variant | LOW | c.3132G>A | p.Gln1044Gln | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 25/41 | 3223/5994 | 3132/5817 | 1044/1938 | chr17 | 10320476 | ||
| chr17:10324058
|
C | T | 1 | a0001c0111 | 1 | HG01109.hp1 | synonymous_variant | LOW | c.2898G>A | p.Thr966Thr | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/41 | 2989/5994 | 2898/5817 | 966/1938 | chr17 | 10324058 | ||
| chr17:10328100
|
C | T | 37 | a0001c0007a0001c0012a0001c0039others(34): Show | 116 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(113): Show |
synonymous_variant | LOW | c.2457G>A | p.Gln819Gln | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/41 | 2548/5994 | 2457/5817 | 819/1938 | chr17 | 10328100 | ||
| chr17:10332138
|
G | A | 1 | a0003c0091 | 1 | HG02970.hp1 | synonymous_variant | LOW | c.2259C>T | p.Ile753Ile | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 20/41 | 2350/5994 | 2259/5817 | 753/1938 | chr17 | 10332138 | ||
| chr17:10333148
|
G | A | 47 | a0001c0003a0001c0004a0001c0027others(44): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
synonymous_variant | LOW | c.2100C>T | p.Asn700Asn | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 19/41 | 2191/5994 | 2100/5817 | 700/1938 | chr17 | 10333148 | ||
| chr17:10333160
|
C | T | 1 | a0001c0075 | 1 | HG02027.hp2 | synonymous_variant | LOW | c.2088G>A | p.Gln696Gln | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 19/41 | 2179/5994 | 2088/5817 | 696/1938 | chr17 | 10333160 | ||
| chr17:10340154
|
A | G | 2 | a0001c0105a0008c0104 | 2 | HG03942.hp2 HG04115.hp1 |
synonymous_variant | LOW | c.2052T>C | p.Thr684Thr | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/41 | 2143/5994 | 2052/5817 | 684/1938 | chr17 | 10340154 | ||
| chr17:10340400
|
G | A | 92 | a0001c0003a0001c0004a0001c0007others(89): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
splice_region_variant&synonymous_variant | LOW | c.1896C>T | p.Gly632Gly | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 17/41 | 1987/5994 | 1896/5817 | 632/1938 | chr17 | 10340400 | ||
| chr17:10343882
|
G | A | 10 | a0001c0027a0001c0034a0001c0105others(7): Show | 21 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(18): Show |
synonymous_variant | LOW | c.1812C>T | p.Asn604Asn | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/41 | 1903/5994 | 1812/5817 | 604/1938 | chr17 | 10343882 | ||
| chr17:10354743
|
G | A | 1 | a0001c0110 | 1 | HG02165.hp2 | synonymous_variant | LOW | c.942C>T | p.Phe314Phe | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/41 | 1033/5994 | 942/5817 | 314/1938 | chr17 | 10354743 | ||
| chr17:10359999
|
G | A | 1 | a0001c0111 | 1 | HG01109.hp1 | synonymous_variant | LOW | c.606C>T | p.Thr202Thr | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 7/41 | 697/5994 | 606/5817 | 202/1938 | chr17 | 10359999 | ||
| chr17:10362375
|
T | C | 1 | a0001c0113 | 1 | HG02055.hp2 | synonymous_variant | LOW | c.333A>G | p.Ala111Ala | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 4/41 | 424/5994 | 333/5817 | 111/1938 | chr17 | 10362375 | ||
| chr17:10362444
|
G | A | 2 | a0001c0118a0001c0119 | 2 | HG02257.hp2 HG02886.hp2 |
synonymous_variant | LOW | c.264C>T | p.Ile88Ile | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 4/41 | 355/5994 | 264/5817 | 88/1938 | chr17 | 10362444 | ||
| chr17:10364438
|
T | C | 1 | a0001c0120 | 1 | HG01192.hp2 | synonymous_variant | LOW | c.93A>G | p.Pro31Pro | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 3/41 | 184/5994 | 93/5817 | 31/1938 | chr17 | 10364438 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:10372991
|
C | G | 1 | a0003c0009t0002 | 1 | HG04204.hp2 | 5_prime_UTR_variant | MODIFIER | c.-76G>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 1/41 | 8461 | chr17 | 10372991 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:10301084
|
C | T | 8 | a0001c0040t0001g0117a0001c0040t0001g0137a0001c0050t0001g0042others(5): Show | 8 | HG00140.hp2 HG00323.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.5803-119G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 40/40 | chr17 | 10301084 | ||||||
| chr17:10301133
|
G | A | 1 | a0001c0014t0001g0219 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.5803-168C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 40/40 | chr17 | 10301133 | ||||||
| chr17:10301357
|
C | T | 1 | a0001c0007t0001g0107 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.5802+212G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 40/40 | chr17 | 10301357 | ||||||
| chr17:10301402
|
G | C | 11 | a0001c0039t0001g0113a0001c0039t0001g0115a0002c0001t0001g0334others(8): Show | 11 | NA18939.hp2 NA18941.hp2 NA18946.hp1 others(8): Show |
intron_variant | MODIFIER | c.5802+167C>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 40/40 | chr17 | 10301402 | ||||||
| chr17:10301462
|
T | C | 1 | a0015c0053t0001g0047 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.5802+107A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 40/40 | chr17 | 10301462 | ||||||
| chr17:10301480
|
C | T | 5 | a0002c0011t0001g0186a0002c0011t0001g0234a0002c0011t0001g0235others(2): Show | 5 | HG02717.hp1 HG02723.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.5802+89G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 40/40 | chr17 | 10301480 | ||||||
| chr17:10301517
|
T | C | 1 | a0001c0014t0001g0110 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.5802+52A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 40/40 | chr17 | 10301517 | ||||||
| chr17:10301730
|
C | G | 117 | a0001c0003t0001g0008a0001c0003t0001g0043a0001c0003t0001g0044others(114): Show | 117 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.5668-27G>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 39/40 | chr17 | 10301730 | ||||||
| chr17:10301750
|
C | T | 379 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(376): Show | 381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.5668-47G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 39/40 | chr17 | 10301750 | ||||||
| chr17:10301760
|
G | A | 1 | a0004c0021t0001g0109 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.5668-57C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 39/40 | chr17 | 10301760 | ||||||
| chr17:10301777
|
G | C | 1 | a0001c0015t0001g0371 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.5668-74C>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 39/40 | chr17 | 10301777 | ||||||
| chr17:10301963
|
A | G | 1 | a0005c0016t0001g0091 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.5668-260T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 39/40 | chr17 | 10301963 | ||||||
| chr17:10301983
|
C | T | 4 | a0001c0007t0001g0376a0005c0028t0001g0363a0007c0083t0001g0096others(1): Show | 4 | HG02622.hp2 HG03225.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.5668-280G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 39/40 | chr17 | 10301983 | ||||||
| chr17:10302274
|
A | G | 1 | a0002c0001t0001g0352 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.5668-571T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 39/40 | chr17 | 10302274 | ||||||
| chr17:10302343
|
G | T | 1 | a0003c0041t0001g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.5668-640C>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 39/40 | chr17 | 10302343 | ||||||
| chr17:10302474
|
A | G | 19 | a0001c0003t0001g0233a0001c0012t0001g0267a0001c0012t0001g0272others(16): Show | 19 | HG00741.hp1 HG01109.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.5667+722T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 39/40 | chr17 | 10302474 | ||||||
| chr17:10302679
|
T | C | 128 | a0001c0003t0001g0063a0001c0007t0001g0284a0001c0007t0001g0312others(125): Show | 128 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.5667+517A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 39/40 | chr17 | 10302679 | ||||||
| chr17:10302685
|
T | G | 3 | a0005c0028t0001g0363a0007c0083t0001g0096a0012c0058t0001g0142 | 3 | HG02622.hp2 HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.5667+511A>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 39/40 | chr17 | 10302685 | ||||||
| chr17:10302925
|
G | T | 1 | a0002c0001t0001g0040 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.5667+271C>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 39/40 | chr17 | 10302925 | ||||||
| chr17:10302943
|
C | T | 1 | a0015c0053t0001g0055 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.5667+253G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 39/40 | chr17 | 10302943 | ||||||
| chr17:10303057
|
T | G | 3 | a0006c0024t0001g0095a0006c0033t0001g0185a0007c0083t0001g0096 | 3 | HG02622.hp2 HG02647.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.5667+139A>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 39/40 | chr17 | 10303057 | ||||||
| chr17:10303391
|
T | C | 1 | a0003c0008t0001g0361 | 1 | NA19074.hp1 | splice_region_variant&intron_variant | LOW | c.5571+3A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 38/40 | chr17 | 10303391 | ||||||
| chr17:10303605
|
A | G | 8 | a0002c0019t0001g0054a0002c0019t0001g0188a0002c0019t0001g0189others(5): Show | 8 | NA18939.hp2 NA18941.hp2 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.5467-107T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 37/40 | chr17 | 10303605 | ||||||
| chr17:10303641
|
T | G | 1 | a0002c0094t0001g0226 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.5467-143A>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 37/40 | chr17 | 10303641 | ||||||
| chr17:10303676
|
G | C | 69 | a0002c0001t0001g0004a0002c0001t0001g0040a0002c0001t0001g0048others(66): Show | 69 | HG00423.hp1 HG00438.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.5467-178C>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 37/40 | chr17 | 10303676 | ||||||
| chr17:10303879
|
C | T | 3 | a0003c0005t0001g0122a0012c0035t0001g0143a0012c0035t0001g0145 | 3 | HG03098.hp2 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.5467-381G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 37/40 | chr17 | 10303879 | ||||||
| chr17:10303944
|
A | G | 5 | a0002c0011t0001g0186a0002c0011t0001g0234a0002c0011t0001g0235others(2): Show | 5 | HG02717.hp1 HG02723.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.5467-446T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 37/40 | chr17 | 10303944 | ||||||
| chr17:10304088
|
A | C | 8 | a0002c0019t0001g0054a0002c0019t0001g0188a0002c0019t0001g0189others(5): Show | 8 | NA18939.hp2 NA18941.hp2 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.5467-590T>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 37/40 | chr17 | 10304088 | ||||||
| chr17:10304205
|
G | A | 8 | a0002c0019t0001g0054a0002c0019t0001g0188a0002c0019t0001g0189others(5): Show | 8 | NA18939.hp2 NA18941.hp2 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.5467-707C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 37/40 | chr17 | 10304205 | ||||||
| chr17:10304330
|
T | G | 1 | a0001c0007t0001g0260 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.5467-832A>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 37/40 | chr17 | 10304330 | ||||||
| chr17:10304445
|
T | C | 68 | a0002c0001t0001g0004a0002c0001t0001g0040a0002c0001t0001g0048others(65): Show | 68 | HG00423.hp1 HG00438.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.5467-947A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 37/40 | chr17 | 10304445 | ||||||
| chr17:10304482
|
G | A | 1 | a0006c0068t0001g0366 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.5467-984C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 37/40 | chr17 | 10304482 | ||||||
| chr17:10304587
|
C | T | 7 | a0001c0015t0001g0092a0001c0015t0001g0098a0001c0015t0001g0378others(4): Show | 7 | HG01891.hp1 HG02451.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.5467-1089G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 37/40 | chr17 | 10304587 | ||||||
| chr17:10304659
|
G | A | 1 | a0001c0004t0001g0194 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.5467-1161C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 37/40 | chr17 | 10304659 | ||||||
| chr17:10304768
|
T | C | 1 | a0001c0017t0001g0128 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.5467-1270A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 37/40 | chr17 | 10304768 | ||||||
| chr17:10305286
|
T | C | 1 | a0004c0002t0001g0212 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.5466+1173A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 37/40 | chr17 | 10305286 | ||||||
| chr17:10305376
|
T | C | 7 | a0001c0003t0001g0237a0001c0003t0001g0269a0006c0099t0001g0270others(4): Show | 7 | HG01243.hp2 HG01884.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.5466+1083A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 37/40 | chr17 | 10305376 | ||||||
| chr17:10305400
|
G | C | 5 | a0004c0002t0001g0212a0010c0023t0001g0311a0010c0023t0001g0347others(2): Show | 5 | HG00438.hp1 NA18967.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.5466+1059C>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 37/40 | chr17 | 10305400 | ||||||
| chr17:10305428
|
A | G | 43 | a0001c0004t0001g0025a0001c0004t0001g0027a0001c0004t0001g0028others(40): Show | 43 | HG00735.hp1 HG01099.hp1 HG01106.hp1 others(40): Show |
intron_variant | MODIFIER | c.5466+1031T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 37/40 | chr17 | 10305428 | ||||||
| chr17:10305765
|
G | A | 1 | a0001c0017t0001g0129 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.5466+694C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 37/40 | chr17 | 10305765 | ||||||
| chr17:10305788
|
T | C | 115 | a0001c0004t0001g0025a0001c0004t0001g0027a0001c0004t0001g0028others(112): Show | 115 | HG00423.hp1 HG00438.hp2 HG00621.hp1 others(112): Show |
intron_variant | MODIFIER | c.5466+671A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 37/40 | chr17 | 10305788 | ||||||
| chr17:10305836
|
A | G | 1 | a0001c0017t0001g0129 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.5466+623T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 37/40 | chr17 | 10305836 | ||||||
| chr17:10305874
|
A | G | 1 | a0002c0011t0001g0081 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.5466+585T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 37/40 | chr17 | 10305874 | ||||||
| chr17:10305895
|
C | A | 47 | a0001c0003t0001g0043a0001c0003t0001g0044a0001c0003t0001g0045others(44): Show | 48 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.5466+564G>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 37/40 | chr17 | 10305895 | ||||||
| chr17:10305901
|
T | C | 2 | a0001c0014t0001g0374a0003c0005t0001g0294 | 2 | HG02717.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.5466+558A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 37/40 | chr17 | 10305901 | ||||||
| chr17:10306030
|
T | C | 339 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(336): Show | 341 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(338): Show |
intron_variant | MODIFIER | c.5466+429A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 37/40 | chr17 | 10306030 | ||||||
| chr17:10306220
|
A | ATG | 65 | a0001c0003t0001g0008a0001c0003t0001g0044a0001c0003t0001g0203others(62): Show | 66 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.5466+237_5466+238d others(4): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 37/40 | chr17 | 10306220 | ||||||
| chr17:10306220
|
A | ATGTG | 32 | a0001c0003t0001g0241a0001c0003t0001g0243a0001c0007t0001g0006others(29): Show | 32 | HG00408.hp2 HG00733.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.5466+235_5466+238d others(6): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 37/40 | chr17 | 10306220 | ||||||
| chr17:10306220
|
A | ATGTGTG | 15 | a0001c0003t0001g0269a0001c0007t0001g0376a0001c0040t0001g0137others(12): Show | 15 | HG01243.hp2 HG01255.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.5466+233_5466+238d others(8): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 37/40 | chr17 | 10306220 | ||||||
| chr17:10306220
|
A | ATGTGTGT others(1): Show |
13 | a0001c0003t0001g0049a0001c0034t0001g0168a0001c0046t0001g0271others(10): Show | 14 | HG00323.hp2 HG00741.hp1 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.5466+231_5466+238d others(10): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 37/40 | chr17 | 10306220 | ||||||
| chr17:10306220
|
A | ATGTGTGT others(3): Show |
13 | a0001c0006t0001g0132a0004c0002t0001g0192a0004c0002t0001g0214others(10): Show | 13 | HG01123.hp1 HG02486.hp2 HG02602.hp2 others(10): Show |
intron_variant | MODIFIER | c.5466+229_5466+238d others(12): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 37/40 | chr17 | 10306220 | ||||||
| chr17:10306220
|
A | ATGTGTGT others(5): Show |
6 | a0004c0002t0001g0075a0004c0002t0001g0134a0004c0002t0001g0135others(3): Show | 6 | HG00733.hp2 HG02735.hp2 NA18974.hp2 others(3): Show |
intron_variant | MODIFIER | c.5466+227_5466+238d others(14): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 37/40 | chr17 | 10306220 | ||||||
| chr17:10306220
|
A | ATGTGTGT others(7): Show |
5 | a0004c0002t0001g0211a0004c0010t0001g0073a0004c0026t0001g0153others(2): Show | 5 | HG00544.hp2 HG01891.hp2 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.5466+225_5466+238d others(16): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 37/40 | chr17 | 10306220 | ||||||
| chr17:10306220
|
A | ATGTGTGT others(9): Show |
1 | a0035c0086t0001g0300 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.5466+223_5466+238d others(18): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 37/40 | chr17 | 10306220 | ||||||
| chr17:10306220
|
A | ATGTGTGT others(11): Show |
1 | a0008c0063t0001g0298 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.5466+221_5466+238d others(20): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 37/40 | chr17 | 10306220 | ||||||
| chr17:10306220
|
ATG | A | 32 | a0001c0003t0001g0032a0001c0003t0001g0043a0001c0003t0001g0045others(29): Show | 32 | HG00639.hp1 HG00639.hp2 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.5466+237_5466+238d others(4): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 37/40 | chr17 | 10306220 | ||||||
| chr17:10306220
|
ATGTG | A | 25 | a0001c0004t0001g0062a0001c0007t0001g0107a0001c0012t0001g0297others(22): Show | 25 | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.5466+235_5466+238d others(6): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 37/40 | chr17 | 10306220 | ||||||
| chr17:10306220
|
ATGTGTG | A | 57 | a0001c0004t0001g0169a0001c0004t0001g0170a0001c0014t0001g0100others(54): Show | 57 | HG00621.hp1 HG00738.hp1 HG01081.hp1 others(54): Show |
intron_variant | MODIFIER | c.5466+233_5466+238d others(8): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 37/40 | chr17 | 10306220 | ||||||
| chr17:10306220
|
ATGTGTGT others(1): Show |
A | 11 | a0001c0004t0001g0071a0001c0004t0001g0236a0001c0027t0001g0266others(8): Show | 11 | HG01106.hp1 HG01109.hp1 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.5466+231_5466+238d others(10): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 37/40 | chr17 | 10306220 | ||||||
| chr17:10306220
|
ATGTGTGT others(3): Show |
A | 34 | a0001c0004t0001g0025a0001c0004t0001g0027a0001c0004t0001g0028others(31): Show | 34 | HG00423.hp1 HG00735.hp1 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.5466+229_5466+238d others(12): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 37/40 | chr17 | 10306220 | ||||||
| chr17:10306220
|
ATGTGTGT others(5): Show |
A | 2 | a0001c0004t0001g0194a0001c0017t0001g0129 | 2 | HG03130.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.5466+227_5466+238d others(14): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 37/40 | chr17 | 10306220 | ||||||
| chr17:10306220
|
ATGTGTGT others(9): Show |
A | 4 | a0001c0003t0001g0051a0001c0003t0001g0069a0001c0012t0001g0353others(1): Show | 4 | HG03704.hp1 NA18972.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.5466+223_5466+238d others(18): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 37/40 | chr17 | 10306220 | ||||||
| chr17:10306220
|
ATGTGTGT others(13): Show |
A | 2 | a0002c0001t0001g0040a0002c0038t0001g0133 | 2 | NA18969.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.5466+219_5466+238d others(22): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 37/40 | chr17 | 10306220 | ||||||
| chr17:10306266
|
G | T | 1 | a0003c0005t0001g0122 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5466+193C>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 37/40 | chr17 | 10306266 | ||||||
| chr17:10306269
|
T | TGTGTGTG others(6): Show |
1 | a0004c0021t0001g0094 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.5466+189_5466+190i others(15): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 37/40 | chr17 | 10306269 | ||||||
| chr17:10307312
|
T | G | 1 | a0005c0016t0001g0060 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.5170-248A>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 35/40 | chr17 | 10307312 | ||||||
| chr17:10307436
|
C | A | 1 | a0001c0015t0001g0378 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.5170-372G>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 35/40 | chr17 | 10307436 | ||||||
| chr17:10307437
|
G | A | 60 | a0002c0001t0001g0004a0002c0001t0001g0040a0002c0001t0001g0048others(57): Show | 60 | HG00621.hp1 HG01081.hp1 HG01346.hp2 others(57): Show |
intron_variant | MODIFIER | c.5170-373C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 35/40 | chr17 | 10307437 | ||||||
| chr17:10307484
|
C | G | 1 | a0001c0007t0001g0312 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.5170-420G>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 35/40 | chr17 | 10307484 | ||||||
| chr17:10307610
|
A | G | 1 | a0037c0100t0001g0064 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.5170-546T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 35/40 | chr17 | 10307610 | ||||||
| chr17:10307627
|
C | G | 1 | a0001c0090t0001g0364 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.5170-563G>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 35/40 | chr17 | 10307627 | ||||||
| chr17:10307750
|
T | C | 3 | a0001c0089t0001g0184a0005c0028t0001g0363a0012c0058t0001g0142 | 3 | HG02486.hp1 HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.5170-686A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 35/40 | chr17 | 10307750 | ||||||
| chr17:10308248
|
T | C | 318 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(315): Show | 320 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(317): Show |
intron_variant | MODIFIER | c.5169+986A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 35/40 | chr17 | 10308248 | ||||||
| chr17:10308301
|
C | T | 61 | a0002c0001t0001g0004a0002c0001t0001g0040a0002c0001t0001g0048others(58): Show | 61 | HG00438.hp2 HG00621.hp1 HG01081.hp1 others(58): Show |
intron_variant | MODIFIER | c.5169+933G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 35/40 | chr17 | 10308301 | ||||||
| chr17:10308327
|
C | CA | 77 | a0001c0004t0001g0025a0001c0004t0001g0027a0001c0004t0001g0028others(74): Show | 77 | HG00423.hp1 HG00621.hp2 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.5169+906dupT | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 35/40 | chr17 | 10308327 | ||||||
| chr17:10308327
|
C | CAA | 60 | a0001c0017t0001g0128a0002c0001t0001g0004a0002c0001t0001g0040others(57): Show | 60 | HG00438.hp2 HG00621.hp1 HG01081.hp1 others(57): Show |
intron_variant | MODIFIER | c.5169+905_5169+906d others(4): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 35/40 | chr17 | 10308327 | ||||||
| chr17:10308327
|
CA | C | 179 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(176): Show | 181 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.5169+906delT | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 35/40 | chr17 | 10308327 | ||||||
| chr17:10308405
|
C | A | 1 | a0006c0033t0001g0213 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.5169+829G>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 35/40 | chr17 | 10308405 | ||||||
| chr17:10308409
|
G | T | 318 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(315): Show | 320 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(317): Show |
intron_variant | MODIFIER | c.5169+825C>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 35/40 | chr17 | 10308409 | ||||||
| chr17:10308411
|
C | CTA | 310 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(307): Show | 312 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(309): Show |
intron_variant | MODIFIER | c.5169+821_5169+822d others(4): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 35/40 | chr17 | 10308411 | ||||||
| chr17:10308411
|
C | CTATA | 8 | a0002c0019t0001g0054a0002c0019t0001g0188a0002c0019t0001g0189others(5): Show | 8 | NA18939.hp2 NA18941.hp2 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.5169+819_5169+822d others(6): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 35/40 | chr17 | 10308411 | ||||||
| chr17:10308443
|
C | CT | 11 | a0001c0027t0001g0009a0003c0005t0001g0112a0003c0009t0001g0330others(8): Show | 11 | HG00544.hp1 HG01175.hp1 HG03516.hp2 others(8): Show |
intron_variant | MODIFIER | c.5169+790dupA | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 35/40 | chr17 | 10308443 | ||||||
| chr17:10308443
|
CTTTT | C | 74 | a0001c0015t0001g0098a0001c0015t0001g0371a0001c0042t0001g0120others(71): Show | 74 | HG00438.hp2 HG00621.hp1 HG01081.hp1 others(71): Show |
intron_variant | MODIFIER | c.5169+787_5169+790d others(6): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 35/40 | chr17 | 10308443 | ||||||
| chr17:10308443
|
CTTTTT | C | 234 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(231): Show | 236 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.5169+786_5169+790d others(7): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 35/40 | chr17 | 10308443 | ||||||
| chr17:10308555
|
A | G | 1 | a0002c0043t0001g0333 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.5169+679T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 35/40 | chr17 | 10308555 | ||||||
| chr17:10308556
|
T | C | 200 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(197): Show | 202 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.5169+678A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 35/40 | chr17 | 10308556 | ||||||
| chr17:10308747
|
G | A | 2 | a0001c0004t0001g0236a0001c0017t0001g0131 | 2 | HG01981.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.5169+487C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 35/40 | chr17 | 10308747 | ||||||
| chr17:10308988
|
C | G | 2 | a0006c0024t0001g0095a0006c0033t0001g0185 | 2 | HG02647.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.5169+246G>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 35/40 | chr17 | 10308988 | ||||||
| chr17:10309488
|
C | T | 8 | a0002c0019t0001g0054a0002c0019t0001g0188a0002c0019t0001g0189others(5): Show | 8 | NA18939.hp2 NA18941.hp2 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.4965+34G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 34/40 | chr17 | 10309488 | ||||||
| chr17:10309905
|
G | A | 8 | a0002c0019t0001g0054a0002c0019t0001g0188a0002c0019t0001g0189others(5): Show | 8 | NA18939.hp2 NA18941.hp2 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.4657-75C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 33/40 | chr17 | 10309905 | ||||||
| chr17:10309915
|
G | A | 1 | a0004c0002t0001g0072 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.4657-85C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 33/40 | chr17 | 10309915 | ||||||
| chr17:10309945
|
A | T | 1 | a0002c0030t0001g0097 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.4657-115T>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 33/40 | chr17 | 10309945 | ||||||
| chr17:10309946
|
A | AT | 51 | a0001c0006t0001g0140a0001c0007t0001g0006a0001c0007t0001g0007others(48): Show | 51 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.4657-117dupA | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 33/40 | chr17 | 10309946 | ||||||
| chr17:10309946
|
A | T | 5 | a0002c0011t0001g0186a0002c0011t0001g0234a0002c0011t0001g0235others(2): Show | 5 | HG02717.hp1 HG02723.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.4657-116T>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 33/40 | chr17 | 10309946 | ||||||
| chr17:10309946
|
AT | A | 66 | a0002c0001t0001g0004a0002c0001t0001g0040a0002c0001t0001g0048others(63): Show | 66 | HG00621.hp1 HG01081.hp1 HG01346.hp2 others(63): Show |
intron_variant | MODIFIER | c.4657-117delA | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 33/40 | chr17 | 10309946 | ||||||
| chr17:10310036
|
C | T | 4 | a0001c0006t0001g0001a0001c0012t0001g0310a0001c0120t0001g0178others(1): Show | 5 | HG01192.hp2 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.4657-206G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 33/40 | chr17 | 10310036 | ||||||
| chr17:10310094
|
G | GT | 155 | a0001c0004t0001g0025a0001c0004t0001g0027a0001c0004t0001g0028others(152): Show | 156 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.4657-265dupA | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 33/40 | chr17 | 10310094 | ||||||
| chr17:10310094
|
G | GTT | 16 | a0001c0004t0001g0071a0001c0007t0001g0289a0001c0017t0001g0128others(13): Show | 16 | HG01109.hp1 HG02074.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.4657-266_4657-265d others(4): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 33/40 | chr17 | 10310094 | ||||||
| chr17:10310122
|
A | G | 317 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(314): Show | 319 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(316): Show |
intron_variant | MODIFIER | c.4657-292T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 33/40 | chr17 | 10310122 | ||||||
| chr17:10310200
|
C | T | 1 | a0001c0027t0001g0266 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.4657-370G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 33/40 | chr17 | 10310200 | ||||||
| chr17:10310216
|
G | A | 1 | a0040c0076t0001g0343 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.4657-386C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 33/40 | chr17 | 10310216 | ||||||
| chr17:10310338
|
C | T | 1 | a0001c0111t0001g0078 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.4657-508G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 33/40 | chr17 | 10310338 | ||||||
| chr17:10310388
|
C | T | 48 | a0001c0004t0001g0025a0001c0004t0001g0027a0001c0004t0001g0028others(45): Show | 48 | HG00423.hp1 HG00621.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.4657-558G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 33/40 | chr17 | 10310388 | ||||||
| chr17:10310497
|
G | C | 5 | a0009c0032t0001g0171a0009c0032t0001g0172a0009c0032t0001g0175others(2): Show | 5 | HG02630.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.4656+606C>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 33/40 | chr17 | 10310497 | ||||||
| chr17:10310507
|
T | G | 8 | a0002c0019t0001g0054a0002c0019t0001g0188a0002c0019t0001g0189others(5): Show | 8 | NA18939.hp2 NA18941.hp2 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.4656+596A>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 33/40 | chr17 | 10310507 | ||||||
| chr17:10310669
|
G | A | 8 | a0002c0019t0001g0054a0002c0019t0001g0188a0002c0019t0001g0189others(5): Show | 8 | NA18939.hp2 NA18941.hp2 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.4656+434C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 33/40 | chr17 | 10310669 | ||||||
| chr17:10310725
|
G | A | 202 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(199): Show | 204 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.4656+378C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 33/40 | chr17 | 10310725 | ||||||
| chr17:10310993
|
A | G | 46 | a0001c0004t0001g0025a0001c0004t0001g0027a0001c0004t0001g0028others(43): Show | 46 | HG00423.hp1 HG00621.hp2 HG01099.hp1 others(43): Show |
intron_variant | MODIFIER | c.4656+110T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 33/40 | chr17 | 10310993 | ||||||
| chr17:10311311
|
C | T | 202 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(199): Show | 204 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.4532-84G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 32/40 | chr17 | 10311311 | ||||||
| chr17:10311334
|
A | G | 1 | a0006c0068t0001g0366 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4532-107T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 32/40 | chr17 | 10311334 | ||||||
| chr17:10311508
|
G | A | 1 | a0025c0074t0001g0076 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4532-281C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 32/40 | chr17 | 10311508 | ||||||
| chr17:10311682
|
C | T | 1 | a0005c0018t0001g0206 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.4531+229G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 32/40 | chr17 | 10311682 | ||||||
| chr17:10311724
|
C | T | 8 | a0002c0019t0001g0054a0002c0019t0001g0188a0002c0019t0001g0189others(5): Show | 8 | NA18939.hp2 NA18941.hp2 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.4531+187G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 32/40 | chr17 | 10311724 | ||||||
| chr17:10311727
|
