| geneid | 202333 |
|---|---|
| ensemblid | ENSG00000164309.15 |
| hgncid | 14305 |
| symbol | CMYA5 |
| name | cardiomyopathy associated 5 |
| refseq_nuc | NM_153610.5 |
| refseq_prot | NP_705838.3 |
| ensembl_nuc | ENST00000446378.3 |
| ensembl_prot | ENSP00000394770.2 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 79689836 |
| end | 79800222 |
| strand | + |
| ver | v1.2 |
| region | chr5:79689836-79800222 |
| region5000 | chr5:79684836-79805222 |
| regionname0 | CMYA5_chr5_79689836_79800222 |
| regionname5000 | CMYA5_chr5_79684836_79805222 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 4069 | 60 | 3 | 13 | 25 | 4 | 14 | 15 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0002 | 0/0 | 4069 | 37 | 1 | 3 | 31 | 0 | 2 | 27 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0003 | 0/0 | 4069 | 28 | 12 | 5 | 8 | 2 | 1 | 7 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0004 | 0/0 | 4069 | 25 | 0 | 0 | 24 | 0 | 1 | 20 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0005 | 0/0 | 4069 | 17 | 1 | 7 | 5 | 0 | 4 | 3 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0006 | 0/0 | 4069 | 14 | 0 | 1 | 12 | 0 | 1 | 7 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0007 | 0/0 | 4069 | 11 | 9 | 1 | 0 | 0 | 1 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0008 | 0/0 | 4069 | 11 | 0 | 0 | 11 | 0 | 0 | 8 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0009 | 0/0 | 4069 | 9 | 8 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0010 | 0/0 | 4069 | 8 | 1 | 2 | 2 | 1 | 2 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0011 | 0/0 | 4069 | 7 | 0 | 7 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0012 | 0/0 | 4069 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0013 | 0/0 | 4069 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0014 | 0/0 | 4069 | 5 | 0 | 0 | 5 | 0 | 0 | 5 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0015 | 0/0 | 4069 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0016 | 0/0 | 4069 | 4 | 0 | 0 | 4 | 0 | 0 | 3 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0017 | 0/0 | 4069 | 4 | 1 | 3 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0018 | 0/0 | 4069 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0019 | 0/0 | 4069 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0020 | 0/0 | 4069 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0021 | 0/0 | 4069 | 3 | 0 | 2 | 1 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0022 | 0/0 | 4069 | 3 | 0 | 0 | 2 | 0 | 1 | 2 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0023 | 0/0 | 4069 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0024 | 0/1 | 4069 | 3 | 0 | 0 | 1 | 0 | 1 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0025 | 0/0 | 4069 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0026 | 0/0 | 4069 | 3 | 0 | 0 | 3 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0027 | 0/0 | 4069 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0028 | 0/0 | 4069 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0029 | 0/0 | 4069 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0030 | 0/0 | 4069 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0031 | 0/0 | 4069 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0032 | 0/0 | 4069 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0033 | 0/0 | 4069 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0034 | 0/0 | 4069 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0035 | 0/0 | 4069 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0036 | 0/0 | 4069 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0037 | 0/0 | 4069 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0038 | 0/0 | 4069 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0039 | 0/0 | 4069 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0040 | 0/0 | 4069 | 2 | 1 | 0 | 0 | 0 | 1 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0041 | 0/0 | 4069 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0042 | 0/0 | 4069 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0043 | 0/0 | 4069 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0044 | 0/0 | 4069 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0045 | 0/0 | 4069 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0046 | 0/0 | 4069 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0047 | 0/0 | 4069 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0048 | 0/0 | 4069 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0049 | 0/0 | 4069 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0050 | 0/0 | 4069 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0051 | 0/0 | 4069 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0052 | 0/0 | 4069 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0053 | 0/0 | 4069 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0054 | 0/0 | 4069 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0055 | 0/0 | 4069 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0056 | 0/0 | 4069 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0057 | 0/0 | 4069 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0058 | 0/0 | 4069 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0059 | 0/0 | 4069 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0060 | 0/0 | 4069 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0061 | 0/0 | 732 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0062 | 0/0 | 4069 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0063 | 0/0 | 4069 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0064 | 0/0 | 4069 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0065 | 0/0 | 4069 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0066 | 0/0 | 4069 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0067 | 0/0 | 4069 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0068 | 0/0 | 4069 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0069 | 0/0 | 4069 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0070 | 0/0 | 4069 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0071 | 0/0 | 4069 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0072 | 0/0 | 4069 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0073 | 0/0 | 1436 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0074 | 0/0 | 4069 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0075 | 0/0 | 4069 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0076 | 0/0 | 4069 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0077 | 0/0 | 4069 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0078 | 0/0 | 4069 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0079 | 0/0 | 4069 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0080 | 0/0 | 4069 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0081 | 0/0 | 4069 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0082 | 0/0 | 4069 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0083 | 0/0 | 4069 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0084 | 0/0 | 4069 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 12210 | 49 | 3 | 11 | 18 | 4 | 12 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0002 | 0/0 | 12210 | 31 | 0 | 3 | 26 | 0 | 2 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0003 | 0/0 | 12210 | 25 | 10 | 4 | 8 | 2 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0004 | 0/0 | 12210 | 14 | 0 | 1 | 12 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0005 | 0/0 | 12210 | 13 | 0 | 6 | 4 | 0 | 3 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0006 | 0/0 | 12210 | 12 | 0 | 0 | 11 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0007 | 0/0 | 12210 | 10 | 0 | 0 | 10 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0008 | 0/0 | 12210 | 10 | 9 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0009 | 0/0 | 12210 | 9 | 8 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0010 | 0/0 | 12210 | 7 | 1 | 2 | 1 | 1 | 2 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0011 | 0/0 | 12210 | 7 | 0 | 0 | 7 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0012 | 0/0 | 12210 | 6 | 0 | 6 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0013 | 0/0 | 12210 | 6 | 0 | 1 | 5 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0014 | 0/0 | 12210 | 6 | 0 | 0 | 6 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0015 | 0/0 | 12210 | 5 | 5 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0016 | 0/0 | 12210 | 5 | 5 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0017 | 0/0 | 12210 | 4 | 0 | 0 | 4 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0018 | 0/0 | 12210 | 4 | 0 | 0 | 4 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0019 | 0/0 | 12210 | 4 | 1 | 3 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0020 | 0/0 | 12210 | 4 | 0 | 0 | 4 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0021 | 0/0 | 12210 | 3 | 0 | 0 | 2 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0022 | 0/0 | 12210 | 3 | 3 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0023 | 0/0 | 12210 | 3 | 0 | 0 | 3 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0024 | 0/0 | 12210 | 3 | 3 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0025 | 0/0 | 12210 | 3 | 3 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0026 | 0/0 | 12210 | 3 | 0 | 2 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0027 | 0/0 | 12210 | 3 | 0 | 0 | 3 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0028 | 0/0 | 12210 | 2 | 0 | 0 | 2 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0029 | 0/0 | 12210 | 2 | 0 | 0 | 2 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0030 | 0/0 | 12210 | 2 | 2 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0031 | 0/0 | 12210 | 2 | 0 | 0 | 2 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0032 | 0/0 | 12210 | 2 | 2 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0033 | 0/0 | 12210 | 2 | 0 | 1 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0034 | 0/0 | 12210 | 2 | 2 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0035 | 0/0 | 12210 | 2 | 0 | 0 | 0 | 0 | 2 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0036 | 0/0 | 12210 | 2 | 0 | 0 | 0 | 0 | 2 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0037 | 0/0 | 12210 | 2 | 2 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0038 | 0/0 | 12210 | 2 | 2 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0039 | 0/0 | 12210 | 2 | 0 | 0 | 2 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0040 | 0/0 | 12210 | 2 | 1 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0041 | 0/0 | 12210 | 2 | 2 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0042 | 0/0 | 12210 | 2 | 2 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0043 | 0/0 | 12210 | 2 | 2 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0044 | 0/0 | 12210 | 2 | 2 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0045 | 0/0 | 12210 | 2 | 0 | 0 | 2 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0046 | 0/0 | 12210 | 2 | 2 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0047 | 0/0 | 12210 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0048 | 0/0 | 12210 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0049 | 0/0 | 12210 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0050 | 0/0 | 12210 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0051 | 0/0 | 12210 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0052 | 0/0 | 12210 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0053 | 0/0 | 12210 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0054 | 0/0 | 12210 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0055 | 0/0 | 12210 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0056 | 0/0 | 12210 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0057 | 0/0 | 12210 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0058 | 0/0 | 12210 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0059 | 0/0 | 12210 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0060 | 0/0 | 12210 | 1 | 0 | 0 | 0 | 1 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0061 | 0/0 | 12210 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0062 | 0/0 | 12210 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0063 | 0/0 | 12210 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0064 | 0/0 | 12210 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0065 | 0/0 | 12210 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0066 | 0/0 | 12210 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0067 | 0/0 | 12210 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0068 | 0/0 | 12210 | 1 | 0 | 0 | 0 | 1 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0069 | 0/0 | 12210 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0070 | 0/0 | 12210 | 1 | 0 | 0 | 0 | 1 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0071 | 0/0 | 12210 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0072 | 0/0 | 12210 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0073 | 0/0 | 12210 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0074 | 0/0 | 12210 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0075 | 0/0 | 12210 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0076 | 0/0 | 12210 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0077 | 0/0 | 12210 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0078 | 0/0 | 12210 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0079 | 0/0 | 12210 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0080 | 0/0 | 12210 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0081 | 0/0 | 12210 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0082 | 0/0 | 12210 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0083 | 0/0 | 12210 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0084 | 0/1 | 12210 | 1 | 0 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0085 | 0/0 | 12210 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0086 | 0/0 | 12210 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0087 | 0/0 | 12210 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0088 | 0/0 | 12210 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0089 | 0/0 | 12210 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0090 | 0/0 | 12210 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0091 | 0/0 | 12210 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0092 | 0/0 | 12210 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0093 | 0/0 | 12210 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0094 | 0/0 | 12210 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0095 | 0/0 | 12210 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0096 | 0/0 | 12210 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0097 | 0/0 | 12210 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0098 | 0/0 | 12210 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0099 | 0/0 | 12210 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0100 | 0/0 | 12210 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0101 | 0/0 | 12210 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0102 | 0/0 | 12210 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0103 | 0/0 | 12210 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0104 | 0/0 | 12210 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0105 | 0/0 | 12210 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0106 | 0/0 | 12210 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0107 | 0/0 | 12210 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0108 | 0/0 | 12210 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0109 | 0/0 | 12210 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0110 | 0/0 | 12210 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0111 | 0/0 | 12210 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0112 | 0/0 | 12210 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0113 | 0/0 | 12210 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| c0114 | 0/0 | 12210 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 679 | 174 | 34 | 31 | 73 | 6 | 28 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| t0002 | 0/0 | 678 | 114 | 14 | 18 | 71 | 2 | 9 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| t0003 | 0/0 | 679 | 24 | 6 | 4 | 11 | 2 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| t0004 | 0/0 | 685 | 11 | 10 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| t0005 | 0/0 | 684 | 7 | 7 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| t0006 | 0/0 | 678 | 6 | 0 | 0 | 5 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| t0007 | 0/0 | 685 | 6 | 6 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| t0008 | 0/0 | 685 | 3 | 3 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| t0009 | 0/0 | 679 | 2 | 2 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| t0010 | 0/0 | 679 | 2 | 0 | 2 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| t0011 | 0/0 | 679 | 2 | 2 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| t0012 | 0/0 | 685 | 2 | 2 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| t0013 | 0/0 | 678 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| t0014 | 0/0 | 679 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| t0015 | 0/0 | 679 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| t0016 | 0/0 | 684 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| t0017 | 0/0 | 685 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0098 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0172 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 12210 | 49 | 3 | 11 | 18 | 4 | 12 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0001c0013 | 0/0 | 12210 | 6 | 0 | 1 | 5 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0001c0033 | 0/0 | 12210 | 2 | 0 | 1 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0001c0055 | 0/0 | 12210 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0001c0056 | 0/0 | 12210 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0001c0058 | 0/0 | 12210 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0002c0002 | 0/0 | 12210 | 31 | 0 | 3 | 26 | 0 | 2 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0002c0020 | 0/0 | 12210 | 4 | 0 | 0 | 4 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0002c0106 | 0/0 | 12210 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0002c0114 | 0/0 | 12210 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0003c0003 | 0/0 | 12210 | 25 | 10 | 4 | 8 | 2 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0003c0034 | 0/0 | 12210 | 2 | 2 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0003c0069 | 0/0 | 12210 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0004c0006 | 0/0 | 12210 | 12 | 0 | 0 | 11 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0004c0011 | 0/0 | 12210 | 7 | 0 | 0 | 7 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0004c0014 | 0/0 | 12210 | 6 | 0 | 0 | 6 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0005c0005 | 0/0 | 12210 | 13 | 0 | 6 | 4 | 0 | 3 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0005c0077 | 0/0 | 12210 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0005c0079 | 0/0 | 12210 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0005c0085 | 0/0 | 12210 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0005c0089 | 0/0 | 12210 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0006c0004 | 0/0 | 12210 | 14 | 0 | 1 | 12 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0007c0008 | 0/0 | 12210 | 10 | 9 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0007c0097 | 0/0 | 12210 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0008c0007 | 0/0 | 12210 | 10 | 0 | 0 | 10 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0008c0067 | 0/0 | 12210 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0009c0009 | 0/0 | 12210 | 9 | 8 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0010c0010 | 0/0 | 12210 | 7 | 1 | 2 | 1 | 1 | 2 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0010c0065 | 0/0 | 12210 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0011c0012 | 0/0 | 12210 | 6 | 0 | 6 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0011c0052 | 0/0 | 12210 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0012c0015 | 0/0 | 12210 | 5 | 5 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0012c0074 | 0/0 | 12210 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0013c0016 | 0/0 | 12210 | 5 | 5 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0014c0027 | 0/0 | 12210 | 3 | 0 | 0 | 3 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0014c0045 | 0/0 | 12210 | 2 | 0 | 0 | 2 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0015c0032 | 0/0 | 12210 | 2 | 2 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0015c0038 | 0/0 | 12210 | 2 | 2 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0015c0073 | 0/0 | 12210 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0016c0018 | 0/0 | 12210 | 4 | 0 | 0 | 4 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0017c0019 | 0/0 | 12210 | 4 | 1 | 3 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0018c0017 | 0/0 | 12210 | 4 | 0 | 0 | 4 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0019c0024 | 0/0 | 12210 | 3 | 3 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0020c0025 | 0/0 | 12210 | 3 | 3 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0021c0026 | 0/0 | 12210 | 3 | 0 | 2 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0022c0021 | 0/0 | 12210 | 3 | 0 | 0 | 2 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0023c0022 | 0/0 | 12210 | 3 | 3 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0024c0082 | 0/0 | 12210 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0024c0084 | 0/1 | 12210 | 1 | 0 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0024c0087 | 0/0 | 12210 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0025c0023 | 0/0 | 12210 | 3 | 0 | 0 | 3 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0026c0028 | 0/0 | 12210 | 2 | 0 | 0 | 2 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0026c0049 | 0/0 | 12210 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0027c0042 | 0/0 | 12210 | 2 | 2 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0028c0043 | 0/0 | 12210 | 2 | 2 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0029c0044 | 0/0 | 12210 | 2 | 2 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0030c0095 | 0/0 | 12210 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0030c0096 | 0/0 | 12210 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0031c0046 | 0/0 | 12210 | 2 | 2 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0032c0109 | 0/0 | 12210 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0032c0110 | 0/0 | 12210 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0033c0039 | 0/0 | 12210 | 2 | 0 | 0 | 2 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0034c0031 | 0/0 | 12210 | 2 | 0 | 0 | 2 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0035c0037 | 0/0 | 12210 | 2 | 2 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0036c0068 | 0/0 | 12210 | 1 | 0 | 0 | 0 | 1 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0036c0070 | 0/0 | 12210 | 1 | 0 | 0 | 0 | 1 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0037c0036 | 0/0 | 12210 | 2 | 0 | 0 | 0 | 0 | 2 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0038c0035 | 0/0 | 12210 | 2 | 0 | 0 | 0 | 0 | 2 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0039c0030 | 0/0 | 12210 | 2 | 2 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0040c0040 | 0/0 | 12210 | 2 | 1 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0041c0041 | 0/0 | 12210 | 2 | 2 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0042c0029 | 0/0 | 12210 | 2 | 0 | 0 | 2 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0043c0094 | 0/0 | 12210 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0044c0093 | 0/0 | 12210 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0045c0099 | 0/0 | 12210 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0046c0098 | 0/0 | 12210 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0047c0105 | 0/0 | 12210 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0048c0107 | 0/0 | 12210 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0049c0103 | 0/0 | 12210 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0050c0104 | 0/0 | 12210 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0051c0100 | 0/0 | 12210 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0052c0102 | 0/0 | 12210 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0053c0101 | 0/0 | 12210 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0054c0108 | 0/0 | 12210 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0055c0113 | 0/0 | 12210 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0056c0112 | 0/0 | 12210 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0057c0111 | 0/0 | 12210 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0058c0092 | 0/0 | 12210 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0059c0075 | 0/0 | 12210 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0060c0051 | 0/0 | 12210 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0061c0053 | 0/0 | 12210 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0062c0072 | 0/0 | 12210 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0063c0064 | 0/0 | 12210 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0064c0063 | 0/0 | 12210 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0065c0060 | 0/0 | 12210 | 1 | 0 | 0 | 0 | 1 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0066c0057 | 0/0 | 12210 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0067c0059 | 0/0 | 12210 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0068c0061 | 0/0 | 12210 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0069c0062 | 0/0 | 12210 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0070c0066 | 0/0 | 12210 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0071c0054 | 0/0 | 12210 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0072c0071 | 0/0 | 12210 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0073c0076 | 0/0 | 12210 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0074c0078 | 0/0 | 12210 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0075c0086 | 0/0 | 12210 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0076c0088 | 0/0 | 12210 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0077c0083 | 0/0 | 12210 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0078c0080 | 0/0 | 12210 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0079c0081 | 0/0 | 12210 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0080c0090 | 0/0 | 12210 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0081c0091 | 0/0 | 12210 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0082c0047 | 0/0 | 12210 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0083c0048 | 0/0 | 12210 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0084c0050 | 0/0 | 12210 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 12888 | 36 | 2 | 7 | 13 | 4 | 9 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0001c0001t0002 | 0/0 | 12887 | 11 | 1 | 2 | 5 | 0 | 3 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0001c0001t0010 | 0/0 | 12888 | 2 | 0 | 2 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0001c0013t0001 | 0/0 | 12888 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0001c0013t0002 | 0/0 | 12887 | 2 | 0 | 0 | 2 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0001c0013t0003 | 0/0 | 12888 | 2 | 0 | 1 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0001c0013t0006 | 0/0 | 12887 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0001c0033t0001 | 0/0 | 12888 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0001c0033t0002 | 0/0 | 12887 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0001c0055t0001 | 0/0 | 12888 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0001c0056t0001 | 0/0 | 12888 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0001c0058t0002 | 0/0 | 12887 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0002c0002t0001 | 0/0 | 12888 | 12 | 0 | 3 | 8 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0002c0002t0002 | 0/0 | 12887 | 17 | 0 | 0 | 16 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0002c0002t0006 | 0/0 | 12887 | 2 | 0 | 0 | 2 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0002c0020t0001 | 0/0 | 12888 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0002c0020t0002 | 0/0 | 12887 | 3 | 0 | 0 | 3 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0002c0106t0007 | 0/0 | 12894 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0002c0114t0001 | 0/0 | 12888 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0003c0003t0001 | 0/0 | 12888 | 10 | 4 | 1 | 4 | 1 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0003c0003t0002 | 0/0 | 12887 | 7 | 1 | 1 | 3 | 1 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0003c0003t0003 | 0/0 | 12888 | 3 | 1 | 1 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0003c0003t0005 | 0/0 | 12893 | 2 | 2 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0003c0003t0008 | 0/0 | 12894 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0003c0003t0009 | 0/0 | 12888 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0003c0003t0013 | 0/0 | 12887 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0003c0034t0009 | 0/0 | 12888 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0003c0034t0012 | 0/0 | 12894 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0003c0069t0002 | 0/0 | 12887 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0004c0006t0001 | 0/0 | 12888 | 4 | 0 | 0 | 3 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0004c0006t0002 | 0/0 | 12887 | 5 | 0 | 0 | 5 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0004c0006t0003 | 0/0 | 12888 | 3 | 0 | 0 | 3 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0004c0011t0001 | 0/0 | 12888 | 4 | 0 | 0 | 4 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0004c0011t0002 | 0/0 | 12887 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0004c0011t0003 | 0/0 | 12888 | 2 | 0 | 0 | 2 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0004c0014t0002 | 0/0 | 12887 | 6 | 0 | 0 | 6 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0005c0005t0001 | 0/0 | 12888 | 9 | 0 | 5 | 2 | 0 | 2 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0005c0005t0002 | 0/0 | 12887 | 3 | 0 | 1 | 2 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0005c0005t0004 | 0/0 | 12894 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0005c0077t0001 | 0/0 | 12888 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0005c0079t0003 | 0/0 | 12888 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0005c0085t0001 | 0/0 | 12888 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0005c0089t0001 | 0/0 | 12888 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0006c0004t0001 | 0/0 | 12888 | 10 | 0 | 0 | 9 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0006c0004t0002 | 0/0 | 12887 | 3 | 0 | 1 | 2 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0006c0004t0006 | 0/0 | 12887 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0007c0008t0001 | 0/0 | 12888 | 4 | 3 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0007c0008t0002 | 0/0 | 12887 | 3 | 3 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0007c0008t0004 | 0/0 | 12894 | 2 | 2 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0007c0008t0011 | 0/0 | 12888 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0007c0097t0002 | 0/0 | 12887 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0008c0007t0001 | 0/0 | 12888 | 3 | 0 | 0 | 3 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0008c0007t0002 | 0/0 | 12887 | 7 | 0 | 0 | 7 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0008c0067t0001 | 0/0 | 12888 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0009c0009t0001 | 0/0 | 12888 | 6 | 6 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0009c0009t0002 | 0/0 | 12887 | 2 | 1 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0009c0009t0014 | 0/0 | 12888 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0010c0010t0001 | 0/0 | 12888 | 4 | 1 | 1 | 1 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0010c0010t0002 | 0/0 | 12887 | 3 | 0 | 1 | 0 | 1 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0010c0065t0002 | 0/0 | 12887 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0011c0012t0001 | 0/0 | 12888 | 3 | 0 | 3 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0011c0012t0002 | 0/0 | 12887 | 3 | 0 | 3 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0011c0052t0001 | 0/0 | 12888 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0012c0015t0004 | 0/0 | 12894 | 4 | 4 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0012c0015t0016 | 0/0 | 12893 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0012c0074t0001 | 0/0 | 12888 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0013c0016t0001 | 0/0 | 12888 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0013c0016t0003 | 0/0 | 12888 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0013c0016t0004 | 0/0 | 12894 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0013c0016t0007 | 0/0 | 12894 | 2 | 2 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0014c0027t0001 | 0/0 | 12888 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0014c0027t0002 | 0/0 | 12887 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0014c0027t0003 | 0/0 | 12888 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0014c0045t0002 | 0/0 | 12887 | 2 | 0 | 0 | 2 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0015c0032t0007 | 0/0 | 12894 | 2 | 2 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0015c0038t0002 | 0/0 | 12887 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0015c0038t0004 | 0/0 | 12894 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0015c0073t0015 | 0/0 | 12888 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0016c0018t0001 | 0/0 | 12888 | 2 | 0 | 0 | 2 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0016c0018t0002 | 0/0 | 12887 | 2 | 0 | 0 | 2 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0017c0019t0001 | 0/0 | 12888 | 4 | 1 | 3 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0018c0017t0001 | 0/0 | 12888 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0018c0017t0002 | 0/0 | 12887 | 3 | 0 | 0 | 3 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0019c0024t0001 | 0/0 | 12888 | 2 | 2 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0019c0024t0017 | 0/0 | 12894 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0020c0025t0001 | 0/0 | 12888 | 3 | 3 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0021c0026t0001 | 0/0 | 12888 | 2 | 0 | 2 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0021c0026t0002 | 0/0 | 12887 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0022c0021t0001 | 0/0 | 12888 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0022c0021t0002 | 0/0 | 12887 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0022c0021t0006 | 0/0 | 12887 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0023c0022t0001 | 0/0 | 12888 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0023c0022t0008 | 0/0 | 12894 | 2 | 2 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0024c0082t0001 | 0/0 | 12888 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0024c0084t0001 | 0/1 | 12888 | 1 | 0 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0024c0087t0001 | 0/0 | 12888 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0025c0023t0001 | 0/0 | 12888 | 2 | 0 | 0 | 2 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0025c0023t0002 | 0/0 | 12887 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0026c0028t0001 | 0/0 | 12888 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0026c0028t0002 | 0/0 | 12887 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0026c0049t0006 | 0/0 | 12887 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0027c0042t0001 | 0/0 | 12888 | 2 | 2 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0028c0043t0001 | 0/0 | 12888 | 2 | 2 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0029c0044t0004 | 0/0 | 12894 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0029c0044t0012 | 0/0 | 12894 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0030c0095t0003 | 0/0 | 12888 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0030c0096t0001 | 0/0 | 12888 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0031c0046t0001 | 0/0 | 12888 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0031c0046t0002 | 0/0 | 12887 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0032c0109t0002 | 0/0 | 12887 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0032c0110t0002 | 0/0 | 12887 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0033c0039t0001 | 0/0 | 12888 | 2 | 0 | 0 | 2 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0034c0031t0003 | 0/0 | 12888 | 2 | 0 | 0 | 2 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0035c0037t0001 | 0/0 | 12888 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0035c0037t0011 | 0/0 | 12888 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0036c0068t0001 | 0/0 | 12888 | 1 | 0 | 0 | 0 | 1 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0036c0070t0003 | 0/0 | 12888 | 1 | 0 | 0 | 0 | 1 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0037c0036t0001 | 0/0 | 12888 | 2 | 0 | 0 | 0 | 0 | 2 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0038c0035t0001 | 0/0 | 12888 | 2 | 0 | 0 | 0 | 0 | 2 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0039c0030t0002 | 0/0 | 12887 | 2 | 2 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0040c0040t0003 | 0/0 | 12888 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0040c0040t0007 | 0/0 | 12894 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0041c0041t0005 | 0/0 | 12893 | 2 | 2 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0042c0029t0001 | 0/0 | 12888 | 2 | 0 | 0 | 2 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0043c0094t0002 | 0/0 | 12887 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0044c0093t0001 | 0/0 | 12888 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0045c0099t0002 | 0/0 | 12887 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0046c0098t0005 | 0/0 | 12893 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0047c0105t0001 | 0/0 | 12888 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0048c0107t0004 | 0/0 | 12894 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0049c0103t0003 | 0/0 | 12888 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0050c0104t0003 | 0/0 | 12888 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0051c0100t0002 | 0/0 | 12887 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0052c0102t0002 | 0/0 | 12887 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0053c0101t0001 | 0/0 | 12888 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0054c0108t0001 | 0/0 | 12888 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0055c0113t0001 | 0/0 | 12888 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0056c0112t0001 | 0/0 | 12888 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0057c0111t0002 | 0/0 | 12887 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0058c0092t0003 | 0/0 | 12888 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0059c0075t0001 | 0/0 | 12888 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0060c0051t0001 | 0/0 | 12888 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0061c0053t0001 | 0/0 | 12888 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0062c0072t0002 | 0/0 | 12887 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0063c0064t0002 | 0/0 | 12887 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0064c0063t0003 | 0/0 | 12888 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0065c0060t0003 | 0/0 | 12888 | 1 | 0 | 0 | 0 | 1 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0066c0057t0003 | 0/0 | 12888 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0067c0059t0001 | 0/0 | 12888 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0068c0061t0001 | 0/0 | 12888 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0069c0062t0001 | 0/0 | 12888 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0070c0066t0005 | 0/0 | 12893 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0071c0054t0002 | 0/0 | 12887 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0072c0071t0002 | 0/0 | 12887 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0073c0076t0001 | 0/0 | 12888 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0074c0078t0001 | 0/0 | 12888 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0075c0086t0001 | 0/0 | 12888 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0076c0088t0002 | 0/0 | 12887 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0077c0083t0002 | 0/0 | 12887 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0078c0080t0002 | 0/0 | 12887 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0079c0081t0002 | 0/0 | 12887 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0080c0090t0002 | 0/0 | 12887 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0081c0091t0005 | 0/0 | 12893 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0082c0047t0002 | 0/0 | 12887 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0083c0048t0001 | 0/0 | 12888 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| a0084c0050t0001 | 0/0 | 12888 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | copy fasta | chr5 | 79684836 | 79805222 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0001t0001g0098 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0001t0002g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0001t0010g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0001t0010g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0013t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0013t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0013t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0013t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0013t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0013t0006g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0033t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0033t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0055t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0056t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0001c0058t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0002c0002t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0002c0002t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0002c0002t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0002c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0002c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0002c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0002c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0002c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0002c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0002c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0002c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0002c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0002c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0002c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0002c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0002c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0002c0002t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0002c0002t0002g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0002c0002t0006g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0002c0002t0006g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0002c0020t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0002c0020t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0002c0020t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0002c0020t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0002c0106t0007g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0002c0114t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0003c0003t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0003c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0003c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0003c0003t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0003c0003t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0003c0003t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0003c0003t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0003c0003t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0003c0003t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0003c0003t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0003c0003t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0003c0003t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0003c0003t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0003c0003t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0003c0003t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0003c0003t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0003c0003t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0003c0003t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0003c0003t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0003c0003t0003g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0003c0003t0005g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0003c0003t0005g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0003c0003t0008g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0003c0003t0009g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0003c0003t0013g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0003c0034t0009g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0003c0034t0012g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0003c0069t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0004c0006t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0004c0006t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0004c0006t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0004c0006t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0004c0006t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0004c0006t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0004c0006t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0004c0006t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0004c0006t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0004c0006t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0004c0006t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0004c0006t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0004c0011t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0004c0011t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0004c0011t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0004c0011t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0004c0011t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0004c0011t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0004c0011t0003g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0004c0014t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0004c0014t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0004c0014t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0004c0014t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0004c0014t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0004c0014t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0005c0005t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0005c0005t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0005c0005t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0005c0005t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0005c0005t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0005c0005t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0005c0005t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0005c0005t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0005c0005t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0005c0005t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0005c0005t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0005c0005t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0005c0005t0004g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0005c0077t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0005c0079t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0005c0085t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0005c0089t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0006c0004t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0006c0004t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0006c0004t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0006c0004t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0006c0004t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0006c0004t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0006c0004t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0006c0004t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0006c0004t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0006c0004t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0006c0004t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0006c0004t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0006c0004t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0006c0004t0006g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0007c0008t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0007c0008t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0007c0008t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0007c0008t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0007c0008t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0007c0008t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0007c0008t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0007c0008t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0007c0008t0004g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0007c0008t0011g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0007c0097t0002g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0008c0007t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0008c0007t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0008c0007t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0008c0007t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0008c0007t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0008c0007t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0008c0007t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0008c0007t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0008c0007t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0008c0007t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0008c0067t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0009c0009t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0009c0009t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0009c0009t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0009c0009t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0009c0009t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0009c0009t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0009c0009t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0009c0009t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0009c0009t0014g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0010c0010t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0010c0010t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0010c0010t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0010c0010t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0010c0010t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0010c0010t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0010c0010t0002g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0010c0065t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0011c0012t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0011c0012t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0011c0012t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0011c0012t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0011c0012t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0011c0012t0002g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0011c0052t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0012c0015t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0012c0015t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0012c0015t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0012c0015t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0012c0015t0016g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0012c0074t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0013c0016t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0013c0016t0003g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0013c0016t0004g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0013c0016t0007g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0013c0016t0007g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0014c0027t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0014c0027t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0014c0027t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0014c0045t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0014c0045t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0015c0032t0007g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0015c0032t0007g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0015c0038t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0015c0038t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0015c0073t0015g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0016c0018t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0016c0018t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0016c0018t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0016c0018t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0017c0019t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0017c0019t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0017c0019t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0017c0019t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0018c0017t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0018c0017t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0018c0017t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0018c0017t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0019c0024t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0019c0024t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0019c0024t0017g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0020c0025t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0020c0025t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0020c0025t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0021c0026t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0021c0026t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0021c0026t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0022c0021t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0022c0021t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0022c0021t0006g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0023c0022t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0023c0022t0008g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0023c0022t0008g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0024c0082t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0024c0084t0001g0172 