Item | Value |
---|---|
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 | 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 | MSSDA others(1933): Show |
chr17 | 10295865 | 10378006 |
a0002 | 1/0 | 1938 | 54 | 11 | 12 | 20 | 3 | 7 | 16 | MYH13_chr17_10295865_10378006 | MYH13 | MSSDA others(1933): Show |
chr17 | 10295865 | 10378006 |
a0003 | 0/0 | 1938 | 55 | 6 | 9 | 36 | 0 | 4 | 31 | MYH13_chr17_10295865_10378006 | MYH13 | MSSDA others(1933): Show |
chr17 | 10295865 | 10378006 |
a0004 | 0/1 | 1938 | 44 | 2 | 12 | 25 | 1 | 3 | 22 | MYH13_chr17_10295865_10378006 | MYH13 | MSSDA others(1933): Show |
chr17 | 10295865 | 10378006 |
a0005 | 0/0 | 1938 | 23 | 6 | 3 | 12 | 0 | 2 | 11 | MYH13_chr17_10295865_10378006 | MYH13 | MSSDA others(1933): Show |
chr17 | 10295865 | 10378006 |
a0006 | 0/0 | 1938 | 14 | 4 | 2 | 8 | 0 | 0 | 6 | MYH13_chr17_10295865_10378006 | MYH13 | MSSDA others(1933): Show |
chr17 | 10295865 | 10378006 |
a0007 | 0/0 | 1938 | 8 | 4 | 1 | 1 | 0 | 2 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | MSSDA others(1933): Show |
chr17 | 10295865 | 10378006 |
a0008 | 0/0 | 1938 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | MSSDA others(1933): Show |
chr17 | 10295865 | 10378006 |
a0009 | 0/0 | 1938 | 5 | 0 | 0 | 0 | 0 | 5 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | MSSDA others(1933): Show |
chr17 | 10295865 | 10378006 |
a0010 | 0/0 | 1938 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | MYH13_chr17_10295865_10378006 | MYH13 | MSSDA others(1933): Show |
chr17 | 10295865 | 10378006 |
a0011 | 0/0 | 1938 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | MSSDA others(1933): Show |
chr17 | 10295865 | 10378006 |
a0012 | 0/0 | 1938 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | MSSDA others(1933): Show |
chr17 | 10295865 | 10378006 |
a0013 | 0/0 | 1938 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | MSSDA others(1933): Show |
chr17 | 10295865 | 10378006 |
a0014 | 0/0 | 1938 | 2 | 0 | 0 | 0 | 1 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | MSSDA others(1933): Show |
chr17 | 10295865 | 10378006 |
a0015 | 0/0 | 1938 | 2 | 0 | 1 | 1 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | MSSDA others(1933): Show |
chr17 | 10295865 | 10378006 |
a0016 | 0/0 | 1938 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | MSSDA others(1933): Show |
chr17 | 10295865 | 10378006 |
a0017 | 0/0 | 1938 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | MSSDA others(1933): Show |
chr17 | 10295865 | 10378006 |
a0018 | 0/0 | 1938 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | MSSDA others(1933): Show |
chr17 | 10295865 | 10378006 |
a0019 | 0/0 | 1938 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | MSSDA others(1933): Show |
chr17 | 10295865 | 10378006 |
a0020 | 0/0 | 1938 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | MSSDA others(1933): Show |
chr17 | 10295865 | 10378006 |
a0021 | 0/0 | 1938 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | MSSDA others(1933): Show |
chr17 | 10295865 | 10378006 |
a0022 | 0/0 | 1938 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | MSSDA others(1933): Show |
chr17 | 10295865 | 10378006 |
a0023 | 0/0 | 1938 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | MSSDA others(1933): Show |
chr17 | 10295865 | 10378006 |
a0024 | 0/0 | 1938 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | MSSDA others(1933): Show |
chr17 | 10295865 | 10378006 |
a0025 | 0/0 | 1938 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | MSSDA others(1933): Show |
chr17 | 10295865 | 10378006 |
a0026 | 0/0 | 1938 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | MSSDA others(1933): Show |
chr17 | 10295865 | 10378006 |
a0027 | 0/0 | 1938 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | MSSDA others(1933): Show |
chr17 | 10295865 | 10378006 |
a0028 | 0/0 | 1938 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | MSSDA others(1933): Show |
chr17 | 10295865 | 10378006 |
a0029 | 0/0 | 1938 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | MSSDA others(1933): Show |
chr17 | 10295865 | 10378006 |
a0030 | 0/0 | 1938 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | MSSDA others(1933): Show |
chr17 | 10295865 | 10378006 |
a0031 | 0/0 | 1938 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | MSSDA others(1933): Show |
chr17 | 10295865 | 10378006 |
a0032 | 0/0 | 1938 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | MSSDA others(1933): Show |
chr17 | 10295865 | 10378006 |
a0033 | 0/0 | 1938 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | MSSDA others(1933): Show |
chr17 | 10295865 | 10378006 |
a0034 | 0/0 | 1938 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | MSSDA others(1933): Show |
chr17 | 10295865 | 10378006 |
a0035 | 0/0 | 1938 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | MSSDA others(1933): Show |
chr17 | 10295865 | 10378006 |
a0036 | 0/0 | 1938 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | MSSDA others(1933): Show |
chr17 | 10295865 | 10378006 |
a0037 | 0/0 | 1938 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | MSSDA others(1933): Show |
chr17 | 10295865 | 10378006 |
a0038 | 0/0 | 1938 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | MSSDA others(1933): Show |
chr17 | 10295865 | 10378006 |
a0039 | 0/0 | 1938 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | MSSDA others(1933): Show |
chr17 | 10295865 | 10378006 |
a0040 | 0/0 | 1938 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | MSSDA others(1933): Show |
chr17 | 10295865 | 10378006 |
a0041 | 0/0 | 1938 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | MSSDA others(1933): Show |
chr17 | 10295865 | 10378006 |
a0042 | 0/0 | 1938 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | MSSDA others(1933): Show |
chr17 | 10295865 | 10378006 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0003 | 0/0 | 5814 | 24 | 4 | 12 | 8 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0001c0004 | 0/0 | 5814 | 18 | 3 | 2 | 11 | 2 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0001c0006 | 0/0 | 5814 | 11 | 3 | 3 | 1 | 2 | 2 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0001c0007 | 0/0 | 5814 | 11 | 2 | 1 | 7 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0001c0012 | 0/0 | 5814 | 8 | 2 | 0 | 4 | 0 | 2 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0001c0014 | 0/0 | 5814 | 7 | 4 | 2 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0001c0015 | 0/0 | 5814 | 7 | 5 | 0 | 2 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0001c0017 | 0/0 | 5814 | 6 | 1 | 1 | 2 | 0 | 2 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0001c0022 | 0/0 | 5814 | 4 | 4 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0001c0027 | 0/0 | 5814 | 4 | 0 | 3 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0001c0034 | 0/0 | 5814 | 3 | 0 | 2 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0001c0039 | 0/0 | 5814 | 2 | 0 | 0 | 2 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0001c0040 | 0/0 | 5814 | 2 | 1 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0001c0042 | 0/0 | 5814 | 2 | 2 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0001c0046 | 0/0 | 5814 | 2 | 1 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0001c0050 | 0/0 | 5814 | 2 | 0 | 1 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0001c0051 | 0/0 | 5814 | 2 | 0 | 0 | 2 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0001c0062 | 0/0 | 5814 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0001c0072 | 0/0 | 5814 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0001c0075 | 0/0 | 5814 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0001c0089 | 0/0 | 5814 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0001c0090 | 0/0 | 5814 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0001c0103 | 0/0 | 5814 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0001c0105 | 0/0 | 5814 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0001c0108 | 0/0 | 5814 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0001c0110 | 0/0 | 5814 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0001c0111 | 0/0 | 5814 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0001c0113 | 0/0 | 5814 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0001c0118 | 0/0 | 5814 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0001c0119 | 0/0 | 5814 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0001c0120 | 0/0 | 5814 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0002c0005 | 1/0 | 5814 | 17 | 4 | 6 | 2 | 0 | 4 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0002c0008 | 0/0 | 5814 | 11 | 1 | 5 | 3 | 2 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0002c0009 | 0/0 | 5814 | 10 | 2 | 0 | 7 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0002c0013 | 0/0 | 5814 | 7 | 1 | 0 | 6 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0002c0025 | 0/0 | 5814 | 4 | 0 | 1 | 0 | 1 | 2 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0002c0041 | 0/0 | 5814 | 2 | 2 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0002c0061 | 0/0 | 5814 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0002c0071 | 0/0 | 5814 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0002c0091 | 0/0 | 5814 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0003c0001 | 0/0 | 5814 | 25 | 0 | 5 | 17 | 0 | 3 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0003c0011 | 0/0 | 5814 | 9 | 3 | 3 | 2 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0003c0019 | 0/0 | 5814 | 6 | 0 | 0 | 6 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0003c0030 | 0/0 | 5814 | 3 | 1 | 0 | 2 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0003c0038 | 0/0 | 5814 | 2 | 1 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0003c0043 | 0/0 | 5814 | 2 | 0 | 0 | 2 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0003c0045 | 0/0 | 5814 | 2 | 0 | 0 | 2 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0003c0064 | 0/0 | 5814 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0003c0065 | 0/0 | 5814 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0003c0070 | 0/0 | 5814 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0003c0078 | 0/0 | 5814 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0003c0081 | 0/0 | 5814 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0003c0094 | 0/0 | 5814 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0004c0002 | 0/1 | 5814 | 24 | 0 | 5 | 18 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0004c0010 | 0/0 | 5814 | 9 | 0 | 2 | 6 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0004c0021 | 0/0 | 5814 | 4 | 1 | 2 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0004c0026 | 0/0 | 5814 | 4 | 1 | 2 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0004c0048 | 0/0 | 5814 | 2 | 0 | 0 | 1 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0004c0106 | 0/0 | 5814 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0005c0016 | 0/0 | 5814 | 7 | 1 | 0 | 4 | 0 | 2 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0005c0018 | 0/0 | 5814 | 6 | 0 | 0 | 6 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0005c0028 | 0/0 | 5814 | 3 | 3 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0005c0037 | 0/0 | 5814 | 2 | 2 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0005c0047 | 0/0 | 5814 | 2 | 0 | 2 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0005c0079 | 0/0 | 5814 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0005c0087 | 0/0 | 5814 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0005c0095 | 0/0 | 5814 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0006c0024 | 0/0 | 5814 | 4 | 1 | 0 | 3 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0006c0029 | 0/0 | 5814 | 3 | 0 | 0 | 3 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0006c0033 | 0/0 | 5814 | 3 | 1 | 0 | 2 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0006c0052 | 0/0 | 5814 | 2 | 0 | 2 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0006c0068 | 0/0 | 5814 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0006c0099 | 0/0 | 5814 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0007c0020 | 0/0 | 5814 | 4 | 2 | 1 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0007c0083 | 0/0 | 5814 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0007c0096 | 0/0 | 5814 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0007c0097 | 0/0 | 5814 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0007c0107 | 0/0 | 5814 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0008c0032 | 0/0 | 5814 | 3 | 3 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0008c0049 | 0/0 | 5814 | 2 | 2 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0009c0044 | 0/0 | 5814 | 2 | 0 | 0 | 0 | 0 | 2 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0009c0063 | 0/0 | 5814 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0009c0093 | 0/0 | 5814 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0009c0104 | 0/0 | 5814 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0010c0023 | 0/0 | 5814 | 4 | 0 | 0 | 4 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0011c0031 | 0/0 | 5814 | 3 | 0 | 3 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0012c0035 | 0/0 | 5814 | 2 | 2 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0012c0058 | 0/0 | 5814 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0013c0053 | 0/0 | 5814 | 2 | 0 | 1 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0014c0059 | 0/0 | 5814 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0014c0060 | 0/0 | 5814 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0015c0054 | 0/0 | 5814 | 2 | 0 | 1 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0016c0116 | 0/0 | 5814 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0016c0117 | 0/0 | 5814 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0017c0036 | 0/0 | 5814 | 2 | 2 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0018c0100 | 0/0 | 5814 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0019c0076 | 0/0 | 5814 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0020c0092 | 0/0 | 5814 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0021c0056 | 0/0 | 5814 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0022c0101 | 0/0 | 5814 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0023c0074 | 0/0 | 5814 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0024c0088 | 0/0 | 5814 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0025c0115 | 0/0 | 5814 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0026c0055 | 0/0 | 5814 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0027c0069 | 0/0 | 5814 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0028c0066 | 0/0 | 5814 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0029c0098 | 0/0 | 5814 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0030c0077 | 0/0 | 5814 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0031c0086 | 0/0 | 5814 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0032c0114 | 0/0 | 5814 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0033c0102 | 0/0 | 5814 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0034c0112 | 0/0 | 5814 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0035c0085 | 0/0 | 5814 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0036c0073 | 0/0 | 5814 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0037c0109 | 0/0 | 5814 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0038c0084 | 0/0 | 5814 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0039c0082 | 0/0 | 5814 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0040c0080 | 0/0 | 5814 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0041c0067 | 0/0 | 5814 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
chr17 | 10295865 | 10378006 | ||
a0042c0057 | 0/0 | 5814 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | ATGAG others(5809): Show |
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 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0001c0004t0001 | 0/0 | 5994 | 18 | 3 | 2 | 11 | 2 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0001c0006t0001 | 0/0 | 5994 | 11 | 3 | 3 | 1 | 2 | 2 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0001c0007t0001 | 0/0 | 5994 | 11 | 2 | 1 | 7 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0001c0012t0001 | 0/0 | 5994 | 8 | 2 | 0 | 4 | 0 | 2 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0001c0014t0001 | 0/0 | 5994 | 7 | 4 | 2 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0001c0015t0001 | 0/0 | 5994 | 7 | 5 | 0 | 2 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0001c0017t0001 | 0/0 | 5994 | 6 | 1 | 1 | 2 | 0 | 2 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0001c0022t0001 | 0/0 | 5994 | 4 | 4 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0001c0027t0001 | 0/0 | 5994 | 4 | 0 | 3 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0001c0034t0001 | 0/0 | 5994 | 3 | 0 | 2 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0001c0039t0001 | 0/0 | 5994 | 2 | 0 | 0 | 2 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0001c0040t0001 | 0/0 | 5994 | 2 | 1 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0001c0042t0001 | 0/0 | 5994 | 2 | 2 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0001c0046t0001 | 0/0 | 5994 | 2 | 1 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0001c0050t0001 | 0/0 | 5994 | 2 | 0 | 1 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0001c0051t0001 | 0/0 | 5994 | 2 | 0 | 0 | 2 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0001c0062t0001 | 0/0 | 5994 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0001c0072t0001 | 0/0 | 5994 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0001c0075t0001 | 0/0 | 5994 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0001c0089t0001 | 0/0 | 5994 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0001c0090t0001 | 0/0 | 5994 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0001c0103t0001 | 0/0 | 5994 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0001c0105t0001 | 0/0 | 5994 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0001c0108t0001 | 0/0 | 5994 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0001c0110t0001 | 0/0 | 5994 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0001c0111t0001 | 0/0 | 5994 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0001c0113t0001 | 0/0 | 5994 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0001c0118t0001 | 0/0 | 5994 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0001c0119t0001 | 0/0 | 5994 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0001c0120t0001 | 0/0 | 5994 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0002c0005t0001 | 1/0 | 5994 | 17 | 4 | 6 | 2 | 0 | 4 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0002c0008t0001 | 0/0 | 5994 | 11 | 1 | 5 | 3 | 2 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0002c0009t0001 | 0/0 | 5994 | 9 | 2 | 0 | 7 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0002c0009t0002 | 0/0 | 5994 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0002c0013t0001 | 0/0 | 5994 | 7 | 1 | 0 | 6 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0002c0025t0001 | 0/0 | 5994 | 4 | 0 | 1 | 0 | 1 | 2 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0002c0041t0001 | 0/0 | 5994 | 2 | 2 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0002c0061t0001 | 0/0 | 5994 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0002c0071t0001 | 0/0 | 5994 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0002c0091t0001 | 0/0 | 5994 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0003c0001t0001 | 0/0 | 5994 | 25 | 0 | 5 | 17 | 0 | 3 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0003c0011t0001 | 0/0 | 5994 | 9 | 3 | 3 | 2 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0003c0019t0001 | 0/0 | 5994 | 6 | 0 | 0 | 6 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0003c0030t0001 | 0/0 | 5994 | 3 | 1 | 0 | 2 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0003c0038t0001 | 0/0 | 5994 | 2 | 1 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0003c0043t0001 | 0/0 | 5994 | 2 | 0 | 0 | 2 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0003c0045t0001 | 0/0 | 5994 | 2 | 0 | 0 | 2 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0003c0064t0001 | 0/0 | 5994 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0003c0065t0001 | 0/0 | 5994 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0003c0070t0001 | 0/0 | 5994 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0003c0078t0001 | 0/0 | 5994 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0003c0081t0001 | 0/0 | 5994 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0003c0094t0001 | 0/0 | 5994 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0004c0002t0001 | 0/1 | 5994 | 24 | 0 | 5 | 18 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0004c0010t0001 | 0/0 | 5994 | 9 | 0 | 2 | 6 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0004c0021t0001 | 0/0 | 5994 | 4 | 1 | 2 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0004c0026t0001 | 0/0 | 5994 | 4 | 1 | 2 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0004c0048t0001 | 0/0 | 5994 | 2 | 0 | 0 | 1 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0004c0106t0001 | 0/0 | 5994 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0005c0016t0001 | 0/0 | 5994 | 7 | 1 | 0 | 4 | 0 | 2 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0005c0018t0001 | 0/0 | 5994 | 6 | 0 | 0 | 6 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0005c0028t0001 | 0/0 | 5994 | 3 | 3 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0005c0037t0001 | 0/0 | 5994 | 2 | 2 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0005c0047t0001 | 0/0 | 5994 | 2 | 0 | 2 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0005c0079t0001 | 0/0 | 5994 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0005c0087t0001 | 0/0 | 5994 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0005c0095t0001 | 0/0 | 5994 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0006c0024t0001 | 0/0 | 5994 | 4 | 1 | 0 | 3 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0006c0029t0001 | 0/0 | 5994 | 3 | 0 | 0 | 3 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0006c0033t0001 | 0/0 | 5994 | 3 | 1 | 0 | 2 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0006c0052t0001 | 0/0 | 5994 | 2 | 0 | 2 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0006c0068t0001 | 0/0 | 5994 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0006c0099t0001 | 0/0 | 5994 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0007c0020t0001 | 0/0 | 5994 | 4 | 2 | 1 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0007c0083t0001 | 0/0 | 5994 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0007c0096t0001 | 0/0 | 5994 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0007c0097t0001 | 0/0 | 5994 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0007c0107t0001 | 0/0 | 5994 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0008c0032t0001 | 0/0 | 5994 | 3 | 3 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0008c0049t0001 | 0/0 | 5994 | 2 | 2 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0009c0044t0001 | 0/0 | 5994 | 2 | 0 | 0 | 0 | 0 | 2 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0009c0063t0001 | 0/0 | 5994 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0009c0093t0001 | 0/0 | 5994 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0009c0104t0001 | 0/0 | 5994 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0010c0023t0001 | 0/0 | 5994 | 4 | 0 | 0 | 4 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0011c0031t0001 | 0/0 | 5994 | 3 | 0 | 3 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0012c0035t0001 | 0/0 | 5994 | 2 | 2 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0012c0058t0001 | 0/0 | 5994 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0013c0053t0001 | 0/0 | 5994 | 2 | 0 | 1 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0014c0059t0001 | 0/0 | 5994 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0014c0060t0001 | 0/0 | 5994 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0015c0054t0001 | 0/0 | 5994 | 2 | 0 | 1 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0016c0116t0001 | 0/0 | 5994 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0016c0117t0001 | 0/0 | 5994 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0017c0036t0001 | 0/0 | 5994 | 2 | 2 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0018c0100t0001 | 0/0 | 5994 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0019c0076t0001 | 0/0 | 5994 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0020c0092t0001 | 0/0 | 5994 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0021c0056t0001 | 0/0 | 5994 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0022c0101t0001 | 0/0 | 5994 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0023c0074t0001 | 0/0 | 5994 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0024c0088t0001 | 0/0 | 5994 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0025c0115t0001 | 0/0 | 5994 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0026c0055t0001 | 0/0 | 5994 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0027c0069t0001 | 0/0 | 5994 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0028c0066t0001 | 0/0 | 5994 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0029c0098t0001 | 0/0 | 5994 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0030c0077t0001 | 0/0 | 5994 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0031c0086t0001 | 0/0 | 5994 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0032c0114t0001 | 0/0 | 5994 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0033c0102t0001 | 0/0 | 5994 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0034c0112t0001 | 0/0 | 5994 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0035c0085t0001 | 0/0 | 5994 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0036c0073t0001 | 0/0 | 5994 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0037c0109t0001 | 0/0 | 5994 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0038c0084t0001 | 0/0 | 5994 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0039c0082t0001 | 0/0 | 5994 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0040c0080t0001 | 0/0 | 5994 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0041c0067t0001 | 0/0 | 5994 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