C | T | 8 | a0002c0019t0001g0054a0002c0019t0001g0188a0002c0019t0001g0189others(5): Show | 8 | NA18939.hp2 NA18941.hp2 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.4531+184G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 32/40 | chr17 | 10311727 | ||||||
| chr17:10311732
|
G | A | 4 | a0009c0032t0001g0172a0009c0032t0001g0175a0009c0049t0001g0151others(1): Show | 4 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.4531+179C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 32/40 | chr17 | 10311732 | ||||||
| chr17:10311802
|
G | A | 1 | a0002c0011t0001g0234 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.4531+109C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 32/40 | chr17 | 10311802 | ||||||
| chr17:10312094
|
G | A | 1 | a0003c0008t0001g0036 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.4366-18C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 31/40 | chr17 | 10312094 | ||||||
| chr17:10312178
|
C | T | 8 | a0002c0019t0001g0054a0002c0019t0001g0188a0002c0019t0001g0189others(5): Show | 8 | NA18939.hp2 NA18941.hp2 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.4366-102G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 31/40 | chr17 | 10312178 | ||||||
| chr17:10312293
|
C | G | 15 | a0001c0014t0001g0375a0003c0008t0001g0053a0003c0025t0001g0155others(12): Show | 15 | HG01167.hp1 HG01169.hp1 HG01515.hp1 others(12): Show |
intron_variant | MODIFIER | c.4366-217G>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 31/40 | chr17 | 10312293 | ||||||
| chr17:10312427
|
C | G | 1 | a0002c0001t0001g0316 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.4365+147G>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 31/40 | chr17 | 10312427 | ||||||
| chr17:10312522
|
A | G | 2 | a0005c0028t0001g0363a0012c0058t0001g0142 | 2 | HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.4365+52T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 31/40 | chr17 | 10312522 | ||||||
| chr17:10312771
|
AT | A | 8 | a0002c0019t0001g0054a0002c0019t0001g0188a0002c0019t0001g0189others(5): Show | 8 | NA18939.hp2 NA18941.hp2 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.4182-15delA | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 30/40 | chr17 | 10312771 | ||||||
| chr17:10312788
|
C | T | 7 | a0003c0008t0001g0053a0003c0025t0001g0155a0005c0016t0001g0210others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.4182-31G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 30/40 | chr17 | 10312788 | ||||||
| chr17:10313028
|
G | A | 6 | a0002c0001t0001g0004a0002c0001t0001g0048a0002c0001t0001g0280others(3): Show | 6 | HG00621.hp1 HG02165.hp1 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.4181+130C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 30/40 | chr17 | 10313028 | ||||||
| chr17:10313041
|
G | A | 8 | a0002c0019t0001g0054a0002c0019t0001g0188a0002c0019t0001g0189others(5): Show | 8 | NA18939.hp2 NA18941.hp2 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.4181+117C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 30/40 | chr17 | 10313041 | ||||||
| chr17:10313114
|
G | A | 1 | a0002c0001t0001g0040 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.4181+44C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 30/40 | chr17 | 10313114 | ||||||
| chr17:10313125
|
C | A | 245 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(242): Show | 247 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.4181+33G>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 30/40 | chr17 | 10313125 | ||||||
| chr17:10313368
|
C | T | 2 | a0010c0023t0001g0311a0034c0085t0001g0315 | 2 | NA18974.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.3985-14G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 29/40 | chr17 | 10313368 | ||||||
| chr17:10313369
|
G | A | 24 | a0001c0027t0001g0009a0003c0005t0001g0046a0003c0005t0001g0112others(21): Show | 24 | HG00738.hp2 HG01123.hp2 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.3985-15C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 29/40 | chr17 | 10313369 | ||||||
| chr17:10313427
|
C | T | 8 | a0002c0019t0001g0054a0002c0019t0001g0188a0002c0019t0001g0189others(5): Show | 8 | NA18939.hp2 NA18941.hp2 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.3985-73G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 29/40 | chr17 | 10313427 | ||||||
| chr17:10313488
|
T | G | 2 | a0015c0053t0001g0047a0038c0102t0001g0066 | 2 | HG01257.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.3985-134A>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 29/40 | chr17 | 10313488 | ||||||
| chr17:10313493
|
TG | T | 8 | a0002c0019t0001g0054a0002c0019t0001g0188a0002c0019t0001g0189others(5): Show | 8 | NA18939.hp2 NA18941.hp2 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.3985-140delC | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 29/40 | chr17 | 10313493 | ||||||
| chr17:10313693
|
G | T | 8 | a0002c0019t0001g0054a0002c0019t0001g0188a0002c0019t0001g0189others(5): Show | 8 | NA18939.hp2 NA18941.hp2 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.3985-339C>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 29/40 | chr17 | 10313693 | ||||||
| chr17:10313713
|
T | C | 8 | a0002c0019t0001g0054a0002c0019t0001g0188a0002c0019t0001g0189others(5): Show | 8 | NA18939.hp2 NA18941.hp2 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.3985-359A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 29/40 | chr17 | 10313713 | ||||||
| chr17:10313742
|
G | A | 8 | a0002c0019t0001g0054a0002c0019t0001g0188a0002c0019t0001g0189others(5): Show | 8 | NA18939.hp2 NA18941.hp2 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.3985-388C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 29/40 | chr17 | 10313742 | ||||||
| chr17:10313831
|
G | C | 3 | a0003c0009t0001g0330a0003c0009t0001g0332a0003c0009t0001g0362 | 3 | HG02080.hp2 NA19000.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.3985-477C>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 29/40 | chr17 | 10313831 | ||||||
| chr17:10313916
|
G | A | 179 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(176): Show | 181 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.3985-562C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 29/40 | chr17 | 10313916 | ||||||
| chr17:10313978
|
G | T | 8 | a0002c0019t0001g0054a0002c0019t0001g0188a0002c0019t0001g0189others(5): Show | 8 | NA18939.hp2 NA18941.hp2 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.3985-624C>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 29/40 | chr17 | 10313978 | ||||||
| chr17:10314034
|
G | A | 1 | a0001c0108t0001g0156 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.3985-680C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 29/40 | chr17 | 10314034 | ||||||
| chr17:10314145
|
C | T | 8 | a0002c0019t0001g0054a0002c0019t0001g0188a0002c0019t0001g0189others(5): Show | 8 | NA18939.hp2 NA18941.hp2 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.3985-791G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 29/40 | chr17 | 10314145 | ||||||
| chr17:10314267
|
A | G | 8 | a0002c0019t0001g0054a0002c0019t0001g0188a0002c0019t0001g0189others(5): Show | 8 | NA18939.hp2 NA18941.hp2 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.3985-913T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 29/40 | chr17 | 10314267 | ||||||
| chr17:10314352
|
T | A | 9 | a0004c0010t0001g0329a0004c0021t0001g0093a0004c0021t0001g0094others(6): Show | 9 | HG00733.hp2 HG01069.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.3985-998A>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 29/40 | chr17 | 10314352 | ||||||
| chr17:10314415
|
C | CA | 9 | a0001c0004t0001g0028a0001c0006t0001g0140a0001c0012t0001g0267others(6): Show | 9 | HG01175.hp2 HG01934.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.3985-1062dupT | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 29/40 | chr17 | 10314415 | ||||||
| chr17:10314415
|
C | CAAAAAAA others(1): Show |
8 | a0002c0019t0001g0054a0002c0019t0001g0188a0002c0019t0001g0189others(5): Show | 8 | NA18939.hp2 NA18941.hp2 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.3985-1069_3985-106 others(12): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 29/40 | chr17 | 10314415 | ||||||
| chr17:10314421
|
A | C | 1 | a0002c0064t0001g0196 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3985-1067T>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 29/40 | chr17 | 10314421 | ||||||
| chr17:10314463
|
A | AAACTC | 8 | a0002c0019t0001g0054a0002c0019t0001g0188a0002c0019t0001g0189others(5): Show | 8 | NA18939.hp2 NA18941.hp2 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.3985-1114_3985-111 others(9): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 29/40 | chr17 | 10314463 | ||||||
| chr17:10314502
|
G | A | 178 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(175): Show | 180 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.3985-1148C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 29/40 | chr17 | 10314502 | ||||||
| chr17:10314516
|
T | C | 8 | a0002c0019t0001g0054a0002c0019t0001g0188a0002c0019t0001g0189others(5): Show | 8 | NA18939.hp2 NA18941.hp2 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.3985-1162A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 29/40 | chr17 | 10314516 | ||||||
| chr17:10314522
|
C | A | 10 | a0003c0008t0001g0053a0003c0025t0001g0155a0005c0016t0001g0091others(7): Show | 10 | HG01167.hp1 HG01169.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.3985-1168G>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 29/40 | chr17 | 10314522 | ||||||
| chr17:10314678
|
T | G | 1 | a0001c0004t0001g0367 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.3984+1015A>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 29/40 | chr17 | 10314678 | ||||||
| chr17:10314810
|
A | G | 5 | a0009c0032t0001g0171a0009c0032t0001g0172a0009c0032t0001g0175others(2): Show | 5 | HG02630.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.3984+883T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 29/40 | chr17 | 10314810 | ||||||
| chr17:10314918
|
A | G | 1 | a0004c0010t0001g0073 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.3984+775T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 29/40 | chr17 | 10314918 | ||||||
| chr17:10314937
|
G | A | 8 | a0002c0019t0001g0054a0002c0019t0001g0188a0002c0019t0001g0189others(5): Show | 8 | NA18939.hp2 NA18941.hp2 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.3984+756C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 29/40 | chr17 | 10314937 | ||||||
| chr17:10314960
|
A | G | 10 | a0003c0008t0001g0053a0003c0025t0001g0155a0005c0016t0001g0091others(7): Show | 10 | HG01167.hp1 HG01169.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.3984+733T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 29/40 | chr17 | 10314960 | ||||||
| chr17:10315129
|
A | G | 8 | a0002c0019t0001g0054a0002c0019t0001g0188a0002c0019t0001g0189others(5): Show | 8 | NA18939.hp2 NA18941.hp2 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.3984+564T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 29/40 | chr17 | 10315129 | ||||||
| chr17:10315177
|
A | T | 1 | a0005c0018t0001g0018 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.3984+516T>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 29/40 | chr17 | 10315177 | ||||||
| chr17:10315194
|
C | T | 26 | a0001c0022t0001g0149a0001c0022t0001g0181a0001c0022t0001g0292others(23): Show | 26 | HG00741.hp1 HG00741.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.3984+499G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 29/40 | chr17 | 10315194 | ||||||
| chr17:10315223
|
A | T | 1 | a0005c0087t0001g0290 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.3984+470T>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 29/40 | chr17 | 10315223 | ||||||
| chr17:10315247
|
A | C | 1 | a0001c0022t0001g0181 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3984+446T>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 29/40 | chr17 | 10315247 | ||||||
| chr17:10315354
|
G | A | 3 | a0001c0004t0001g0236a0001c0017t0001g0131a0001c0027t0001g0266 | 3 | HG01106.hp1 HG01981.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.3984+339C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 29/40 | chr17 | 10315354 | ||||||
| chr17:10315378
|
C | T | 8 | a0002c0019t0001g0054a0002c0019t0001g0188a0002c0019t0001g0189others(5): Show | 8 | NA18939.hp2 NA18941.hp2 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.3984+315G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 29/40 | chr17 | 10315378 | ||||||
| chr17:10315380
|
C | A | 3 | a0001c0014t0001g0374a0003c0005t0001g0294a0007c0083t0001g0096 | 3 | HG02622.hp2 HG02717.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.3984+313G>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 29/40 | chr17 | 10315380 | ||||||
| chr17:10315393
|
A | G | 1 | a0005c0016t0001g0210 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3984+300T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 29/40 | chr17 | 10315393 | ||||||
| chr17:10315471
|
T | G | 1 | a0001c0014t0001g0375 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3984+222A>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 29/40 | chr17 | 10315471 | ||||||
| chr17:10315485
|
G | A | 1 | a0028c0098t0001g0024 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.3984+208C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 29/40 | chr17 | 10315485 | ||||||
| chr17:10315635
|
C | T | 1 | a0001c0014t0001g0375 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3984+58G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 29/40 | chr17 | 10315635 | ||||||
| chr17:10316049
|
C | T | 315 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(312): Show | 317 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(314): Show |
intron_variant | MODIFIER | c.3739-24G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 27/40 | chr17 | 10316049 | ||||||
| chr17:10316143
|
A | G | 8 | a0002c0019t0001g0054a0002c0019t0001g0188a0002c0019t0001g0189others(5): Show | 8 | NA18939.hp2 NA18941.hp2 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.3739-118T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 27/40 | chr17 | 10316143 | ||||||
| chr17:10316153
|
A | T | 220 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(217): Show | 222 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.3739-128T>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 27/40 | chr17 | 10316153 | ||||||
| chr17:10316169
|
A | G | 23 | a0001c0027t0001g0009a0003c0005t0001g0046a0003c0005t0001g0112others(20): Show | 23 | HG00738.hp2 HG01123.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.3739-144T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 27/40 | chr17 | 10316169 | ||||||
| chr17:10316198
|
C | T | 1 | a0004c0021t0001g0109 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3739-173G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 27/40 | chr17 | 10316198 | ||||||
| chr17:10316216
|
T | C | 1 | a0001c0015t0001g0378 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3739-191A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 27/40 | chr17 | 10316216 | ||||||
| chr17:10316400
|
G | T | 1 | a0003c0009t0001g0039 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.3739-375C>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 27/40 | chr17 | 10316400 | ||||||
| chr17:10316457
|
G | A | 36 | a0001c0003t0001g0008a0001c0003t0001g0043a0001c0003t0001g0044others(33): Show | 37 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.3739-432C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 27/40 | chr17 | 10316457 | ||||||
| chr17:10316461
|
C | CA | 79 | a0001c0004t0001g0169a0001c0014t0001g0100a0001c0014t0001g0110others(76): Show | 79 | HG00621.hp1 HG01081.hp1 HG01167.hp1 others(76): Show |
intron_variant | MODIFIER | c.3739-437dupT | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 27/40 | chr17 | 10316461 | ||||||
| chr17:10316461
|
CA | C | 8 | a0002c0019t0001g0054a0002c0019t0001g0188a0002c0019t0001g0189others(5): Show | 8 | NA18939.hp2 NA18941.hp2 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.3739-437delT | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 27/40 | chr17 | 10316461 | ||||||
| chr17:10316731
|
C | A | 80 | a0001c0089t0001g0184a0002c0001t0001g0004a0002c0001t0001g0040others(77): Show | 80 | HG00621.hp1 HG01081.hp1 HG01167.hp1 others(77): Show |
intron_variant | MODIFIER | c.3739-706G>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 27/40 | chr17 | 10316731 | ||||||
| chr17:10316826
|
GC | G | 80 | a0001c0089t0001g0184a0002c0001t0001g0004a0002c0001t0001g0040others(77): Show | 80 | HG00621.hp1 HG01081.hp1 HG01167.hp1 others(77): Show |
intron_variant | MODIFIER | c.3739-802delG | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 27/40 | chr17 | 10316826 | ||||||
| chr17:10316829
|
G | T | 80 | a0001c0089t0001g0184a0002c0001t0001g0004a0002c0001t0001g0040others(77): Show | 80 | HG00621.hp1 HG01081.hp1 HG01167.hp1 others(77): Show |
intron_variant | MODIFIER | c.3739-804C>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 27/40 | chr17 | 10316829 | ||||||
| chr17:10316959
|
G | A | 8 | a0002c0019t0001g0054a0002c0019t0001g0188a0002c0019t0001g0189others(5): Show | 8 | NA18939.hp2 NA18941.hp2 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.3739-934C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 27/40 | chr17 | 10316959 | ||||||
| chr17:10317032
|
G | A | 86 | a0001c0089t0001g0184a0002c0001t0001g0004a0002c0001t0001g0040others(83): Show | 86 | HG00621.hp1 HG01081.hp1 HG01167.hp1 others(83): Show |
intron_variant | MODIFIER | c.3739-1007C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 27/40 | chr17 | 10317032 | ||||||
| chr17:10317070
|
C | A | 262 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(259): Show | 264 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(261): Show |
intron_variant | MODIFIER | c.3739-1045G>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 27/40 | chr17 | 10317070 | ||||||
| chr17:10317103
|
C | G | 1 | a0005c0018t0001g0018 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.3739-1078G>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 27/40 | chr17 | 10317103 | ||||||
| chr17:10317176
|
G | A | 10 | a0003c0008t0001g0053a0003c0025t0001g0155a0005c0016t0001g0091others(7): Show | 10 | HG01167.hp1 HG01169.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.3739-1151C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 27/40 | chr17 | 10317176 | ||||||
| chr17:10317281
|
G | A | 6 | a0003c0005t0001g0114a0003c0005t0001g0116a0003c0025t0001g0158others(3): Show | 6 | HG01123.hp2 HG01358.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.3739-1256C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 27/40 | chr17 | 10317281 | ||||||
| chr17:10317353
|
G | C | 86 | a0001c0089t0001g0184a0002c0001t0001g0004a0002c0001t0001g0040others(83): Show | 86 | HG00621.hp1 HG01081.hp1 HG01167.hp1 others(83): Show |
intron_variant | MODIFIER | c.3739-1328C>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 27/40 | chr17 | 10317353 | ||||||
| chr17:10317370
|
C | A | 5 | a0002c0011t0001g0186a0002c0011t0001g0234a0002c0011t0001g0235others(2): Show | 5 | HG02717.hp1 HG02723.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.3739-1345G>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 27/40 | chr17 | 10317370 | ||||||
| chr17:10317374
|
G | C | 5 | a0009c0032t0001g0171a0009c0032t0001g0172a0009c0032t0001g0175others(2): Show | 5 | HG02630.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.3739-1349C>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 27/40 | chr17 | 10317374 | ||||||
| chr17:10317443
|
G | A | 101 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(98): Show | 102 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.3738+1347C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 27/40 | chr17 | 10317443 | ||||||
| chr17:10317964
|
A | T | 1 | a0001c0006t0001g0268 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3738+826T>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 27/40 | chr17 | 10317964 | ||||||
| chr17:10318005
|
G | A | 1 | a0001c0004t0001g0236 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3738+785C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 27/40 | chr17 | 10318005 | ||||||
| chr17:10318110
|
C | T | 1 | a0005c0016t0001g0091 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3738+680G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 27/40 | chr17 | 10318110 | ||||||
| chr17:10318216
|
T | TG | 6 | a0001c0004t0001g0025a0001c0004t0001g0027a0001c0004t0001g0028others(3): Show | 6 | NA18950.hp2 NA18961.hp2 NA19060.hp2 others(3): Show |
intron_variant | MODIFIER | c.3738+573dupC | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 27/40 | chr17 | 10318216 | ||||||
| chr17:10318344
|
G | A | 101 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(98): Show | 102 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.3738+446C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 27/40 | chr17 | 10318344 | ||||||
| chr17:10318534
|
C | T | 178 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(175): Show | 180 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.3738+256G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 27/40 | chr17 | 10318534 | ||||||
| chr17:10318639
|
A | G | 82 | a0001c0089t0001g0184a0002c0001t0001g0004a0002c0001t0001g0040others(79): Show | 82 | HG00621.hp1 HG01081.hp1 HG01167.hp1 others(79): Show |
intron_variant | MODIFIER | c.3738+151T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 27/40 | chr17 | 10318639 | ||||||
| chr17:10318653
|
A | G | 82 | a0001c0089t0001g0184a0002c0001t0001g0004a0002c0001t0001g0040others(79): Show | 82 | HG00621.hp1 HG01081.hp1 HG01167.hp1 others(79): Show |
intron_variant | MODIFIER | c.3738+137T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 27/40 | chr17 | 10318653 | ||||||
| chr17:10318744
|
G | A | 102 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(99): Show | 103 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.3738+46C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 27/40 | chr17 | 10318744 | ||||||
| chr17:10319258
|
T | C | 1 | a0002c0064t0001g0196 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3349-79A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 26/40 | chr17 | 10319258 | ||||||
| chr17:10319326
|
T | C | 1 | a0004c0002t0001g0135 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.3349-147A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 26/40 | chr17 | 10319326 | ||||||
| chr17:10319366
|
G | A | 82 | a0001c0089t0001g0184a0002c0001t0001g0004a0002c0001t0001g0040others(79): Show | 82 | HG00621.hp1 HG01081.hp1 HG01167.hp1 others(79): Show |
intron_variant | MODIFIER | c.3349-187C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 26/40 | chr17 | 10319366 | ||||||
| chr17:10319382
|
G | C | 81 | a0001c0089t0001g0184a0002c0001t0001g0004a0002c0001t0001g0040others(78): Show | 81 | HG00621.hp1 HG01081.hp1 HG01167.hp1 others(78): Show |
intron_variant | MODIFIER | c.3349-203C>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 26/40 | chr17 | 10319382 | ||||||
| chr17:10319401
|
C | T | 82 | a0001c0089t0001g0184a0002c0001t0001g0004a0002c0001t0001g0040others(79): Show | 82 | HG00621.hp1 HG01081.hp1 HG01167.hp1 others(79): Show |
intron_variant | MODIFIER | c.3349-222G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 26/40 | chr17 | 10319401 | ||||||
| chr17:10319490
|
C | T | 176 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(173): Show | 178 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.3349-311G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 26/40 | chr17 | 10319490 | ||||||
| chr17:10319508
|
C | CAAAAA | 70 | a0001c0089t0001g0184a0002c0001t0001g0004a0002c0001t0001g0040others(67): Show | 70 | HG00621.hp1 HG01081.hp1 HG01167.hp1 others(67): Show |
intron_variant | MODIFIER | c.3349-334_3349-330d others(7): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 26/40 | chr17 | 10319508 | ||||||
| chr17:10319508
|
C | CAAAAAA | 10 | a0002c0001t0001g0323a0002c0019t0001g0054a0002c0019t0001g0188others(7): Show | 10 | NA18939.hp2 NA18941.hp2 NA18946.hp1 others(7): Show |
intron_variant | MODIFIER | c.3349-335_3349-330d others(8): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 26/40 | chr17 | 10319508 | ||||||
| chr17:10319520
|
AG | A | 220 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(217): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.3349-342delC | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 26/40 | chr17 | 10319520 | ||||||
| chr17:10319521
|
G | A | 154 | a0001c0004t0001g0028a0001c0006t0001g0132a0001c0006t0001g0268others(151): Show | 155 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.3349-342C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 26/40 | chr17 | 10319521 | ||||||
| chr17:10319655
|
C | T | 5 | a0002c0011t0001g0186a0002c0011t0001g0234a0002c0011t0001g0235others(2): Show | 5 | HG02717.hp1 HG02723.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.3349-476G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 26/40 | chr17 | 10319655 | ||||||
| chr17:10319705
|
A | G | 82 | a0001c0089t0001g0184a0002c0001t0001g0004a0002c0001t0001g0040others(79): Show | 82 | HG00621.hp1 HG01081.hp1 HG01167.hp1 others(79): Show |
intron_variant | MODIFIER | c.3348+448T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 26/40 | chr17 | 10319705 | ||||||
| chr17:10319754
|
A | T | 9 | a0004c0002t0001g0002a0004c0002t0001g0212a0004c0010t0001g0322others(6): Show | 10 | HG00438.hp1 HG01257.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.3348+399T>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 26/40 | chr17 | 10319754 | ||||||
| chr17:10319903
|
C | T | 310 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(307): Show | 312 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(309): Show |
intron_variant | MODIFIER | c.3348+250G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 26/40 | chr17 | 10319903 | ||||||
| chr17:10320041
|
T | C | 1 | a0001c0003t0001g0204 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.3348+112A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 26/40 | chr17 | 10320041 | ||||||
| chr17:10320105
|
G | A | 87 | a0001c0007t0001g0284a0001c0007t0001g0285a0001c0007t0001g0289others(84): Show | 87 | HG00621.hp1 HG01081.hp1 HG01167.hp1 others(84): Show |
intron_variant | MODIFIER | c.3348+48C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 26/40 | chr17 | 10320105 | ||||||
| chr17:10320256
|
TA | T | 91 | a0002c0001t0001g0004a0002c0001t0001g0040a0002c0001t0001g0048others(88): Show | 91 | HG00621.hp1 HG01081.hp1 HG01167.hp1 others(88): Show |
intron_variant | MODIFIER | c.3258-14delT | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 25/40 | chr17 | 10320256 | ||||||
| chr17:10320269
|
A | G | 91 | a0002c0001t0001g0004a0002c0001t0001g0040a0002c0001t0001g0048others(88): Show | 91 | HG00621.hp1 HG01081.hp1 HG01167.hp1 others(88): Show |
intron_variant | MODIFIER | c.3258-26T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 25/40 | chr17 | 10320269 | ||||||
| chr17:10320283
|
A | C | 1 | a0003c0005t0001g0295 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3258-40T>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 25/40 | chr17 | 10320283 | ||||||
| chr17:10320539
|
A | G | 1 | a0037c0100t0001g0064 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.3112-43T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 24/40 | chr17 | 10320539 | ||||||
| chr17:10320764
|
T | C | 5 | a0002c0011t0001g0186a0002c0011t0001g0234a0002c0011t0001g0235others(2): Show | 5 | HG02717.hp1 HG02723.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.3112-268A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 24/40 | chr17 | 10320764 | ||||||
| chr17:10320827
|
C | T | 1 | a0001c0089t0001g0184 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3112-331G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 24/40 | chr17 | 10320827 | ||||||
| chr17:10320938
|
T | C | 95 | a0001c0003t0001g0237a0001c0003t0001g0269a0002c0001t0001g0004others(92): Show | 95 | HG00621.hp1 HG00741.hp2 HG01081.hp1 others(92): Show |
intron_variant | MODIFIER | c.3112-442A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 24/40 | chr17 | 10320938 | ||||||
| chr17:10320967
|
A | C | 95 | a0001c0003t0001g0237a0001c0003t0001g0269a0002c0001t0001g0004others(92): Show | 95 | HG00621.hp1 HG00741.hp2 HG01081.hp1 others(92): Show |
intron_variant | MODIFIER | c.3112-471T>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 24/40 | chr17 | 10320967 | ||||||
| chr17:10321318
|
C | T | 1 | a0005c0018t0001g0018 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.3111+214G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 24/40 | chr17 | 10321318 | ||||||
| chr17:10321398
|
T | TG | 6 | a0001c0015t0001g0098a0001c0015t0001g0371a0001c0015t0001g0372others(3): Show | 6 | HG01891.hp1 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.3111+133dupC | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 24/40 | chr17 | 10321398 | ||||||
| chr17:10321486
|
T | C | 1 | a0006c0024t0001g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3111+46A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 24/40 | chr17 | 10321486 | ||||||
| chr17:10321730
|
T | G | 8 | a0001c0050t0001g0042a0001c0050t0001g0065a0005c0016t0001g0091others(5): Show | 8 | HG00323.hp1 HG01167.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.2935-22A>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10321730 | ||||||
| chr17:10321899
|
C | G | 6 | a0001c0015t0001g0098a0001c0015t0001g0371a0001c0015t0001g0372others(3): Show | 6 | HG01891.hp1 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2935-191G>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10321899 | ||||||
| chr17:10321930
|
A | G | 1 | a0006c0068t0001g0366 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2935-222T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10321930 | ||||||
| chr17:10321935
|
A | G | 2 | a0002c0081t0001g0005a0002c0094t0001g0226 | 2 | HG02074.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.2935-227T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10321935 | ||||||
| chr17:10321951
|
C | T | 6 | a0001c0015t0001g0098a0001c0015t0001g0371a0001c0015t0001g0372others(3): Show | 6 | HG01891.hp1 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2935-243G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10321951 | ||||||
| chr17:10321952
|
G | A | 29 | a0001c0003t0001g0233a0001c0007t0001g0312a0001c0012t0001g0267others(26): Show | 29 | HG00323.hp1 HG00544.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.2935-244C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10321952 | ||||||
| chr17:10322036
|
T | G | 2 | a0001c0012t0001g0310a0004c0021t0001g0127 | 2 | HG02735.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2935-328A>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10322036 | ||||||
| chr17:10322093
|
C | G | 36 | a0001c0003t0001g0233a0001c0004t0001g0170a0001c0004t0001g0194others(33): Show | 36 | HG00140.hp1 HG00423.hp1 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.2935-385G>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10322093 | ||||||
| chr17:10322101
|
AGAAAATT others(15): Show |
A | 3 | a0002c0001t0001g0040a0002c0001t0001g0253a0002c0038t0001g0133 | 3 | NA18969.hp2 NA18990.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.2935-415_2935-394d others(24): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10322101 | ||||||
| chr17:10322120
|
C | T | 1 | a0002c0001t0001g0335 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2935-412G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10322120 | ||||||
| chr17:10322124
|
G | A | 5 | a0001c0004t0001g0170a0001c0004t0001g0194a0001c0007t0001g0107others(2): Show | 5 | HG00741.hp2 HG02622.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2935-416C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10322124 | ||||||
| chr17:10322167
|
C | T | 1 | a0026c0092t0001g0368 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2935-459G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10322167 | ||||||
| chr17:10322207
|
A | G | 5 | a0001c0003t0001g0008a0001c0003t0001g0043a0001c0003t0001g0044others(2): Show | 5 | HG00639.hp1 HG01081.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.2935-499T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10322207 | ||||||
| chr17:10322236
|
C | CA | 24 | a0001c0014t0001g0010a0001c0015t0001g0011a0001c0015t0001g0014others(21): Show | 24 | HG00423.hp2 HG00544.hp1 HG02027.hp1 others(21): Show |
intron_variant | MODIFIER | c.2935-529dupT | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10322236 | ||||||
| chr17:10322236
|
CA | C | 293 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(290): Show | 295 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(292): Show |
intron_variant | MODIFIER | c.2935-529delT | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10322236 | ||||||
| chr17:10322259
|
A | G | 3 | a0003c0005t0001g0299a0004c0010t0001g0329a0008c0063t0001g0298 | 3 | HG02698.hp1 HG03239.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.2935-551T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10322259 | ||||||
| chr17:10322266
|
T | C | 1 | a0003c0005t0001g0046 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2935-558A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10322266 | ||||||