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0024c0087t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0025c0023t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0025c0023t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0025c0023t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0026c0028t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0026c0028t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0026c0049t0006g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0027c0042t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0027c0042t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0028c0043t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0028c0043t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0029c0044t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0029c0044t0012g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0030c0095t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0030c0096t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0031c0046t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0031c0046t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0032c0109t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0032c0110t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0033c0039t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0033c0039t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0034c0031t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0034c0031t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0035c0037t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0035c0037t0011g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0036c0068t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0036c0070t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0037c0036t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0037c0036t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0038c0035t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0038c0035t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0039c0030t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0039c0030t0002g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0040c0040t0003g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0040c0040t0007g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0041c0041t0005g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0042c0029t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0042c0029t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0043c0094t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0044c0093t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0045c0099t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0046c0098t0005g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0047c0105t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0048c0107t0004g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0049c0103t0003g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0050c0104t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0051c0100t0002g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0052c0102t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0053c0101t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0054c0108t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0055c0113t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0056c0112t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0057c0111t0002g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0058c0092t0003g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0059c0075t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0060c0051t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0061c0053t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0062c0072t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0063c0064t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0064c0063t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0065c0060t0003g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0066c0057t0003g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0067c0059t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0068c0061t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0069c0062t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0070c0066t0005g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0071c0054t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0072c0071t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0073c0076t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0074c0078t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0075c0086t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0076c0088t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0077c0083t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0078c0080t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0079c0081t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0080c0090t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0081c0091t0005g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0082c0047t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0083c0048t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| a0084c0050t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0003 | t0002 | g0290 | EUR | GBR | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG00099 | hp2 | a0010 | c0010 | t0002 | g0330 | EUR | GBR | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG00323 | hp1 | a0036 | c0068 | t0001 | g0133 | EUR | FIN | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG00323 | hp2 | a0065 | c0060 | t0003 | g0083 | EUR | FIN | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG00408 | hp1 | a0006 | c0004 | t0001 | g0152 | EAS | CHS | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG00408 | hp2 | a0026 | c0028 | t0002 | g0075 | EAS | CHS | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG00438 | hp1 | a0002 | c0002 | t0002 | g0354 | EAS | CHS | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG00438 | hp2 | a0004 | c0014 | t0002 | g0158 | EAS | CHS | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG00544 | hp1 | a0016 | c0018 | t0001 | g0169 | EAS | CHS | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG00544 | hp2 | a0004 | c0014 | t0002 | g0040 | EAS | CHS | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG00558 | hp1 | a0078 | c0080 | t0002 | g0118 | EAS | CHS | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG00558 | hp2 | a0010 | c0065 | t0002 | g0080 | EAS | CHS | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG00597 | hp1 | a0001 | c0013 | t0002 | g0204 | EAS | CHS | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | CHS | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG00621 | hp1 | a0004 | c0011 | t0003 | g0251 | EAS | CHS | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG00621 | hp2 | a0006 | c0004 | t0006 | g0156 | EAS | CHS | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG00642 | hp1 | a0017 | c0019 | t0001 | g0280 | AMR | PUR | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG00642 | hp2 | a0079 | c0081 | t0002 | g0091 | AMR | PUR | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0332 | EAS | CHS | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG00673 | hp2 | a0008 | c0007 | t0002 | g0114 | EAS | CHS | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0294 | AMR | PUR | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG00741 | hp1 | a0009 | c0009 | t0002 | g0268 | AMR | PUR | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG00741 | hp2 | a0021 | c0026 | t0001 | g0189 | AMR | PUR | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG01069 | hp1 | a0005 | c0005 | t0001 | g0045 | AMR | PUR | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG01074 | hp1 | a0007 | c0008 | t0001 | g0168 | AMR | PUR | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG01074 | hp2 | a0021 | c0026 | t0001 | g0089 | AMR | PUR | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG01081 | hp1 | a0011 | c0012 | t0002 | g0350 | AMR | PUR | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG01081 | hp2 | a0001 | c0013 | t0003 | g0087 | AMR | PUR | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG01099 | hp1 | a0080 | c0090 | t0002 | g0094 | AMR | PUR | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG01099 | hp2 | a0017 | c0019 | t0001 | g0295 | AMR | PUR | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG01106 | hp1 | a0017 | c0019 | t0001 | g0096 | AMR | PUR | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG01109 | hp1 | a0010 | c0010 | t0001 | g0336 | AMR | PUR | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG01109 | hp2 | a0003 | c0069 | t0002 | g0310 | AMR | PUR | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG01167 | hp1 | a0001 | c0001 | t0010 | g0085 | AMR | PUR | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG01167 | hp2 | a0044 | c0093 | t0001 | g0276 | AMR | PUR | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG01169 | hp1 | a0001 | c0001 | t0010 | g0084 | AMR | PUR | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG01169 | hp2 | a0003 | c0003 | t0013 | g0090 | AMR | PUR | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG01175 | hp1 | a0066 | c0057 | t0003 | g0219 | AMR | PUR | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0324 | AMR | PUR | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG01192 | hp1 | a0010 | c0010 | t0002 | g0254 | AMR | PUR | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG01243 | hp1 | a0072 | c0071 | t0002 | g0191 | AMR | PUR | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG01243 | hp2 | a0005 | c0005 | t0001 | g0270 | AMR | PUR | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0338 | AMR | CLM | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG01257 | hp1 | a0011 | c0012 | t0002 | g0273 | AMR | CLM | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG01257 | hp2 | a0005 | c0005 | t0001 | g0216 | AMR | CLM | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG01258 | hp1 | a0005 | c0005 | t0001 | g0217 | AMR | CLM | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0253 | AMR | CLM | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG01361 | hp2 | a0003 | c0003 | t0003 | g0105 | AMR | CLM | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG01433 | hp1 | a0005 | c0005 | t0002 | g0214 | AMR | CLM | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG01433 | hp2 | a0011 | c0012 | t0001 | g0287 | AMR | CLM | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG01496 | hp1 | a0003 | c0003 | t0001 | g0192 | AMR | CLM | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG01496 | hp2 | a0076 | c0088 | t0002 | g0215 | AMR | CLM | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0285 | EUR | IBS | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | IBS | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | PEL | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG01928 | hp2 | a0005 | c0005 | t0001 | g0218 | AMR | PEL | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG01975 | hp1 | a0003 | c0003 | t0002 | g0213 | AMR | PEL | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG01975 | hp2 | a0001 | c0033 | t0002 | g0286 | AMR | PEL | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG01978 | hp1 | a0062 | c0072 | t0002 | g0255 | AMR | PEL | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG01978 | hp2 | a0071 | c0054 | t0002 | g0275 | AMR | PEL | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0222 | AMR | PEL | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG01981 | hp2 | a0011 | c0052 | t0001 | g0284 | AMR | PEL | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG01993 | hp1 | a0011 | c0012 | t0002 | g0248 | AMR | PEL | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG01993 | hp2 | a0005 | c0079 | t0003 | g0082 | AMR | PEL | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02004 | hp1 | a0011 | c0012 | t0001 | g0306 | AMR | PEL | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02004 | hp2 | a0075 | c0086 | t0001 | g0250 | AMR | PEL | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02015 | hp1 | a0001 | c0013 | t0002 | g0041 | EAS | KHV | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02015 | hp2 | a0025 | c0023 | t0001 | g0106 | EAS | KHV | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02027 | hp1 | a0001 | c0013 | t0003 | g0205 | EAS | KHV | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02027 | hp2 | a0005 | c0005 | t0002 | g0004 | EAS | KHV | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02040 | hp1 | a0003 | c0003 | t0001 | g0046 | EAS | KHV | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0129 | EAS | KHV | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02055 | hp1 | a0054 | c0108 | t0001 | g0187 | AFR | ACB | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02055 | hp2 | a0013 | c0016 | t0004 | g0019 | AFR | ACB | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02056 | hp1 | a0053 | c0101 | t0001 | g0202 | EAS | KHV | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02056 | hp2 | a0006 | c0004 | t0001 | g0079 | EAS | KHV | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02074 | hp1 | a0006 | c0004 | t0001 | g0193 | EAS | KHV | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | KHV | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02080 | hp1 | a0005 | c0005 | t0002 | g0170 | EAS | KHV | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02080 | hp2 | a0001 | c0055 | t0001 | g0116 | EAS | KHV | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02132 | hp1 | a0008 | c0007 | t0001 | g0226 | EAS | KHV | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02132 | hp2 | a0006 | c0004 | t0001 | g0122 | EAS | KHV | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02135 | hp2 | a0002 | c0114 | t0001 | g0196 | EAS | KHV | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02145 | hp2 | a0007 | c0008 | t0011 | g0341 | AFR | ACB | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02148 | hp1 | a0074 | c0078 | t0001 | g0289 | AMR | PEL | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02148 | hp2 | a0006 | c0004 | t0002 | g0100 | AMR | PEL | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02165 | hp1 | a0004 | c0014 | t0002 | g0119 | EAS | CDX | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02165 | hp2 | a0008 | c0067 | t0001 | g0305 | EAS | CDX | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0137 | AFR | ACB | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02257 | hp2 | a0039 | c0030 | t0002 | g0314 | AFR | ACB | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02258 | hp1 | a0009 | c0009 | t0001 | g0357 | AFR | ACB | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02258 | hp2 | a0007 | c0008 | t0001 | g0138 | AFR | ACB | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02273 | hp1 | a0060 | c0051 | t0001 | g0298 | AMR | PEL | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02273 | hp2 | a0011 | c0012 | t0001 | g0261 | AMR | PEL | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02280 | hp1 | a0045 | c0099 | t0002 | g0316 | AFR | ACB | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02280 | hp2 | a0003 | c0003 | t0003 | g0081 | AFR | ACB | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02451 | hp1 | a0030 | c0095 | t0003 | g0271 | AFR | ACB | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02451 | hp2 | a0015 | c0032 | t0007 | g0034 | AFR | ACB | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02523 | hp1 | a0064 | c0063 | t0003 | g0200 | EAS | KHV | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02523 | hp2 | a0002 | c0020 | t0001 | g0117 | EAS | KHV | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02572 | hp1 | a0081 | c0091 | t0005 | g0038 | AFR | GWD | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02572 | hp2 | a0007 | c0008 | t0004 | g0032 | AFR | GWD | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02602 | hp1 | a0001 | c0033 | t0001 | g0139 | SAS | PJL | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02615 | hp1 | a0049 | c0103 | t0003 | g0328 | AFR | GWD | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02615 | hp2 | a0013 | c0016 | t0007 | g0315 | AFR | GWD | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02630 | hp1 | a0046 | c0098 | t0005 | g0259 | AFR | GWD | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02630 | hp2 | a0003 | c0003 | t0008 | g0018 | AFR | GWD | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02647 | hp1 | a0003 | c0003 | t0001 | g0188 | AFR | GWD | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02647 | hp2 | a0010 | c0010 | t0001 | g0262 | AFR | GWD | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02683 | hp1 | a0073 | c0076 | t0001 | g0101 | SAS | PJL | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02683 | hp2 | a0007 | c0097 | t0002 | g0347 | SAS | PJL | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0329 | SAS | PJL | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02698 | hp2 | a0069 | c0062 | t0001 | g0088 | SAS | PJL | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02717 | hp1 | a0012 | c0015 | t0016 | g0318 | AFR | GWD | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02717 | hp2 | a0003 | c0003 | t0001 | g0153 | AFR | GWD | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02723 | hp1 | a0007 | c0008 | t0004 | g0030 | AFR | GWD | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02723 | hp2 | a0015 | c0038 | t0002 | g0312 | AFR | GWD | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02735 | hp1 | a0056 | c0112 | t0001 | g0072 | SAS | PJL | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0056 | SAS | PJL | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02809 | hp1 | a0007 | c0008 | t0002 | g0179 | AFR | GWD | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02809 | hp2 | a0019 | c0024 | t0017 | g0355 | AFR | GWD | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02886 | hp1 | a0009 | c0009 | t0001 | g0322 | AFR | GWD | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02886 | hp2 | a0007 | c0008 | t0002 | g0308 | AFR | GWD | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02895 | hp1 | a0041 | c0041 | t0005 | g0001 | AFR | GWD | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02895 | hp2 | a0003 | c0003 | t0005 | g0020 | AFR | GWD | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02896 | hp1 | a0023 | c0022 | t0008 | g0025 | AFR | GWD | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02896 | hp2 | a0003 | c0003 | t0009 | g0313 | AFR | GWD | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02897 | hp1 | a0041 | c0041 | t0005 | g0001 | AFR | GWD | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02897 | hp2 | a0023 | c0022 | t0008 | g0016 | AFR | GWD | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02922 | hp1 | a0012 | c0015 | t0004 | g0022 | AFR | ESN | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02922 | hp2 | a0035 | c0037 | t0011 | g0319 | AFR | ESN | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02965 | hp1 | a0058 | c0092 | t0003 | g0263 | AFR | ESN | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02965 | hp2 | a0007 | c0008 | t0001 | g0311 | AFR | ESN | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02970 | hp1 | a0030 | c0096 | t0001 | g0274 | AFR | ESN | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02970 | hp2 | a0023 | c0022 | t0001 | g0185 | AFR | ESN | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02976 | hp1 | a0003 | c0003 | t0001 | g0178 | AFR | ESN | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02976 | hp2 | a0035 | c0037 | t0001 | g0177 | AFR | ESN | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0335 | SAS | PJL | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG03041 | hp1 | a0009 | c0009 | t0001 | g0323 | AFR | GWD | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG03041 | hp2 | a0019 | c0024 | t0001 | g0181 | AFR | GWD | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG03130 | hp1 | a0040 | c0040 | t0007 | g0031 | AFR | ESN | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG03130 | hp2 | a0003 | c0003 | t0001 | g0015 | AFR | ESN | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG03139 | hp1 | a0015 | c0073 | t0015 | g0343 | AFR | ESN | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG03139 | hp2 | a0028 | c0043 | t0001 | g0267 | AFR | ESN | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG03195 | hp1 | a0015 | c0038 | t0004 | g0260 | AFR | ESN | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG03195 | hp2 | a0020 | c0025 | t0001 | g0344 | AFR | ESN | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG03209 | hp1 | a0050 | c0104 | t0003 | g0272 | AFR | MSL | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG03209 | hp2 | a0019 | c0024 | t0001 | g0184 | AFR | MSL | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG03225 | hp1 | a0043 | c0094 | t0002 | g0011 | AFR | MSL | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG03225 | hp2 | a0029 | c0044 | t0012 | g0036 | AFR | MSL | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG03239 | hp1 | a0005 | c0005 | t0004 | g0017 | SAS | PJL | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG03239 | hp2 | a0037 | c0036 | t0001 | g0103 | SAS | PJL | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG03453 | hp1 | a0027 | c0042 | t0001 | g0134 | AFR | MSL | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG03453 | hp2 | a0009 | c0009 | t0014 | g0266 | AFR | MSL | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG03486 | hp1 | a0028 | c0043 | t0001 | g0183 | AFR | MSL | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG03486 | hp2 | a0003 | c0034 | t0009 | g0320 | AFR | MSL | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG03490 | hp1 | a0005 | c0005 | t0001 | g0220 | SAS | PJL | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG03490 | hp2 | a0001 | c0056 | t0001 | g0086 | SAS | PJL | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG03516 | hp1 | a0012 | c0015 | t0004 | g0028 | AFR | ESN | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG03516 | hp2 | a0031 | c0046 | t0001 | g0186 | AFR | ESN | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG03540 | hp1 | a0003 | c0003 | t0005 | g0035 | AFR | GWD | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG03540 | hp2 | a0027 | c0042 | t0001 | g0342 | AFR | GWD | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG03579 | hp1 | a0013 | c0016 | t0001 | g0180 | AFR | MSL | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG03579 | hp2 | a0003 | c0034 | t0012 | g0021 | AFR | MSL | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG03669 | hp1 | a0010 | c0010 | t0002 | g0245 | SAS | PJL | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG03669 | hp2 | a0059 | c0075 | t0001 | g0327 | SAS | PJL | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG03688 | hp1 | a0005 | c0005 | t0001 | g0337 | SAS | STU | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG03688 | hp2 | a0057 | c0111 | t0002 | g0321 | SAS | STU | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG03704 | hp2 | a0022 | c0021 | t0006 | g0351 | SAS | PJL | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG03710 | hp1 | a0040 | c0040 | t0003 | g0325 | SAS | PJL | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG03710 | hp2 | a0003 | c0003 | t0002 | g0070 | SAS | PJL | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | BEB | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0333 | SAS | BEB | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | BEB | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG03834 | hp2 | a0005 | c0085 | t0001 | g0223 | SAS | BEB | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0076 | SAS | BEB | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG03927 | hp2 | a0037 | c0036 | t0001 | g0326 | SAS | BEB | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG03942 | hp1 | a0010 | c0010 | t0001 | g0291 | SAS | BEB | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG03942 | hp2 | a0038 | c0035 | t0001 | g0093 | SAS | BEB | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG04184 | hp1 | a0002 | c0002 | t0002 | g0054 | SAS | BEB | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0246 | SAS | BEB | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG04199 | hp1 | a0063 | c0064 | t0002 | g0282 | SAS | STU | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG04199 | hp2 | a0004 | c0006 | t0001 | g0078 | SAS | STU | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0173 | SAS | STU | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG04204 | hp2 | a0038 | c0035 | t0001 | g0092 | SAS | STU | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG04228 | hp1 | a0024 | c0082 | t0001 | g0297 | SAS | STU | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG04228 | hp2 | a0061 | c0053 | t0001 | g0155 | SAS | STU | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18522 | hp1 | a0009 | c0009 | t0001 | g0014 | AFR | YRI | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18522 | hp2 | a0020 | c0025 | t0001 | g0278 | AFR | YRI | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18612 | hp1 | a0052 | c0102 | t0002 | g0211 | EAS | CHB | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18612 | hp2 | a0026 | c0028 | t0001 | g0044 | EAS | CHB | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18906 | hp1 | a0020 | c0025 | t0001 | g0309 | AFR | YRI | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18906 | hp2 | a0013 | c0016 | t0007 | g0024 | AFR | YRI | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18939 | hp1 | a0014 | c0027 | t0001 | g0052 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18939 | hp2 | a0002 | c0002 | t0002 | g0130 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18941 | hp1 | a0021 | c0026 | t0002 | g0252 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18941 | hp2 | a0008 | c0007 | t0002 | g0104 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18942 | hp1 | a0006 | c0004 | t0002 | g0199 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18942 | hp2 | a0008 | c0007 | t0002 | g0115 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18943 | hp1 | a0006 | c0004 | t0001 | g0161 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18943 | hp2 | a0004 | c0014 | t0002 | g0195 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18945 | hp1 | a0004 | c0011 | t0001 | g0233 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18945 | hp2 | a0004 | c0006 | t0001 | g0304 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18946 | hp2 | a0003 | c0003 | t0003 | g0352 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18948 | hp1 | a0003 | c0003 | t0001 | g0242 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18948 | hp2 | a0002 | c0002 | t0006 | g0120 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18949 | hp2 | a0002 | c0002 | t0002 | g0229 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18952 | hp1 | a0006 | c0004 | t0001 | g0201 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18952 | hp2 | a0055 | c0113 | t0001 | g0151 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18953 | hp1 | a0083 | c0048 | t0001 | g0057 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18953 | hp2 | a0008 | c0007 | t0002 | g0111 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18954 | hp1 | a0008 | c0007 | t0002 | g0006 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18954 | hp2 | a0032 | c0109 | t0002 | g0231 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18956 | hp1 | a0002 | c0002 | t0002 | g0209 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18956 | hp2 | a0008 | c0007 | t0002 | g0145 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18957 | hp1 | a0022 | c0021 | t0001 | g0300 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18957 | hp2 | a0024 | c0087 | t0001 | g0010 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18960 | hp1 | a0002 | c0002 | t0002 | g0061 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18960 | hp2 | a0008 | c0007 | t0001 | g0009 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18963 | hp1 | a0004 | c0006 | t0002 | g0144 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18963 | hp2 | a0008 | c0007 | t0002 | g0113 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18964 | hp1 | a0001 | c0013 | t0006 | g0140 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18964 | hp2 | a0002 | c0002 | t0002 | g0066 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18965 | hp1 | a0018 | c0017 | t0001 | g0067 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18965 | hp2 | a0004 | c0014 | t0002 | g0244 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18967 | hp2 | a0004 | c0006 | t0002 | g0210 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18968 | hp2 | a0002 | c0002 | t0002 | g0141 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18969 | hp1 | a0002 | c0020 | t0002 | g0293 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18969 | hp2 | a0042 | c0029 | t0001 | g0108 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18970 | hp1 | a0014 | c0027 | t0002 | g0053 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18970 | hp2 | a0003 | c0003 | t0002 | g0149 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0331 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18971 | hp2 | a0003 | c0003 | t0001 | g0232 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18972 | hp1 | a0016 | c0018 | t0002 | g0146 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18972 | hp2 | a0004 | c0006 | t0002 | g0303 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18973 | hp2 | a0006 | c0004 | t0002 | g0123 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18974 | hp1 | a0003 | c0003 | t0002 | g0050 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18974 | hp2 | a0004 | c0006 | t0001 | g0048 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18977 | hp1 | a0004 | c0006 | t0003 | g0236 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18977 | hp2 | a0018 | c0017 | t0002 | g0002 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18979 | hp1 | a0018 | c0017 | t0002 | g0069 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18979 | hp2 | a0033 | c0039 | t0001 | g0279 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18983 | hp1 | a0004 | c0011 | t0003 | g0349 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18983 | hp2 | a0005 | c0005 | t0001 | g0039 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18984 | hp1 | a0068 | c0061 | t0001 | g0005 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18984 | hp2 | a0002 | c0002 | t0002 | g0112 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18988 | hp1 | a0042 | c0029 | t0001 | g0109 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18988 | hp2 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18989 | hp1 | a0004 | c0011 | t0001 | g0277 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18989 | hp2 | a0084 | c0050 | t0001 | g0107 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18990 | hp1 | a0082 | c0047 | t0002 | g0110 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18990 | hp2 | a0047 | c0105 | t0001 | g0042 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18993 | hp1 | a0004 | c0006 | t0002 | g0249 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18993 | hp2 | a0016 | c0018 | t0001 | g0176 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18994 | hp2 | a0004 | c0006 | t0003 | g0258 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18995 | hp1 | a0025 | c0023 | t0002 | g0203 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18997 | hp1 | a0004 | c0006 | t0002 | g0055 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18997 | hp2 | a0005 | c0005 | t0001 | g0353 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18999 | hp1 | a0006 | c0004 | t0001 | g0162 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18999 | hp2 | a0032 | c0110 | t0002 | g0074 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA19000 | hp1 | a0002 | c0002 | t0002 | g0143 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA19000 | hp2 | a0033 | c0039 | t0001 | g0003 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA19002 | hp1 | a0016 | c0018 | t0002 | g0283 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA19002 | hp2 | a0026 | c0049 | t0006 | g0073 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA19003 | hp1 | a0014 | c0045 | t0002 | g0230 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA19003 | hp2 | a0034 | c0031 | t0003 | g0228 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA19006 | hp1 | a0014 | c0027 | t0003 | g0051 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA19006 | hp2 | a0004 | c0011 | t0001 | g0160 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA19009 | hp1 | a0004 | c0011 | t0001 | g0206 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA19009 | hp2 | a0005 | c0089 | t0001 | g0348 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA19010 | hp1 | a0010 | c0010 | t0001 | g0207 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA19010 | hp2 | a0002 | c0002 | t0002 | g0148 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA19030 | hp1 | a0051 | c0100 | t0002 | g0356 | AFR | LWK | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA19030 | hp2 | a0009 | c0009 | t0002 | g0265 | AFR | LWK | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA19043 | hp1 | a0039 | c0030 | t0002 | g0269 | AFR | LWK | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA19043 | hp2 | a0002 | c0106 | t0007 | g0029 | AFR | LWK | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA19056 | hp2 | a0004 | c0006 | t0001 | g0256 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA19057 | hp2 | a0006 | c0004 | t0001 | g0247 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA19058 | hp1 | a0002 | c0020 | t0002 | g0190 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA19058 | hp2 | a0002 | c0002 | t0002 | g0071 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA19064 | hp1 | a0001 | c0058 | t0002 | g0339 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA19064 | hp2 | a0067 | c0059 | t0001 | g0299 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA19065 | hp1 | a0002 | c0002 | t0002 | g0159 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA19065 | hp2 | a0002 | c0020 | t0002 | g0121 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA19066 | hp1 | a0004 | c0006 | t0003 | g0062 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0127 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA19067 | hp1 | a0022 | c0021 | t0002 | g0302 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA19067 | hp2 | a0006 | c0004 | t0001 | g0225 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA19068 | hp1 | a0003 | c0003 | t0002 | g0167 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA19068 | hp2 | a0034 | c0031 | t0003 | g0237 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA19070 | hp1 | a0002 | c0002 | t0006 | g0164 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA19074 | hp1 | a0014 | c0045 | t0002 | g0194 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA19074 | hp2 | a0004 | c0014 | t0002 | g0227 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA19075 | hp1 | a0008 | c0007 | t0001 | g0047 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA19080 | hp1 | a0001 | c0013 | t0001 | g0154 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA19080 | hp2 | a0002 | c0002 | t0001 | g0128 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA19081 | hp1 | a0002 | c0002 | t0002 | g0288 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA19081 | hp2 | a0025 | c0023 | t0001 | g0234 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA19082 | hp1 | a0002 | c0002 | t0002 | g0334 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA19082 | hp2 | a0004 | c0011 | t0002 | g0049 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA19084 | hp1 | a0002 | c0002 | t0002 | g0208 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA19084 | hp2 | a0018 | c0017 | t0002 | g0068 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0131 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA19240 | hp1 | a0007 | c0008 | t0001 | g0340 | AFR | YRI | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA19240 | hp2 | a0015 | c0032 | t0007 | g0027 | AFR | YRI | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA20129 | hp1 | a0003 | c0003 | t0002 | g0058 | AFR | ASW | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA20129 | hp2 | a0009 | c0009 | t0001 | g0346 | AFR | ASW | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA20752 | hp1 | a0036 | c0070 | t0003 | g0060 | EUR | TSI | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA20752 | hp2 | a0003 | c0003 | t0001 | g0099 | EUR | TSI | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0136 | EUR | TSI | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0095 | EUR | TSI | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0292 | SAS | GIH | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA20905 | hp2 | a0006 | c0004 | t0001 | g0059 | SAS | GIH | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02109 | hp2 | a0012 | c0015 | t0004 | g0033 | AFR | ACB | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02486 | hp1 | a0013 | c0016 | t0003 | g0307 | AFR | ACB | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02486 | hp2 | a0048 | c0107 | t0004 | g0317 | AFR | ACB | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02559 | hp1 | a0012 | c0015 | t0004 | g0023 | AFR | ACB | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG02559 | hp2 | a0007 | c0008 | t0002 | g0301 | AFR | ACB | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG03471 | hp1 | a0012 | c0074 | t0001 | g0345 | AFR | MSL | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG03471 | hp2 | a0031 | c0046 | t0002 | g0182 | AFR | MSL | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG06807 | hp1 | a0017 | c0019 | t0001 | g0132 | AFR | USA | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| HG06807 | hp2 | a0005 | c0077 | t0001 | g0221 | AFR | USA | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18955 | hp1 | a0002 | c0002 | t0002 | g0238 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA18955 | hp2 | a0003 | c0003 | t0001 | g0243 | EAS | JPT | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA20300 | hp1 | a0077 | c0083 | t0002 | g0224 | AFR | USA | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA20300 | hp2 | a0009 | c0009 | t0001 | g0264 | AFR | USA | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA21309 | hp1 | a0029 | c0044 | t0004 | g0026 | AFR | LWK | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| NA21309 | hp2 | a0070 | c0066 | t0005 | g0037 | AFR | LWK | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| homoSapiens_chm13v2 | hp1 | a0024 | c0084 | t0001 | g0172 | REF | REF | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0098 | REF | REF | CMYA5_chr5_79684836_79805222 | CMYA5 | chr5 | 79684836 | 79805222 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:79690010
|
G | A | 5 | a0026a0042a0082others(2): Show | 8 | HG00408.hp2 NA18612.hp2 NA18953.hp1 others(5): Show |
missense_variant | MODERATE | c.103G>A | p.Glu35Lys | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/13 | 175/12888 | 103/12210 | 35/4069 | chr5 | 79690010 | ||
| chr5:79728956
|
A | G | 32 | a0002a0004a0007others(29): Show | 131 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(128): Show |
missense_variant | MODERATE | c.191A>G | p.Tyr64Cys | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 263/12888 | 191/12210 | 64/4069 | chr5 | 79728956 | ||
| chr5:79729093
|
G | A | 1 | a0058 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.328G>A | p.Glu110Lys | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 400/12888 | 328/12210 | 110/4069 | chr5 | 79729093 | ||
| chr5:79729174
|
A | C | 1 | a0041 | 2 | HG02895.hp1 HG02897.hp1 |
missense_variant | MODERATE | c.409A>C | p.Lys137Gln | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 481/12888 | 409/12210 | 137/4069 | chr5 | 79729174 | ||
| chr5:79729205
|
G | A | 6 | a0013a0019a0027others(3): Show | 14 | HG01167.hp2 HG02055.hp2 HG02486.hp1 others(11): Show |
missense_variant | MODERATE | c.440G>A | p.Arg147Gln | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 512/12888 | 440/12210 | 147/4069 | chr5 | 79729205 | ||
| chr5:79729223
|
G | T | 1 | a0045 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.458G>T | p.Arg153Ile | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 530/12888 | 458/12210 | 153/4069 | chr5 | 79729223 | ||
| chr5:79729232
|
T | C | 1 | a0018 | 4 | NA18965.hp1 NA18977.hp2 NA18979.hp1 others(1): Show |
missense_variant | MODERATE | c.467T>C | p.Phe156Ser | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 539/12888 | 467/12210 | 156/4069 | chr5 | 79729232 | ||
| chr5:79729262
|
A | G | 6 | a0004a0032a0042others(3): Show | 32 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(29): Show |
missense_variant | MODERATE | c.497A>G | p.Lys166Arg | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 569/12888 | 497/12210 | 166/4069 | chr5 | 79729262 | ||
| chr5:79729290
|
G | T | 2 | a0045a0046 | 2 | HG02280.hp1 HG02630.hp1 |
missense_variant | MODERATE | c.525G>T | p.Gln175His | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 597/12888 | 525/12210 | 175/4069 | chr5 | 79729290 | ||
| chr5:79729334
|
A | G | 15 | a0005a0006a0023others(12): Show | 51 | HG00408.hp1 HG00558.hp1 HG00621.hp2 others(48): Show |
missense_variant | MODERATE | c.569A>G | p.Asp190Gly | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 641/12888 | 569/12210 | 190/4069 | chr5 | 79729334 | ||
| chr5:79729811
|
G | A | 29 | a0002a0004a0007others(26): Show | 119 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(116): Show |
missense_variant | MODERATE | c.1046G>A | p.Gly349Asp | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 1118/12888 | 1046/12210 | 349/4069 | chr5 | 79729811 | ||
| chr5:79729864
|
C | T | 1 | a0073 | 1 | HG02683.hp1 | missense_variant | MODERATE | c.1099C>T | p.Pro367Ser | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 1171/12888 | 1099/12210 | 367/4069 | chr5 | 79729864 | ||
| chr5:79730176
|
G | A | 1 | a0039 | 2 | HG02257.hp2 NA19043.hp1 |
missense_variant | MODERATE | c.1411G>A | p.Ala471Thr | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 1483/12888 | 1411/12210 | 471/4069 | chr5 | 79730176 | ||
| chr5:79730449
|
C | T | 1 | a0059 | 1 | HG03669.hp2 | missense_variant | MODERATE | c.1684C>T | p.Leu562Phe | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 1756/12888 | 1684/12210 | 562/4069 | chr5 | 79730449 | ||
| chr5:79730497
|
T | C | 1 | a0060 | 1 | HG02273.hp1 | missense_variant | MODERATE | c.1732T>C | p.Ser578Pro | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 1804/12888 | 1732/12210 | 578/4069 | chr5 | 79730497 | ||
| chr5:79730537
|
G | A | 30 | a0002a0004a0007others(27): Show | 128 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(125): Show |
missense_variant | MODERATE | c.1772G>A | p.Gly591Asp | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 1844/12888 | 1772/12210 | 591/4069 | chr5 | 79730537 | ||
| chr5:79730547
|
T | G | 6 | a0004a0032a0042others(3): Show | 32 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(29): Show |
missense_variant | MODERATE | c.1782T>G | p.Phe594Leu | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 1854/12888 | 1782/12210 | 594/4069 | chr5 | 79730547 | ||
| chr5:79730611
|
G | A | 2 | a0011a0060 | 8 | HG01081.hp1 HG01257.hp1 HG01433.hp2 others(5): Show |
missense_variant | MODERATE | c.1846G>A | p.Val616Ile | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 1918/12888 | 1846/12210 | 616/4069 | chr5 | 79730611 | ||
| chr5:79730716
|
A | C | 30 | a0002a0004a0007others(27): Show | 128 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(125): Show |
missense_variant | MODERATE | c.1951A>C | p.Ser651Arg | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 2023/12888 | 1951/12210 | 651/4069 | chr5 | 79730716 | ||
| chr5:79730963
|
C | A | 1 | a0061 | 1 | HG04228.hp2 | stop_gained | HIGH | c.2198C>A | p.Ser733* | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 2270/12888 | 2198/12210 | 733/4069 | chr5 | 79730963 | ||
| chr5:79731043
|
G | A | 1 | a0032 | 2 | NA18954.hp2 NA18999.hp2 |
missense_variant | MODERATE | c.2278G>A | p.Glu760Lys | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 2350/12888 | 2278/12210 | 760/4069 | chr5 | 79731043 | ||
| chr5:79731133
|
C | T | 1 | a0033 | 2 | NA18979.hp2 NA19000.hp2 |
missense_variant | MODERATE | c.2368C>T | p.Arg790Cys | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 2440/12888 | 2368/12210 | 790/4069 | chr5 | 79731133 | ||
| chr5:79731638
|
C | T | 1 | a0047 | 1 | NA18990.hp2 | missense_variant | MODERATE | c.2873C>T | p.Pro958Leu | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 2945/12888 | 2873/12210 | 958/4069 | chr5 | 79731638 | ||
| chr5:79731641
|
C | T | 1 | a0048 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.2876C>T | p.Pro959Leu | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 2948/12888 | 2876/12210 | 959/4069 | chr5 | 79731641 | ||
| chr5:79731782
|
T | C | 31 | a0002a0004a0007others(28): Show | 130 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(127): Show |
missense_variant | MODERATE | c.3017T>C | p.Val1006Ala | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 3089/12888 | 3017/12210 | 1006/4069 | chr5 | 79731782 | ||
| chr5:79731797
|
T | C | 1 | a0059 | 1 | HG03669.hp2 | missense_variant | MODERATE | c.3032T>C | p.Phe1011Ser | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 3104/12888 | 3032/12210 | 1011/4069 | chr5 | 79731797 | ||
| chr5:79731877
|
T | C | 15 | a0002a0004a0014others(12): Show | 84 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(81): Show |
missense_variant | MODERATE | c.3112T>C | p.Phe1038Leu | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 3184/12888 | 3112/12210 | 1038/4069 | chr5 | 79731877 | ||
| chr5:79731911
|
C | T | 1 | a0062 | 1 | HG01978.hp1 | missense_variant | MODERATE | c.3146C>T | p.Thr1049Ile | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 3218/12888 | 3146/12210 | 1049/4069 | chr5 | 79731911 | ||
| chr5:79732007
|
C | T | 1 | a0014 | 5 | NA18939.hp1 NA18970.hp1 NA19003.hp1 others(2): Show |
missense_variant | MODERATE | c.3242C>T | p.Pro1081Leu | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 3314/12888 | 3242/12210 | 1081/4069 | chr5 | 79732007 | ||
| chr5:79732649
|
C | T | 53 | a0002a0003a0004others(50): Show | 228 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(225): Show |
missense_variant | MODERATE | c.3884C>T | p.Ala1295Val | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 3956/12888 | 3884/12210 | 1295/4069 | chr5 | 79732649 | ||
| chr5:79732690
|
A | G | 18 | a0002a0004a0009others(15): Show | 95 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(92): Show |
missense_variant | MODERATE | c.3925A>G | p.Ile1309Val | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 3997/12888 | 3925/12210 | 1309/4069 | chr5 | 79732690 | ||
| chr5:79732763
|
C | T | 18 | a0002a0004a0009others(15): Show | 95 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(92): Show |
missense_variant | MODERATE | c.3998C>T | p.Ala1333Val | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 4070/12888 | 3998/12210 | 1333/4069 | chr5 | 79732763 | ||
| chr5:79732903
|
A | G | 8 | a0003a0035a0036others(5): Show | 40 | HG00099.hp1 HG00323.hp1 HG01099.hp1 others(37): Show |
missense_variant | MODERATE | c.4138A>G | p.Ile1380Val | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 4210/12888 | 4138/12210 | 1380/4069 | chr5 | 79732903 | ||
| chr5:79733075
|
C | A | 1 | a0073 | 1 | HG02683.hp1 | stop_gained | HIGH | c.4310C>A | p.Ser1437* | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 4382/12888 | 4310/12210 | 1437/4069 | chr5 | 79733075 | ||
| chr5:79733252
|
A | G | 1 | a0050 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.4487A>G | p.Asp1496Gly | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 4559/12888 | 4487/12210 | 1496/4069 | chr5 | 79733252 | ||
| chr5:79733341
|
G | A | 1 | a0071 | 1 | HG01978.hp2 | missense_variant | MODERATE | c.4576G>A | p.Glu1526Lys | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 4648/12888 | 4576/12210 | 1526/4069 | chr5 | 79733341 | ||
| chr5:79733465
|
C | A | 32 | a0002a0004a0007others(29): Show | 131 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(128): Show |
missense_variant | MODERATE | c.4700C>A | p.Ala1567Glu | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 4772/12888 | 4700/12210 | 1567/4069 | chr5 | 79733465 | ||
| chr5:79733488
|
A | T | 4 | a0009a0030a0058others(1): Show | 13 | HG00741.hp1 HG02258.hp1 HG02451.hp1 others(10): Show |
missense_variant | MODERATE | c.4723A>T | p.Asn1575Tyr | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 4795/12888 | 4723/12210 | 1575/4069 | chr5 | 79733488 | ||
| chr5:79733533
|
G | A | 1 | a0053 | 1 | HG02056.hp1 | missense_variant | MODERATE | c.4768G>A | p.Asp1590Asn | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 4840/12888 | 4768/12210 | 1590/4069 | chr5 | 79733533 | ||
| chr5:79733560
|
T | G | 32 | a0002a0004a0007others(29): Show | 131 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(128): Show |
missense_variant | MODERATE | c.4795T>G | p.Ser1599Ala | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 4867/12888 | 4795/12210 | 1599/4069 | chr5 | 79733560 | ||
| chr5:79733771
|
T | C | 7 | a0003a0035a0036others(4): Show | 39 | HG00099.hp1 HG00323.hp1 HG01109.hp2 others(36): Show |
missense_variant | MODERATE | c.5006T>C | p.Leu1669Ser | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 5078/12888 | 5006/12210 | 1669/4069 | chr5 | 79733771 | ||
| chr5:79733789
|
A | T | 1 | a0070 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.5024A>T | p.Glu1675Val | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 5096/12888 | 5024/12210 | 1675/4069 | chr5 | 79733789 | ||
| chr5:79733852
|
C | G | 1 | a0048 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.5087C>G | p.Ala1696Gly | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 5159/12888 | 5087/12210 | 1696/4069 | chr5 | 79733852 | ||
| chr5:79733903
|
T | A | 19 | a0002a0004a0009others(16): Show | 96 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(93): Show |
missense_variant | MODERATE | c.5138T>A | p.Ile1713Asn | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 5210/12888 | 5138/12210 | 1713/4069 | chr5 | 79733903 | ||
| chr5:79733926
|
A | G | 32 | a0002a0004a0007others(29): Show | 131 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(128): Show |
missense_variant | MODERATE | c.5161A>G | p.Ile1721Val | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 5233/12888 | 5161/12210 | 1721/4069 | chr5 | 79733926 | ||
| chr5:79734389
|
C | T | 12 | a0002a0004a0014others(9): Show | 80 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(77): Show |
missense_variant | MODERATE | c.5624C>T | p.Ala1875Val | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 5696/12888 | 5624/12210 | 1875/4069 | chr5 | 79734389 | ||
| chr5:79734515
|
A | G | 12 | a0002a0004a0014others(9): Show | 80 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(77): Show |
missense_variant | MODERATE | c.5750A>G | p.Asp1917Gly | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 5822/12888 | 5750/12210 | 1917/4069 | chr5 | 79734515 | ||
| chr5:79734523
|
A | G | 31 | a0002a0004a0007others(28): Show | 130 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(127): Show |
missense_variant | MODERATE | c.5758A>G | p.Ser1920Gly | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 5830/12888 | 5758/12210 | 1920/4069 | chr5 | 79734523 | ||
| chr5:79734647
|
C | T | 2 | a0019a0028 | 5 | HG02809.hp2 HG03041.hp2 HG03139.hp2 others(2): Show |
missense_variant | MODERATE | c.5882C>T | p.Ala1961Val | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 5954/12888 | 5882/12210 | 1961/4069 | chr5 | 79734647 | ||
| chr5:79734815
|
A | G | 1 | a0012 | 6 | HG02109.hp2 HG02559.hp1 HG02717.hp1 others(3): Show |
missense_variant | MODERATE | c.6050A>G | p.Glu2017Gly | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 6122/12888 | 6050/12210 | 2017/4069 | chr5 | 79734815 | ||
| chr5:79735103
|
T | C | 1 | a0013 | 5 | HG02055.hp2 HG02486.hp1 HG02615.hp2 others(2): Show |
missense_variant | MODERATE | c.6338T>C | p.Ile2113Thr | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 6410/12888 | 6338/12210 | 2113/4069 | chr5 | 79735103 | ||
| chr5:79735216
|
G | T | 1 | a0063 | 1 | HG04199.hp1 | missense_variant | MODERATE | c.6451G>T | p.Val2151Leu | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 6523/12888 | 6451/12210 | 2151/4069 | chr5 | 79735216 | ||
| chr5:79735222
|
C | G | 1 | a0064 | 1 | HG02523.hp1 | missense_variant | MODERATE | c.6457C>G | p.Gln2153Glu | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 6529/12888 | 6457/12210 | 2153/4069 | chr5 | 79735222 | ||
| chr5:79735256
|
C | T | 1 | a0044 | 1 | HG01167.hp2 | missense_variant | MODERATE | c.6491C>T | p.Pro2164Leu | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 6563/12888 | 6491/12210 | 2164/4069 | chr5 | 79735256 | ||
| chr5:79735284
|
A | C | 1 | a0069 | 1 | HG02698.hp2 | missense_variant | MODERATE | c.6519A>C | p.Lys2173Asn | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 6591/12888 | 6519/12210 | 2173/4069 | chr5 | 79735284 | ||
| chr5:79735549
|
G | C | 30 | a0002a0004a0007others(27): Show | 128 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(125): Show |
missense_variant | MODERATE | c.6784G>C | p.Val2262Leu | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 6856/12888 | 6784/12210 | 2262/4069 | chr5 | 79735549 | ||
| chr5:79735723
|
T | C | 3 | a0016a0034a0082 | 7 | HG00544.hp1 NA18972.hp1 NA18990.hp1 others(4): Show |
missense_variant | MODERATE | c.6958T>C | p.Tyr2320His | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 7030/12888 | 6958/12210 | 2320/4069 | chr5 | 79735723 | ||
| chr5:79735735
|
G | A | 12 | a0005a0006a0008others(9): Show | 56 | HG00408.hp1 HG00558.hp1 HG00621.hp2 others(53): Show |
missense_variant | MODERATE | c.6970G>A | p.Gly2324Ser | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 7042/12888 | 6970/12210 | 2324/4069 | chr5 | 79735735 | ||
| chr5:79735756
|
G | A | 1 | a0058 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.6991G>A | p.Glu2331Lys | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 7063/12888 | 6991/12210 | 2331/4069 | chr5 | 79735756 | ||
| chr5:79735888
|
C | T | 1 | a0058 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.7123C>T | p.Leu2375Phe | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 7195/12888 | 7123/12210 | 2375/4069 | chr5 | 79735888 | ||