a0042c0057t0001 | 0/0 | 5994 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | GAAAT others(5989): Show |
chr17 | 10295865 | 10378006 |
actghapid | grch38/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 |
a0001c0003t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0003t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0003t0001g0040 | 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 |
a0001c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0003t0001g0062 | 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 |
a0001c0003t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0003t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0003t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0003t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0003t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0003t0001g0226 | 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 |
a0001c0003t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0003t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0003t0001g0242 | 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 |
a0001c0003t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0003t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0003t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0004t0001g0026 | 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 |
a0001c0004t0001g0061 | 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 |
a0001c0004t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0004t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0004t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0004t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0004t0001g0354 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0004t0001g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0004t0001g0356 | 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 |
a0001c0006t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0006t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0006t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0006t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0006t0001g0121 | 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 |
a0001c0006t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0006t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0006t0001g0337 | 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 |
a0001c0007t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0007t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0007t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0007t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0007t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0007t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0007t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0007t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
a0001c0012t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0012t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0012t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0012t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0012t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0012t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0012t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0012t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 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 |
a0001c0014t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0014t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0014t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0014t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0014t0001g0372 | 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 |
a0001c0015t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0015t0001g0134 | 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 |
a0001c0015t0001g0373 | 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 |
a0001c0017t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0017t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0017t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0017t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0017t0001g0119 | 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 |
a0001c0022t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0022t0001g0335 | 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 |
a0001c0027t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0027t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0027t0001g0322 | 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 |
a0001c0034t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0039t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0039t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0040t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0040t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0042t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0042t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0046t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0046t0001g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0050t0001g0037 | 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 |
a0001c0051t0001g0060 | 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 |
a0001c0062t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0072t0001g0163 | 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 |
a0001c0105t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0108t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0110t0001g0126 | 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 |
a0001c0113t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0118t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0001c0119t0001g0351 | 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 |
a0002c0005t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0002c0005t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0002c0005t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0002c0005t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0002c0005t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0002c0005t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0002c0005t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0002c0005t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0002c0005t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0002c0005t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0002c0005t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0002c0005t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0002c0005t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0002c0005t0001g0237 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0002c0005t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0002c0005t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0002c0005t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0002c0008t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0002c0008t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0002c0008t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0002c0008t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0002c0008t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0002c0008t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0002c0008t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0002c0008t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0002c0008t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0002c0008t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0002c0008t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0002c0009t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0002c0009t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0002c0009t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0002c0009t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0002c0009t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0002c0009t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0002c0009t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0002c0009t0001g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0002c0009t0001g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0002c0009t0002g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0002c0013t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0002c0013t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0002c0013t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0002c0013t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0002c0013t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0002c0013t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0002c0013t0001g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0002c0025t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0002c0025t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0002c0025t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0002c0025t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0002c0041t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0002c0041t0001g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0002c0061t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0002c0071t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0002c0091t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0001t0001g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0011t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0011t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0011t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0011t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0011t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0011t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0011t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0011t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0011t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0019t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0019t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0019t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0019t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0019t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0019t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0030t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0030t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0030t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0038t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0038t0001g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0043t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0043t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0045t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0045t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0064t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0065t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0070t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0078t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0081t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0003c0094t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0004c0002t0001g0025 | 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 |
a0004c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0004c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0004c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0004c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0004c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0004c0002t0001g0210 | 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 |
a0004c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0004c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0004c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0004c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0004c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0004c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0004c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0004c0002t0001g0271 | 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 |
a0004c0010t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0004c0010t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0004c0010t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0004c0010t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0004c0010t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0004c0010t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0004c0010t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0004c0021t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0004c0021t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0004c0021t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0004c0021t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 |
a0004c0026t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0004c0026t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0004c0026t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0004c0048t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0004c0048t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0004c0106t0001g0177 | 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 |
a0005c0016t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0005c0016t0001g0058 | 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 |
a0005c0016t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0005c0016t0001g0218 | 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 |
a0005c0018t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0005c0018t0001g0205 | 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 |
a0005c0018t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0005c0018t0001g0291 | 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 |
a0005c0028t0001g0084 | 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 |
a0005c0037t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0005c0047t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0005c0047t0001g0136 | 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 |
a0005c0087t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0005c0095t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0006c0024t0001g0128 | 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 |
a0006c0024t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0006c0029t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0006c0029t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0006c0029t0001g0311 | 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 |
a0006c0033t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0006c0052t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0006c0052t0001g0243 | 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 |
a0006c0099t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0007c0020t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0007c0020t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0007c0020t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0007c0020t0001g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0007c0083t0001g0127 | 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 |
a0007c0107t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0008c0032t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0008c0032t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0008c0032t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0008c0049t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0008c0049t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0009c0044t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0009c0044t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0009c0063t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0009c0093t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0009c0104t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0010c0023t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0010c0023t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0010c0023t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0010c0023t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0011c0031t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0011c0031t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0011c0031t0001g0063 | 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 |
a0013c0053t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0013c0053t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0014c0059t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0014c0060t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0015c0054t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0015c0054t0001g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0016c0116t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0016c0117t0001g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
a0018c0100t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0019c0076t0001g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0020c0092t0001g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0021c0056t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0022c0101t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0023c0074t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0024c0088t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0025c0115t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0026c0055t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0027c0069t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0028c0066t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0029c0098t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0030c0077t0001g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0031c0086t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0032c0114t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0033c0102t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0034c0112t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0035c0085t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0036c0073t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0037c0109t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0038c0084t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0039c0082t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0040c0080t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
a0041c0067t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | a0002 | c0008 | t0001 | g0054 | EUR | GBR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG00099 | hp2 | a0013 | c0053 | t0001 | g0051 | EUR | GBR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG00140 | hp1 | a0002 | c0025 | t0001 | g0162 | EUR | GBR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG00140 | hp2 | a0014 | c0059 | t0001 | g0044 | 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 | a0018 | 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 | g0331 | EAS | CHS | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG00544 | hp1 | a0002 | c0013 | t0001 | g0019 | 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 | a0003 | c0001 | t0001 | g0004 | EAS | CHS | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG00621 | hp2 | a0001 | c0004 | t0001 | g0061 | EAS | CHS | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG00639 | hp1 | a0001 | c0003 | t0001 | g0040 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG00639 | hp2 | a0001 | c0006 | t0001 | g0232 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG00733 | hp1 | a0019 | c0076 | t0001 | g0352 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG00733 | hp2 | a0004 | c0026 | t0001 | g0164 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG00735 | hp1 | a0001 | c0004 | t0001 | g0355 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG00735 | hp2 | a0002 | c0025 | t0001 | g0154 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG00738 | hp1 | a0001 | c0034 | t0001 | g0321 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG00738 | hp2 | a0002 | c0008 | t0001 | g0036 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG00741 | hp1 | a0001 | c0046 | t0001 | g0343 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG00741 | hp2 | a0005 | c0087 | t0001 | g0332 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG01069 | hp1 | a0004 | c0021 | t0001 | g0092 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG01069 | hp2 | a0001 | c0003 | t0001 | g0225 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG01070 | hp1 | a0002 | c0005 | t0001 | g0112 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG01070 | hp2 | a0001 | c0108 | t0001 | g0158 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG01071 | hp1 | a0002 | c0005 | t0001 | g0111 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG01071 | hp2 | a0001 | c0003 | t0001 | g0226 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG01074 | hp1 | a0004 | c0021 | t0001 | g0091 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG01074 | hp2 | a0001 | c0003 | t0001 | g0228 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG01081 | hp1 | a0003 | c0011 | t0001 | g0198 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG01081 | hp2 | a0001 | c0003 | t0001 | g0038 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG01099 | hp1 | a0001 | c0027 | t0001 | g0165 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG01099 | hp2 | a0020 | c0092 | t0001 | g0368 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG01106 | hp1 | a0001 | c0027 | t0001 | g0322 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG01106 | hp2 | a0001 | c0007 | t0001 | g0283 | 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 | g0131 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG01167 | hp2 | a0001 | c0072 | t0001 | g0163 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG01169 | hp1 | a0005 | c0047 | t0001 | g0136 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG01169 | hp2 | a0002 | c0008 | t0001 | g0048 | 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 | g0045 | 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 | g0201 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG01243 | hp2 | a0007 | c0020 | t0001 | g0333 | AMR | PUR | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG01255 | hp1 | a0001 | c0014 | t0001 | g0125 | AMR | CLM | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG01255 | hp2 | a0004 | c0106 | t0001 | g0177 | AMR | CLM | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG01256 | hp1 | a0002 | c0008 | t0001 | g0229 | AMR | CLM | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG01256 | hp2 | a0004 | c0026 | t0001 | g0166 | 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 | a0013 | c0053 | t0001 | g0042 | AMR | CLM | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG01258 | hp1 | a0002 | c0008 | t0001 | g0227 | 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 | a0002 | c0005 | t0001 | g0147 | AMR | CLM | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG01261 | hp2 | a0002 | c0008 | t0001 | g0348 | AMR | CLM | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG01346 | hp1 | a0001 | c0006 | t0001 | g0108 | AMR | CLM | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG01346 | hp2 | a0003 | c0001 | t0001 | g0306 | 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 | g0059 | AMR | CLM | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG01361 | hp1 | a0002 | c0005 | t0001 | g0118 | AMR | CLM | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG01361 | hp2 | a0011 | c0031 | t0001 | g0063 | AMR | CLM | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG01433 | hp1 | a0003 | c0001 | t0001 | g0325 | AMR | CLM | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG01433 | hp2 | a0011 | c0031 | t0001 | g0052 | AMR | CLM | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG01496 | hp1 | a0001 | c0003 | t0001 | g0039 | AMR | CLM | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG01496 | hp2 | a0001 | c0050 | t0001 | g0037 | AMR | CLM | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG01515 | hp1 | a0002 | c0008 | t0001 | g0047 | EUR | IBS | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG01515 | hp2 | a0001 | c0004 | t0001 | g0356 | EUR | IBS | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG01516 | hp1 | a0021 | 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 | g0354 | 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 | g0339 | AFR | ACB | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG01884 | hp2 | a0001 | c0006 | t0001 | g0337 | AFR | ACB | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG01891 | hp1 | a0001 | c0042 | t0001 | g0105 | 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 | g0309 | AMR | PEL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG01934 | hp1 | a0003 | c0070 | t0001 | g0109 | AMR | PEL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG01934 | hp2 | a0001 | c0003 | t0001 | g0241 | AMR | PEL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG01943 | hp1 | a0001 | c0003 | t0001 | g0200 | AMR | PEL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG01943 | hp2 | a0006 | c0052 | t0001 | g0243 | AMR | PEL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG01952 | hp1 | a0015 | c0054 | t0001 | g0150 | AMR | PEL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG01952 | hp2 | a0002 | c0005 | t0001 | g0098 | 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 | a0003 | c0011 | t0001 | g0248 | AMR | PEL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG01978 | hp1 | a0003 | c0001 | t0001 | g0359 | AMR | PEL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG01978 | hp2 | a0022 | c0101 | t0001 | g0074 | AMR | PEL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG01981 | hp1 | a0003 | c0001 | t0001 | g0258 | AMR | PEL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG01981 | hp2 | a0001 | c0004 | t0001 | g0208 | AMR | PEL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG02004 | hp1 | a0003 | c0011 | t0001 | g0287 | AMR | PEL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG02004 | hp2 | a0001 | c0003 | t0001 | g0197 | AMR | PEL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG02027 | hp1 | a0002 | c0008 | t0001 | g0329 | 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 | g0120 | AFR | ACB | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG02055 | hp2 | a0001 | c0113 | t0001 | g0135 | AFR | ACB | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG02074 | hp1 | a0003 | c0094 | t0001 | g0220 | EAS | KHV | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG02074 | hp2 | a0016 | c0116 | t0001 | g0090 | EAS | KHV | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG02080 | hp1 | a0003 | c0001 | t0001 | g0310 | EAS | KHV | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG02080 | hp2 | a0002 | c0009 | t0001 | g0362 | EAS | KHV | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG02083 | hp1 | a0001 | c0007 | t0001 | g0301 | EAS | KHV | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG02083 | hp2 | a0005 | c0018 | t0001 | g0291 | EAS | KHV | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG02135 | hp1 | a0006 | c0029 | t0001 | g0256 | 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 | g0187 | AFR | ACB | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG02145 | hp2 | a0002 | c0013 | t0001 | g0370 | AFR | ACB | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG02148 | hp1 | a0006 | c0052 | t0001 | g0196 | AMR | PEL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG02148 | hp2 | a0001 | c0040 | t0001 | g0101 | AMR | PEL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG02155 | hp1 | a0002 | c0009 | t0001 | g0298 | EAS | CDX | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG02155 | hp2 | a0001 | c0051 | t0001 | g0060 | EAS | CDX | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG02165 | hp1 | a0003 | c0001 | t0001 | g0281 | EAS | CDX | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG02165 | hp2 | a0001 | c0110 | t0001 | g0126 | EAS | CDX | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG02257 | hp1 | a0001 | c0040 | t0001 | g0102 | AFR | ACB | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG02257 | hp2 | a0001 | c0119 | t0001 | g0351 | AFR | ACB | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG02258 | hp1 | a0001 | c0046 | t0001 | g0319 | AFR | ACB | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG02258 | hp2 | a0023 | c0074 | t0001 | g0076 | AFR | ACB | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG02280 | hp1 | a0007 | c0020 | t0001 | g0106 | 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 | g0307 | 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 | g0199 | AMR | PEL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG02300 | hp2 | a0003 | c0001 | t0001 | g0292 | AMR | PEL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG02451 | hp1 | a0001 | c0022 | t0001 | g0334 | AFR | ACB | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG02451 | hp2 | a0001 | c0015 | t0001 | g0134 | 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 | a0003 | c0011 | t0001 | g0213 | EAS | KHV | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG02602 | hp1 | a0003 | c0011 | t0001 | g0081 | SAS | PJL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG02602 | hp2 | a0004 | c0048 | t0001 | g0265 | SAS | PJL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG02622 | hp1 | a0001 | c0007 | t0001 | g0117 | AFR | GWD | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG02622 | hp2 | a0007 | c0083 | t0001 | g0127 | AFR | GWD | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG02630 | hp1 | a0008 | 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 | a0003 | c0038 | t0001 | g0369 | AFR | GWD | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG02698 | hp1 | a0002 | c0005 | t0001 | g0261 | SAS | PJL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG02698 | hp2 | a0001 | c0007 | t0001 | g0326 | SAS | PJL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG02717 | hp1 | a0003 | c0011 | t0001 | g0186 | AFR | GWD | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG02717 | hp2 | a0001 | c0014 | t0001 | g0372 | AFR | GWD | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG02723 | hp1 | a0001 | c0015 | t0001 | g0130 | AFR | GWD | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG02723 | hp2 | a0003 | c0011 | t0001 | g0202 | AFR | GWD | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG02735 | hp1 | a0001 | c0012 | t0001 | g0285 | SAS | PJL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG02735 | hp2 | a0025 | c0115 | t0001 | g0267 | SAS | PJL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG02809 | hp1 | a0001 | c0015 | t0001 | g0373 | 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 | g0335 | AFR | GWD | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG02886 | hp2 | a0001 | c0118 | t0001 | g0350 | AFR | GWD | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG02895 | hp1 | a0001 | c0012 | t0001 | g0345 | AFR | GWD | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG02895 | hp2 | a0008 | c0032 | t0001 | g0172 | AFR | GWD | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG02897 | hp1 | a0001 | c0012 | t0001 | g0336 | AFR | GWD | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG02897 | hp2 | a0008 | 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 | a0002 | c0005 | t0001 | g0224 | AFR | ESN | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG02965 | hp1 | a0002 | c0009 | t0001 | g0377 | AFR | ESN | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG02965 | hp2 | a0001 | c0062 | t0001 | g0273 | AFR | ESN | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG02970 | hp1 | a0002 | c0091 | t0001 | g0133 | 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 | g0234 | AFR | ESN | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG02976 | hp2 | a0003 | c0011 | t0001 | g0203 | AFR | ESN | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG03041 | hp1 | a0003 | c0030 | t0001 | g0129 | AFR | GWD | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG03041 | hp2 | a0008 | c0049 | t0001 | g0151 | AFR | GWD | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG03098 | hp1 | a0002 | c0008 | t0001 | g0222 | AFR | MSL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG03098 | hp2 | a0002 | c0005 | t0001 | g0107 | AFR | MSL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG03130 | hp1 | a0002 | c0005 | t0001 | g0338 | AFR | ESN | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG03130 | hp2 | a0001 | c0004 | t0001 | g0188 | AFR | ESN | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG03139 | hp1 | a0006 | c0099 | t0001 | g0340 | AFR | ESN | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG03139 | hp2 | a0001 | c0014 | t0001 | g0132 | AFR | ESN | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG03209 | hp1 | a0001 | c0014 | t0001 | g0094 | 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 | g0315 | SAS | PJL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG03239 | hp2 | a0002 | c0025 | t0001 | g0157 | SAS | PJL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG03453 | hp1 | a0001 | c0006 | t0001 | g0233 | AFR | MSL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG03453 | hp2 | a0006 | c0024 | t0001 | g0128 | 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 | a0027 | c0069 | t0001 | g0236 | AFR | MSL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG03491 | hp1 | a0003 | c0001 | t0001 | g0277 | SAS | PJL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG03491 | hp2 | a0009 | c0044 | t0001 | g0138 | SAS | PJL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG03492 | hp1 | a0009 | c0044 | t0001 | g0139 | SAS | PJL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG03492 | hp2 | a0005 | c0016 | t0001 | g0058 | 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 | a0028 | 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 | g0238 | AFR | GWD | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG03579 | hp1 | a0008 | c0049 | t0001 | g0244 | AFR | MSL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG03579 | hp2 | a0002 | c0041 | t0001 | g0365 | AFR | MSL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG03654 | hp1 | a0001 | c0006 | t0001 | g0113 | SAS | PJL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG03654 | hp2 | a0029 | c0098 | t0001 | g0024 | SAS | PJL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG03669 | hp1 | a0007 | c0107 | t0001 | g0167 | SAS | PJL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG03669 | hp2 | a0030 | c0077 | t0001 | g0353 | SAS | PJL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG03688 | hp1 | a0003 | c0001 | t0001 | g0318 | SAS | STU | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG03688 | hp2 | a0003 | c0001 | t0001 | g0250 | SAS | STU | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG03704 | hp1 | a0005 | c0016 | t0001 | g0218 | SAS | PJL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG03704 | hp2 | a0031 | c0086 | t0001 | g0262 | SAS | PJL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG03710 | hp1 | a0032 | c0114 | t0001 | g0330 | SAS | PJL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG03710 | hp2 | a0001 | c0006 | t0001 | g0087 | SAS | PJL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG03834 | hp1 | a0001 | c0017 | t0001 | g0116 | SAS | BEB | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG03834 | hp2 | a0009 | c0093 | t0001 | g0259 | SAS | BEB | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG03927 | hp1 | a0009 | c0063 | t0001 | g0260 | SAS | BEB | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG03927 | hp2 | a0007 | c0020 | t0001 | g0349 | SAS | BEB | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG03942 | hp1 | a0001 | c0017 | t0001 | g0119 | SAS | BEB | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG03942 | hp2 | a0009 | c0104 | t0001 | g0161 | SAS | BEB | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG04115 | hp1 | a0001 | c0105 | t0001 | g0160 | SAS | STU | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG04115 | hp2 | a0002 | c0005 | t0001 | g0110 | SAS | STU | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG04199 | hp1 | a0033 | c0102 | t0001 | g0066 | SAS | STU | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG04199 | hp2 | a0002 | c0005 | t0001 | g0041 | SAS | STU | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG04204 | hp1 | a0014 | c0060 | t0001 | g0095 | SAS | STU | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG04204 | hp2 | a0002 | c0009 | t0002 | g0003 | SAS | STU | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG04228 | hp1 | a0002 | c0005 | t0001 | g0097 | SAS | STU | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG04228 | hp2 | a0001 | c0012 | t0001 | g0289 | SAS | STU | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18522 | hp1 | a0001 | c0003 | t0001 | g0214 | 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 | g0083 | AFR | YRI | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18906 | hp2 | a0002 | c0009 | t0001 | g0374 | AFR | YRI | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18939 | hp1 | a0034 | c0112 | t0001 | g0067 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18939 | hp2 | a0003 | c0019 | t0001 | g0190 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18941 | hp1 | a0003 | c0001 | t0001 | g0264 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18941 | hp2 | a0003 | c0019 | t0001 | g0049 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18942 | hp1 | a0004 | c0002 | t0001 | g0219 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18942 | hp2 | a0003 | c0045 | t0001 | g0328 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18943 | hp1 | a0001 | c0003 | t0001 | g0062 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18943 | hp2 | a0003 | c0001 | t0001 | g0313 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18944 | hp1 | a0004 | c0002 | t0001 | g0216 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18944 | hp2 | a0003 | c0030 | t0001 | g0017 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18946 | hp1 | a0003 | c0019 | t0001 | g0195 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18946 | hp2 | a0003 | c0001 | t0001 | g0297 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18947 | hp1 | a0003 | c0011 | t0001 | g0239 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18947 | hp2 | a0001 | c0003 | t0001 | g0247 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18948 | hp1 | a0006 | c0029 | t0001 | g0280 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18948 | hp2 | a0003 | c0045 | t0001 | g0033 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18950 | hp1 | a0001 | c0007 | t0001 | g0288 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18950 | hp2 | a0001 | c0004 | t0001 | g0027 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18951 | hp1 | a0002 | c0061 | t0001 | g0104 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18951 | hp2 | a0001 | c0012 | t0001 | g0275 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18952 | hp1 | a0001 | c0003 | t0001 | g0347 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18952 | hp2 | a0002 | c0005 | t0001 | g0086 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18953 | hp1 | a0003 | c0030 | t0001 | g0023 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18953 | hp2 | a0002 | c0005 | t0001 | g0089 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18954 | hp1 | a0004 | c0002 | t0001 | g0207 | 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 | a0003 | c0001 | t0001 | g0043 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18959 | hp2 | a0003 | c0078 | t0001 | g0279 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18961 | hp1 | a0004 | c0002 | t0001 | g0221 | 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 | a0002 | c0008 | t0001 | g0255 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18962 | hp2 | a0003 | 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 | g0271 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18965 | hp2 | a0002 | c0071 | t0001 | g0103 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18967 | hp1 | a0010 | c0023 | t0001 | g0317 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18967 | hp2 | a0003 | c0001 | t0001 | g0268 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18968 | hp1 | a0004 | c0002 | t0001 | g0210 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18968 | hp2 | a0001 | c0003 | t0001 | g0242 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18969 | hp1 | a0002 | c0009 | t0001 | g0055 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18969 | hp2 | a0003 | c0038 | t0001 | g0122 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18972 | hp1 | a0004 | c0002 | t0001 | g0235 | 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 | a0003 | c0019 | t0001 | g0191 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18973 | hp2 | a0004 | c0002 | t0001 | g0269 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18974 | hp1 | a0005 | c0018 | t0001 | g0205 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18974 | hp2 | a0035 | c0085 | t0001 | g0293 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18975 | hp1 | a0004 | c0010 | t0001 | g0299 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18975 | hp2 | a0001 | c0004 | t0001 | g0346 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18978 | hp1 | a0005 | c0095 | t0001 | g0057 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18978 | hp2 | a0005 | c0018 | t0001 | g0282 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18979 | hp1 | a0003 | c0065 | t0001 | g0079 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18979 | hp2 | a0004 | c0010 | t0001 | g0263 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18980 | hp1 | a0003 | c0001 | t0001 | g0294 | 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 | g0270 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18983 | hp2 | a0003 | c0001 | t0001 | g0303 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18984 | hp1 | a0001 | c0004 | t0001 | g0314 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18984 | hp2 | a0004 | c0002 | t0001 | g0217 | 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 | g0290 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18988 | hp1 | a0001 | c0003 | t0001 | g0050 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18988 | hp2 | a0001 | c0007 | t0001 | g0278 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18990 | hp1 | a0015 | c0054 | t0001 | g0379 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18990 | hp2 | a0003 | c0001 | t0001 | g0056 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18991 | hp1 | a0036 | c0073 | t0001 | g0046 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18991 | hp2 | a0001 | c0007 | t0001 | g0327 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18992 | hp1 | a0001 | c0039 | t0001 | g0096 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18992 | hp2 | a0004 | c0002 | t0001 | g0194 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18993 | hp1 | a0003 | c0001 | t0001 | g0284 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18993 | hp2 | a0004 | c0002 | t0001 | g0211 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18995 | hp1 | a0006 | c0024 | t0001 | g0183 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18995 | hp2 | a0002 | c0013 | t0001 | g0018 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18998 | hp1 | a0010 | c0023 | t0001 | g0286 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18998 | hp2 | a0003 | c0001 | t0001 | g0253 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18999 | hp1 | a0001 | c0012 | t0001 | g0302 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18999 | hp2 | a0037 | c0109 | t0001 | g0305 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA19000 | hp1 | a0004 | c0002 | t0001 | g0025 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA19000 | hp2 | a0002 | c0009 | t0001 | g0316 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA19003 | hp1 | a0004 | c0048 | t0001 | g0206 | 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 | g0088 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA19004 | hp2 | a0001 | c0012 | t0001 | g0304 | 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 | g0300 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA19010 | hp1 | a0002 | c0013 | t0001 | g0022 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA19010 | hp2 | a0006 | c0033 | t0001 | g0215 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA19043 | hp1 | a0001 | c0006 | t0001 | g0121 | AFR | LWK | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA19043 | hp2 | a0003 | c0064 | t0001 | g0230 | AFR | LWK | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA19055 | hp1 | a0004 | c0010 | t0001 | g0312 | 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 | g0099 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA19056 | hp2 | a0002 | 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 | g0182 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA19063 | hp1 | a0003 | c0001 | t0001 | g0357 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA19063 | hp2 | a0038 | c0084 | t0001 | g0254 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA19064 | hp1 | a0001 | c0006 | t0001 | g0085 | 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 | a0002 | c0009 | t0001 | g0320 | 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 | g0311 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA19067 | hp1 | a0039 | 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 | g0020 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA19068 | hp2 | a0004 | c0002 | t0001 | g0189 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA19070 | hp1 | a0010 | c0023 | t0001 | g0296 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA19070 | hp2 | a0003 | c0019 | t0001 | g0192 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA19072 | hp1 | a0004 | c0002 | t0001 | g0123 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA19072 | hp2 | a0003 | c0019 | t0001 | g0193 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA19074 | hp1 | a0002 | c0008 | t0001 | g0361 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA19074 | hp2 | a0003 | c0001 | t0001 | g0308 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA19078 | hp1 | a0002 | c0013 | t0001 | g0012 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA19078 | hp2 | a0016 | c0117 | t0001 | g0380 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA19079 | hp1 | a0003 | c0081 | t0001 | g0005 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA19079 | hp2 | a0005 | c0016 | t0001 | g0053 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA19083 | hp1 | a0001 | c0017 | t0001 | g0115 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA19083 | hp2 | a0010 | c0023 | t0001 | g0266 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA19084 | hp1 | a0002 | c0009 | t0001 | g0274 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA19084 | hp2 | a0004 | c0002 | t0001 | g0124 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA19085 | hp1 | a0002 | c0013 | t0001 | g0016 | 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 | g0342 | 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 | a0003 | c0001 | t0001 | g0324 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA19088 | hp2 | a0002 | c0009 | t0001 | g0295 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA19091 | hp1 | a0001 | c0004 | t0001 | g0026 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA19091 | hp2 | a0001 | c0012 | t0001 | g0344 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA19240 | hp1 | a0004 | c0021 | t0001 | g0137 | 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 | a0040 | c0080 | t0001 | g0204 | 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 | g0176 | EUR | TSI | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA20752 | hp2 | a0001 | c0027 | t0001 | g0155 | EUR | TSI | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA20805 | hp1 | a0041 | c0067 | t0001 | g0093 | 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 | a0002 | c0025 | t0001 | g0156 | SAS | GIH | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA20905 | hp2 | a0004 | c0021 | t0001 | g0114 | SAS | GIH | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG01123 | hp1 | a0004 | c0002 | t0001 | g0223 | AMR | CLM | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG01123 | hp2 | a0002 | c0005 | t0001 | g0100 | 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 | g0084 | 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 | a0024 | c0088 | t0001 | g0257 | 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 | a0026 | c0055 | t0001 | g0276 | AFR | MSL | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