| chr17:10322267
|
G | A | 1 | a0003c0005t0001g0046 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2935-559C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10322267 | ||||||
| chr17:10322268
|
G | C | 22 | a0001c0012t0001g0314a0001c0039t0001g0113a0001c0039t0001g0115others(19): Show | 22 | HG00099.hp2 HG00140.hp2 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.2935-560C>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10322268 | ||||||
| chr17:10322268
|
G | T | 1 | a0003c0005t0001g0046 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2935-560C>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10322268 | ||||||
| chr17:10322291
|
A | G | 1 | a0006c0033t0001g0213 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2935-583T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10322291 | ||||||
| chr17:10322312
|
C | T | 1 | a0004c0002t0001g0134 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.2935-604G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10322312 | ||||||
| chr17:10322330
|
A | G | 2 | a0003c0005t0001g0123a0003c0009t0002g0003 | 2 | HG04115.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.2935-622T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10322330 | ||||||
| chr17:10322352
|
T | C | 8 | a0001c0015t0001g0378a0002c0011t0001g0234a0003c0005t0001g0122others(5): Show | 8 | HG02055.hp1 HG02723.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.2935-644A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10322352 | ||||||
| chr17:10322383
|
C | T | 5 | a0003c0009t0001g0330a0003c0041t0001g0197a0004c0010t0001g0320others(2): Show | 5 | HG06807.hp2 NA18975.hp1 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.2935-675G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10322383 | ||||||
| chr17:10322400
|
A | G | 1 | a0010c0023t0001g0351 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2935-692T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10322400 | ||||||
| chr17:10322434
|
C | T | 1 | a0004c0026t0001g0177 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2935-726G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10322434 | ||||||
| chr17:10322551
|
A | G | 1 | a0009c0032t0001g0172 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2935-843T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10322551 | ||||||
| chr17:10322630
|
G | GT | 42 | a0001c0003t0001g0008a0001c0003t0001g0043a0001c0003t0001g0044others(39): Show | 42 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.2935-923dupA | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10322630 | ||||||
| chr17:10322630
|
G | T | 2 | a0004c0002t0001g0214a0005c0016t0001g0210 | 2 | HG01123.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.2935-922C>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10322630 | ||||||
| chr17:10322630
|
GT | G | 31 | a0001c0003t0001g0051a0001c0003t0001g0069a0001c0003t0001g0203others(28): Show | 32 | HG00140.hp2 HG00323.hp1 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.2935-923delA | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10322630 | ||||||
| chr17:10322630
|
GTT | G | 7 | a0001c0022t0001g0292a0001c0090t0001g0364a0001c0113t0001g0102others(4): Show | 7 | HG02055.hp2 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.2935-924_2935-923d others(4): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10322630 | ||||||
| chr17:10322630
|
GTTT | G | 75 | a0001c0003t0001g0063a0001c0003t0001g0227a0001c0003t0001g0228others(72): Show | 76 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.2935-925_2935-923d others(5): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10322630 | ||||||
| chr17:10322633
|
T | G | 1 | a0012c0035t0001g0143 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2935-925A>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10322633 | ||||||
| chr17:10322656
|
G | C | 15 | a0001c0027t0001g0154a0001c0027t0001g0161a0001c0072t0001g0160others(12): Show | 15 | HG00140.hp1 HG00733.hp2 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.2935-948C>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10322656 | ||||||
| chr17:10322671
|
T | C | 1 | a0004c0106t0001g0176 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2935-963A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10322671 | ||||||
| chr17:10322722
|
C | T | 1 | a0001c0017t0001g0129 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2935-1014G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10322722 | ||||||
| chr17:10322727
|
G | A | 2 | a0002c0019t0001g0189a0003c0005t0001g0116 | 2 | HG01123.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.2935-1019C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10322727 | ||||||
| chr17:10322745
|
G | T | 67 | a0001c0003t0001g0063a0001c0004t0001g0169a0001c0004t0001g0170others(64): Show | 68 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.2935-1037C>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10322745 | ||||||
| chr17:10322758
|
T | C | 1 | a0002c0001t0001g0250 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2935-1050A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10322758 | ||||||
| chr17:10322778
|
C | T | 1 | a0007c0020t0001g0121 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2935-1070G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10322778 | ||||||
| chr17:10322783
|
G | A | 3 | a0001c0007t0001g0107a0001c0089t0001g0184a0004c0002t0001g0214 | 3 | HG01123.hp1 HG02486.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2935-1075C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10322783 | ||||||
| chr17:10322790
|
C | T | 2 | a0001c0034t0001g0288a0004c0002t0001g0360 | 2 | HG00738.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.2935-1082G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10322790 | ||||||
| chr17:10322835
|
A | G | 1 | a0002c0001t0001g0250 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2935-1127T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10322835 | ||||||
| chr17:10322855
|
G | C | 2 | a0004c0106t0001g0176a0026c0092t0001g0368 | 2 | HG01099.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.2935-1147C>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10322855 | ||||||
| chr17:10322868
|
C | T | 1 | a0001c0003t0001g0356 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2934+1154G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10322868 | ||||||
| chr17:10322869
|
G | A | 12 | a0001c0014t0001g0010a0001c0015t0001g0011a0001c0015t0001g0014others(9): Show | 12 | HG00423.hp2 HG00544.hp1 NA18944.hp2 others(9): Show |
intron_variant | MODIFIER | c.2934+1153C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10322869 | ||||||
| chr17:10322923
|
G | A | 1 | a0001c0027t0001g0154 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2934+1099C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10322923 | ||||||
| chr17:10322951
|
C | T | 3 | a0001c0012t0001g0267a0001c0012t0001g0272a0001c0014t0001g0375 | 3 | HG02895.hp1 HG02897.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2934+1071G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10322951 | ||||||
| chr17:10322963
|
G | A | 25 | a0001c0004t0001g0344a0001c0004t0001g0345a0001c0004t0001g0346others(22): Show | 25 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.2934+1059C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10322963 | ||||||
| chr17:10322999
|
G | A | 1 | a0003c0061t0001g0119 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2934+1023C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10322999 | ||||||
| chr17:10323019
|
C | T | 4 | a0001c0006t0001g0084a0001c0006t0001g0085a0003c0005t0001g0088others(1): Show | 4 | HG03710.hp2 NA18952.hp2 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.2934+1003G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323019 | ||||||
| chr17:10323020
|
G | A | 5 | a0001c0022t0001g0181a0001c0034t0001g0152a0001c0034t0001g0168others(2): Show | 5 | HG00323.hp2 HG01109.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.2934+1002C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323020 | ||||||
| chr17:10323062
|
G | A | 1 | a0009c0032t0001g0172 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2934+960C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323062 | ||||||
| chr17:10323157
|
G | A | 114 | a0001c0007t0001g0006a0001c0007t0001g0007a0001c0007t0001g0107others(111): Show | 114 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.2934+865C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323157 | ||||||
| chr17:10323193
|
T | A | 1 | a0006c0052t0001g0201 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2934+829A>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323193 | ||||||
| chr17:10323249
|
T | C | 1 | a0002c0001t0001g0283 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2934+773A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323249 | ||||||
| chr17:10323281
|
G | A | 12 | a0001c0014t0001g0010a0001c0015t0001g0011a0001c0015t0001g0014others(9): Show | 12 | HG00423.hp2 HG00544.hp1 NA18944.hp2 others(9): Show |
intron_variant | MODIFIER | c.2934+741C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323281 | ||||||
| chr17:10323284
|
A | AC | 13 | a0001c0003t0001g0069a0001c0004t0001g0028a0001c0012t0001g0353others(10): Show | 13 | HG01109.hp1 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.2934+737dupG | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323284 | ||||||
| chr17:10323287
|
C | T | 39 | a0001c0004t0001g0344a0001c0004t0001g0345a0001c0004t0001g0346others(36): Show | 39 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.2934+735G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323287 | ||||||
| chr17:10323511
|
A | T | 74 | a0001c0003t0001g0203a0001c0003t0001g0204a0001c0003t0001g0205others(71): Show | 75 | HG00438.hp1 HG01099.hp2 HG01109.hp1 others(72): Show |
intron_variant | MODIFIER | c.2934+511T>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323511 | ||||||
| chr17:10323614
|
C | T | 1 | a0001c0014t0001g0219 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2934+408G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323614 | ||||||
| chr17:10323764
|
CAAAAAAA others(3): Show |
C | 5 | a0001c0003t0001g0246a0001c0110t0001g0108a0002c0011t0001g0239others(2): Show | 5 | HG01928.hp1 HG01934.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.2934+248_2934+257d others(12): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323764 | ||||||
| chr17:10323764
|
CAAAAAAA others(4): Show |
C | 8 | a0001c0003t0001g0203a0001c0003t0001g0204a0001c0003t0001g0205others(5): Show | 9 | HG01257.hp1 HG01258.hp2 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.2934+247_2934+257d others(13): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323764 | ||||||
| chr17:10323776
|
AAAAAAAA others(7): Show |
A | 1 | a0002c0011t0001g0247 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2934+232_2934+245d others(16): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323776 | ||||||
| chr17:10323777
|
AAAAAAAA others(9): Show |
A | 1 | a0001c0003t0001g0249 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2934+229_2934+244d others(18): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323777 | ||||||
| chr17:10323777
|
AAAAAAAA others(12): Show |
A | 1 | a0001c0089t0001g0184 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2934+226_2934+244d others(21): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323777 | ||||||
| chr17:10323777
|
AAAAAAAA others(15): Show |
A | 1 | a0001c0111t0001g0078 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2934+223_2934+244d others(24): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323777 | ||||||
| chr17:10323778
|
A | AAAGAAGA others(11): Show |
1 | a0001c0004t0001g0170 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2934+243_2934+244i others(20): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323778 | ||||||
| chr17:10323778
|
AAAAAAAA others(5): Show |
A | 2 | a0001c0007t0001g0376a0003c0009t0001g0373 | 2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2934+232_2934+243d others(14): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323778 | ||||||
| chr17:10323778
|
AAAAAAAA others(8): Show |
A | 5 | a0001c0003t0001g0008a0001c0003t0001g0043a0001c0003t0001g0044others(2): Show | 5 | HG00639.hp1 HG01081.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.2934+229_2934+243d others(17): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323778 | ||||||
| chr17:10323779
|
AAAAAAAA others(4): Show |
A | 13 | a0001c0004t0001g0344a0001c0004t0001g0345a0001c0004t0001g0346others(10): Show | 13 | HG00140.hp1 HG00323.hp2 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.2934+232_2934+242d others(13): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323779 | ||||||
| chr17:10323779
|
AAAAAAAA others(7): Show |
A | 5 | a0001c0004t0001g0328a0001c0050t0001g0042a0003c0005t0001g0124others(2): Show | 5 | HG01070.hp1 HG01071.hp1 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.2934+229_2934+242d others(16): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323779 | ||||||
| chr17:10323779
|
AAAAAAAA others(10): Show |
A | 51 | a0001c0003t0001g0032a0001c0003t0001g0049a0001c0003t0001g0051others(48): Show | 51 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.2934+226_2934+242d others(19): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323779 | ||||||
| chr17:10323779
|
AAAAAAAA others(13): Show |
A | 1 | a0003c0008t0001g0053 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2934+223_2934+242d others(22): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323779 | ||||||
| chr17:10323779
|
AAAAAAAA others(16): Show |
A | 1 | a0008c0093t0001g0257 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2934+220_2934+242d others(25): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323779 | ||||||
| chr17:10323779
|
AAAAAAAA others(28): Show |
A | 1 | a0005c0016t0001g0091 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2934+208_2934+242d others(37): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323779 | ||||||
| chr17:10323780
|
AAAAAAAA others(6): Show |
A | 4 | a0001c0027t0001g0161a0004c0026t0001g0153a0004c0026t0001g0167others(1): Show | 4 | HG00733.hp2 HG01099.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.2934+229_2934+241d others(15): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323780 | ||||||
| chr17:10323780
|
AAAAAAAA others(9): Show |
A | 5 | a0001c0004t0001g0062a0001c0004t0001g0071a0004c0002t0001g0134others(2): Show | 5 | HG00423.hp1 HG00621.hp2 NA19055.hp2 others(2): Show |
intron_variant | MODIFIER | c.2934+226_2934+241d others(18): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323780 | ||||||
| chr17:10323780
|
AAAAAAAA others(12): Show |
A | 1 | a0001c0119t0001g0274 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2934+223_2934+241d others(21): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323780 | ||||||
| chr17:10323781
|
A | AAG | 6 | a0002c0019t0001g0188a0004c0002t0001g0221a0004c0002t0001g0222others(3): Show | 6 | NA18939.hp2 NA18942.hp1 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.2934+240_2934+241i others(4): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323781 | ||||||
| chr17:10323781
|
A | AAGAAGAA others(4): Show |
2 | a0003c0008t0001g0238a0009c0032t0001g0172 | 2 | HG02895.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2934+240_2934+241i others(13): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323781 | ||||||
| chr17:10323781
|
A | AG | 6 | a0002c0019t0001g0189a0002c0019t0001g0191a0002c0019t0001g0193others(3): Show | 6 | NA18946.hp1 NA18955.hp1 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.2934+240_2934+241i others(3): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323781 | ||||||
| chr17:10323781
|
A | AGAAG | 7 | a0001c0120t0001g0178a0002c0019t0001g0190a0002c0043t0001g0251others(4): Show | 7 | HG01192.hp2 NA18962.hp1 NA18962.hp2 others(4): Show |
intron_variant | MODIFIER | c.2934+240_2934+241i others(6): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323781 | ||||||
| chr17:10323781
|
A | AGAAGAAG | 6 | a0003c0008t0001g0361a0004c0002t0001g0212a0004c0002t0001g0360others(3): Show | 6 | HG00438.hp1 HG01099.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.2934+240_2934+241i others(9): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323781 | ||||||
| chr17:10323781
|
A | AGAAGAAG others(3): Show |
10 | a0001c0003t0001g0233a0001c0003t0001g0269a0001c0004t0001g0169others(7): Show | 10 | HG01123.hp1 HG01884.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.2934+240_2934+241i others(12): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323781 | ||||||
| chr17:10323781
|
A | AGAAGAAG others(6): Show |
7 | a0001c0003t0001g0237a0001c0004t0001g0236a0001c0103t0001g0174others(4): Show | 7 | HG01981.hp2 HG02074.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2934+240_2934+241i others(15): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323781 | ||||||
| chr17:10323781
|
A | AGAAGAAG others(9): Show |
1 | a0004c0002t0001g0231 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.2934+240_2934+241i others(18): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323781 | ||||||
| chr17:10323781
|
A | G | 5 | a0001c0004t0001g0170a0002c0011t0001g0186a0002c0011t0001g0235others(2): Show | 5 | HG02717.hp1 HG02976.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.2934+241T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323781 | ||||||
| chr17:10323781
|
AAAAAAAA others(11): Show |
A | 4 | a0001c0046t0001g0265a0001c0046t0001g0271a0001c0062t0001g0262others(1): Show | 4 | HG00741.hp1 HG02258.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2934+223_2934+240d others(20): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323781 | ||||||
| chr17:10323784
|
A | AGAAGAAG others(6): Show |
1 | a0005c0028t0001g0363 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2934+237_2934+238i others(15): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323784 | ||||||
| chr17:10323784
|
A | G | 63 | a0001c0003t0001g0233a0001c0003t0001g0237a0001c0003t0001g0269others(60): Show | 63 | HG00438.hp1 HG00639.hp2 HG00738.hp1 others(60): Show |
intron_variant | MODIFIER | c.2934+238T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323784 | ||||||
| chr17:10323785
|
AAAAAGAA others(7): Show |
A | 2 | a0006c0024t0001g0095a0007c0083t0001g0096 | 2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2934+223_2934+236d others(16): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323785 | ||||||
| chr17:10323786
|
AAAAGAAG others(3): Show |
A | 1 | a0004c0106t0001g0176 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2934+226_2934+235d others(12): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323786 | ||||||
| chr17:10323786
|
AAAAGAAG others(9): Show |
A | 1 | a0003c0005t0001g0299 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2934+220_2934+235d others(18): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323786 | ||||||
| chr17:10323787
|
A | G | 67 | a0001c0003t0001g0233a0001c0003t0001g0237a0001c0003t0001g0243others(64): Show | 67 | HG00438.hp1 HG00639.hp2 HG00738.hp1 others(64): Show |
intron_variant | MODIFIER | c.2934+235T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323787 | ||||||
| chr17:10323787
|
AAAG | A | 28 | a0001c0003t0001g0063a0001c0006t0001g0001a0001c0006t0001g0105others(25): Show | 29 | HG00140.hp2 HG01069.hp1 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.2934+232_2934+234d others(5): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323787 | ||||||
| chr17:10323787
|
AAAGAAGA others(2): Show |
A | 35 | a0001c0007t0001g0307a0001c0012t0001g0267a0001c0012t0001g0272others(32): Show | 35 | HG00544.hp2 HG01243.hp2 HG01346.hp2 others(32): Show |
intron_variant | MODIFIER | c.2934+226_2934+234d others(11): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323787 | ||||||
| chr17:10323787
|
AAAGAAGA others(5): Show |
A | 1 | a0003c0005t0001g0122 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2934+223_2934+234d others(14): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323787 | ||||||
| chr17:10323787
|
AAAGAAGA others(8): Show |
A | 1 | a0008c0063t0001g0298 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2934+220_2934+234d others(17): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323787 | ||||||
| chr17:10323788
|
AAG | A | 7 | a0001c0015t0001g0092a0001c0017t0001g0141a0001c0113t0001g0102others(4): Show | 7 | HG01358.hp1 HG02055.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.2934+232_2934+233d others(4): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323788 | ||||||
| chr17:10323788
|
AAGAAGAA others(4): Show |
A | 9 | a0002c0001t0001g0283a0002c0001t0001g0303a0002c0001t0001g0349others(6): Show | 9 | HG00733.hp1 HG02080.hp1 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.2934+223_2934+233d others(13): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323788 | ||||||
| chr17:10323788
|
AAGAAGAA others(10): Show |
A | 8 | a0001c0014t0001g0010a0001c0015t0001g0014a0002c0030t0001g0020others(5): Show | 8 | HG00423.hp2 HG00544.hp1 NA18944.hp2 others(5): Show |
intron_variant | MODIFIER | c.2934+217_2934+233d others(19): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323788 | ||||||
| chr17:10323789
|
AGAAGAAG | A | 8 | a0001c0012t0001g0310a0001c0118t0001g0273a0002c0001t0001g0316others(5): Show | 8 | HG01433.hp1 HG01928.hp2 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.2934+226_2934+232d others(9): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323789 | ||||||
| chr17:10323789
|
AGAAGAAG others(3): Show |
A | 62 | a0001c0007t0001g0006a0001c0007t0001g0007a0001c0007t0001g0107others(59): Show | 62 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.2934+223_2934+232d others(12): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323789 | ||||||
| chr17:10323789
|
AGAAGAAG others(6): Show |
A | 1 | a0005c0018t0001g0281 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2934+220_2934+232d others(15): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323789 | ||||||
| chr17:10323789
|
AGAAGAAG others(9): Show |
A | 4 | a0001c0015t0001g0011a0003c0013t0001g0012a0003c0013t0001g0016others(1): Show | 4 | NA18995.hp2 NA19007.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.2934+217_2934+232d others(18): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323789 | ||||||
| chr17:10323799
|
G | A | 35 | a0001c0007t0001g0307a0001c0012t0001g0267a0001c0012t0001g0272others(32): Show | 35 | HG00544.hp2 HG01081.hp1 HG01346.hp2 others(32): Show |
intron_variant | MODIFIER | c.2934+223C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323799 | ||||||
| chr17:10323808
|
G | A | 12 | a0001c0014t0001g0010a0001c0015t0001g0011a0001c0015t0001g0014others(9): Show | 12 | HG00423.hp2 HG00544.hp1 NA18944.hp2 others(9): Show |
intron_variant | MODIFIER | c.2934+214C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10323808 | ||||||
| chr17:10324391
|
C | T | 184 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(181): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.2692-127G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10324391 | ||||||
| chr17:10324392
|
G | A | 1 | a0006c0024t0001g0340 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2692-128C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10324392 | ||||||
| chr17:10324421
|
G | A | 1 | a0002c0019t0001g0054 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2692-157C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10324421 | ||||||
| chr17:10324421
|
GTACA | G | 14 | a0001c0006t0001g0132a0001c0006t0001g0198a0001c0006t0001g0218others(11): Show | 14 | HG00639.hp2 HG01243.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.2692-161_2692-158d others(6): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10324421 | ||||||
| chr17:10324756
|
G | GT | 24 | a0001c0003t0001g0063a0001c0006t0001g0140a0001c0014t0001g0100others(21): Show | 24 | HG01074.hp1 HG01167.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.2692-493dupA | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10324756 | ||||||
| chr17:10324756
|
G | GTT | 6 | a0001c0014t0001g0219a0001c0113t0001g0102a0004c0021t0001g0094others(3): Show | 6 | HG01069.hp1 HG01243.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.2692-494_2692-493d others(4): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10324756 | ||||||
| chr17:10324756
|
G | GTTTT | 27 | a0001c0003t0001g0237a0001c0006t0001g0132a0001c0006t0001g0198others(24): Show | 27 | HG00140.hp1 HG00639.hp2 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.2692-496_2692-493d others(6): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10324756 | ||||||
| chr17:10324756
|
G | GTTTTT | 15 | a0001c0003t0001g0233a0001c0004t0001g0344a0001c0004t0001g0346others(12): Show | 15 | HG00323.hp2 HG01071.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.2692-497_2692-493d others(7): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10324756 | ||||||
| chr17:10324756
|
G | GTTTTTT | 30 | a0001c0004t0001g0169a0001c0004t0001g0170a0001c0004t0001g0194others(27): Show | 30 | HG00438.hp1 HG00735.hp1 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.2692-498_2692-493d others(8): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10324756 | ||||||
| chr17:10324756
|
G | GTTTTTTT | 8 | a0001c0119t0001g0274a0002c0011t0001g0247a0002c0019t0001g0193others(5): Show | 8 | HG01123.hp1 HG01516.hp1 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.2692-499_2692-493d others(9): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10324756 | ||||||
| chr17:10324756
|
G | GTTTTTTT others(1): Show |
13 | a0001c0003t0001g0203a0001c0003t0001g0204a0001c0003t0001g0205others(10): Show | 14 | HG01192.hp2 HG01257.hp1 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.2692-500_2692-493d others(10): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10324756 | ||||||
| chr17:10324756
|
G | GTTTTTTT others(2): Show |
8 | a0001c0003t0001g0243a0001c0003t0001g0249a0001c0089t0001g0184others(5): Show | 8 | HG01934.hp1 HG01934.hp2 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.2692-501_2692-493d others(11): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10324756 | ||||||
| chr17:10324756
|
G | GTTTTTTT others(3): Show |
1 | a0001c0003t0001g0246 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2692-502_2692-493d others(12): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10324756 | ||||||
| chr17:10324756
|
G | GTTTTTTT others(6): Show |
2 | a0001c0007t0001g0376a0003c0009t0001g0377 | 2 | HG02965.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2692-505_2692-493d others(15): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10324756 | ||||||
| chr17:10324756
|
G | GTTTTTTT others(7): Show |
1 | a0003c0009t0001g0373 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2692-506_2692-493d others(16): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10324756 | ||||||
| chr17:10324756
|
GT | G | 107 | a0001c0007t0001g0006a0001c0007t0001g0007a0001c0007t0001g0107others(104): Show | 107 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.2692-493delA | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10324756 | ||||||
| chr17:10324756
|
GTT | G | 6 | a0001c0012t0001g0272a0001c0012t0001g0310a0001c0111t0001g0078others(3): Show | 6 | HG01109.hp1 HG01433.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.2692-494_2692-493d others(4): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10324756 | ||||||
| chr17:10324756
|
GTTTTTT | G | 6 | a0001c0014t0001g0374a0001c0015t0001g0371a0001c0015t0001g0372others(3): Show | 6 | HG02145.hp2 HG02717.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2692-498_2692-493d others(8): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10324756 | ||||||
| chr17:10324756
|
GTTTTTTT others(2): Show |
G | 64 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(61): Show | 64 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.2692-501_2692-493d others(11): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10324756 | ||||||
| chr17:10324791
|
A | G | 185 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(182): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.2692-527T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10324791 | ||||||
| chr17:10325380
|
T | C | 5 | a0001c0003t0001g0246a0002c0011t0001g0239a0002c0011t0001g0247others(2): Show | 5 | HG01928.hp1 HG01934.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.2692-1116A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10325380 | ||||||
| chr17:10325389
|
G | A | 1 | a0004c0002t0001g0212 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2692-1125C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10325389 | ||||||
| chr17:10325498
|
A | G | 185 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(182): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.2692-1234T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10325498 | ||||||
| chr17:10325557
|
A | G | 1 | a0031c0080t0001g0220 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2692-1293T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10325557 | ||||||
| chr17:10325738
|
G | A | 1 | a0003c0025t0001g0155 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2692-1474C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10325738 | ||||||
| chr17:10325833
|
T | C | 186 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(183): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.2692-1569A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10325833 | ||||||
| chr17:10325848
|
T | G | 186 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(183): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.2692-1584A>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10325848 | ||||||
| chr17:10325922
|
G | A | 2 | a0003c0009t0001g0319a0030c0084t0001g0254 | 2 | HG02155.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.2692-1658C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10325922 | ||||||
| chr17:10326141
|
T | G | 3 | a0001c0007t0001g0284a0001c0007t0001g0285a0001c0007t0001g0289 | 3 | HG02083.hp1 NA18991.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.2691+1725A>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10326141 | ||||||
| chr17:10326512
|
C | T | 186 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(183): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.2691+1354G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10326512 | ||||||
| chr17:10326534
|
G | C | 116 | a0001c0007t0001g0006a0001c0007t0001g0007a0001c0007t0001g0107others(113): Show | 116 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.2691+1332C>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10326534 | ||||||
| chr17:10326616
|
G | A | 1 | a0002c0001t0001g0048 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2691+1250C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10326616 | ||||||
| chr17:10326637
|
A | AT | 14 | a0001c0003t0001g0249a0001c0014t0001g0010a0001c0015t0001g0011others(11): Show | 14 | HG00423.hp2 HG00544.hp1 NA18944.hp2 others(11): Show |
intron_variant | MODIFIER | c.2691+1228dupA | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10326637 | ||||||
| chr17:10326637
|
AT | A | 119 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(116): Show | 119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.2691+1228delA | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10326637 | ||||||
| chr17:10326768
|
C | T | 187 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(184): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.2691+1098G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10326768 | ||||||
| chr17:10326778
|
A | G | 3 | a0002c0001t0001g0334a0002c0078t0001g0308a0023c0109t0001g0287 | 3 | NA18959.hp2 NA18999.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.2691+1088T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10326778 | ||||||
| chr17:10326821
|
C | CT | 11 | a0001c0014t0001g0010a0001c0015t0001g0011a0001c0015t0001g0014others(8): Show | 11 | HG00423.hp2 HG00544.hp1 NA18944.hp2 others(8): Show |
intron_variant | MODIFIER | c.2691+1044dupA | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10326821 | ||||||
| chr17:10326922
|
T | C | 187 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(184): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.2691+944A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10326922 | ||||||
| chr17:10326977
|
A | G | 314 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(311): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.2691+889T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10326977 | ||||||
| chr17:10326981
|
G | GT | 51 | a0001c0003t0001g0063a0001c0003t0001g0203a0001c0003t0001g0204others(48): Show | 52 | HG00140.hp1 HG00140.hp2 HG00741.hp2 others(49): Show |
intron_variant | MODIFIER | c.2691+884dupA | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10326981 | ||||||
| chr17:10326981
|
G | GTT | 35 | a0001c0004t0001g0344a0001c0004t0001g0346a0001c0006t0001g0001others(32): Show | 36 | HG00323.hp2 HG00438.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.2691+883_2691+884d others(4): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10326981 | ||||||
| chr17:10326981
|