| chr5:79735909
|
G | T | 2 | a0022a0064 | 4 | HG02523.hp1 HG03704.hp2 NA18957.hp1 others(1): Show |
missense_variant | MODERATE | c.7144G>T | p.Asp2382Tyr | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 7216/12888 | 7144/12210 | 2382/4069 | chr5 | 79735909 | ||
| chr5:79735912
|
A | G | 1 | a0012 | 6 | HG02109.hp2 HG02559.hp1 HG02717.hp1 others(3): Show |
missense_variant | MODERATE | c.7147A>G | p.Lys2383Glu | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 7219/12888 | 7147/12210 | 2383/4069 | chr5 | 79735912 | ||
| chr5:79736237
|
T | C | 1 | a0057 | 1 | HG03688.hp2 | missense_variant | MODERATE | c.7472T>C | p.Ile2491Thr | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 7544/12888 | 7472/12210 | 2491/4069 | chr5 | 79736237 | ||
| chr5:79736244
|
G | T | 2 | a0031a0054 | 3 | HG02055.hp1 HG03471.hp2 HG03516.hp2 |
missense_variant | MODERATE | c.7479G>T | p.Lys2493Asn | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 7551/12888 | 7479/12210 | 2493/4069 | chr5 | 79736244 | ||
| chr5:79736303
|
T | C | 1 | a0050 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.7538T>C | p.Met2513Thr | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 7610/12888 | 7538/12210 | 2513/4069 | chr5 | 79736303 | ||
| chr5:79736567
|
T | C | 1 | a0012 | 6 | HG02109.hp2 HG02559.hp1 HG02717.hp1 others(3): Show |
missense_variant | MODERATE | c.7802T>C | p.Met2601Thr | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 7874/12888 | 7802/12210 | 2601/4069 | chr5 | 79736567 | ||
| chr5:79736818
|
G | T | 2 | a0015a0039 | 7 | HG02257.hp2 HG02451.hp2 HG02723.hp2 others(4): Show |
missense_variant | MODERATE | c.8053G>T | p.Gly2685Cys | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 8125/12888 | 8053/12210 | 2685/4069 | chr5 | 79736818 | ||
| chr5:79736843
|
C | T | 19 | a0002a0004a0009others(16): Show | 96 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(93): Show |
missense_variant | MODERATE | c.8078C>T | p.Thr2693Ile | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 8150/12888 | 8078/12210 | 2693/4069 | chr5 | 79736843 | ||
| chr5:79736888
|
G | A | 18 | a0002a0004a0009others(15): Show | 95 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(92): Show |
missense_variant | MODERATE | c.8123G>A | p.Arg2708His | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 8195/12888 | 8123/12210 | 2708/4069 | chr5 | 79736888 | ||
| chr5:79737109
|
A | T | 1 | a0035 | 2 | HG02922.hp2 HG02976.hp2 |
missense_variant | MODERATE | c.8344A>T | p.Met2782Leu | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 8416/12888 | 8344/12210 | 2782/4069 | chr5 | 79737109 | ||
| chr5:79737155
|
G | A | 7 | a0009a0029a0030others(4): Show | 17 | HG00741.hp1 HG02258.hp1 HG02451.hp1 others(14): Show |
missense_variant | MODERATE | c.8390G>A | p.Arg2797His | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 8462/12888 | 8390/12210 | 2797/4069 | chr5 | 79737155 | ||
| chr5:79737299
|
G | A | 1 | a0057 | 1 | HG03688.hp2 | missense_variant | MODERATE | c.8534G>A | p.Arg2845Lys | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 8606/12888 | 8534/12210 | 2845/4069 | chr5 | 79737299 | ||
| chr5:79737483
|
A | C | 29 | a0002a0004a0007others(26): Show | 125 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(122): Show |
missense_variant | MODERATE | c.8718A>C | p.Lys2906Asn | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 8790/12888 | 8718/12210 | 2906/4069 | chr5 | 79737483 | ||
| chr5:79737568
|
G | A | 6 | a0006a0025a0040others(3): Show | 22 | HG00408.hp1 HG00558.hp1 HG00621.hp2 others(19): Show |
missense_variant | MODERATE | c.8803G>A | p.Gly2935Arg | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 8875/12888 | 8803/12210 | 2935/4069 | chr5 | 79737568 | ||
| chr5:79737637
|
G | T | 1 | a0068 | 1 | NA18984.hp1 | missense_variant | MODERATE | c.8872G>T | p.Ala2958Ser | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 8944/12888 | 8872/12210 | 2958/4069 | chr5 | 79737637 | ||
| chr5:79738204
|
G | T | 1 | a0035 | 2 | HG02922.hp2 HG02976.hp2 |
missense_variant | MODERATE | c.9439G>T | p.Asp3147Tyr | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 9511/12888 | 9439/12210 | 3147/4069 | chr5 | 79738204 | ||
| chr5:79738517
|
C | T | 1 | a0063 | 1 | HG04199.hp1 | missense_variant | MODERATE | c.9752C>T | p.Thr3251Ile | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 9824/12888 | 9752/12210 | 3251/4069 | chr5 | 79738517 | ||
| chr5:79738564
|
G | C | 1 | a0051 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.9799G>C | p.Val3267Leu | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 9871/12888 | 9799/12210 | 3267/4069 | chr5 | 79738564 | ||
| chr5:79738817
|
G | A | 1 | a0052 | 1 | NA18612.hp1 | missense_variant | MODERATE | c.10052G>A | p.Arg3351His | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 10124/12888 | 10052/12210 | 3351/4069 | chr5 | 79738817 | ||
| chr5:79738839
|
C | G | 18 | a0002a0004a0009others(15): Show | 95 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(92): Show |
missense_variant | MODERATE | c.10074C>G | p.His3358Gln | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 10146/12888 | 10074/12210 | 3358/4069 | chr5 | 79738839 | ||
| chr5:79738873
|
A | G | 1 | a0031 | 2 | HG03471.hp2 HG03516.hp2 |
missense_variant | MODERATE | c.10108A>G | p.Asn3370Asp | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 10180/12888 | 10108/12210 | 3370/4069 | chr5 | 79738873 | ||
| chr5:79738904
|
C | T | 1 | a0065 | 1 | HG00323.hp2 | missense_variant | MODERATE | c.10139C>T | p.Pro3380Leu | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 10211/12888 | 10139/12210 | 3380/4069 | chr5 | 79738904 | ||
| chr5:79738925
|
G | T | 1 | a0067 | 1 | NA19064.hp2 | missense_variant | MODERATE | c.10160G>T | p.Gly3387Val | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 10232/12888 | 10160/12210 | 3387/4069 | chr5 | 79738925 | ||
| chr5:79739002
|
C | T | 1 | a0025 | 3 | HG02015.hp2 NA18995.hp1 NA19081.hp2 |
missense_variant | MODERATE | c.10237C>T | p.Arg3413Cys | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 10309/12888 | 10237/12210 | 3413/4069 | chr5 | 79739002 | ||
| chr5:79739321
|
C | A | 2 | a0031a0054 | 3 | HG02055.hp1 HG03471.hp2 HG03516.hp2 |
missense_variant | MODERATE | c.10556C>A | p.Pro3519Gln | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 10628/12888 | 10556/12210 | 3519/4069 | chr5 | 79739321 | ||
| chr5:79745234
|
A | G | 7 | a0005a0024a0045others(4): Show | 25 | HG01069.hp1 HG01243.hp2 HG01257.hp2 others(22): Show |
missense_variant | MODERATE | c.10747A>G | p.Lys3583Glu | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 4/13 | 10819/12888 | 10747/12210 | 3583/4069 | chr5 | 79745234 | ||
| chr5:79745274
|
T | G | 1 | a0077 | 1 | NA20300.hp1 | missense_variant | MODERATE | c.10787T>G | p.Met3596Arg | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 4/13 | 10859/12888 | 10787/12210 | 3596/4069 | chr5 | 79745274 | ||
| chr5:79745418
|
G | A | 1 | a0072 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.10931G>A | p.Arg3644Lys | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 4/13 | 11003/12888 | 10931/12210 | 3644/4069 | chr5 | 79745418 | ||
| chr5:79752776
|
A | G | 1 | a0034 | 2 | NA19003.hp2 NA19068.hp2 |
missense_variant | MODERATE | c.11092A>G | p.Met3698Val | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/13 | 11164/12888 | 11092/12210 | 3698/4069 | chr5 | 79752776 | ||
| chr5:79758776
|
C | T | 1 | a0079 | 1 | HG00642.hp2 | missense_variant | MODERATE | c.11134C>T | p.Pro3712Ser | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 7/13 | 11206/12888 | 11134/12210 | 3712/4069 | chr5 | 79758776 | ||
| chr5:79763131
|
G | A | 4 | a0019a0020a0029others(1): Show | 9 | HG02630.hp1 HG02809.hp2 HG03041.hp2 others(6): Show |
missense_variant | MODERATE | c.11477G>A | p.Arg3826Gln | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/13 | 11549/12888 | 11477/12210 | 3826/4069 | chr5 | 79763131 | ||
| chr5:79788997
|
A | G | 1 | a0076 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.11582A>G | p.Gln3861Arg | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 10/13 | 11654/12888 | 11582/12210 | 3861/4069 | chr5 | 79788997 | ||
| chr5:79791029
|
G | C | 1 | a0038 | 2 | HG03942.hp2 HG04204.hp2 |
missense_variant | MODERATE | c.11749G>C | p.Gly3917Arg | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 11/13 | 11821/12888 | 11749/12210 | 3917/4069 | chr5 | 79791029 | ||
| chr5:79791060
|
G | A | 11 | a0010a0013a0021others(8): Show | 28 | HG00099.hp2 HG00323.hp1 HG00558.hp2 others(25): Show |
missense_variant | MODERATE | c.11780G>A | p.Arg3927Gln | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 11/13 | 11852/12888 | 11780/12210 | 3927/4069 | chr5 | 79791060 | ||
| chr5:79793516
|
T | C | 1 | a0078 | 1 | HG00558.hp1 | missense_variant | MODERATE | c.11869T>C | p.Tyr3957His | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/13 | 11941/12888 | 11869/12210 | 3957/4069 | chr5 | 79793516 | ||
| chr5:79799476
|
A | G | 1 | a0066 | 1 | HG01175.hp1 | missense_variant | MODERATE | c.12070A>G | p.Asn4024Asp | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 13/13 | 12142/12888 | 12070/12210 | 4024/4069 | chr5 | 79799476 | ||
| chr5:79799594
|
C | T | 5 | a0017a0037a0056others(2): Show | 9 | HG00642.hp1 HG01099.hp2 HG01106.hp1 others(6): Show |
missense_variant | MODERATE | c.12188C>T | p.Pro4063Leu | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 13/13 | 12260/12888 | 12188/12210 | 4063/4069 | chr5 | 79799594 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:79729092
|
G | C | 16 | a0007c0008a0007c0097a0009c0009others(13): Show | 44 | HG00741.hp1 HG01074.hp1 HG01167.hp2 others(41): Show |
synonymous_variant | LOW | c.327G>C | p.Arg109Arg | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 399/12888 | 327/12210 | 109/4069 | chr5 | 79729092 | ||
| chr5:79729218
|
A | G | 1 | a0002c0114 | 1 | HG02135.hp2 | synonymous_variant | LOW | c.453A>G | p.Arg151Arg | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 525/12888 | 453/12210 | 151/4069 | chr5 | 79729218 | ||
| chr5:79729467
|
G | A | 1 | a0005c0077 | 1 | HG06807.hp2 | synonymous_variant | LOW | c.702G>A | p.Ser234Ser | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 774/12888 | 702/12210 | 234/4069 | chr5 | 79729467 | ||
| chr5:79729494
|
A | G | 41 | a0002c0002a0002c0020a0002c0106others(38): Show | 131 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(128): Show |
synonymous_variant | LOW | c.729A>G | p.Gln243Gln | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 801/12888 | 729/12210 | 243/4069 | chr5 | 79729494 | ||
| chr5:79729680
|
C | T | 1 | a0007c0097 | 1 | HG02683.hp2 | synonymous_variant | LOW | c.915C>T | p.Gly305Gly | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 987/12888 | 915/12210 | 305/4069 | chr5 | 79729680 | ||
| chr5:79729866
|
A | G | 1 | a0048c0107 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.1101A>G | p.Pro367Pro | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 1173/12888 | 1101/12210 | 367/4069 | chr5 | 79729866 | ||
| chr5:79729977
|
A | G | 1 | a0048c0107 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.1212A>G | p.Gly404Gly | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 1284/12888 | 1212/12210 | 404/4069 | chr5 | 79729977 | ||
| chr5:79730394
|
C | T | 1 | a0002c0106 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.1629C>T | p.Ser543Ser | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 1701/12888 | 1629/12210 | 543/4069 | chr5 | 79730394 | ||
| chr5:79730767
|
C | T | 1 | a0012c0074 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.2002C>T | p.Leu668Leu | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 2074/12888 | 2002/12210 | 668/4069 | chr5 | 79730767 | ||
| chr5:79730952
|
C | T | 1 | a0030c0096 | 1 | HG02970.hp1 | synonymous_variant | LOW | c.2187C>T | p.Tyr729Tyr | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 2259/12888 | 2187/12210 | 729/4069 | chr5 | 79730952 | ||
| chr5:79731273
|
C | T | 3 | a0015c0038a0015c0073a0039c0030 | 5 | HG02257.hp2 HG02723.hp2 HG03139.hp1 others(2): Show |
synonymous_variant | LOW | c.2508C>T | p.Asp836Asp | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 2580/12888 | 2508/12210 | 836/4069 | chr5 | 79731273 | ||
| chr5:79731987
|
G | A | 1 | a0014c0045 | 2 | NA19003.hp1 NA19074.hp1 |
synonymous_variant | LOW | c.3222G>A | p.Pro1074Pro | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 3294/12888 | 3222/12210 | 1074/4069 | chr5 | 79731987 | ||
| chr5:79732641
|
A | G | 1 | a0030c0096 | 1 | HG02970.hp1 | synonymous_variant | LOW | c.3876A>G | p.Gly1292Gly | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 3948/12888 | 3876/12210 | 1292/4069 | chr5 | 79732641 | ||
| chr5:79733364
|
A | G | 1 | a0029c0044 | 2 | HG03225.hp2 NA21309.hp1 |
synonymous_variant | LOW | c.4599A>G | p.Leu1533Leu | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 4671/12888 | 4599/12210 | 1533/4069 | chr5 | 79733364 | ||
| chr5:79733844
|
G | A | 1 | a0005c0079 | 1 | HG01993.hp2 | synonymous_variant | LOW | c.5079G>A | p.Thr1693Thr | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 5151/12888 | 5079/12210 | 1693/4069 | chr5 | 79733844 | ||
| chr5:79734222
|
A | G | 79 | a0001c0033a0002c0002a0002c0020others(76): Show | 241 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(238): Show |
synonymous_variant | LOW | c.5457A>G | p.Val1819Val | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 5529/12888 | 5457/12210 | 1819/4069 | chr5 | 79734222 | ||
| chr5:79734936
|
G | A | 2 | a0015c0032a0043c0094 | 3 | HG02451.hp2 HG03225.hp1 NA19240.hp2 |
synonymous_variant | LOW | c.6171G>A | p.Val2057Val | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 6243/12888 | 6171/12210 | 2057/4069 | chr5 | 79734936 | ||
| chr5:79734951
|
A | G | 1 | a0072c0071 | 1 | HG01243.hp1 | synonymous_variant | LOW | c.6186A>G | p.Ser2062Ser | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 6258/12888 | 6186/12210 | 2062/4069 | chr5 | 79734951 | ||
| chr5:79735167
|
C | G | 1 | a0010c0065 | 1 | HG00558.hp2 | synonymous_variant | LOW | c.6402C>G | p.Pro2134Pro | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 6474/12888 | 6402/12210 | 2134/4069 | chr5 | 79735167 | ||
| chr5:79735257
|
G | A | 2 | a0011c0052a0060c0051 | 2 | HG01981.hp2 HG02273.hp1 |
synonymous_variant | LOW | c.6492G>A | p.Pro2164Pro | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 6564/12888 | 6492/12210 | 2164/4069 | chr5 | 79735257 | ||
| chr5:79735593
|
A | G | 1 | a0036c0070 | 1 | NA20752.hp1 | synonymous_variant | LOW | c.6828A>G | p.Gln2276Gln | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 6900/12888 | 6828/12210 | 2276/4069 | chr5 | 79735593 | ||
| chr5:79736616
|
C | T | 5 | a0009c0009a0030c0095a0030c0096others(2): Show | 13 | HG00741.hp1 HG02258.hp1 HG02451.hp1 others(10): Show |
synonymous_variant | LOW | c.7851C>T | p.Thr2617Thr | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 7923/12888 | 7851/12210 | 2617/4069 | chr5 | 79736616 | ||
| chr5:79737072
|
A | G | 1 | a0048c0107 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.8307A>G | p.Leu2769Leu | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 8379/12888 | 8307/12210 | 2769/4069 | chr5 | 79737072 | ||
| chr5:79737189
|
G | A | 2 | a0049c0103a0050c0104 | 2 | HG02615.hp1 HG03209.hp1 |
synonymous_variant | LOW | c.8424G>A | p.Pro2808Pro | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 8496/12888 | 8424/12210 | 2808/4069 | chr5 | 79737189 | ||
| chr5:79737642
|
G | A | 1 | a0024c0082 | 1 | HG04228.hp1 | synonymous_variant | LOW | c.8877G>A | p.Pro2959Pro | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 8949/12888 | 8877/12210 | 2959/4069 | chr5 | 79737642 | ||
| chr5:79738758
|
G | A | 1 | a0001c0055 | 1 | HG02080.hp2 | synonymous_variant | LOW | c.9993G>A | p.Val3331Val | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 10065/12888 | 9993/12210 | 3331/4069 | chr5 | 79738758 | ||
| chr5:79738905
|
G | A | 1 | a0025c0023 | 3 | HG02015.hp2 NA18995.hp1 NA19081.hp2 |
synonymous_variant | LOW | c.10140G>A | p.Pro3380Pro | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 10212/12888 | 10140/12210 | 3380/4069 | chr5 | 79738905 | ||
| chr5:79739214
|
C | T | 1 | a0032c0110 | 1 | NA18999.hp2 | synonymous_variant | LOW | c.10449C>T | p.Ser3483Ser | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/13 | 10521/12888 | 10449/12210 | 3483/4069 | chr5 | 79739214 | ||
| chr5:79743871
|
G | A | 1 | a0072c0071 | 1 | HG01243.hp1 | synonymous_variant | LOW | c.10683G>A | p.Leu3561Leu | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 3/13 | 10755/12888 | 10683/12210 | 3561/4069 | chr5 | 79743871 | ||
| chr5:79745281
|
G | A | 2 | a0015c0032a0049c0103 | 3 | HG02451.hp2 HG02615.hp1 NA19240.hp2 |
synonymous_variant | LOW | c.10794G>A | p.Lys3598Lys | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 4/13 | 10866/12888 | 10794/12210 | 3598/4069 | chr5 | 79745281 | ||
| chr5:79752739
|
C | T | 32 | a0001c0013a0002c0002a0002c0106others(29): Show | 108 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(105): Show |
synonymous_variant | LOW | c.11055C>T | p.Phe3685Phe | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/13 | 11127/12888 | 11055/12210 | 3685/4069 | chr5 | 79752739 | ||
| chr5:79761833
|
G | A | 1 | a0001c0056 | 1 | HG03490.hp2 | synonymous_variant | LOW | c.11283G>A | p.Leu3761Leu | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 8/13 | 11355/12888 | 11283/12210 | 3761/4069 | chr5 | 79761833 | ||
| chr5:79761890
|
A | G | 3 | a0001c0058a0004c0014a0005c0089 | 8 | HG00438.hp2 HG00544.hp2 HG02165.hp1 others(5): Show |
synonymous_variant | LOW | c.11340A>G | p.Gln3780Gln | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 8/13 | 11412/12888 | 11340/12210 | 3780/4069 | chr5 | 79761890 | ||
| chr5:79789040
|
T | C | 2 | a0003c0034a0015c0073 | 3 | HG03139.hp1 HG03486.hp2 HG03579.hp2 |
synonymous_variant | LOW | c.11625T>C | p.Tyr3875Tyr | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 10/13 | 11697/12888 | 11625/12210 | 3875/4069 | chr5 | 79789040 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:79689878
|
T | TCCGGCC | 22 | a0002c0106t0007a0003c0003t0005a0003c0003t0008others(19): Show | 31 | HG02055.hp2 HG02109.hp2 HG02451.hp2 others(28): Show |
5_prime_UTR_variant | MODIFIER | c.-22_-17dupCGGCCC | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/13 | 16 | INFO_REALIGN_3_PRIME | chr5 | 79689878 | ||||
| chr5:79689907
|
G | A | 1 | a0003c0003t0013 | 1 | HG01169.hp2 | 5_prime_UTR_variant | MODIFIER | c.-1G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/13 | 1 | chr5 | 79689907 | |||||
| chr5:79799630
|
G | A | 2 | a0003c0003t0008a0023c0022t0008 | 3 | HG02630.hp2 HG02896.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*14G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 13/13 | 14 | chr5 | 79799630 | |||||
| chr5:79799647
|
G | A | 1 | a0009c0009t0014 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*31G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 13/13 | 31 | chr5 | 79799647 | |||||
| chr5:79799660
|
G | A | 2 | a0003c0003t0009a0003c0034t0009 | 2 | HG02896.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*44G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 13/13 | 44 | chr5 | 79799660 | |||||
| chr5:79799664
|
G | A | 5 | a0001c0013t0006a0002c0002t0006a0006c0004t0006others(2): Show | 6 | HG00621.hp2 HG03704.hp2 NA18948.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*48G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 13/13 | 48 | chr5 | 79799664 | |||||
| chr5:79799712
|
C | A | 1 | a0009c0009t0014 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*96C>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 13/13 | 96 | chr5 | 79799712 | |||||
| chr5:79799715
|
C | T | 3 | a0003c0034t0012a0015c0073t0015a0029c0044t0012 | 3 | HG03139.hp1 HG03225.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*99C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 13/13 | 99 | chr5 | 79799715 | |||||
| chr5:79799898
|
G | A | 21 | a0001c0013t0003a0002c0106t0007a0003c0003t0003others(18): Show | 30 | HG00323.hp2 HG00621.hp1 HG01081.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*282G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 13/13 | 282 | chr5 | 79799898 | |||||
| chr5:79799978
|
G | A | 1 | a0001c0001t0010 | 2 | HG01167.hp1 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*362G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 13/13 | 362 | chr5 | 79799978 | |||||
| chr5:79799997
|
C | T | 5 | a0003c0003t0009a0003c0034t0009a0007c0008t0011others(2): Show | 5 | HG02145.hp2 HG02809.hp2 HG02896.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*381C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 13/13 | 381 | chr5 | 79799997 | |||||
| chr5:79800079
|
C | G | 1 | a0012c0015t0016 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*463C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 13/13 | 463 | chr5 | 79800079 | |||||
| chr5:79800123
|
CT | C | 60 | a0001c0001t0002a0001c0013t0002a0001c0013t0006others(57): Show | 129 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*508delT | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 13/13 | 508 | chr5 | 79800123 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:79690460
|
G | C | 1 | a0018c0017t0002g0002 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.149+404G>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79690460 | ||||||
| chr5:79690517
|
A | G | 2 | a0009c0009t0001g0357a0051c0100t0002g0356 | 2 | HG02258.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.149+461A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79690517 | ||||||
| chr5:79690603
|
T | C | 8 | a0001c0001t0001g0007a0002c0002t0001g0008a0005c0005t0002g0004others(5): Show | 8 | HG02027.hp2 NA18954.hp1 NA18957.hp2 others(5): Show |
intron_variant | MODIFIER | c.149+547T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79690603 | ||||||
| chr5:79690633
|
T | G | 1 | a0043c0094t0002g0011 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.149+577T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79690633 | ||||||
| chr5:79690664
|
A | G | 1 | a0019c0024t0017g0355 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.149+608A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79690664 | ||||||
| chr5:79691191
|
G | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG01516.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.149+1135G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79691191 | ||||||
| chr5:79691206
|
G | A | 2 | a0003c0003t0001g0015a0009c0009t0001g0014 | 2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.149+1150G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79691206 | ||||||
| chr5:79691239
|
C | T | 1 | a0009c0009t0001g0357 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.149+1183C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79691239 | ||||||
| chr5:79691330
|
C | A | 25 | a0002c0106t0007g0029a0003c0003t0005g0020a0003c0003t0005g0035others(22): Show | 26 | HG02055.hp2 HG02109.hp2 HG02451.hp2 others(23): Show |
intron_variant | MODIFIER | c.149+1274C>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79691330 | ||||||
| chr5:79691428
|
A | G | 7 | a0002c0002t0002g0354a0003c0003t0003g0352a0004c0011t0003g0349others(4): Show | 7 | HG00438.hp1 HG01081.hp1 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.149+1372A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79691428 | ||||||
| chr5:79691432
|
A | C | 1 | a0019c0024t0017g0355 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.149+1376A>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79691432 | ||||||
| chr5:79691512
|
G | A | 1 | a0005c0005t0001g0039 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.149+1456G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79691512 | ||||||
| chr5:79691541
|
C | G | 96 | a0001c0001t0001g0281a0001c0001t0001g0285a0001c0001t0001g0292others(93): Show | 96 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.149+1485C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79691541 | ||||||
| chr5:79691576
|
C | G | 106 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(103): Show | 107 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(104): Show |
intron_variant | MODIFIER | c.149+1520C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79691576 | ||||||
| chr5:79691722
|
C | T | 43 | a0001c0001t0001g0333a0001c0001t0001g0335a0001c0001t0002g0329others(40): Show | 43 | HG00099.hp2 HG00673.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.149+1666C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79691722 | ||||||
| chr5:79691961
|
T | G | 3 | a0001c0013t0002g0041a0004c0014t0002g0040a0047c0105t0001g0042 | 3 | HG00544.hp2 HG02015.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.149+1905T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79691961 | ||||||
| chr5:79692380
|
TGATATAT others(13): Show |
T | 107 | a0001c0001t0001g0150a0001c0001t0001g0157a0001c0001t0001g0163others(104): Show | 107 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.149+2326_149+2345d others(22): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79692380 | |||||
| chr5:79692605
|
C | G | 31 | a0001c0001t0001g0333a0001c0001t0001g0335a0001c0001t0002g0329others(28): Show | 31 | HG00099.hp2 HG00673.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.149+2549C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79692605 | ||||||
| chr5:79692833
|
G | A | 13 | a0001c0001t0001g0150a0001c0001t0002g0142a0001c0013t0006g0140others(10): Show | 13 | HG00408.hp1 NA18952.hp2 NA18956.hp2 others(10): Show |
intron_variant | MODIFIER | c.149+2777G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79692833 | ||||||
| chr5:79692869
|
C | G | 8 | a0003c0003t0001g0188a0019c0024t0001g0181a0019c0024t0001g0184others(5): Show | 8 | HG02055.hp1 HG02647.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.149+2813C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79692869 | ||||||
| chr5:79692946
|
A | C | 262 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(259): Show | 263 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.149+2890A>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79692946 | ||||||
| chr5:79693336
|
AT | A | 254 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0136others(251): Show | 255 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.149+3298delT | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79693336 | |||||
| chr5:79693336
|
ATT | A | 6 | a0002c0020t0002g0190a0003c0003t0001g0153a0005c0005t0004g0017others(3): Show | 6 | HG00741.hp2 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.149+3297_149+3298d others(4): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79693336 | |||||
| chr5:79693431
|
A | G | 2 | a0002c0020t0002g0190a0004c0006t0001g0256 | 2 | NA19056.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.149+3375A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79693431 | ||||||
| chr5:79693471
|
G | A | 2 | a0003c0003t0001g0192a0072c0071t0002g0191 | 2 | HG01243.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.149+3415G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79693471 | ||||||
| chr5:79693489
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.149+3433C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79693489 | ||||||
| chr5:79693504
|
C | T | 261 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(258): Show | 262 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.149+3448C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79693504 | ||||||
| chr5:79693542
|
G | A | 261 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(258): Show | 262 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.149+3486G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79693542 | ||||||
| chr5:79693603
|
A | C | 8 | a0003c0003t0001g0188a0019c0024t0001g0181a0019c0024t0001g0184others(5): Show | 8 | HG02055.hp1 HG02647.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.149+3547A>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79693603 | ||||||
| chr5:79693663
|
C | T | 262 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(259): Show | 263 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.149+3607C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79693663 | ||||||
| chr5:79693683
|
A | G | 3 | a0002c0002t0001g0253a0010c0010t0002g0254a0062c0072t0002g0255 | 3 | HG01192.hp1 HG01361.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.149+3627A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79693683 | ||||||
| chr5:79693685
|
G | A | 1 | a0003c0003t0001g0046 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.149+3629G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79693685 | ||||||
| chr5:79693807
|
T | C | 1 | a0011c0012t0001g0261 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.149+3751T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79693807 | ||||||
| chr5:79694216
|
A | G | 2 | a0017c0019t0001g0132a0036c0068t0001g0133 | 2 | HG00323.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.149+4160A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79694216 | ||||||
| chr5:79694283
|
T | C | 1 | a0008c0007t0001g0047 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.149+4227T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79694283 | ||||||
| chr5:79694284
|
A | T | 1 | a0008c0007t0001g0047 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.149+4228A>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79694284 | ||||||
| chr5:79694347
|
A | C | 1 | a0008c0007t0001g0047 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.149+4291A>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79694347 | ||||||
| chr5:79694662
|
T | C | 37 | a0001c0001t0001g0150a0001c0001t0001g0157a0001c0001t0001g0163others(34): Show | 37 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.149+4606T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79694662 | ||||||
| chr5:79694805
|
G | A | 1 | a0010c0010t0001g0262 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.149+4749G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79694805 | ||||||
| chr5:79694844
|
G | A | 35 | a0001c0001t0001g0136a0001c0001t0001g0333a0001c0001t0001g0335others(32): Show | 35 | HG00099.hp2 HG00673.hp1 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.149+4788G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79694844 | ||||||
| chr5:79694980
|
C | T | 1 | a0021c0026t0002g0252 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.149+4924C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79694980 | ||||||
| chr5:79695091
|
C | A | 261 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(258): Show | 261 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(258): Show |
intron_variant | MODIFIER | c.149+5035C>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79695091 | ||||||
| chr5:79695092
|
A | C | 2 | a0015c0038t0004g0260a0046c0098t0005g0259 | 2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.149+5036A>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79695092 | ||||||
| chr5:79695102
|
A | G | 40 | a0001c0001t0001g0136a0001c0001t0001g0333a0001c0001t0001g0335others(37): Show | 40 | HG00099.hp2 HG00673.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.149+5046A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79695102 | ||||||
| chr5:79695315
|
A | G | 1 | a0007c0097t0002g0347 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.149+5259A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79695315 | ||||||
| chr5:79695550
|
A | G | 155 | a0001c0001t0001g0136a0001c0001t0001g0150a0001c0001t0001g0157others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.149+5494A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79695550 | ||||||
| chr5:79695572
|
C | A | 6 | a0003c0003t0009g0313a0003c0069t0002g0310a0007c0008t0001g0311others(3): Show | 6 | HG01109.hp2 HG02257.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.149+5516C>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79695572 | ||||||
| chr5:79695769
|
A | G | 8 | a0003c0003t0001g0188a0019c0024t0001g0181a0019c0024t0001g0184others(5): Show | 8 | HG02055.hp1 HG02647.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.149+5713A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79695769 | ||||||
| chr5:79695792
|
C | T | 1 | a0004c0011t0003g0251 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.149+5736C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79695792 | ||||||
| chr5:79695798
|
A | G | 1 | a0013c0016t0003g0307 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.149+5742A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79695798 | ||||||
| chr5:79696011
|
C | T | 1 | a0011c0012t0001g0306 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.149+5955C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79696011 | ||||||
| chr5:79696101
|
G | T | 1 | a0008c0067t0001g0305 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.149+6045G>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79696101 | ||||||
| chr5:79696250
|
C | A | 1 | a0008c0007t0001g0047 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.149+6194C>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79696250 | ||||||
| chr5:79696310
|
G | A | 1 | a0058c0092t0003g0263 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.149+6254G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79696310 | ||||||
| chr5:79696374
|
A | G | 1 | a0016c0018t0001g0176 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.149+6318A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79696374 | ||||||
| chr5:79696408
|
A | G | 1 | a0008c0007t0001g0047 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.149+6352A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79696408 | ||||||
| chr5:79696413
|
C | T | 1 | a0039c0030t0002g0314 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.149+6357C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79696413 | ||||||
| chr5:79696442
|
A | C | 42 | a0001c0001t0001g0150a0001c0001t0001g0157a0001c0001t0001g0163others(39): Show | 42 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.149+6386A>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79696442 | ||||||
| chr5:79696474
|
C | T | 21 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0002g0126others(18): Show | 21 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.149+6418C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79696474 | ||||||
| chr5:79696565
|
G | C | 1 | a0009c0009t0001g0264 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.149+6509G>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79696565 | ||||||
| chr5:79696783
|
G | A | 264 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(261): Show | 265 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.149+6727G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79696783 | ||||||
| chr5:79696836
|
G | A | 44 | a0001c0001t0001g0150a0001c0001t0001g0157a0001c0001t0001g0163others(41): Show | 44 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.149+6780G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79696836 | ||||||
| chr5:79696863
|
C | T | 46 | a0001c0001t0001g0281a0001c0001t0001g0285a0001c0001t0001g0292others(43): Show | 46 | HG00099.hp1 HG00438.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.149+6807C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79696863 | ||||||
| chr5:79696864
|
G | C | 1 | a0008c0007t0001g0047 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.149+6808G>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79696864 | ||||||
| chr5:79696868
|
A | G | 266 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(263): Show | 267 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(264): Show |
intron_variant | MODIFIER | c.149+6812A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79696868 | ||||||
| chr5:79696910
|
G | A | 1 | a0021c0026t0002g0252 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.149+6854G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79696910 | ||||||
| chr5:79697007
|
C | CA | 16 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0198others(13): Show | 16 | HG00621.hp1 HG00741.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.149+6963dupA | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79697007 | |||||
| chr5:79697020
|
T | A | 1 | a0046c0098t0005g0259 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.149+6964T>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79697020 | ||||||
| chr5:79697348
|
C | A | 1 | a0001c0013t0001g0154 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.149+7292C>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79697348 | ||||||
| chr5:79697603
|
A | G | 11 | a0003c0003t0001g0188a0012c0015t0016g0318a0013c0016t0007g0315others(8): Show | 11 | HG02055.hp1 HG02280.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.149+7547A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79697603 | ||||||
| chr5:79697661
|
C | T | 82 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(79): Show | 82 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.149+7605C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79697661 | ||||||
| chr5:79697726
|
T | G | 4 | a0012c0015t0016g0318a0013c0016t0007g0315a0045c0099t0002g0316others(1): Show | 4 | HG02280.hp1 HG02486.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.149+7670T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79697726 | ||||||
| chr5:79697855
|
A | G | 1 | a0029c0044t0012g0036 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.149+7799A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79697855 | ||||||
| chr5:79697929
|
A | C | 43 | a0001c0001t0001g0136a0001c0001t0001g0333a0001c0001t0001g0335others(40): Show | 43 | HG00099.hp2 HG00673.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.149+7873A>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79697929 | ||||||
| chr5:79698147
|
C | T | 58 | a0001c0001t0001g0281a0001c0001t0001g0285a0001c0001t0001g0292others(55): Show | 58 | HG00099.hp1 HG00438.hp1 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.149+8091C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79698147 | ||||||
| chr5:79698174
|
A | T | 3 | a0001c0001t0001g0150a0006c0004t0001g0152a0055c0113t0001g0151 | 3 | HG00408.hp1 NA18952.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.149+8118A>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79698174 | ||||||
| chr5:79698201
|
C | T | 3 | a0004c0006t0001g0304a0004c0006t0002g0303a0022c0021t0002g0302 | 3 | NA18945.hp2 NA18972.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.149+8145C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79698201 | ||||||
| chr5:79698202
|
G | A | 107 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(104): Show | 108 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(105): Show |
intron_variant | MODIFIER | c.149+8146G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79698202 | ||||||
| chr5:79698304
|
CAAAAAAC others(7): Show |
C | 1 | a0035c0037t0011g0319 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.149+8255_149+8268d others(16): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79698304 | |||||
| chr5:79698317
|
CA | C | 183 | a0001c0001t0001g0136a0001c0001t0001g0150a0001c0001t0001g0157others(180): Show | 184 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.149+8272delA | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79698317 | |||||
| chr5:79698323
|
A | C | 84 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(81): Show | 84 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.149+8267A>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79698323 | ||||||
| chr5:79698539
|
C | T | 37 | a0001c0001t0001g0136a0001c0001t0001g0333a0001c0001t0001g0335others(34): Show | 37 | HG00099.hp2 HG00673.hp1 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.149+8483C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79698539 | ||||||
| chr5:79698618
|
G | A | 52 | a0001c0001t0001g0150a0001c0001t0001g0157a0001c0001t0001g0163others(49): Show | 52 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.149+8562G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79698618 | ||||||
| chr5:79698656
|
A | G | 269 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(266): Show | 270 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(267): Show |
intron_variant | MODIFIER | c.149+8600A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79698656 | ||||||
| chr5:79698939
|
C | G | 37 | a0001c0001t0001g0136a0001c0001t0001g0333a0001c0001t0001g0335others(34): Show | 37 | HG00099.hp2 HG00673.hp1 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.149+8883C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79698939 | ||||||
| chr5:79699025
|
G | A | 44 | a0001c0001t0001g0150a0001c0001t0001g0157a0001c0001t0001g0163others(41): Show | 44 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.149+8969G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79699025 | ||||||
| chr5:79699037
|
A | C | 103 | a0001c0001t0001g0136a0001c0001t0001g0281a0001c0001t0001g0285others(100): Show | 103 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.149+8981A>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79699037 | ||||||
| chr5:79699158
|
A | AAAC | 48 | a0001c0001t0001g0150a0001c0001t0001g0157a0001c0001t0001g0163others(45): Show | 48 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.149+9120_149+9122d others(5): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79699158 | |||||
| chr5:79699176
|
C | A | 1 | a0003c0034t0009g0320 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.149+9120C>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79699176 | ||||||
| chr5:79699218
|
G | T | 1 | a0009c0009t0001g0346 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.149+9162G>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79699218 | ||||||
| chr5:79699240
|
T | A | 105 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(102): Show | 106 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(103): Show |
intron_variant | MODIFIER | c.149+9184T>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79699240 | ||||||
| chr5:79699289
|
T | G | 2 | a0010c0010t0001g0262a0030c0096t0001g0274 | 2 | HG02647.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.149+9233T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79699289 | ||||||
| chr5:79699332
|
C | A | 1 | a0003c0003t0008g0018 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.149+9276C>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79699332 | ||||||
| chr5:79699441
|
A | T | 44 | a0001c0001t0001g0150a0001c0001t0001g0157a0001c0001t0001g0163others(41): Show | 44 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.149+9385A>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79699441 | ||||||
| chr5:79699500
|
T | C | 83 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(80): Show | 83 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.149+9444T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79699500 | ||||||
| chr5:79699587
|
A | G | 60 | a0001c0001t0001g0281a0001c0001t0001g0285a0001c0001t0001g0292others(57): Show | 60 | HG00099.hp1 HG00438.hp1 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.149+9531A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79699587 | ||||||
| chr5:79699880
|
C | T | 60 | a0001c0001t0001g0281a0001c0001t0001g0285a0001c0001t0001g0292others(57): Show | 60 | HG00099.hp1 HG00438.hp1 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.149+9824C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79699880 | ||||||
| chr5:79699968
|
C | G | 59 | a0001c0001t0001g0150a0001c0001t0001g0157a0001c0001t0001g0163others(56): Show | 59 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.149+9912C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79699968 | ||||||
| chr5:79700172
|
A | G | 1 | a0015c0038t0004g0260 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.149+10116A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79700172 | ||||||
| chr5:79700227
|
A | G | 173 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(170): Show | 174 | HG00099.hp1 HG00438.hp1 HG00597.hp1 others(171): Show |
intron_variant | MODIFIER | c.149+10171A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79700227 | ||||||
| chr5:79700379
|
C | CTG | 164 | a0001c0001t0001g0136a0001c0001t0001g0150a0001c0001t0001g0157others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.149+10324_149+1032 others(6): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79700379 | |||||
| chr5:79700421
|
A | G | 164 | a0001c0001t0001g0136a0001c0001t0001g0150a0001c0001t0001g0157others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.149+10365A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79700421 | ||||||
| chr5:79700502
|
A | T | 4 | a0012c0015t0016g0318a0013c0016t0007g0315a0045c0099t0002g0316others(1): Show | 4 | HG02280.hp1 HG02486.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.149+10446A>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79700502 | ||||||
| chr5:79700784
|
C | T | 8 | a0003c0003t0001g0188a0019c0024t0001g0181a0019c0024t0001g0184others(5): Show | 8 | HG02055.hp1 HG02647.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.149+10728C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79700784 | ||||||
| chr5:79700832
|
C | G | 1 | a0075c0086t0001g0250 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.149+10776C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79700832 | ||||||
| chr5:79700834
|
G | T | 1 | a0005c0005t0001g0353 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.149+10778G>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79700834 | ||||||
| chr5:79700966
|
T | C | 202 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(199): Show | 203 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(200): Show |
intron_variant | MODIFIER | c.149+10910T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79700966 | ||||||
| chr5:79701090
|
C | CA | 37 | a0001c0001t0001g0136a0001c0001t0001g0333a0001c0001t0001g0335others(34): Show | 37 | HG00099.hp2 HG00673.hp1 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.149+11052dupA | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79701090 | |||||
| chr5:79701090
|
C | CCAAAA | 9 | a0003c0003t0001g0188a0015c0032t0007g0034a0019c0024t0001g0181others(6): Show | 9 | HG02055.hp1 HG02451.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.149+11034_149+1103 others(9): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79701090 | ||||||
| chr5:79701090
|
C | CCAAAAA | 8 | a0002c0106t0007g0029a0007c0008t0004g0030a0007c0008t0004g0032others(5): Show | 9 | HG02109.hp2 HG02572.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.149+11034_149+1103 others(10): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79701090 | ||||||
| chr5:79701090
|
C | CCAAAAAA | 12 | a0003c0003t0005g0020a0003c0003t0008g0018a0003c0034t0012g0021others(9): Show | 12 | HG02559.hp1 HG02630.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.149+11034_149+1103 others(11): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79701090 | ||||||
| chr5:79701090
|
C | CCAAAAAA others(1): Show |
6 | a0003c0003t0001g0192a0004c0006t0002g0249a0011c0012t0002g0248others(3): Show | 6 | HG01243.hp1 HG01496.hp1 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.149+11034_149+1103 others(12): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79701090 | ||||||
| chr5:79701090
|
C | CCAAAAAA others(2): Show |
66 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(63): Show | 66 | HG00609.hp1 HG00621.hp1 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.149+11034_149+1103 others(13): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79701090 | ||||||
| chr5:79701090
|
C | CCAAAAAA others(3): Show |
12 | a0001c0013t0002g0204a0001c0013t0003g0205a0002c0002t0001g0253others(9): Show | 12 | HG00597.hp1 HG01361.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.149+11034_149+1103 others(14): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79701090 | ||||||
| chr5:79701090
|
CA | C | 51 | a0001c0001t0001g0150a0001c0001t0001g0157a0001c0001t0001g0163others(48): Show | 51 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.149+11052delA | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79701090 | |||||
| chr5:79701135
|
A | G | 172 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(169): Show | 173 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(170): Show |
intron_variant | MODIFIER | c.149+11079A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79701135 | ||||||
| chr5:79701198
|
G | C | 3 | a0008c0007t0002g0113a0008c0007t0002g0114a0008c0007t0002g0115 | 3 | HG00673.hp2 NA18942.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.149+11142G>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79701198 | ||||||
| chr5:79701235
|
C | CAAAT | 53 | a0001c0001t0001g0150a0001c0001t0001g0157a0001c0001t0001g0163others(50): Show | 53 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.149+11183_149+1118 others(8): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79701235 | |||||
| chr5:79701431
|
G | A | 14 | a0003c0003t0001g0188a0003c0003t0009g0313a0003c0069t0002g0310others(11): Show | 14 | HG01109.hp2 HG02055.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.149+11375G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79701431 | ||||||
| chr5:79701495
|
ATAAAT | A | 14 | a0003c0003t0001g0188a0003c0003t0009g0313a0003c0069t0002g0310others(11): Show | 14 | HG01109.hp2 HG02055.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.149+11444_149+1144 others(9): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79701495 | |||||
| chr5:79701555
|
T | C | 48 | a0001c0001t0001g0150a0001c0001t0001g0157a0001c0001t0001g0163others(45): Show | 48 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.149+11499T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79701555 | ||||||
| chr5:79701584
|
G | A | 1 | a0043c0094t0002g0011 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.149+11528G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79701584 | ||||||
| chr5:79701593
|
A | C | 1 | a0015c0073t0015g0343 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.149+11537A>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79701593 | ||||||
| chr5:79701744
|
C | T | 8 | a0003c0003t0001g0188a0019c0024t0001g0181a0019c0024t0001g0184others(5): Show | 8 | HG02055.hp1 HG02647.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.149+11688C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79701744 | ||||||
| chr5:79701777
|
C | T | 8 | a0003c0003t0001g0188a0019c0024t0001g0181a0019c0024t0001g0184others(5): Show | 8 | HG02055.hp1 HG02647.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.149+11721C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79701777 | ||||||
| chr5:79701930
|
A | G | 8 | a0003c0003t0001g0188a0019c0024t0001g0181a0019c0024t0001g0184others(5): Show | 8 | HG02055.hp1 HG02647.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.149+11874A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79701930 | ||||||
| chr5:79702077
|
C | T | 2 | a0001c0001t0001g0174a0001c0001t0002g0175 | 2 | NA18949.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.149+12021C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79702077 | ||||||
| chr5:79702112
|
G | A | 8 | a0003c0003t0001g0188a0019c0024t0001g0181a0019c0024t0001g0184others(5): Show | 8 | HG02055.hp1 HG02647.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.149+12056G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79702112 | ||||||
| chr5:79702112
|
G | C | 48 | a0001c0001t0001g0150a0001c0001t0001g0157a0001c0001t0001g0163others(45): Show | 48 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.149+12056G>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79702112 | ||||||
| chr5:79702145
|
T | C | 8 | a0003c0003t0001g0188a0019c0024t0001g0181a0019c0024t0001g0184others(5): Show | 8 | HG02055.hp1 HG02647.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.149+12089T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79702145 | ||||||
| chr5:79702168
|
A | G | 22 | a0002c0106t0007g0029a0003c0003t0005g0020a0003c0003t0008g0018others(19): Show | 23 | HG02055.hp2 HG02109.hp2 HG02451.hp2 others(20): Show |
intron_variant | MODIFIER | c.149+12112A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79702168 | ||||||
| chr5:79702190
|
G | A | 1 | a0001c0001t0001g0150 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.149+12134G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79702190 | ||||||
| chr5:79702217
|
C | G | 3 | a0004c0006t0001g0304a0004c0006t0002g0303a0022c0021t0002g0302 | 3 | NA18945.hp2 NA18972.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.149+12161C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79702217 | ||||||
| chr5:79702217
|
C | T | 9 | a0003c0003t0001g0188a0019c0024t0001g0181a0019c0024t0001g0184others(6): Show | 9 | HG02055.hp1 HG02647.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.149+12161C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79702217 | ||||||
| chr5:79702492
|
T | A | 60 | a0001c0001t0001g0281a0001c0001t0001g0285a0001c0001t0001g0292others(57): Show | 60 | HG00099.hp1 HG00438.hp1 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.149+12436T>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79702492 | ||||||
| chr5:79702533
|
A | G | 8 | a0003c0003t0001g0188a0019c0024t0001g0181a0019c0024t0001g0184others(5): Show | 8 | HG02055.hp1 HG02647.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.149+12477A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79702533 | ||||||
| chr5:79702630
|
T | C | 1 | a0057c0111t0002g0321 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.149+12574T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79702630 | ||||||
| chr5:79702650
|
T | C | 8 | a0003c0003t0001g0188a0019c0024t0001g0181a0019c0024t0001g0184others(5): Show | 8 | HG02055.hp1 HG02647.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.149+12594T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79702650 | ||||||
| chr5:79702655
|
G | A | 8 | a0003c0003t0001g0188a0019c0024t0001g0181a0019c0024t0001g0184others(5): Show | 8 | HG02055.hp1 HG02647.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.149+12599G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79702655 | ||||||
| chr5:79703004
|
G | A | 8 | a0003c0003t0001g0188a0019c0024t0001g0181a0019c0024t0001g0184others(5): Show | 8 | HG02055.hp1 HG02647.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.149+12948G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79703004 | ||||||
| chr5:79703080
|
C | T | 47 | a0001c0001t0001g0150a0001c0001t0001g0157a0001c0001t0001g0163others(44): Show | 47 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.149+13024C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79703080 | ||||||
| chr5:79703111
|
C | T | 8 | a0003c0003t0001g0188a0019c0024t0001g0181a0019c0024t0001g0184others(5): Show | 8 | HG02055.hp1 HG02647.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.149+13055C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79703111 | ||||||