HG03471 | hp2 | a0002 | c0005 | t0001 | g0341 | 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 | a0003 | c0043 | t0001 | g0323 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA18955 | hp2 | a0003 | c0001 | t0001 | g0252 | EAS | JPT | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
NA20300 | hp1 | a0007 | c0020 | t0001 | g0272 | 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 | a0002 | c0041 | t0001 | g0231 | AFR | LWK | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
homoSapiens | chm13v2 | a0004 | c0002 | t0001 | g0075 | REF | REF | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
homoSapiens | grch38p0 | a0002 | c0005 | t0001 | g0237 | REF | REF | MYH13_chr17_10295865_10378006 | MYH13 | chr17 | 10295865 | 10378006 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:10303278 | T | C | 12 | a0003 a0006 a0007 others(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 | a0038 | 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 | a0013 a0033 a0041 |
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 | a0018 | 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 | a0028 | 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 | a0040 | 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 | a0031 | 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 | a0039 | 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 | a0022 | 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 | a0008 | 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 | a0029 | 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 | a0004 a0009 a0010 others(8): Show |
60 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(57): 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 | a0010 a0035 |
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 | a0037 | 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 | a0030 | 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 | a0003 a0005 a0009 others(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 | a0001 a0004 a0006 others(17): Show |
213 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(210): 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 | a0019 | 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 | a0027 | 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 | a0020 | 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 | a0014 | 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 | a0023 | 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 | a0036 | 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 | a0037 | 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 | a0012 a0017 |
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 | a0021 | 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 | a0026 | 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 | a0034 | 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 | a0025 a0032 |
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 | a0015 a0016 |
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 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
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 | a0003c0064 | 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 | a0003c0078 | 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 | a0032c0114 | 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 | a0001c0003 a0001c0006 a0001c0012 others(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 | a0003c0019 a0003c0043 |
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 | a0003c0019 a0003c0043 |
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 | a0003c0019 a0003c0043 |
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 | a0007c0096 a0016c0116 |
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 | a0003c0081 a0003c0094 |
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 | a0001c0089 a0003c0001 a0003c0011 others(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 | a0001c0022 a0001c0046 a0001c0062 others(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 | a0003c0019 a0003c0043 |
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 | a0001c0040 a0001c0050 a0001c0105 others(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 | a0001c0007 a0001c0012 a0001c0039 others(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 | a0002c0091 | 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 | a0001c0003 a0001c0004 a0001c0027 others(44): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): 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 | a0001c0105 a0009c0104 |
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 | a0001c0003 a0001c0004 a0001c0007 others(89): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): 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 | a0001c0027 a0001c0034 a0001c0105 others(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 | a0001c0118 a0001c0119 |
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 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:10372991 | C | G | 1 | a0002c0009t0002 | 1 | HG04204.hp2 | 5_prime_UTR_variant | MODIFIER | c.-76G>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 1/41 | 8461 | chr17 | 10372991 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:10301084 | C | T | 8 | a0001c0040t0001g0101 a0001c0040t0001g0102 a0001c0050t0001g0037 others(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 | a0001c0014t0001g0201 | 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 | a0001c0007t0001g0117 | 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 | a0001c0039t0001g0096 a0001c0039t0001g0099 a0003c0001t0001g0324 others(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 | a0013c0053t0001g0042 | 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 | a0003c0011t0001g0186 a0003c0011t0001g0202 a0003c0011t0001g0203 others(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 | a0001c0014t0001g0094 | 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 | 116 | a0001c0003t0001g0008 a0001c0003t0001g0038 a0001c0003t0001g0039 others(113): Show |
116 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.5668-27G>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 39/40 | chr17 | 10301730 | |||||||
chr17:10301760 | G | A | 1 | a0004c0021t0001g0137 | 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 | a0005c0016t0001g0120 | 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 | a0001c0007t0001g0376 a0005c0028t0001g0363 a0007c0083t0001g0127 others(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 | a0003c0001t0001g0284 | 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 | a0002c0041t0001g0231 | 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 | a0001c0003t0001g0238 a0001c0012t0001g0336 a0001c0012t0001g0345 others(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 | a0001c0003t0001g0062 a0001c0007t0001g0288 a0001c0007t0001g0300 others(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 | a0005c0028t0001g0363 a0007c0083t0001g0127 a0012c0058t0001g0142 |
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 | a0003c0001t0001g0056 | 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 | a0013c0053t0001g0051 | 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 | a0006c0024t0001g0128 a0006c0033t0001g0185 a0007c0083t0001g0127 |
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 | a0002c0008t0001g0361 | 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 | a0003c0019t0001g0049 a0003c0019t0001g0190 a0003c0019t0001g0191 others(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 | a0003c0094t0001g0220 | 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 | a0003c0001t0001g0004 a0003c0001t0001g0043 a0003c0001t0001g0056 others(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 | a0002c0005t0001g0107 a0012c0035t0001g0143 a0012c0035t0001g0145 |
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 | a0003c0011t0001g0186 a0003c0011t0001g0202 a0003c0011t0001g0203 others(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 | a0003c0019t0001g0049 a0003c0019t0001g0190 a0003c0019t0001g0191 others(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 | a0003c0019t0001g0049 a0003c0019t0001g0190 a0003c0019t0001g0191 others(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 | a0001c0007t0001g0283 | 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 | a0003c0001t0001g0004 a0003c0001t0001g0043 a0003c0001t0001g0056 others(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 | a0001c0015t0001g0130 a0001c0015t0001g0134 a0001c0015t0001g0378 others(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 | a0001c0004t0001g0188 | 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 | a0001c0017t0001g0115 | 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 | a0001c0003t0001g0214 a0001c0003t0001g0339 a0006c0099t0001g0340 others(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 | a0004c0002t0001g0212 a0010c0023t0001g0286 a0010c0023t0001g0296 others(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 | a0001c0004t0001g0026 a0001c0004t0001g0027 a0001c0004t0001g0028 others(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 | a0001c0017t0001g0116 | 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 | a0001c0004t0001g0026 a0001c0004t0001g0027 a0001c0004t0001g0028 others(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 | a0001c0017t0001g0116 | 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 | a0003c0011t0001g0081 | 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 | a0001c0003t0001g0038 a0001c0003t0001g0039 a0001c0003t0001g0040 others(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 | a0001c0014t0001g0372 a0002c0005t0001g0338 |
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 | 338 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(335): Show |
340 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(337): 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 | a0001c0003t0001g0008 a0001c0003t0001g0039 a0001c0003t0001g0197 others(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 | a0001c0003t0001g0241 a0001c0003t0001g0242 a0001c0007t0001g0006 others(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 | a0001c0003t0001g0339 a0001c0007t0001g0376 a0001c0040t0001g0102 others(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 | a0001c0003t0001g0045 a0001c0034t0001g0168 a0001c0046t0001g0343 others(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 | a0001c0006t0001g0121 a0004c0002t0001g0194 a0004c0002t0001g0223 others(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 |
5 | a0004c0002t0001g0123 a0004c0002t0001g0124 a0004c0026t0001g0164 others(2): Show |
5 | HG00733.hp2 HG02735.hp2 NA18974.hp2 others(2): 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 | a0004c0002t0001g0221 a0004c0010t0001g0073 a0004c0026t0001g0153 others(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 | a0031c0086t0001g0262 | 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 | a0009c0063t0001g0260 | 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 | a0001c0003t0001g0032 a0001c0003t0001g0038 a0001c0003t0001g0040 others(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 | a0001c0004t0001g0061 a0001c0007t0001g0117 a0001c0012t0001g0344 others(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 | a0001c0004t0001g0169 a0001c0004t0001g0170 a0001c0014t0001g0094 others(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 | a0001c0004t0001g0071 a0001c0004t0001g0208 a0001c0027t0001g0322 others(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 | a0001c0004t0001g0026 a0001c0004t0001g0027 a0001c0004t0001g0028 others(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 | a0001c0004t0001g0188 a0001c0017t0001g0116 |
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 | a0001c0003t0001g0050 a0001c0003t0001g0069 a0001c0012t0001g0304 others(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 | a0003c0001t0001g0056 a0003c0038t0001g0122 |
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 | a0002c0005t0001g0107 | 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 | a0004c0021t0001g0092 | 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 | a0005c0016t0001g0058 | 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 | a0003c0001t0001g0004 a0003c0001t0001g0043 a0003c0001t0001g0056 others(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 | a0001c0007t0001g0288 | 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 | a0018c0100t0001g0064 | 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 | a0001c0089t0001g0184 a0005c0028t0001g0363 a0012c0058t0001g0142 |
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 | 317 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(314): Show |
319 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(316): 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 | a0003c0001t0001g0004 a0003c0001t0001g0043 a0003c0001t0001g0056 others(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 | a0001c0004t0001g0026 a0001c0004t0001g0027 a0001c0004t0001g0028 others(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 | a0001c0017t0001g0115 a0002c0009t0002g0003 a0003c0001t0001g0004 others(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 | 178 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(175): Show |
180 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.5169+906delT | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 35/40 | chr17 | 10308327 | |||||||
chr17:10308405 | C | A | 1 | a0006c0033t0001g0215 | 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 | 317 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(314): Show |
319 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(316): Show |
intron_variant | MODIFIER | c.5169+825C>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 35/40 | chr17 | 10308409 | |||||||
chr17:10308411 | C | CTA | 309 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(306): Show |
311 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(308): 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 | a0003c0019t0001g0049 a0003c0019t0001g0190 a0003c0019t0001g0191 others(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 | a0001c0027t0001g0009 a0002c0005t0001g0097 a0002c0009t0001g0316 others(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 | a0001c0015t0001g0130 a0001c0015t0001g0371 a0001c0042t0001g0105 others(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 | 233 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(230): Show |
235 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(232): 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 | a0003c0043t0001g0323 | 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 | 199 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(196): Show |
201 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(198): 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 | a0001c0004t0001g0208 a0001c0017t0001g0119 |
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 | a0006c0024t0001g0128 a0006c0033t0001g0185 |
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 | a0003c0019t0001g0049 a0003c0019t0001g0190 a0003c0019t0001g0191 others(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 | a0003c0019t0001g0049 a0003c0019t0001g0190 a0003c0019t0001g0191 others(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 | a0003c0030t0001g0129 | 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 | a0001c0006t0001g0140 a0001c0007t0001g0006 a0001c0007t0001g0007 others(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 | a0003c0011t0001g0186 a0003c0011t0001g0202 a0003c0011t0001g0203 others(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 | a0003c0001t0001g0004 a0003c0001t0001g0043 a0003c0001t0001g0056 others(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 | a0001c0006t0001g0001 a0001c0012t0001g0285 a0001c0120t0001g0178 others(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 | 154 | a0001c0004t0001g0026 a0001c0004t0001g0027 a0001c0004t0001g0028 others(151): Show |
155 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.4657-265dupA | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 33/40 | chr17 | 10310094 | |||||||
chr17:10310094 | G | GTT | 16 | a0001c0004t0001g0071 a0001c0007t0001g0327 a0001c0017t0001g0115 others(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 | 316 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(313): Show |
318 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(315): 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 | a0001c0027t0001g0322 | 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 | a0019c0076t0001g0352 | 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 | a0001c0004t0001g0026 a0001c0004t0001g0027 a0001c0004t0001g0028 others(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 | a0008c0032t0001g0171 a0008c0032t0001g0172 a0008c0032t0001g0175 others(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 | a0003c0019t0001g0049 a0003c0019t0001g0190 a0003c0019t0001g0191 others(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 | a0003c0019t0001g0049 a0003c0019t0001g0190 a0003c0019t0001g0191 others(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 | 201 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(198): Show |
203 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(200): 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 | a0001c0004t0001g0026 a0001c0004t0001g0027 a0001c0004t0001g0028 others(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 | 201 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(198): Show |
203 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(200): 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 | a0023c0074t0001g0076 | 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 | a0005c0018t0001g0205 | 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 | a0003c0019t0001g0049 a0003c0019t0001g0190 a0003c0019t0001g0191 others(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 | a0003c0019t0001g0049 a0003c0019t0001g0190 a0003c0019t0001g0191 others(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 | a0008c0032t0001g0172 a0008c0032t0001g0175 a0008c0049t0001g0151 others(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 | a0003c0011t0001g0202 | 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 | a0002c0008t0001g0036 | 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 | a0003c0019t0001g0049 a0003c0019t0001g0190 a0003c0019t0001g0191 others(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 | a0001c0014t0001g0375 a0002c0008t0001g0047 a0002c0025t0001g0157 others(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 | a0003c0001t0001g0292 | 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 | a0005c0028t0001g0363 a0012c0058t0001g0142 |
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 | a0003c0019t0001g0049 a0003c0019t0001g0190 a0003c0019t0001g0191 others(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 | a0002c0008t0001g0047 a0002c0025t0001g0157 a0005c0016t0001g0218 others(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 | a0003c0001t0001g0004 a0003c0001t0001g0043 a0003c0001t0001g0264 others(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 | a0003c0019t0001g0049 a0003c0019t0001g0190 a0003c0019t0001g0191 others(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 | a0003c0001t0001g0056 | 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 | 244 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(241): Show |
246 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(243): 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 | a0010c0023t0001g0286 a0035c0085t0001g0293 |
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 | a0001c0027t0001g0009 a0002c0005t0001g0041 a0002c0005t0001g0097 others(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 | a0003c0019t0001g0049 a0003c0019t0001g0190 a0003c0019t0001g0191 others(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 | a0013c0053t0001g0042 a0033c0102t0001g0066 |
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 | a0003c0019t0001g0049 a0003c0019t0001g0190 a0003c0019t0001g0191 others(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 | a0003c0019t0001g0049 a0003c0019t0001g0190 a0003c0019t0001g0191 others(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 | a0003c0019t0001g0049 a0003c0019t0001g0190 a0003c0019t0001g0191 others(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 | a0003c0019t0001g0049 a0003c0019t0001g0190 a0003c0019t0001g0191 others(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 | a0002c0009t0001g0316 a0002c0009t0001g0320 a0002c0009t0001g0362 |
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 | 178 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(175): Show |
180 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(177): 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 | a0003c0019t0001g0049 a0003c0019t0001g0190 a0003c0019t0001g0191 others(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 | a0001c0108t0001g0158 | 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 | a0003c0019t0001g0049 a0003c0019t0001g0190 a0003c0019t0001g0191 others(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 | a0003c0019t0001g0049 a0003c0019t0001g0190 a0003c0019t0001g0191 others(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 | a0004c0010t0001g0315 a0004c0021t0001g0091 a0004c0021t0001g0092 others(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 | a0001c0004t0001g0028 a0001c0006t0001g0140 a0001c0012t0001g0336 others(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 | a0003c0019t0001g0049 a0003c0019t0001g0190 a0003c0019t0001g0191 others(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 | a0003c0064t0001g0230 | 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 | a0003c0019t0001g0049 a0003c0019t0001g0190 a0003c0019t0001g0191 others(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 | 177 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(174): Show |
179 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(176): 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 | a0003c0019t0001g0049 a0003c0019t0001g0190 a0003c0019t0001g0191 others(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 | a0002c0008t0001g0047 a0002c0025t0001g0157 a0005c0016t0001g0120 others(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 | a0008c0032t0001g0171 a0008c0032t0001g0172 a0008c0032t0001g0175 others(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 | a0003c0019t0001g0049 a0003c0019t0001g0190 a0003c0019t0001g0191 others(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 | a0002c0008t0001g0047 a0002c0025t0001g0157 a0005c0016t0001g0120 others(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 | a0003c0019t0001g0049 a0003c0019t0001g0190 a0003c0019t0001g0191 others(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 | a0005c0018t0001g0020 | 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 | a0001c0022t0001g0149 a0001c0022t0001g0181 a0001c0022t0001g0334 others(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 | a0005c0087t0001g0332 | 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 | a0001c0004t0001g0208 a0001c0017t0001g0119 a0001c0027t0001g0322 |
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 | a0003c0019t0001g0049 a0003c0019t0001g0190 a0003c0019t0001g0191 others(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 | a0001c0014t0001g0372 a0002c0005t0001g0338 a0007c0083t0001g0127 |
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 | a0005c0016t0001g0218 | 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 | a0029c0098t0001g0024 | 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 | 314 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(311): Show |