G | GTTT | 14 | a0001c0004t0001g0345a0001c0012t0001g0297a0001c0017t0001g0128others(11): Show | 14 | HG00733.hp2 HG00735.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.2691+882_2691+884d others(5): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10326981 | ||||||
| chr17:10326981
|
G | GTTTT | 7 | a0001c0014t0001g0110a0001c0113t0001g0102a0002c0043t0001g0251others(4): Show | 7 | HG00735.hp2 HG01891.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.2691+881_2691+884d others(6): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10326981 | ||||||
| chr17:10326981
|
G | GTTTTTTT others(1): Show |
18 | a0001c0003t0001g0044a0001c0003t0001g0045a0001c0003t0001g0228others(15): Show | 18 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.2691+877_2691+884d others(10): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10326981 | ||||||
| chr17:10326981
|
G | GTTTTTTT others(2): Show |
23 | a0001c0003t0001g0008a0001c0003t0001g0043a0001c0003t0001g0049others(20): Show | 23 | HG00423.hp1 HG00738.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.2691+876_2691+884d others(11): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10326981 | ||||||
| chr17:10326981
|
G | GTTTTTTT others(3): Show |
2 | a0006c0033t0001g0185a0009c0032t0001g0171 | 2 | HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.2691+875_2691+884d others(12): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10326981 | ||||||
| chr17:10326981
|
G | GTTTTTTT others(4): Show |
1 | a0001c0004t0001g0169 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2691+874_2691+884d others(13): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10326981 | ||||||
| chr17:10326981
|
G | GTTTTTTT others(5): Show |
9 | a0001c0003t0001g0051a0001c0004t0001g0170a0001c0004t0001g0341others(6): Show | 9 | HG03098.hp1 NA18975.hp2 NA18988.hp1 others(6): Show |
intron_variant | MODIFIER | c.2691+873_2691+884d others(14): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10326981 | ||||||
| chr17:10326981
|
G | GTTTTTTT others(6): Show |
12 | a0001c0003t0001g0069a0001c0004t0001g0367a0001c0014t0001g0010others(9): Show | 12 | HG00423.hp2 HG00544.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.2691+872_2691+884d others(15): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10326981 | ||||||
| chr17:10326981
|
G | GTTTTTTT others(7): Show |
5 | a0001c0003t0001g0237a0002c0011t0001g0081a0002c0030t0001g0020others(2): Show | 5 | HG01952.hp1 HG02602.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.2691+871_2691+884d others(16): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10326981 | ||||||
| chr17:10326981
|
G | GTTTTTTT others(9): Show |
1 | a0005c0016t0001g0060 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2691+869_2691+884d others(18): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10326981 | ||||||
| chr17:10326981
|
G | GTTTTTTT others(10): Show |
1 | a0004c0002t0001g0070 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2691+868_2691+884d others(19): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10326981 | ||||||
| chr17:10326981
|
G | GTTTTTTT others(11): Show |
1 | a0004c0002t0001g0072 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2691+867_2691+884d others(20): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10326981 | ||||||
| chr17:10326981
|
G | GTTTTTTT others(12): Show |
2 | a0001c0004t0001g0062a0003c0008t0001g0038 | 2 | HG00621.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.2691+866_2691+884d others(21): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10326981 | ||||||
| chr17:10326981
|
G | GTTTTTTT others(13): Show |
1 | a0001c0004t0001g0071 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.2691+865_2691+884d others(22): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10326981 | ||||||
| chr17:10326981
|
GT | G | 31 | a0001c0007t0001g0260a0001c0046t0001g0265a0001c0089t0001g0184others(28): Show | 31 | HG00621.hp1 HG01106.hp2 HG01978.hp1 others(28): Show |
intron_variant | MODIFIER | c.2691+884delA | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10326981 | ||||||
| chr17:10326981
|
GTT | G | 42 | a0001c0007t0001g0107a0001c0007t0001g0312a0001c0012t0001g0310others(39): Show | 42 | HG00408.hp1 HG00544.hp2 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.2691+883_2691+884d others(4): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10326981 | ||||||
| chr17:10326981
|
GTTT | G | 11 | a0001c0003t0001g0243a0001c0075t0001g0358a0001c0110t0001g0108others(8): Show | 11 | HG01934.hp2 HG02027.hp2 HG02165.hp2 others(8): Show |
intron_variant | MODIFIER | c.2691+882_2691+884d others(5): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10326981 | ||||||
| chr17:10326981
|
GTTTT | G | 14 | a0001c0003t0001g0244a0001c0003t0001g0246a0001c0003t0001g0249others(11): Show | 14 | HG00438.hp2 HG00733.hp1 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.2691+881_2691+884d others(6): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10326981 | ||||||
| chr17:10326981
|
GTTTTT | G | 11 | a0001c0003t0001g0241a0001c0015t0001g0372a0001c0015t0001g0378others(8): Show | 11 | HG01934.hp1 HG01943.hp2 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.2691+880_2691+884d others(7): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10326981 | ||||||
| chr17:10326981
|
GTTTTTTT others(6): Show |
G | 2 | a0001c0004t0001g0236a0001c0022t0001g0181 | 2 | HG01981.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.2691+872_2691+884d others(15): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10326981 | ||||||
| chr17:10326981
|
GTTTTTTT others(7): Show |
G | 8 | a0001c0006t0001g0198a0001c0006t0001g0218a0001c0014t0001g0100others(5): Show | 8 | HG00639.hp2 HG02922.hp2 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.2691+871_2691+884d others(16): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10326981 | ||||||
| chr17:10326981
|
GTTTTTTT others(8): Show |
G | 4 | a0001c0006t0001g0268a0001c0014t0001g0375a0005c0016t0001g0068others(1): Show | 4 | HG01884.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2691+870_2691+884d others(17): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10326981 | ||||||
| chr17:10326981
|
GTTTTTTT others(9): Show |
G | 9 | a0001c0003t0001g0233a0001c0006t0001g0132a0001c0014t0001g0219others(6): Show | 9 | HG01243.hp1 HG02717.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.2691+869_2691+884d others(18): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10326981 | ||||||
| chr17:10326981
|
GTTTTTTT others(10): Show |
G | 3 | a0001c0003t0001g0356a0001c0007t0001g0006a0001c0007t0001g0007 | 3 | HG00408.hp2 NA18952.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.2691+868_2691+884d others(19): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10326981 | ||||||
| chr17:10326981
|
GTTTTTTT others(11): Show |
G | 5 | a0001c0012t0001g0267a0001c0012t0001g0272a0005c0016t0001g0035others(2): Show | 5 | HG02895.hp1 HG02897.hp1 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.2691+867_2691+884d others(20): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10326981 | ||||||
| chr17:10326981
|
GTTTTTTT others(17): Show |
G | 2 | a0001c0015t0001g0098a0002c0030t0001g0097 | 2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2691+861_2691+884d others(26): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10326981 | ||||||
| chr17:10327032
|
C | T | 38 | a0001c0003t0001g0203a0001c0003t0001g0204a0001c0003t0001g0205others(35): Show | 39 | HG00438.hp1 HG01123.hp1 HG01192.hp2 others(36): Show |
intron_variant | MODIFIER | c.2691+834G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10327032 | ||||||
| chr17:10327064
|
C | G | 323 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(320): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.2691+802G>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10327064 | ||||||
| chr17:10327070
|
C | T | 1 | a0001c0006t0001g0132 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2691+796G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10327070 | ||||||
| chr17:10327071
|
A | G | 323 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(320): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.2691+795T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10327071 | ||||||
| chr17:10327095
|
A | G | 357 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(354): Show | 358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.2691+771T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10327095 | ||||||
| chr17:10327121
|
C | T | 2 | a0001c0004t0001g0341a0001c0004t0001g0367 | 2 | NA18975.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.2691+745G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10327121 | ||||||
| chr17:10327292
|
C | T | 3 | a0001c0022t0001g0149a0001c0042t0001g0120a0001c0042t0001g0199 | 3 | HG01891.hp1 HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2691+574G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10327292 | ||||||
| chr17:10327309
|
G | A | 1 | a0001c0111t0001g0078 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2691+557C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10327309 | ||||||
| chr17:10327352
|
C | A | 1 | a0001c0004t0001g0236 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2691+514G>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10327352 | ||||||
| chr17:10327426
|
A | G | 187 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(184): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.2691+440T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10327426 | ||||||
| chr17:10327812
|
C | A | 1 | a0001c0089t0001g0184 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2691+54G>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10327812 | ||||||
| chr17:10328181
|
A | C | 288 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(285): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.2436-60T>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 21/40 | chr17 | 10328181 | ||||||
| chr17:10328181
|
A | T | 14 | a0001c0006t0001g0132a0001c0006t0001g0198a0001c0006t0001g0218others(11): Show | 14 | HG00639.hp2 HG01243.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.2436-60T>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 21/40 | chr17 | 10328181 | ||||||
| chr17:10328208
|
C | T | 14 | a0001c0006t0001g0132a0001c0006t0001g0198a0001c0006t0001g0218others(11): Show | 14 | HG00639.hp2 HG01243.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.2436-87G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 21/40 | chr17 | 10328208 | ||||||
| chr17:10328415
|
G | A | 1 | a0001c0014t0001g0136 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2436-294C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 21/40 | chr17 | 10328415 | ||||||
| chr17:10328558
|
C | T | 312 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(309): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.2436-437G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 21/40 | chr17 | 10328558 | ||||||
| chr17:10328643
|
T | A | 1 | a0016c0060t0001g0111 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2436-522A>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 21/40 | chr17 | 10328643 | ||||||
| chr17:10328645
|
G | T | 1 | a0001c0089t0001g0184 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2436-524C>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 21/40 | chr17 | 10328645 | ||||||
| chr17:10328677
|
C | T | 1 | a0001c0017t0001g0129 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2436-556G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 21/40 | chr17 | 10328677 | ||||||
| chr17:10328678
|
G | GT | 24 | a0001c0006t0001g0084a0001c0012t0001g0267a0001c0012t0001g0272others(21): Show | 24 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(21): Show |
intron_variant | MODIFIER | c.2436-558dupA | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 21/40 | chr17 | 10328678 | ||||||
| chr17:10328678
|
GT | G | 27 | a0001c0003t0001g0069a0001c0003t0001g0233a0001c0004t0001g0028others(24): Show | 27 | HG01070.hp2 HG01109.hp1 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.2436-558delA | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 21/40 | chr17 | 10328678 | ||||||
| chr17:10328678
|
GTT | G | 139 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(136): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.2436-559_2436-558d others(4): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 21/40 | chr17 | 10328678 | ||||||
| chr17:10328994
|
G | A | 312 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(309): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.2436-873C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 21/40 | chr17 | 10328994 | ||||||
| chr17:10329176
|
C | T | 1 | a0002c0001t0001g0303 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2436-1055G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 21/40 | chr17 | 10329176 | ||||||
| chr17:10329280
|
A | G | 3 | a0001c0027t0001g0266a0001c0034t0001g0288a0042c0057t0001g0159 | 3 | HG00738.hp1 HG01106.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2435+1107T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 21/40 | chr17 | 10329280 | ||||||
| chr17:10329309
|
G | C | 1 | a0002c0001t0001g0048 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2435+1078C>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 21/40 | chr17 | 10329309 | ||||||
| chr17:10329594
|
C | T | 6 | a0001c0014t0001g0374a0001c0015t0001g0371a0001c0015t0001g0372others(3): Show | 6 | HG02145.hp2 HG02717.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2435+793G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 21/40 | chr17 | 10329594 | ||||||
| chr17:10329617
|
A | G | 1 | a0031c0080t0001g0220 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2435+770T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 21/40 | chr17 | 10329617 | ||||||
| chr17:10329669
|
G | A | 133 | a0001c0006t0001g0132a0001c0006t0001g0198a0001c0006t0001g0218others(130): Show | 133 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.2435+718C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 21/40 | chr17 | 10329669 | ||||||
| chr17:10329708
|
C | T | 117 | a0001c0007t0001g0006a0001c0007t0001g0007a0001c0007t0001g0107others(114): Show | 117 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.2435+679G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 21/40 | chr17 | 10329708 | ||||||
| chr17:10329741
|
GGGAGGCC others(9): Show |
G | 3 | a0002c0038t0001g0369a0005c0037t0001g0148a0005c0037t0001g0195 | 3 | HG02145.hp1 HG02647.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2435+630_2435+645d others(18): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 21/40 | chr17 | 10329741 | ||||||
| chr17:10329758
|
G | A | 1 | a0002c0001t0001g0352 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2435+629C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 21/40 | chr17 | 10329758 | ||||||
| chr17:10329997
|
C | CT | 12 | a0001c0014t0001g0010a0001c0015t0001g0011a0001c0015t0001g0014others(9): Show | 12 | HG00423.hp2 HG00544.hp1 NA18944.hp2 others(9): Show |
intron_variant | MODIFIER | c.2435+389dupA | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 21/40 | chr17 | 10329997 | ||||||
| chr17:10329998
|
T | TA | 17 | a0001c0006t0001g0132a0001c0006t0001g0198a0001c0006t0001g0218others(14): Show | 17 | HG00639.hp2 HG01123.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.2435+388dupT | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 21/40 | chr17 | 10329998 | ||||||
| chr17:10330013
|
A | G | 1 | a0005c0095t0001g0059 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2435+374T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 21/40 | chr17 | 10330013 | ||||||
| chr17:10330076
|
G | A | 1 | a0004c0002t0001g0002 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.2435+311C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 21/40 | chr17 | 10330076 | ||||||
| chr17:10330222
|
C | T | 6 | a0001c0014t0001g0374a0001c0015t0001g0371a0001c0015t0001g0372others(3): Show | 6 | HG02145.hp2 HG02717.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2435+165G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 21/40 | chr17 | 10330222 | ||||||
| chr17:10330300
|
T | C | 1 | a0003c0008t0001g0053 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2435+87A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 21/40 | chr17 | 10330300 | ||||||
| chr17:10330345
|
G | A | 17 | a0001c0006t0001g0132a0001c0006t0001g0198a0001c0006t0001g0218others(14): Show | 17 | HG00639.hp2 HG01109.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.2435+42C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 21/40 | chr17 | 10330345 | ||||||
| chr17:10330554
|
T | A | 1 | a0036c0067t0001g0104 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2299-31A>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 20/40 | chr17 | 10330554 | ||||||
| chr17:10330556
|
T | C | 6 | a0001c0014t0001g0374a0001c0015t0001g0371a0001c0015t0001g0372others(3): Show | 6 | HG02145.hp2 HG02717.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2299-33A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 20/40 | chr17 | 10330556 | ||||||
| chr17:10330575
|
C | A | 1 | a0001c0103t0001g0174 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2299-52G>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 20/40 | chr17 | 10330575 | ||||||
| chr17:10330581
|
C | T | 1 | a0001c0014t0001g0136 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2299-58G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 20/40 | chr17 | 10330581 | ||||||
| chr17:10330874
|
G | A | 3 | a0001c0007t0001g0376a0003c0009t0001g0373a0003c0009t0001g0377 | 3 | HG02965.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2299-351C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 20/40 | chr17 | 10330874 | ||||||
| chr17:10330966
|
G | C | 116 | a0001c0007t0001g0006a0001c0007t0001g0007a0001c0007t0001g0107others(113): Show | 116 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.2299-443C>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 20/40 | chr17 | 10330966 | ||||||
| chr17:10331030
|
C | T | 1 | a0003c0009t0001g0305 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2299-507G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 20/40 | chr17 | 10331030 | ||||||
| chr17:10331085
|
C | A | 1 | a0001c0111t0001g0078 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2299-562G>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 20/40 | chr17 | 10331085 | ||||||
| chr17:10331093
|
G | A | 3 | a0001c0007t0001g0284a0001c0007t0001g0285a0001c0007t0001g0289 | 3 | HG02083.hp1 NA18991.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.2299-570C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 20/40 | chr17 | 10331093 | ||||||
| chr17:10331237
|
T | C | 378 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(375): Show | 380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.2299-714A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 20/40 | chr17 | 10331237 | ||||||
| chr17:10331252
|
C | T | 161 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(158): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.2299-729G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 20/40 | chr17 | 10331252 | ||||||
| chr17:10331274
|
C | T | 116 | a0001c0007t0001g0006a0001c0007t0001g0007a0001c0007t0001g0107others(113): Show | 116 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.2299-751G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 20/40 | chr17 | 10331274 | ||||||
| chr17:10331517
|
C | T | 28 | a0001c0004t0001g0344a0001c0004t0001g0345a0001c0004t0001g0346others(25): Show | 28 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.2298+582G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 20/40 | chr17 | 10331517 | ||||||
| chr17:10331648
|
C | A | 1 | a0001c0006t0001g0132 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2298+451G>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 20/40 | chr17 | 10331648 | ||||||
| chr17:10331779
|
C | T | 6 | a0001c0014t0001g0374a0001c0015t0001g0371a0001c0015t0001g0372others(3): Show | 6 | HG02145.hp2 HG02717.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2298+320G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 20/40 | chr17 | 10331779 | ||||||
| chr17:10331798
|
C | T | 17 | a0001c0006t0001g0132a0001c0006t0001g0198a0001c0006t0001g0218others(14): Show | 17 | HG00639.hp2 HG01109.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.2298+301G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 20/40 | chr17 | 10331798 | ||||||
| chr17:10331835
|
C | G | 2 | a0004c0010t0001g0302a0006c0029t0001g0259 | 2 | HG02135.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.2298+264G>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 20/40 | chr17 | 10331835 | ||||||
| chr17:10331917
|
C | T | 116 | a0001c0007t0001g0006a0001c0007t0001g0007a0001c0007t0001g0107others(113): Show | 116 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.2298+182G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 20/40 | chr17 | 10331917 | ||||||
| chr17:10331980
|
C | T | 10 | a0001c0012t0001g0279a0001c0012t0001g0286a0002c0001t0001g0250others(7): Show | 10 | HG00733.hp1 HG02622.hp2 HG03453.hp2 others(7): Show |
intron_variant | MODIFIER | c.2298+119G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 20/40 | chr17 | 10331980 | ||||||
| chr17:10332043
|
G | C | 311 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(308): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.2298+56C>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 20/40 | chr17 | 10332043 | ||||||
| chr17:10332056
|
G | A | 1 | a0007c0020t0001g0342 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2298+43C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 20/40 | chr17 | 10332056 | ||||||
| chr17:10332284
|
C | A | 16 | a0001c0006t0001g0132a0001c0006t0001g0198a0001c0006t0001g0218others(13): Show | 16 | HG00099.hp1 HG00639.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.2175-62G>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 19/40 | chr17 | 10332284 | ||||||
| chr17:10332328
|
G | GA | 3 | a0001c0012t0001g0279a0001c0012t0001g0286a0006c0029t0001g0309 | 3 | NA18948.hp1 NA18951.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.2175-107dupT | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 19/40 | chr17 | 10332328 | ||||||
| chr17:10332333
|
C | T | 17 | a0001c0006t0001g0132a0001c0006t0001g0198a0001c0006t0001g0218others(14): Show | 17 | HG00639.hp2 HG01109.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.2175-111G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 19/40 | chr17 | 10332333 | ||||||
| chr17:10332454
|
G | A | 1 | a0001c0119t0001g0274 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2175-232C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 19/40 | chr17 | 10332454 | ||||||
| chr17:10332473
|
G | A | 116 | a0001c0007t0001g0006a0001c0007t0001g0007a0001c0007t0001g0107others(113): Show | 116 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.2175-251C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 19/40 | chr17 | 10332473 | ||||||
| chr17:10332492
|
G | C | 1 | a0001c0004t0001g0028 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2175-270C>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 19/40 | chr17 | 10332492 | ||||||
| chr17:10332597
|
C | G | 6 | a0001c0014t0001g0374a0001c0015t0001g0371a0001c0015t0001g0372others(3): Show | 6 | HG02145.hp2 HG02717.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2175-375G>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 19/40 | chr17 | 10332597 | ||||||
| chr17:10332691
|
T | C | 1 | a0003c0008t0001g0058 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2174+383A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 19/40 | chr17 | 10332691 | ||||||
| chr17:10332739
|
C | G | 1 | a0003c0005t0001g0046 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2174+335G>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 19/40 | chr17 | 10332739 | ||||||
| chr17:10332881
|
G | A | 1 | a0005c0018t0001g0264 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2174+193C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 19/40 | chr17 | 10332881 | ||||||
| chr17:10332882
|
A | C | 133 | a0001c0006t0001g0132a0001c0006t0001g0198a0001c0006t0001g0218others(130): Show | 133 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.2174+192T>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 19/40 | chr17 | 10332882 | ||||||
| chr17:10333244
|
A | T | 1 | a0003c0041t0001g0365 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2057-53T>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10333244 | ||||||
| chr17:10333678
|
G | A | 69 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(66): Show | 69 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.2057-487C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10333678 | ||||||
| chr17:10333705
|
G | A | 4 | a0004c0021t0001g0093a0004c0021t0001g0094a0007c0107t0001g0162others(1): Show | 4 | HG01069.hp1 HG01074.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.2057-514C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10333705 | ||||||
| chr17:10333776
|
C | T | 19 | a0001c0004t0001g0344a0001c0004t0001g0345a0001c0004t0001g0346others(16): Show | 19 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.2057-585G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10333776 | ||||||
| chr17:10333842
|
G | C | 6 | a0001c0014t0001g0374a0001c0015t0001g0371a0001c0015t0001g0372others(3): Show | 6 | HG02145.hp2 HG02717.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2057-651C>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10333842 | ||||||
| chr17:10333873
|
A | C | 1 | a0001c0090t0001g0364 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2057-682T>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10333873 | ||||||
| chr17:10333908
|
C | CA | 6 | a0001c0014t0001g0374a0001c0015t0001g0371a0001c0015t0001g0372others(3): Show | 6 | HG02145.hp2 HG02717.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2057-718dupT | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10333908 | ||||||
| chr17:10333908
|
CA | C | 6 | a0001c0012t0001g0267a0001c0012t0001g0353a0002c0001t0001g0331others(3): Show | 6 | HG02293.hp1 HG02809.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2057-718delT | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10333908 | ||||||
| chr17:10333925
|
G | T | 1 | a0007c0020t0001g0261 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2057-734C>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10333925 | ||||||
| chr17:10333966
|
C | T | 1 | a0002c0019t0001g0188 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2057-775G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10333966 | ||||||
| chr17:10334231
|
G | C | 69 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(66): Show | 69 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.2057-1040C>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10334231 | ||||||
| chr17:10334394
|
C | A | 3 | a0001c0004t0001g0062a0001c0004t0001g0071a0001c0004t0001g0077 | 3 | HG00621.hp2 HG02523.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.2057-1203G>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10334394 | ||||||
| chr17:10334468
|
C | T | 128 | a0001c0003t0001g0241a0001c0003t0001g0243a0001c0003t0001g0244others(125): Show | 128 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.2057-1277G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10334468 | ||||||
| chr17:10334630
|
C | T | 21 | a0001c0003t0001g0203a0001c0003t0001g0204a0001c0003t0001g0205others(18): Show | 22 | HG01081.hp1 HG01257.hp1 HG01258.hp2 others(19): Show |
intron_variant | MODIFIER | c.2057-1439G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10334630 | ||||||
| chr17:10334741
|
T | A | 116 | a0001c0007t0001g0006a0001c0007t0001g0007a0001c0007t0001g0107others(113): Show | 116 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.2057-1550A>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10334741 | ||||||
| chr17:10335193
|
C | T | 1 | a0001c0119t0001g0274 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2057-2002G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10335193 | ||||||
| chr17:10335460
|
A | G | 1 | a0001c0119t0001g0274 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2057-2269T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10335460 | ||||||
| chr17:10335475
|
C | G | 16 | a0001c0006t0001g0132a0001c0006t0001g0198a0001c0006t0001g0218others(13): Show | 16 | HG00639.hp2 HG01109.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.2057-2284G>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10335475 | ||||||
| chr17:10335493
|
T | C | 116 | a0001c0007t0001g0006a0001c0007t0001g0007a0001c0007t0001g0107others(113): Show | 116 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.2057-2302A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10335493 | ||||||
| chr17:10335565
|
C | G | 116 | a0001c0007t0001g0006a0001c0007t0001g0007a0001c0007t0001g0107others(113): Show | 116 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.2057-2374G>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10335565 | ||||||
| chr17:10335605
|
G | T | 132 | a0001c0006t0001g0132a0001c0006t0001g0198a0001c0006t0001g0218others(129): Show | 132 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.2057-2414C>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10335605 | ||||||
| chr17:10335703
|
T | A | 1 | a0001c0006t0001g0132 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2057-2512A>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10335703 | ||||||
| chr17:10335711
|
C | T | 1 | a0001c0015t0001g0378 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2057-2520G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10335711 | ||||||
| chr17:10335763
|
AAGAG | A | 12 | a0001c0014t0001g0010a0001c0015t0001g0011a0001c0015t0001g0014others(9): Show | 12 | HG00423.hp2 HG00544.hp1 NA18944.hp2 others(9): Show |
intron_variant | MODIFIER | c.2057-2576_2057-257 others(8): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10335763 | ||||||
| chr17:10335863
|
G | A | 8 | a0001c0027t0001g0161a0001c0034t0001g0152a0001c0034t0001g0168others(5): Show | 8 | HG00323.hp2 HG00733.hp2 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.2057-2672C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10335863 | ||||||
| chr17:10336012
|
C | T | 86 | a0001c0007t0001g0006a0001c0007t0001g0007a0001c0007t0001g0284others(83): Show | 86 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.2057-2821G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10336012 | ||||||
| chr17:10336017
|
T | C | 16 | a0001c0006t0001g0132a0001c0006t0001g0198a0001c0006t0001g0218others(13): Show | 16 | HG00639.hp2 HG01109.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.2057-2826A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10336017 | ||||||
| chr17:10336049
|
G | A | 1 | a0005c0018t0001g0264 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2057-2858C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10336049 | ||||||
| chr17:10336146
|
T | C | 5 | a0002c0019t0001g0188a0002c0019t0001g0189a0002c0019t0001g0190others(2): Show | 5 | NA18939.hp2 NA18946.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.2057-2955A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10336146 | ||||||
| chr17:10336417
|
C | T | 117 | a0001c0007t0001g0006a0001c0007t0001g0007a0001c0007t0001g0107others(114): Show | 117 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.2057-3226G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10336417 | ||||||
| chr17:10336428
|
G | A | 1 | a0025c0074t0001g0076 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2057-3237C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10336428 | ||||||
| chr17:10336469
|
A | G | 1 | a0007c0096t0001g0034 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2057-3278T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10336469 | ||||||
| chr17:10336472
|
C | T | 2 | a0003c0013t0001g0019a0004c0048t0001g0207 | 2 | NA19003.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.2057-3281G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10336472 | ||||||
| chr17:10336518
|
C | T | 1 | a0001c0040t0001g0117 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2057-3327G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10336518 | ||||||
| chr17:10336519
|
G | A | 2 | a0003c0013t0001g0021a0003c0013t0001g0023 | 2 | NA19010.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.2057-3328C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10336519 | ||||||
| chr17:10336523
|
C | A | 3 | a0018c0114t0001g0339a0035c0086t0001g0300a0040c0076t0001g0343 | 3 | HG00733.hp1 HG03704.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.2057-3332G>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10336523 | ||||||
| chr17:10336564
|
C | T | 1 | a0001c0119t0001g0274 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2057-3373G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10336564 | ||||||
| chr17:10336620
|
A | G | 1 | a0003c0008t0001g0338 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2057-3429T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10336620 | ||||||
| chr17:10336687
|
A | G | 301 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(298): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.2056+3463T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10336687 | ||||||