| chr5:79703402
|
A | G | 8 | a0003c0003t0001g0188a0019c0024t0001g0181a0019c0024t0001g0184others(5): Show | 8 | HG02055.hp1 HG02647.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.149+13346A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79703402 | ||||||
| chr5:79703415
|
C | G | 3 | a0004c0006t0001g0304a0004c0006t0002g0303a0022c0021t0002g0302 | 3 | NA18945.hp2 NA18972.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.149+13359C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79703415 | ||||||
| chr5:79703462
|
A | G | 8 | a0003c0003t0001g0188a0019c0024t0001g0181a0019c0024t0001g0184others(5): Show | 8 | HG02055.hp1 HG02647.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.149+13406A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79703462 | ||||||
| chr5:79703717
|
G | A | 8 | a0003c0003t0001g0188a0019c0024t0001g0181a0019c0024t0001g0184others(5): Show | 8 | HG02055.hp1 HG02647.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.149+13661G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79703717 | ||||||
| chr5:79703870
|
T | C | 4 | a0012c0015t0016g0318a0013c0016t0007g0315a0045c0099t0002g0316others(1): Show | 4 | HG02280.hp1 HG02486.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.149+13814T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79703870 | ||||||
| chr5:79703907
|
A | G | 1 | a0007c0008t0002g0301 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.149+13851A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79703907 | ||||||
| chr5:79704005
|
C | T | 3 | a0007c0008t0004g0032a0012c0015t0004g0033a0015c0032t0007g0034 | 3 | HG02109.hp2 HG02451.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.149+13949C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79704005 | ||||||
| chr5:79704088
|
T | TA | 12 | a0003c0003t0001g0188a0012c0015t0016g0318a0013c0016t0007g0315others(9): Show | 12 | HG02055.hp1 HG02280.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.149+14042dupA | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79704088 | |||||
| chr5:79704155
|
T | C | 4 | a0012c0015t0016g0318a0013c0016t0007g0315a0045c0099t0002g0316others(1): Show | 4 | HG02280.hp1 HG02486.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.149+14099T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79704155 | ||||||
| chr5:79704204
|
G | GA | 8 | a0003c0003t0002g0050a0003c0003t0009g0313a0003c0034t0009g0320others(5): Show | 8 | HG01109.hp2 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.149+14161dupA | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79704204 | |||||
| chr5:79704526
|
T | C | 8 | a0003c0003t0001g0188a0019c0024t0001g0181a0019c0024t0001g0184others(5): Show | 8 | HG02055.hp1 HG02647.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.149+14470T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79704526 | ||||||
| chr5:79704618
|
C | G | 37 | a0001c0001t0001g0136a0001c0001t0001g0333a0001c0001t0001g0335others(34): Show | 37 | HG00099.hp2 HG00673.hp1 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.149+14562C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79704618 | ||||||
| chr5:79704678
|
T | TGA | 8 | a0003c0003t0001g0188a0019c0024t0001g0181a0019c0024t0001g0184others(5): Show | 8 | HG02055.hp1 HG02647.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.149+14634_149+1463 others(6): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79704678 | |||||
| chr5:79704934
|
C | T | 8 | a0003c0003t0001g0188a0019c0024t0001g0181a0019c0024t0001g0184others(5): Show | 8 | HG02055.hp1 HG02647.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.149+14878C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79704934 | ||||||
| chr5:79705042
|
G | GT | 13 | a0003c0003t0005g0020a0003c0003t0008g0018a0003c0034t0012g0021others(10): Show | 13 | HG02055.hp2 HG02559.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.149+14987dupT | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79705042 | |||||
| chr5:79705083
|
CT | C | 8 | a0003c0003t0001g0188a0019c0024t0001g0181a0019c0024t0001g0184others(5): Show | 8 | HG02055.hp1 HG02647.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.149+15028delT | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79705083 | ||||||
| chr5:79705126
|
A | G | 231 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(228): Show | 232 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(229): Show |
intron_variant | MODIFIER | c.149+15070A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79705126 | ||||||
| chr5:79705418
|
A | AT | 96 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(93): Show | 97 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.149+15376dupT | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79705418 | |||||
| chr5:79705418
|
A | ATT | 73 | a0001c0001t0001g0281a0001c0001t0001g0285a0001c0001t0001g0292others(70): Show | 73 | HG00099.hp1 HG00438.hp1 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.149+15375_149+1537 others(6): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79705418 | |||||
| chr5:79705418
|
AT | A | 58 | a0001c0001t0001g0150a0001c0001t0001g0157a0001c0001t0001g0163others(55): Show | 58 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.149+15376delT | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79705418 | |||||
| chr5:79705418
|
ATT | A | 12 | a0002c0002t0001g0043a0003c0003t0001g0188a0014c0027t0001g0052others(9): Show | 12 | HG02055.hp1 HG02647.hp1 HG02970.hp2 others(9): Show |
intron_variant | MODIFIER | c.149+15375_149+1537 others(6): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79705418 | |||||
| chr5:79705583
|
C | G | 6 | a0003c0003t0009g0313a0003c0069t0002g0310a0007c0008t0001g0311others(3): Show | 6 | HG01109.hp2 HG02257.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.149+15527C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79705583 | ||||||
| chr5:79705730
|
C | A | 8 | a0003c0003t0001g0188a0019c0024t0001g0181a0019c0024t0001g0184others(5): Show | 8 | HG02055.hp1 HG02647.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.149+15674C>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79705730 | ||||||
| chr5:79705731
|
G | A | 2 | a0001c0001t0001g0135a0001c0001t0002g0056 | 2 | HG01192.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.149+15675G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79705731 | ||||||
| chr5:79705749
|
A | G | 2 | a0003c0003t0009g0313a0015c0038t0002g0312 | 2 | HG02723.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.149+15693A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79705749 | ||||||
| chr5:79705886
|
G | A | 1 | a0083c0048t0001g0057 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.149+15830G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79705886 | ||||||
| chr5:79706065
|
G | A | 41 | a0001c0001t0001g0150a0001c0001t0001g0157a0001c0001t0001g0163others(38): Show | 41 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.149+16009G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79706065 | ||||||
| chr5:79706099
|
A | G | 8 | a0003c0003t0001g0188a0019c0024t0001g0181a0019c0024t0001g0184others(5): Show | 8 | HG02055.hp1 HG02647.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.149+16043A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79706099 | ||||||
| chr5:79706112
|
C | T | 8 | a0003c0003t0001g0188a0019c0024t0001g0181a0019c0024t0001g0184others(5): Show | 8 | HG02055.hp1 HG02647.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.149+16056C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79706112 | ||||||
| chr5:79706125
|
C | T | 8 | a0003c0003t0001g0188a0019c0024t0001g0181a0019c0024t0001g0184others(5): Show | 8 | HG02055.hp1 HG02647.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.149+16069C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79706125 | ||||||
| chr5:79706126
|
G | A | 1 | a0006c0004t0006g0156 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.149+16070G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79706126 | ||||||
| chr5:79706161
|
T | C | 9 | a0003c0003t0001g0188a0003c0003t0002g0058a0019c0024t0001g0181others(6): Show | 9 | HG02055.hp1 HG02647.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.149+16105T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79706161 | ||||||
| chr5:79706228
|
G | C | 1 | a0019c0024t0017g0355 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.149+16172G>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79706228 | ||||||
| chr5:79706598
|
G | A | 8 | a0003c0003t0001g0188a0019c0024t0001g0181a0019c0024t0001g0184others(5): Show | 8 | HG02055.hp1 HG02647.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.149+16542G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79706598 | ||||||
| chr5:79706620
|
A | G | 52 | a0001c0001t0001g0150a0001c0001t0001g0157a0001c0001t0001g0163others(49): Show | 52 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.149+16564A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79706620 | ||||||
| chr5:79706699
|
T | C | 8 | a0003c0003t0001g0188a0019c0024t0001g0181a0019c0024t0001g0184others(5): Show | 8 | HG02055.hp1 HG02647.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.149+16643T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79706699 | ||||||
| chr5:79706719
|
C | T | 75 | a0001c0001t0001g0136a0001c0001t0001g0281a0001c0001t0001g0285others(72): Show | 75 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.149+16663C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79706719 | ||||||
| chr5:79706724
|
T | TG | 8 | a0003c0003t0001g0188a0019c0024t0001g0181a0019c0024t0001g0184others(5): Show | 8 | HG02055.hp1 HG02647.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.149+16674dupG | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79706724 | |||||
| chr5:79706741
|
C | T | 48 | a0001c0001t0001g0007a0001c0001t0001g0235a0001c0001t0001g0239others(45): Show | 48 | HG00597.hp1 HG00609.hp1 HG02004.hp2 others(45): Show |
intron_variant | MODIFIER | c.149+16685C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79706741 | ||||||
| chr5:79706744
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.149+16688G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79706744 | ||||||
| chr5:79706844
|
T | C | 8 | a0003c0003t0001g0188a0019c0024t0001g0181a0019c0024t0001g0184others(5): Show | 8 | HG02055.hp1 HG02647.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.149+16788T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79706844 | ||||||
| chr5:79706846
|
T | C | 8 | a0003c0003t0001g0188a0019c0024t0001g0181a0019c0024t0001g0184others(5): Show | 8 | HG02055.hp1 HG02647.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.149+16790T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79706846 | ||||||
| chr5:79707010
|
C | T | 8 | a0003c0003t0001g0188a0019c0024t0001g0181a0019c0024t0001g0184others(5): Show | 8 | HG02055.hp1 HG02647.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.149+16954C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79707010 | ||||||
| chr5:79707025
|
T | G | 1 | a0003c0003t0002g0058 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.149+16969T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79707025 | ||||||
| chr5:79707126
|
T | C | 1 | a0019c0024t0017g0355 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.149+17070T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79707126 | ||||||
| chr5:79707195
|
G | T | 4 | a0012c0015t0016g0318a0013c0016t0007g0315a0045c0099t0002g0316others(1): Show | 4 | HG02280.hp1 HG02486.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.149+17139G>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79707195 | ||||||
| chr5:79707329
|
A | G | 8 | a0003c0003t0001g0188a0019c0024t0001g0181a0019c0024t0001g0184others(5): Show | 8 | HG02055.hp1 HG02647.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.149+17273A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79707329 | ||||||
| chr5:79707492
|
A | G | 8 | a0003c0003t0001g0188a0019c0024t0001g0181a0019c0024t0001g0184others(5): Show | 8 | HG02055.hp1 HG02647.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.149+17436A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79707492 | ||||||
| chr5:79707537
|
C | T | 76 | a0001c0001t0001g0136a0001c0001t0001g0281a0001c0001t0001g0285others(73): Show | 76 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.149+17481C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79707537 | ||||||
| chr5:79707662
|
C | T | 1 | a0050c0104t0003g0272 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.149+17606C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79707662 | ||||||
| chr5:79707749
|
G | A | 1 | a0002c0002t0002g0354 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.149+17693G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79707749 | ||||||
| chr5:79707759
|
G | T | 1 | a0039c0030t0002g0314 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.149+17703G>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79707759 | ||||||
| chr5:79707849
|
G | A | 8 | a0003c0003t0001g0188a0019c0024t0001g0181a0019c0024t0001g0184others(5): Show | 8 | HG02055.hp1 HG02647.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.149+17793G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79707849 | ||||||
| chr5:79707977
|
T | A | 8 | a0003c0003t0001g0188a0019c0024t0001g0181a0019c0024t0001g0184others(5): Show | 8 | HG02055.hp1 HG02647.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.149+17921T>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79707977 | ||||||
| chr5:79708024
|
C | G | 8 | a0003c0003t0001g0188a0019c0024t0001g0181a0019c0024t0001g0184others(5): Show | 8 | HG02055.hp1 HG02647.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.149+17968C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79708024 | ||||||
| chr5:79708060
|
C | T | 1 | a0002c0002t0001g0131 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.149+18004C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79708060 | ||||||
| chr5:79708223
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.149+18167G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79708223 | ||||||
| chr5:79708235
|
G | C | 5 | a0003c0003t0001g0153a0003c0003t0001g0178a0007c0008t0002g0179others(2): Show | 5 | HG02717.hp2 HG02809.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.149+18179G>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79708235 | ||||||
| chr5:79708346
|
G | T | 2 | a0003c0003t0001g0015a0005c0005t0004g0017 | 2 | HG03130.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.149+18290G>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79708346 | ||||||
| chr5:79708360
|
G | A | 2 | a0006c0004t0001g0059a0036c0070t0003g0060 | 2 | NA20752.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.149+18304G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79708360 | ||||||
| chr5:79708388
|
G | A | 1 | a0009c0009t0001g0014 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.149+18332G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79708388 | ||||||
| chr5:79708398
|
G | A | 3 | a0009c0009t0001g0322a0009c0009t0001g0323a0035c0037t0011g0319 | 3 | HG02886.hp1 HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.149+18342G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79708398 | ||||||
| chr5:79708531
|
G | A | 39 | a0001c0001t0001g0281a0001c0001t0001g0285a0001c0001t0001g0292others(36): Show | 39 | HG00099.hp1 HG00438.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.149+18475G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79708531 | ||||||
| chr5:79708692
|
C | G | 47 | a0001c0001t0001g0150a0001c0001t0001g0157a0001c0001t0001g0163others(44): Show | 47 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.149+18636C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79708692 | ||||||
| chr5:79708732
|
A | C | 1 | a0002c0002t0001g0173 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.149+18676A>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79708732 | ||||||
| chr5:79708849
|
G | A | 1 | a0019c0024t0017g0355 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.149+18793G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79708849 | ||||||
| chr5:79708850
|
G | T | 76 | a0001c0001t0001g0136a0001c0001t0001g0281a0001c0001t0001g0285others(73): Show | 76 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.149+18794G>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79708850 | ||||||
| chr5:79708865
|
C | G | 1 | a0037c0036t0001g0103 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.149+18809C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79708865 | ||||||
| chr5:79708951
|
T | A | 1 | a0033c0039t0001g0279 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.149+18895T>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79708951 | ||||||
| chr5:79708982
|
G | A | 1 | a0006c0004t0001g0225 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.149+18926G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79708982 | ||||||
| chr5:79709016
|
G | A | 1 | a0013c0016t0007g0315 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.149+18960G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79709016 | ||||||
| chr5:79709093
|
A | C | 1 | a0027c0042t0001g0342 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.149+19037A>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79709093 | ||||||
| chr5:79709454
|
G | C | 82 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(79): Show | 82 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.149+19398G>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79709454 | ||||||
| chr5:79709535
|
G | A | 13 | a0003c0003t0005g0020a0003c0003t0008g0018a0003c0034t0012g0021others(10): Show | 13 | HG02055.hp2 HG02559.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.150-19380G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79709535 | ||||||
| chr5:79709650
|
T | G | 1 | a0002c0002t0002g0141 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.150-19265T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79709650 | ||||||
| chr5:79709659
|
G | A | 22 | a0003c0003t0005g0035a0005c0005t0001g0270a0007c0008t0002g0301others(19): Show | 22 | HG00741.hp1 HG01167.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.150-19256G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79709659 | ||||||
| chr5:79709683
|
C | T | 1 | a0001c0001t0001g0102 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.150-19232C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79709683 | ||||||
| chr5:79709740
|
T | C | 1 | a0002c0114t0001g0196 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.150-19175T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79709740 | ||||||
| chr5:79709773
|
C | T | 8 | a0003c0003t0001g0188a0019c0024t0001g0181a0019c0024t0001g0184others(5): Show | 8 | HG02055.hp1 HG02647.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.150-19142C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79709773 | ||||||
| chr5:79709824
|
T | G | 273 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(270): Show | 274 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(271): Show |
intron_variant | MODIFIER | c.150-19091T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79709824 | ||||||
| chr5:79709838
|
G | A | 6 | a0003c0003t0003g0352a0004c0011t0003g0349a0005c0005t0001g0353others(3): Show | 6 | HG01081.hp1 HG03704.hp2 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.150-19077G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79709838 | ||||||
| chr5:79709885
|
C | T | 6 | a0003c0003t0009g0313a0003c0069t0002g0310a0007c0008t0001g0311others(3): Show | 6 | HG01109.hp2 HG02257.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.150-19030C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79709885 | ||||||
| chr5:79709893
|
G | A | 11 | a0001c0001t0001g0007a0002c0002t0001g0008a0002c0002t0002g0061others(8): Show | 11 | HG02027.hp2 HG02132.hp1 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.150-19022G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79709893 | ||||||
| chr5:79709960
|
C | CA | 175 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0064others(172): Show | 176 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.150-18927dupA | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79709960 | |||||
| chr5:79709960
|
C | CAA | 84 | a0001c0001t0001g0007a0001c0001t0001g0063a0001c0001t0001g0198others(81): Show | 84 | HG00438.hp2 HG00609.hp1 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.150-18928_150-1892 others(6): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79709960 | |||||
| chr5:79709960
|
C | CAAA | 17 | a0001c0013t0002g0204a0001c0013t0003g0205a0001c0033t0001g0139others(14): Show | 17 | HG00597.hp1 HG02027.hp1 HG02602.hp1 others(14): Show |
intron_variant | MODIFIER | c.150-18929_150-1892 others(7): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79709960 | |||||
| chr5:79709960
|
CAAAAA | C | 7 | a0003c0003t0001g0188a0019c0024t0001g0184a0023c0022t0001g0185others(4): Show | 7 | HG02055.hp1 HG02647.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.150-18931_150-1892 others(9): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79709960 | |||||
| chr5:79709986
|
AAAG | A | 6 | a0003c0003t0002g0213a0005c0005t0001g0216a0005c0005t0001g0217others(3): Show | 6 | HG01257.hp2 HG01258.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.150-18926_150-1892 others(7): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79709986 | |||||
| chr5:79710030
|
A | G | 2 | a0009c0009t0001g0357a0051c0100t0002g0356 | 2 | HG02258.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.150-18885A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79710030 | ||||||
| chr5:79710288
|
C | T | 45 | a0001c0001t0001g0150a0001c0001t0001g0157a0001c0001t0001g0163others(42): Show | 45 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.150-18627C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79710288 | ||||||
| chr5:79710300
|
G | A | 2 | a0001c0001t0001g0174a0001c0001t0002g0175 | 2 | NA18949.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.150-18615G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79710300 | ||||||
| chr5:79710434
|
GT | G | 8 | a0003c0003t0001g0188a0019c0024t0001g0181a0019c0024t0001g0184others(5): Show | 8 | HG02055.hp1 HG02647.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.150-18477delT | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79710434 | |||||
| chr5:79710566
|
T | A | 2 | a0027c0042t0001g0134a0043c0094t0002g0011 | 2 | HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.150-18349T>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79710566 | ||||||
| chr5:79710566
|
T | C | 300 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(297): Show | 301 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(298): Show |
intron_variant | MODIFIER | c.150-18349T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79710566 | ||||||
| chr5:79710606
|
A | G | 91 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(88): Show | 91 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.150-18309A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79710606 | ||||||
| chr5:79710692
|
T | A | 270 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(267): Show | 271 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.150-18223T>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79710692 | ||||||
| chr5:79710740
|
C | G | 1 | a0005c0005t0002g0004 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.150-18175C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79710740 | ||||||
| chr5:79710911
|
A | G | 2 | a0007c0008t0001g0340a0007c0008t0011g0341 | 2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.150-18004A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79710911 | ||||||
| chr5:79710974
|
A | G | 1 | a0002c0002t0001g0173 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.150-17941A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79710974 | ||||||
| chr5:79711079
|
G | C | 13 | a0003c0003t0005g0020a0003c0003t0008g0018a0003c0034t0012g0021others(10): Show | 13 | HG02055.hp2 HG02559.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.150-17836G>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79711079 | ||||||
| chr5:79711137
|
CT | C | 5 | a0003c0003t0009g0313a0003c0069t0002g0310a0007c0008t0001g0311others(2): Show | 5 | HG01109.hp2 HG02723.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.150-17777delT | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79711137 | ||||||
| chr5:79711258
|
A | G | 8 | a0003c0003t0001g0188a0019c0024t0001g0181a0019c0024t0001g0184others(5): Show | 8 | HG02055.hp1 HG02647.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.150-17657A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79711258 | ||||||
| chr5:79711356
|
C | T | 4 | a0003c0003t0002g0050a0004c0006t0003g0062a0022c0021t0001g0300others(1): Show | 4 | NA18957.hp1 NA18974.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.150-17559C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79711356 | ||||||
| chr5:79711367
|
G | A | 1 | a0006c0004t0001g0059 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.150-17548G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79711367 | ||||||
| chr5:79711411
|
A | G | 3 | a0001c0001t0001g0257a0053c0101t0001g0202a0064c0063t0003g0200 | 3 | HG02056.hp1 HG02523.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.150-17504A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79711411 | ||||||
| chr5:79711418
|
A | T | 1 | a0002c0002t0002g0354 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.150-17497A>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79711418 | ||||||
| chr5:79711459
|
C | G | 138 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(135): Show | 139 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(136): Show |
intron_variant | MODIFIER | c.150-17456C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79711459 | ||||||
| chr5:79711513
|
T | A | 6 | a0003c0003t0009g0313a0003c0069t0002g0310a0007c0008t0001g0311others(3): Show | 6 | HG01109.hp2 HG02257.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.150-17402T>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79711513 | ||||||
| chr5:79711572
|
A | G | 52 | a0001c0001t0001g0150a0001c0001t0001g0157a0001c0001t0001g0163others(49): Show | 52 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.150-17343A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79711572 | ||||||
| chr5:79711953
|
C | T | 82 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(79): Show | 82 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.150-16962C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79711953 | ||||||
| chr5:79711954
|
G | A | 41 | a0001c0001t0001g0150a0001c0001t0001g0157a0001c0001t0001g0163others(38): Show | 41 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.150-16961G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79711954 | ||||||
| chr5:79712007
|
C | T | 22 | a0002c0106t0007g0029a0003c0003t0005g0020a0003c0003t0008g0018others(19): Show | 23 | HG02055.hp2 HG02109.hp2 HG02451.hp2 others(20): Show |
intron_variant | MODIFIER | c.150-16908C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79712007 | ||||||
| chr5:79712065
|
A | G | 1 | a0002c0114t0001g0196 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.150-16850A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79712065 | ||||||
| chr5:79712155
|
C | T | 1 | a0004c0011t0001g0277 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.150-16760C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79712155 | ||||||
| chr5:79712179
|
G | A | 22 | a0002c0106t0007g0029a0003c0003t0005g0020a0003c0003t0008g0018others(19): Show | 23 | HG02055.hp2 HG02109.hp2 HG02451.hp2 others(20): Show |
intron_variant | MODIFIER | c.150-16736G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79712179 | ||||||
| chr5:79712223
|
A | G | 8 | a0003c0003t0001g0188a0019c0024t0001g0181a0019c0024t0001g0184others(5): Show | 8 | HG02055.hp1 HG02647.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.150-16692A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79712223 | ||||||
| chr5:79712282
|
C | T | 1 | a0003c0003t0002g0149 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.150-16633C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79712282 | ||||||
| chr5:79712290
|
C | T | 4 | a0013c0016t0007g0315a0045c0099t0002g0316a0048c0107t0004g0317others(1): Show | 4 | HG02280.hp1 HG02486.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.150-16625C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79712290 | ||||||
| chr5:79712298
|
T | C | 201 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(198): Show | 202 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(199): Show |
intron_variant | MODIFIER | c.150-16617T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79712298 | ||||||
| chr5:79712316
|
C | T | 20 | a0001c0001t0002g0175a0003c0003t0005g0035a0005c0005t0001g0270others(17): Show | 20 | HG00741.hp1 HG01243.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.150-16599C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79712316 | ||||||
| chr5:79712397
|
T | G | 137 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(134): Show | 138 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(135): Show |
intron_variant | MODIFIER | c.150-16518T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79712397 | ||||||
| chr5:79712508
|
C | T | 1 | a0060c0051t0001g0298 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.150-16407C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79712508 | ||||||
| chr5:79712577
|
A | G | 1 | a0012c0015t0004g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.150-16338A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79712577 | ||||||
| chr5:79712636
|
A | G | 6 | a0003c0003t0001g0153a0003c0003t0001g0178a0007c0008t0001g0340others(3): Show | 6 | HG02717.hp2 HG02809.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.150-16279A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79712636 | ||||||
| chr5:79712974
|
A | G | 16 | a0003c0003t0001g0153a0003c0003t0001g0178a0007c0008t0001g0340others(13): Show | 16 | HG01167.hp2 HG02451.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.150-15941A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79712974 | ||||||
| chr5:79713068
|
C | T | 28 | a0001c0001t0001g0150a0001c0001t0001g0171a0001c0001t0001g0174others(25): Show | 28 | HG00544.hp1 HG01069.hp1 HG01928.hp2 others(25): Show |
intron_variant | MODIFIER | c.150-15847C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79713068 | ||||||
| chr5:79713124
|
C | G | 2 | a0002c0002t0002g0209a0006c0004t0002g0199 | 2 | NA18942.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.150-15791C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79713124 | ||||||
| chr5:79713148
|
T | A | 38 | a0001c0001t0001g0150a0001c0001t0001g0212a0001c0001t0001g0246others(35): Show | 38 | HG00323.hp2 HG00544.hp1 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.150-15767T>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79713148 | ||||||
| chr5:79713164
|
G | A | 90 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0063others(87): Show | 91 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.150-15751G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79713164 | ||||||
| chr5:79713172
|
A | G | 9 | a0003c0003t0009g0313a0009c0009t0001g0014a0009c0009t0002g0265others(6): Show | 9 | HG00741.hp1 HG02723.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.150-15743A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79713172 | ||||||
| chr5:79713249
|
C | T | 2 | a0039c0030t0002g0314a0050c0104t0003g0272 | 2 | HG02257.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.150-15666C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79713249 | ||||||
| chr5:79713293
|
CCCCG | C | 197 | a0001c0001t0001g0007a0001c0001t0001g0063a0001c0001t0001g0077others(194): Show | 198 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.150-15618_150-1561 others(8): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79713293 | |||||
| chr5:79713297
|
G | C | 3 | a0003c0003t0001g0153a0016c0018t0001g0169a0042c0029t0001g0108 | 3 | HG00544.hp1 HG02717.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.150-15618G>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79713297 | ||||||
| chr5:79713297
|
GCCCCCA | G | 5 | a0001c0001t0001g0013a0002c0002t0001g0253a0009c0009t0001g0346others(2): Show | 5 | HG01361.hp1 HG02145.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.150-15612_150-1560 others(10): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79713297 | |||||
| chr5:79713297
|
GCCCCCAC | G | 6 | a0001c0001t0002g0338a0002c0002t0002g0148a0007c0008t0001g0138others(3): Show | 6 | HG01255.hp1 HG02109.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.150-15608_150-1560 others(11): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79713297 | |||||
| chr5:79713303
|
A | G | 1 | a0072c0071t0002g0191 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.150-15612A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79713303 | ||||||
| chr5:79713307
|
C | G | 1 | a0003c0034t0012g0021 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.150-15608C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79713307 | ||||||
| chr5:79713314
|
G | A | 21 | a0001c0001t0001g0157a0001c0001t0001g0163a0001c0001t0001g0239others(18): Show | 22 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.150-15601G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79713314 | ||||||
| chr5:79713317
|
G | A | 124 | a0001c0001t0001g0007a0001c0001t0001g0095a0001c0001t0001g0102others(121): Show | 125 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.150-15598G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79713317 | ||||||
| chr5:79713528
|
A | G | 2 | a0007c0008t0001g0138a0019c0024t0001g0181 | 2 | HG02258.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.150-15387A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79713528 | ||||||
| chr5:79713551
|
G | A | 1 | a0005c0005t0001g0039 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.150-15364G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79713551 | ||||||
| chr5:79713677
|
A | G | 2 | a0006c0004t0001g0161a0006c0004t0001g0162 | 2 | NA18943.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.150-15238A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79713677 | ||||||
| chr5:79713696
|
G | GGA | 146 | a0001c0001t0001g0007a0001c0001t0001g0124a0001c0001t0001g0135others(143): Show | 146 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.150-15214_150-1521 others(6): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79713696 | |||||
| chr5:79713781
|
G | A | 3 | a0031c0046t0001g0186a0031c0046t0002g0182a0054c0108t0001g0187 | 3 | HG02055.hp1 HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.150-15134G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79713781 | ||||||
| chr5:79713822
|
T | C | 1 | a0037c0036t0001g0326 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.150-15093T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79713822 | ||||||
| chr5:79713867
|
C | T | 3 | a0031c0046t0001g0186a0031c0046t0002g0182a0054c0108t0001g0187 | 3 | HG02055.hp1 HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.150-15048C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79713867 | ||||||
| chr5:79713868
|
G | A | 1 | a0011c0012t0002g0350 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.150-15047G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79713868 | ||||||
| chr5:79713954
|
G | GT | 152 | a0001c0001t0001g0171a0001c0001t0001g0198a0001c0001t0001g0212others(149): Show | 152 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.150-14959dupT | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79713954 | |||||
| chr5:79714101
|
C | G | 1 | a0046c0098t0005g0259 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.150-14814C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79714101 | ||||||
| chr5:79714197
|
C | A | 3 | a0031c0046t0001g0186a0031c0046t0002g0182a0054c0108t0001g0187 | 3 | HG02055.hp1 HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.150-14718C>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79714197 | ||||||
| chr5:79714391
|
T | G | 1 | a0005c0005t0002g0214 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.150-14524T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79714391 | ||||||
| chr5:79714431
|
C | CT | 10 | a0001c0001t0001g0013a0001c0001t0001g0198a0001c0001t0001g0241others(7): Show | 10 | HG01433.hp2 HG01978.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.150-14464dupT | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79714431 | |||||
| chr5:79714431
|
C | CTTTTTCT others(1): Show |
163 | a0001c0001t0001g0171a0001c0001t0001g0212a0001c0001t0001g0235others(160): Show | 164 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(161): Show |
intron_variant | MODIFIER | c.150-14479_150-1447 others(12): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79714431 | |||||
| chr5:79714431
|
C | CTTTTTCT others(2): Show |
17 | a0001c0058t0002g0339a0002c0002t0001g0127a0002c0002t0001g0128others(14): Show | 17 | HG00544.hp2 HG01243.hp2 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.150-14479_150-1447 others(13): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79714431 | |||||
| chr5:79714431
|
C | CTTTTTCT others(3): Show |
1 | a0047c0105t0001g0042 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.150-14479_150-1447 others(14): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79714431 | |||||
| chr5:79714431
|
CT | C | 10 | a0001c0001t0001g0102a0001c0001t0001g0165a0003c0003t0001g0192others(7): Show | 10 | HG01169.hp2 HG01496.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.150-14464delT | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79714431 | |||||
| chr5:79714465
|
G | A | 1 | a0003c0003t0001g0188 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.150-14450G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79714465 | ||||||
| chr5:79714561
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.150-14354C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79714561 | ||||||
| chr5:79714597
|
C | T | 2 | a0009c0009t0001g0323a0030c0096t0001g0274 | 2 | HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.150-14318C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79714597 | ||||||
| chr5:79714640
|
A | C | 6 | a0009c0009t0001g0323a0030c0096t0001g0274a0031c0046t0001g0186others(3): Show | 6 | HG02055.hp1 HG02615.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.150-14275A>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79714640 | ||||||
| chr5:79714729
|
C | T | 1 | a0019c0024t0017g0355 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.150-14186C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79714729 | ||||||
| chr5:79714750
|
C | T | 186 | a0001c0001t0001g0171a0001c0001t0001g0212a0001c0001t0001g0235others(183): Show | 187 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(184): Show |
intron_variant | MODIFIER | c.150-14165C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79714750 | ||||||
| chr5:79714860
|
C | T | 194 | a0001c0001t0001g0171a0001c0001t0001g0212a0001c0001t0001g0235others(191): Show | 195 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(192): Show |
intron_variant | MODIFIER | c.150-14055C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79714860 | ||||||
| chr5:79715045
|
A | G | 196 | a0001c0001t0001g0171a0001c0001t0001g0212a0001c0001t0001g0235others(193): Show | 197 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(194): Show |
intron_variant | MODIFIER | c.150-13870A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79715045 | ||||||
| chr5:79715047
|
T | C | 1 | a0009c0009t0001g0323 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.150-13868T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79715047 | ||||||
| chr5:79715293
|
A | AT | 192 | a0001c0001t0001g0171a0001c0001t0001g0212a0001c0001t0001g0235others(189): Show | 192 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(189): Show |
intron_variant | MODIFIER | c.150-13612dupT | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79715293 | |||||
| chr5:79715327
|
A | G | 197 | a0001c0001t0001g0171a0001c0001t0001g0212a0001c0001t0001g0235others(194): Show | 198 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.150-13588A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79715327 | ||||||
| chr5:79715351
|
G | A | 5 | a0009c0009t0001g0323a0030c0096t0001g0274a0031c0046t0001g0186others(2): Show | 5 | HG02055.hp1 HG02970.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.150-13564G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79715351 | ||||||
| chr5:79715436
|
C | T | 2 | a0009c0009t0001g0323a0030c0096t0001g0274 | 2 | HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.150-13479C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79715436 | ||||||
| chr5:79715440
|
A | T | 197 | a0001c0001t0001g0171a0001c0001t0001g0212a0001c0001t0001g0235others(194): Show | 198 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.150-13475A>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79715440 | ||||||
| chr5:79715449
|
G | A | 1 | a0009c0009t0001g0323 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.150-13466G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79715449 | ||||||
| chr5:79715533
|
C | T | 2 | a0009c0009t0001g0323a0030c0096t0001g0274 | 2 | HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.150-13382C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79715533 | ||||||
| chr5:79715796
|
C | T | 5 | a0009c0009t0001g0323a0030c0096t0001g0274a0031c0046t0001g0186others(2): Show | 5 | HG02055.hp1 HG02970.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.150-13119C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79715796 | ||||||
| chr5:79716087
|
A | G | 193 | a0001c0001t0001g0171a0001c0001t0001g0212a0001c0001t0001g0235others(190): Show | 194 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(191): Show |
intron_variant | MODIFIER | c.150-12828A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79716087 | ||||||
| chr5:79716456
|
C | T | 3 | a0001c0001t0001g0212a0009c0009t0001g0323a0030c0096t0001g0274 | 3 | HG01106.hp2 HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.150-12459C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79716456 | ||||||
| chr5:79716515
|
T | G | 198 | a0001c0001t0001g0171a0001c0001t0001g0212a0001c0001t0001g0235others(195): Show | 199 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(196): Show |
intron_variant | MODIFIER | c.150-12400T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79716515 | ||||||
| chr5:79716529
|
C | A | 198 | a0001c0001t0001g0171a0001c0001t0001g0212a0001c0001t0001g0235others(195): Show | 199 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(196): Show |
intron_variant | MODIFIER | c.150-12386C>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79716529 | ||||||
| chr5:79716663
|
C | A | 28 | a0003c0003t0001g0046a0003c0003t0001g0153a0003c0003t0001g0178others(25): Show | 28 | HG00741.hp1 HG01169.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.150-12252C>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79716663 | ||||||
| chr5:79716733
|
T | G | 42 | a0001c0058t0002g0339a0002c0002t0001g0043a0002c0002t0001g0127others(39): Show | 42 | HG00438.hp1 HG00741.hp2 HG01175.hp2 others(39): Show |
intron_variant | MODIFIER | c.150-12182T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79716733 | ||||||
| chr5:79716736
|
C | A | 2 | a0003c0003t0002g0058a0037c0036t0001g0103 | 2 | HG03239.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.150-12179C>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79716736 | ||||||
| chr5:79716743
|
C | T | 195 | a0001c0001t0001g0171a0001c0001t0001g0212a0001c0001t0001g0235others(192): Show | 196 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(193): Show |
intron_variant | MODIFIER | c.150-12172C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79716743 | ||||||
| chr5:79716789
|
C | T | 190 | a0001c0001t0001g0171a0001c0001t0001g0212a0001c0001t0001g0235others(187): Show | 191 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(188): Show |
intron_variant | MODIFIER | c.150-12126C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79716789 | ||||||
| chr5:79716856
|
C | T | 195 | a0001c0001t0001g0171a0001c0001t0001g0212a0001c0001t0001g0235others(192): Show | 196 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(193): Show |
intron_variant | MODIFIER | c.150-12059C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79716856 | ||||||
| chr5:79716910
|
G | T | 39 | a0002c0002t0001g0043a0002c0002t0001g0127a0002c0002t0001g0128others(36): Show | 39 | HG00438.hp1 HG00741.hp2 HG01175.hp2 others(36): Show |
intron_variant | MODIFIER | c.150-12005G>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79716910 | ||||||
| chr5:79717185
|
G | C | 5 | a0009c0009t0001g0323a0030c0096t0001g0274a0031c0046t0001g0186others(2): Show | 5 | HG02055.hp1 HG02970.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.150-11730G>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79717185 | ||||||
| chr5:79717300
|
A | G | 3 | a0031c0046t0001g0186a0031c0046t0002g0182a0054c0108t0001g0187 | 3 | HG02055.hp1 HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.150-11615A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79717300 | ||||||
| chr5:79717334
|
A | G | 3 | a0008c0007t0001g0047a0008c0007t0002g0104a0008c0007t0002g0145 | 3 | NA18941.hp2 NA18956.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.150-11581A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79717334 | ||||||
| chr5:79717378
|
A | G | 99 | a0001c0001t0001g0171a0001c0001t0001g0212a0001c0001t0001g0296others(96): Show | 99 | HG00099.hp1 HG00408.hp1 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.150-11537A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79717378 | ||||||
| chr5:79717390
|
C | A | 194 | a0001c0001t0001g0171a0001c0001t0001g0212a0001c0001t0001g0235others(191): Show | 195 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(192): Show |
intron_variant | MODIFIER | c.150-11525C>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79717390 | ||||||
| chr5:79717477
|
A | T | 1 | a0001c0001t0001g0246 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.150-11438A>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79717477 | ||||||
| chr5:79717479
|
C | T | 194 | a0001c0001t0001g0171a0001c0001t0001g0212a0001c0001t0001g0235others(191): Show | 195 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(192): Show |
intron_variant | MODIFIER | c.150-11436C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79717479 | ||||||
| chr5:79717701
|
A | G | 1 | a0001c0001t0001g0063 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.150-11214A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79717701 | ||||||
| chr5:79717740
|
A | G | 1 | a0015c0073t0015g0343 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.150-11175A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79717740 | ||||||
| chr5:79717797
|
A | G | 1 | a0005c0005t0001g0045 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.150-11118A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79717797 | ||||||
| chr5:79717879
|
AAGCTATT others(300): Show |
A | 196 | a0001c0001t0001g0171a0001c0001t0001g0212a0001c0001t0001g0235others(193): Show | 197 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(194): Show |
intron_variant | MODIFIER | c.150-11026_150-1072 others(4): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79717879 | |||||
| chr5:79717884
|
A | AT | 8 | a0001c0001t0001g0240a0001c0001t0002g0142a0008c0007t0002g0145others(5): Show | 8 | HG01109.hp1 HG01257.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.150-11009dupT | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79717884 | |||||
| chr5:79717884
|
A | ATT | 6 | a0009c0009t0001g0264a0009c0009t0001g0322a0009c0009t0001g0357others(3): Show | 6 | HG00741.hp1 HG02258.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.150-11010_150-1100 others(6): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79717884 | |||||
| chr5:79717884
|
A | ATTTTTTT others(3): Show |
1 | a0048c0107t0004g0317 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.150-11018_150-1100 others(14): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79717884 | |||||
| chr5:79717884
|
AT | A | 6 | a0003c0003t0001g0188a0008c0007t0002g0006a0008c0007t0002g0104others(3): Show | 6 | HG00323.hp1 HG02647.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.150-11009delT | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79717884 | |||||
| chr5:79718022
|
A | G | 1 | a0050c0104t0003g0272 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.150-10893A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79718022 | ||||||
| chr5:79718034
|
A | G | 1 | a0050c0104t0003g0272 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.150-10881A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79718034 | ||||||
| chr5:79718045
|
C | T | 1 | a0058c0092t0003g0263 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.150-10870C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79718045 | ||||||
| chr5:79718260
|
T | C | 1 | a0016c0018t0001g0176 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.150-10655T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79718260 | ||||||
| chr5:79718274
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.150-10641G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79718274 | ||||||
| chr5:79718503
|
C | T | 1 | a0044c0093t0001g0276 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.150-10412C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79718503 | ||||||
| chr5:79718506
|
C | T | 1 | a0058c0092t0003g0263 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.150-10409C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79718506 | ||||||
| chr5:79718510
|
T | A | 3 | a0031c0046t0001g0186a0031c0046t0002g0182a0054c0108t0001g0187 | 3 | HG02055.hp1 HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.150-10405T>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79718510 | ||||||
| chr5:79718564
|
A | G | 2 | a0009c0009t0001g0323a0030c0096t0001g0274 | 2 | HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.150-10351A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79718564 | ||||||
| chr5:79718734
|
T | A | 29 | a0001c0001t0001g0064a0001c0001t0001g0095a0001c0001t0001g0102others(26): Show | 29 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.150-10181T>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79718734 | ||||||
| chr5:79718833
|
T | C | 196 | a0001c0001t0001g0171a0001c0001t0001g0212a0001c0001t0001g0235others(193): Show | 197 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(194): Show |
intron_variant | MODIFIER | c.150-10082T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79718833 | ||||||
| chr5:79719068
|
A | G | 2 | a0009c0009t0001g0323a0030c0096t0001g0274 | 2 | HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.150-9847A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79719068 | ||||||
| chr5:79719077
|
AT | A | 190 | a0001c0001t0001g0171a0001c0001t0001g0212a0001c0001t0001g0235others(187): Show | 191 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(188): Show |
intron_variant | MODIFIER | c.150-9835delT | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79719077 | |||||
| chr5:79719154
|
A | G | 9 | a0009c0009t0001g0014a0009c0009t0001g0264a0009c0009t0001g0322others(6): Show | 9 | HG00741.hp1 HG02258.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.150-9761A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79719154 | ||||||
| chr5:79719251
|
T | A | 2 | a0009c0009t0001g0323a0030c0096t0001g0274 | 2 | HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.150-9664T>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79719251 | ||||||
| chr5:79719281
|
A | T | 1 | a0002c0002t0002g0066 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.150-9634A>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79719281 | ||||||
| chr5:79719307
|
A | G | 2 | a0009c0009t0001g0323a0030c0096t0001g0274 | 2 | HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.150-9608A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79719307 | ||||||
| chr5:79719308
|
T | C | 1 | a0072c0071t0002g0191 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.150-9607T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79719308 | ||||||
| chr5:79719373
|
A | G | 1 | a0006c0004t0001g0059 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.150-9542A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79719373 | ||||||
| chr5:79719481
|
C | T | 9 | a0009c0009t0001g0014a0009c0009t0001g0264a0009c0009t0001g0322others(6): Show | 9 | HG00741.hp1 HG02258.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.150-9434C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79719481 | ||||||
| chr5:79719589
|
G | A | 5 | a0003c0069t0002g0310a0012c0015t0004g0022a0012c0015t0004g0023others(2): Show | 5 | HG01109.hp2 HG02559.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.150-9326G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79719589 | ||||||
| chr5:79719605
|
T | A | 196 | a0001c0001t0001g0171a0001c0001t0001g0212a0001c0001t0001g0235others(193): Show | 197 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(194): Show |
intron_variant | MODIFIER | c.150-9310T>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79719605 | ||||||
| chr5:79719638
|
G | A | 196 | a0001c0001t0001g0171a0001c0001t0001g0212a0001c0001t0001g0235others(193): Show | 197 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(194): Show |
intron_variant | MODIFIER | c.150-9277G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79719638 | ||||||
| chr5:79719639
|
T | C | 124 | a0001c0001t0001g0235a0002c0002t0001g0043a0002c0002t0001g0127others(121): Show | 125 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.150-9276T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79719639 | ||||||
| chr5:79719697
|
A | G | 1 | a0001c0001t0001g0292 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.150-9218A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79719697 | ||||||
| chr5:79719713
|
T | C | 2 | a0015c0032t0007g0027a0015c0032t0007g0034 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.150-9202T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79719713 | ||||||
| chr5:79719758
|
G | T | 196 | a0001c0001t0001g0171a0001c0001t0001g0212a0001c0001t0001g0235others(193): Show | 197 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(194): Show |
intron_variant | MODIFIER | c.150-9157G>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79719758 | ||||||
| chr5:79719795
|
A | G | 5 | a0001c0001t0001g0135a0010c0010t0002g0245a0010c0010t0002g0254others(2): Show | 5 | HG01099.hp2 HG01175.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.150-9120A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79719795 | ||||||
| chr5:79720267
|