316 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(313): 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 | a0003c0019t0001g0049 a0003c0019t0001g0190 a0003c0019t0001g0191 others(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 | 219 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(216): Show |
221 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(218): 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 | a0001c0027t0001g0009 a0002c0005t0001g0041 a0002c0005t0001g0097 others(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 | a0004c0021t0001g0137 | 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 | a0002c0009t0001g0055 | 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 | a0001c0003t0001g0008 a0001c0003t0001g0038 a0001c0003t0001g0039 others(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 | a0001c0004t0001g0169 a0001c0014t0001g0094 a0001c0014t0001g0125 others(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 | a0003c0019t0001g0049 a0003c0019t0001g0190 a0003c0019t0001g0191 others(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 | a0001c0089t0001g0184 a0002c0008t0001g0047 a0002c0025t0001g0157 others(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 | a0001c0089t0001g0184 a0002c0008t0001g0047 a0002c0025t0001g0157 others(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 | a0001c0089t0001g0184 a0002c0008t0001g0047 a0002c0025t0001g0157 others(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 | a0003c0019t0001g0049 a0003c0019t0001g0190 a0003c0019t0001g0191 others(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 | a0001c0089t0001g0184 a0002c0008t0001g0047 a0002c0025t0001g0157 others(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 | 261 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(258): Show |
263 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(260): 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 | a0005c0018t0001g0020 | 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 | a0002c0008t0001g0047 a0002c0025t0001g0157 a0005c0016t0001g0120 others(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 | a0002c0005t0001g0098 a0002c0005t0001g0100 a0002c0025t0001g0156 others(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 | a0001c0089t0001g0184 a0002c0008t0001g0047 a0002c0025t0001g0157 others(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 | a0003c0011t0001g0186 a0003c0011t0001g0202 a0003c0011t0001g0203 others(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 | a0008c0032t0001g0171 a0008c0032t0001g0172 a0008c0032t0001g0175 others(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 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(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 | a0001c0006t0001g0337 | 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 | a0001c0004t0001g0208 | 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 | a0005c0016t0001g0120 | 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 | a0001c0004t0001g0026 a0001c0004t0001g0027 a0001c0004t0001g0028 others(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 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(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 | 177 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(174): Show |
179 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(176): 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 | a0001c0089t0001g0184 a0003c0001t0001g0004 a0003c0001t0001g0043 others(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 | a0001c0089t0001g0184 a0003c0001t0001g0004 a0003c0001t0001g0043 others(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 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(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 | a0003c0064t0001g0230 | 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 | a0004c0002t0001g0124 | 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 | a0001c0089t0001g0184 a0003c0001t0001g0004 a0003c0001t0001g0043 others(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 | a0001c0089t0001g0184 a0003c0001t0001g0004 a0003c0001t0001g0043 others(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 | a0001c0089t0001g0184 a0003c0001t0001g0004 a0003c0001t0001g0043 others(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 | 175 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(172): Show |
177 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(174): 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 | a0001c0089t0001g0184 a0003c0001t0001g0004 a0003c0001t0001g0043 others(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 | a0003c0001t0001g0308 a0003c0019t0001g0049 a0003c0019t0001g0190 others(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 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(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 | 153 | a0001c0004t0001g0028 a0001c0006t0001g0121 a0001c0006t0001g0337 others(150): Show |
154 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(151): 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 | a0003c0011t0001g0186 a0003c0011t0001g0202 a0003c0011t0001g0203 others(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 | a0001c0089t0001g0184 a0003c0001t0001g0004 a0003c0001t0001g0043 others(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 | a0004c0002t0001g0002 a0004c0002t0001g0212 a0004c0010t0001g0307 others(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 | 309 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(306): Show |
311 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(308): 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 | a0001c0003t0001g0200 | 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 | a0001c0007t0001g0300 a0001c0007t0001g0301 a0001c0007t0001g0327 others(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 | a0003c0001t0001g0004 a0003c0001t0001g0043 a0003c0001t0001g0056 others(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 | a0003c0001t0001g0004 a0003c0001t0001g0043 a0003c0001t0001g0056 others(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 | a0002c0005t0001g0341 | 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 | a0018c0100t0001g0064 | 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 | a0003c0011t0001g0186 a0003c0011t0001g0202 a0003c0011t0001g0203 others(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 | a0001c0003t0001g0214 a0001c0003t0001g0339 a0003c0001t0001g0004 others(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 | a0001c0003t0001g0214 a0001c0003t0001g0339 a0003c0001t0001g0004 others(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 | a0005c0018t0001g0020 | 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 | a0001c0015t0001g0130 a0001c0015t0001g0371 a0001c0015t0001g0373 others(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 | a0006c0024t0001g0128 | 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 | a0001c0050t0001g0037 a0001c0050t0001g0065 a0005c0016t0001g0120 others(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 | a0001c0015t0001g0130 a0001c0015t0001g0371 a0001c0015t0001g0373 others(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 | a0003c0081t0001g0005 a0003c0094t0001g0220 |
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 | a0001c0015t0001g0130 a0001c0015t0001g0371 a0001c0015t0001g0373 others(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 | a0001c0003t0001g0238 a0001c0007t0001g0288 a0001c0012t0001g0336 others(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 | a0001c0012t0001g0285 a0004c0021t0001g0114 |
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 | a0001c0003t0001g0238 a0001c0004t0001g0170 a0001c0004t0001g0188 others(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 | a0003c0001t0001g0056 a0003c0001t0001g0253 a0003c0038t0001g0122 |
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 | a0003c0001t0001g0325 | 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 | a0001c0004t0001g0170 a0001c0004t0001g0188 a0001c0007t0001g0117 others(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 | a0020c0092t0001g0368 | 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 | a0001c0003t0001g0008 a0001c0003t0001g0038 a0001c0003t0001g0039 others(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 | a0001c0014t0001g0010 a0001c0015t0001g0011 a0001c0015t0001g0014 others(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 | 292 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(289): Show |
294 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.2935-529delT | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 23/40 | chr17 | 10322236 | |||||||
chr17:10322259 | A | G | 3 | a0002c0005t0001g0261 a0004c0010t0001g0315 a0009c0063t0001g0260 |
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 | a0002c0005t0001g0041 | 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 | a0002c0005t0001g0041 | 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 | a0001c0012t0001g0289 a0001c0039t0001g0096 a0001c0039t0001g0099 others(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 | a0002c0005t0001g0041 | 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 | a0006c0033t0001g0215 | 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 | a0004c0002t0001g0123 | 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 | a0002c0005t0001g0110 a0002c0009t0002g0003 |
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 | a0001c0015t0001g0378 a0002c0005t0001g0107 a0002c0041t0001g0231 others(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 | a0002c0009t0001g0316 a0002c0041t0001g0231 a0004c0010t0001g0299 others(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 | a0010c0023t0001g0266 | 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 | a0004c0026t0001g0176 | 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 | a0008c0032t0001g0172 | 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 | a0001c0003t0001g0008 a0001c0003t0001g0038 a0001c0003t0001g0039 others(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 | a0004c0002t0001g0223 a0005c0016t0001g0218 |
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 | a0001c0003t0001g0050 a0001c0003t0001g0069 a0001c0003t0001g0197 others(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 | a0001c0022t0001g0334 a0001c0090t0001g0364 a0001c0113t0001g0135 others(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 | a0001c0003t0001g0062 a0001c0003t0001g0225 a0001c0003t0001g0226 others(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 | a0001c0027t0001g0155 a0001c0027t0001g0165 a0001c0072t0001g0163 others(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 | a0004c0106t0001g0177 | 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 | a0001c0017t0001g0116 | 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 | a0002c0005t0001g0100 a0003c0019t0001g0191 |
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 | a0001c0003t0001g0062 a0001c0004t0001g0169 a0001c0004t0001g0170 others(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 | a0003c0001t0001g0250 | 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 | a0007c0020t0001g0106 | 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 | a0001c0007t0001g0117 a0001c0089t0001g0184 a0004c0002t0001g0223 |
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 | a0001c0034t0001g0321 a0004c0002t0001g0360 |
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 | a0003c0001t0001g0250 | 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 | a0004c0106t0001g0177 a0020c0092t0001g0368 |
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 | a0001c0003t0001g0347 | 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 | a0001c0014t0001g0010 a0001c0015t0001g0011 a0001c0015t0001g0014 others(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 | a0001c0027t0001g0155 | 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 | a0001c0012t0001g0336 a0001c0012t0001g0345 a0001c0014t0001g0375 |
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 | a0001c0004t0001g0354 a0001c0004t0001g0355 a0001c0004t0001g0356 others(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 | a0002c0061t0001g0104 | 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 | a0001c0006t0001g0085 a0001c0006t0001g0087 a0002c0005t0001g0086 others(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 | a0001c0022t0001g0181 a0001c0034t0001g0152 a0001c0034t0001g0168 others(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 | a0008c0032t0001g0172 | 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 | a0001c0007t0001g0006 a0001c0007t0001g0007 a0001c0007t0001g0117 others(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 | a0006c0052t0001g0196 | 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 | a0003c0001t0001g0297 | 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 | a0001c0014t0001g0010 a0001c0015t0001g0011 a0001c0015t0001g0014 others(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 | a0001c0003t0001g0069 a0001c0004t0001g0028 a0001c0012t0001g0304 others(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 | a0001c0004t0001g0354 a0001c0004t0001g0355 a0001c0004t0001g0356 others(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 | a0001c0003t0001g0197 a0001c0003t0001g0199 a0001c0003t0001g0200 others(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 | a0001c0014t0001g0201 | 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 | a0001c0003t0001g0246 a0001c0110t0001g0126 a0003c0011t0001g0239 others(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 | a0001c0003t0001g0197 a0001c0003t0001g0199 a0001c0003t0001g0200 others(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 | a0003c0011t0001g0248 | 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 | a0001c0007t0001g0376 a0002c0009t0001g0374 |
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 | a0001c0003t0001g0008 a0001c0003t0001g0038 a0001c0003t0001g0039 others(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 | a0001c0004t0001g0354 a0001c0004t0001g0355 a0001c0004t0001g0356 others(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 | a0001c0004t0001g0314 a0001c0050t0001g0037 a0002c0005t0001g0111 others(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 | 50 | a0001c0003t0001g0032 a0001c0003t0001g0045 a0001c0003t0001g0050 others(47): Show |
50 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(47): 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 | a0002c0008t0001g0047 | 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 | a0009c0093t0001g0259 | 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 | a0005c0016t0001g0120 | 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 | a0001c0027t0001g0165 a0004c0026t0001g0153 a0004c0026t0001g0164 others(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 | a0001c0004t0001g0061 a0001c0004t0001g0071 a0004c0002t0001g0123 others(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 | a0001c0119t0001g0351 | 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 | a0003c0019t0001g0190 a0004c0002t0001g0210 a0004c0002t0001g0211 others(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 | a0002c0008t0001g0222 a0008c0032t0001g0172 |
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 | a0003c0019t0001g0191 a0003c0019t0001g0193 a0003c0019t0001g0195 others(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 | a0001c0120t0001g0178 a0002c0008t0001g0255 a0003c0019t0001g0192 others(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 | a0002c0008t0001g0361 a0004c0002t0001g0212 a0004c0002t0001g0360 others(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 | a0001c0003t0001g0238 a0001c0003t0001g0339 a0001c0004t0001g0169 others(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 | a0001c0003t0001g0214 a0001c0004t0001g0208 a0001c0103t0001g0174 others(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 | a0004c0002t0001g0235 | 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 | a0001c0004t0001g0170 a0002c0041t0001g0231 a0002c0041t0001g0365 others(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 | a0001c0046t0001g0319 a0001c0046t0001g0343 a0001c0062t0001g0273 others(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 | a0001c0003t0001g0214 a0001c0003t0001g0238 a0001c0003t0001g0339 others(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 | a0006c0024t0001g0128 a0007c0083t0001g0127 |
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 | a0004c0106t0001g0177 | 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 | a0002c0005t0001g0261 | 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 | a0001c0003t0001g0214 a0001c0003t0001g0238 a0001c0003t0001g0241 others(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 | a0001c0003t0001g0062 a0001c0006t0001g0001 a0001c0006t0001g0108 others(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 | a0001c0007t0001g0278 a0001c0012t0001g0302 a0001c0012t0001g0336 others(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 | a0002c0005t0001g0107 | 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 | a0009c0063t0001g0260 | 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 | a0001c0015t0001g0134 a0001c0017t0001g0141 a0001c0113t0001g0135 others(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 | a0002c0009t0001g0295 a0003c0001t0001g0264 a0003c0001t0001g0297 others(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 | a0001c0014t0001g0010 a0001c0015t0001g0014 a0002c0013t0001g0016 others(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 | a0001c0012t0001g0285 a0001c0118t0001g0350 a0003c0001t0001g0292 others(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 | a0001c0007t0001g0006 a0001c0007t0001g0007 a0001c0007t0001g0117 others(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 | a0005c0018t0001g0290 | 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 | a0001c0015t0001g0011 a0002c0013t0001g0012 a0002c0013t0001g0018 others(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 | a0001c0007t0001g0278 a0001c0012t0001g0302 a0001c0012t0001g0336 others(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 | a0001c0014t0001g0010 a0001c0015t0001g0011 a0001c0015t0001g0014 others(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 | 183 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(180): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): 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 | a0006c0024t0001g0331 | 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 | a0003c0019t0001g0049 | 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 | a0001c0006t0001g0121 a0001c0006t0001g0232 a0001c0006t0001g0233 others(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 | a0001c0003t0001g0062 a0001c0006t0001g0140 a0001c0014t0001g0094 others(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 | a0001c0014t0001g0201 a0001c0113t0001g0135 a0004c0021t0001g0092 others(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 | a0001c0003t0001g0214 a0001c0006t0001g0121 a0001c0006t0001g0232 others(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 | a0001c0003t0001g0238 a0001c0004t0001g0354 a0001c0004t0001g0356 others(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 | a0001c0004t0001g0169 a0001c0004t0001g0170 a0001c0004t0001g0188 others(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 | a0001c0119t0001g0351 a0003c0011t0001g0248 a0003c0019t0001g0195 others(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 | a0001c0003t0001g0197 a0001c0003t0001g0199 a0001c0003t0001g0200 others(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 | a0001c0003t0001g0241 a0001c0003t0001g0249 a0001c0089t0001g0184 others(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 | a0001c0007t0001g0376 a0002c0009t0001g0377 |
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 | a0002c0009t0001g0374 | 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 | a0001c0007t0001g0006 a0001c0007t0001g0007 a0001c0007t0001g0117 others(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 | a0001c0012t0001g0285 a0001c0012t0001g0345 a0001c0111t0001g0078 others(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 | a0001c0014t0001g0372 a0001c0015t0001g0371 a0001c0015t0001g0373 others(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 | 63 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(60): Show |
63 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(60): 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 | 184 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(181): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): 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 | a0001c0003t0001g0246 a0003c0011t0001g0239 a0003c0011t0001g0248 others(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 | 184 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(181): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): 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 | a0040c0080t0001g0204 | 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 | a0002c0025t0001g0157 | 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 | 185 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(182): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.2692-1569A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10325833 | |||||||
chr17:10325848 | T | G | 185 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(182): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): 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 | a0002c0009t0001g0298 a0038c0084t0001g0254 |
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 | a0001c0007t0001g0300 a0001c0007t0001g0301 a0001c0007t0001g0327 |
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 | 185 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(182): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): 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 | a0001c0007t0001g0006 a0001c0007t0001g0007 a0001c0007t0001g0117 others(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 | a0003c0001t0001g0043 | 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 | a0001c0003t0001g0249 a0001c0014t0001g0010 a0001c0015t0001g0011 others(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 | 118 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(115): Show |
118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.2691+1228delA | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10326637 | |||||||
chr17:10326768 | C | T | 186 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(183): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): 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 | a0003c0001t0001g0324 a0003c0078t0001g0279 a0037c0109t0001g0305 |
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 | a0001c0014t0001g0010 a0001c0015t0001g0011 a0001c0015t0001g0014 others(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 | 186 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(183): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.2691+944A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10326922 | |||||||
chr17:10326977 | A | G | 313 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(310): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): 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 | a0001c0003t0001g0062 a0001c0003t0001g0197 a0001c0003t0001g0199 others(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 | a0001c0004t0001g0354 a0001c0004t0001g0356 a0001c0006t0001g0001 others(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 | a0001c0004t0001g0355 a0001c0012t0001g0344 a0001c0017t0001g0115 others(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 | a0001c0014t0001g0094 a0001c0113t0001g0135 a0002c0009t0001g0374 others(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 | a0001c0003t0001g0039 a0001c0003t0001g0040 a0001c0003t0001g0226 others(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 |
22 | a0001c0003t0001g0008 a0001c0003t0001g0038 a0001c0003t0001g0045 others(19): Show |
22 | HG00423.hp1 HG00738.hp2 HG01069.hp2 others(19): 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 | a0006c0033t0001g0185 a0008c0032t0001g0171 |
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 | a0001c0003t0001g0050 a0001c0004t0001g0170 a0001c0004t0001g0346 others(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 | a0001c0003t0001g0069 a0001c0004t0001g0367 a0001c0014t0001g0010 others(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 | a0001c0003t0001g0214 a0003c0011t0001g0081 a0003c0030t0001g0017 others(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 | a0005c0016t0001g0058 | 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 | a0001c0004t0001g0061 a0002c0008t0001g0048 |