| chr17:10336781
|
A | G | 1 | a0001c0015t0001g0378 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2056+3369T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10336781 | ||||||
| chr17:10336815
|
G | A | 230 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(227): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.2056+3335C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10336815 | ||||||
| chr17:10336818
|
G | T | 13 | a0001c0003t0001g0049a0001c0003t0001g0227a0001c0003t0001g0228others(10): Show | 13 | HG00323.hp1 HG01069.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.2056+3332C>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10336818 | ||||||
| chr17:10336897
|
G | T | 1 | a0003c0005t0001g0294 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2056+3253C>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10336897 | ||||||
| chr17:10336921
|
C | CT | 68 | a0001c0003t0001g0203a0001c0003t0001g0204a0001c0003t0001g0205others(65): Show | 69 | HG00438.hp1 HG01081.hp1 HG01099.hp2 others(66): Show |
intron_variant | MODIFIER | c.2056+3228dupA | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10336921 | ||||||
| chr17:10336921
|
CT | C | 225 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(222): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.2056+3228delA | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10336921 | ||||||
| chr17:10336928
|
T | C | 1 | a0001c0089t0001g0184 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2056+3222A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10336928 | ||||||
| chr17:10337110
|
T | A | 1 | a0001c0089t0001g0184 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2056+3040A>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10337110 | ||||||
| chr17:10337178
|
C | T | 299 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(296): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.2056+2972G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10337178 | ||||||
| chr17:10337190
|
C | T | 1 | a0001c0006t0001g0218 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2056+2960G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10337190 | ||||||
| chr17:10337209
|
G | C | 299 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(296): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.2056+2941C>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10337209 | ||||||
| chr17:10337361
|
A | G | 1 | a0001c0014t0001g0110 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2056+2789T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10337361 | ||||||
| chr17:10337436
|
G | A | 299 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(296): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.2056+2714C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10337436 | ||||||
| chr17:10337442
|
T | C | 299 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(296): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.2056+2708A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10337442 | ||||||
| chr17:10337454
|
T | C | 301 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(298): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.2056+2696A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10337454 | ||||||
| chr17:10337455
|
G | A | 299 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(296): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.2056+2695C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10337455 | ||||||
| chr17:10337615
|
C | G | 299 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(296): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.2056+2535G>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10337615 | ||||||
| chr17:10337647
|
T | C | 299 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(296): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.2056+2503A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10337647 | ||||||
| chr17:10337648
|
C | A | 299 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(296): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.2056+2502G>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10337648 | ||||||
| chr17:10337783
|
G | A | 1 | a0001c0007t0001g0376 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2056+2367C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10337783 | ||||||
| chr17:10337830
|
A | C | 134 | a0001c0004t0001g0328a0001c0006t0001g0132a0001c0006t0001g0198others(131): Show | 134 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.2056+2320T>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10337830 | ||||||
| chr17:10337865
|
T | C | 299 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(296): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.2056+2285A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10337865 | ||||||
| chr17:10337920
|
A | G | 299 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(296): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.2056+2230T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10337920 | ||||||
| chr17:10338038
|
C | T | 1 | a0001c0089t0001g0184 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2056+2112G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10338038 | ||||||
| chr17:10338067
|
G | A | 2 | a0004c0010t0001g0329a0033c0077t0001g0355 | 2 | HG03239.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.2056+2083C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10338067 | ||||||
| chr17:10338130
|
C | T | 299 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(296): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.2056+2020G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10338130 | ||||||
| chr17:10338170
|
C | T | 1 | a0001c0105t0001g0163 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2056+1980G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10338170 | ||||||
| chr17:10338188
|
A | G | 299 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(296): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.2056+1962T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10338188 | ||||||
| chr17:10338200
|
C | T | 299 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(296): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.2056+1950G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10338200 | ||||||
| chr17:10338238
|
C | CA | 299 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(296): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.2056+1911_2056+191 others(5): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10338238 | ||||||
| chr17:10338248
|
A | G | 283 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(280): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.2056+1902T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10338248 | ||||||
| chr17:10338322
|
C | T | 1 | a0002c0001t0001g0321 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2056+1828G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10338322 | ||||||
| chr17:10338344
|
CAT | C | 299 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(296): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.2056+1804_2056+180 others(6): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10338344 | ||||||
| chr17:10338434
|
A | G | 1 | a0004c0010t0001g0302 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2056+1716T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10338434 | ||||||
| chr17:10338458
|
G | C | 21 | a0001c0004t0001g0344a0001c0004t0001g0345a0001c0004t0001g0346others(18): Show | 21 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.2056+1692C>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10338458 | ||||||
| chr17:10338462
|
A | C | 283 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(280): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.2056+1688T>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10338462 | ||||||
| chr17:10338689
|
G | GTT | 37 | a0001c0003t0001g0203a0001c0003t0001g0204a0001c0003t0001g0205others(34): Show | 38 | HG00438.hp1 HG01081.hp1 HG01123.hp1 others(35): Show |
intron_variant | MODIFIER | c.2056+1459_2056+146 others(6): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10338689 | ||||||
| chr17:10338689
|
G | GTTT | 6 | a0002c0001t0001g0040a0003c0008t0001g0230a0004c0002t0001g0221others(3): Show | 6 | HG01099.hp2 HG01256.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.2056+1458_2056+146 others(7): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10338689 | ||||||
| chr17:10338689
|
G | GTTTT | 61 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(58): Show | 61 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.2056+1457_2056+146 others(8): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10338689 | ||||||
| chr17:10338689
|
G | GTTTTT | 7 | a0001c0003t0001g0051a0001c0004t0001g0025a0013c0117t0001g0380others(4): Show | 7 | HG00099.hp2 HG00423.hp1 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.2056+1456_2056+146 others(9): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10338689 | ||||||
| chr17:10338698
|
T | G | 1 | a0041c0069t0001g0200 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2056+1452A>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10338698 | ||||||
| chr17:10338698
|
T | TG | 12 | a0001c0014t0001g0010a0001c0015t0001g0011a0001c0015t0001g0014others(9): Show | 12 | HG00423.hp2 HG00544.hp1 NA18944.hp2 others(9): Show |
intron_variant | MODIFIER | c.2056+1451_2056+145 others(5): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10338698 | ||||||
| chr17:10338701
|
T | TTG | 17 | a0001c0003t0001g0233a0001c0003t0001g0237a0001c0003t0001g0269others(14): Show | 17 | HG01884.hp1 HG02109.hp1 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.2056+1448_2056+144 others(6): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10338701 | ||||||
| chr17:10338702
|
T | G | 91 | a0001c0006t0001g0001a0001c0006t0001g0084a0001c0006t0001g0085others(88): Show | 92 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.2056+1448A>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10338702 | ||||||
| chr17:10338702
|
T | TTG | 15 | a0001c0006t0001g0132a0002c0019t0001g0188a0002c0019t0001g0189others(12): Show | 15 | HG03041.hp2 HG03579.hp1 NA18939.hp2 others(12): Show |
intron_variant | MODIFIER | c.2056+1447_2056+144 others(6): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10338702 | ||||||
| chr17:10338702
|
T | TTTG | 32 | a0001c0004t0001g0344a0001c0004t0001g0345a0001c0004t0001g0346others(29): Show | 32 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.2056+1447_2056+144 others(7): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10338702 | ||||||
| chr17:10338702
|
T | TTTTG | 104 | a0001c0004t0001g0328a0001c0007t0001g0006a0001c0007t0001g0007others(101): Show | 104 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.2056+1444_2056+144 others(8): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10338702 | ||||||
| chr17:10338706
|
G | T | 1 | a0005c0016t0001g0080 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2056+1444C>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10338706 | ||||||
| chr17:10338710
|
G | GT | 12 | a0001c0014t0001g0010a0001c0015t0001g0011a0001c0015t0001g0014others(9): Show | 12 | HG00423.hp2 HG00544.hp1 NA18944.hp2 others(9): Show |
intron_variant | MODIFIER | c.2056+1439dupA | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10338710 | ||||||
| chr17:10338752
|
A | G | 2 | a0003c0013t0001g0019a0004c0048t0001g0207 | 2 | NA19003.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.2056+1398T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10338752 | ||||||
| chr17:10338818
|
G | A | 302 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(299): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.2056+1332C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10338818 | ||||||
| chr17:10338845
|
C | T | 2 | a0003c0005t0001g0299a0008c0063t0001g0298 | 2 | HG02698.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.2056+1305G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10338845 | ||||||
| chr17:10338849
|
C | T | 23 | a0001c0027t0001g0009a0001c0027t0001g0154a0001c0027t0001g0161others(20): Show | 23 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.2056+1301G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10338849 | ||||||
| chr17:10338893
|
G | C | 2 | a0001c0015t0001g0011a0001c0015t0001g0014 | 2 | HG00423.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.2056+1257C>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10338893 | ||||||
| chr17:10338938
|
T | G | 288 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(285): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.2056+1212A>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10338938 | ||||||
| chr17:10338949
|
A | C | 1 | a0001c0006t0001g0268 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2056+1201T>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10338949 | ||||||
| chr17:10338990
|
T | C | 303 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(300): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.2056+1160A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10338990 | ||||||
| chr17:10338991
|
G | A | 1 | a0001c0017t0001g0086 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2056+1159C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10338991 | ||||||
| chr17:10338992
|
T | C | 1 | a0001c0017t0001g0086 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2056+1158A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10338992 | ||||||
| chr17:10339094
|
C | T | 151 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(148): Show | 152 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.2056+1056G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10339094 | ||||||
| chr17:10339099
|
C | T | 1 | a0001c0014t0001g0110 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2056+1051G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10339099 | ||||||
| chr17:10339225
|
G | A | 1 | a0031c0080t0001g0220 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2056+925C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10339225 | ||||||
| chr17:10339317
|
G | A | 1 | a0004c0048t0001g0301 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2056+833C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10339317 | ||||||
| chr17:10339353
|
T | C | 108 | a0001c0004t0001g0328a0001c0007t0001g0006a0001c0007t0001g0007others(105): Show | 108 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.2056+797A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10339353 | ||||||
| chr17:10339371
|
G | T | 2 | a0010c0023t0001g0350a0010c0023t0001g0351 | 2 | NA18967.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.2056+779C>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10339371 | ||||||
| chr17:10339518
|
T | C | 1 | a0006c0029t0001g0325 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2056+632A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10339518 | ||||||
| chr17:10339639
|
A | G | 2 | a0003c0008t0001g0036a0011c0031t0001g0041 | 2 | HG00738.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.2056+511T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10339639 | ||||||
| chr17:10339667
|
G | A | 289 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(286): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.2056+483C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10339667 | ||||||
| chr17:10339679
|
C | A | 4 | a0001c0120t0001g0178a0004c0002t0001g0214a0005c0016t0001g0210others(1): Show | 4 | HG01123.hp1 HG01192.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2056+471G>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10339679 | ||||||
| chr17:10339817
|
A | T | 1 | a0013c0116t0001g0087 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2056+333T>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10339817 | ||||||
| chr17:10339854
|
G | T | 2 | a0001c0014t0001g0219a0025c0074t0001g0076 | 2 | HG01243.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.2056+296C>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10339854 | ||||||
| chr17:10339891
|
G | A | 2 | a0001c0014t0001g0219a0025c0074t0001g0076 | 2 | HG01243.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.2056+259C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10339891 | ||||||
| chr17:10339907
|
C | T | 1 | a0016c0060t0001g0111 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2056+243G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10339907 | ||||||
| chr17:10339909
|
T | C | 1 | a0001c0007t0001g0006 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2056+241A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10339909 | ||||||
| chr17:10339993
|
T | C | 1 | a0001c0022t0001g0293 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2056+157A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10339993 | ||||||
| chr17:10340071
|
C | T | 1 | a0032c0082t0001g0180 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.2056+79G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10340071 | ||||||
| chr17:10340105
|
C | T | 1 | a0001c0089t0001g0184 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2056+45G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10340105 | ||||||
| chr17:10340263
|
A | G | 1 | a0003c0008t0001g0338 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1969-26T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 17/40 | chr17 | 10340263 | ||||||
| chr17:10340272
|
C | A | 293 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(290): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.1969-35G>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 17/40 | chr17 | 10340272 | ||||||
| chr17:10340472
|
T | C | 293 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(290): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.1895-71A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10340472 | ||||||
| chr17:10340541
|
C | T | 291 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(288): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.1895-140G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10340541 | ||||||
| chr17:10340611
|
C | T | 1 | a0001c0014t0001g0374 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1895-210G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10340611 | ||||||
| chr17:10340711
|
A | G | 293 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(290): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.1895-310T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10340711 | ||||||
| chr17:10340754
|
G | T | 293 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(290): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.1895-353C>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10340754 | ||||||
| chr17:10340791
|
T | G | 293 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(290): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.1895-390A>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10340791 | ||||||
| chr17:10341017
|
C | CT | 174 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(171): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.1895-617dupA | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10341017 | ||||||
| chr17:10341107
|
A | G | 1 | a0003c0005t0001g0046 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1895-706T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10341107 | ||||||
| chr17:10341164
|
T | C | 91 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(88): Show | 91 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(88): Show |
intron_variant | MODIFIER | c.1895-763A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10341164 | ||||||
| chr17:10341172
|
A | G | 12 | a0001c0014t0001g0010a0001c0015t0001g0011a0001c0015t0001g0014others(9): Show | 12 | HG00423.hp2 HG00544.hp1 NA18944.hp2 others(9): Show |
intron_variant | MODIFIER | c.1895-771T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10341172 | ||||||
| chr17:10341278
|
C | T | 1 | a0004c0002t0001g0075 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1895-877G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10341278 | ||||||
| chr17:10341387
|
T | C | 91 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(88): Show | 91 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(88): Show |
intron_variant | MODIFIER | c.1895-986A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10341387 | ||||||
| chr17:10341527
|
A | G | 293 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(290): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.1895-1126T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10341527 | ||||||
| chr17:10341546
|
G | A | 293 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(290): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.1895-1145C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10341546 | ||||||
| chr17:10341567
|
A | G | 7 | a0001c0004t0001g0169a0001c0004t0001g0170a0001c0103t0001g0174others(4): Show | 7 | HG02109.hp1 HG02559.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1895-1166T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10341567 | ||||||
| chr17:10341605
|
C | T | 91 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(88): Show | 91 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(88): Show |
intron_variant | MODIFIER | c.1895-1204G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10341605 | ||||||
| chr17:10341677
|
T | G | 293 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(290): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.1895-1276A>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10341677 | ||||||
| chr17:10341697
|
C | T | 91 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(88): Show | 91 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(88): Show |
intron_variant | MODIFIER | c.1895-1296G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10341697 | ||||||
| chr17:10341714
|
C | T | 1 | a0005c0028t0001g0363 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1895-1313G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10341714 | ||||||
| chr17:10341729
|
T | C | 1 | a0001c0110t0001g0108 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1895-1328A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10341729 | ||||||
| chr17:10341779
|
A | G | 1 | a0005c0028t0001g0363 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1895-1378T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10341779 | ||||||
| chr17:10342119
|
C | T | 1 | a0001c0111t0001g0078 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1894+1681G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10342119 | ||||||
| chr17:10342146
|
T | C | 2 | a0001c0012t0001g0353a0002c0001t0001g0331 | 2 | HG03688.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.1894+1654A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10342146 | ||||||
| chr17:10342166
|
T | C | 293 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(290): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.1894+1634A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10342166 | ||||||
| chr17:10342174
|
T | A | 1 | a0032c0082t0001g0180 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1894+1626A>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10342174 | ||||||
| chr17:10342341
|
A | G | 293 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(290): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.1894+1459T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10342341 | ||||||
| chr17:10342351
|
G | A | 1 | a0001c0004t0001g0062 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1894+1449C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10342351 | ||||||
| chr17:10342368
|
C | T | 136 | a0001c0003t0001g0241a0001c0003t0001g0243a0001c0003t0001g0244others(133): Show | 136 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.1894+1432G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10342368 | ||||||
| chr17:10342450
|
G | A | 1 | a0010c0023t0001g0311 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1894+1350C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10342450 | ||||||
| chr17:10342492
|
A | G | 293 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(290): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.1894+1308T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10342492 | ||||||
| chr17:10342547
|
G | A | 293 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(290): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.1894+1253C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10342547 | ||||||
| chr17:10342557
|
C | T | 8 | a0001c0003t0001g0241a0001c0003t0001g0243a0001c0003t0001g0244others(5): Show | 8 | HG01928.hp1 HG01934.hp2 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.1894+1243G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10342557 | ||||||
| chr17:10342677
|
T | TGAGA | 293 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(290): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.1894+1122_1894+112 others(8): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10342677 | ||||||
| chr17:10342709
|
A | G | 1 | a0005c0028t0001g0363 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1894+1091T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10342709 | ||||||
| chr17:10342737
|
G | T | 1 | a0005c0016t0001g0080 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1894+1063C>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10342737 | ||||||
| chr17:10342799
|
C | A | 1 | a0001c0017t0001g0086 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1894+1001G>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10342799 | ||||||
| chr17:10342827
|
G | A | 293 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(290): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.1894+973C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10342827 | ||||||
| chr17:10342958
|
C | T | 11 | a0001c0014t0001g0010a0001c0015t0001g0011a0001c0015t0001g0014others(8): Show | 11 | HG00423.hp2 HG00544.hp1 NA18944.hp2 others(8): Show |
intron_variant | MODIFIER | c.1894+842G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10342958 | ||||||
| chr17:10342988
|
G | C | 293 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(290): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.1894+812C>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10342988 | ||||||
| chr17:10343070
|
A | C | 293 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(290): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.1894+730T>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10343070 | ||||||
| chr17:10343088
|
C | CA | 11 | a0002c0065t0001g0079a0002c0070t0001g0106a0003c0005t0001g0089others(8): Show | 11 | HG01261.hp1 HG01934.hp1 HG03098.hp2 others(8): Show |
intron_variant | MODIFIER | c.1894+711dupT | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10343088 | ||||||
| chr17:10343088
|
CAAAAAA | C | 12 | a0001c0003t0001g0233a0001c0007t0001g0107a0001c0007t0001g0260others(9): Show | 12 | HG00741.hp1 HG01106.hp2 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1894+706_1894+711d others(8): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10343088 | ||||||
| chr17:10343088
|
CAAAAAAA | C | 199 | a0001c0003t0001g0203a0001c0003t0001g0204a0001c0003t0001g0205others(196): Show | 200 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.1894+705_1894+711d others(9): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10343088 | ||||||
| chr17:10343088
|
CAAAAAAA others(2): Show |
C | 77 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(74): Show | 77 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.1894+703_1894+711d others(11): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10343088 | ||||||
| chr17:10343088
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0003t0001g0069 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1894+702_1894+711d others(12): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10343088 | ||||||
| chr17:10343128
|
G | A | 293 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(290): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.1894+672C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10343128 | ||||||
| chr17:10343135
|
T | C | 293 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(290): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.1894+665A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10343135 | ||||||
| chr17:10343136
|
G | A | 1 | a0005c0028t0001g0363 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1894+664C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10343136 | ||||||
| chr17:10343204
|
A | AT | 57 | a0001c0003t0001g0203a0001c0003t0001g0204a0001c0003t0001g0205others(54): Show | 58 | HG00438.hp1 HG01081.hp1 HG01123.hp1 others(55): Show |
intron_variant | MODIFIER | c.1894+595dupA | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10343204 | ||||||
| chr17:10343279
|
C | T | 39 | a0001c0003t0001g0203a0001c0003t0001g0204a0001c0003t0001g0205others(36): Show | 40 | HG00438.hp1 HG01081.hp1 HG01123.hp1 others(37): Show |
intron_variant | MODIFIER | c.1894+521G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10343279 | ||||||
| chr17:10343319
|
G | T | 20 | a0001c0027t0001g0009a0001c0027t0001g0154a0001c0027t0001g0161others(17): Show | 20 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.1894+481C>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10343319 | ||||||
| chr17:10343343
|
A | G | 293 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(290): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.1894+457T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10343343 | ||||||
| chr17:10343386
|
T | C | 293 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(290): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.1894+414A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10343386 | ||||||
| chr17:10343387
|
G | A | 1 | a0004c0048t0001g0301 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1894+413C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10343387 | ||||||
| chr17:10343440
|
G | A | 1 | a0007c0020t0001g0342 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1894+360C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10343440 | ||||||
| chr17:10343517
|
T | G | 1 | a0004c0002t0001g0212 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1894+283A>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10343517 | ||||||
| chr17:10343759
|
A | G | 1 | a0002c0038t0001g0369 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1894+41T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10343759 | ||||||
| chr17:10343766
|
G | A | 20 | a0001c0027t0001g0009a0001c0027t0001g0154a0001c0027t0001g0161others(17): Show | 20 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.1894+34C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10343766 | ||||||
| chr17:10344112
|
G | A | 12 | a0001c0014t0001g0010a0001c0015t0001g0011a0001c0015t0001g0014others(9): Show | 12 | HG00423.hp2 HG00544.hp1 NA18944.hp2 others(9): Show |
splice_region_variant&intron_variant | LOW | c.1585-3C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 15/40 | chr17 | 10344112 | ||||||
| chr17:10344128
|
A | G | 6 | a0001c0003t0001g0241a0001c0003t0001g0244a0001c0003t0001g0246others(3): Show | 6 | HG01928.hp1 HG01975.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.1585-19T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 15/40 | chr17 | 10344128 | ||||||
| chr17:10344227
|
C | T | 73 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(70): Show | 73 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.1585-118G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 15/40 | chr17 | 10344227 | ||||||
| chr17:10344456
|
G | A | 3 | a0001c0027t0001g0266a0001c0034t0001g0288a0042c0057t0001g0159 | 3 | HG00738.hp1 HG01106.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1585-347C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 15/40 | chr17 | 10344456 | ||||||
| chr17:10344547
|
G | A | 3 | a0018c0114t0001g0339a0035c0086t0001g0300a0040c0076t0001g0343 | 3 | HG00733.hp1 HG03704.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1585-438C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 15/40 | chr17 | 10344547 | ||||||
| chr17:10344681
|
C | T | 1 | a0026c0092t0001g0368 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1584+521G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 15/40 | chr17 | 10344681 | ||||||
| chr17:10344729
|
G | A | 1 | a0003c0005t0001g0046 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1584+473C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 15/40 | chr17 | 10344729 | ||||||
| chr17:10344767
|
T | G | 306 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(303): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.1584+435A>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 15/40 | chr17 | 10344767 | ||||||
| chr17:10344820
|
C | CA | 10 | a0001c0003t0001g0063a0001c0004t0001g0028a0001c0004t0001g0194others(7): Show | 10 | HG01070.hp2 HG01516.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1584+381dupT | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 15/40 | chr17 | 10344820 | ||||||
| chr17:10344820
|