A | C | 196 | a0001c0001t0001g0171a0001c0001t0001g0212a0001c0001t0001g0235others(193): Show | 197 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(194): Show |
intron_variant | MODIFIER | c.150-8648A>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79720267 | ||||||
| chr5:79720337
|
T | G | 1 | a0001c0001t0001g0163 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.150-8578T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79720337 | ||||||
| chr5:79720427
|
AATTT | A | 4 | a0031c0046t0001g0186a0031c0046t0002g0182a0039c0030t0002g0269others(1): Show | 4 | HG02055.hp1 HG03471.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.150-8487_150-8484d others(6): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79720427 | ||||||
| chr5:79720427
|
AATTTT | A | 28 | a0001c0055t0001g0116a0002c0002t0001g0129a0002c0002t0001g0253others(25): Show | 28 | HG00642.hp2 HG01069.hp1 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.150-8487_150-8483d others(7): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79720427 | ||||||
| chr5:79720427
|
AATTTTT | A | 124 | a0001c0001t0001g0171a0001c0001t0001g0212a0001c0001t0001g0296others(121): Show | 125 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.150-8487_150-8482d others(8): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79720427 | ||||||
| chr5:79720427
|
AATTTTTT | A | 7 | a0001c0058t0002g0339a0002c0002t0001g0043a0002c0020t0001g0117others(4): Show | 7 | HG02280.hp2 HG02523.hp2 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.150-8487_150-8481d others(9): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79720427 | ||||||
| chr5:79720427
|
AATTTTTT others(2): Show |
A | 31 | a0001c0001t0001g0235a0004c0006t0001g0048a0004c0006t0001g0078others(28): Show | 31 | HG00438.hp2 HG00544.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.150-8487_150-8479d others(11): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79720427 | ||||||
| chr5:79720427
|
AATTTTTT others(3): Show |
A | 1 | a0002c0002t0006g0120 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.150-8487_150-8478d others(12): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79720427 | ||||||
| chr5:79720428
|
A | AT | 20 | a0001c0001t0001g0135a0001c0001t0001g0150a0001c0001t0001g0198others(17): Show | 20 | HG00673.hp1 HG01099.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.150-8462dupT | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79720428 | |||||
| chr5:79720428
|
A | ATT | 11 | a0009c0009t0001g0014a0009c0009t0001g0264a0009c0009t0001g0357others(8): Show | 11 | HG00741.hp1 HG02109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.150-8463_150-8462d others(4): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79720428 | |||||
| chr5:79720428
|
AT | A | 8 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0335others(5): Show | 8 | HG00558.hp2 HG01255.hp2 HG01993.hp1 others(5): Show |
intron_variant | MODIFIER | c.150-8462delT | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79720428 | |||||
| chr5:79720822
|
TC | T | 8 | a0005c0005t0001g0216a0005c0005t0001g0217a0005c0005t0001g0218others(5): Show | 8 | HG01257.hp2 HG01258.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.150-8089delC | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79720822 | |||||
| chr5:79720848
|
A | G | 90 | a0001c0033t0001g0139a0002c0002t0001g0043a0002c0002t0001g0127others(87): Show | 91 | HG00438.hp1 HG00741.hp2 HG01074.hp1 others(88): Show |
intron_variant | MODIFIER | c.150-8067A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79720848 | ||||||
| chr5:79720889
|
G | A | 1 | a0007c0008t0001g0168 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.150-8026G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79720889 | ||||||
| chr5:79721073
|
T | C | 1 | a0073c0076t0001g0101 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.150-7842T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79721073 | ||||||
| chr5:79721080
|
A | G | 3 | a0031c0046t0001g0186a0031c0046t0002g0182a0054c0108t0001g0187 | 3 | HG02055.hp1 HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.150-7835A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79721080 | ||||||
| chr5:79721088
|
C | T | 2 | a0039c0030t0002g0269a0039c0030t0002g0314 | 2 | HG02257.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.150-7827C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79721088 | ||||||
| chr5:79721362
|
G | GA | 5 | a0015c0038t0002g0312a0015c0038t0004g0260a0015c0073t0015g0343others(2): Show | 5 | HG02257.hp2 HG02723.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.150-7548dupA | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79721362 | |||||
| chr5:79721413
|
G | A | 1 | a0030c0096t0001g0274 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.150-7502G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79721413 | ||||||
| chr5:79721553
|
A | G | 1 | a0015c0038t0004g0260 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.150-7362A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79721553 | ||||||
| chr5:79721554
|
A | C | 102 | a0001c0013t0006g0140a0002c0106t0007g0029a0003c0003t0001g0232others(99): Show | 102 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.150-7361A>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79721554 | ||||||
| chr5:79721555
|
G | A | 1 | a0006c0004t0001g0059 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.150-7360G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79721555 | ||||||
| chr5:79721970
|
T | C | 1 | a0044c0093t0001g0276 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.150-6945T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79721970 | ||||||
| chr5:79722070
|
G | A | 130 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(127): Show | 130 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(127): Show |
intron_variant | MODIFIER | c.150-6845G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79722070 | ||||||
| chr5:79722084
|
T | C | 3 | a0031c0046t0001g0186a0031c0046t0002g0182a0054c0108t0001g0187 | 3 | HG02055.hp1 HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.150-6831T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79722084 | ||||||
| chr5:79722212
|
A | G | 39 | a0003c0003t0001g0015a0003c0003t0001g0046a0003c0003t0001g0099others(36): Show | 40 | HG00099.hp1 HG00323.hp1 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.150-6703A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79722212 | ||||||
| chr5:79722359
|
G | A | 33 | a0004c0006t0001g0048a0004c0006t0001g0078a0004c0006t0001g0256others(30): Show | 33 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.150-6556G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79722359 | ||||||
| chr5:79722608
|
C | T | 2 | a0015c0032t0007g0027a0015c0032t0007g0034 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.150-6307C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79722608 | ||||||
| chr5:79722676
|
C | CA | 72 | a0001c0001t0001g0135a0001c0001t0001g0171a0001c0001t0001g0212others(69): Show | 72 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.150-6217dupA | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79722676 | |||||
| chr5:79722676
|
CA | C | 51 | a0001c0056t0001g0086a0001c0058t0002g0339a0002c0002t0001g0147others(48): Show | 51 | HG00438.hp1 HG00642.hp2 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.150-6217delA | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79722676 | |||||
| chr5:79722676
|
CAA | C | 67 | a0002c0002t0002g0229a0002c0106t0007g0029a0004c0006t0001g0048others(64): Show | 67 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.150-6218_150-6217d others(4): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79722676 | |||||
| chr5:79722676
|
CAAA | C | 14 | a0009c0009t0001g0014a0009c0009t0001g0264a0009c0009t0001g0322others(11): Show | 14 | HG00741.hp1 HG02258.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.150-6219_150-6217d others(5): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79722676 | |||||
| chr5:79722713
|
A | G | 130 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(127): Show | 130 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(127): Show |
intron_variant | MODIFIER | c.150-6202A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79722713 | ||||||
| chr5:79722716
|
G | A | 1 | a0001c0001t0002g0329 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.150-6199G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79722716 | ||||||
| chr5:79722795
|
G | A | 130 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(127): Show | 130 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(127): Show |
intron_variant | MODIFIER | c.150-6120G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79722795 | ||||||
| chr5:79722904
|
AAAAAC | A | 84 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(81): Show | 84 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.150-6006_150-6002d others(7): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79722904 | |||||
| chr5:79722911
|
A | T | 1 | a0001c0001t0001g0241 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.150-6004A>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79722911 | ||||||
| chr5:79723085
|
C | T | 1 | a0037c0036t0001g0103 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.150-5830C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79723085 | ||||||
| chr5:79723149
|
A | C | 1 | a0048c0107t0004g0317 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.150-5766A>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79723149 | ||||||
| chr5:79723162
|
C | T | 3 | a0020c0025t0001g0278a0020c0025t0001g0309a0020c0025t0001g0344 | 3 | HG03195.hp2 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.150-5753C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79723162 | ||||||
| chr5:79723268
|
A | G | 130 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(127): Show | 130 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(127): Show |
intron_variant | MODIFIER | c.150-5647A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79723268 | ||||||
| chr5:79723277
|
A | G | 50 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(47): Show | 50 | HG00438.hp1 HG00741.hp2 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.150-5638A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79723277 | ||||||
| chr5:79723332
|
G | C | 2 | a0005c0085t0001g0223a0024c0084t0001g0172 | 2 | HG03834.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.150-5583G>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79723332 | ||||||
| chr5:79723407
|
T | C | 128 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(125): Show | 128 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.150-5508T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79723407 | ||||||
| chr5:79723443
|
G | GA | 215 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0064others(212): Show | 215 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(212): Show |
intron_variant | MODIFIER | c.150-5456dupA | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79723443 | |||||
| chr5:79723443
|
G | GAA | 18 | a0001c0001t0001g0097a0001c0001t0001g0150a0001c0001t0002g0076others(15): Show | 18 | HG01109.hp1 HG01167.hp2 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.150-5457_150-5456d others(4): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79723443 | |||||
| chr5:79723443
|
GA | G | 39 | a0003c0003t0001g0015a0003c0003t0001g0046a0003c0003t0001g0099others(36): Show | 40 | HG00099.hp1 HG00323.hp1 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.150-5456delA | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79723443 | |||||
| chr5:79723459
|
A | G | 1 | a0039c0030t0002g0269 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.150-5456A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79723459 | ||||||
| chr5:79723513
|
T | A | 130 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(127): Show | 130 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(127): Show |
intron_variant | MODIFIER | c.150-5402T>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79723513 | ||||||
| chr5:79723570
|
T | TG | 226 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(223): Show | 227 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.150-5343dupG | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79723570 | |||||
| chr5:79723743
|
C | T | 5 | a0015c0038t0002g0312a0015c0038t0004g0260a0015c0073t0015g0343others(2): Show | 5 | HG02257.hp2 HG02723.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.150-5172C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79723743 | ||||||
| chr5:79723748
|
C | T | 3 | a0031c0046t0001g0186a0031c0046t0002g0182a0054c0108t0001g0187 | 3 | HG02055.hp1 HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.150-5167C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79723748 | ||||||
| chr5:79723749
|
G | A | 1 | a0030c0096t0001g0274 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.150-5166G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79723749 | ||||||
| chr5:79723752
|
T | A | 84 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(81): Show | 84 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.150-5163T>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79723752 | ||||||
| chr5:79723776
|
G | GA | 137 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(134): Show | 137 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(134): Show |
intron_variant | MODIFIER | c.150-5127dupA | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79723776 | |||||
| chr5:79723830
|
T | C | 83 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(80): Show | 83 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.150-5085T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79723830 | ||||||
| chr5:79723892
|
T | C | 84 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(81): Show | 84 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.150-5023T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79723892 | ||||||
| chr5:79723899
|
T | C | 1 | a0030c0095t0003g0271 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.150-5016T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79723899 | ||||||
| chr5:79723909
|
G | A | 47 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(44): Show | 47 | HG00438.hp1 HG00741.hp2 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.150-5006G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79723909 | ||||||
| chr5:79723952
|
T | C | 1 | a0072c0071t0002g0191 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.150-4963T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79723952 | ||||||
| chr5:79724051
|
C | T | 84 | a0003c0003t0001g0015a0003c0003t0001g0046a0003c0003t0001g0099others(81): Show | 85 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.150-4864C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79724051 | ||||||
| chr5:79724141
|
T | A | 215 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(212): Show | 216 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.150-4774T>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79724141 | ||||||
| chr5:79724149
|
C | G | 2 | a0006c0004t0001g0193a0078c0080t0002g0118 | 2 | HG00558.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.150-4766C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79724149 | ||||||
| chr5:79724155
|
TA | T | 81 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(78): Show | 81 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.150-4748delA | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79724155 | |||||
| chr5:79724210
|
T | G | 130 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(127): Show | 130 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(127): Show |
intron_variant | MODIFIER | c.150-4705T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79724210 | ||||||
| chr5:79724279
|
G | T | 84 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(81): Show | 84 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.150-4636G>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79724279 | ||||||
| chr5:79724421
|
G | T | 1 | a0050c0104t0003g0272 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.150-4494G>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79724421 | ||||||
| chr5:79724514
|
G | A | 3 | a0031c0046t0001g0186a0031c0046t0002g0182a0054c0108t0001g0187 | 3 | HG02055.hp1 HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.150-4401G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79724514 | ||||||
| chr5:79724603
|
A | G | 130 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(127): Show | 130 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(127): Show |
intron_variant | MODIFIER | c.150-4312A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79724603 | ||||||
| chr5:79724666
|
A | G | 1 | a0003c0003t0001g0153 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.150-4249A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79724666 | ||||||
| chr5:79724801
|
T | C | 84 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(81): Show | 84 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.150-4114T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79724801 | ||||||
| chr5:79724893
|
T | A | 1 | a0026c0028t0002g0075 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.150-4022T>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79724893 | ||||||
| chr5:79725141
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.150-3774C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79725141 | ||||||
| chr5:79725215
|
A | G | 222 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(219): Show | 223 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.150-3700A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79725215 | ||||||
| chr5:79725228
|
G | A | 2 | a0049c0103t0003g0328a0050c0104t0003g0272 | 2 | HG02615.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.150-3687G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79725228 | ||||||
| chr5:79725454
|
G | A | 85 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(82): Show | 85 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.150-3461G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79725454 | ||||||
| chr5:79725551
|
C | T | 2 | a0029c0044t0004g0026a0029c0044t0012g0036 | 2 | HG03225.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.150-3364C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79725551 | ||||||
| chr5:79725640
|
C | T | 330 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0064others(327): Show | 331 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(328): Show |
intron_variant | MODIFIER | c.150-3275C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79725640 | ||||||
| chr5:79725671
|
G | A | 1 | a0004c0014t0002g0119 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.150-3244G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79725671 | ||||||
| chr5:79725700
|
C | T | 50 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(47): Show | 50 | HG00438.hp1 HG00741.hp2 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.150-3215C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79725700 | ||||||
| chr5:79725727
|
A | C | 1 | a0066c0057t0003g0219 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.150-3188A>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79725727 | ||||||
| chr5:79725729
|
C | G | 31 | a0003c0003t0001g0046a0003c0003t0001g0099a0003c0003t0001g0153others(28): Show | 31 | HG00099.hp1 HG00323.hp1 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.150-3186C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79725729 | ||||||
| chr5:79725862
|
A | C | 87 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(84): Show | 87 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.150-3053A>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79725862 | ||||||
| chr5:79725944
|
AAG | A | 47 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(44): Show | 47 | HG00438.hp1 HG00741.hp2 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.150-2969_150-2968d others(4): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79725944 | |||||
| chr5:79726067
|
A | G | 34 | a0002c0106t0007g0029a0004c0006t0001g0048a0004c0006t0001g0078others(31): Show | 34 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.150-2848A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79726067 | ||||||
| chr5:79726079
|
G | A | 47 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(44): Show | 47 | HG00438.hp1 HG00741.hp2 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.150-2836G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79726079 | ||||||
| chr5:79726146
|
C | T | 6 | a0005c0005t0001g0216a0005c0005t0001g0217a0005c0005t0001g0218others(3): Show | 6 | HG01257.hp2 HG01258.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.150-2769C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79726146 | ||||||
| chr5:79726198
|
T | C | 1 | a0002c0002t0001g0127 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.150-2717T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79726198 | ||||||
| chr5:79726232
|
A | G | 1 | a0072c0071t0002g0191 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.150-2683A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79726232 | ||||||
| chr5:79726378
|
G | A | 1 | a0057c0111t0002g0321 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.150-2537G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79726378 | ||||||
| chr5:79726379
|
G | A | 1 | a0001c0001t0001g0241 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.150-2536G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79726379 | ||||||
| chr5:79726434
|
A | G | 132 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(129): Show | 132 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.150-2481A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79726434 | ||||||
| chr5:79726595
|
G | A | 6 | a0019c0024t0001g0181a0019c0024t0001g0184a0019c0024t0017g0355others(3): Show | 6 | HG01167.hp2 HG02809.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.150-2320G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79726595 | ||||||
| chr5:79726624
|
G | A | 3 | a0006c0004t0001g0201a0006c0004t0001g0225a0006c0004t0002g0199 | 3 | NA18942.hp1 NA18952.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.150-2291G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79726624 | ||||||
| chr5:79726770
|
T | G | 1 | a0002c0106t0007g0029 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.150-2145T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79726770 | ||||||
| chr5:79726792
|
C | T | 7 | a0003c0003t0001g0015a0003c0003t0005g0020a0003c0003t0008g0018others(4): Show | 8 | HG02630.hp2 HG02895.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.150-2123C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79726792 | ||||||
| chr5:79726827
|
C | G | 2 | a0031c0046t0001g0186a0031c0046t0002g0182 | 2 | HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.150-2088C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79726827 | ||||||
| chr5:79726888
|
C | G | 131 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(128): Show | 131 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.150-2027C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79726888 | ||||||
| chr5:79726909
|
A | AT | 52 | a0001c0001t0001g0246a0001c0001t0002g0175a0001c0013t0001g0154others(49): Show | 53 | HG00099.hp1 HG00408.hp1 HG01099.hp1 others(50): Show |
intron_variant | MODIFIER | c.150-1983dupT | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79726909 | |||||
| chr5:79726909
|
A | ATT | 7 | a0002c0020t0002g0293a0003c0003t0003g0081a0003c0069t0002g0310others(4): Show | 7 | HG00323.hp1 HG01109.hp2 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.150-1984_150-1983d others(4): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79726909 | |||||
| chr5:79726909
|
A | ATTTTTT | 6 | a0007c0097t0002g0347a0019c0024t0001g0181a0019c0024t0001g0184others(3): Show | 6 | HG02683.hp2 HG02809.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.150-1988_150-1983d others(8): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79726909 | |||||
| chr5:79726909
|
A | ATTTTTTT | 19 | a0007c0008t0001g0138a0007c0008t0001g0311a0007c0008t0001g0340others(16): Show | 19 | HG02258.hp2 HG02280.hp1 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.150-1989_150-1983d others(9): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79726909 | |||||
| chr5:79726909
|
A | ATTTTTTT others(1): Show |
8 | a0007c0008t0001g0168a0007c0008t0011g0341a0013c0016t0001g0180others(5): Show | 8 | HG01074.hp1 HG01167.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.150-1990_150-1983d others(10): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79726909 | |||||
| chr5:79726909
|
A | ATTTTTTT others(2): Show |
7 | a0009c0009t0001g0264a0009c0009t0001g0346a0009c0009t0001g0357others(4): Show | 7 | HG02258.hp1 HG02451.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.150-1991_150-1983d others(11): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79726909 | |||||
| chr5:79726909
|
A | ATTTTTTT others(3): Show |
5 | a0004c0006t0001g0256a0009c0009t0001g0323a0009c0009t0002g0265others(2): Show | 5 | HG00741.hp1 HG03041.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.150-1992_150-1983d others(12): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79726909 | |||||
| chr5:79726909
|
A | ATTTTTTT others(4): Show |
12 | a0004c0006t0002g0249a0004c0006t0003g0236a0004c0006t0003g0258others(9): Show | 12 | HG00438.hp2 HG02165.hp1 HG03688.hp2 others(9): Show |
intron_variant | MODIFIER | c.150-1993_150-1983d others(13): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79726909 | |||||
| chr5:79726909
|
A | ATTTTTTT others(5): Show |
10 | a0004c0006t0001g0048a0004c0006t0002g0144a0004c0006t0002g0210others(7): Show | 10 | HG00544.hp2 HG00621.hp1 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.150-1994_150-1983d others(14): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79726909 | |||||
| chr5:79726909
|
A | ATTTTTTT others(6): Show |
4 | a0004c0006t0002g0055a0004c0011t0002g0049a0004c0011t0003g0349others(1): Show | 4 | NA18952.hp2 NA18983.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.150-1995_150-1983d others(15): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79726909 | |||||
| chr5:79726909
|
A | ATTTTTTT others(7): Show |
2 | a0004c0006t0001g0078a0009c0009t0001g0014 | 2 | HG04199.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.150-1996_150-1983d others(16): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79726909 | |||||
| chr5:79726909
|
A | ATTTTTTT others(8): Show |
1 | a0009c0009t0001g0322 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.150-1997_150-1983d others(17): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79726909 | |||||
| chr5:79726909
|
A | ATTTTTTT others(9): Show |
3 | a0002c0002t0001g0147a0004c0006t0001g0304a0004c0011t0001g0233 | 3 | NA18945.hp1 NA18945.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.150-1998_150-1983d others(18): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79726909 | |||||
| chr5:79726909
|
A | ATTTTTTT others(10): Show |
25 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0129others(22): Show | 25 | HG00438.hp1 HG00741.hp2 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.150-1999_150-1983d others(19): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79726909 | |||||
| chr5:79726909
|
A | ATTTTTTT others(11): Show |
16 | a0002c0002t0001g0222a0002c0002t0001g0253a0002c0002t0001g0324others(13): Show | 16 | HG01175.hp2 HG01361.hp1 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.150-2000_150-1983d others(20): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79726909 | |||||
| chr5:79726909
|
A | ATTTTTTT others(12): Show |
1 | a0002c0002t0002g0334 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.150-2001_150-1983d others(21): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79726909 | |||||
| chr5:79726909
|
A | ATTTTTTT others(13): Show |
1 | a0031c0046t0001g0186 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.150-2002_150-1983d others(22): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79726909 | |||||
| chr5:79726909
|
A | ATTTTTTT others(14): Show |
3 | a0002c0002t0001g0131a0031c0046t0002g0182a0054c0108t0001g0187 | 3 | HG02055.hp1 HG03471.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.150-2003_150-1983d others(23): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79726909 | |||||
| chr5:79726909
|
A | ATTTTTTT others(15): Show |
2 | a0002c0002t0001g0127a0002c0002t0001g0128 | 2 | NA19066.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.150-2004_150-1983d others(24): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79726909 | |||||
| chr5:79726909
|
A | ATTTTTTT others(16): Show |
1 | a0002c0106t0007g0029 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.150-2005_150-1983d others(25): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79726909 | |||||
| chr5:79726909
|
AT | A | 6 | a0005c0005t0002g0214a0005c0085t0001g0223a0012c0015t0004g0033others(3): Show | 6 | HG01433.hp1 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.150-1983delT | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79726909 | |||||
| chr5:79726977
|
G | A | 1 | a0006c0004t0001g0152 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.150-1938G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79726977 | ||||||
| chr5:79727002
|
G | A | 1 | a0005c0077t0001g0221 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.150-1913G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79727002 | ||||||
| chr5:79727040
|
T | C | 131 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(128): Show | 131 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.150-1875T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79727040 | ||||||
| chr5:79727062
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.150-1853C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79727062 | ||||||
| chr5:79727081
|
A | G | 1 | a0012c0015t0016g0318 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.150-1834A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79727081 | ||||||
| chr5:79727097
|
G | T | 4 | a0023c0022t0001g0185a0023c0022t0008g0016a0023c0022t0008g0025others(1): Show | 4 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.150-1818G>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79727097 | ||||||
| chr5:79727168
|
G | A | 14 | a0013c0016t0001g0180a0013c0016t0003g0307a0013c0016t0004g0019others(11): Show | 14 | HG01167.hp2 HG02055.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.150-1747G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79727168 | ||||||
| chr5:79727196
|
G | A | 1 | a0060c0051t0001g0298 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.150-1719G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79727196 | ||||||
| chr5:79727343
|
A | G | 1 | a0006c0004t0001g0059 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.150-1572A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79727343 | ||||||
| chr5:79727435
|
G | A | 9 | a0009c0009t0001g0014a0009c0009t0001g0264a0009c0009t0001g0322others(6): Show | 9 | HG00741.hp1 HG02258.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.150-1480G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79727435 | ||||||
| chr5:79727621
|
G | A | 2 | a0001c0001t0001g0125a0001c0001t0002g0126 | 2 | NA18946.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.150-1294G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79727621 | ||||||
| chr5:79727622
|
C | T | 131 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(128): Show | 131 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.150-1293C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79727622 | ||||||
| chr5:79727676
|
A | G | 131 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(128): Show | 131 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.150-1239A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79727676 | ||||||
| chr5:79727939
|
C | T | 131 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(128): Show | 131 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.150-976C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79727939 | ||||||
| chr5:79728059
|
T | A | 131 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(128): Show | 131 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.150-856T>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79728059 | ||||||
| chr5:79728066
|
G | A | 85 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(82): Show | 85 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.150-849G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79728066 | ||||||
| chr5:79728076
|
T | C | 85 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(82): Show | 85 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.150-839T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79728076 | ||||||
| chr5:79728088
|
T | G | 1 | a0001c0001t0002g0056 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.150-827T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79728088 | ||||||
| chr5:79728213
|
C | T | 1 | a0044c0093t0001g0276 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.150-702C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79728213 | ||||||
| chr5:79728331
|
TTC | T | 84 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(81): Show | 84 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.150-582_150-581del others(2): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 79728331 | |||||
| chr5:79728332
|
TC | T | 47 | a0004c0011t0001g0160a0007c0008t0001g0138a0007c0008t0001g0168others(44): Show | 47 | HG00741.hp1 HG01074.hp1 HG01167.hp2 others(44): Show |
intron_variant | MODIFIER | c.150-582delC | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79728332 | ||||||
| chr5:79728428
|
G | C | 4 | a0002c0002t0002g0208a0002c0002t0002g0209a0002c0002t0002g0229others(1): Show | 4 | NA18949.hp2 NA18955.hp1 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.150-487G>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79728428 | ||||||
| chr5:79728621
|
A | G | 131 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(128): Show | 131 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.150-294A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79728621 | ||||||
| chr5:79728653
|
T | C | 1 | a0013c0016t0004g0019 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.150-262T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79728653 | ||||||
| chr5:79728899
|
T | C | 131 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(128): Show | 131 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.150-16T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79728899 | ||||||
| chr5:79728911
|
A | G | 219 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(216): Show | 220 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(217): Show |
splice_region_variant&intron_variant | LOW | c.150-4A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 1/12 | chr5 | 79728911 | ||||||
| chr5:79739665
|
A | AAC | 13 | a0007c0008t0001g0311a0012c0015t0004g0022a0012c0015t0004g0023others(10): Show | 13 | HG02109.hp2 HG02486.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.10638+282_10638+28 others(6): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 79739665 | |||||
| chr5:79739702
|
G | T | 1 | a0001c0056t0001g0086 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.10638+299G>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | chr5 | 79739702 | ||||||
| chr5:79739748
|
C | T | 46 | a0005c0005t0001g0039a0005c0005t0001g0045a0005c0005t0001g0216others(43): Show | 46 | HG00408.hp1 HG00558.hp1 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.10638+345C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | chr5 | 79739748 | ||||||
| chr5:79739907
|
C | T | 1 | a0007c0008t0001g0138 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.10638+504C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | chr5 | 79739907 | ||||||
| chr5:79739908
|
A | G | 180 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(177): Show | 180 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(177): Show |
intron_variant | MODIFIER | c.10638+505A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | chr5 | 79739908 | ||||||
| chr5:79739956
|
C | G | 1 | a0039c0030t0002g0314 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.10638+553C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | chr5 | 79739956 | ||||||
| chr5:79740225
|
C | T | 49 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(46): Show | 49 | HG00438.hp1 HG00438.hp2 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.10638+822C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | chr5 | 79740225 | ||||||
| chr5:79740443
|
A | G | 1 | a0050c0104t0003g0272 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.10638+1040A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | chr5 | 79740443 | ||||||
| chr5:79740628
|
T | C | 9 | a0009c0009t0001g0014a0009c0009t0001g0264a0009c0009t0001g0322others(6): Show | 9 | HG00741.hp1 HG02258.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.10638+1225T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | chr5 | 79740628 | ||||||
| chr5:79740862
|
T | G | 1 | a0002c0106t0007g0029 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.10638+1459T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | chr5 | 79740862 | ||||||
| chr5:79740873
|
G | T | 1 | a0002c0106t0007g0029 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.10638+1470G>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | chr5 | 79740873 | ||||||
| chr5:79740944
|
C | G | 2 | a0004c0006t0001g0304a0004c0006t0002g0303 | 2 | NA18945.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.10638+1541C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | chr5 | 79740944 | ||||||
| chr5:79740957
|
C | T | 3 | a0019c0024t0001g0181a0019c0024t0017g0355a0050c0104t0003g0272 | 3 | HG02809.hp2 HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.10638+1554C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | chr5 | 79740957 | ||||||
| chr5:79740977
|
C | T | 1 | a0005c0005t0002g0170 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.10638+1574C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | chr5 | 79740977 | ||||||
| chr5:79740979
|
C | A | 48 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(45): Show | 48 | HG00438.hp1 HG00741.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.10638+1576C>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | chr5 | 79740979 | ||||||
| chr5:79741069
|
G | A | 32 | a0004c0006t0001g0048a0004c0006t0001g0078a0004c0006t0001g0256others(29): Show | 32 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.10638+1666G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | chr5 | 79741069 | ||||||
| chr5:79741116
|
C | T | 48 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(45): Show | 48 | HG00438.hp1 HG00741.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.10638+1713C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | chr5 | 79741116 | ||||||
| chr5:79741448
|
T | A | 212 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(209): Show | 213 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.10638+2045T>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | chr5 | 79741448 | ||||||
| chr5:79741521
|
GA | G | 6 | a0001c0001t0001g0136a0001c0001t0001g0285a0001c0013t0003g0087others(3): Show | 6 | HG01081.hp2 HG01109.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.10638+2119delA | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | chr5 | 79741521 | ||||||
| chr5:79741531
|
C | T | 1 | a0003c0003t0001g0192 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.10638+2128C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | chr5 | 79741531 | ||||||
| chr5:79741661
|
C | T | 217 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(214): Show | 218 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.10639-2166C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | chr5 | 79741661 | ||||||
| chr5:79741662
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.10639-2165G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | chr5 | 79741662 | ||||||
| chr5:79741748
|
TTATCTC | T | 48 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(45): Show | 48 | HG00438.hp1 HG00741.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.10639-2075_10639-2 others(12): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 79741748 | |||||
| chr5:79741810
|
T | G | 1 | a0002c0002t0002g0054 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.10639-2017T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | chr5 | 79741810 | ||||||
| chr5:79741875
|
T | C | 3 | a0019c0024t0001g0181a0019c0024t0017g0355a0050c0104t0003g0272 | 3 | HG02809.hp2 HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.10639-1952T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | chr5 | 79741875 | ||||||
| chr5:79741920
|
T | A | 1 | a0006c0004t0001g0161 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.10639-1907T>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | chr5 | 79741920 | ||||||
| chr5:79742019
|
C | T | 47 | a0005c0005t0001g0039a0005c0005t0001g0045a0005c0005t0001g0216others(44): Show | 47 | HG00408.hp1 HG00558.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.10639-1808C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | chr5 | 79742019 | ||||||
| chr5:79742048
|
C | CTCT | 3 | a0010c0010t0001g0262a0015c0038t0004g0260a0069c0062t0001g0088 | 3 | HG02647.hp2 HG02698.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.10639-1729_10639-1 others(9): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 79742048 | |||||
| chr5:79742048
|
C | CTCTTCTT others(5): Show |
1 | a0039c0030t0002g0269 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.10639-1738_10639-1 others(18): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 79742048 | |||||
| chr5:79742048
|
C | CTCTTCTT others(8): Show |
1 | a0039c0030t0002g0314 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.10639-1741_10639-1 others(21): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 79742048 | |||||
| chr5:79742048
|
C | CTCTTCTT others(17): Show |
1 | a0015c0038t0002g0312 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.10639-1750_10639-1 others(30): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 79742048 | |||||
| chr5:79742048
|
CTCT | C | 24 | a0001c0001t0001g0077a0001c0001t0001g0097a0001c0001t0001g0157others(21): Show | 24 | HG00544.hp1 HG01081.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.10639-1729_10639-1 others(9): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 79742048 | |||||
| chr5:79742048
|
CTCTTCT | C | 51 | a0001c0001t0001g0012a0001c0001t0001g0064a0001c0001t0001g0065others(48): Show | 51 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.10639-1732_10639-1 others(12): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 79742048 | |||||
| chr5:79742048
|
CTCTTCTT others(2): Show |
C | 31 | a0001c0001t0001g0063a0001c0001t0001g0102a0001c0001t0001g0125others(28): Show | 31 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.10639-1735_10639-1 others(15): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 79742048 | |||||
| chr5:79742048
|
CTCTTCTT others(5): Show |
C | 12 | a0001c0001t0001g0013a0001c0001t0001g0150a0001c0001t0002g0332others(9): Show | 12 | HG00673.hp1 HG02015.hp1 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.10639-1738_10639-1 others(18): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 79742048 | |||||
| chr5:79742048
|
CTCTTCTT others(8): Show |
C | 4 | a0031c0046t0001g0186a0031c0046t0002g0182a0054c0108t0001g0187others(1): Show | 4 | HG02055.hp1 HG03471.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.10639-1741_10639-1 others(21): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 79742048 | |||||
| chr5:79742048
|
CTCTTCTT others(11): Show |
C | 7 | a0001c0001t0001g0240a0012c0015t0004g0022a0012c0015t0004g0023others(4): Show | 7 | HG02109.hp2 HG02523.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.10639-1744_10639-1 others(24): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 79742048 | |||||
| chr5:79742048
|
CTCTTCTT others(14): Show |
C | 2 | a0012c0015t0004g0028a0015c0032t0007g0034 | 2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.10639-1747_10639-1 others(27): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 79742048 | |||||
| chr5:79742048
|
CTCTTCTT others(20): Show |
C | 3 | a0019c0024t0001g0181a0019c0024t0017g0355a0050c0104t0003g0272 | 3 | HG02809.hp2 HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.10639-1753_10639-1 others(33): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 79742048 | |||||
| chr5:79742048
|
CTCTTCTT others(23): Show |
C | 107 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(104): Show | 107 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.10639-1756_10639-1 others(36): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 79742048 | |||||
| chr5:79742048
|
CTCTTCTT others(26): Show |
C | 3 | a0020c0025t0001g0278a0020c0025t0001g0309a0042c0029t0001g0108 | 3 | NA18522.hp2 NA18906.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.10639-1759_10639-1 others(39): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 79742048 | |||||
| chr5:79742051
|
T | C | 99 | a0003c0003t0001g0015a0003c0003t0001g0046a0003c0003t0001g0099others(96): Show | 100 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.10639-1776T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | chr5 | 79742051 | ||||||
| chr5:79742069
|
TTC | T | 97 | a0003c0003t0001g0015a0003c0003t0001g0046a0003c0003t0001g0099others(94): Show | 98 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.10639-1756_10639-1 others(8): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 79742069 | |||||
| chr5:79742077
|
CTTCTTCT others(27): Show |
C | 1 | a0075c0086t0001g0250 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.10639-1748_10639-1 others(40): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 79742077 | |||||
| chr5:79742080
|
CTTCTTCT others(24): Show |
C | 97 | a0003c0003t0001g0015a0003c0003t0001g0046a0003c0003t0001g0099others(94): Show | 98 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.10639-1745_10639-1 others(37): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 79742080 | |||||
| chr5:79742081
|
T | C | 107 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(104): Show | 107 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.10639-1746T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | chr5 | 79742081 | ||||||
| chr5:79742083
|
CTTCTTCT others(21): Show |
C | 1 | a0030c0095t0003g0271 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.10639-1742_10639-1 others(34): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 79742083 | |||||
| chr5:79742084
|
T | C | 3 | a0020c0025t0001g0278a0020c0025t0001g0309a0042c0029t0001g0108 | 3 | NA18522.hp2 NA18906.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.10639-1743T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | chr5 | 79742084 | ||||||
| chr5:79742113
|
C | T | 48 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(45): Show | 48 | HG00438.hp1 HG00741.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.10639-1714C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | chr5 | 79742113 | ||||||
| chr5:79742248
|
G | A | 4 | a0002c0002t0001g0253a0002c0002t0001g0324a0002c0002t0002g0071others(1): Show | 4 | HG00741.hp2 HG01175.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.10639-1579G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | chr5 | 79742248 | ||||||
| chr5:79742251
|
G | A | 15 | a0007c0008t0001g0138a0007c0008t0001g0168a0007c0008t0001g0311others(12): Show | 15 | HG01074.hp1 HG02145.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.10639-1576G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | chr5 | 79742251 | ||||||
| chr5:79742261
|
T | C | 3 | a0019c0024t0001g0181a0019c0024t0017g0355a0050c0104t0003g0272 | 3 | HG02809.hp2 HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.10639-1566T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | chr5 | 79742261 | ||||||
| chr5:79742291
|
A | G | 3 | a0019c0024t0001g0181a0019c0024t0017g0355a0050c0104t0003g0272 | 3 | HG02809.hp2 HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.10639-1536A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | chr5 | 79742291 | ||||||
| chr5:79742630
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.10639-1197C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | chr5 | 79742630 | ||||||
| chr5:79742746
|
C | T | 92 | a0003c0003t0001g0015a0003c0003t0001g0046a0003c0003t0001g0099others(89): Show | 93 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.10639-1081C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | chr5 | 79742746 | ||||||
| chr5:79742760
|
GA | G | 140 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(137): Show | 141 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.10639-1055delA | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 79742760 | |||||
| chr5:79742762
|
A | G | 137 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(134): Show | 138 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.10639-1065A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | chr5 | 79742762 | ||||||
| chr5:79742963
|
A | C | 17 | a0009c0009t0001g0014a0009c0009t0001g0264a0009c0009t0001g0322others(14): Show | 17 | HG00741.hp1 HG02257.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.10639-864A>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | chr5 | 79742963 | ||||||
| chr5:79743049
|
G | A | 1 | a0049c0103t0003g0328 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.10639-778G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | chr5 | 79743049 | ||||||
| chr5:79743104
|
T | C | 47 | a0005c0005t0001g0039a0005c0005t0001g0045a0005c0005t0001g0216others(44): Show | 47 | HG00408.hp1 HG00558.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.10639-723T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | chr5 | 79743104 | ||||||
| chr5:79743114
|
T | G | 3 | a0025c0023t0001g0106a0025c0023t0001g0234a0025c0023t0002g0203 | 3 | HG02015.hp2 NA18995.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.10639-713T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | chr5 | 79743114 | ||||||
| chr5:79743226
|
C | T | 48 | a0004c0011t0001g0206a0005c0005t0001g0039a0005c0005t0001g0045others(45): Show | 48 | HG00408.hp1 HG00558.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.10639-601C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | chr5 | 79743226 | ||||||
| chr5:79743265
|
G | A | 28 | a0007c0008t0001g0138a0007c0008t0001g0168a0007c0008t0001g0311others(25): Show | 28 | HG01074.hp1 HG01167.hp2 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.10639-562G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | chr5 | 79743265 | ||||||
| chr5:79743342
|
C | T | 1 | a0048c0107t0004g0317 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.10639-485C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | chr5 | 79743342 | ||||||
| chr5:79743372
|
A | G | 179 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(176): Show | 180 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.10639-455A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | chr5 | 79743372 | ||||||
| chr5:79743492
|
T | C | 32 | a0004c0006t0001g0048a0004c0006t0001g0078a0004c0006t0001g0256others(29): Show | 32 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.10639-335T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | chr5 | 79743492 | ||||||
| chr5:79743547
|
A | G | 2 | a0048c0107t0004g0317a0072c0071t0002g0191 | 2 | HG01243.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.10639-280A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | chr5 | 79743547 | ||||||
| chr5:79743576
|
CT | C | 52 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(49): Show | 52 | HG00438.hp1 HG00741.hp2 HG01074.hp2 others(49): Show |
intron_variant | MODIFIER | c.10639-248delT | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 79743576 | |||||
| chr5:79743597
|
T | C | 52 | a0003c0003t0001g0015a0003c0003t0001g0046a0003c0003t0001g0099others(49): Show | 53 | HG00099.hp1 HG00323.hp1 HG01109.hp2 others(50): Show |
intron_variant | MODIFIER | c.10639-230T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | chr5 | 79743597 | ||||||
| chr5:79743678
|
T | A | 1 | a0026c0049t0006g0073 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.10639-149T>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | chr5 | 79743678 | ||||||
| chr5:79743732
|
G | A | 1 | a0001c0001t0001g0239 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.10639-95G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 2/12 | chr5 | 79743732 | ||||||
| chr5:79744005
|
T | C | 49 | a0003c0003t0001g0015a0003c0003t0001g0046a0003c0003t0001g0099others(46): Show | 50 | HG00099.hp1 HG00323.hp1 HG01109.hp2 others(47): Show |
intron_variant | MODIFIER | c.10734+83T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 3/12 | chr5 | 79744005 | ||||||
| chr5:79744048
|
G | A | 1 | a0002c0002t0002g0066 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.10734+126G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 3/12 | chr5 | 79744048 | ||||||
| chr5:79744084
|
C | G | 1 | a0062c0072t0002g0255 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.10734+162C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 3/12 | chr5 | 79744084 | ||||||
| chr5:79744160
|
C | T | 6 | a0012c0015t0004g0022a0012c0015t0004g0023a0012c0015t0004g0028others(3): Show | 6 | HG02109.hp2 HG02559.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.10734+238C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 3/12 | chr5 | 79744160 | ||||||
| chr5:79744385
|
A | G | 1 | a0058c0092t0003g0263 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.10734+463A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 3/12 | chr5 | 79744385 | ||||||
| chr5:79744403
|
C | A | 2 | a0001c0001t0001g0212a0069c0062t0001g0088 | 2 | HG01106.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.10734+481C>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 3/12 | chr5 | 79744403 | ||||||
| chr5:79744447
|
G | A | 1 | a0006c0004t0002g0123 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.10734+525G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 3/12 | chr5 | 79744447 | ||||||
| chr5:79744601
|
C | G | 1 | a0058c0092t0003g0263 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.10735-621C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 3/12 | chr5 | 79744601 | ||||||
| chr5:79744611
|
GT | G | 6 | a0012c0015t0004g0022a0012c0015t0004g0023a0012c0015t0004g0028others(3): Show | 6 | HG02109.hp2 HG02559.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.10735-609delT | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 79744611 | |||||
| chr5:79744644
|
G | A | 1 | a0016c0018t0001g0176 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.10735-578G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 3/12 | chr5 | 79744644 | ||||||