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 | a0001c0007t0001g0283 a0001c0046t0001g0319 a0001c0089t0001g0184 others(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 | a0001c0007t0001g0117 a0001c0007t0001g0288 a0001c0012t0001g0285 others(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 | a0001c0003t0001g0241 a0001c0075t0001g0358 a0001c0110t0001g0126 others(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 | a0001c0003t0001g0246 a0001c0003t0001g0247 a0001c0003t0001g0249 others(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 | a0001c0003t0001g0242 a0001c0015t0001g0373 a0001c0015t0001g0378 others(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 | a0001c0004t0001g0208 a0001c0022t0001g0181 |
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 | a0001c0006t0001g0232 a0001c0006t0001g0233 a0001c0014t0001g0132 others(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 | a0001c0006t0001g0337 a0001c0014t0001g0375 a0005c0016t0001g0068 others(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 | a0001c0003t0001g0238 a0001c0006t0001g0121 a0001c0014t0001g0201 others(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 | a0001c0003t0001g0347 a0001c0007t0001g0006 a0001c0007t0001g0007 |
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 | a0001c0012t0001g0336 a0001c0012t0001g0345 a0005c0016t0001g0035 others(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 | a0001c0015t0001g0130 a0003c0030t0001g0129 |
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 | a0001c0003t0001g0197 a0001c0003t0001g0199 a0001c0003t0001g0200 others(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 | 322 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(319): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): 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 | a0001c0006t0001g0121 | 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 | 322 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(319): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.2691+795T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 22/40 | chr17 | 10327071 | |||||||
chr17:10327095 | A | G | 356 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(353): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): 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 | a0001c0004t0001g0346 a0001c0004t0001g0367 |
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 | a0001c0022t0001g0149 a0001c0042t0001g0105 a0001c0042t0001g0234 |
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 | a0001c0004t0001g0208 | 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 | 186 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(183): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): 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 | 287 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(284): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): 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 | a0001c0006t0001g0121 a0001c0006t0001g0232 a0001c0006t0001g0233 others(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 | a0001c0006t0001g0121 a0001c0006t0001g0232 a0001c0006t0001g0233 others(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 | a0001c0014t0001g0125 | 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 | 311 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(308): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): 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 | a0014c0060t0001g0095 | 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 | a0001c0017t0001g0116 | 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 | a0001c0006t0001g0085 a0001c0012t0001g0336 a0001c0012t0001g0345 others(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 | a0001c0003t0001g0069 a0001c0003t0001g0238 a0001c0004t0001g0028 others(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 | 138 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(135): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): 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 | 311 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(308): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): 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 | a0003c0001t0001g0264 | 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 | a0001c0027t0001g0322 a0001c0034t0001g0321 a0042c0057t0001g0159 |
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 | a0003c0001t0001g0043 | 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 | a0001c0014t0001g0372 a0001c0015t0001g0371 a0001c0015t0001g0373 others(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 | a0040c0080t0001g0204 | 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 | a0001c0006t0001g0121 a0001c0006t0001g0232 a0001c0006t0001g0233 others(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 | a0001c0007t0001g0006 a0001c0007t0001g0007 a0001c0007t0001g0117 others(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 | a0003c0038t0001g0369 a0005c0037t0001g0148 a0005c0037t0001g0187 |
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 | a0003c0001t0001g0284 | 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 | a0001c0014t0001g0010 a0001c0015t0001g0011 a0001c0015t0001g0014 others(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 | a0001c0006t0001g0121 a0001c0006t0001g0232 a0001c0006t0001g0233 others(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 | a0005c0095t0001g0057 | 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 | a0001c0014t0001g0372 a0001c0015t0001g0371 a0001c0015t0001g0373 others(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 | a0002c0008t0001g0047 | 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 | a0001c0006t0001g0121 a0001c0006t0001g0232 a0001c0006t0001g0233 others(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 | a0041c0067t0001g0093 | 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 | a0001c0014t0001g0372 a0001c0015t0001g0371 a0001c0015t0001g0373 others(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 | a0001c0014t0001g0125 | 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 | a0001c0007t0001g0376 a0002c0009t0001g0374 a0002c0009t0001g0377 |
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 | a0001c0007t0001g0006 a0001c0007t0001g0007 a0001c0007t0001g0117 others(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 | a0002c0009t0001g0274 | 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 | a0001c0007t0001g0300 a0001c0007t0001g0301 a0001c0007t0001g0327 |
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 | 377 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(374): Show |
379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.2299-714A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 20/40 | chr17 | 10331237 | |||||||
chr17:10331252 | C | T | 160 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(157): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): 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 | a0001c0007t0001g0006 a0001c0007t0001g0007 a0001c0007t0001g0117 others(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 | a0001c0004t0001g0354 a0001c0004t0001g0355 a0001c0004t0001g0356 others(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 | a0001c0006t0001g0121 | 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 | a0001c0014t0001g0372 a0001c0015t0001g0371 a0001c0015t0001g0373 others(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 | a0001c0006t0001g0121 a0001c0006t0001g0232 a0001c0006t0001g0233 others(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 | a0004c0010t0001g0263 a0006c0029t0001g0256 |
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 | a0001c0007t0001g0006 a0001c0007t0001g0007 a0001c0007t0001g0117 others(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 | a0001c0012t0001g0275 a0001c0012t0001g0302 a0003c0001t0001g0250 others(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 | 310 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(307): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): 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 | a0007c0020t0001g0349 | 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 | 15 | a0001c0006t0001g0121 a0001c0006t0001g0232 a0001c0006t0001g0233 others(12): Show |
15 | HG00099.hp1 HG00639.hp2 HG01243.hp1 others(12): 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 | a0001c0012t0001g0275 a0001c0012t0001g0302 a0006c0029t0001g0280 |
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 | a0001c0006t0001g0121 a0001c0006t0001g0232 a0001c0006t0001g0233 others(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 | a0001c0119t0001g0351 | 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 | a0001c0007t0001g0006 a0001c0007t0001g0007 a0001c0007t0001g0117 others(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 | a0001c0014t0001g0372 a0001c0015t0001g0371 a0001c0015t0001g0373 others(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 | a0002c0008t0001g0054 | 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 | a0002c0005t0001g0041 | 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 | a0005c0018t0001g0282 | 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 | a0001c0006t0001g0121 a0001c0006t0001g0232 a0001c0006t0001g0233 others(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 | a0002c0041t0001g0365 | 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 | 68 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(65): Show |
68 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(65): 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 | a0004c0021t0001g0091 a0004c0021t0001g0092 a0007c0107t0001g0167 others(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 | a0001c0004t0001g0354 a0001c0004t0001g0355 a0001c0004t0001g0356 others(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 | a0001c0014t0001g0372 a0001c0015t0001g0371 a0001c0015t0001g0373 others(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 | a0001c0014t0001g0372 a0001c0015t0001g0371 a0001c0015t0001g0373 others(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 | a0001c0012t0001g0304 a0001c0012t0001g0336 a0002c0013t0001g0016 others(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 | a0007c0020t0001g0272 | 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 | a0003c0019t0001g0190 | 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 | 68 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(65): Show |
68 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(65): 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 | a0001c0004t0001g0061 a0001c0004t0001g0071 a0001c0004t0001g0077 |
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 | a0001c0003t0001g0241 a0001c0003t0001g0242 a0001c0003t0001g0246 others(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 | a0001c0003t0001g0197 a0001c0003t0001g0199 a0001c0003t0001g0200 others(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 | a0001c0007t0001g0006 a0001c0007t0001g0007 a0001c0007t0001g0117 others(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 | a0001c0119t0001g0351 | 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 | a0001c0119t0001g0351 | 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 | a0001c0006t0001g0121 a0001c0006t0001g0232 a0001c0006t0001g0233 others(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 | a0001c0007t0001g0006 a0001c0007t0001g0007 a0001c0007t0001g0117 others(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 | a0001c0007t0001g0006 a0001c0007t0001g0007 a0001c0007t0001g0117 others(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 | a0001c0006t0001g0121 a0001c0006t0001g0232 a0001c0006t0001g0233 others(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 | a0001c0006t0001g0121 | 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 | a0001c0014t0001g0010 a0001c0015t0001g0011 a0001c0015t0001g0014 others(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 | a0001c0027t0001g0165 a0001c0034t0001g0152 a0001c0034t0001g0168 others(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 | a0001c0007t0001g0006 a0001c0007t0001g0007 a0001c0007t0001g0278 others(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 | a0001c0006t0001g0121 a0001c0006t0001g0232 a0001c0006t0001g0233 others(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 | a0005c0018t0001g0282 | 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 | a0003c0019t0001g0190 a0003c0019t0001g0191 a0003c0019t0001g0192 others(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 | a0001c0007t0001g0006 a0001c0007t0001g0007 a0001c0007t0001g0117 others(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 | a0023c0074t0001g0076 | 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 | a0002c0013t0001g0016 a0004c0048t0001g0206 |
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 | a0001c0040t0001g0101 | 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 | a0002c0013t0001g0021 a0002c0013t0001g0022 |
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 | a0019c0076t0001g0352 a0031c0086t0001g0262 a0032c0114t0001g0330 |
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 | a0001c0119t0001g0351 | 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 | a0002c0008t0001g0329 | 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 | 300 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(297): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): 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 | 229 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(226): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): 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 | a0001c0003t0001g0045 a0001c0003t0001g0225 a0001c0003t0001g0226 others(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 | a0002c0005t0001g0338 | 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 | a0001c0003t0001g0197 a0001c0003t0001g0199 a0001c0003t0001g0200 others(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 | 224 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(221): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): 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 | 298 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(295): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): 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 | a0001c0006t0001g0232 | 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 | 298 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(295): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): 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 | a0001c0014t0001g0094 | 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 | 298 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(295): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.2056+2714C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10337436 | |||||||
chr17:10337442 | T | C | 298 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(295): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.2056+2708A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10337442 | |||||||
chr17:10337454 | T | C | 300 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(297): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.2056+2696A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10337454 | |||||||
chr17:10337455 | G | A | 298 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(295): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.2056+2695C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10337455 | |||||||
chr17:10337615 | C | G | 298 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(295): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.2056+2535G>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10337615 | |||||||
chr17:10337647 | T | C | 298 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(295): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.2056+2503A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10337647 | |||||||
chr17:10337648 | C | A | 298 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(295): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): 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 | a0001c0004t0001g0314 a0001c0006t0001g0121 a0001c0006t0001g0232 others(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 | 298 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(295): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.2056+2285A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10337865 | |||||||
chr17:10337920 | A | G | 298 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(295): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): 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 | a0004c0010t0001g0315 a0030c0077t0001g0353 |
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 | 298 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(295): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): 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 | a0001c0105t0001g0160 | 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 | 298 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(295): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.2056+1962T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10338188 | |||||||
chr17:10338200 | C | T | 298 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(295): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.2056+1950G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 18/40 | chr17 | 10338200 | |||||||
chr17:10338238 | C | CA | 298 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(295): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): 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 | 282 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(279): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): 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 | a0003c0001t0001g0306 | 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 | 298 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(295): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): 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 | a0004c0010t0001g0263 | 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 | a0001c0004t0001g0354 a0001c0004t0001g0355 a0001c0004t0001g0356 others(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 | 282 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(279): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): 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 | a0001c0003t0001g0197 a0001c0003t0001g0199 a0001c0003t0001g0200 others(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 | a0002c0008t0001g0229 a0003c0001t0001g0056 a0004c0002t0001g0210 others(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 | 60 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(57): Show |
60 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(57): 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 | a0001c0003t0001g0050 a0001c0004t0001g0027 a0013c0053t0001g0051 others(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 | a0027c0069t0001g0236 | 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 | a0001c0014t0001g0010 a0001c0015t0001g0011 a0001c0015t0001g0014 others(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 | a0001c0003t0001g0214 a0001c0003t0001g0238 a0001c0003t0001g0339 others(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 | a0001c0006t0001g0001 a0001c0006t0001g0085 a0001c0006t0001g0087 others(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 | a0001c0006t0001g0121 a0002c0008t0001g0255 a0003c0019t0001g0190 others(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 | a0001c0004t0001g0354 a0001c0004t0001g0355 a0001c0004t0001g0356 others(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 | a0001c0004t0001g0314 a0001c0007t0001g0006 a0001c0007t0001g0007 others(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 | a0001c0014t0001g0010 a0001c0015t0001g0011 a0001c0015t0001g0014 others(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 | a0002c0013t0001g0016 a0004c0048t0001g0206 |
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 | 301 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(298): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): 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 | a0002c0005t0001g0261 a0009c0063t0001g0260 |
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 | a0001c0027t0001g0009 a0001c0027t0001g0155 a0001c0027t0001g0165 others(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 | a0001c0015t0001g0011 a0001c0015t0001g0014 |
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 | 287 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(284): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): 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 | a0001c0006t0001g0337 | 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 | 302 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(299): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): 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 | a0001c0017t0001g0088 | 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 | a0001c0017t0001g0088 | 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 | 150 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(147): Show |
151 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(148): 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 | a0001c0014t0001g0094 | 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 | a0040c0080t0001g0204 | 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 | a0004c0048t0001g0265 | 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 | a0001c0004t0001g0314 a0001c0007t0001g0006 a0001c0007t0001g0007 others(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 | a0010c0023t0001g0266 a0010c0023t0001g0317 |
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 | a0006c0029t0001g0311 | 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 | a0002c0008t0001g0036 a0011c0031t0001g0063 |
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 | 288 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(285): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): 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 | a0001c0120t0001g0178 a0004c0002t0001g0223 a0005c0016t0001g0218 others(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 | a0016c0116t0001g0090 | 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 | a0001c0014t0001g0201 a0023c0074t0001g0076 |
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 | a0001c0014t0001g0201 a0023c0074t0001g0076 |
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 | a0014c0060t0001g0095 | 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 | a0001c0022t0001g0335 | 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 | a0039c0082t0001g0180 | 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 | a0002c0008t0001g0329 | 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 | 292 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(289): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.1969-35G>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 17/40 | chr17 | 10340272 | |||||||
chr17:10340472 | T | C | 292 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(289): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.1895-71A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10340472 | |||||||
chr17:10340541 | C | T | 290 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(287): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): 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 | a0001c0014t0001g0372 | 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 | 292 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(289): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.1895-310T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10340711 | |||||||
chr17:10340754 | G | T | 292 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(289): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.1895-353C>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10340754 | |||||||
chr17:10340791 | T | G | 292 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(289): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.1895-390A>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10340791 | |||||||
chr17:10341017 | C | CT | 173 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(170): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.1895-617dupA | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10341017 | |||||||
chr17:10341107 | A | G | 1 | a0002c0005t0001g0041 | 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 | 90 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(87): Show |