CA | C | 57 | a0001c0004t0001g0030a0001c0006t0001g0084a0001c0006t0001g0085others(54): Show | 57 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.1584+381delT | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 15/40 | chr17 | 10344820 | ||||||
| chr17:10344840
|
AAAG | A | 16 | a0001c0003t0001g0241a0001c0003t0001g0243a0001c0003t0001g0244others(13): Show | 16 | HG00733.hp1 HG01928.hp1 HG01934.hp2 others(13): Show |
intron_variant | MODIFIER | c.1584+359_1584+361d others(5): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 15/40 | chr17 | 10344840 | ||||||
| chr17:10344841
|
AAG | A | 35 | a0001c0004t0001g0328a0001c0004t0001g0344a0001c0004t0001g0345others(32): Show | 35 | HG00438.hp2 HG00735.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.1584+359_1584+360d others(4): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 15/40 | chr17 | 10344841 | ||||||
| chr17:10344842
|
AG | A | 78 | a0001c0007t0001g0006a0001c0007t0001g0007a0001c0007t0001g0107others(75): Show | 78 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.1584+359delC | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 15/40 | chr17 | 10344842 | ||||||
| chr17:10344843
|
G | A | 2 | a0001c0089t0001g0184a0001c0090t0001g0364 | 2 | HG02280.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1584+359C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 15/40 | chr17 | 10344843 | ||||||
| chr17:10345395
|
A | G | 3 | a0001c0004t0001g0344a0001c0004t0001g0345a0001c0004t0001g0346 | 3 | HG00735.hp1 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1414-23T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 14/40 | chr17 | 10345395 | ||||||
| chr17:10345765
|
C | T | 1 | a0002c0001t0001g0331 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1264-149G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 13/40 | chr17 | 10345765 | ||||||
| chr17:10345766
|
G | A | 1 | a0001c0111t0001g0078 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1264-150C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 13/40 | chr17 | 10345766 | ||||||
| chr17:10345770
|
G | A | 137 | a0001c0003t0001g0241a0001c0003t0001g0243a0001c0003t0001g0244others(134): Show | 137 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(134): Show |
intron_variant | MODIFIER | c.1264-154C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 13/40 | chr17 | 10345770 | ||||||
| chr17:10345821
|
C | T | 2 | a0003c0005t0001g0124a0003c0005t0001g0125 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1264-205G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 13/40 | chr17 | 10345821 | ||||||
| chr17:10345854
|
G | T | 1 | a0004c0002t0001g0222 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1264-238C>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 13/40 | chr17 | 10345854 | ||||||
| chr17:10345885
|
C | T | 1 | a0009c0049t0001g0248 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1264-269G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 13/40 | chr17 | 10345885 | ||||||
| chr17:10345991
|
C | CA | 109 | a0001c0004t0001g0328a0001c0004t0001g0344a0001c0004t0001g0345others(106): Show | 110 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.1264-376dupT | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 13/40 | chr17 | 10345991 | ||||||
| chr17:10345991
|
C | CAA | 40 | a0001c0003t0001g0241a0001c0003t0001g0243a0001c0003t0001g0244others(37): Show | 40 | HG01099.hp2 HG01346.hp2 HG01433.hp1 others(37): Show |
intron_variant | MODIFIER | c.1264-377_1264-376d others(4): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 13/40 | chr17 | 10345991 | ||||||
| chr17:10345991
|
C | CAAA | 46 | a0001c0003t0001g0204a0001c0003t0001g0205a0001c0003t0001g0233others(43): Show | 47 | HG01081.hp1 HG01192.hp2 HG01257.hp1 others(44): Show |
intron_variant | MODIFIER | c.1264-378_1264-376d others(5): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 13/40 | chr17 | 10345991 | ||||||
| chr17:10345991
|
C | CAAAA | 9 | a0001c0003t0001g0203a0002c0001t0001g0275a0002c0019t0001g0193others(6): Show | 9 | HG00438.hp1 HG01123.hp1 HG02300.hp1 others(6): Show |
intron_variant | MODIFIER | c.1264-379_1264-376d others(6): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 13/40 | chr17 | 10345991 | ||||||
| chr17:10345991
|
CAA | C | 18 | a0001c0004t0001g0031a0001c0027t0001g0009a0001c0027t0001g0154others(15): Show | 18 | HG00140.hp1 HG00323.hp2 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.1264-377_1264-376d others(4): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 13/40 | chr17 | 10345991 | ||||||
| chr17:10345991
|
CAAA | C | 74 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(71): Show | 74 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.1264-378_1264-376d others(5): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 13/40 | chr17 | 10345991 | ||||||
| chr17:10346014
|
C | A | 4 | a0001c0003t0001g0249a0001c0014t0001g0374a0003c0013t0001g0023others(1): Show | 4 | HG02145.hp2 HG02717.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.1264-398G>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 13/40 | chr17 | 10346014 | ||||||
| chr17:10346017
|
A | C | 3 | a0001c0003t0001g0249a0001c0014t0001g0374a0003c0013t0001g0370 | 3 | HG02145.hp2 HG02717.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1264-401T>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 13/40 | chr17 | 10346017 | ||||||
| chr17:10346018
|
A | C | 1 | a0001c0119t0001g0274 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1264-402T>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 13/40 | chr17 | 10346018 | ||||||
| chr17:10346018
|
A | G | 1 | a0004c0002t0001g0222 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1264-402T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 13/40 | chr17 | 10346018 | ||||||
| chr17:10346019
|
G | A | 5 | a0001c0003t0001g0249a0001c0014t0001g0374a0001c0119t0001g0274others(2): Show | 5 | HG02145.hp2 HG02257.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1264-403C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 13/40 | chr17 | 10346019 | ||||||
| chr17:10346022
|
A | G | 3 | a0001c0003t0001g0249a0001c0014t0001g0374a0003c0013t0001g0370 | 3 | HG02145.hp2 HG02717.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1264-406T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 13/40 | chr17 | 10346022 | ||||||
| chr17:10346023
|
A | G | 1 | a0001c0119t0001g0274 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1264-407T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 13/40 | chr17 | 10346023 | ||||||
| chr17:10346024
|
AAAG | A | 134 | a0001c0003t0001g0241a0001c0003t0001g0243a0001c0003t0001g0244others(131): Show | 134 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(131): Show |
intron_variant | MODIFIER | c.1264-411_1264-409d others(5): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 13/40 | chr17 | 10346024 | ||||||
| chr17:10346027
|
G | A | 4 | a0001c0003t0001g0249a0001c0014t0001g0374a0001c0119t0001g0274others(1): Show | 4 | HG02145.hp2 HG02257.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1264-411C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 13/40 | chr17 | 10346027 | ||||||
| chr17:10346082
|
A | C | 1 | a0004c0002t0001g0222 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1264-466T>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 13/40 | chr17 | 10346082 | ||||||
| chr17:10346112
|
T | C | 295 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(292): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.1264-496A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 13/40 | chr17 | 10346112 | ||||||
| chr17:10346288
|
T | C | 1 | a0032c0082t0001g0180 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1263+392A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 13/40 | chr17 | 10346288 | ||||||
| chr17:10346571
|
G | GA | 293 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(290): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.1263+108dupT | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 13/40 | chr17 | 10346571 | ||||||
| chr17:10346623
|
A | G | 2 | a0002c0030t0001g0020a0002c0030t0001g0022 | 2 | NA18944.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.1263+57T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 13/40 | chr17 | 10346623 | ||||||
| chr17:10346842
|
G | A | 4 | a0001c0120t0001g0178a0004c0002t0001g0214a0005c0016t0001g0210others(1): Show | 4 | HG01123.hp1 HG01192.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1145-44C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 12/40 | chr17 | 10346842 | ||||||
| chr17:10346851
|
T | G | 1 | a0004c0002t0001g0192 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1145-53A>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 12/40 | chr17 | 10346851 | ||||||
| chr17:10347058
|
T | C | 5 | a0001c0003t0001g0203a0001c0003t0001g0204a0001c0003t0001g0205others(2): Show | 6 | HG01081.hp1 HG01257.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1145-260A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 12/40 | chr17 | 10347058 | ||||||
| chr17:10347141
|
G | A | 4 | a0001c0072t0001g0160a0002c0011t0001g0081a0003c0005t0001g0130others(1): Show | 4 | HG01167.hp2 HG01361.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.1145-343C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 12/40 | chr17 | 10347141 | ||||||
| chr17:10347281
|
C | T | 1 | a0038c0102t0001g0066 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1145-483G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 12/40 | chr17 | 10347281 | ||||||
| chr17:10347413
|
C | T | 1 | a0005c0028t0001g0363 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1145-615G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 12/40 | chr17 | 10347413 | ||||||
| chr17:10347520
|
G | A | 1 | a0001c0012t0001g0297 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1145-722C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 12/40 | chr17 | 10347520 | ||||||
| chr17:10347629
|
G | A | 1 | a0001c0015t0001g0098 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1145-831C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 12/40 | chr17 | 10347629 | ||||||
| chr17:10347655
|
G | T | 347 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(344): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.1145-857C>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 12/40 | chr17 | 10347655 | ||||||
| chr17:10347712
|
C | CT | 53 | a0001c0003t0001g0049a0001c0003t0001g0241a0001c0003t0001g0243others(50): Show | 53 | HG00423.hp2 HG00438.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.1145-915dupA | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 12/40 | chr17 | 10347712 | ||||||
| chr17:10347712
|
C | CTT | 100 | a0001c0003t0001g0246a0001c0004t0001g0328a0001c0004t0001g0344others(97): Show | 100 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.1145-916_1145-915d others(4): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 12/40 | chr17 | 10347712 | ||||||
| chr17:10347712
|
C | CTTT | 17 | a0001c0007t0001g0260a0001c0014t0001g0375a0001c0111t0001g0078others(14): Show | 17 | HG00621.hp1 HG01106.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1145-917_1145-915d others(5): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 12/40 | chr17 | 10347712 | ||||||
| chr17:10347712
|
C | CTTTTT | 59 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(56): Show | 59 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.1145-919_1145-915d others(7): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 12/40 | chr17 | 10347712 | ||||||
| chr17:10347712
|
C | CTTTTTT | 13 | a0001c0003t0001g0063a0001c0004t0001g0030a0001c0004t0001g0031others(10): Show | 13 | HG01257.hp2 HG01258.hp1 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.1145-920_1145-915d others(8): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 12/40 | chr17 | 10347712 | ||||||
| chr17:10347712
|
CT | C | 23 | a0001c0027t0001g0009a0001c0027t0001g0154a0001c0027t0001g0161others(20): Show | 23 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.1145-915delA | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 12/40 | chr17 | 10347712 | ||||||
| chr17:10347750
|
T | G | 308 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(305): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.1145-952A>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 12/40 | chr17 | 10347750 | ||||||
| chr17:10347753
|
A | G | 1 | a0002c0001t0001g0040 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1145-955T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 12/40 | chr17 | 10347753 | ||||||
| chr17:10347862
|
C | T | 2 | a0001c0003t0001g0243a0006c0052t0001g0242 | 2 | HG01934.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.1145-1064G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 12/40 | chr17 | 10347862 | ||||||
| chr17:10347874
|
G | C | 20 | a0001c0027t0001g0009a0001c0027t0001g0154a0001c0027t0001g0161others(17): Show | 20 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.1145-1076C>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 12/40 | chr17 | 10347874 | ||||||
| chr17:10347910
|
G | C | 1 | a0004c0010t0001g0326 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1145-1112C>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 12/40 | chr17 | 10347910 | ||||||
| chr17:10347956
|
A | T | 1 | a0004c0002t0001g0221 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1145-1158T>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 12/40 | chr17 | 10347956 | ||||||
| chr17:10347972
|
A | G | 74 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(71): Show | 74 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.1145-1174T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 12/40 | chr17 | 10347972 | ||||||
| chr17:10348019
|
T | C | 20 | a0001c0027t0001g0009a0001c0027t0001g0154a0001c0027t0001g0161others(17): Show | 20 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.1145-1221A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 12/40 | chr17 | 10348019 | ||||||
| chr17:10348274
|
G | T | 1 | a0004c0021t0001g0127 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1145-1476C>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 12/40 | chr17 | 10348274 | ||||||
| chr17:10348357
|
C | T | 1 | a0001c0111t0001g0078 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1145-1559G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 12/40 | chr17 | 10348357 | ||||||
| chr17:10348494
|
A | G | 94 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(91): Show | 94 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(91): Show |
intron_variant | MODIFIER | c.1145-1696T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 12/40 | chr17 | 10348494 | ||||||
| chr17:10348713
|
C | T | 258 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(255): Show | 259 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.1144+1843G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 12/40 | chr17 | 10348713 | ||||||
| chr17:10348800
|
G | T | 74 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(71): Show | 74 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.1144+1756C>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 12/40 | chr17 | 10348800 | ||||||
| chr17:10348990
|
T | TCCTTCCT others(30): Show |
1 | a0002c0001t0001g0327 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1144+1529_1144+156 others(41): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 12/40 | chr17 | 10348990 | ||||||
| chr17:10349074
|
CCTTCT | C | 16 | a0001c0003t0001g0241a0001c0003t0001g0243a0001c0003t0001g0244others(13): Show | 16 | HG01099.hp2 HG01928.hp1 HG01934.hp2 others(13): Show |
intron_variant | MODIFIER | c.1144+1477_1144+148 others(9): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 12/40 | chr17 | 10349074 | ||||||
| chr17:10349083
|
CCT | C | 60 | a0001c0003t0001g0203a0001c0003t0001g0204a0001c0003t0001g0205others(57): Show | 61 | HG00438.hp1 HG01081.hp1 HG01123.hp1 others(58): Show |
intron_variant | MODIFIER | c.1144+1471_1144+147 others(6): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 12/40 | chr17 | 10349083 | ||||||
| chr17:10349270
|
T | C | 30 | a0001c0003t0001g0241a0001c0003t0001g0243a0001c0003t0001g0244others(27): Show | 30 | HG00423.hp2 HG00544.hp1 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.1144+1286A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 12/40 | chr17 | 10349270 | ||||||
| chr17:10349285
|
G | A | 308 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(305): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.1144+1271C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 12/40 | chr17 | 10349285 | ||||||
| chr17:10349291
|
G | A | 16 | a0001c0003t0001g0241a0001c0003t0001g0243a0001c0003t0001g0244others(13): Show | 16 | HG01099.hp2 HG01928.hp1 HG01934.hp2 others(13): Show |
intron_variant | MODIFIER | c.1144+1265C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 12/40 | chr17 | 10349291 | ||||||
| chr17:10349326
|
A | C | 90 | a0001c0003t0001g0203a0001c0003t0001g0204a0001c0003t0001g0205others(87): Show | 91 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.1144+1230T>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 12/40 | chr17 | 10349326 | ||||||
| chr17:10349327
|
T | C | 1 | a0001c0119t0001g0274 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1144+1229A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 12/40 | chr17 | 10349327 | ||||||
| chr17:10349400
|
T | C | 1 | a0005c0028t0001g0363 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1144+1156A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 12/40 | chr17 | 10349400 | ||||||
| chr17:10349441
|
A | G | 1 | a0003c0008t0001g0053 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1144+1115T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 12/40 | chr17 | 10349441 | ||||||
| chr17:10349472
|
C | G | 1 | a0002c0094t0001g0226 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1144+1084G>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 12/40 | chr17 | 10349472 | ||||||
| chr17:10349549
|
G | A | 3 | a0001c0007t0001g0376a0003c0009t0001g0373a0003c0009t0001g0377 | 3 | HG02965.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1144+1007C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 12/40 | chr17 | 10349549 | ||||||
| chr17:10349605
|
G | A | 1 | a0001c0040t0001g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1144+951C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 12/40 | chr17 | 10349605 | ||||||
| chr17:10349837
|
C | T | 1 | a0001c0089t0001g0184 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1144+719G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 12/40 | chr17 | 10349837 | ||||||
| chr17:10349934
|
C | T | 1 | a0005c0016t0001g0091 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1144+622G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 12/40 | chr17 | 10349934 | ||||||
| chr17:10349971
|
T | C | 32 | a0001c0003t0001g0241a0001c0003t0001g0243a0001c0003t0001g0244others(29): Show | 32 | HG00423.hp2 HG00544.hp1 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.1144+585A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 12/40 | chr17 | 10349971 | ||||||
| chr17:10350024
|
G | A | 1 | a0001c0004t0001g0328 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1144+532C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 12/40 | chr17 | 10350024 | ||||||
| chr17:10350043
|
G | A | 1 | a0001c0006t0001g0126 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1144+513C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 12/40 | chr17 | 10350043 | ||||||
| chr17:10350048
|
T | A | 1 | a0001c0089t0001g0184 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1144+508A>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 12/40 | chr17 | 10350048 | ||||||
| chr17:10350313
|
C | G | 33 | a0001c0003t0001g0241a0001c0003t0001g0243a0001c0003t0001g0244others(30): Show | 33 | HG00423.hp2 HG00544.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.1144+243G>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 12/40 | chr17 | 10350313 | ||||||
| chr17:10350416
|
A | G | 1 | a0001c0111t0001g0078 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1144+140T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 12/40 | chr17 | 10350416 | ||||||
| chr17:10350531
|
G | T | 7 | a0001c0004t0001g0169a0001c0004t0001g0170a0001c0103t0001g0174others(4): Show | 7 | HG02109.hp1 HG02559.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1144+25C>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 12/40 | chr17 | 10350531 | ||||||
| chr17:10350817
|
G | A | 2 | a0008c0044t0001g0138a0008c0044t0001g0139 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1006-123C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10350817 | ||||||
| chr17:10350880
|
A | G | 373 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(370): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.1006-186T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10350880 | ||||||
| chr17:10350895
|
A | G | 2 | a0001c0003t0001g0227a0001c0003t0001g0228 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1006-201T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10350895 | ||||||
| chr17:10350897
|
A | G | 14 | a0001c0014t0001g0010a0001c0015t0001g0011a0001c0015t0001g0014others(11): Show | 14 | HG00423.hp2 HG00544.hp1 NA18944.hp2 others(11): Show |
intron_variant | MODIFIER | c.1006-203T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10350897 | ||||||
| chr17:10350948
|
G | A | 1 | a0004c0010t0001g0329 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1006-254C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10350948 | ||||||
| chr17:10350992
|
C | T | 1 | a0002c0094t0001g0226 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1006-298G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10350992 | ||||||
| chr17:10350993
|
A | G | 1 | a0002c0094t0001g0226 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1006-299T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10350993 | ||||||
| chr17:10351001
|
T | C | 1 | a0002c0094t0001g0226 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1006-307A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10351001 | ||||||
| chr17:10351004
|
G | A | 1 | a0002c0094t0001g0226 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1006-310C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10351004 | ||||||
| chr17:10351015
|
T | A | 1 | a0002c0094t0001g0226 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1006-321A>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10351015 | ||||||
| chr17:10351017
|
T | C | 1 | a0002c0094t0001g0226 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1006-323A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10351017 | ||||||
| chr17:10351018
|
G | A | 1 | a0002c0094t0001g0226 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1006-324C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10351018 | ||||||
| chr17:10351040
|
C | T | 247 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(244): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.1006-346G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10351040 | ||||||
| chr17:10351043
|
C | A | 2 | a0001c0089t0001g0184a0001c0111t0001g0078 | 2 | HG01109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1006-349G>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10351043 | ||||||
| chr17:10351171
|
A | G | 1 | a0003c0005t0001g0046 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1006-477T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10351171 | ||||||
| chr17:10351177
|
T | C | 2 | a0001c0089t0001g0184a0001c0111t0001g0078 | 2 | HG01109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1006-483A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10351177 | ||||||
| chr17:10351201
|
A | T | 1 | a0009c0049t0001g0248 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1006-507T>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10351201 | ||||||
| chr17:10351219
|
T | TAAAAAAA others(12): Show |
1 | a0004c0002t0001g0134 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1006-526_1006-525i others(21): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10351219 | ||||||
| chr17:10351220
|
C | A | 1 | a0004c0002t0001g0134 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1006-526G>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10351220 | ||||||
| chr17:10351220
|
C | CAAAAAAA | 7 | a0001c0012t0001g0267a0001c0012t0001g0272a0001c0027t0001g0266others(4): Show | 7 | HG01106.hp1 HG02486.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1006-533_1006-527d others(9): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10351220 | ||||||
| chr17:10351220
|
C | CAAAAAAA others(2): Show |
14 | a0001c0007t0001g0307a0001c0014t0001g0219a0001c0075t0001g0358others(11): Show | 14 | HG01243.hp1 HG02027.hp2 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.1006-535_1006-527d others(11): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10351220 | ||||||
| chr17:10351220
|
C | CAAAAAAA others(3): Show |
76 | a0001c0004t0001g0328a0001c0004t0001g0344a0001c0004t0001g0346others(73): Show | 76 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.1006-536_1006-527d others(12): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10351220 | ||||||
| chr17:10351220
|
C | CAAAAAAA others(4): Show |
27 | a0001c0004t0001g0345a0001c0007t0001g0289a0001c0007t0001g0336others(24): Show | 27 | HG00735.hp1 HG01167.hp1 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.1006-537_1006-527d others(13): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10351220 | ||||||
| chr17:10351220
|
C | CAAAAAAA others(5): Show |
4 | a0001c0003t0001g0008a0001c0089t0001g0184a0003c0009t0002g0003others(1): Show | 4 | HG02145.hp2 HG02486.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.1006-538_1006-527d others(14): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10351220 | ||||||
| chr17:10351220
|
C | CAAAAAAA others(6): Show |
16 | a0001c0027t0001g0154a0001c0027t0001g0161a0001c0034t0001g0168others(13): Show | 16 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.1006-539_1006-527d others(15): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10351220 | ||||||
| chr17:10351220
|
C | CAAAAAAA others(7): Show |
8 | a0001c0027t0001g0009a0001c0034t0001g0152a0003c0013t0001g0019others(5): Show | 8 | HG01099.hp2 HG01109.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.1006-540_1006-527d others(16): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10351220 | ||||||
| chr17:10351220
|
C | CAAAAAAA others(8): Show |
8 | a0001c0014t0001g0010a0001c0015t0001g0011a0001c0015t0001g0014others(5): Show | 8 | HG00423.hp2 HG04115.hp1 NA18944.hp2 others(5): Show |
intron_variant | MODIFIER | c.1006-541_1006-527d others(17): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10351220 | ||||||
| chr17:10351220
|
C | CAAAAAAA others(9): Show |
2 | a0003c0013t0001g0017a0005c0079t0001g0013 | 2 | HG00544.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1006-527_1006-526i others(18): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10351220 | ||||||
| chr17:10351220
|
C | CAAAAAAA others(10): Show |
2 | a0005c0018t0001g0018a0025c0074t0001g0076 | 2 | HG02258.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1006-527_1006-526i others(19): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10351220 | ||||||
| chr17:10351220
|
C | CAAAAAAA others(11): Show |
6 | a0001c0004t0001g0027a0001c0119t0001g0274a0002c0011t0001g0081others(3): Show | 6 | HG01169.hp2 HG01515.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1006-527_1006-526i others(20): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10351220 | ||||||
| chr17:10351220
|
C | CAAAAAAA others(12): Show |
35 | a0001c0003t0001g0032a0001c0003t0001g0043a0001c0003t0001g0044others(32): Show | 35 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.1006-527_1006-526i others(21): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10351220 | ||||||
| chr17:10351220
|
C | CAAAAAAA others(13): Show |
21 | a0001c0003t0001g0045a0001c0003t0001g0049a0001c0003t0001g0069others(18): Show | 21 | HG00423.hp1 HG00621.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.1006-527_1006-526i others(22): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10351220 | ||||||
| chr17:10351220
|
C | CAAAAAAA others(14): Show |
7 | a0001c0003t0001g0063a0001c0004t0001g0030a0001c0007t0001g0007others(4): Show | 7 | HG00408.hp2 HG00738.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.1006-527_1006-526i others(23): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10351220 | ||||||
| chr17:10351220
|
C | CAAAAAAA others(15): Show |
2 | a0013c0116t0001g0087a0028c0098t0001g0024 | 2 | HG02074.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1006-527_1006-526i others(24): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10351220 | ||||||
| chr17:10351234
|
A | AAAAAAAA others(5): Show |
2 | a0001c0003t0001g0249a0001c0051t0001g0245 | 2 | HG02135.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1006-541_1006-540i others(14): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10351234 | ||||||
| chr17:10351234
|
A | AAAAAAAA others(4): Show |
6 | a0001c0003t0001g0241a0001c0003t0001g0243a0001c0003t0001g0244others(3): Show | 6 | HG01928.hp1 HG01934.hp2 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.1006-541_1006-540i others(13): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10351234 | ||||||
| chr17:10351236
|
G | A | 1 | a0001c0111t0001g0078 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1006-542C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10351236 | ||||||
| chr17:10351573
|
C | T | 19 | a0001c0014t0001g0100a0001c0014t0001g0110a0001c0014t0001g0136others(16): Show | 19 | HG01167.hp1 HG01169.hp1 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.1006-879G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10351573 | ||||||
| chr17:10351622
|
A | T | 73 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(70): Show | 73 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.1006-928T>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10351622 | ||||||
| chr17:10351633
|
A | G | 8 | a0001c0003t0001g0241a0001c0003t0001g0243a0001c0003t0001g0244others(5): Show | 8 | HG01928.hp1 HG01934.hp2 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.1006-939T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10351633 | ||||||
| chr17:10351695
|
G | C | 141 | a0001c0004t0001g0328a0001c0004t0001g0344a0001c0004t0001g0345others(138): Show | 141 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.1006-1001C>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10351695 | ||||||
| chr17:10351699
|
C | T | 30 | a0001c0003t0001g0241a0001c0003t0001g0243a0001c0003t0001g0244others(27): Show | 30 | HG00423.hp2 HG00544.hp1 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.1006-1005G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10351699 | ||||||
| chr17:10351888
|
C | G | 32 | a0001c0003t0001g0241a0001c0003t0001g0243a0001c0003t0001g0244others(29): Show | 32 | HG00423.hp2 HG00544.hp1 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.1006-1194G>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10351888 | ||||||
| chr17:10351942
|
A | G | 3 | a0001c0089t0001g0184a0001c0111t0001g0078a0009c0049t0001g0248 | 3 | HG01109.hp1 HG02486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1006-1248T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10351942 | ||||||
| chr17:10351943
|
T | G | 1 | a0001c0119t0001g0274 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1006-1249A>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10351943 | ||||||
| chr17:10351959
|
C | T | 1 | a0001c0004t0001g0236 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1006-1265G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10351959 | ||||||
| chr17:10352270
|
A | C | 1 | a0002c0001t0001g0275 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1006-1576T>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10352270 | ||||||
| chr17:10352271
|
A | T | 1 | a0002c0001t0001g0275 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1006-1577T>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10352271 | ||||||
| chr17:10352274
|
G | A | 1 | a0002c0001t0001g0275 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1006-1580C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10352274 | ||||||
| chr17:10352275
|
G | T | 1 | a0002c0001t0001g0275 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1006-1581C>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10352275 | ||||||
| chr17:10352276
|
A | C | 1 | a0002c0001t0001g0275 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1006-1582T>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10352276 | ||||||
| chr17:10352278
|
A | C | 1 | a0002c0001t0001g0275 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1006-1584T>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10352278 | ||||||
| chr17:10352279
|
C | G | 1 | a0002c0001t0001g0275 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1006-1585G>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10352279 | ||||||
| chr17:10352281
|
A | G | 1 | a0002c0001t0001g0275 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1006-1587T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10352281 | ||||||
| chr17:10352284
|
C | T | 1 | a0002c0001t0001g0275 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1006-1590G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10352284 | ||||||