| chr5:79744656
|
C | T | 12 | a0009c0009t0001g0014a0009c0009t0001g0264a0009c0009t0001g0322others(9): Show | 12 | HG00741.hp1 HG02258.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.10735-566C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 3/12 | chr5 | 79744656 | ||||||
| chr5:79744723
|
G | A | 1 | a0001c0058t0002g0339 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.10735-499G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 3/12 | chr5 | 79744723 | ||||||
| chr5:79744734
|
G | A | 1 | a0050c0104t0003g0272 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.10735-488G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 3/12 | chr5 | 79744734 | ||||||
| chr5:79744755
|
G | A | 1 | a0001c0013t0002g0041 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.10735-467G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 3/12 | chr5 | 79744755 | ||||||
| chr5:79744786
|
T | A | 1 | a0058c0092t0003g0263 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.10735-436T>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 3/12 | chr5 | 79744786 | ||||||
| chr5:79744836
|
T | G | 6 | a0012c0015t0004g0022a0012c0015t0004g0023a0012c0015t0004g0028others(3): Show | 6 | HG02109.hp2 HG02559.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.10735-386T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 3/12 | chr5 | 79744836 | ||||||
| chr5:79744967
|
A | G | 1 | a0058c0092t0003g0263 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.10735-255A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 3/12 | chr5 | 79744967 | ||||||
| chr5:79745149
|
G | A | 2 | a0038c0035t0001g0092a0038c0035t0001g0093 | 2 | HG03942.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.10735-73G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 3/12 | chr5 | 79745149 | ||||||
| chr5:79745154
|
C | CA | 74 | a0001c0001t0001g0007a0001c0001t0001g0102a0001c0001t0001g0150others(71): Show | 75 | HG00099.hp1 HG00323.hp1 HG00673.hp2 others(72): Show |
intron_variant | MODIFIER | c.10735-54dupA | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 79745154 | |||||
| chr5:79745154
|
CAA | C | 6 | a0012c0015t0004g0022a0012c0015t0004g0023a0012c0015t0004g0028others(3): Show | 6 | HG02109.hp2 HG02559.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.10735-55_10735-54d others(4): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 79745154 | |||||
| chr5:79745676
|
G | A | 52 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(49): Show | 52 | HG00438.hp1 HG00741.hp2 HG01074.hp2 others(49): Show |
intron_variant | MODIFIER | c.10968+221G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 4/12 | chr5 | 79745676 | ||||||
| chr5:79745710
|
G | A | 1 | a0001c0055t0001g0116 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.10968+255G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 4/12 | chr5 | 79745710 | ||||||
| chr5:79746084
|
A | C | 2 | a0006c0004t0001g0161a0006c0004t0001g0162 | 2 | NA18943.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.10968+629A>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 4/12 | chr5 | 79746084 | ||||||
| chr5:79746094
|
A | C | 5 | a0015c0038t0002g0312a0015c0038t0004g0260a0015c0073t0015g0343others(2): Show | 5 | HG02257.hp2 HG02723.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.10968+639A>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 4/12 | chr5 | 79746094 | ||||||
| chr5:79746241
|
C | G | 30 | a0004c0006t0001g0048a0004c0006t0001g0078a0004c0006t0001g0256others(27): Show | 30 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.10968+786C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 4/12 | chr5 | 79746241 | ||||||
| chr5:79746289
|
G | A | 15 | a0007c0008t0001g0138a0007c0008t0001g0168a0007c0008t0001g0311others(12): Show | 15 | HG01074.hp1 HG02145.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.10969-802G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 4/12 | chr5 | 79746289 | ||||||
| chr5:79746342
|
A | C | 6 | a0012c0015t0004g0022a0012c0015t0004g0023a0012c0015t0004g0028others(3): Show | 6 | HG02109.hp2 HG02559.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.10969-749A>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 4/12 | chr5 | 79746342 | ||||||
| chr5:79746517
|
T | A | 54 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(51): Show | 54 | HG00438.hp1 HG00741.hp2 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.10969-574T>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 4/12 | chr5 | 79746517 | ||||||
| chr5:79746547
|
T | TA | 97 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0136others(94): Show | 97 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.10969-521dupA | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr5 | 79746547 | |||||
| chr5:79746547
|
T | TAA | 70 | a0001c0001t0002g0137a0002c0002t0001g0008a0002c0002t0001g0043others(67): Show | 70 | HG00741.hp1 HG00741.hp2 HG01074.hp1 others(67): Show |
intron_variant | MODIFIER | c.10969-522_10969-52 others(6): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr5 | 79746547 | |||||
| chr5:79746547
|
T | TAAA | 13 | a0002c0002t0001g0147a0002c0002t0002g0054a0002c0002t0002g0229others(10): Show | 13 | HG00438.hp1 HG01243.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.10969-523_10969-52 others(7): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr5 | 79746547 | |||||
| chr5:79746547
|
TA | T | 41 | a0001c0001t0001g0166a0001c0001t0001g0281a0001c0001t0001g0333others(38): Show | 42 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.10969-521delA | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr5 | 79746547 | |||||
| chr5:79746547
|
TAAA | T | 6 | a0012c0015t0004g0022a0012c0015t0004g0023a0012c0015t0004g0028others(3): Show | 6 | HG02109.hp2 HG02559.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.10969-523_10969-52 others(7): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr5 | 79746547 | |||||
| chr5:79746890
|
C | T | 1 | a0007c0008t0011g0341 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.10969-201C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 4/12 | chr5 | 79746890 | ||||||
| chr5:79746891
|
G | A | 1 | a0010c0010t0002g0245 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.10969-200G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 4/12 | chr5 | 79746891 | ||||||
| chr5:79746973
|
G | A | 1 | a0002c0002t0001g0222 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.10969-118G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 4/12 | chr5 | 79746973 | ||||||
| chr5:79747203
|
C | T | 1 | a0040c0040t0003g0325 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.10991+90C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | chr5 | 79747203 | ||||||
| chr5:79747397
|
T | G | 2 | a0048c0107t0004g0317a0072c0071t0002g0191 | 2 | HG01243.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.10991+284T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | chr5 | 79747397 | ||||||
| chr5:79747450
|
T | G | 1 | a0003c0034t0009g0320 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.10991+337T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | chr5 | 79747450 | ||||||
| chr5:79747945
|
A | G | 2 | a0010c0010t0001g0291a0063c0064t0002g0282 | 2 | HG03942.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.10991+832A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | chr5 | 79747945 | ||||||
| chr5:79748012
|
A | G | 55 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(52): Show | 55 | HG00438.hp1 HG00438.hp2 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.10991+899A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | chr5 | 79748012 | ||||||
| chr5:79748095
|
C | T | 1 | a0030c0096t0001g0274 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.10991+982C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | chr5 | 79748095 | ||||||
| chr5:79748303
|
A | G | 16 | a0007c0008t0001g0138a0007c0008t0001g0168a0007c0008t0001g0311others(13): Show | 16 | HG01074.hp1 HG02145.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.10991+1190A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | chr5 | 79748303 | ||||||
| chr5:79748419
|
G | A | 16 | a0007c0008t0001g0138a0007c0008t0001g0168a0007c0008t0001g0311others(13): Show | 16 | HG01074.hp1 HG02145.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.10991+1306G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | chr5 | 79748419 | ||||||
| chr5:79748516
|
TCTAC | T | 49 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(46): Show | 49 | HG00438.hp1 HG00438.hp2 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.10991+1407_10991+1 others(10): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr5 | 79748516 | |||||
| chr5:79748520
|
C | CCTAT | 12 | a0001c0001t0001g0296a0001c0001t0001g0333a0001c0001t0002g0076others(9): Show | 12 | HG01069.hp2 HG01257.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.10991+1436_10991+1 others(10): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr5 | 79748520 | |||||
| chr5:79748520
|
C | CCTATCTA others(1): Show |
5 | a0001c0001t0001g0063a0011c0012t0002g0350a0023c0022t0001g0185others(2): Show | 5 | HG01081.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.10991+1432_10991+1 others(14): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr5 | 79748520 | |||||
| chr5:79748520
|
C | CCTATCTA others(5): Show |
1 | a0030c0096t0001g0274 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.10991+1428_10991+1 others(18): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr5 | 79748520 | |||||
| chr5:79748520
|
C | T | 7 | a0002c0002t0002g0130a0002c0106t0007g0029a0014c0027t0001g0052others(4): Show | 7 | HG02809.hp2 HG03041.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.10991+1407C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | chr5 | 79748520 | ||||||
| chr5:79748520
|
CCTAT | C | 170 | a0001c0001t0001g0064a0001c0001t0001g0095a0001c0001t0001g0102others(167): Show | 171 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.10991+1436_10991+1 others(10): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr5 | 79748520 | |||||
| chr5:79748520
|
CCTATCTA others(1): Show |
C | 16 | a0007c0008t0001g0138a0007c0008t0001g0168a0007c0008t0001g0311others(13): Show | 16 | HG01074.hp1 HG02145.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.10991+1432_10991+1 others(14): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr5 | 79748520 | |||||
| chr5:79748520
|
CCTATCTA others(13): Show |
C | 6 | a0012c0015t0004g0022a0012c0015t0004g0023a0012c0015t0004g0028others(3): Show | 6 | HG02109.hp2 HG02559.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.10991+1420_10991+1 others(26): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr5 | 79748520 | |||||
| chr5:79748524
|
T | C | 3 | a0002c0002t0002g0130a0014c0027t0001g0052a0024c0087t0001g0010 | 3 | NA18939.hp1 NA18939.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.10991+1411T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | chr5 | 79748524 | ||||||
| chr5:79748528
|
T | C | 53 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(50): Show | 53 | HG00438.hp1 HG00438.hp2 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.10991+1415T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | chr5 | 79748528 | ||||||
| chr5:79748553
|
A | C | 2 | a0001c0001t0001g0166a0001c0001t0002g0338 | 2 | HG01255.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.10991+1440A>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | chr5 | 79748553 | ||||||
| chr5:79748662
|
C | T | 1 | a0060c0051t0001g0298 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.10991+1549C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | chr5 | 79748662 | ||||||
| chr5:79748735
|
A | G | 16 | a0007c0008t0001g0138a0007c0008t0001g0168a0007c0008t0001g0311others(13): Show | 16 | HG01074.hp1 HG02145.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.10991+1622A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | chr5 | 79748735 | ||||||
| chr5:79748743
|
C | T | 1 | a0050c0104t0003g0272 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.10991+1630C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | chr5 | 79748743 | ||||||
| chr5:79748744
|
A | ATGTT | 6 | a0012c0015t0004g0022a0012c0015t0004g0023a0012c0015t0004g0028others(3): Show | 6 | HG02109.hp2 HG02559.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.10991+1632_10991+1 others(10): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr5 | 79748744 | |||||
| chr5:79749132
|
G | T | 1 | a0048c0107t0004g0317 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.10991+2019G>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | chr5 | 79749132 | ||||||
| chr5:79749276
|
C | A | 1 | a0065c0060t0003g0083 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.10991+2163C>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | chr5 | 79749276 | ||||||
| chr5:79749278
|
G | A | 146 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(143): Show | 147 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.10991+2165G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | chr5 | 79749278 | ||||||
| chr5:79749325
|
G | A | 1 | a0003c0003t0001g0153 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.10991+2212G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | chr5 | 79749325 | ||||||
| chr5:79749653
|
A | G | 1 | a0050c0104t0003g0272 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.10991+2540A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | chr5 | 79749653 | ||||||
| chr5:79749665
|
A | G | 1 | a0062c0072t0002g0255 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.10991+2552A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | chr5 | 79749665 | ||||||
| chr5:79749707
|
C | T | 2 | a0023c0022t0008g0016a0023c0022t0008g0025 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.10991+2594C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | chr5 | 79749707 | ||||||
| chr5:79749896
|
T | C | 1 | a0005c0005t0001g0218 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.10992-2780T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | chr5 | 79749896 | ||||||
| chr5:79749975
|
T | G | 1 | a0049c0103t0003g0328 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.10992-2701T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | chr5 | 79749975 | ||||||
| chr5:79750010
|
A | AT | 47 | a0002c0002t0006g0120a0002c0002t0006g0164a0006c0004t0001g0079others(44): Show | 47 | HG00408.hp1 HG00558.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.10992-2652dupT | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr5 | 79750010 | |||||
| chr5:79750010
|
AT | A | 8 | a0002c0002t0002g0334a0012c0015t0004g0022a0012c0015t0004g0023others(5): Show | 8 | HG02109.hp2 HG02451.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.10992-2652delT | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr5 | 79750010 | |||||
| chr5:79750010
|
ATT | A | 91 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0127others(88): Show | 91 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.10992-2653_10992-2 others(8): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr5 | 79750010 | |||||
| chr5:79750010
|
ATTT | A | 50 | a0003c0003t0001g0015a0003c0003t0001g0046a0003c0003t0001g0099others(47): Show | 51 | HG00099.hp1 HG00323.hp1 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.10992-2654_10992-2 others(9): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr5 | 79750010 | |||||
| chr5:79750033
|
C | T | 1 | a0029c0044t0004g0026 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.10992-2643C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | chr5 | 79750033 | ||||||
| chr5:79750056
|
A | G | 16 | a0007c0008t0001g0138a0007c0008t0001g0168a0007c0008t0001g0311others(13): Show | 16 | HG01074.hp1 HG02145.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.10992-2620A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | chr5 | 79750056 | ||||||
| chr5:79750362
|
T | C | 25 | a0007c0008t0001g0168a0007c0008t0001g0311a0007c0008t0001g0340others(22): Show | 25 | HG01074.hp1 HG01167.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.10992-2314T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | chr5 | 79750362 | ||||||
| chr5:79750487
|
A | T | 1 | a0048c0107t0004g0317 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.10992-2189A>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | chr5 | 79750487 | ||||||
| chr5:79750568
|
T | C | 3 | a0001c0001t0002g0056a0007c0097t0002g0347a0073c0076t0001g0101 | 3 | HG02683.hp1 HG02683.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.10992-2108T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | chr5 | 79750568 | ||||||
| chr5:79750592
|
T | C | 35 | a0001c0001t0001g0065a0003c0003t0001g0015a0003c0003t0001g0046others(32): Show | 36 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.10992-2084T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | chr5 | 79750592 | ||||||
| chr5:79750715
|
G | A | 1 | a0072c0071t0002g0191 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.10992-1961G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | chr5 | 79750715 | ||||||
| chr5:79750835
|
C | G | 30 | a0001c0013t0003g0205a0003c0069t0002g0310a0004c0006t0001g0048others(27): Show | 30 | HG00544.hp2 HG00741.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.10992-1841C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | chr5 | 79750835 | ||||||
| chr5:79751049
|
G | A | 1 | a0030c0096t0001g0274 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.10992-1627G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | chr5 | 79751049 | ||||||
| chr5:79751067
|
C | G | 10 | a0013c0016t0003g0307a0013c0016t0007g0024a0015c0032t0007g0027others(7): Show | 10 | HG01167.hp2 HG02451.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.10992-1609C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | chr5 | 79751067 | ||||||
| chr5:79751104
|
T | G | 1 | a0033c0039t0001g0003 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.10992-1572T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | chr5 | 79751104 | ||||||
| chr5:79751113
|
C | G | 1 | a0075c0086t0001g0250 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.10992-1563C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | chr5 | 79751113 | ||||||
| chr5:79751227
|
G | C | 2 | a0001c0001t0001g0296a0017c0019t0001g0280 | 2 | HG00642.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.10992-1449G>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | chr5 | 79751227 | ||||||
| chr5:79751335
|
A | G | 20 | a0003c0003t0001g0015a0003c0003t0005g0020a0003c0003t0008g0018others(17): Show | 21 | HG02055.hp2 HG02257.hp2 HG02615.hp2 others(18): Show |
intron_variant | MODIFIER | c.10992-1341A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | chr5 | 79751335 | ||||||
| chr5:79751442
|
C | T | 1 | a0059c0075t0001g0327 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.10992-1234C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | chr5 | 79751442 | ||||||
| chr5:79751584
|
T | G | 122 | a0001c0001t0001g0065a0001c0001t0001g0097a0001c0001t0001g0136others(119): Show | 123 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.10992-1092T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | chr5 | 79751584 | ||||||
| chr5:79751802
|
AG | A | 52 | a0001c0013t0002g0041a0001c0013t0002g0204a0001c0013t0006g0140others(49): Show | 52 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.10992-873delG | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | chr5 | 79751802 | ||||||
| chr5:79751842
|
G | A | 29 | a0001c0013t0003g0205a0003c0069t0002g0310a0004c0006t0001g0048others(26): Show | 29 | HG00544.hp2 HG00741.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.10992-834G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | chr5 | 79751842 | ||||||
| chr5:79751903
|
C | G | 29 | a0001c0013t0003g0205a0003c0069t0002g0310a0004c0006t0001g0048others(26): Show | 29 | HG00544.hp2 HG00741.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.10992-773C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | chr5 | 79751903 | ||||||
| chr5:79751921
|
A | G | 124 | a0001c0013t0001g0154a0001c0013t0002g0041a0001c0013t0002g0204others(121): Show | 124 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.10992-755A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | chr5 | 79751921 | ||||||
| chr5:79751994
|
T | G | 29 | a0001c0013t0003g0205a0003c0069t0002g0310a0004c0006t0001g0048others(26): Show | 29 | HG00544.hp2 HG00741.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.10992-682T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | chr5 | 79751994 | ||||||
| chr5:79752068
|
G | A | 29 | a0001c0013t0003g0205a0003c0069t0002g0310a0004c0006t0001g0048others(26): Show | 29 | HG00544.hp2 HG00741.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.10992-608G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | chr5 | 79752068 | ||||||
| chr5:79752257
|
G | A | 84 | a0001c0013t0002g0041a0001c0013t0002g0204a0001c0013t0003g0205others(81): Show | 84 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.10992-419G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | chr5 | 79752257 | ||||||
| chr5:79752403
|
T | C | 1 | a0008c0007t0002g0006 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.10992-273T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | chr5 | 79752403 | ||||||
| chr5:79752488
|
C | T | 11 | a0003c0069t0002g0310a0009c0009t0001g0014a0009c0009t0001g0264others(8): Show | 11 | HG00741.hp1 HG01109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.10992-188C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | chr5 | 79752488 | ||||||
| chr5:79752548
|
T | C | 1 | a0016c0018t0002g0146 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.10992-128T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | chr5 | 79752548 | ||||||
| chr5:79752612
|
T | A | 1 | a0050c0104t0003g0272 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.10992-64T>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | chr5 | 79752612 | ||||||
| chr5:79752659
|
G | C | 1 | a0060c0051t0001g0298 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.10992-17G>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | chr5 | 79752659 | ||||||
| chr5:79752673
|
T | C | 1 | a0048c0107t0004g0317 | 1 | HG02486.hp2 | splice_region_variant&intron_variant | LOW | c.10992-3T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 5/12 | chr5 | 79752673 | ||||||
| chr5:79752917
|
T | G | 1 | a0001c0001t0001g0065 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.11110+123T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79752917 | ||||||
| chr5:79753190
|
A | G | 6 | a0003c0003t0001g0015a0003c0003t0005g0020a0003c0003t0008g0018others(3): Show | 6 | HG02630.hp2 HG02895.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.11110+396A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79753190 | ||||||
| chr5:79753201
|
C | T | 2 | a0028c0043t0001g0183a0028c0043t0001g0267 | 2 | HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.11110+407C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79753201 | ||||||
| chr5:79753257
|
A | G | 6 | a0001c0001t0001g0125a0001c0001t0001g0174a0001c0001t0001g0198others(3): Show | 6 | HG02135.hp1 NA18946.hp1 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.11110+463A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79753257 | ||||||
| chr5:79753302
|
A | G | 3 | a0017c0019t0001g0096a0056c0112t0001g0072a0062c0072t0002g0255 | 3 | HG01106.hp1 HG01978.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.11110+508A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79753302 | ||||||
| chr5:79753448
|
G | A | 145 | a0001c0001t0001g0063a0001c0001t0001g0212a0001c0013t0002g0041others(142): Show | 146 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.11110+654G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79753448 | ||||||
| chr5:79753587
|
A | AAAC | 36 | a0001c0001t0001g0157a0001c0001t0001g0163a0001c0001t0001g0212others(33): Show | 36 | HG00408.hp1 HG00609.hp2 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.11110+811_11110+81 others(7): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr5 | 79753587 | |||||
| chr5:79753605
|
C | A | 1 | a0058c0092t0003g0263 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.11110+811C>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79753605 | ||||||
| chr5:79753605
|
C | CAAA | 6 | a0012c0015t0004g0022a0012c0015t0004g0023a0012c0015t0004g0028others(3): Show | 6 | HG02109.hp2 HG02559.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.11110+815_11110+81 others(7): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr5 | 79753605 | |||||
| chr5:79753666
|
A | T | 273 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0063others(270): Show | 274 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(271): Show |
intron_variant | MODIFIER | c.11110+872A>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79753666 | ||||||
| chr5:79753718
|
T | A | 29 | a0001c0001t0001g0065a0001c0001t0001g0235a0001c0001t0002g0197others(26): Show | 29 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.11110+924T>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79753718 | ||||||
| chr5:79753719
|
A | C | 29 | a0001c0001t0001g0065a0001c0001t0001g0235a0001c0001t0002g0197others(26): Show | 29 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.11110+925A>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79753719 | ||||||
| chr5:79753721
|
G | C | 29 | a0001c0001t0001g0065a0001c0001t0001g0235a0001c0001t0002g0197others(26): Show | 29 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.11110+927G>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79753721 | ||||||
| chr5:79753724
|
T | TG | 29 | a0001c0001t0001g0065a0001c0001t0001g0235a0001c0001t0002g0197others(26): Show | 29 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.11110+930_11110+93 others(5): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79753724 | ||||||
| chr5:79753725
|
A | T | 29 | a0001c0001t0001g0065a0001c0001t0001g0235a0001c0001t0002g0197others(26): Show | 29 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.11110+931A>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79753725 | ||||||
| chr5:79753727
|
A | C | 29 | a0001c0001t0001g0065a0001c0001t0001g0235a0001c0001t0002g0197others(26): Show | 29 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.11110+933A>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79753727 | ||||||
| chr5:79753730
|
G | C | 29 | a0001c0001t0001g0065a0001c0001t0001g0235a0001c0001t0002g0197others(26): Show | 29 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.11110+936G>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79753730 | ||||||
| chr5:79753731
|
A | T | 29 | a0001c0001t0001g0065a0001c0001t0001g0235a0001c0001t0002g0197others(26): Show | 29 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.11110+937A>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79753731 | ||||||
| chr5:79753732
|
C | G | 29 | a0001c0001t0001g0065a0001c0001t0001g0235a0001c0001t0002g0197others(26): Show | 29 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.11110+938C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79753732 | ||||||
| chr5:79753737
|
A | T | 29 | a0001c0001t0001g0065a0001c0001t0001g0235a0001c0001t0002g0197others(26): Show | 29 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.11110+943A>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79753737 | ||||||
| chr5:79753739
|
A | C | 29 | a0001c0001t0001g0065a0001c0001t0001g0235a0001c0001t0002g0197others(26): Show | 29 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.11110+945A>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79753739 | ||||||
| chr5:79753741
|
C | T | 29 | a0001c0001t0001g0065a0001c0001t0001g0235a0001c0001t0002g0197others(26): Show | 29 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.11110+947C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79753741 | ||||||
| chr5:79753742
|
A | G | 29 | a0001c0001t0001g0065a0001c0001t0001g0235a0001c0001t0002g0197others(26): Show | 29 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.11110+948A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79753742 | ||||||
| chr5:79753743
|
C | T | 29 | a0001c0001t0001g0065a0001c0001t0001g0235a0001c0001t0002g0197others(26): Show | 29 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.11110+949C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79753743 | ||||||
| chr5:79753744
|
G | GT | 29 | a0001c0001t0001g0065a0001c0001t0001g0235a0001c0001t0002g0197others(26): Show | 29 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.11110+950_11110+95 others(5): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79753744 | ||||||
| chr5:79753746
|
C | CTGTTTGA others(422): Show |
29 | a0001c0001t0001g0065a0001c0001t0001g0235a0001c0001t0002g0197others(26): Show | 29 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.11110+952_11110+95 others(433): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79753746 | ||||||
| chr5:79753818
|
A | G | 29 | a0001c0001t0002g0056a0003c0003t0001g0015a0003c0003t0005g0020others(26): Show | 29 | HG01074.hp1 HG01243.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.11110+1024A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79753818 | ||||||
| chr5:79754061
|
T | G | 2 | a0005c0005t0001g0270a0048c0107t0004g0317 | 2 | HG01243.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.11110+1267T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79754061 | ||||||
| chr5:79754092
|
T | C | 1 | a0012c0015t0004g0022 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.11110+1298T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79754092 | ||||||
| chr5:79754108
|
A | G | 1 | a0003c0003t0013g0090 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.11110+1314A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79754108 | ||||||
| chr5:79754149
|
G | A | 6 | a0019c0024t0001g0181a0019c0024t0001g0184a0019c0024t0017g0355others(3): Show | 6 | HG02630.hp1 HG02809.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.11110+1355G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79754149 | ||||||
| chr5:79754212
|
G | A | 1 | a0049c0103t0003g0328 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.11110+1418G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79754212 | ||||||
| chr5:79754239
|
T | A | 1 | a0002c0002t0001g0147 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.11110+1445T>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79754239 | ||||||
| chr5:79754327
|
G | T | 6 | a0015c0038t0002g0312a0015c0038t0004g0260a0039c0030t0002g0269others(3): Show | 6 | HG02257.hp2 HG02723.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.11110+1533G>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79754327 | ||||||
| chr5:79754635
|
G | A | 2 | a0002c0002t0002g0143a0002c0002t0002g0148 | 2 | NA19000.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.11110+1841G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79754635 | ||||||
| chr5:79754649
|
AT | A | 44 | a0001c0001t0001g0065a0001c0001t0001g0235a0001c0001t0002g0197others(41): Show | 45 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.11110+1865delT | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr5 | 79754649 | |||||
| chr5:79754710
|
T | C | 1 | a0035c0037t0001g0177 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.11110+1916T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79754710 | ||||||
| chr5:79754772
|
C | A | 1 | a0048c0107t0004g0317 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.11110+1978C>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79754772 | ||||||
| chr5:79754860
|
A | G | 26 | a0001c0001t0002g0056a0003c0003t0001g0153a0003c0003t0001g0178others(23): Show | 26 | HG01074.hp1 HG01243.hp1 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.11110+2066A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79754860 | ||||||
| chr5:79754924
|
T | C | 67 | a0001c0001t0001g0163a0001c0001t0001g0212a0001c0001t0001g0240others(64): Show | 67 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.11110+2130T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79754924 | ||||||
| chr5:79754973
|
C | T | 1 | a0035c0037t0011g0319 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.11110+2179C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79754973 | ||||||
| chr5:79755002
|
T | C | 61 | a0001c0001t0001g0163a0001c0001t0001g0212a0001c0001t0001g0240others(58): Show | 61 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.11110+2208T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79755002 | ||||||
| chr5:79755037
|
C | G | 58 | a0001c0001t0001g0063a0001c0013t0002g0041a0001c0013t0002g0204others(55): Show | 58 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.11110+2243C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79755037 | ||||||
| chr5:79755090
|
C | T | 1 | a0003c0003t0005g0035 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.11110+2296C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79755090 | ||||||
| chr5:79755185
|
T | G | 2 | a0001c0001t0010g0084a0001c0001t0010g0085 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.11110+2391T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79755185 | ||||||
| chr5:79755281
|
G | A | 4 | a0015c0032t0007g0027a0015c0032t0007g0034a0030c0095t0003g0271others(1): Show | 4 | HG02451.hp1 HG02451.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.11110+2487G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79755281 | ||||||
| chr5:79755326
|
G | A | 10 | a0001c0013t0003g0205a0004c0006t0001g0048a0004c0006t0002g0210others(7): Show | 10 | HG02027.hp1 HG02451.hp2 NA18945.hp1 others(7): Show |
intron_variant | MODIFIER | c.11110+2532G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79755326 | ||||||
| chr5:79755583
|
G | A | 12 | a0003c0069t0002g0310a0009c0009t0001g0014a0009c0009t0001g0264others(9): Show | 13 | HG00741.hp1 HG01109.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.11110+2789G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79755583 | ||||||
| chr5:79755587
|
A | G | 60 | a0001c0001t0001g0163a0001c0001t0001g0212a0001c0001t0001g0240others(57): Show | 60 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.11110+2793A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79755587 | ||||||
| chr5:79755647
|
G | A | 1 | a0005c0079t0003g0082 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.11110+2853G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79755647 | ||||||
| chr5:79755917
|
C | T | 1 | a0072c0071t0002g0191 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.11111-2836C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79755917 | ||||||
| chr5:79756011
|
A | C | 1 | a0004c0014t0002g0158 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.11111-2742A>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79756011 | ||||||
| chr5:79756143
|
T | C | 172 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0163others(169): Show | 173 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.11111-2610T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79756143 | ||||||
| chr5:79756234
|
G | C | 1 | a0003c0003t0002g0058 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.11111-2519G>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79756234 | ||||||
| chr5:79756367
|
CCT | C | 59 | a0001c0001t0001g0063a0001c0013t0002g0041a0001c0013t0002g0204others(56): Show | 59 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.11111-2383_11111-2 others(8): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr5 | 79756367 | |||||
| chr5:79756603
|
T | G | 8 | a0001c0058t0002g0339a0004c0014t0002g0040a0004c0014t0002g0119others(5): Show | 8 | HG00544.hp2 HG02165.hp1 HG03688.hp2 others(5): Show |
intron_variant | MODIFIER | c.11111-2150T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79756603 | ||||||
| chr5:79756709
|
C | A | 1 | a0013c0016t0004g0019 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.11111-2044C>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79756709 | ||||||
| chr5:79756877
|
C | A | 209 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0163others(206): Show | 210 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.11111-1876C>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79756877 | ||||||
| chr5:79756967
|
G | A | 1 | a0035c0037t0011g0319 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.11111-1786G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79756967 | ||||||
| chr5:79757044
|
A | C | 19 | a0001c0001t0002g0056a0003c0003t0001g0153a0003c0003t0001g0178others(16): Show | 19 | HG01074.hp1 HG02145.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.11111-1709A>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79757044 | ||||||
| chr5:79757056
|
G | A | 62 | a0001c0001t0001g0163a0001c0001t0001g0212a0001c0001t0001g0240others(59): Show | 62 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.11111-1697G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79757056 | ||||||
| chr5:79757120
|
A | G | 1 | a0005c0005t0001g0270 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.11111-1633A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79757120 | ||||||
| chr5:79757194
|
C | CA | 108 | a0001c0001t0001g0007a0001c0001t0001g0063a0001c0001t0001g0065others(105): Show | 109 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.11111-1542dupA | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr5 | 79757194 | |||||
| chr5:79757194
|
C | CAA | 16 | a0001c0013t0002g0041a0001c0013t0002g0204a0002c0002t0001g0043others(13): Show | 16 | HG00597.hp1 HG02015.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.11111-1543_11111-1 others(8): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr5 | 79757194 | |||||
| chr5:79757194
|
CA | C | 6 | a0001c0001t0001g0125a0001c0001t0001g0174a0001c0001t0002g0126others(3): Show | 6 | HG02965.hp1 NA18946.hp1 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.11111-1542delA | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr5 | 79757194 | |||||
| chr5:79757331
|
A | G | 8 | a0013c0016t0003g0307a0013c0016t0007g0024a0023c0022t0001g0185others(5): Show | 8 | HG01167.hp2 HG02486.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.11111-1422A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79757331 | ||||||
| chr5:79757351
|
C | T | 1 | a0006c0004t0001g0201 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.11111-1402C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79757351 | ||||||
| chr5:79757514
|
A | G | 1 | a0005c0005t0001g0270 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.11111-1239A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79757514 | ||||||
| chr5:79757553
|
G | A | 1 | a0005c0085t0001g0223 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.11111-1200G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79757553 | ||||||
| chr5:79757640
|
T | C | 1 | a0003c0003t0002g0070 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.11111-1113T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79757640 | ||||||
| chr5:79757711
|
C | T | 177 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0163others(174): Show | 178 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.11111-1042C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79757711 | ||||||
| chr5:79757755
|
A | G | 1 | a0059c0075t0001g0327 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.11111-998A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79757755 | ||||||
| chr5:79757802
|
G | C | 1 | a0001c0001t0002g0294 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.11111-951G>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79757802 | ||||||
| chr5:79757928
|
T | C | 3 | a0023c0022t0008g0016a0023c0022t0008g0025a0081c0091t0005g0038 | 3 | HG02572.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.11111-825T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79757928 | ||||||
| chr5:79758063
|
C | G | 18 | a0001c0001t0001g0007a0001c0001t0001g0135a0001c0001t0001g0165others(15): Show | 18 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.11111-690C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79758063 | ||||||
| chr5:79758115
|
A | G | 7 | a0002c0106t0007g0029a0015c0038t0002g0312a0015c0038t0004g0260others(4): Show | 7 | HG02257.hp2 HG02723.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.11111-638A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79758115 | ||||||
| chr5:79758159
|
G | T | 2 | a0007c0008t0002g0179a0007c0008t0004g0032 | 2 | HG02572.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.11111-594G>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79758159 | ||||||
| chr5:79758217
|
A | C | 5 | a0009c0009t0001g0346a0031c0046t0001g0186a0031c0046t0002g0182others(2): Show | 5 | HG02055.hp1 HG02486.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.11111-536A>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79758217 | ||||||
| chr5:79758237
|
T | C | 26 | a0001c0001t0002g0056a0003c0003t0001g0153a0003c0003t0001g0178others(23): Show | 26 | HG01074.hp1 HG01243.hp1 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.11111-516T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79758237 | ||||||
| chr5:79758405
|
G | A | 1 | a0049c0103t0003g0328 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.11111-348G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79758405 | ||||||
| chr5:79758487
|
G | A | 1 | a0078c0080t0002g0118 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.11111-266G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | chr5 | 79758487 | ||||||
| chr5:79758645
|
CTATG | C | 60 | a0001c0001t0001g0163a0001c0001t0001g0212a0001c0001t0001g0240others(57): Show | 60 | HG00408.hp1 HG00408.hp2 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.11111-104_11111-10 others(8): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr5 | 79758645 | |||||
| chr5:79759408
|
C | A | 5 | a0009c0009t0001g0346a0031c0046t0001g0186a0031c0046t0002g0182others(2): Show | 5 | HG02055.hp1 HG02486.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.11260+506C>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 7/12 | chr5 | 79759408 | ||||||
| chr5:79759433
|
C | T | 4 | a0009c0009t0001g0346a0031c0046t0001g0186a0031c0046t0002g0182others(1): Show | 4 | HG02055.hp1 HG03471.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.11260+531C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 7/12 | chr5 | 79759433 | ||||||
| chr5:79759561
|
A | G | 10 | a0003c0003t0001g0015a0003c0003t0005g0020a0003c0003t0008g0018others(7): Show | 10 | HG02055.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.11260+659A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 7/12 | chr5 | 79759561 | ||||||
| chr5:79759739
|
A | G | 1 | a0049c0103t0003g0328 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.11260+837A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 7/12 | chr5 | 79759739 | ||||||
| chr5:79759872
|
T | C | 1 | a0001c0001t0001g0285 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.11260+970T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 7/12 | chr5 | 79759872 | ||||||
| chr5:79760025
|
G | A | 1 | a0004c0006t0001g0048 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.11260+1123G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 7/12 | chr5 | 79760025 | ||||||
| chr5:79760168
|
A | AAAG | 109 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0235others(106): Show | 110 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.11260+1267_11260+1 others(9): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr5 | 79760168 | |||||
| chr5:79760170
|
T | A | 109 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0235others(106): Show | 110 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.11260+1268T>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 7/12 | chr5 | 79760170 | ||||||
| chr5:79760172
|
G | A | 116 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0235others(113): Show | 117 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.11260+1270G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 7/12 | chr5 | 79760172 | ||||||
| chr5:79760188
|
CT | C | 204 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0163others(201): Show | 205 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.11260+1301delT | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr5 | 79760188 | |||||
| chr5:79760436
|
A | T | 5 | a0015c0038t0002g0312a0015c0038t0004g0260a0039c0030t0002g0269others(2): Show | 5 | HG02257.hp2 HG02723.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.11261-1375A>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 7/12 | chr5 | 79760436 | ||||||
| chr5:79760507
|
T | C | 59 | a0001c0001t0001g0063a0001c0013t0002g0041a0001c0013t0002g0204others(56): Show | 59 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.11261-1304T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 7/12 | chr5 | 79760507 | ||||||
| chr5:79760518
|
A | G | 59 | a0001c0001t0001g0063a0001c0013t0002g0041a0001c0013t0002g0204others(56): Show | 59 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.11261-1293A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 7/12 | chr5 | 79760518 | ||||||
| chr5:79761022
|
G | C | 2 | a0013c0016t0003g0307a0013c0016t0007g0024 | 2 | HG02486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.11261-789G>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 7/12 | chr5 | 79761022 | ||||||
| chr5:79761023
|
G | C | 22 | a0001c0001t0001g0102a0001c0001t0001g0124a0001c0001t0001g0125others(19): Show | 22 | HG00597.hp2 HG00673.hp1 HG02080.hp2 others(19): Show |
intron_variant | MODIFIER | c.11261-788G>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 7/12 | chr5 | 79761023 | ||||||
| chr5:79761208
|
T | C | 1 | a0033c0039t0001g0003 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.11261-603T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 7/12 | chr5 | 79761208 | ||||||
| chr5:79761226
|
A | G | 1 | a0001c0013t0002g0041 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.11261-585A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 7/12 | chr5 | 79761226 | ||||||
| chr5:79761564
|
T | A | 1 | a0080c0090t0002g0094 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.11261-247T>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 7/12 | chr5 | 79761564 | ||||||
| chr5:79761654
|
C | T | 115 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0235others(112): Show | 116 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.11261-157C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 7/12 | chr5 | 79761654 | ||||||
| chr5:79761663
|
T | C | 1 | a0002c0002t0002g0112 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.11261-148T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 7/12 | chr5 | 79761663 | ||||||
| chr5:79761687
|
G | A | 5 | a0015c0038t0002g0312a0015c0038t0004g0260a0039c0030t0002g0269others(2): Show | 5 | HG02257.hp2 HG02723.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.11261-124G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 7/12 | chr5 | 79761687 | ||||||
| chr5:79761762
|
T | C | 10 | a0003c0003t0001g0015a0003c0003t0005g0020a0003c0003t0008g0018others(7): Show | 10 | HG02055.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.11261-49T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 7/12 | chr5 | 79761762 | ||||||
| chr5:79761809
|
A | G | 1 | a0005c0005t0001g0353 | 1 | NA18997.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.11261-2A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 7/12 | chr5 | 79761809 | ||||||
| chr5:79762126
|
C | T | 3 | a0009c0009t0001g0014a0009c0009t0001g0322a0015c0073t0015g0343 | 3 | HG02886.hp1 HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.11407+169C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 8/12 | chr5 | 79762126 | ||||||
| chr5:79762190
|
A | T | 1 | a0005c0005t0001g0270 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.11407+233A>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 8/12 | chr5 | 79762190 | ||||||
| chr5:79762322
|
C | T | 3 | a0015c0032t0007g0027a0015c0032t0007g0034a0030c0095t0003g0271 | 3 | HG02451.hp1 HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.11407+365C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 8/12 | chr5 | 79762322 | ||||||
| chr5:79762477
|
G | A | 1 | a0048c0107t0004g0317 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.11407+520G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 8/12 | chr5 | 79762477 | ||||||
| chr5:79762796
|
A | G | 37 | a0001c0001t0001g0163a0001c0001t0001g0212a0001c0001t0001g0240others(34): Show | 37 | HG00408.hp1 HG00438.hp2 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.11408-266A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 8/12 | chr5 | 79762796 | ||||||
| chr5:79762819
|
A | T | 109 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0235others(106): Show | 110 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.11408-243A>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 8/12 | chr5 | 79762819 | ||||||
| chr5:79762840
|
C | T | 29 | a0001c0001t0002g0056a0003c0003t0001g0178a0003c0003t0001g0188others(26): Show | 29 | HG01074.hp1 HG01243.hp1 HG02145.hp2 others(26): Show |
intron_variant | MODIFIER | c.11408-222C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 8/12 | chr5 | 79762840 | ||||||
| chr5:79762994
|
C | T | 29 | a0001c0001t0001g0065a0001c0001t0001g0235a0001c0001t0002g0197others(26): Show | 29 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.11408-68C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 8/12 | chr5 | 79762994 | ||||||
| chr5:79763338
|
C | T | 12 | a0002c0002t0001g0147a0002c0002t0001g0331a0002c0002t0002g0141others(9): Show | 12 | HG00438.hp1 NA18612.hp1 NA18949.hp2 others(9): Show |
intron_variant | MODIFIER | c.11555+129C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79763338 | ||||||
| chr5:79763456
|
T | C | 1 | a0043c0094t0002g0011 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.11555+247T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79763456 | ||||||
| chr5:79763531
|
C | A | 1 | a0005c0005t0001g0270 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.11555+322C>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79763531 | ||||||
| chr5:79763578
|
T | A | 2 | a0004c0006t0001g0304a0004c0006t0002g0303 | 2 | NA18945.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.11555+369T>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79763578 | ||||||
| chr5:79763594
|
T | C | 94 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0235others(91): Show | 95 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.11555+385T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79763594 | ||||||
| chr5:79763722
|
C | T | 7 | a0001c0058t0002g0339a0004c0014t0002g0040a0004c0014t0002g0119others(4): Show | 7 | HG00544.hp2 HG02165.hp1 NA18943.hp2 others(4): Show |
intron_variant | MODIFIER | c.11555+513C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79763722 | ||||||
| chr5:79763725
|
A | T | 203 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0163others(200): Show | 204 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.11555+516A>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79763725 | ||||||
| chr5:79764012
|
T | A | 1 | a0035c0037t0001g0177 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.11555+803T>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79764012 | ||||||
| chr5:79764126
|
T | C | 8 | a0001c0001t0002g0056a0002c0106t0007g0029a0003c0003t0005g0020others(5): Show | 8 | HG02451.hp1 HG02451.hp2 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.11555+917T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79764126 | ||||||
| chr5:79764164
|
C | T | 1 | a0005c0005t0001g0270 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.11555+955C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79764164 | ||||||
| chr5:79764222
|
A | G | 10 | a0019c0024t0001g0181a0019c0024t0001g0184a0019c0024t0017g0355others(7): Show | 10 | HG01243.hp1 HG02630.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.11555+1013A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79764222 | ||||||
| chr5:79764361
|
C | T | 1 | a0002c0106t0007g0029 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.11555+1152C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79764361 | ||||||
| chr5:79764455
|
G | A | 11 | a0009c0009t0001g0014a0009c0009t0001g0264a0009c0009t0001g0322others(8): Show | 12 | HG00741.hp1 HG02258.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.11555+1246G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79764455 | ||||||
| chr5:79764599
|
A | G | 1 | a0039c0030t0002g0269 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.11555+1390A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79764599 | ||||||
| chr5:79764751
|
G | T | 1 | a0001c0001t0001g0007 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.11555+1542G>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79764751 | ||||||
| chr5:79764766
|
T | C | 1 | a0002c0114t0001g0196 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.11555+1557T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79764766 | ||||||
| chr5:79764837
|
G | T | 69 | a0001c0001t0001g0163a0001c0001t0001g0212a0001c0001t0001g0240others(66): Show | 69 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.11555+1628G>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79764837 | ||||||
| chr5:79764848
|
T | C | 71 | a0001c0001t0001g0163a0001c0001t0001g0212a0001c0001t0001g0240others(68): Show | 71 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.11555+1639T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79764848 | ||||||
| chr5:79765056
|
A | C | 16 | a0002c0002t0002g0208a0002c0002t0002g0209a0002c0002t0002g0229others(13): Show | 16 | HG00099.hp1 HG00323.hp1 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.11555+1847A>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79765056 | ||||||
| chr5:79765107
|
T | G | 2 | a0005c0005t0001g0270a0030c0096t0001g0274 | 2 | HG01243.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.11555+1898T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79765107 | ||||||
| chr5:79765126
|
T | C | 1 | a0001c0001t0001g0292 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.11555+1917T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79765126 | ||||||
| chr5:79765172
|
A | G | 94 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0235others(91): Show | 95 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.11555+1963A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79765172 | ||||||
| chr5:79765294
|
A | G | 333 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0063others(330): Show | 334 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(331): Show |
intron_variant | MODIFIER | c.11555+2085A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79765294 | ||||||
| chr5:79765402
|
T | C | 6 | a0019c0024t0001g0181a0019c0024t0001g0184a0019c0024t0017g0355others(3): Show | 6 | HG02630.hp1 HG02809.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.11555+2193T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79765402 | ||||||
| chr5:79765533
|