90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): 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 | a0001c0014t0001g0010 a0001c0015t0001g0011 a0001c0015t0001g0014 others(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 | |||||||
chr17:10341387 | T | C | 90 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(87): Show |
90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.1895-986A>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10341387 | |||||||
chr17:10341527 | A | G | 292 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(289): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.1895-1126T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10341527 | |||||||
chr17:10341546 | G | A | 292 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(289): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): 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 | a0001c0004t0001g0169 a0001c0004t0001g0170 a0001c0103t0001g0174 others(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 | 90 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(87): Show |
90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.1895-1204G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10341605 | |||||||
chr17:10341677 | T | G | 292 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(289): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.1895-1276A>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10341677 | |||||||
chr17:10341697 | C | T | 90 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(87): Show |
90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): 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 | a0001c0110t0001g0126 | 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 | a0001c0012t0001g0304 a0003c0001t0001g0318 |
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 | 292 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(289): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): 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 | a0039c0082t0001g0180 | 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 | 292 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(289): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): 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 | a0001c0004t0001g0061 | 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 | a0001c0003t0001g0241 a0001c0003t0001g0242 a0001c0003t0001g0246 others(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 | a0010c0023t0001g0286 | 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 | 292 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(289): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.1894+1308T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10342492 | |||||||
chr17:10342547 | G | A | 292 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(289): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): 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 | a0001c0003t0001g0241 a0001c0003t0001g0242 a0001c0003t0001g0246 others(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 | 292 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(289): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): 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 | a0001c0017t0001g0088 | 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 | 292 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(289): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): 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 | a0001c0014t0001g0010 a0001c0015t0001g0011 a0001c0015t0001g0014 others(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 | 292 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(289): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.1894+812C>G | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10342988 | |||||||
chr17:10343070 | A | C | 292 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(289): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): 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 | a0002c0005t0001g0089 a0002c0005t0001g0107 a0002c0005t0001g0110 others(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 | a0001c0003t0001g0238 a0001c0007t0001g0117 a0001c0007t0001g0283 others(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 | a0001c0003t0001g0197 a0001c0003t0001g0199 a0001c0003t0001g0200 others(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 | 76 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(73): Show |
76 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(73): 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 | 292 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(289): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.1894+672C>T | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10343128 | |||||||
chr17:10343135 | T | C | 292 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(289): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): 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 | a0001c0003t0001g0197 a0001c0003t0001g0199 a0001c0003t0001g0200 others(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 | a0001c0003t0001g0197 a0001c0003t0001g0199 a0001c0003t0001g0200 others(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 | a0001c0027t0001g0009 a0001c0027t0001g0155 a0001c0027t0001g0165 others(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 | 292 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(289): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.1894+457T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 16/40 | chr17 | 10343343 | |||||||
chr17:10343386 | T | C | 292 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(289): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): 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 | a0004c0048t0001g0265 | 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 | a0007c0020t0001g0349 | 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 | a0003c0038t0001g0369 | 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 | a0001c0027t0001g0009 a0001c0027t0001g0155 a0001c0027t0001g0165 others(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 | a0001c0014t0001g0010 a0001c0015t0001g0011 a0001c0015t0001g0014 others(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 | a0001c0003t0001g0242 a0001c0003t0001g0246 a0001c0003t0001g0247 others(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 | 72 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(69): Show |
72 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(69): 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 | a0001c0027t0001g0322 a0001c0034t0001g0321 a0042c0057t0001g0159 |
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 | a0019c0076t0001g0352 a0031c0086t0001g0262 a0032c0114t0001g0330 |
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 | a0020c0092t0001g0368 | 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 | a0002c0005t0001g0041 | 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 | 305 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(302): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): 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 | a0001c0003t0001g0062 a0001c0004t0001g0028 a0001c0004t0001g0188 others(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 | a0001c0004t0001g0030 a0001c0006t0001g0085 a0001c0006t0001g0087 others(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 | a0001c0003t0001g0241 a0001c0003t0001g0242 a0001c0003t0001g0246 others(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 | a0001c0004t0001g0314 a0001c0004t0001g0354 a0001c0004t0001g0355 others(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 | a0001c0007t0001g0006 a0001c0007t0001g0007 a0001c0007t0001g0117 others(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 | a0001c0089t0001g0184 a0001c0090t0001g0364 |
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 | a0001c0004t0001g0354 a0001c0004t0001g0355 a0001c0004t0001g0356 |
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 | a0003c0001t0001g0318 | 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 | a0001c0003t0001g0241 a0001c0003t0001g0242 a0001c0003t0001g0246 others(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 | a0002c0005t0001g0111 a0002c0005t0001g0112 |
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 | a0004c0002t0001g0211 | 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 | a0008c0049t0001g0244 | 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 | a0001c0004t0001g0314 a0001c0004t0001g0354 a0001c0004t0001g0355 others(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 | a0001c0003t0001g0241 a0001c0003t0001g0242 a0001c0003t0001g0246 others(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 | a0001c0003t0001g0197 a0001c0003t0001g0200 a0001c0003t0001g0214 others(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 | a0001c0003t0001g0199 a0002c0008t0001g0222 a0003c0001t0001g0268 others(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 | a0001c0004t0001g0031 a0001c0027t0001g0009 a0001c0027t0001g0155 others(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 | 73 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(70): Show |
73 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(70): 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 | a0001c0003t0001g0249 a0001c0014t0001g0372 a0002c0013t0001g0022 others(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 | a0001c0003t0001g0249 a0001c0014t0001g0372 a0002c0013t0001g0370 |
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 | a0001c0119t0001g0351 | 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 | a0004c0002t0001g0211 | 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 | a0001c0003t0001g0249 a0001c0014t0001g0372 a0001c0119t0001g0351 others(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 | a0001c0003t0001g0249 a0001c0014t0001g0372 a0002c0013t0001g0370 |
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 | a0001c0119t0001g0351 | 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 | a0001c0003t0001g0241 a0001c0003t0001g0242 a0001c0003t0001g0246 others(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 | a0001c0003t0001g0249 a0001c0014t0001g0372 a0001c0119t0001g0351 others(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 | a0004c0002t0001g0211 | 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 | 294 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(291): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): 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 | a0039c0082t0001g0180 | 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 | 292 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(289): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.1263+108dupT | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 13/40 | chr17 | 10346571 | |||||||
chr17:10346623 | A | G | 2 | a0003c0030t0001g0017 a0003c0030t0001g0023 |
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 | a0001c0120t0001g0178 a0004c0002t0001g0223 a0005c0016t0001g0218 others(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 | a0004c0002t0001g0194 | 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 | a0001c0003t0001g0197 a0001c0003t0001g0199 a0001c0003t0001g0200 others(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 | a0001c0072t0001g0163 a0002c0005t0001g0118 a0003c0011t0001g0081 others(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 | a0033c0102t0001g0066 | 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 | a0001c0012t0001g0344 | 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 | a0001c0015t0001g0130 | 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 | 346 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(343): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): 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 | a0001c0003t0001g0045 a0001c0003t0001g0241 a0001c0003t0001g0242 others(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 | a0001c0003t0001g0246 a0001c0004t0001g0314 a0001c0004t0001g0354 others(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 | a0001c0007t0001g0283 a0001c0014t0001g0375 a0001c0111t0001g0078 others(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 | 58 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(55): Show |
58 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(55): 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 | a0001c0003t0001g0062 a0001c0004t0001g0030 a0001c0004t0001g0031 others(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 | a0001c0027t0001g0009 a0001c0027t0001g0155 a0001c0027t0001g0165 others(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 | 307 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(304): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): 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 | a0003c0001t0001g0056 | 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 | a0001c0003t0001g0241 a0006c0052t0001g0243 |
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 | a0001c0027t0001g0009 a0001c0027t0001g0155 a0001c0027t0001g0165 others(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 | a0004c0010t0001g0312 | 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 | a0004c0002t0001g0210 | 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 | 73 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(70): Show |
73 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(70): 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 | a0001c0027t0001g0009 a0001c0027t0001g0155 a0001c0027t0001g0165 others(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 | a0004c0021t0001g0114 | 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 | 93 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(90): Show |
93 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(90): Show |
intron_variant | MODIFIER | c.1145-1696T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 12/40 | chr17 | 10348494 | |||||||
chr17:10348713 | C | T | 257 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(254): Show |
258 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.1144+1843G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 12/40 | chr17 | 10348713 | |||||||
chr17:10348800 | G | T | 73 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(70): Show |
73 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(70): 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 | a0003c0001t0001g0313 | 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 | a0001c0003t0001g0241 a0001c0003t0001g0242 a0001c0003t0001g0246 others(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 | a0001c0003t0001g0197 a0001c0003t0001g0199 a0001c0003t0001g0200 others(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 | a0001c0003t0001g0241 a0001c0003t0001g0242 a0001c0003t0001g0246 others(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 | 307 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(304): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): 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 | a0001c0003t0001g0241 a0001c0003t0001g0242 a0001c0003t0001g0246 others(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 | a0001c0003t0001g0197 a0001c0003t0001g0199 a0001c0003t0001g0200 others(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 | a0001c0119t0001g0351 | 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 | a0002c0008t0001g0047 | 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 | a0003c0094t0001g0220 | 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 | a0001c0007t0001g0376 a0002c0009t0001g0374 a0002c0009t0001g0377 |
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 | a0001c0040t0001g0102 | 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 | a0005c0016t0001g0120 | 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 | a0001c0003t0001g0241 a0001c0003t0001g0242 a0001c0003t0001g0246 others(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 | a0001c0004t0001g0314 | 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 | a0001c0006t0001g0113 | 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 | a0001c0003t0001g0241 a0001c0003t0001g0242 a0001c0003t0001g0246 others(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 | a0001c0004t0001g0169 a0001c0004t0001g0170 a0001c0103t0001g0174 others(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 | a0009c0044t0001g0138 a0009c0044t0001g0139 |
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 | 372 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(369): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): 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 | a0001c0003t0001g0225 a0001c0003t0001g0226 |
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 | a0001c0014t0001g0010 a0001c0015t0001g0011 a0001c0015t0001g0014 others(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 | a0004c0010t0001g0315 | 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 | a0003c0094t0001g0220 | 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 | a0003c0094t0001g0220 | 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 | a0003c0094t0001g0220 | 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 | a0003c0094t0001g0220 | 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 | a0003c0094t0001g0220 | 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 | a0003c0094t0001g0220 | 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 | a0003c0094t0001g0220 | 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 | 246 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(243): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): 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 | a0001c0089t0001g0184 a0001c0111t0001g0078 |
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 | a0002c0005t0001g0041 | 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 | a0001c0089t0001g0184 a0001c0111t0001g0078 |
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 | a0008c0049t0001g0244 | 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 | a0004c0002t0001g0123 | 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 | a0004c0002t0001g0123 | 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 | a0001c0012t0001g0336 a0001c0012t0001g0345 a0001c0027t0001g0322 others(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 | a0001c0007t0001g0278 a0001c0014t0001g0201 a0001c0075t0001g0358 others(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 | a0001c0004t0001g0314 a0001c0004t0001g0354 a0001c0004t0001g0356 others(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 | a0001c0004t0001g0355 a0001c0007t0001g0326 a0001c0007t0001g0327 others(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 | a0001c0003t0001g0008 a0001c0089t0001g0184 a0002c0009t0002g0003 others(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 | a0001c0027t0001g0155 a0001c0027t0001g0165 a0001c0034t0001g0168 others(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 | a0001c0027t0001g0009 a0001c0034t0001g0152 a0002c0013t0001g0016 others(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 | a0001c0014t0001g0010 a0001c0015t0001g0011 a0001c0015t0001g0014 others(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 | a0002c0013t0001g0019 a0005c0079t0001g0013 |
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 | a0005c0018t0001g0020 a0023c0074t0001g0076 |
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 | a0001c0004t0001g0026 a0001c0119t0001g0351 a0002c0008t0001g0047 others(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 |
34 | a0001c0003t0001g0032 a0001c0003t0001g0038 a0001c0003t0001g0039 others(31): Show |
34 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(31): 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 | a0001c0003t0001g0040 a0001c0003t0001g0045 a0001c0003t0001g0069 others(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 | a0001c0003t0001g0062 a0001c0004t0001g0030 a0001c0007t0001g0007 others(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 | a0016c0116t0001g0090 a0029c0098t0001g0024 |
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 | a0001c0003t0001g0249 a0001c0051t0001g0245 |
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 | a0001c0003t0001g0241 a0001c0003t0001g0242 a0001c0003t0001g0246 others(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 | a0001c0014t0001g0094 a0001c0014t0001g0125 a0001c0014t0001g0132 others(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 | 72 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(69): Show |
72 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(69): 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 | a0001c0003t0001g0241 a0001c0003t0001g0242 a0001c0003t0001g0246 others(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 | a0001c0004t0001g0314 a0001c0004t0001g0354 a0001c0004t0001g0355 others(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 | a0001c0003t0001g0241 a0001c0003t0001g0242 a0001c0003t0001g0246 others(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 | a0001c0003t0001g0241 a0001c0003t0001g0242 a0001c0003t0001g0246 others(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 | a0001c0089t0001g0184 a0001c0111t0001g0078 a0008c0049t0001g0244 |
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 | a0001c0119t0001g0351 | 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 | a0001c0004t0001g0208 | 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 | a0003c0001t0001g0268 | 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 | a0003c0001t0001g0268 | 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 | a0003c0001t0001g0268 | 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 | a0003c0001t0001g0268 | 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 | a0003c0001t0001g0268 | 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 | a0003c0001t0001g0268 | 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 | a0003c0001t0001g0268 | 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 | a0003c0001t0001g0268 | 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 | a0003c0001t0001g0268 | 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 | a0036c0073t0001g0046 | 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 | a0001c0006t0001g0108 a0002c0005t0001g0147 a0003c0070t0001g0109 |
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 | a0001c0003t0001g0197 a0001c0003t0001g0199 a0001c0003t0001g0200 others(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 | a0003c0001t0001g0258 | 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 | a0001c0089t0001g0184 a0001c0111t0001g0078 |
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 | a0001c0004t0001g0314 a0001c0004t0001g0354 a0001c0004t0001g0355 others(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 | a0001c0007t0001g0006 a0001c0007t0001g0007 a0018c0100t0001g0064 |
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 | a0001c0119t0001g0351 | 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 | a0001c0089t0001g0184 a0001c0111t0001g0078 |
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 | a0001c0003t0001g0197 a0001c0003t0001g0199 a0001c0003t0001g0200 others(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 | a0001c0014t0001g0201 | 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 | a0001c0014t0001g0201 | 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 | a0001c0004t0001g0314 a0001c0004t0001g0354 a0001c0004t0001g0355 others(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 | a0001c0003t0001g0197 a0001c0003t0001g0199 a0001c0003t0001g0200 others(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 | a0001c0089t0001g0184 a0001c0111t0001g0078 |
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 | a0002c0013t0001g0021 | 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 | a0001c0089t0001g0184 a0001c0111t0001g0078 |
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 | a0001c0089t0001g0184 a0001c0111t0001g0078 |
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 | a0001c0003t0001g0241 a0001c0003t0001g0242 a0001c0003t0001g0246 others(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 | a0001c0089t0001g0184 a0001c0111t0001g0078 |
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 | a0001c0003t0001g0200 | 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 | a0001c0089t0001g0184 a0001c0111t0001g0078 |
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 | 251 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(248): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.1005+995G>A | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 11/40 | chr17 | 10353685 | |||||||