| chr17:10352289
|
C | A | 1 | a0001c0004t0001g0077 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1006-1595G>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10352289 | ||||||
| chr17:10352294
|
T | A | 1 | a0024c0073t0001g0050 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1006-1600A>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10352294 | ||||||
| chr17:10352317
|
C | T | 3 | a0001c0006t0001g0105a0002c0070t0001g0106a0003c0005t0001g0147 | 3 | HG01261.hp1 HG01346.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.1006-1623G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10352317 | ||||||
| chr17:10352341
|
C | T | 62 | a0001c0003t0001g0203a0001c0003t0001g0204a0001c0003t0001g0205others(59): Show | 63 | HG00438.hp1 HG01081.hp1 HG01123.hp1 others(60): Show |
intron_variant | MODIFIER | c.1006-1647G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10352341 | ||||||
| chr17:10352356
|
C | T | 1 | a0002c0001t0001g0258 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1006-1662G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10352356 | ||||||
| chr17:10352378
|
C | T | 2 | a0001c0089t0001g0184a0001c0111t0001g0078 | 2 | HG01109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1006-1684G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10352378 | ||||||
| chr17:10352587
|
C | CA | 125 | a0001c0004t0001g0328a0001c0004t0001g0344a0001c0004t0001g0345others(122): Show | 125 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.1006-1894dupT | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10352587 | ||||||
| chr17:10352611
|
C | A | 3 | a0001c0007t0001g0006a0001c0007t0001g0007a0037c0100t0001g0064 | 3 | HG00408.hp2 HG00423.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1006-1917G>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10352611 | ||||||
| chr17:10352647
|
G | A | 1 | a0001c0119t0001g0274 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1006-1953C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10352647 | ||||||
| chr17:10352667
|
T | C | 2 | a0001c0089t0001g0184a0001c0111t0001g0078 | 2 | HG01109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1006-1973A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10352667 | ||||||
| chr17:10352696
|
T | A | 22 | a0001c0003t0001g0203a0001c0003t0001g0204a0001c0003t0001g0205others(19): Show | 23 | HG01081.hp1 HG01257.hp1 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.1005+1984A>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10352696 | ||||||
| chr17:10352778
|
G | A | 1 | a0001c0014t0001g0219 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1005+1902C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10352778 | ||||||
| chr17:10352815
|
A | G | 1 | a0001c0014t0001g0219 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1005+1865T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10352815 | ||||||
| chr17:10353068
|
A | AT | 123 | a0001c0004t0001g0328a0001c0004t0001g0344a0001c0004t0001g0345others(120): Show | 123 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.1005+1611dupA | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10353068 | ||||||
| chr17:10353141
|
T | C | 1 | a0001c0089t0001g0184 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1005+1539A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10353141 | ||||||
| chr17:10353209
|
T | C | 62 | a0001c0003t0001g0203a0001c0003t0001g0204a0001c0003t0001g0205others(59): Show | 63 | HG00438.hp1 HG01081.hp1 HG01123.hp1 others(60): Show |
intron_variant | MODIFIER | c.1005+1471A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10353209 | ||||||
| chr17:10353244
|
A | G | 2 | a0001c0089t0001g0184a0001c0111t0001g0078 | 2 | HG01109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1005+1436T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10353244 | ||||||
| chr17:10353406
|
C | A | 1 | a0003c0013t0001g0021 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1005+1274G>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10353406 | ||||||
| chr17:10353464
|
A | C | 2 | a0001c0089t0001g0184a0001c0111t0001g0078 | 2 | HG01109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1005+1216T>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10353464 | ||||||
| chr17:10353477
|
G | A | 2 | a0001c0089t0001g0184a0001c0111t0001g0078 | 2 | HG01109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1005+1203C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10353477 | ||||||
| chr17:10353515
|
C | T | 30 | a0001c0003t0001g0241a0001c0003t0001g0243a0001c0003t0001g0244others(27): Show | 30 | HG00423.hp2 HG00544.hp1 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.1005+1165G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10353515 | ||||||
| chr17:10353549
|
T | A | 2 | a0001c0089t0001g0184a0001c0111t0001g0078 | 2 | HG01109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1005+1131A>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10353549 | ||||||
| chr17:10353611
|
T | C | 1 | a0001c0003t0001g0204 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1005+1069A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10353611 | ||||||
| chr17:10353639
|
T | C | 2 | a0001c0089t0001g0184a0001c0111t0001g0078 | 2 | HG01109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1005+1041A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10353639 | ||||||
| chr17:10353685
|
C | T | 252 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(249): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.1005+995G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10353685 | ||||||
| chr17:10353908
|
G | A | 317 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(314): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.1005+772C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10353908 | ||||||
| chr17:10353931
|
A | AGAAG | 44 | a0001c0003t0001g0205a0001c0004t0001g0344a0001c0004t0001g0345others(41): Show | 45 | HG00621.hp1 HG00735.hp1 HG01070.hp1 others(42): Show |
intron_variant | MODIFIER | c.1005+745_1005+748d others(6): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10353931 | ||||||
| chr17:10353931
|
A | AGAAGGAA others(1): Show |
18 | a0001c0003t0001g0203a0001c0003t0001g0204a0001c0006t0001g0198others(15): Show | 18 | HG00639.hp2 HG00738.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.1005+741_1005+748d others(10): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10353931 | ||||||
| chr17:10353931
|
A | AGAAGGAA others(5): Show |
15 | a0001c0027t0001g0009a0001c0027t0001g0154a0001c0027t0001g0161others(12): Show | 15 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.1005+737_1005+748d others(14): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10353931 | ||||||
| chr17:10353931
|
A | AGAAGGAA others(9): Show |
9 | a0001c0015t0001g0014a0001c0111t0001g0078a0002c0030t0001g0020others(6): Show | 9 | HG00423.hp2 HG00735.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1005+733_1005+748d others(18): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10353931 | ||||||
| chr17:10353931
|
A | AGAAGGAA others(13): Show |
9 | a0001c0014t0001g0010a0001c0015t0001g0011a0002c0030t0001g0022others(6): Show | 9 | HG00544.hp1 NA18953.hp1 NA18954.hp2 others(6): Show |
intron_variant | MODIFIER | c.1005+729_1005+748d others(22): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10353931 | ||||||
| chr17:10353931
|
AGAAG | A | 92 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(89): Show | 92 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.1005+745_1005+748d others(6): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10353931 | ||||||
| chr17:10353963
|
G | A | 1 | a0004c0010t0001g0073 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1005+717C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10353963 | ||||||
| chr17:10353973
|
G | A | 1 | a0001c0014t0001g0219 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1005+707C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10353973 | ||||||
| chr17:10353986
|
A | G | 16 | a0001c0003t0001g0241a0001c0003t0001g0243a0001c0003t0001g0244others(13): Show | 16 | HG01099.hp2 HG01928.hp1 HG01934.hp2 others(13): Show |
intron_variant | MODIFIER | c.1005+694T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10353986 | ||||||
| chr17:10354314
|
A | T | 316 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(313): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.1005+366T>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10354314 | ||||||
| chr17:10354338
|
T | C | 2 | a0002c0001t0001g0253a0030c0084t0001g0254 | 2 | NA18998.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1005+342A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10354338 | ||||||
| chr17:10354356
|
G | A | 3 | a0001c0027t0001g0161a0004c0026t0001g0153a0004c0026t0001g0167 | 3 | HG00733.hp2 HG01099.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.1005+324C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10354356 | ||||||
| chr17:10354416
|
G | C | 30 | a0001c0003t0001g0241a0001c0003t0001g0243a0001c0003t0001g0244others(27): Show | 30 | HG00423.hp2 HG00544.hp1 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.1005+264C>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10354416 | ||||||
| chr17:10354551
|
C | G | 1 | a0001c0111t0001g0078 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1005+129G>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10354551 | ||||||
| chr17:10354620
|
C | T | 6 | a0001c0003t0001g0227a0001c0003t0001g0228a0001c0003t0001g0232others(3): Show | 6 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.1005+60G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10354620 | ||||||
| chr17:10354835
|
T | G | 1 | a0007c0020t0001g0121 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.902-52A>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 10/40 | chr17 | 10354835 | ||||||
| chr17:10354836
|
GT | G | 219 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.902-54delA | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 10/40 | chr17 | 10354836 | ||||||
| chr17:10354838
|
T | C | 219 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.902-55A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 10/40 | chr17 | 10354838 | ||||||
| chr17:10354844
|
T | C | 1 | a0001c0090t0001g0364 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.901+51A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 10/40 | chr17 | 10354844 | ||||||
| chr17:10355165
|
G | A | 2 | a0001c0089t0001g0184a0001c0111t0001g0078 | 2 | HG01109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.739-18C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 8/40 | chr17 | 10355165 | ||||||
| chr17:10355177
|
G | A | 1 | a0001c0119t0001g0274 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.739-30C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 8/40 | chr17 | 10355177 | ||||||
| chr17:10355470
|
G | A | 19 | a0001c0014t0001g0100a0001c0014t0001g0110a0001c0014t0001g0136others(16): Show | 19 | HG01167.hp1 HG01169.hp1 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.739-323C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 8/40 | chr17 | 10355470 | ||||||
| chr17:10355542
|
A | G | 1 | a0001c0015t0001g0092 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.739-395T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 8/40 | chr17 | 10355542 | ||||||
| chr17:10355664
|
G | C | 23 | a0001c0027t0001g0009a0001c0027t0001g0154a0001c0027t0001g0161others(20): Show | 23 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.739-517C>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 8/40 | chr17 | 10355664 | ||||||
| chr17:10355828
|
C | CT | 9 | a0001c0006t0001g0140a0002c0011t0001g0081a0003c0005t0001g0046others(6): Show | 9 | HG01069.hp1 HG01074.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.739-682dupA | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 8/40 | chr17 | 10355828 | ||||||
| chr17:10355828
|
CT | C | 13 | a0001c0006t0001g0001a0001c0006t0001g0085a0001c0006t0001g0105others(10): Show | 14 | HG00140.hp2 HG01261.hp1 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.739-682delA | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 8/40 | chr17 | 10355828 | ||||||
| chr17:10355828
|
CTT | C | 8 | a0001c0006t0001g0132a0002c0038t0001g0133a0002c0064t0001g0196others(5): Show | 8 | HG01934.hp1 NA18522.hp2 NA18951.hp1 others(5): Show |
intron_variant | MODIFIER | c.739-683_739-682del others(2): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 8/40 | chr17 | 10355828 | ||||||
| chr17:10355828
|
CTTT | C | 8 | a0001c0006t0001g0198a0001c0006t0001g0218a0001c0022t0001g0149others(5): Show | 8 | HG00639.hp2 HG01891.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.739-684_739-682del others(3): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 8/40 | chr17 | 10355828 | ||||||
| chr17:10355828
|
CTTTTTTT others(6): Show |
C | 2 | a0004c0002t0001g0208a0004c0002t0001g0231 | 2 | NA18954.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.739-694_739-682del others(13): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 8/40 | chr17 | 10355828 | ||||||
| chr17:10355828
|
CTTTTTTT others(7): Show |
C | 3 | a0001c0004t0001g0169a0002c0001t0001g0275a0006c0033t0001g0185 | 3 | HG02559.hp1 HG02647.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.739-695_739-682del others(14): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 8/40 | chr17 | 10355828 | ||||||
| chr17:10355828
|
CTTTTTTT others(8): Show |
C | 64 | a0001c0003t0001g0049a0001c0003t0001g0203a0001c0003t0001g0204others(61): Show | 65 | HG00438.hp1 HG01081.hp1 HG01123.hp1 others(62): Show |
intron_variant | MODIFIER | c.739-696_739-682del others(15): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 8/40 | chr17 | 10355828 | ||||||
| chr17:10355828
|
CTTTTTTT others(9): Show |
C | 168 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.739-697_739-682del others(16): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 8/40 | chr17 | 10355828 | ||||||
| chr17:10355828
|
CTTTTTTT others(10): Show |
C | 50 | a0001c0004t0001g0031a0001c0007t0001g0376a0001c0012t0001g0267others(47): Show | 50 | HG00140.hp1 HG00323.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.739-698_739-682del others(17): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 8/40 | chr17 | 10355828 | ||||||
| chr17:10355828
|
CTTTTTTT others(11): Show |
C | 16 | a0001c0014t0001g0010a0001c0015t0001g0011a0001c0015t0001g0014others(13): Show | 16 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(13): Show |
intron_variant | MODIFIER | c.739-699_739-682del others(18): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 8/40 | chr17 | 10355828 | ||||||
| chr17:10355828
|
CTTTTTTT others(15): Show |
C | 2 | a0001c0089t0001g0184a0001c0119t0001g0274 | 2 | HG02257.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.739-703_739-682del others(22): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 8/40 | chr17 | 10355828 | ||||||
| chr17:10355828
|
CTTTTTTT others(17): Show |
C | 8 | a0001c0003t0001g0241a0001c0003t0001g0243a0001c0003t0001g0244others(5): Show | 8 | HG01928.hp1 HG01934.hp2 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.739-705_739-682del others(24): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 8/40 | chr17 | 10355828 | ||||||
| chr17:10355991
|
A | T | 2 | a0001c0089t0001g0184a0001c0111t0001g0078 | 2 | HG01109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.739-844T>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 8/40 | chr17 | 10355991 | ||||||
| chr17:10356084
|
A | G | 2 | a0004c0048t0001g0207a0005c0018t0001g0206 | 2 | NA18974.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.739-937T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 8/40 | chr17 | 10356084 | ||||||
| chr17:10356105
|
C | T | 2 | a0001c0014t0001g0219a0003c0009t0001g0305 | 2 | HG01243.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.739-958G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 8/40 | chr17 | 10356105 | ||||||
| chr17:10356123
|
T | C | 211 | a0001c0003t0001g0203a0001c0003t0001g0204a0001c0003t0001g0205others(208): Show | 212 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.739-976A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 8/40 | chr17 | 10356123 | ||||||
| chr17:10356230
|
G | A | 1 | a0006c0052t0001g0242 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.739-1083C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 8/40 | chr17 | 10356230 | ||||||
| chr17:10356303
|
A | G | 2 | a0001c0089t0001g0184a0001c0111t0001g0078 | 2 | HG01109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.739-1156T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 8/40 | chr17 | 10356303 | ||||||
| chr17:10356711
|
G | A | 30 | a0001c0003t0001g0241a0001c0003t0001g0243a0001c0003t0001g0244others(27): Show | 30 | HG00423.hp2 HG00544.hp1 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.738+1024C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 8/40 | chr17 | 10356711 | ||||||
| chr17:10356826
|
G | C | 2 | a0001c0014t0001g0136a0001c0110t0001g0108 | 2 | HG01255.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.738+909C>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 8/40 | chr17 | 10356826 | ||||||
| chr17:10356886
|
G | A | 1 | a0001c0007t0001g0107 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.738+849C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 8/40 | chr17 | 10356886 | ||||||
| chr17:10356937
|
A | G | 1 | a0005c0087t0001g0290 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.738+798T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 8/40 | chr17 | 10356937 | ||||||
| chr17:10356983
|
C | T | 1 | a0001c0075t0001g0358 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.738+752G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 8/40 | chr17 | 10356983 | ||||||
| chr17:10357003
|
C | T | 114 | a0001c0004t0001g0328a0001c0004t0001g0344a0001c0004t0001g0345others(111): Show | 114 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.738+732G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 8/40 | chr17 | 10357003 | ||||||
| chr17:10357029
|
C | T | 14 | a0001c0012t0001g0267a0001c0012t0001g0272a0001c0022t0001g0292others(11): Show | 14 | HG00438.hp2 HG00741.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.738+706G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 8/40 | chr17 | 10357029 | ||||||
| chr17:10357030
|
G | A | 3 | a0001c0007t0001g0376a0003c0009t0001g0373a0003c0009t0001g0377 | 3 | HG02965.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.738+705C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 8/40 | chr17 | 10357030 | ||||||
| chr17:10357036
|
C | T | 13 | a0001c0003t0001g0233a0001c0004t0001g0169a0001c0004t0001g0170others(10): Show | 13 | HG02109.hp1 HG02559.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.738+699G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 8/40 | chr17 | 10357036 | ||||||
| chr17:10357043
|
C | T | 1 | a0009c0049t0001g0248 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.738+692G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 8/40 | chr17 | 10357043 | ||||||
| chr17:10357063
|
C | T | 1 | a0001c0014t0001g0219 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.738+672G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 8/40 | chr17 | 10357063 | ||||||
| chr17:10357134
|
G | T | 1 | a0005c0028t0001g0363 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.738+601C>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 8/40 | chr17 | 10357134 | ||||||
| chr17:10357210
|
C | G | 1 | a0001c0017t0001g0129 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.738+525G>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 8/40 | chr17 | 10357210 | ||||||
| chr17:10357252
|
G | A | 1 | a0003c0008t0001g0238 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.738+483C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 8/40 | chr17 | 10357252 | ||||||
| chr17:10357253
|
C | T | 16 | a0001c0003t0001g0241a0001c0003t0001g0243a0001c0003t0001g0244others(13): Show | 16 | HG01099.hp2 HG01928.hp1 HG01934.hp2 others(13): Show |
intron_variant | MODIFIER | c.738+482G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 8/40 | chr17 | 10357253 | ||||||
| chr17:10357369
|
C | T | 3 | a0001c0022t0001g0181a0003c0005t0001g0215a0041c0069t0001g0200 | 3 | HG02559.hp2 HG02922.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.738+366G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 8/40 | chr17 | 10357369 | ||||||
| chr17:10357397
|
T | C | 32 | a0001c0003t0001g0241a0001c0003t0001g0243a0001c0003t0001g0244others(29): Show | 32 | HG00423.hp2 HG00544.hp1 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.738+338A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 8/40 | chr17 | 10357397 | ||||||
| chr17:10357618
|
C | G | 31 | a0001c0003t0001g0241a0001c0003t0001g0243a0001c0003t0001g0244others(28): Show | 31 | HG00423.hp2 HG00544.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.738+117G>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 8/40 | chr17 | 10357618 | ||||||
| chr17:10358036
|
G | C | 1 | a0002c0001t0001g0250 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.646-209C>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 7/40 | chr17 | 10358036 | ||||||
| chr17:10358039
|
T | C | 6 | a0001c0006t0001g0084a0001c0006t0001g0085a0001c0017t0001g0086others(3): Show | 6 | HG03710.hp2 NA18952.hp2 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.646-212A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 7/40 | chr17 | 10358039 | ||||||
| chr17:10358203
|
C | G | 31 | a0001c0003t0001g0241a0001c0003t0001g0243a0001c0003t0001g0244others(28): Show | 31 | HG00423.hp2 HG00544.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.646-376G>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 7/40 | chr17 | 10358203 | ||||||
| chr17:10358233
|
G | A | 1 | a0001c0015t0001g0092 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.646-406C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 7/40 | chr17 | 10358233 | ||||||
| chr17:10358366
|
G | A | 2 | a0001c0089t0001g0184a0001c0111t0001g0078 | 2 | HG01109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.646-539C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 7/40 | chr17 | 10358366 | ||||||
| chr17:10358404
|
T | C | 62 | a0001c0003t0001g0203a0001c0003t0001g0204a0001c0003t0001g0205others(59): Show | 63 | HG00438.hp1 HG01081.hp1 HG01123.hp1 others(60): Show |
intron_variant | MODIFIER | c.646-577A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 7/40 | chr17 | 10358404 | ||||||
| chr17:10358440
|
A | G | 70 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(67): Show | 70 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.646-613T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 7/40 | chr17 | 10358440 | ||||||
| chr17:10358506
|
T | C | 3 | a0001c0006t0001g0132a0002c0065t0001g0079a0003c0005t0001g0122 | 3 | HG03098.hp2 NA18979.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.646-679A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 7/40 | chr17 | 10358506 | ||||||
| chr17:10358551
|
G | A | 3 | a0001c0006t0001g0105a0002c0070t0001g0106a0003c0005t0001g0147 | 3 | HG01261.hp1 HG01346.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.646-724C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 7/40 | chr17 | 10358551 | ||||||
| chr17:10358625
|
G | A | 1 | a0001c0007t0001g0336 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.646-798C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 7/40 | chr17 | 10358625 | ||||||
| chr17:10358628
|
G | A | 1 | a0025c0074t0001g0076 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.646-801C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 7/40 | chr17 | 10358628 | ||||||
| chr17:10358663
|
A | G | 1 | a0005c0028t0001g0363 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.646-836T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 7/40 | chr17 | 10358663 | ||||||
| chr17:10358665
|
G | A | 1 | a0009c0049t0001g0248 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.646-838C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 7/40 | chr17 | 10358665 | ||||||
| chr17:10358705
|
G | C | 1 | a0009c0049t0001g0248 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.646-878C>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 7/40 | chr17 | 10358705 | ||||||
| chr17:10358985
|
A | G | 1 | a0001c0089t0001g0184 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.645+975T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 7/40 | chr17 | 10358985 | ||||||
| chr17:10359132
|
T | A | 1 | a0002c0001t0001g0250 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.645+828A>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 7/40 | chr17 | 10359132 | ||||||
| chr17:10359132
|
T | C | 61 | a0001c0003t0001g0203a0001c0003t0001g0204a0001c0003t0001g0205others(58): Show | 62 | HG00438.hp1 HG01081.hp1 HG01123.hp1 others(59): Show |
intron_variant | MODIFIER | c.645+828A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 7/40 | chr17 | 10359132 | ||||||
| chr17:10359258
|
A | G | 2 | a0001c0089t0001g0184a0001c0111t0001g0078 | 2 | HG01109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.645+702T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 7/40 | chr17 | 10359258 | ||||||
| chr17:10359496
|
A | C | 1 | a0020c0112t0001g0067 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.645+464T>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 7/40 | chr17 | 10359496 | ||||||
| chr17:10359542
|
C | T | 29 | a0001c0003t0001g0241a0001c0003t0001g0243a0001c0003t0001g0244others(26): Show | 29 | HG00423.hp2 HG00544.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.645+418G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 7/40 | chr17 | 10359542 | ||||||
| chr17:10359555
|
C | T | 31 | a0001c0003t0001g0241a0001c0003t0001g0243a0001c0003t0001g0244others(28): Show | 31 | HG00423.hp2 HG00544.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.645+405G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 7/40 | chr17 | 10359555 | ||||||
| chr17:10359618
|
A | G | 1 | a0003c0041t0001g0365 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.645+342T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 7/40 | chr17 | 10359618 | ||||||
| chr17:10359619
|
G | A | 1 | a0003c0005t0001g0299 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.645+341C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 7/40 | chr17 | 10359619 | ||||||
| chr17:10359625
|
G | A | 1 | a0033c0077t0001g0355 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.645+335C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 7/40 | chr17 | 10359625 | ||||||
| chr17:10359672
|
C | T | 1 | a0003c0025t0001g0166 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.645+288G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 7/40 | chr17 | 10359672 | ||||||
| chr17:10359683
|
G | A | 18 | a0001c0027t0001g0009a0001c0027t0001g0154a0001c0027t0001g0161others(15): Show | 18 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.645+277C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 7/40 | chr17 | 10359683 | ||||||
| chr17:10359727
|
G | C | 14 | a0001c0014t0001g0010a0001c0015t0001g0011a0001c0015t0001g0014others(11): Show | 14 | HG00423.hp2 HG00544.hp1 NA18944.hp2 others(11): Show |
intron_variant | MODIFIER | c.645+233C>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 7/40 | chr17 | 10359727 | ||||||
| chr17:10359792
|
A | T | 3 | a0004c0021t0001g0093a0004c0021t0001g0094a0036c0067t0001g0104 | 3 | HG01069.hp1 HG01074.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.645+168T>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 7/40 | chr17 | 10359792 | ||||||
| chr17:10359795
|
C | T | 29 | a0001c0003t0001g0241a0001c0003t0001g0243a0001c0003t0001g0244others(26): Show | 29 | HG00423.hp2 HG00544.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.645+165G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 7/40 | chr17 | 10359795 | ||||||
| chr17:10359845
|
A | G | 29 | a0001c0003t0001g0241a0001c0003t0001g0243a0001c0003t0001g0244others(26): Show | 29 | HG00423.hp2 HG00544.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.645+115T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 7/40 | chr17 | 10359845 | ||||||
| chr17:10359861
|
G | A | 29 | a0001c0003t0001g0241a0001c0003t0001g0243a0001c0003t0001g0244others(26): Show | 29 | HG00423.hp2 HG00544.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.645+99C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 7/40 | chr17 | 10359861 | ||||||
| chr17:10359938
|
G | A | 14 | a0001c0014t0001g0010a0001c0015t0001g0011a0001c0015t0001g0014others(11): Show | 14 | HG00423.hp2 HG00544.hp1 NA18944.hp2 others(11): Show |
intron_variant | MODIFIER | c.645+22C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 7/40 | chr17 | 10359938 | ||||||
| chr17:10359944
|
A | G | 1 | a0041c0069t0001g0200 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.645+16T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 7/40 | chr17 | 10359944 | ||||||
| chr17:10360255
|
A | T | 18 | a0001c0027t0001g0009a0001c0027t0001g0154a0001c0027t0001g0161others(15): Show | 18 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.506-67T>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 5/40 | chr17 | 10360255 | ||||||
| chr17:10360276
|
T | C | 1 | a0003c0005t0001g0295 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.506-88A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 5/40 | chr17 | 10360276 | ||||||
| chr17:10360281
|
T | C | 11 | a0001c0006t0001g0084a0001c0006t0001g0085a0001c0006t0001g0126others(8): Show | 11 | HG01070.hp1 HG01071.hp1 HG03654.hp1 others(8): Show |
intron_variant | MODIFIER | c.506-93A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 5/40 | chr17 | 10360281 | ||||||
| chr17:10360300
|
A | G | 1 | a0001c0111t0001g0078 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.506-112T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 5/40 | chr17 | 10360300 | ||||||
| chr17:10360307
|
A | G | 1 | a0001c0111t0001g0078 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.506-119T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 5/40 | chr17 | 10360307 | ||||||
| chr17:10360650
|
G | C | 2 | a0004c0026t0001g0165a0007c0107t0001g0162 | 2 | HG01256.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.506-462C>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 5/40 | chr17 | 10360650 | ||||||
| chr17:10360711
|
A | G | 115 | a0001c0003t0001g0203a0001c0003t0001g0204a0001c0003t0001g0205others(112): Show | 116 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.506-523T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 5/40 | chr17 | 10360711 | ||||||
| chr17:10360905
|
A | G | 111 | a0001c0003t0001g0269a0001c0004t0001g0328a0001c0004t0001g0344others(108): Show | 111 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.506-717T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 5/40 | chr17 | 10360905 | ||||||
| chr17:10360948
|
A | G | 1 | a0001c0090t0001g0364 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.506-760T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 5/40 | chr17 | 10360948 | ||||||
| chr17:10360982
|
C | T | 1 | a0006c0024t0001g0340 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.506-794G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 5/40 | chr17 | 10360982 | ||||||
| chr17:10361088
|
T | A | 1 | a0003c0008t0001g0338 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.506-900A>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 5/40 | chr17 | 10361088 | ||||||
| chr17:10361149
|
A | G | 1 | a0012c0058t0001g0142 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.506-961T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 5/40 | chr17 | 10361149 | ||||||
| chr17:10361235
|
A | G | 80 | a0001c0003t0001g0203a0001c0003t0001g0204a0001c0003t0001g0205others(77): Show | 81 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.505+883T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 5/40 | chr17 | 10361235 | ||||||
| chr17:10361292
|
C | CT | 119 | a0001c0003t0001g0269a0001c0004t0001g0328a0001c0004t0001g0344others(116): Show | 119 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.505+825dupA | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 5/40 | chr17 | 10361292 | ||||||
| chr17:10361292
|
CT | C | 11 | a0001c0007t0001g0376a0001c0014t0001g0375a0001c0042t0001g0199others(8): Show | 11 | HG02897.hp2 HG02965.hp1 HG02976.hp1 others(8): Show |
intron_variant | MODIFIER | c.505+825delA | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 5/40 | chr17 | 10361292 | ||||||
| chr17:10361353
|
G | A | 1 | a0001c0111t0001g0078 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.505+765C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 5/40 | chr17 | 10361353 | ||||||
| chr17:10361458
|
A | AT | 24 | a0001c0003t0001g0241a0001c0003t0001g0243a0001c0003t0001g0244others(21): Show | 24 | HG01099.hp2 HG01928.hp1 HG01934.hp2 others(21): Show |
intron_variant | MODIFIER | c.505+659dupA | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 5/40 | chr17 | 10361458 | ||||||
| chr17:10361545
|
C | T | 21 | a0001c0027t0001g0009a0001c0027t0001g0154a0001c0027t0001g0161others(18): Show | 21 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.505+573G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 5/40 | chr17 | 10361545 | ||||||