G | T | 26 | a0003c0003t0001g0153a0003c0003t0001g0178a0003c0003t0001g0188others(23): Show | 26 | HG01074.hp1 HG01243.hp1 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.11555+2324G>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79765533 | ||||||
| chr5:79765682
|
T | A | 4 | a0009c0009t0001g0346a0031c0046t0001g0186a0031c0046t0002g0182others(1): Show | 4 | HG02055.hp1 HG03471.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.11555+2473T>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79765682 | ||||||
| chr5:79765683
|
T | G | 11 | a0012c0015t0004g0022a0012c0015t0004g0023a0012c0015t0004g0028others(8): Show | 11 | HG02109.hp2 HG02257.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.11555+2474T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79765683 | ||||||
| chr5:79765720
|
T | G | 26 | a0003c0003t0001g0153a0003c0003t0001g0178a0003c0003t0001g0188others(23): Show | 26 | HG01074.hp1 HG01243.hp1 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.11555+2511T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79765720 | ||||||
| chr5:79765941
|
C | A | 203 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0163others(200): Show | 204 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.11555+2732C>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79765941 | ||||||
| chr5:79766110
|
T | A | 1 | a0049c0103t0003g0328 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.11555+2901T>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79766110 | ||||||
| chr5:79766121
|
C | T | 4 | a0009c0009t0001g0346a0031c0046t0001g0186a0031c0046t0002g0182others(1): Show | 4 | HG02055.hp1 HG03471.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.11555+2912C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79766121 | ||||||
| chr5:79766223
|
C | T | 1 | a0058c0092t0003g0263 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.11555+3014C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79766223 | ||||||
| chr5:79766244
|
G | A | 16 | a0003c0003t0001g0153a0003c0003t0001g0178a0003c0003t0001g0188others(13): Show | 16 | HG01074.hp1 HG02145.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.11555+3035G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79766244 | ||||||
| chr5:79766390
|
G | A | 2 | a0005c0005t0001g0270a0030c0096t0001g0274 | 2 | HG01243.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.11555+3181G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79766390 | ||||||
| chr5:79766425
|
G | A | 39 | a0001c0001t0001g0095a0001c0001t0001g0102a0001c0001t0001g0124others(36): Show | 39 | HG00597.hp2 HG00673.hp1 HG01255.hp1 others(36): Show |
intron_variant | MODIFIER | c.11555+3216G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79766425 | ||||||
| chr5:79766797
|
T | C | 92 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0235others(89): Show | 93 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.11555+3588T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79766797 | ||||||
| chr5:79766818
|
A | T | 1 | a0030c0096t0001g0274 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.11555+3609A>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79766818 | ||||||
| chr5:79766890
|
C | T | 12 | a0003c0069t0002g0310a0009c0009t0001g0014a0009c0009t0001g0264others(9): Show | 13 | HG00741.hp1 HG01109.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.11555+3681C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79766890 | ||||||
| chr5:79766903
|
T | C | 94 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0235others(91): Show | 95 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.11555+3694T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79766903 | ||||||
| chr5:79766943
|
T | A | 2 | a0005c0005t0001g0270a0030c0096t0001g0274 | 2 | HG01243.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.11555+3734T>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79766943 | ||||||
| chr5:79766994
|
G | T | 3 | a0001c0001t0002g0056a0003c0003t0005g0020a0007c0097t0002g0347 | 3 | HG02683.hp2 HG02735.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.11555+3785G>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79766994 | ||||||
| chr5:79767096
|
G | A | 3 | a0001c0001t0002g0056a0003c0003t0005g0020a0007c0097t0002g0347 | 3 | HG02683.hp2 HG02735.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.11555+3887G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79767096 | ||||||
| chr5:79767128
|
A | G | 4 | a0009c0009t0001g0346a0031c0046t0001g0186a0031c0046t0002g0182others(1): Show | 4 | HG02055.hp1 HG03471.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.11555+3919A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79767128 | ||||||
| chr5:79767252
|
G | T | 16 | a0003c0003t0001g0153a0003c0003t0001g0178a0003c0003t0001g0188others(13): Show | 16 | HG01074.hp1 HG02145.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.11555+4043G>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79767252 | ||||||
| chr5:79767261
|
T | G | 11 | a0012c0015t0004g0022a0012c0015t0004g0023a0012c0015t0004g0028others(8): Show | 11 | HG02109.hp2 HG02257.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.11555+4052T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79767261 | ||||||
| chr5:79767279
|
G | C | 92 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0235others(89): Show | 93 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.11555+4070G>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79767279 | ||||||
| chr5:79767283
|
T | C | 45 | a0001c0001t0001g0065a0001c0001t0001g0235a0001c0001t0002g0197others(42): Show | 46 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.11555+4074T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79767283 | ||||||
| chr5:79767296
|
A | G | 2 | a0003c0003t0001g0153a0007c0008t0001g0340 | 2 | HG02717.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.11555+4087A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79767296 | ||||||
| chr5:79767448
|
A | T | 88 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0235others(85): Show | 89 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.11555+4239A>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79767448 | ||||||
| chr5:79767452
|
T | G | 4 | a0009c0009t0001g0346a0031c0046t0001g0186a0031c0046t0002g0182others(1): Show | 4 | HG02055.hp1 HG03471.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.11555+4243T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79767452 | ||||||
| chr5:79767460
|
A | C | 11 | a0012c0015t0004g0022a0012c0015t0004g0023a0012c0015t0004g0028others(8): Show | 11 | HG02109.hp2 HG02257.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.11555+4251A>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79767460 | ||||||
| chr5:79767470
|
T | C | 71 | a0001c0001t0001g0163a0001c0001t0001g0212a0001c0001t0001g0240others(68): Show | 71 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.11555+4261T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79767470 | ||||||
| chr5:79767620
|
A | C | 45 | a0001c0001t0001g0065a0001c0001t0001g0235a0001c0001t0002g0197others(42): Show | 46 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.11555+4411A>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79767620 | ||||||
| chr5:79767806
|
A | C | 1 | a0001c0001t0001g0198 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.11555+4597A>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79767806 | ||||||
| chr5:79767944
|
G | T | 12 | a0003c0069t0002g0310a0009c0009t0001g0014a0009c0009t0001g0264others(9): Show | 13 | HG00741.hp1 HG01109.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.11555+4735G>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79767944 | ||||||
| chr5:79767979
|
G | A | 10 | a0019c0024t0001g0181a0019c0024t0001g0184a0019c0024t0017g0355others(7): Show | 10 | HG01243.hp1 HG02630.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.11555+4770G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79767979 | ||||||
| chr5:79768028
|
A | G | 105 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0235others(102): Show | 106 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.11555+4819A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79768028 | ||||||
| chr5:79768054
|
C | T | 3 | a0020c0025t0001g0278a0020c0025t0001g0309a0020c0025t0001g0344 | 3 | HG03195.hp2 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.11555+4845C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79768054 | ||||||
| chr5:79768067
|
C | G | 1 | a0002c0002t0001g0173 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.11555+4858C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79768067 | ||||||
| chr5:79768097
|
T | C | 1 | a0030c0096t0001g0274 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.11555+4888T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79768097 | ||||||
| chr5:79768103
|
C | T | 1 | a0049c0103t0003g0328 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.11555+4894C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79768103 | ||||||
| chr5:79768144
|
A | G | 2 | a0005c0005t0001g0216a0005c0005t0001g0217 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.11555+4935A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79768144 | ||||||
| chr5:79768145
|
T | G | 2 | a0015c0032t0007g0027a0015c0032t0007g0034 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.11555+4936T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79768145 | ||||||
| chr5:79768318
|
T | A | 93 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0235others(90): Show | 94 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.11555+5109T>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79768318 | ||||||
| chr5:79768418
|
GT | G | 44 | a0001c0001t0001g0065a0001c0001t0001g0235a0001c0001t0002g0197others(41): Show | 45 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.11555+5214delT | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79768418 | |||||
| chr5:79768567
|
G | A | 2 | a0023c0022t0008g0016a0023c0022t0008g0025 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.11555+5358G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79768567 | ||||||
| chr5:79768762
|
A | AT | 94 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0235others(91): Show | 95 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.11555+5555dupT | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79768762 | |||||
| chr5:79768831
|
G | A | 1 | a0058c0092t0003g0263 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.11555+5622G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79768831 | ||||||
| chr5:79768918
|
CTT | C | 69 | a0001c0001t0001g0163a0001c0001t0001g0212a0001c0001t0001g0240others(66): Show | 69 | HG00408.hp1 HG00408.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.11555+5711_11555+5 others(8): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79768918 | |||||
| chr5:79768935
|
C | G | 1 | a0001c0001t0001g0063 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.11555+5726C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79768935 | ||||||
| chr5:79769101
|
G | C | 1 | a0001c0001t0001g0171 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.11555+5892G>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79769101 | ||||||
| chr5:79769109
|
G | A | 70 | a0001c0001t0001g0163a0001c0001t0001g0212a0001c0001t0001g0240others(67): Show | 70 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.11555+5900G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79769109 | ||||||
| chr5:79769202
|
T | C | 2 | a0015c0032t0007g0027a0015c0032t0007g0034 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.11555+5993T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79769202 | ||||||
| chr5:79769288
|
C | T | 1 | a0002c0106t0007g0029 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.11555+6079C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79769288 | ||||||
| chr5:79769320
|
G | A | 2 | a0015c0032t0007g0027a0015c0032t0007g0034 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.11555+6111G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79769320 | ||||||
| chr5:79769323
|
T | C | 203 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0163others(200): Show | 204 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.11555+6114T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79769323 | ||||||
| chr5:79769448
|
G | A | 1 | a0005c0005t0001g0270 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.11555+6239G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79769448 | ||||||
| chr5:79769491
|
G | A | 92 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0235others(89): Show | 93 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.11555+6282G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79769491 | ||||||
| chr5:79769653
|
G | T | 1 | a0030c0096t0001g0274 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.11555+6444G>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79769653 | ||||||
| chr5:79769694
|
C | T | 2 | a0023c0022t0008g0016a0023c0022t0008g0025 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.11555+6485C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79769694 | ||||||
| chr5:79769696
|
C | G | 1 | a0004c0006t0003g0062 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.11555+6487C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79769696 | ||||||
| chr5:79769849
|
T | C | 1 | a0030c0096t0001g0274 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.11555+6640T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79769849 | ||||||
| chr5:79769850
|
C | G | 1 | a0030c0096t0001g0274 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.11555+6641C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79769850 | ||||||
| chr5:79769884
|
T | G | 5 | a0015c0038t0002g0312a0015c0038t0004g0260a0039c0030t0002g0269others(2): Show | 5 | HG02257.hp2 HG02723.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.11555+6675T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79769884 | ||||||
| chr5:79769919
|
A | C | 4 | a0004c0006t0001g0304a0004c0006t0002g0303a0014c0027t0002g0053others(1): Show | 4 | NA18945.hp2 NA18970.hp1 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.11555+6710A>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79769919 | ||||||
| chr5:79769953
|
A | C | 71 | a0001c0001t0001g0163a0001c0001t0001g0212a0001c0001t0001g0240others(68): Show | 71 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.11555+6744A>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79769953 | ||||||
| chr5:79769965
|
C | T | 71 | a0001c0001t0001g0163a0001c0001t0001g0212a0001c0001t0001g0240others(68): Show | 71 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.11555+6756C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79769965 | ||||||
| chr5:79770028
|
C | T | 1 | a0005c0005t0001g0270 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.11555+6819C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79770028 | ||||||
| chr5:79770141
|
A | G | 92 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0235others(89): Show | 93 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.11555+6932A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79770141 | ||||||
| chr5:79770143
|
G | A | 1 | a0048c0107t0004g0317 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.11555+6934G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79770143 | ||||||
| chr5:79770147
|
C | G | 1 | a0005c0005t0001g0270 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.11555+6938C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79770147 | ||||||
| chr5:79770177
|
T | C | 97 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0235others(94): Show | 98 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.11555+6968T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79770177 | ||||||
| chr5:79770237
|
G | T | 90 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0235others(87): Show | 91 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.11555+7028G>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79770237 | ||||||
| chr5:79770260
|
G | T | 1 | a0005c0005t0001g0270 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.11555+7051G>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79770260 | ||||||
| chr5:79770261
|
A | G | 1 | a0005c0005t0001g0270 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.11555+7052A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79770261 | ||||||
| chr5:79770264
|
T | C | 1 | a0003c0003t0001g0046 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.11555+7055T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79770264 | ||||||
| chr5:79770380
|
G | C | 10 | a0019c0024t0001g0181a0019c0024t0001g0184a0019c0024t0017g0355others(7): Show | 10 | HG01243.hp1 HG02630.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.11555+7171G>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79770380 | ||||||
| chr5:79770399
|
C | T | 1 | a0008c0007t0001g0009 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.11555+7190C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79770399 | ||||||
| chr5:79770422
|
G | GC | 356 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(353): Show | 357 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(354): Show |
intron_variant | MODIFIER | c.11555+7215dupC | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79770422 | |||||
| chr5:79770442
|
G | A | 6 | a0004c0014t0002g0244a0015c0038t0002g0312a0015c0038t0004g0260others(3): Show | 6 | HG02257.hp2 HG02723.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.11555+7233G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79770442 | ||||||
| chr5:79770506
|
G | T | 1 | a0079c0081t0002g0091 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.11555+7297G>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79770506 | ||||||
| chr5:79770514
|
C | T | 1 | a0024c0084t0001g0172 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.11555+7305C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79770514 | ||||||
| chr5:79770568
|
G | A | 47 | a0001c0001t0001g0095a0001c0001t0001g0102a0001c0001t0001g0124others(44): Show | 47 | HG00597.hp2 HG00673.hp1 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.11555+7359G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79770568 | ||||||
| chr5:79770679
|
T | G | 1 | a0005c0005t0001g0270 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.11555+7470T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79770679 | ||||||
| chr5:79770716
|
G | A | 1 | a0057c0111t0002g0321 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.11555+7507G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79770716 | ||||||
| chr5:79770771
|
C | G | 2 | a0001c0001t0002g0137a0001c0001t0002g0338 | 2 | HG01255.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.11555+7562C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79770771 | ||||||
| chr5:79770909
|
G | A | 1 | a0051c0100t0002g0356 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.11555+7700G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79770909 | ||||||
| chr5:79770949
|
G | T | 4 | a0015c0038t0002g0312a0015c0038t0004g0260a0039c0030t0002g0269others(1): Show | 4 | HG02257.hp2 HG02723.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.11555+7740G>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79770949 | ||||||
| chr5:79771058
|
A | G | 3 | a0020c0025t0001g0278a0020c0025t0001g0309a0020c0025t0001g0344 | 3 | HG03195.hp2 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.11555+7849A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79771058 | ||||||
| chr5:79771068
|
G | GA | 14 | a0001c0001t0001g0281a0001c0001t0002g0332a0004c0006t0002g0249others(11): Show | 14 | HG00621.hp1 HG00673.hp1 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.11555+7877dupA | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79771068 | |||||
| chr5:79771068
|
GA | G | 55 | a0001c0001t0001g0063a0001c0001t0002g0056a0001c0001t0010g0085others(52): Show | 55 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.11555+7877delA | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79771068 | |||||
| chr5:79771092
|
CT | C | 3 | a0008c0007t0002g0006a0008c0007t0002g0113a0008c0007t0002g0115 | 3 | NA18942.hp2 NA18954.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.11555+7887delT | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79771092 | |||||
| chr5:79771210
|
T | G | 71 | a0001c0001t0001g0163a0001c0001t0001g0212a0001c0001t0001g0240others(68): Show | 71 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.11555+8001T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79771210 | ||||||
| chr5:79771281
|
C | T | 6 | a0004c0014t0002g0040a0004c0014t0002g0119a0004c0014t0002g0195others(3): Show | 6 | HG00544.hp2 HG02165.hp1 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.11555+8072C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79771281 | ||||||
| chr5:79771367
|
C | T | 2 | a0013c0016t0001g0180a0013c0016t0004g0019 | 2 | HG02055.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.11555+8158C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79771367 | ||||||
| chr5:79771566
|
G | A | 1 | a0007c0008t0002g0179 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.11555+8357G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79771566 | ||||||
| chr5:79771763
|
T | C | 4 | a0009c0009t0001g0346a0031c0046t0001g0186a0031c0046t0002g0182others(1): Show | 4 | HG02055.hp1 HG03471.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.11555+8554T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79771763 | ||||||
| chr5:79771818
|
T | C | 1 | a0050c0104t0003g0272 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.11555+8609T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79771818 | ||||||
| chr5:79771843
|
A | T | 93 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0235others(90): Show | 94 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.11555+8634A>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79771843 | ||||||
| chr5:79771844
|
G | T | 6 | a0004c0014t0002g0040a0004c0014t0002g0119a0004c0014t0002g0195others(3): Show | 6 | HG00544.hp2 HG02165.hp1 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.11555+8635G>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79771844 | ||||||
| chr5:79772121
|
G | GA | 71 | a0001c0001t0001g0163a0001c0001t0001g0212a0001c0001t0001g0240others(68): Show | 71 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.11555+8922dupA | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79772121 | |||||
| chr5:79772134
|
C | A | 2 | a0002c0002t0006g0120a0002c0002t0006g0164 | 2 | NA18948.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.11555+8925C>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79772134 | ||||||
| chr5:79772182
|
G | A | 1 | a0002c0106t0007g0029 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.11555+8973G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79772182 | ||||||
| chr5:79772266
|
C | T | 221 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0163others(218): Show | 222 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.11555+9057C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79772266 | ||||||
| chr5:79772268
|
G | A | 6 | a0012c0015t0004g0022a0012c0015t0004g0023a0012c0015t0004g0028others(3): Show | 6 | HG02109.hp2 HG02559.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.11555+9059G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79772268 | ||||||
| chr5:79772288
|
A | G | 1 | a0004c0006t0002g0303 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.11555+9079A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79772288 | ||||||
| chr5:79772322
|
T | C | 2 | a0028c0043t0001g0183a0028c0043t0001g0267 | 2 | HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.11555+9113T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79772322 | ||||||
| chr5:79772332
|
G | A | 1 | a0004c0006t0001g0078 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.11555+9123G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79772332 | ||||||
| chr5:79772477
|
G | A | 47 | a0001c0001t0001g0063a0001c0013t0002g0041a0001c0013t0002g0204others(44): Show | 47 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.11555+9268G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79772477 | ||||||
| chr5:79772516
|
C | G | 5 | a0015c0038t0002g0312a0015c0038t0004g0260a0039c0030t0002g0269others(2): Show | 5 | HG02257.hp2 HG02723.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.11555+9307C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79772516 | ||||||
| chr5:79772775
|
G | A | 1 | a0019c0024t0001g0181 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.11555+9566G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79772775 | ||||||
| chr5:79772845
|
C | T | 1 | a0001c0001t0001g0136 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.11555+9636C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79772845 | ||||||
| chr5:79772906
|
A | G | 10 | a0019c0024t0001g0181a0019c0024t0001g0184a0019c0024t0017g0355others(7): Show | 10 | HG01243.hp1 HG02630.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.11555+9697A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79772906 | ||||||
| chr5:79773036
|
A | G | 25 | a0003c0003t0001g0153a0003c0003t0001g0178a0003c0003t0001g0188others(22): Show | 25 | HG01074.hp1 HG01243.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.11555+9827A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79773036 | ||||||
| chr5:79773226
|
G | A | 4 | a0015c0038t0002g0312a0015c0038t0004g0260a0039c0030t0002g0269others(1): Show | 4 | HG02257.hp2 HG02723.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.11555+10017G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79773226 | ||||||
| chr5:79773301
|
T | A | 3 | a0001c0013t0001g0154a0005c0005t0002g0170a0026c0028t0002g0075 | 3 | HG00408.hp2 HG02080.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.11555+10092T>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79773301 | ||||||
| chr5:79773646
|
C | T | 4 | a0015c0038t0002g0312a0015c0038t0004g0260a0039c0030t0002g0269others(1): Show | 4 | HG02257.hp2 HG02723.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.11555+10437C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79773646 | ||||||
| chr5:79773696
|
G | GTGAA | 9 | a0004c0014t0002g0040a0004c0014t0002g0119a0004c0014t0002g0195others(6): Show | 9 | HG00544.hp2 HG02165.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.11555+10512_11555+ others(12): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79773696 | |||||
| chr5:79773696
|
GTGAA | G | 40 | a0001c0001t0001g0063a0001c0013t0002g0041a0002c0002t0001g0147others(37): Show | 40 | HG00438.hp1 HG00544.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.11555+10512_11555+ others(12): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79773696 | |||||
| chr5:79773776
|
G | A | 1 | a0002c0020t0002g0121 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.11555+10567G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79773776 | ||||||
| chr5:79773795
|
A | G | 1 | a0026c0049t0006g0073 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.11555+10586A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79773795 | ||||||
| chr5:79774002
|
T | C | 1 | a0030c0095t0003g0271 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.11555+10793T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79774002 | ||||||
| chr5:79774168
|
G | A | 1 | a0001c0001t0001g0241 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.11555+10959G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79774168 | ||||||
| chr5:79774198
|
C | T | 2 | a0003c0003t0001g0099a0062c0072t0002g0255 | 2 | HG01978.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.11555+10989C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79774198 | ||||||
| chr5:79774580
|
C | T | 1 | a0072c0071t0002g0191 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.11555+11371C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79774580 | ||||||
| chr5:79774665
|
C | G | 1 | a0004c0006t0001g0256 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.11555+11456C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79774665 | ||||||
| chr5:79774672
|
A | T | 1 | a0003c0003t0002g0167 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.11555+11463A>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79774672 | ||||||
| chr5:79774691
|
G | T | 1 | a0001c0001t0001g0335 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.11555+11482G>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79774691 | ||||||
| chr5:79774732
|
T | G | 2 | a0001c0033t0001g0139a0008c0067t0001g0305 | 2 | HG02165.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.11555+11523T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79774732 | ||||||
| chr5:79774828
|
A | G | 2 | a0001c0001t0001g0165a0040c0040t0003g0325 | 2 | HG03017.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.11555+11619A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79774828 | ||||||
| chr5:79775278
|
C | G | 1 | a0001c0001t0001g0285 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.11555+12069C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79775278 | ||||||
| chr5:79775561
|
A | G | 2 | a0003c0003t0001g0015a0009c0009t0014g0266 | 2 | HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.11555+12352A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79775561 | ||||||
| chr5:79775623
|
T | C | 4 | a0010c0010t0001g0207a0010c0065t0002g0080a0026c0028t0001g0044others(1): Show | 4 | HG00558.hp2 NA18612.hp2 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.11555+12414T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79775623 | ||||||
| chr5:79775728
|
C | T | 2 | a0028c0043t0001g0183a0028c0043t0001g0267 | 2 | HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.11555+12519C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79775728 | ||||||
| chr5:79775778
|
A | C | 1 | a0002c0106t0007g0029 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.11555+12569A>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79775778 | ||||||
| chr5:79775958
|
A | G | 83 | a0001c0001t0001g0007a0001c0001t0001g0063a0001c0001t0001g0102others(80): Show | 83 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.11555+12749A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79775958 | ||||||
| chr5:79776029
|
A | G | 4 | a0009c0009t0001g0346a0020c0025t0001g0278a0020c0025t0001g0309others(1): Show | 4 | HG03195.hp2 NA18522.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.11555+12820A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79776029 | ||||||
| chr5:79776156
|
G | A | 2 | a0058c0092t0003g0263a0072c0071t0002g0191 | 2 | HG01243.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.11556-12815G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79776156 | ||||||
| chr5:79776566
|
G | A | 1 | a0073c0076t0001g0101 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.11556-12405G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79776566 | ||||||
| chr5:79776568
|
G | T | 1 | a0019c0024t0017g0355 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.11556-12403G>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79776568 | ||||||
| chr5:79776736
|
A | G | 5 | a0003c0003t0008g0018a0003c0003t0009g0313a0023c0022t0008g0016others(2): Show | 5 | HG02572.hp1 HG02630.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.11556-12235A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79776736 | ||||||
| chr5:79776833
|
C | CT | 41 | a0001c0001t0001g0246a0001c0001t0001g0292a0002c0002t0001g0043others(38): Show | 41 | HG01074.hp1 HG01243.hp1 HG02015.hp2 others(38): Show |
intron_variant | MODIFIER | c.11556-12137dupT | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79776833 | |||||
| chr5:79776884
|
T | A | 9 | a0003c0003t0001g0153a0003c0034t0009g0320a0003c0034t0012g0021others(6): Show | 9 | HG01074.hp1 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.11556-12087T>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79776884 | ||||||
| chr5:79776934
|
G | C | 2 | a0013c0016t0001g0180a0013c0016t0004g0019 | 2 | HG02055.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.11556-12037G>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79776934 | ||||||
| chr5:79777044
|
G | A | 3 | a0015c0032t0007g0027a0015c0032t0007g0034a0050c0104t0003g0272 | 3 | HG02451.hp2 HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.11556-11927G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79777044 | ||||||
| chr5:79777096
|
C | A | 4 | a0011c0052t0001g0284a0033c0039t0001g0279a0042c0029t0001g0108others(1): Show | 4 | HG01981.hp2 HG02148.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.11556-11875C>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79777096 | ||||||
| chr5:79777208
|
G | A | 54 | a0001c0001t0001g0102a0001c0001t0001g0150a0001c0001t0001g0163others(51): Show | 54 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.11556-11763G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79777208 | ||||||
| chr5:79777389
|
A | G | 32 | a0001c0001t0010g0084a0001c0001t0010g0085a0002c0106t0007g0029others(29): Show | 32 | HG01074.hp1 HG01167.hp1 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.11556-11582A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79777389 | ||||||
| chr5:79777395
|
G | A | 5 | a0019c0024t0017g0355a0030c0095t0003g0271a0035c0037t0011g0319others(2): Show | 5 | HG01243.hp1 HG02451.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.11556-11576G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79777395 | ||||||
| chr5:79777569
|
T | C | 213 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0064others(210): Show | 213 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(210): Show |
intron_variant | MODIFIER | c.11556-11402T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79777569 | ||||||
| chr5:79777691
|
T | C | 268 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0063others(265): Show | 269 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(266): Show |
intron_variant | MODIFIER | c.11556-11280T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79777691 | ||||||
| chr5:79777729
|
T | G | 1 | a0059c0075t0001g0327 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.11556-11242T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79777729 | ||||||
| chr5:79777771
|
A | G | 4 | a0003c0003t0008g0018a0023c0022t0008g0016a0023c0022t0008g0025others(1): Show | 4 | HG02572.hp1 HG02630.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.11556-11200A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79777771 | ||||||
| chr5:79777793
|
T | TA | 3 | a0002c0106t0007g0029a0028c0043t0001g0183a0028c0043t0001g0267 | 3 | HG03139.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.11556-11175dupA | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79777793 | |||||
| chr5:79777796
|
A | AT | 229 | a0001c0001t0001g0063a0001c0001t0001g0095a0001c0001t0001g0102others(226): Show | 230 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(227): Show |
intron_variant | MODIFIER | c.11556-11166dupT | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79777796 | |||||
| chr5:79777847
|
C | G | 190 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0064others(187): Show | 190 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(187): Show |
intron_variant | MODIFIER | c.11556-11124C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79777847 | ||||||
| chr5:79777885
|
G | A | 1 | a0001c0001t0001g0235 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.11556-11086G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79777885 | ||||||
| chr5:79777887
|
C | T | 1 | a0030c0096t0001g0274 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.11556-11084C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79777887 | ||||||
| chr5:79777912
|
G | C | 190 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0064others(187): Show | 190 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(187): Show |
intron_variant | MODIFIER | c.11556-11059G>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79777912 | ||||||
| chr5:79777983
|
A | G | 1 | a0002c0002t0001g0129 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.11556-10988A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79777983 | ||||||
| chr5:79777993
|
A | G | 268 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0063others(265): Show | 269 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(266): Show |
intron_variant | MODIFIER | c.11556-10978A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79777993 | ||||||
| chr5:79778034
|
C | T | 7 | a0003c0003t0001g0153a0007c0008t0001g0168a0007c0008t0001g0340others(4): Show | 7 | HG01074.hp1 HG02717.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.11556-10937C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79778034 | ||||||
| chr5:79778135
|
A | C | 2 | a0003c0034t0009g0320a0003c0034t0012g0021 | 2 | HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.11556-10836A>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79778135 | ||||||
| chr5:79778135
|
A | G | 18 | a0001c0001t0001g0246a0001c0001t0001g0292a0001c0058t0002g0339others(15): Show | 18 | HG02015.hp2 HG02165.hp1 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.11556-10836A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79778135 | ||||||
| chr5:79778328
|
T | C | 5 | a0003c0003t0008g0018a0003c0003t0009g0313a0023c0022t0008g0016others(2): Show | 5 | HG02572.hp1 HG02630.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.11556-10643T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79778328 | ||||||
| chr5:79778393
|
G | A | 1 | a0007c0008t0001g0168 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.11556-10578G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79778393 | ||||||
| chr5:79778406
|
T | C | 268 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0063others(265): Show | 269 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(266): Show |
intron_variant | MODIFIER | c.11556-10565T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79778406 | ||||||
| chr5:79778665
|
G | C | 4 | a0002c0106t0007g0029a0015c0032t0007g0027a0015c0032t0007g0034others(1): Show | 4 | HG02451.hp2 HG03209.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.11556-10306G>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79778665 | ||||||
| chr5:79778684
|
A | C | 4 | a0002c0106t0007g0029a0015c0032t0007g0027a0015c0032t0007g0034others(1): Show | 4 | HG02451.hp2 HG03209.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.11556-10287A>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79778684 | ||||||
| chr5:79778697
|
G | C | 18 | a0001c0001t0001g0246a0001c0001t0001g0292a0001c0058t0002g0339others(15): Show | 18 | HG02015.hp2 HG02165.hp1 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.11556-10274G>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79778697 | ||||||
| chr5:79778734
|
A | G | 4 | a0003c0003t0001g0015a0007c0008t0001g0138a0009c0009t0001g0014others(1): Show | 4 | HG02258.hp2 HG03130.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.11556-10237A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79778734 | ||||||
| chr5:79778756
|
A | T | 8 | a0001c0001t0010g0084a0001c0001t0010g0085a0005c0005t0001g0270others(5): Show | 8 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.11556-10215A>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79778756 | ||||||
| chr5:79778800
|
C | T | 2 | a0001c0013t0002g0041a0002c0020t0001g0117 | 2 | HG02015.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.11556-10171C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79778800 | ||||||
| chr5:79778811
|
C | CTGTGTGT others(7): Show |
1 | a0002c0002t0001g0128 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.11556-10148_11556- others(22): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79778811 | |||||
| chr5:79778811
|
C | CTGTGTGT others(15): Show |
1 | a0067c0059t0001g0299 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.11556-10143_11556- others(30): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79778811 | |||||
| chr5:79778811
|
C | CTGTGTGT others(11): Show |
15 | a0001c0001t0001g0246a0002c0002t0002g0209a0002c0002t0002g0229others(12): Show | 15 | HG02015.hp2 HG02165.hp1 HG02698.hp2 others(12): Show |
intron_variant | MODIFIER | c.11556-10152_11556- others(26): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79778811 | |||||
| chr5:79778811
|
C | CTGTGTGT others(15): Show |
3 | a0001c0001t0001g0174a0001c0001t0002g0137a0026c0028t0001g0044 | 3 | HG02257.hp1 NA18612.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.11556-10141_11556- others(30): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79778811 | |||||
| chr5:79778811
|
C | CTGTGTGT others(17): Show |
57 | a0001c0001t0001g0095a0001c0001t0001g0124a0001c0001t0001g0125others(54): Show | 57 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.11556-10141_11556- others(32): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79778811 | |||||
| chr5:79778811
|
C | CTGTGTGT others(19): Show |
7 | a0004c0011t0001g0233a0009c0009t0001g0346a0020c0025t0001g0278others(4): Show | 7 | HG02486.hp2 HG02970.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.11556-10141_11556- others(34): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79778811 | |||||
| chr5:79778811
|
C | CTGTGTGT others(19): Show |
1 | a0011c0012t0001g0287 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.11556-10141_11556- others(34): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79778811 | |||||
| chr5:79778811
|
C | CTGTGTGT others(13): Show |
2 | a0001c0001t0001g0292a0002c0002t0001g0043 | 2 | NA19056.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.11556-10154_11556- others(28): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79778811 | |||||
| chr5:79778811
|
C | CTGTGTGT others(15): Show |
1 | a0007c0008t0001g0311 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.11556-10139_11556- others(30): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79778811 | |||||
| chr5:79778811
|
C | CTGTGTGT others(17): Show |
1 | a0019c0024t0001g0181 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.11556-10139_11556- others(32): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79778811 | |||||
| chr5:79778811
|
C | CTGTGTGT others(19): Show |
34 | a0001c0001t0001g0064a0001c0001t0001g0077a0001c0001t0001g0135others(31): Show | 34 | HG01081.hp2 HG01099.hp1 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.11556-10139_11556- others(34): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79778811 | |||||
| chr5:79778811
|
C | CTGTGTGT others(21): Show |
8 | a0001c0001t0010g0084a0001c0001t0010g0085a0005c0005t0001g0270others(5): Show | 8 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.11556-10139_11556- others(36): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79778811 | |||||
| chr5:79778811
|
C | CTGTGTGT others(15): Show |
1 | a0001c0001t0001g0012 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.11556-10156_11556- others(30): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79778811 | |||||
| chr5:79778811
|
C | CTGTGTGT others(21): Show |
1 | a0007c0008t0001g0138 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.11556-10137_11556- others(36): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79778811 | |||||
| chr5:79778811
|
C | CTGTGTGT others(17): Show |
1 | a0001c0001t0001g0013 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.11556-10158_11556- others(32): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79778811 | |||||
| chr5:79778811
|
C | CTGTGTGT others(19): Show |
10 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0241others(7): Show | 10 | NA18942.hp1 NA18945.hp2 NA18952.hp1 others(7): Show |
intron_variant | MODIFIER | c.11556-10156_11556- others(34): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79778811 | |||||
| chr5:79778811
|
C | CTGTGTGT others(21): Show |
1 | a0022c0021t0002g0302 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.11556-10135_11556- others(36): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79778811 | |||||
| chr5:79778811
|
C | CTGTGTGT others(25): Show |
2 | a0003c0034t0009g0320a0003c0034t0012g0021 | 2 | HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.11556-10135_11556- others(40): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79778811 | |||||
| chr5:79778811
|
C | CTGTGTGT others(27): Show |
4 | a0007c0008t0001g0168a0009c0009t0001g0323a0015c0038t0002g0312others(1): Show | 4 | HG01074.hp1 HG02723.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.11556-10135_11556- others(42): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79778811 | |||||
| chr5:79778811
|
C | CTGTGTGT others(29): Show |
1 | a0015c0038t0004g0260 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.11556-10135_11556- others(44): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79778811 | |||||
| chr5:79778811
|
C | CTGTGTGT others(31): Show |
2 | a0003c0003t0001g0153a0007c0008t0001g0340 | 2 | HG02717.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.11556-10135_11556- others(46): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79778811 | |||||
| chr5:79778811
|
CTGTG | C | 4 | a0003c0003t0008g0018a0003c0003t0009g0313a0023c0022t0008g0016others(1): Show | 4 | HG02630.hp2 HG02896.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.11556-10138_11556- others(12): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79778811 | |||||
| chr5:79778813
|
G | GTGTGTGT others(11): Show |
5 | a0018c0017t0002g0002a0018c0017t0002g0068a0018c0017t0002g0069others(2): Show | 5 | HG02451.hp1 HG02965.hp1 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.11556-10141_11556- others(26): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79778813 | |||||
| chr5:79778813
|
G | GTGTGTGT others(17): Show |
47 | a0001c0001t0001g0198a0001c0013t0002g0041a0001c0013t0002g0204others(44): Show | 48 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.11556-10141_11556- others(32): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79778813 | |||||
| chr5:79778813
|
G | GTGTGTGT others(13): Show |
3 | a0019c0024t0017g0355a0035c0037t0011g0319a0072c0071t0002g0191 | 3 | HG01243.hp1 HG02809.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.11556-10139_11556- others(28): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79778813 | |||||
| chr5:79778813
|
G | GTGTGTGT others(19): Show |
4 | a0002c0106t0007g0029a0015c0032t0007g0027a0015c0032t0007g0034others(1): Show | 4 | HG02451.hp2 HG03209.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.11556-10139_11556- others(34): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79778813 | |||||
| chr5:79778813
|
G | GTGTGTGT others(15): Show |
2 | a0028c0043t0001g0183a0028c0043t0001g0267 | 2 | HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.11556-10137_11556- others(30): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79778813 | |||||
| chr5:79778813
|
G | GTGTGTGT others(17): Show |
29 | a0001c0001t0001g0102a0001c0001t0001g0150a0001c0001t0001g0163others(26): Show | 29 | HG00609.hp2 HG01169.hp2 HG02040.hp1 others(26): Show |
intron_variant | MODIFIER | c.11556-10154_11556- others(32): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79778813 | |||||
| chr5:79778813
|
G | GTGTGTGT others(19): Show |
9 | a0002c0002t0001g0008a0002c0002t0001g0129a0003c0003t0001g0242others(6): Show | 9 | HG02040.hp2 HG02056.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.11556-10135_11556- others(34): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79778813 | |||||
| chr5:79778815
|
G | GTGTGTGT others(15): Show |
2 | a0001c0001t0001g0063a0002c0002t0001g0131 | 2 | HG03831.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.11556-10141_11556- others(30): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79778815 | |||||
| chr5:79778815
|
G | GTGTGTGT others(15): Show |
7 | a0001c0001t0001g0235a0002c0002t0001g0222a0006c0004t0001g0079others(4): Show | 7 | HG00408.hp1 HG00609.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.11556-10152_11556- others(30): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79778815 | |||||
| chr5:79778880
|
T | C | 5 | a0019c0024t0017g0355a0030c0095t0003g0271a0035c0037t0011g0319others(2): Show | 5 | HG01243.hp1 HG02451.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.11556-10091T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79778880 | ||||||
| chr5:79778900
|
AT | A | 81 | a0001c0001t0001g0097a0001c0001t0001g0102a0001c0001t0001g0150others(78): Show | 81 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.11556-10060delT | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79778900 | |||||
| chr5:79778900
|
ATT | A | 9 | a0001c0001t0010g0084a0001c0001t0010g0085a0005c0005t0001g0270others(6): Show | 9 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.11556-10061_11556- others(10): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79778900 | |||||
| chr5:79778910
|
TTA | T | 60 | a0001c0001t0001g0063a0001c0001t0001g0198a0001c0013t0002g0041others(57): Show | 61 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.11556-10060_11556- others(10): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79778910 | ||||||
| chr5:79778911
|
T | A | 3 | a0003c0003t0008g0018a0023c0022t0008g0016a0023c0022t0008g0025 | 3 | HG02630.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.11556-10060T>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79778911 | ||||||
| chr5:79778912
|
AATT | A | 3 | a0003c0003t0008g0018a0023c0022t0008g0016a0023c0022t0008g0025 | 3 | HG02630.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.11556-10058_11556- others(11): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79778912 | ||||||
| chr5:79778913
|
AT | A | 21 | a0001c0001t0002g0329a0001c0013t0001g0154a0001c0033t0002g0286others(18): Show | 21 | HG01069.hp1 HG01081.hp1 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.11556-10046delT | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79778913 | |||||
| chr5:79778914
|
T | A | 60 | a0001c0001t0001g0063a0001c0001t0001g0198a0001c0013t0002g0041others(57): Show | 61 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.11556-10057T>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79778914 | ||||||
| chr5:79778940
|
T | A | 1 | a0027c0042t0001g0134 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.11556-10031T>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79778940 | ||||||
| chr5:79779002
|
C | T | 3 | a0030c0095t0003g0271a0058c0092t0003g0263a0072c0071t0002g0191 | 3 | HG01243.hp1 HG02451.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.11556-9969C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79779002 | ||||||
| chr5:79779058
|
C | A | 4 | a0002c0106t0007g0029a0015c0032t0007g0027a0015c0032t0007g0034others(1): Show | 4 | HG02451.hp2 HG03209.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.11556-9913C>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79779058 | ||||||
| chr5:79779062
|
C | G | 5 | a0019c0024t0017g0355a0030c0095t0003g0271a0035c0037t0011g0319others(2): Show | 5 | HG01243.hp1 HG02451.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.11556-9909C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79779062 | ||||||
| chr5:79779062
|
C | T | 73 | a0001c0001t0001g0102a0001c0001t0001g0150a0001c0001t0001g0163others(70): Show | 73 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.11556-9909C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79779062 | ||||||
| chr5:79779069
|
C | T | 4 | a0003c0003t0008g0018a0003c0003t0009g0313a0023c0022t0008g0016others(1): Show | 4 | HG02630.hp2 HG02896.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.11556-9902C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79779069 | ||||||
| chr5:79779096
|
A | G | 64 | a0001c0001t0001g0063a0001c0001t0001g0198a0001c0013t0002g0041others(61): Show | 65 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.11556-9875A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79779096 | ||||||
| chr5:79779117
|
T | C | 5 | a0019c0024t0017g0355a0030c0095t0003g0271a0035c0037t0011g0319others(2): Show | 5 | HG01243.hp1 HG02451.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.11556-9854T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79779117 | ||||||
| chr5:79779127
|
T | C | 1 | a0041c0041t0005g0001 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.11556-9844T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79779127 | ||||||
| chr5:79779159
|
C | T | 1 | a0046c0098t0005g0259 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.11556-9812C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79779159 | ||||||
| chr5:79779160
|
G | A | 3 | a0002c0002t0002g0209a0002c0002t0002g0229a0002c0002t0002g0238 | 3 | NA18949.hp2 NA18955.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.11556-9811G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79779160 | ||||||
| chr5:79779193
|
T | A | 1 | a0004c0014t0002g0158 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.11556-9778T>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79779193 | ||||||
| chr5:79779314
|
T | C | 1 | a0033c0039t0001g0003 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.11556-9657T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79779314 | ||||||
| chr5:79779366
|
A | G | 6 | a0009c0009t0001g0264a0009c0009t0001g0357a0009c0009t0002g0265others(3): Show | 7 | HG00741.hp1 HG02258.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.11556-9605A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79779366 | ||||||
| chr5:79779376
|
G | A | 3 | a0002c0002t0002g0288a0025c0023t0001g0106a0025c0023t0002g0203 | 3 | HG02015.hp2 NA18995.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.11556-9595G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79779376 | ||||||
| chr5:79779484
|
G | A | 73 | a0001c0001t0001g0102a0001c0001t0001g0150a0001c0001t0001g0163others(70): Show | 73 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.11556-9487G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79779484 | ||||||
| chr5:79779665
|
T | C | 6 | a0009c0009t0001g0346a0020c0025t0001g0278a0020c0025t0001g0309others(3): Show | 6 | HG02486.hp2 HG02970.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.11556-9306T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79779665 | ||||||
| chr5:79779700
|
C | T | 5 | a0009c0009t0001g0346a0020c0025t0001g0278a0020c0025t0001g0309others(2): Show | 5 | HG02486.hp2 HG03195.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.11556-9271C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79779700 | ||||||
| chr5:79779740
|
C | T | 60 | a0001c0001t0001g0063a0001c0001t0001g0198a0001c0013t0002g0041others(57): Show | 61 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.11556-9231C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79779740 | ||||||
| chr5:79779788
|
G | C | 192 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0063others(189): Show | 193 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(190): Show |
intron_variant | MODIFIER | c.11556-9183G>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79779788 | ||||||
| chr5:79779836
|