chr17:10353908 | G | A | 316 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(313): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): 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 | a0001c0003t0001g0197 a0001c0004t0001g0354 a0001c0004t0001g0355 others(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 | a0001c0003t0001g0199 a0001c0003t0001g0200 a0001c0006t0001g0232 others(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 | a0001c0027t0001g0009 a0001c0027t0001g0155 a0001c0027t0001g0165 others(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 | a0001c0015t0001g0014 a0001c0111t0001g0078 a0002c0013t0001g0016 others(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 | a0001c0014t0001g0010 a0001c0015t0001g0011 a0002c0013t0001g0012 others(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 | 91 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(88): Show |
91 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(88): 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 | a0001c0014t0001g0201 | 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 | a0001c0003t0001g0241 a0001c0003t0001g0242 a0001c0003t0001g0246 others(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 | 315 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(312): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): 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 | a0003c0001t0001g0253 a0038c0084t0001g0254 |
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 | a0001c0027t0001g0165 a0004c0026t0001g0153 a0004c0026t0001g0164 |
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 | a0001c0003t0001g0241 a0001c0003t0001g0242 a0001c0003t0001g0246 others(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 | a0001c0003t0001g0225 a0001c0003t0001g0226 a0001c0003t0001g0228 others(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 | a0007c0020t0001g0106 | 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 | 218 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(215): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.902-54delA | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 10/40 | chr17 | 10354836 | |||||||
chr17:10354838 | T | C | 218 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(215): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): 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 | a0001c0089t0001g0184 a0001c0111t0001g0078 |
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 | a0001c0119t0001g0351 | 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 | a0001c0014t0001g0094 a0001c0014t0001g0125 a0001c0014t0001g0132 others(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 | a0001c0015t0001g0134 | 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 | a0001c0027t0001g0009 a0001c0027t0001g0155 a0001c0027t0001g0165 others(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 | a0001c0006t0001g0140 a0002c0005t0001g0041 a0002c0005t0001g0110 others(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 | a0001c0006t0001g0001 a0001c0006t0001g0087 a0001c0006t0001g0108 others(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 | a0001c0006t0001g0121 a0002c0041t0001g0231 a0002c0061t0001g0104 others(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 | a0001c0006t0001g0232 a0001c0006t0001g0233 a0001c0022t0001g0149 others(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 | a0004c0002t0001g0207 a0004c0002t0001g0235 |
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 | a0001c0004t0001g0169 a0003c0001t0001g0268 a0006c0033t0001g0185 |
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 | a0001c0003t0001g0045 a0001c0003t0001g0197 a0001c0003t0001g0199 others(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 | 167 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(164): Show |
167 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(164): 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 | a0001c0004t0001g0031 a0001c0007t0001g0376 a0001c0012t0001g0336 others(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 | a0001c0014t0001g0010 a0001c0015t0001g0011 a0001c0015t0001g0014 others(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 | a0001c0089t0001g0184 a0001c0119t0001g0351 |
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 | a0001c0003t0001g0241 a0001c0003t0001g0242 a0001c0003t0001g0246 others(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 | a0001c0089t0001g0184 a0001c0111t0001g0078 |
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 | a0004c0048t0001g0206 a0005c0018t0001g0205 |
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 | a0001c0014t0001g0201 a0002c0009t0001g0274 |
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 | a0001c0003t0001g0197 a0001c0003t0001g0199 a0001c0003t0001g0200 others(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 | a0006c0052t0001g0243 | 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 | a0001c0089t0001g0184 a0001c0111t0001g0078 |
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 | a0001c0003t0001g0241 a0001c0003t0001g0242 a0001c0003t0001g0246 others(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 | a0001c0014t0001g0125 a0001c0110t0001g0126 |
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 | a0001c0007t0001g0117 | 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 | a0005c0087t0001g0332 | 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 | a0001c0004t0001g0314 a0001c0004t0001g0354 a0001c0004t0001g0355 others(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 | a0001c0012t0001g0336 a0001c0012t0001g0345 a0001c0022t0001g0334 others(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 | a0001c0007t0001g0376 a0002c0009t0001g0374 a0002c0009t0001g0377 |
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 | a0001c0003t0001g0238 a0001c0004t0001g0169 a0001c0004t0001g0170 others(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 | a0008c0049t0001g0244 | 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 | a0001c0014t0001g0201 | 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 | a0001c0017t0001g0116 | 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 | a0002c0008t0001g0222 | 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 | a0001c0003t0001g0241 a0001c0003t0001g0242 a0001c0003t0001g0246 others(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 | a0001c0022t0001g0181 a0002c0005t0001g0224 a0027c0069t0001g0236 |
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 | a0001c0003t0001g0241 a0001c0003t0001g0242 a0001c0003t0001g0246 others(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 | a0001c0003t0001g0241 a0001c0003t0001g0242 a0001c0003t0001g0246 others(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 | a0003c0001t0001g0250 | 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 | a0001c0006t0001g0085 a0001c0006t0001g0087 a0001c0017t0001g0088 others(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 | a0001c0003t0001g0241 a0001c0003t0001g0242 a0001c0003t0001g0246 others(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 | a0001c0015t0001g0134 | 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 | a0001c0089t0001g0184 a0001c0111t0001g0078 |
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 | a0001c0003t0001g0197 a0001c0003t0001g0199 a0001c0003t0001g0200 others(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 | 69 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(66): Show |
69 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(66): 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 | a0001c0006t0001g0121 a0002c0005t0001g0107 a0003c0065t0001g0079 |
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 | a0001c0006t0001g0108 a0002c0005t0001g0147 a0003c0070t0001g0109 |
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 | a0001c0007t0001g0326 | 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 | a0023c0074t0001g0076 | 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 | a0008c0049t0001g0244 | 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 | a0008c0049t0001g0244 | 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 | a0003c0001t0001g0250 | 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 | a0001c0003t0001g0197 a0001c0003t0001g0199 a0001c0003t0001g0200 others(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 | a0001c0089t0001g0184 a0001c0111t0001g0078 |
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 | a0034c0112t0001g0067 | 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 | a0001c0003t0001g0241 a0001c0003t0001g0242 a0001c0003t0001g0246 others(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 | a0001c0003t0001g0241 a0001c0003t0001g0242 a0001c0003t0001g0246 others(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 | a0002c0041t0001g0365 | 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 | a0002c0005t0001g0261 | 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 | a0030c0077t0001g0353 | 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 | a0002c0025t0001g0162 | 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 | a0001c0027t0001g0009 a0001c0027t0001g0155 a0001c0027t0001g0165 others(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 | a0001c0014t0001g0010 a0001c0015t0001g0011 a0001c0015t0001g0014 others(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 | a0004c0021t0001g0091 a0004c0021t0001g0092 a0041c0067t0001g0093 |
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 | a0001c0003t0001g0241 a0001c0003t0001g0242 a0001c0003t0001g0246 others(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 | a0001c0003t0001g0241 a0001c0003t0001g0242 a0001c0003t0001g0246 others(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 | a0001c0003t0001g0241 a0001c0003t0001g0242 a0001c0003t0001g0246 others(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 | a0001c0014t0001g0010 a0001c0015t0001g0011 a0001c0015t0001g0014 others(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 | a0027c0069t0001g0236 | 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 | a0001c0027t0001g0009 a0001c0027t0001g0155 a0001c0027t0001g0165 others(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 | a0002c0005t0001g0341 | 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 | a0001c0006t0001g0085 a0001c0006t0001g0087 a0001c0006t0001g0113 others(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 | a0004c0026t0001g0166 a0007c0107t0001g0167 |
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 | a0001c0003t0001g0197 a0001c0003t0001g0199 a0001c0003t0001g0200 others(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 | a0001c0003t0001g0339 a0001c0004t0001g0314 a0001c0004t0001g0354 others(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 | a0006c0024t0001g0331 | 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 | a0002c0008t0001g0329 | 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 | a0001c0003t0001g0197 a0001c0003t0001g0199 a0001c0003t0001g0200 others(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 | a0001c0003t0001g0339 a0001c0004t0001g0314 a0001c0004t0001g0354 others(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 | a0001c0007t0001g0376 a0001c0014t0001g0375 a0001c0042t0001g0234 others(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 | a0001c0003t0001g0241 a0001c0003t0001g0242 a0001c0003t0001g0246 others(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 | a0001c0027t0001g0009 a0001c0027t0001g0155 a0001c0027t0001g0165 others(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 | a0001c0003t0001g0241 a0001c0003t0001g0242 a0001c0003t0001g0246 others(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 | a0001c0003t0001g0339 a0001c0004t0001g0314 a0001c0004t0001g0354 others(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 | a0001c0003t0001g0241 a0001c0003t0001g0242 a0001c0003t0001g0246 others(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 | a0001c0003t0001g0339 a0001c0006t0001g0337 a0001c0012t0001g0336 others(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 | a0001c0014t0001g0010 a0001c0015t0001g0011 a0001c0015t0001g0014 others(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 | a0001c0003t0001g0197 a0001c0003t0001g0199 a0001c0003t0001g0200 others(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 | 74 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(71): Show |
74 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(71): Show |
intron_variant | MODIFIER | c.205-465dupT | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 3/40 | chr17 | 10362967 | |||||||
chr17:10363052 | G | A | 303 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(300): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): 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 | a0001c0089t0001g0184 a0004c0021t0001g0137 a0006c0068t0001g0366 others(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 | a0001c0003t0001g0339 a0001c0004t0001g0314 a0001c0004t0001g0354 others(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 | a0009c0044t0001g0138 a0009c0044t0001g0139 |
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 | a0001c0017t0001g0116 | 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 | a0012c0035t0001g0143 a0012c0035t0001g0145 a0012c0058t0001g0142 others(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 | a0006c0024t0001g0128 a0007c0083t0001g0127 |
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 | 166 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(163): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.205-813dupT | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 3/40 | chr17 | 10363315 | |||||||
chr17:10363315 | C | CAA | 28 | a0001c0003t0001g0069 a0001c0003t0001g0241 a0001c0003t0001g0242 others(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 | a0001c0003t0001g0197 a0001c0003t0001g0199 a0001c0003t0001g0200 others(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 | a0001c0090t0001g0364 a0001c0111t0001g0078 a0001c0118t0001g0350 others(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 | a0007c0020t0001g0349 | 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 | a0001c0027t0001g0009 a0001c0027t0001g0155 a0001c0027t0001g0165 others(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 | a0001c0027t0001g0009 a0001c0027t0001g0155 a0001c0027t0001g0165 others(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 | a0003c0038t0001g0369 | 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 | a0001c0027t0001g0009 a0001c0027t0001g0155 a0001c0027t0001g0165 others(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 | 303 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(300): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): 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 | a0008c0049t0001g0244 | 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 | a0001c0027t0001g0009 a0001c0027t0001g0155 a0001c0027t0001g0165 others(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 | a0001c0089t0001g0184 a0004c0021t0001g0137 a0006c0068t0001g0366 others(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 | a0001c0027t0001g0009 a0001c0027t0001g0155 a0001c0027t0001g0165 others(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 | a0001c0006t0001g0001 a0001c0006t0001g0085 a0001c0006t0001g0087 others(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 | a0001c0003t0001g0241 a0001c0003t0001g0242 a0001c0003t0001g0246 others(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 | a0001c0027t0001g0009 a0001c0027t0001g0155 a0001c0027t0001g0165 others(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 | a0001c0014t0001g0010 a0001c0015t0001g0011 a0001c0015t0001g0014 others(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 | a0001c0090t0001g0364 a0002c0041t0001g0365 a0004c0021t0001g0137 others(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 | a0001c0003t0001g0008 a0001c0003t0001g0038 a0001c0003t0001g0039 others(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 | a0001c0027t0001g0009 a0001c0027t0001g0155 a0001c0027t0001g0165 others(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 | a0001c0003t0001g0241 a0001c0003t0001g0242 a0001c0003t0001g0246 others(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 | a0019c0076t0001g0352 | 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 | a0030c0077t0001g0353 | 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 | a0001c0004t0001g0354 a0001c0004t0001g0355 a0001c0004t0001g0356 |
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 | a0001c0006t0001g0233 a0001c0007t0001g0283 a0001c0027t0001g0009 others(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 | a0001c0006t0001g0232 a0001c0007t0001g0300 a0001c0007t0001g0301 others(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 | a0001c0003t0001g0225 a0001c0003t0001g0226 a0001c0003t0001g0242 others(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 | a0001c0003t0001g0228 a0001c0003t0001g0238 a0001c0006t0001g0001 others(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 | a0001c0003t0001g0214 a0001c0003t0001g0241 a0001c0004t0001g0208 others(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 | 49 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(46): Show |
49 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(46): 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 | a0001c0003t0001g0347 a0001c0040t0001g0102 a0004c0026t0001g0153 others(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 | a0001c0014t0001g0010 a0001c0015t0001g0011 a0001c0015t0001g0014 others(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 | a0008c0049t0001g0151 | 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 | 105 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(102): Show |
105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): 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 | a0001c0027t0001g0009 a0001c0027t0001g0155 a0001c0027t0001g0165 others(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 | a0001c0003t0001g0241 a0001c0003t0001g0242 a0001c0003t0001g0249 others(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 | a0008c0049t0001g0151 | 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 | a0001c0007t0001g0376 a0001c0014t0001g0375 a0002c0009t0001g0377 |
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 | a0001c0014t0001g0372 a0001c0015t0001g0373 a0001c0015t0001g0378 others(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 | a0001c0015t0001g0371 a0001c0111t0001g0078 a0002c0013t0001g0022 others(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 | a0001c0027t0001g0165 a0001c0072t0001g0163 a0001c0105t0001g0160 others(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 | a0001c0015t0001g0011 a0001c0015t0001g0014 a0001c0027t0001g0009 others(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 | a0001c0014t0001g0010 a0001c0034t0001g0152 a0004c0026t0001g0153 |
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 | 57 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(54): Show |
57 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(54): 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 | a0001c0003t0001g0241 a0001c0003t0001g0242 a0001c0003t0001g0246 others(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 | a0003c0001t0001g0357 | 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 | a0003c0011t0001g0239 | 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 | a0022c0101t0001g0074 | 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 | 2 | a0001c0006t0001g0140 a0001c0017t0001g0141 |
2 | HG01175.hp2 HG01358.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 | a0001c0007t0001g0376 a0001c0014t0001g0372 a0001c0014t0001g0375 others(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 | a0001c0027t0001g0009 a0001c0027t0001g0155 a0001c0027t0001g0165 others(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 | a0003c0011t0001g0186 | 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 | a0001c0027t0001g0009 a0001c0027t0001g0155 a0001c0027t0001g0165 others(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 | a0003c0001t0001g0252 a0003c0001t0001g0253 a0038c0084t0001g0254 |
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 | a0001c0003t0001g0241 a0001c0003t0001g0242 a0001c0003t0001g0246 others(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 | a0008c0049t0001g0151 | 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 | a0012c0035t0001g0143 a0012c0035t0001g0145 a0012c0058t0001g0142 others(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 | a0001c0027t0001g0009 a0001c0027t0001g0155 a0001c0027t0001g0165 others(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 | a0002c0005t0001g0147 | 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 | a0003c0001t0001g0359 | 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 | a0003c0043t0001g0251 | 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 | a0001c0027t0001g0009 a0001c0027t0001g0155 a0001c0027t0001g0165 others(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 | a0003c0001t0001g0250 | 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 | a0001c0003t0001g0339 a0001c0003t0001g0347 a0001c0004t0001g0314 others(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 | a0001c0027t0001g0009 a0001c0027t0001g0155 a0001c0027t0001g0165 others(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 | a0006c0024t0001g0182 a0006c0024t0001g0183 |
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 | a0001c0027t0001g0009 a0001c0027t0001g0155 a0001c0027t0001g0165 others(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 | a0002c0008t0001g0361 a0002c0009t0001g0362 a0004c0002t0001g0360 |
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 | a0001c0003t0001g0032 a0003c0045t0001g0033 a0007c0096t0001g0034 |
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 | a0001c0027t0001g0009 a0001c0027t0001g0155 a0001c0027t0001g0165 others(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 | a0001c0027t0001g0009 a0001c0027t0001g0155 a0001c0027t0001g0165 others(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 | a0001c0014t0001g0010 a0001c0015t0001g0011 a0001c0015t0001g0014 others(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 | a0023c0074t0001g0076 | 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 | a0001c0027t0001g0009 a0001c0027t0001g0155 a0001c0027t0001g0165 others(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 | a0001c0007t0001g0376 a0001c0014t0001g0372 a0001c0014t0001g0375 others(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 | a0004c0010t0001g0179 a0039c0082t0001g0180 |
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 | a0001c0120t0001g0178 a0004c0026t0001g0176 a0004c0106t0001g0177 |
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 | a0001c0004t0001g0169 a0001c0004t0001g0170 a0001c0103t0001g0174 others(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 | a0001c0007t0001g0376 a0001c0014t0001g0372 a0001c0014t0001g0375 others(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 | a0001c0027t0001g0009 a0001c0027t0001g0155 a0001c0027t0001g0165 others(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 | a0001c0004t0001g0026 a0001c0004t0001g0027 a0001c0004t0001g0028 others(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 | a0001c0007t0001g0376 a0001c0014t0001g0010 a0001c0014t0001g0372 others(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 | a0015c0054t0001g0150 | 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 | a0003c0011t0001g0081 | 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 | a0003c0065t0001g0079 a0005c0016t0001g0080 |
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 | a0001c0007t0001g0376 a0001c0014t0001g0010 a0001c0014t0001g0372 others(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 | a0001c0006t0001g0001 a0001c0006t0001g0085 a0001c0006t0001g0087 others(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 | a0029c0098t0001g0024 | 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 | 56 | a0001c0003t0001g0008 a0001c0003t0001g0032 a0001c0003t0001g0038 others(53): Show |
56 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(53): 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 | a0001c0014t0001g0010 a0001c0015t0001g0011 a0001c0015t0001g0014 others(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 | a0001c0007t0001g0376 a0001c0014t0001g0372 a0001c0014t0001g0375 others(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 | a0015c0054t0001g0379 a0016c0117t0001g0380 |
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 | a0001c0007t0001g0006 a0001c0007t0001g0007 |
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 | a0003c0001t0001g0004 a0003c0081t0001g0005 |
2 | HG00621.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.-64+320T>C | MYH13 | ENSG00000006788.14 | transcript | ENST00000252172.9 | protein_coding | 1/40 | chr17 | 10372659 |