| chr17:10361698
|
C | T | 34 | a0001c0003t0001g0241a0001c0003t0001g0243a0001c0003t0001g0244others(31): Show | 34 | HG00423.hp2 HG00544.hp1 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.505+420G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 5/40 | chr17 | 10361698 | ||||||
| chr17:10361901
|
G | A | 111 | a0001c0003t0001g0269a0001c0004t0001g0328a0001c0004t0001g0344others(108): Show | 111 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.505+217C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 5/40 | chr17 | 10361901 | ||||||
| chr17:10362049
|
C | T | 56 | a0001c0003t0001g0241a0001c0003t0001g0243a0001c0003t0001g0244others(53): Show | 56 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.505+69G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 5/40 | chr17 | 10362049 | ||||||
| chr17:10362741
|
G | A | 1 | a0001c0111t0001g0078 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.205-238C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 3/40 | chr17 | 10362741 | ||||||
| chr17:10362834
|
G | A | 17 | a0001c0003t0001g0269a0001c0006t0001g0268a0001c0012t0001g0267others(14): Show | 17 | HG00438.hp2 HG00741.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.205-331C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 3/40 | chr17 | 10362834 | ||||||
| chr17:10362956
|
C | G | 14 | a0001c0014t0001g0010a0001c0015t0001g0011a0001c0015t0001g0014others(11): Show | 14 | HG00423.hp2 HG00544.hp1 NA18944.hp2 others(11): Show |
intron_variant | MODIFIER | c.205-453G>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 3/40 | chr17 | 10362956 | ||||||
| chr17:10362964
|
T | C | 74 | a0001c0003t0001g0203a0001c0003t0001g0204a0001c0003t0001g0205others(71): Show | 75 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.205-461A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 3/40 | chr17 | 10362964 | ||||||
| chr17:10362967
|
C | CA | 75 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(72): Show | 75 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(72): Show |
intron_variant | MODIFIER | c.205-465dupT | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 3/40 | chr17 | 10362967 | ||||||
| chr17:10363052
|
G | A | 304 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(301): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.205-549C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 3/40 | chr17 | 10363052 | ||||||
| chr17:10363058
|
TG | T | 4 | a0001c0089t0001g0184a0004c0021t0001g0109a0006c0068t0001g0366others(1): Show | 4 | HG02486.hp1 HG03579.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.205-556delC | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 3/40 | chr17 | 10363058 | ||||||
| chr17:10363200
|
C | T | 115 | a0001c0003t0001g0269a0001c0004t0001g0328a0001c0004t0001g0344others(112): Show | 115 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(112): Show |
intron_variant | MODIFIER | c.205-697G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 3/40 | chr17 | 10363200 | ||||||
| chr17:10363246
|
G | A | 2 | a0008c0044t0001g0138a0008c0044t0001g0139 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.205-743C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 3/40 | chr17 | 10363246 | ||||||
| chr17:10363248
|
G | A | 1 | a0001c0017t0001g0129 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.205-745C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 3/40 | chr17 | 10363248 | ||||||
| chr17:10363277
|
C | G | 5 | a0012c0035t0001g0143a0012c0035t0001g0145a0012c0058t0001g0142others(2): Show | 5 | HG02809.hp2 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.205-774G>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 3/40 | chr17 | 10363277 | ||||||
| chr17:10363311
|
G | A | 2 | a0006c0024t0001g0095a0007c0083t0001g0096 | 2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.205-808C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 3/40 | chr17 | 10363311 | ||||||
| chr17:10363315
|
C | CA | 167 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(164): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.205-813dupT | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 3/40 | chr17 | 10363315 | ||||||
| chr17:10363315
|
C | CAA | 28 | a0001c0003t0001g0069a0001c0003t0001g0241a0001c0003t0001g0243others(25): Show | 28 | HG00423.hp2 HG01169.hp1 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.205-814_205-813dup others(2): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 3/40 | chr17 | 10363315 | ||||||
| chr17:10363315
|
C | CAAAAAAA others(5): Show |
1 | a0005c0028t0001g0363 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.205-824_205-813dup others(12): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 3/40 | chr17 | 10363315 | ||||||
| chr17:10363315
|
CA | C | 19 | a0001c0003t0001g0203a0001c0003t0001g0204a0001c0003t0001g0205others(16): Show | 20 | HG00733.hp1 HG00735.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.205-813delT | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 3/40 | chr17 | 10363315 | ||||||
| chr17:10363394
|
C | T | 6 | a0001c0090t0001g0364a0001c0111t0001g0078a0001c0118t0001g0273others(3): Show | 6 | HG01109.hp1 HG02257.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.205-891G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 3/40 | chr17 | 10363394 | ||||||
| chr17:10363570
|
T | C | 1 | a0007c0020t0001g0342 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.204+757A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 3/40 | chr17 | 10363570 | ||||||
| chr17:10363653
|
T | C | 21 | a0001c0027t0001g0009a0001c0027t0001g0154a0001c0027t0001g0161others(18): Show | 21 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.204+674A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 3/40 | chr17 | 10363653 | ||||||
| chr17:10363678
|
G | A | 22 | a0001c0027t0001g0009a0001c0027t0001g0154a0001c0027t0001g0161others(19): Show | 22 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.204+649C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 3/40 | chr17 | 10363678 | ||||||
| chr17:10363785
|
C | T | 1 | a0002c0038t0001g0369 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.204+542G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 3/40 | chr17 | 10363785 | ||||||
| chr17:10363887
|
C | T | 20 | a0001c0027t0001g0009a0001c0027t0001g0154a0001c0027t0001g0161others(17): Show | 20 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.204+440G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 3/40 | chr17 | 10363887 | ||||||
| chr17:10363914
|
A | G | 304 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(301): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.204+413T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 3/40 | chr17 | 10363914 | ||||||
| chr17:10363921
|
C | T | 1 | a0009c0049t0001g0248 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.204+406G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 3/40 | chr17 | 10363921 | ||||||
| chr17:10363922
|
G | A | 20 | a0001c0027t0001g0009a0001c0027t0001g0154a0001c0027t0001g0161others(17): Show | 20 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.204+405C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 3/40 | chr17 | 10363922 | ||||||
| chr17:10364011
|
G | A | 4 | a0001c0089t0001g0184a0004c0021t0001g0109a0006c0068t0001g0366others(1): Show | 4 | HG02486.hp1 HG03579.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.204+316C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 3/40 | chr17 | 10364011 | ||||||
| chr17:10364029
|
G | A | 1 | a0001c0111t0001g0078 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.204+298C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 3/40 | chr17 | 10364029 | ||||||
| chr17:10364067
|
C | A | 20 | a0001c0027t0001g0009a0001c0027t0001g0154a0001c0027t0001g0161others(17): Show | 20 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.204+260G>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 3/40 | chr17 | 10364067 | ||||||
| chr17:10364239
|
G | A | 1 | a0004c0010t0001g0073 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.204+88C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 3/40 | chr17 | 10364239 | ||||||
| chr17:10364293
|
C | T | 52 | a0001c0006t0001g0001a0001c0006t0001g0084a0001c0006t0001g0085others(49): Show | 53 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.204+34G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 3/40 | chr17 | 10364293 | ||||||
| chr17:10364550
|
G | A | 20 | a0001c0003t0001g0241a0001c0003t0001g0243a0001c0003t0001g0244others(17): Show | 20 | HG01099.hp2 HG01928.hp1 HG01934.hp2 others(17): Show |
splice_region_variant&intron_variant | LOW | c.-12-8C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10364550 | ||||||
| chr17:10364625
|
C | CAG | 21 | a0001c0027t0001g0009a0001c0027t0001g0154a0001c0027t0001g0161others(18): Show | 21 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12-84_-12-83insCT | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10364625 | ||||||
| chr17:10364755
|
G | GT | 34 | a0001c0014t0001g0010a0001c0015t0001g0011a0001c0015t0001g0014others(31): Show | 34 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.-12-214dupA | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10364755 | ||||||
| chr17:10364766
|
T | TA | 5 | a0001c0090t0001g0364a0003c0041t0001g0365a0004c0021t0001g0109others(2): Show | 5 | HG02280.hp2 HG03579.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.-12-225dupT | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10364766 | ||||||
| chr17:10364850
|
A | G | 1 | a0001c0004t0001g0169 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-12-308T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10364850 | ||||||
| chr17:10364871
|
A | ACTTT | 8 | a0001c0003t0001g0008a0001c0003t0001g0043a0001c0003t0001g0044others(5): Show | 8 | HG00639.hp1 HG01081.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12-333_-12-330dup others(4): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10364871 | ||||||
| chr17:10364874
|
T | G | 20 | a0001c0027t0001g0009a0001c0027t0001g0154a0001c0027t0001g0161others(17): Show | 20 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-12-332A>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10364874 | ||||||
| chr17:10365046
|
T | A | 8 | a0001c0003t0001g0241a0001c0003t0001g0243a0001c0003t0001g0244others(5): Show | 8 | HG01928.hp1 HG01934.hp2 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.-12-504A>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10365046 | ||||||
| chr17:10365284
|
T | C | 1 | a0040c0076t0001g0343 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-12-742A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10365284 | ||||||
| chr17:10365335
|
T | A | 1 | a0033c0077t0001g0355 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-12-793A>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10365335 | ||||||
| chr17:10365416
|
C | A | 3 | a0001c0004t0001g0344a0001c0004t0001g0345a0001c0004t0001g0346 | 3 | HG00735.hp1 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-12-874G>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10365416 | ||||||
| chr17:10365840
|
G | GGT | 16 | a0001c0006t0001g0198a0001c0007t0001g0260a0001c0027t0001g0009others(13): Show | 16 | HG01070.hp2 HG01099.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.-12-1300_-12-1299d others(4): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10365840 | ||||||
| chr17:10365840
|
GGT | G | 43 | a0001c0006t0001g0218a0001c0007t0001g0284a0001c0007t0001g0285others(40): Show | 43 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.-12-1300_-12-1299d others(4): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10365840 | ||||||
| chr17:10365840
|
GGTGT | G | 116 | a0001c0003t0001g0227a0001c0003t0001g0228a0001c0003t0001g0241others(113): Show | 117 | HG00408.hp1 HG00438.hp2 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.-12-1302_-12-1299d others(6): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10365840 | ||||||
| chr17:10365840
|
GGTGTGT | G | 52 | a0001c0003t0001g0232a0001c0003t0001g0233a0001c0006t0001g0001others(49): Show | 53 | HG01070.hp1 HG01071.hp1 HG01074.hp2 others(50): Show |
intron_variant | MODIFIER | c.-12-1304_-12-1299d others(8): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10365840 | ||||||
| chr17:10365840
|
GGTGTGTG others(1): Show |
G | 24 | a0001c0003t0001g0237a0001c0003t0001g0243a0001c0004t0001g0236others(21): Show | 24 | HG00140.hp2 HG00738.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.-12-1306_-12-1299d others(10): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10365840 | ||||||
| chr17:10365840
|
GGTGTGTG others(3): Show |
G | 50 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(47): Show | 50 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.-12-1308_-12-1299d others(12): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10365840 | ||||||
| chr17:10365840
|
GGTGTGTG others(5): Show |
G | 5 | a0001c0003t0001g0356a0001c0040t0001g0137a0004c0026t0001g0153others(2): Show | 5 | HG00733.hp2 HG01891.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12-1310_-12-1299d others(14): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10365840 | ||||||
| chr17:10365840
|
GGTGTGTG others(9): Show |
G | 1 | a0001c0111t0001g0078 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-12-1314_-12-1299d others(18): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10365840 | ||||||
| chr17:10365840
|
GGTGTGTG others(17): Show |
G | 14 | a0001c0014t0001g0010a0001c0015t0001g0011a0001c0015t0001g0014others(11): Show | 14 | HG00423.hp2 HG00544.hp1 NA18944.hp2 others(11): Show |
intron_variant | MODIFIER | c.-12-1322_-12-1299d others(26): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10365840 | ||||||
| chr17:10365840
|
GGTGTGTG others(25): Show |
G | 1 | a0009c0049t0001g0151 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-12-1330_-12-1299d others(34): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10365840 | ||||||
| chr17:10366124
|
C | T | 1 | a0042c0057t0001g0159 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-12-1582G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10366124 | ||||||
| chr17:10366197
|
C | T | 106 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.-12-1655G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10366197 | ||||||
| chr17:10366202
|
G | T | 20 | a0001c0027t0001g0009a0001c0027t0001g0154a0001c0027t0001g0161others(17): Show | 20 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-12-1660C>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10366202 | ||||||
| chr17:10366381
|
G | GT | 36 | a0001c0003t0001g0241a0001c0003t0001g0243a0001c0003t0001g0249others(33): Show | 36 | HG00738.hp2 HG01934.hp2 HG01943.hp2 others(33): Show |
intron_variant | MODIFIER | c.-12-1840dupA | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10366381 | ||||||
| chr17:10366381
|
G | GTTTGTTT others(12): Show |
1 | a0009c0049t0001g0151 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-12-1840_-12-1839i others(21): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10366381 | ||||||
| chr17:10366381
|
G | GTTTTTTT others(6): Show |
1 | a0001c0034t0001g0168 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-12-1840_-12-1839i others(15): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10366381 | ||||||
| chr17:10366381
|
G | GTTTTTTT others(3): Show |
3 | a0001c0007t0001g0376a0001c0014t0001g0375a0003c0009t0001g0377 | 3 | HG02965.hp1 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-12-1849_-12-1840d others(12): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10366381 | ||||||
| chr17:10366381
|
G | GTTTTTTT others(4): Show |
6 | a0001c0014t0001g0374a0001c0015t0001g0372a0001c0015t0001g0378others(3): Show | 6 | HG01099.hp2 HG02717.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-1850_-12-1840d others(13): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10366381 | ||||||
| chr17:10366381
|
G | GTTTTTTT others(5): Show |
5 | a0001c0015t0001g0371a0001c0111t0001g0078a0002c0030t0001g0022others(2): Show | 5 | HG01109.hp1 HG02145.hp2 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12-1851_-12-1840d others(14): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10366381 | ||||||
| chr17:10366381
|
G | GTTTTTTT others(6): Show |
17 | a0001c0027t0001g0161a0001c0072t0001g0160a0001c0105t0001g0163others(14): Show | 17 | HG00140.hp1 HG00544.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.-12-1852_-12-1840d others(15): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10366381 | ||||||
| chr17:10366381
|
G | GTTTTTTT others(7): Show |
10 | a0001c0015t0001g0011a0001c0015t0001g0014a0001c0027t0001g0009others(7): Show | 10 | HG00423.hp2 HG00735.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.-12-1853_-12-1840d others(16): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10366381 | ||||||
| chr17:10366381
|
G | GTTTTTTT others(8): Show |
3 | a0001c0014t0001g0010a0001c0034t0001g0152a0004c0026t0001g0153 | 3 | HG01109.hp2 HG01891.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.-12-1854_-12-1840d others(17): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10366381 | ||||||
| chr17:10366449
|
C | T | 58 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(55): Show | 58 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(55): Show |
intron_variant | MODIFIER | c.-12-1907G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10366449 | ||||||
| chr17:10366474
|
G | A | 132 | a0001c0003t0001g0241a0001c0003t0001g0243a0001c0003t0001g0244others(129): Show | 132 | HG00408.hp1 HG00438.hp2 HG00621.hp1 others(129): Show |
intron_variant | MODIFIER | c.-12-1932C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10366474 | ||||||
| chr17:10366526
|
G | A | 1 | a0002c0001t0001g0357 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-12-1984C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10366526 | ||||||
| chr17:10366661
|
G | A | 1 | a0002c0011t0001g0239 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-12-2119C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10366661 | ||||||
| chr17:10366678
|
G | A | 1 | a0039c0101t0001g0074 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-12-2136C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10366678 | ||||||
| chr17:10366689
|
G | A | 1 | a0001c0075t0001g0358 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-12-2147C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10366689 | ||||||
| chr17:10366843
|
G | A | 3 | a0001c0006t0001g0140a0001c0017t0001g0141a0004c0002t0001g0075 | 3 | HG01175.hp2 HG01358.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-12-2301C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10366843 | ||||||
| chr17:10367178
|
A | G | 11 | a0001c0007t0001g0376a0001c0014t0001g0374a0001c0014t0001g0375others(8): Show | 11 | HG01099.hp2 HG02145.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.-12-2636T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10367178 | ||||||
| chr17:10367372
|
G | A | 18 | a0001c0027t0001g0009a0001c0027t0001g0154a0001c0027t0001g0161others(15): Show | 18 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.-12-2830C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10367372 | ||||||
| chr17:10367374
|
A | G | 1 | a0002c0011t0001g0186 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-12-2832T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10367374 | ||||||
| chr17:10367420
|
C | T | 1 | a0006c0033t0001g0185 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-12-2878G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10367420 | ||||||
| chr17:10367439
|
C | G | 18 | a0001c0027t0001g0009a0001c0027t0001g0154a0001c0027t0001g0161others(15): Show | 18 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.-12-2897G>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10367439 | ||||||
| chr17:10367638
|
C | T | 3 | a0002c0001t0001g0252a0002c0001t0001g0253a0030c0084t0001g0254 | 3 | NA18955.hp2 NA18998.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.-12-3096G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10367638 | ||||||
| chr17:10367919
|
T | G | 12 | a0001c0003t0001g0241a0001c0003t0001g0243a0001c0003t0001g0244others(9): Show | 12 | HG01928.hp1 HG01934.hp2 HG01943.hp2 others(9): Show |
intron_variant | MODIFIER | c.-13+3290A>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10367919 | ||||||
| chr17:10367943
|
C | T | 1 | a0009c0049t0001g0151 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-13+3266G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10367943 | ||||||
| chr17:10368071
|
GT | G | 5 | a0012c0035t0001g0143a0012c0035t0001g0145a0012c0058t0001g0142others(2): Show | 5 | HG02809.hp2 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13+3137delA | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10368071 | ||||||
| chr17:10368132
|
C | T | 1 | a0001c0089t0001g0184 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-13+3077G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10368132 | ||||||
| chr17:10368169
|
G | C | 20 | a0001c0027t0001g0009a0001c0027t0001g0154a0001c0027t0001g0161others(17): Show | 20 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-13+3040C>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10368169 | ||||||
| chr17:10368257
|
T | G | 1 | a0003c0005t0001g0147 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-13+2952A>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10368257 | ||||||
| chr17:10368296
|
T | A | 1 | a0002c0001t0001g0359 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-13+2913A>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10368296 | ||||||
| chr17:10368311
|
C | T | 1 | a0002c0043t0001g0251 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-13+2898G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10368311 | ||||||
| chr17:10368317
|
G | A | 20 | a0001c0027t0001g0009a0001c0027t0001g0154a0001c0027t0001g0161others(17): Show | 20 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-13+2892C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10368317 | ||||||
| chr17:10368595
|
C | T | 1 | a0002c0001t0001g0250 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-13+2614G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10368595 | ||||||
| chr17:10368599
|
G | A | 1 | a0001c0003t0001g0249 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-13+2610C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10368599 | ||||||
| chr17:10368876
|
G | T | 1 | a0005c0016t0001g0035 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-13+2333C>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10368876 | ||||||
| chr17:10369089
|
T | C | 121 | a0001c0003t0001g0269a0001c0003t0001g0356a0001c0004t0001g0328others(118): Show | 121 | HG00408.hp1 HG00438.hp2 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.-13+2120A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10369089 | ||||||
| chr17:10369161
|
T | TA | 20 | a0001c0027t0001g0009a0001c0027t0001g0154a0001c0027t0001g0161others(17): Show | 20 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-13+2047dupT | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10369161 | ||||||
| chr17:10369162
|
A | C | 2 | a0006c0024t0001g0182a0006c0024t0001g0183 | 2 | NA18995.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.-13+2047T>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10369162 | ||||||
| chr17:10369319
|
A | G | 20 | a0001c0027t0001g0009a0001c0027t0001g0154a0001c0027t0001g0161others(17): Show | 20 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-13+1890T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10369319 | ||||||
| chr17:10369421
|
T | C | 1 | a0005c0037t0001g0148 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-13+1788A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10369421 | ||||||
| chr17:10369422
|
A | AAACCCTC others(17): Show |
1 | a0005c0037t0001g0148 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-13+1786_-13+1787i others(26): Show |
MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10369422 | ||||||
| chr17:10369466
|
C | A | 3 | a0003c0008t0001g0361a0003c0009t0001g0362a0004c0002t0001g0360 | 3 | HG02080.hp2 NA19066.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.-13+1743G>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10369466 | ||||||
| chr17:10369494
|
A | C | 3 | a0001c0003t0001g0032a0002c0045t0001g0033a0007c0096t0001g0034 | 3 | NA18948.hp2 NA18964.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.-13+1715T>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10369494 | ||||||
| chr17:10369574
|
G | A | 18 | a0001c0027t0001g0009a0001c0027t0001g0154a0001c0027t0001g0161others(15): Show | 18 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.-13+1635C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10369574 | ||||||
| chr17:10369693
|
AT | A | 20 | a0001c0027t0001g0009a0001c0027t0001g0154a0001c0027t0001g0161others(17): Show | 20 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-13+1515delA | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10369693 | ||||||
| chr17:10369981
|
C | T | 14 | a0001c0014t0001g0010a0001c0015t0001g0011a0001c0015t0001g0014others(11): Show | 14 | HG00423.hp2 HG00544.hp1 NA18944.hp2 others(11): Show |
intron_variant | MODIFIER | c.-13+1228G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10369981 | ||||||
| chr17:10370171
|
G | C | 1 | a0001c0015t0001g0378 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-13+1038C>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10370171 | ||||||
| chr17:10370224
|
C | T | 1 | a0001c0022t0001g0181 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-13+985G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10370224 | ||||||
| chr17:10370254
|
G | A | 1 | a0025c0074t0001g0076 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-13+955C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10370254 | ||||||
| chr17:10370288
|
T | C | 1 | a0005c0037t0001g0148 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-13+921A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10370288 | ||||||
| chr17:10370314
|
C | T | 1 | a0001c0111t0001g0078 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-13+895G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10370314 | ||||||
| chr17:10370329
|
C | A | 1 | a0001c0022t0001g0149 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-13+880G>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10370329 | ||||||
| chr17:10370648
|
G | A | 20 | a0001c0027t0001g0009a0001c0027t0001g0154a0001c0027t0001g0161others(17): Show | 20 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-13+561C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10370648 | ||||||
| chr17:10370683
|
T | C | 10 | a0001c0007t0001g0376a0001c0014t0001g0374a0001c0014t0001g0375others(7): Show | 10 | HG02145.hp2 HG02647.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.-13+526A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10370683 | ||||||
| chr17:10370713
|
A | G | 1 | a0001c0111t0001g0078 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-13+496T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10370713 | ||||||
| chr17:10370822
|
C | T | 2 | a0004c0010t0001g0179a0032c0082t0001g0180 | 2 | HG00408.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.-13+387G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10370822 | ||||||
| chr17:10370871
|
A | G | 3 | a0001c0120t0001g0178a0004c0026t0001g0177a0004c0106t0001g0176 | 3 | HG01192.hp2 HG01255.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-13+338T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10370871 | ||||||
| chr17:10370970
|
A | G | 7 | a0001c0004t0001g0169a0001c0004t0001g0170a0001c0103t0001g0174others(4): Show | 7 | HG02109.hp1 HG02559.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13+239T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10370970 | ||||||
| chr17:10370989
|
T | C | 11 | a0001c0007t0001g0376a0001c0014t0001g0374a0001c0014t0001g0375others(8): Show | 11 | HG01099.hp2 HG02145.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.-13+220A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10370989 | ||||||
| chr17:10371069
|
A | G | 20 | a0001c0027t0001g0009a0001c0027t0001g0154a0001c0027t0001g0161others(17): Show | 20 | HG00140.hp1 HG00323.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-13+140T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10371069 | ||||||
| chr17:10371114
|
G | T | 1 | a0001c0111t0001g0078 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-13+95C>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 2/40 | chr17 | 10371114 | ||||||
| chr17:10371275
|
GA | G | 7 | a0001c0004t0001g0025a0001c0004t0001g0027a0001c0004t0001g0028others(4): Show | 7 | NA18950.hp2 NA18961.hp2 NA19000.hp1 others(4): Show |
intron_variant | MODIFIER | c.-63-17delT | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 1/40 | chr17 | 10371275 | ||||||
| chr17:10371278
|
A | AC | 49 | a0001c0007t0001g0376a0001c0014t0001g0010a0001c0014t0001g0374others(46): Show | 49 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.-63-20_-63-19insG | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 1/40 | chr17 | 10371278 | ||||||
| chr17:10371298
|
C | A | 1 | a0014c0054t0001g0150 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-63-39G>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 1/40 | chr17 | 10371298 | ||||||
| chr17:10371311
|
C | T | 1 | a0002c0011t0001g0081 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-63-52G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 1/40 | chr17 | 10371311 | ||||||
| chr17:10371374
|
C | A | 1 | a0001c0004t0001g0077 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-63-115G>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 1/40 | chr17 | 10371374 | ||||||
| chr17:10371445
|
A | G | 2 | a0002c0065t0001g0079a0005c0016t0001g0080 | 2 | NA18979.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.-63-186T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 1/40 | chr17 | 10371445 | ||||||
| chr17:10371607
|
T | G | 29 | a0001c0007t0001g0376a0001c0014t0001g0010a0001c0014t0001g0374others(26): Show | 29 | HG00423.hp2 HG00544.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.-63-348A>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 1/40 | chr17 | 10371607 | ||||||
| chr17:10371674
|
C | T | 75 | a0001c0006t0001g0001a0001c0006t0001g0084a0001c0006t0001g0085others(72): Show | 76 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(73): Show |
intron_variant | MODIFIER | c.-63-415G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 1/40 | chr17 | 10371674 | ||||||
| chr17:10371859
|
G | A | 1 | a0001c0004t0001g0367 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-63-600C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 1/40 | chr17 | 10371859 | ||||||
| chr17:10371862
|
A | G | 1 | a0001c0111t0001g0078 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-63-603T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 1/40 | chr17 | 10371862 | ||||||
| chr17:10371955
|
A | T | 1 | a0028c0098t0001g0024 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-63-696T>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 1/40 | chr17 | 10371955 | ||||||
| chr17:10371972
|
G | T | 57 | a0001c0003t0001g0008a0001c0003t0001g0032a0001c0003t0001g0043others(54): Show | 57 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(54): Show |
intron_variant | MODIFIER | c.-63-713C>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 1/40 | chr17 | 10371972 | ||||||
| chr17:10372180
|
A | T | 14 | a0001c0014t0001g0010a0001c0015t0001g0011a0001c0015t0001g0014others(11): Show | 14 | HG00423.hp2 HG00544.hp1 NA18944.hp2 others(11): Show |
intron_variant | MODIFIER | c.-64+799T>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 1/40 | chr17 | 10372180 | ||||||
| chr17:10372204
|
T | A | 11 | a0001c0007t0001g0376a0001c0014t0001g0374a0001c0014t0001g0375others(8): Show | 11 | HG01099.hp2 HG02145.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.-64+775A>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 1/40 | chr17 | 10372204 | ||||||
| chr17:10372214
|
T | C | 2 | a0013c0117t0001g0380a0014c0054t0001g0379 | 2 | NA18990.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.-64+765A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 1/40 | chr17 | 10372214 | ||||||
| chr17:10372257
|
A | G | 1 | a0001c0027t0001g0009 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-64+722T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 1/40 | chr17 | 10372257 | ||||||
| chr17:10372369
|
T | C | 1 | a0004c0002t0001g0002 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-64+610A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 1/40 | chr17 | 10372369 | ||||||
| chr17:10372428
|
C | T | 1 | a0001c0003t0001g0008 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-64+551G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 1/40 | chr17 | 10372428 | ||||||
| chr17:10372604
|
A | T | 2 | a0001c0007t0001g0006a0001c0007t0001g0007 | 2 | HG00408.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.-64+375T>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 1/40 | chr17 | 10372604 | ||||||
| chr17:10372659
|
A | G | 2 | a0002c0001t0001g0004a0002c0081t0001g0005 | 2 | HG00621.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.-64+320T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 1/40 | chr17 | 10372659 |