T | G | 208 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0064others(205): Show | 208 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(205): Show |
intron_variant | MODIFIER | c.11556-9135T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79779836 | ||||||
| chr5:79779838
|
C | T | 2 | a0003c0034t0009g0320a0003c0034t0012g0021 | 2 | HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.11556-9133C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79779838 | ||||||
| chr5:79779839
|
G | A | 1 | a0012c0015t0016g0318 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.11556-9132G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79779839 | ||||||
| chr5:79779861
|
G | A | 5 | a0009c0009t0001g0346a0020c0025t0001g0278a0020c0025t0001g0309others(2): Show | 5 | HG02486.hp2 HG03195.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.11556-9110G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79779861 | ||||||
| chr5:79780046
|
A | C | 3 | a0001c0001t0002g0056a0007c0097t0002g0347a0019c0024t0001g0181 | 3 | HG02683.hp2 HG02735.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.11556-8925A>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79780046 | ||||||
| chr5:79780054
|
C | T | 4 | a0031c0046t0001g0186a0031c0046t0002g0182a0039c0030t0002g0314others(1): Show | 4 | HG02055.hp1 HG02257.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.11556-8917C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79780054 | ||||||
| chr5:79780055
|
G | A | 3 | a0015c0032t0007g0027a0015c0032t0007g0034a0050c0104t0003g0272 | 3 | HG02451.hp2 HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.11556-8916G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79780055 | ||||||
| chr5:79780131
|
A | C | 199 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0064others(196): Show | 199 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(196): Show |
intron_variant | MODIFIER | c.11556-8840A>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79780131 | ||||||
| chr5:79780134
|
G | A | 1 | a0072c0071t0002g0191 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.11556-8837G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79780134 | ||||||
| chr5:79780191
|
T | C | 1 | a0001c0001t0001g0198 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.11556-8780T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79780191 | ||||||
| chr5:79780211
|
G | T | 1 | a0011c0012t0002g0248 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.11556-8760G>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79780211 | ||||||
| chr5:79780233
|
G | A | 2 | a0003c0034t0009g0320a0003c0034t0012g0021 | 2 | HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.11556-8738G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79780233 | ||||||
| chr5:79780425
|
A | C | 2 | a0001c0013t0006g0140a0006c0004t0006g0156 | 2 | HG00621.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.11556-8546A>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79780425 | ||||||
| chr5:79780510
|
T | C | 1 | a0005c0085t0001g0223 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.11556-8461T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79780510 | ||||||
| chr5:79780522
|
C | T | 75 | a0001c0001t0001g0102a0001c0001t0001g0150a0001c0001t0001g0163others(72): Show | 75 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.11556-8449C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79780522 | ||||||
| chr5:79780594
|
G | C | 2 | a0003c0034t0009g0320a0003c0034t0012g0021 | 2 | HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.11556-8377G>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79780594 | ||||||
| chr5:79780695
|
C | A | 14 | a0002c0002t0001g0043a0002c0002t0002g0071a0002c0002t0002g0209others(11): Show | 14 | HG02015.hp2 HG02165.hp1 NA18943.hp2 others(11): Show |
intron_variant | MODIFIER | c.11556-8276C>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79780695 | ||||||
| chr5:79780709
|
C | G | 1 | a0023c0022t0001g0185 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.11556-8262C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79780709 | ||||||
| chr5:79780822
|
C | T | 1 | a0001c0001t0002g0175 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.11556-8149C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79780822 | ||||||
| chr5:79780853
|
G | A | 1 | a0002c0106t0007g0029 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.11556-8118G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79780853 | ||||||
| chr5:79780859
|
A | G | 3 | a0030c0095t0003g0271a0058c0092t0003g0263a0072c0071t0002g0191 | 3 | HG01243.hp1 HG02451.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.11556-8112A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79780859 | ||||||
| chr5:79780872
|
T | G | 1 | a0005c0005t0004g0017 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.11556-8099T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79780872 | ||||||
| chr5:79780922
|
G | A | 4 | a0002c0106t0007g0029a0015c0032t0007g0027a0015c0032t0007g0034others(1): Show | 4 | HG02451.hp2 HG03209.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.11556-8049G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79780922 | ||||||
| chr5:79780924
|
T | G | 1 | a0003c0069t0002g0310 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.11556-8047T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79780924 | ||||||
| chr5:79780964
|
T | C | 262 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0063others(259): Show | 263 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(260): Show |
intron_variant | MODIFIER | c.11556-8007T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79780964 | ||||||
| chr5:79781014
|
G | T | 2 | a0003c0003t0002g0058a0063c0064t0002g0282 | 2 | HG04199.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.11556-7957G>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79781014 | ||||||
| chr5:79781085
|
G | A | 6 | a0002c0106t0007g0029a0003c0034t0009g0320a0003c0034t0012g0021others(3): Show | 6 | HG02451.hp2 HG03209.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.11556-7886G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79781085 | ||||||
| chr5:79781246
|
T | G | 5 | a0001c0001t0010g0084a0001c0001t0010g0085a0005c0005t0001g0270others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.11556-7725T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79781246 | ||||||
| chr5:79781333
|
G | T | 1 | a0054c0108t0001g0187 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.11556-7638G>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79781333 | ||||||
| chr5:79781354
|
C | G | 1 | a0030c0096t0001g0274 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.11556-7617C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79781354 | ||||||
| chr5:79781377
|
C | G | 9 | a0001c0001t0010g0084a0001c0001t0010g0085a0005c0005t0001g0270others(6): Show | 9 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.11556-7594C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79781377 | ||||||
| chr5:79781388
|
G | A | 4 | a0002c0106t0007g0029a0015c0032t0007g0027a0015c0032t0007g0034others(1): Show | 4 | HG02451.hp2 HG03209.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.11556-7583G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79781388 | ||||||
| chr5:79781505
|
T | C | 199 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0064others(196): Show | 199 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(196): Show |
intron_variant | MODIFIER | c.11556-7466T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79781505 | ||||||
| chr5:79781536
|
C | T | 2 | a0019c0024t0001g0184a0029c0044t0012g0036 | 2 | HG03209.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.11556-7435C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79781536 | ||||||
| chr5:79781660
|
C | G | 266 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0063others(263): Show | 267 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(264): Show |
intron_variant | MODIFIER | c.11556-7311C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79781660 | ||||||
| chr5:79781701
|
CGTAGAGG others(280): Show |
C | 1 | a0011c0012t0002g0273 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.11556-7267_11556-6 others(6): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79781701 | |||||
| chr5:79781715
|
T | C | 4 | a0002c0002t0001g0043a0003c0003t0002g0167a0004c0014t0002g0195others(1): Show | 4 | NA18943.hp2 NA19056.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.11556-7256T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79781715 | ||||||
| chr5:79781752
|
C | T | 56 | a0001c0001t0001g0063a0001c0001t0001g0198a0001c0013t0002g0041others(53): Show | 57 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.11556-7219C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79781752 | ||||||
| chr5:79781785
|
T | C | 29 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0064others(26): Show | 29 | HG01081.hp2 HG01192.hp2 HG01258.hp2 others(26): Show |
intron_variant | MODIFIER | c.11556-7186T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79781785 | ||||||
| chr5:79781825
|
T | C | 7 | a0003c0003t0001g0153a0007c0008t0001g0168a0007c0008t0001g0340others(4): Show | 7 | HG01074.hp1 HG02717.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.11556-7146T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79781825 | ||||||
| chr5:79781831
|
C | T | 2 | a0028c0043t0001g0183a0028c0043t0001g0267 | 2 | HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.11556-7140C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79781831 | ||||||
| chr5:79781882
|
G | A | 1 | a0016c0018t0001g0169 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.11556-7089G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79781882 | ||||||
| chr5:79781907
|
T | C | 198 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0064others(195): Show | 198 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(195): Show |
intron_variant | MODIFIER | c.11556-7064T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79781907 | ||||||
| chr5:79781941
|
T | C | 2 | a0028c0043t0001g0183a0028c0043t0001g0267 | 2 | HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.11556-7030T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79781941 | ||||||
| chr5:79781968
|
G | T | 18 | a0001c0001t0001g0246a0001c0001t0001g0292a0002c0002t0001g0043others(15): Show | 18 | HG02015.hp2 HG02165.hp1 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.11556-7003G>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79781968 | ||||||
| chr5:79781998
|
A | T | 1 | a0011c0012t0002g0273 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.11556-6973A>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79781998 | ||||||
| chr5:79782001
|
G | C | 1 | a0011c0012t0002g0273 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.11556-6970G>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79782001 | ||||||
| chr5:79782004
|
A | T | 1 | a0011c0012t0002g0273 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.11556-6967A>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79782004 | ||||||
| chr5:79782006
|
G | A | 1 | a0011c0012t0002g0273 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.11556-6965G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79782006 | ||||||
| chr5:79782009
|
A | T | 1 | a0011c0012t0002g0273 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.11556-6962A>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79782009 | ||||||
| chr5:79782011
|
G | C | 1 | a0011c0012t0002g0273 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.11556-6960G>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79782011 | ||||||
| chr5:79782013
|
TGTCAATT others(271): Show |
T | 1 | a0011c0012t0002g0273 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.11556-6957_11556-6 others(6): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79782013 | ||||||
| chr5:79782071
|
T | C | 203 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0064others(200): Show | 203 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(200): Show |
intron_variant | MODIFIER | c.11556-6900T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79782071 | ||||||
| chr5:79782074
|
A | G | 1 | a0006c0004t0002g0123 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.11556-6897A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79782074 | ||||||
| chr5:79782127
|
C | T | 204 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0064others(201): Show | 204 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(201): Show |
intron_variant | MODIFIER | c.11556-6844C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79782127 | ||||||
| chr5:79782167
|
G | A | 2 | a0001c0001t0001g0171a0021c0026t0002g0252 | 2 | HG02602.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.11556-6804G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79782167 | ||||||
| chr5:79782236
|
A | T | 1 | a0016c0018t0001g0176 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.11556-6735A>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79782236 | ||||||
| chr5:79782250
|
G | C | 2 | a0003c0034t0009g0320a0003c0034t0012g0021 | 2 | HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.11556-6721G>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79782250 | ||||||
| chr5:79782288
|
G | C | 3 | a0030c0095t0003g0271a0058c0092t0003g0263a0072c0071t0002g0191 | 3 | HG01243.hp1 HG02451.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.11556-6683G>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79782288 | ||||||
| chr5:79782293
|
A | T | 1 | a0011c0012t0002g0273 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.11556-6678A>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79782293 | ||||||
| chr5:79782306
|
T | C | 2 | a0009c0009t0001g0346a0020c0025t0001g0344 | 2 | HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.11556-6665T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79782306 | ||||||
| chr5:79782348
|
A | G | 18 | a0001c0001t0001g0246a0001c0001t0001g0292a0002c0002t0001g0043others(15): Show | 18 | HG02015.hp2 HG02165.hp1 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.11556-6623A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79782348 | ||||||
| chr5:79782434
|
T | C | 28 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0064others(25): Show | 28 | HG01081.hp2 HG01099.hp1 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.11556-6537T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79782434 | ||||||
| chr5:79782469
|
T | C | 204 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0064others(201): Show | 204 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(201): Show |
intron_variant | MODIFIER | c.11556-6502T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79782469 | ||||||
| chr5:79782488
|
C | T | 2 | a0003c0034t0009g0320a0003c0034t0012g0021 | 2 | HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.11556-6483C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79782488 | ||||||
| chr5:79782528
|
T | C | 349 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(346): Show | 350 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(347): Show |
intron_variant | MODIFIER | c.11556-6443T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79782528 | ||||||
| chr5:79782551
|
T | C | 201 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0064others(198): Show | 201 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(198): Show |
intron_variant | MODIFIER | c.11556-6420T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79782551 | ||||||
| chr5:79782610
|
G | A | 55 | a0001c0001t0001g0102a0001c0001t0001g0150a0001c0001t0001g0163others(52): Show | 55 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.11556-6361G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79782610 | ||||||
| chr5:79782617
|
A | T | 56 | a0001c0001t0001g0102a0001c0001t0001g0150a0001c0001t0001g0163others(53): Show | 56 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.11556-6354A>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79782617 | ||||||
| chr5:79782646
|
G | A | 2 | a0001c0001t0001g0165a0004c0006t0001g0078 | 2 | HG03017.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.11556-6325G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79782646 | ||||||
| chr5:79782692
|
G | C | 3 | a0030c0095t0003g0271a0058c0092t0003g0263a0072c0071t0002g0191 | 3 | HG01243.hp1 HG02451.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.11556-6279G>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79782692 | ||||||
| chr5:79782746
|
C | T | 1 | a0041c0041t0005g0001 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.11556-6225C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79782746 | ||||||
| chr5:79782764
|
G | T | 73 | a0001c0001t0001g0102a0001c0001t0001g0150a0001c0001t0001g0163others(70): Show | 73 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.11556-6207G>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79782764 | ||||||
| chr5:79782854
|
A | G | 268 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0063others(265): Show | 269 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(266): Show |
intron_variant | MODIFIER | c.11556-6117A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79782854 | ||||||
| chr5:79782914
|
T | C | 11 | a0001c0001t0010g0084a0001c0001t0010g0085a0003c0034t0009g0320others(8): Show | 11 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.11556-6057T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79782914 | ||||||
| chr5:79783057
|
G | A | 189 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0064others(186): Show | 189 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(186): Show |
intron_variant | MODIFIER | c.11556-5914G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79783057 | ||||||
| chr5:79783116
|
A | G | 268 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0063others(265): Show | 269 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(266): Show |
intron_variant | MODIFIER | c.11556-5855A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79783116 | ||||||
| chr5:79783131
|
A | C | 60 | a0001c0001t0001g0063a0001c0001t0001g0198a0001c0013t0002g0041others(57): Show | 61 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.11556-5840A>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79783131 | ||||||
| chr5:79783146
|
A | G | 60 | a0001c0001t0001g0063a0001c0001t0001g0198a0001c0013t0002g0041others(57): Show | 61 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.11556-5825A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79783146 | ||||||
| chr5:79783228
|
G | C | 191 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0064others(188): Show | 191 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(188): Show |
intron_variant | MODIFIER | c.11556-5743G>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79783228 | ||||||
| chr5:79783256
|
C | T | 202 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0064others(199): Show | 202 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(199): Show |
intron_variant | MODIFIER | c.11556-5715C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79783256 | ||||||
| chr5:79783277
|
C | T | 1 | a0023c0022t0001g0185 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.11556-5694C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79783277 | ||||||
| chr5:79783280
|
G | C | 1 | a0001c0001t0001g0235 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.11556-5691G>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79783280 | ||||||
| chr5:79783304
|
C | T | 2 | a0003c0034t0009g0320a0003c0034t0012g0021 | 2 | HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.11556-5667C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79783304 | ||||||
| chr5:79783335
|
C | T | 204 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0064others(201): Show | 204 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(201): Show |
intron_variant | MODIFIER | c.11556-5636C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79783335 | ||||||
| chr5:79783382
|
G | C | 199 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0064others(196): Show | 199 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(196): Show |
intron_variant | MODIFIER | c.11556-5589G>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79783382 | ||||||
| chr5:79783438
|
G | C | 2 | a0003c0034t0009g0320a0003c0034t0012g0021 | 2 | HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.11556-5533G>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79783438 | ||||||
| chr5:79783456
|
T | C | 268 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0063others(265): Show | 269 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(266): Show |
intron_variant | MODIFIER | c.11556-5515T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79783456 | ||||||
| chr5:79783536
|
A | C | 1 | a0007c0008t0002g0301 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.11556-5435A>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79783536 | ||||||
| chr5:79783565
|
T | G | 1 | a0007c0008t0004g0032 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.11556-5406T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79783565 | ||||||
| chr5:79783617
|
C | A | 1 | a0018c0017t0001g0067 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.11556-5354C>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79783617 | ||||||
| chr5:79783624
|
T | C | 1 | a0003c0003t0002g0167 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.11556-5347T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79783624 | ||||||
| chr5:79783650
|
C | T | 7 | a0003c0003t0001g0153a0007c0008t0001g0168a0007c0008t0001g0340others(4): Show | 7 | HG01074.hp1 HG02717.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.11556-5321C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79783650 | ||||||
| chr5:79783651
|
G | A | 5 | a0028c0043t0001g0183a0028c0043t0001g0267a0030c0095t0003g0271others(2): Show | 5 | HG01243.hp1 HG02451.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.11556-5320G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79783651 | ||||||
| chr5:79783651
|
G | C | 18 | a0001c0001t0001g0246a0001c0001t0001g0292a0002c0002t0001g0043others(15): Show | 18 | HG02015.hp2 HG02165.hp1 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.11556-5320G>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79783651 | ||||||
| chr5:79783746
|
C | G | 2 | a0003c0034t0009g0320a0003c0034t0012g0021 | 2 | HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.11556-5225C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79783746 | ||||||
| chr5:79783747
|
G | T | 3 | a0030c0095t0003g0271a0058c0092t0003g0263a0072c0071t0002g0191 | 3 | HG01243.hp1 HG02451.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.11556-5224G>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79783747 | ||||||
| chr5:79783950
|
G | A | 2 | a0003c0069t0002g0310a0079c0081t0002g0091 | 2 | HG00642.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.11556-5021G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79783950 | ||||||
| chr5:79783968
|
C | T | 1 | a0041c0041t0005g0001 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.11556-5003C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79783968 | ||||||
| chr5:79783969
|
G | A | 1 | a0002c0002t0002g0209 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.11556-5002G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79783969 | ||||||
| chr5:79783979
|
A | T | 5 | a0009c0009t0001g0346a0020c0025t0001g0278a0020c0025t0001g0309others(2): Show | 5 | HG02486.hp2 HG03195.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.11556-4992A>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79783979 | ||||||
| chr5:79783998
|
A | G | 268 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0063others(265): Show | 269 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(266): Show |
intron_variant | MODIFIER | c.11556-4973A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79783998 | ||||||
| chr5:79784096
|
G | T | 56 | a0001c0001t0001g0063a0001c0001t0001g0198a0001c0013t0002g0041others(53): Show | 57 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.11556-4875G>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79784096 | ||||||
| chr5:79784101
|
A | G | 1 | a0036c0070t0003g0060 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.11556-4870A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79784101 | ||||||
| chr5:79784120
|
T | G | 1 | a0026c0028t0002g0075 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.11556-4851T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79784120 | ||||||
| chr5:79784166
|
A | G | 2 | a0009c0009t0014g0266a0029c0044t0004g0026 | 2 | HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.11556-4805A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79784166 | ||||||
| chr5:79784172
|
C | G | 1 | a0017c0019t0001g0280 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.11556-4799C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79784172 | ||||||
| chr5:79784175
|
C | T | 52 | a0001c0001t0001g0095a0001c0001t0001g0124a0001c0001t0001g0125others(49): Show | 52 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.11556-4796C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79784175 | ||||||
| chr5:79784181
|
G | A | 52 | a0001c0001t0001g0095a0001c0001t0001g0124a0001c0001t0001g0125others(49): Show | 52 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.11556-4790G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79784181 | ||||||
| chr5:79784197
|
C | T | 1 | a0026c0028t0002g0075 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.11556-4774C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79784197 | ||||||
| chr5:79784216
|
C | T | 1 | a0073c0076t0001g0101 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.11556-4755C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79784216 | ||||||
| chr5:79784229
|
C | T | 1 | a0066c0057t0003g0219 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.11556-4742C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79784229 | ||||||
| chr5:79784230
|
G | A | 1 | a0003c0003t0001g0192 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.11556-4741G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79784230 | ||||||
| chr5:79784234
|
G | C | 6 | a0002c0002t0001g0008a0003c0003t0001g0242a0003c0003t0003g0352others(3): Show | 6 | HG02132.hp1 HG03704.hp2 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.11556-4737G>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79784234 | ||||||
| chr5:79784235
|
T | A | 6 | a0002c0002t0001g0008a0003c0003t0001g0242a0003c0003t0003g0352others(3): Show | 6 | HG02132.hp1 HG03704.hp2 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.11556-4736T>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79784235 | ||||||
| chr5:79784273
|
G | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG01516.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.11556-4698G>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79784273 | ||||||
| chr5:79784364
|
T | A | 1 | a0024c0084t0001g0172 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.11556-4607T>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79784364 | ||||||
| chr5:79784387
|
C | A | 1 | a0016c0018t0002g0146 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.11556-4584C>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79784387 | ||||||
| chr5:79784405
|
A | G | 1 | a0024c0084t0001g0172 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.11556-4566A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79784405 | ||||||
| chr5:79784419
|
G | T | 1 | a0001c0001t0001g0240 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.11556-4552G>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79784419 | ||||||
| chr5:79784434
|
G | C | 39 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0064others(36): Show | 39 | HG01081.hp2 HG01099.hp1 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.11556-4537G>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79784434 | ||||||
| chr5:79784462
|
G | A | 68 | a0001c0001t0001g0095a0001c0001t0001g0124a0001c0001t0001g0125others(65): Show | 68 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.11556-4509G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79784462 | ||||||
| chr5:79784498
|
C | T | 3 | a0001c0001t0001g0241a0002c0002t0001g0173a0004c0006t0001g0256 | 3 | HG04204.hp1 NA18973.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.11556-4473C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79784498 | ||||||
| chr5:79784502
|
A | C | 5 | a0001c0001t0001g0241a0001c0001t0010g0084a0001c0001t0010g0085others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.11556-4469A>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79784502 | ||||||
| chr5:79784549
|
G | A | 7 | a0010c0010t0001g0336a0010c0010t0002g0245a0010c0010t0002g0254others(4): Show | 7 | HG00099.hp2 HG00323.hp1 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.11556-4422G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79784549 | ||||||
| chr5:79784571
|
T | C | 2 | a0003c0069t0002g0310a0079c0081t0002g0091 | 2 | HG00642.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.11556-4400T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79784571 | ||||||
| chr5:79784592
|
T | C | 3 | a0003c0003t0009g0313a0003c0034t0009g0320a0003c0034t0012g0021 | 3 | HG02896.hp2 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.11556-4379T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79784592 | ||||||
| chr5:79784603
|
T | C | 1 | a0005c0005t0002g0214 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.11556-4368T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79784603 | ||||||
| chr5:79784689
|
G | A | 3 | a0030c0095t0003g0271a0058c0092t0003g0263a0072c0071t0002g0191 | 3 | HG01243.hp1 HG02451.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.11556-4282G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79784689 | ||||||
| chr5:79784692
|
C | T | 10 | a0002c0106t0007g0029a0002c0114t0001g0196a0003c0003t0008g0018others(7): Show | 10 | HG02027.hp2 HG02135.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.11556-4279C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79784692 | ||||||
| chr5:79784743
|
C | T | 64 | a0001c0001t0001g0063a0001c0001t0001g0198a0001c0013t0002g0041others(61): Show | 65 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.11556-4228C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79784743 | ||||||
| chr5:79784780
|
T | G | 110 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0063others(107): Show | 111 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.11556-4191T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79784780 | ||||||
| chr5:79784790
|
C | T | 4 | a0006c0004t0001g0161a0006c0004t0001g0162a0006c0004t0001g0225others(1): Show | 4 | NA18943.hp1 NA18957.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.11556-4181C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79784790 | ||||||
| chr5:79784791
|
G | A | 2 | a0004c0014t0002g0244a0030c0096t0001g0274 | 2 | HG02970.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.11556-4180G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79784791 | ||||||
| chr5:79784828
|
A | G | 64 | a0001c0001t0001g0063a0001c0001t0001g0198a0001c0013t0002g0041others(61): Show | 65 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.11556-4143A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79784828 | ||||||
| chr5:79784880
|
G | A | 1 | a0007c0008t0011g0341 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.11556-4091G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79784880 | ||||||
| chr5:79784889
|
A | T | 2 | a0002c0002t0001g0222a0026c0049t0006g0073 | 2 | HG01981.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.11556-4082A>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79784889 | ||||||
| chr5:79784890
|
C | T | 9 | a0007c0008t0001g0311a0007c0008t0004g0030a0009c0009t0001g0322others(6): Show | 9 | HG01167.hp2 HG02109.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.11556-4081C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79784890 | ||||||
| chr5:79784899
|
C | G | 1 | a0036c0070t0003g0060 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.11556-4072C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79784899 | ||||||
| chr5:79784923
|
C | T | 54 | a0001c0001t0001g0102a0001c0001t0001g0150a0001c0001t0001g0163others(51): Show | 54 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.11556-4048C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79784923 | ||||||
| chr5:79785037
|
A | G | 1 | a0072c0071t0002g0191 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.11556-3934A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79785037 | ||||||
| chr5:79785068
|
C | T | 4 | a0003c0003t0008g0018a0003c0003t0009g0313a0023c0022t0008g0016others(1): Show | 4 | HG02630.hp2 HG02896.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.11556-3903C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79785068 | ||||||
| chr5:79785107
|
T | C | 1 | a0002c0106t0007g0029 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.11556-3864T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79785107 | ||||||
| chr5:79785145
|
C | A | 1 | a0015c0073t0015g0343 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.11556-3826C>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79785145 | ||||||
| chr5:79785212
|
T | G | 7 | a0003c0003t0001g0153a0007c0008t0001g0168a0007c0008t0001g0340others(4): Show | 7 | HG01074.hp1 HG02717.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.11556-3759T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79785212 | ||||||
| chr5:79785274
|
A | G | 3 | a0001c0001t0001g0246a0001c0001t0001g0292a0069c0062t0001g0088 | 3 | HG02698.hp2 HG04184.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.11556-3697A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79785274 | ||||||
| chr5:79785501
|
T | G | 1 | a0019c0024t0001g0181 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.11556-3470T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79785501 | ||||||
| chr5:79785611
|
A | G | 3 | a0030c0095t0003g0271a0058c0092t0003g0263a0072c0071t0002g0191 | 3 | HG01243.hp1 HG02451.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.11556-3360A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79785611 | ||||||
| chr5:79785688
|
A | G | 38 | a0001c0001t0001g0063a0001c0001t0001g0198a0001c0013t0002g0041others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.11556-3283A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79785688 | ||||||
| chr5:79785724
|
T | G | 1 | a0008c0007t0002g0006 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.11556-3247T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79785724 | ||||||
| chr5:79785816
|
A | G | 56 | a0001c0001t0001g0063a0001c0001t0001g0198a0001c0013t0002g0041others(53): Show | 57 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.11556-3155A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79785816 | ||||||
| chr5:79785890
|
A | G | 108 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0063others(105): Show | 109 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.11556-3081A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79785890 | ||||||
| chr5:79785915
|
G | A | 1 | a0008c0007t0001g0009 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.11556-3056G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79785915 | ||||||
| chr5:79786018
|
G | A | 50 | a0001c0001t0001g0063a0001c0001t0001g0198a0001c0013t0002g0041others(47): Show | 51 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.11556-2953G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79786018 | ||||||
| chr5:79786269
|
G | A | 6 | a0002c0106t0007g0029a0003c0034t0009g0320a0003c0034t0012g0021others(3): Show | 6 | HG02451.hp2 HG03209.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.11556-2702G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79786269 | ||||||
| chr5:79786339
|
A | T | 1 | a0001c0001t0001g0136 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.11556-2632A>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79786339 | ||||||
| chr5:79786435
|
G | A | 349 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(346): Show | 350 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(347): Show |
intron_variant | MODIFIER | c.11556-2536G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79786435 | ||||||
| chr5:79786524
|
G | A | 16 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0064others(13): Show | 16 | HG01081.hp2 HG01192.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.11556-2447G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79786524 | ||||||
| chr5:79786549
|
T | A | 38 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0064others(35): Show | 38 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(35): Show |
intron_variant | MODIFIER | c.11556-2422T>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79786549 | ||||||
| chr5:79786725
|
A | G | 1 | a0004c0014t0002g0244 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.11556-2246A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79786725 | ||||||
| chr5:79786808
|
T | C | 63 | a0001c0001t0001g0063a0001c0001t0001g0198a0001c0013t0002g0041others(60): Show | 64 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.11556-2163T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79786808 | ||||||
| chr5:79786885
|
G | A | 1 | a0072c0071t0002g0191 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.11556-2086G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79786885 | ||||||
| chr5:79786941
|
C | T | 1 | a0035c0037t0001g0177 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.11556-2030C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79786941 | ||||||
| chr5:79786981
|
G | T | 5 | a0005c0089t0001g0348a0011c0052t0001g0284a0033c0039t0001g0279others(2): Show | 5 | HG01981.hp2 HG02148.hp1 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.11556-1990G>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79786981 | ||||||
| chr5:79787124
|
T | G | 18 | a0001c0001t0001g0246a0001c0001t0001g0292a0002c0002t0001g0043others(15): Show | 18 | HG02015.hp2 HG02165.hp1 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.11556-1847T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79787124 | ||||||
| chr5:79787135
|
G | A | 7 | a0003c0003t0001g0153a0007c0008t0001g0168a0007c0008t0001g0340others(4): Show | 7 | HG01074.hp1 HG02717.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.11556-1836G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79787135 | ||||||
| chr5:79787224
|
C | G | 86 | a0001c0001t0001g0095a0001c0001t0001g0124a0001c0001t0001g0125others(83): Show | 86 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.11556-1747C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79787224 | ||||||
| chr5:79787251
|
C | A | 56 | a0001c0001t0001g0063a0001c0001t0001g0198a0001c0013t0002g0041others(53): Show | 57 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.11556-1720C>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79787251 | ||||||
| chr5:79787608
|
G | T | 1 | a0023c0022t0001g0185 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.11556-1363G>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79787608 | ||||||
| chr5:79787644
|
A | G | 55 | a0001c0001t0001g0102a0001c0001t0001g0150a0001c0001t0001g0163others(52): Show | 55 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.11556-1327A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79787644 | ||||||
| chr5:79787783
|
G | C | 2 | a0001c0001t0002g0175a0008c0007t0002g0104 | 2 | NA18941.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.11556-1188G>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79787783 | ||||||
| chr5:79787791
|
G | C | 2 | a0028c0043t0001g0183a0028c0043t0001g0267 | 2 | HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.11556-1180G>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79787791 | ||||||
| chr5:79787856
|
G | A | 85 | a0001c0001t0001g0095a0001c0001t0001g0124a0001c0001t0001g0125others(82): Show | 85 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.11556-1115G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79787856 | ||||||
| chr5:79787856
|
G | T | 1 | a0001c0001t0001g0257 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.11556-1115G>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79787856 | ||||||
| chr5:79787923
|
G | T | 1 | a0004c0011t0001g0277 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.11556-1048G>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79787923 | ||||||
| chr5:79787934
|
G | GA | 86 | a0001c0001t0001g0095a0001c0001t0001g0124a0001c0001t0001g0125others(83): Show | 86 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.11556-1030dupA | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79787934 | |||||
| chr5:79787952
|
G | A | 60 | a0001c0001t0001g0063a0001c0001t0001g0198a0001c0013t0002g0041others(57): Show | 61 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.11556-1019G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79787952 | ||||||
| chr5:79788007
|
C | CA | 9 | a0007c0008t0001g0311a0007c0008t0004g0030a0009c0009t0001g0322others(6): Show | 9 | HG01167.hp2 HG02109.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.11556-955dupA | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79788007 | |||||
| chr5:79788051
|
T | C | 1 | a0007c0008t0002g0179 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.11556-920T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79788051 | ||||||
| chr5:79788174
|
A | T | 8 | a0003c0003t0008g0018a0003c0003t0009g0313a0007c0008t0011g0341others(5): Show | 8 | HG01243.hp1 HG02145.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.11556-797A>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79788174 | ||||||
| chr5:79788212
|
CT | C | 40 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0064others(37): Show | 40 | HG00408.hp1 HG00609.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.11556-744delT | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79788212 | |||||
| chr5:79788325
|
G | A | 37 | a0001c0001t0001g0285a0001c0001t0001g0296a0002c0002t0001g0253others(34): Show | 37 | HG00099.hp2 HG00323.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.11556-646G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79788325 | ||||||
| chr5:79788466
|
A | AT | 46 | a0001c0001t0001g0198a0001c0013t0002g0041a0001c0013t0002g0204others(43): Show | 47 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.11556-487dupT | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79788466 | |||||
| chr5:79788466
|
AT | A | 123 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0064others(120): Show | 123 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(120): Show |
intron_variant | MODIFIER | c.11556-487delT | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79788466 | |||||
| chr5:79788466
|
ATT | A | 84 | a0001c0001t0001g0095a0001c0001t0001g0124a0001c0001t0001g0125others(81): Show | 84 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.11556-488_11556-48 others(6): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79788466 | |||||
| chr5:79788487
|
A | G | 1 | a0030c0096t0001g0274 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.11556-484A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79788487 | ||||||
| chr5:79788583
|
CATG | C | 12 | a0001c0001t0002g0329a0001c0058t0002g0339a0005c0005t0001g0218others(9): Show | 12 | HG01081.hp1 HG01257.hp1 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.11556-382_11556-38 others(7): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 79788583 | |||||
| chr5:79788590
|
A | T | 4 | a0003c0034t0009g0320a0003c0034t0012g0021a0015c0073t0015g0343others(1): Show | 4 | HG02970.hp2 HG03139.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.11556-381A>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79788590 | ||||||
| chr5:79788714
|
T | G | 1 | a0001c0001t0001g0166 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.11556-257T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79788714 | ||||||
| chr5:79788750
|
G | A | 1 | a0002c0002t0001g0128 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.11556-221G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79788750 | ||||||
| chr5:79788886
|
G | A | 1 | a0036c0070t0003g0060 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.11556-85G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79788886 | ||||||
| chr5:79788892
|
C | G | 4 | a0003c0034t0009g0320a0003c0034t0012g0021a0015c0073t0015g0343others(1): Show | 4 | HG02970.hp2 HG03139.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.11556-79C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 9/12 | chr5 | 79788892 | ||||||
| chr5:79789126
|
G | C | 86 | a0001c0001t0001g0095a0001c0001t0001g0124a0001c0001t0001g0125others(83): Show | 86 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.11689+22G>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 10/12 | chr5 | 79789126 | ||||||
| chr5:79789197
|
C | G | 1 | a0080c0090t0002g0094 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.11689+93C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 10/12 | chr5 | 79789197 | ||||||
| chr5:79789251
|
A | G | 3 | a0007c0008t0001g0168a0009c0009t0001g0323a0015c0038t0004g0260 | 3 | HG01074.hp1 HG03041.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.11689+147A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 10/12 | chr5 | 79789251 | ||||||
| chr5:79789288
|
G | T | 4 | a0003c0034t0009g0320a0003c0034t0012g0021a0015c0073t0015g0343others(1): Show | 4 | HG02970.hp2 HG03139.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.11689+184G>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 10/12 | chr5 | 79789288 | ||||||
| chr5:79789429
|
AT | A | 294 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(291): Show | 295 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(292): Show |
intron_variant | MODIFIER | c.11689+338delT | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr5 | 79789429 | |||||
| chr5:79789535
|
A | C | 1 | a0075c0086t0001g0250 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.11689+431A>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 10/12 | chr5 | 79789535 | ||||||
| chr5:79789690
|
T | G | 224 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(221): Show | 225 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(222): Show |
intron_variant | MODIFIER | c.11689+586T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 10/12 | chr5 | 79789690 | ||||||
| chr5:79789719
|
C | T | 7 | a0003c0003t0001g0153a0007c0008t0001g0168a0007c0008t0001g0340others(4): Show | 7 | HG01074.hp1 HG02717.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.11689+615C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 10/12 | chr5 | 79789719 | ||||||
| chr5:79789728
|
C | A | 54 | a0001c0001t0001g0102a0001c0001t0001g0150a0001c0001t0001g0163others(51): Show | 54 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.11689+624C>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 10/12 | chr5 | 79789728 | ||||||
| chr5:79789903
|
A | G | 90 | a0001c0001t0001g0095a0001c0001t0001g0124a0001c0001t0001g0125others(87): Show | 90 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.11689+799A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 10/12 | chr5 | 79789903 | ||||||
| chr5:79790173
|
C | A | 3 | a0012c0015t0004g0022a0012c0015t0004g0023a0012c0015t0004g0028 | 3 | HG02559.hp1 HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.11690-797C>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 10/12 | chr5 | 79790173 | ||||||
| chr5:79790174
|
G | A | 75 | a0001c0001t0001g0102a0001c0001t0001g0150a0001c0001t0001g0163others(72): Show | 75 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.11690-796G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 10/12 | chr5 | 79790174 | ||||||
| chr5:79790174
|
GA | G | 5 | a0001c0001t0010g0084a0001c0001t0010g0085a0005c0005t0001g0270others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.11690-795delA | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 10/12 | chr5 | 79790174 | ||||||
| chr5:79790261
|
C | T | 1 | a0003c0003t0009g0313 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.11690-709C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 10/12 | chr5 | 79790261 | ||||||
| chr5:79790274
|
A | AT | 50 | a0001c0001t0001g0007a0001c0001t0001g0065a0001c0001t0001g0136others(47): Show | 50 | HG00099.hp1 HG00323.hp2 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.11690-685dupT | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr5 | 79790274 | |||||
| chr5:79790289
|
G | A | 1 | a0036c0070t0003g0060 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.11690-681G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 10/12 | chr5 | 79790289 | ||||||
| chr5:79790338
|
C | T | 1 | a0027c0042t0001g0342 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.11690-632C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 10/12 | chr5 | 79790338 | ||||||
| chr5:79790451
|
G | A | 174 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(171): Show | 174 | HG00099.hp1 HG00323.hp2 HG00544.hp2 others(171): Show |
intron_variant | MODIFIER | c.11690-519G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 10/12 | chr5 | 79790451 | ||||||
| chr5:79790459
|
C | T | 32 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0064others(29): Show | 32 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.11690-511C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 10/12 | chr5 | 79790459 | ||||||
| chr5:79790493
|
G | A | 295 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(292): Show | 296 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(293): Show |
intron_variant | MODIFIER | c.11690-477G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 10/12 | chr5 | 79790493 | ||||||
| chr5:79790565
|
G | T | 3 | a0010c0010t0001g0262a0013c0016t0001g0180a0013c0016t0004g0019 | 3 | HG02055.hp2 HG02647.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.11690-405G>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 10/12 | chr5 | 79790565 | ||||||
| chr5:79790574
|
C | A | 1 | a0003c0003t0002g0070 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.11690-396C>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 10/12 | chr5 | 79790574 | ||||||
| chr5:79790656
|
C | T | 1 | a0029c0044t0004g0026 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.11690-314C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 10/12 | chr5 | 79790656 | ||||||
| chr5:79790722
|
A | G | 1 | a0013c0016t0001g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.11690-248A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 10/12 | chr5 | 79790722 | ||||||
| chr5:79790774
|
C | G | 1 | a0067c0059t0001g0299 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.11690-196C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 10/12 | chr5 | 79790774 | ||||||
| chr5:79790796
|
G | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG01516.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.11690-174G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 10/12 | chr5 | 79790796 | ||||||
| chr5:79790797
|
G | A | 36 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0064others(33): Show | 36 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(33): Show |
intron_variant | MODIFIER | c.11690-173G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 10/12 | chr5 | 79790797 | ||||||
| chr5:79790804
|
C | T | 79 | a0001c0001t0001g0095a0001c0001t0001g0124a0001c0001t0001g0165others(76): Show | 79 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.11690-166C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 10/12 | chr5 | 79790804 | ||||||
| chr5:79790826
|
G | A | 308 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(305): Show | 309 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(306): Show |
intron_variant | MODIFIER | c.11690-144G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 10/12 | chr5 | 79790826 | ||||||
| chr5:79790870
|
G | A | 1 | a0004c0006t0002g0144 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.11690-100G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 10/12 | chr5 | 79790870 | ||||||
| chr5:79791080
|
G | A | 42 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0064others(39): Show | 42 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(39): Show |
intron_variant | MODIFIER | c.11789+11G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 11/12 | chr5 | 79791080 | ||||||
| chr5:79791132
|
G | A | 4 | a0003c0003t0008g0018a0003c0003t0009g0313a0023c0022t0008g0016others(1): Show | 4 | HG02630.hp2 HG02896.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.11789+63G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 11/12 | chr5 | 79791132 | ||||||
| chr5:79791137
|
A | G | 3 | a0009c0009t0002g0265a0009c0009t0002g0268a0012c0015t0016g0318 | 3 | HG00741.hp1 HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.11789+68A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 11/12 | chr5 | 79791137 | ||||||
| chr5:79791150
|
C | T | 6 | a0001c0001t0001g0285a0001c0001t0001g0296a0002c0002t0001g0253others(3): Show | 6 | HG00642.hp1 HG01069.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.11789+81C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 11/12 | chr5 | 79791150 | ||||||
| chr5:79791221
|
G | C | 1 | a0003c0003t0001g0015 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.11789+152G>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 11/12 | chr5 | 79791221 | ||||||
| chr5:79791241
|
C | T | 28 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0064others(25): Show | 28 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.11789+172C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 11/12 | chr5 | 79791241 | ||||||
| chr5:79791242
|
G | A | 77 | a0001c0001t0001g0095a0001c0001t0001g0124a0001c0001t0001g0165others(74): Show | 77 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.11789+173G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 11/12 | chr5 | 79791242 | ||||||
| chr5:79791475
|
C | T | 65 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0165others(62): Show | 65 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.11789+406C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 11/12 | chr5 | 79791475 | ||||||
| chr5:79791479
|
G | A | 214 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0063others(211): Show | 214 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.11789+410G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 11/12 | chr5 | 79791479 | ||||||
| chr5:79791483
|
G | T | 2 | a0001c0001t0002g0056a0007c0097t0002g0347 | 2 | HG02683.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.11789+414G>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 11/12 | chr5 | 79791483 | ||||||
| chr5:79791522
|
A | G | 1 | a0029c0044t0004g0026 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.11789+453A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 11/12 | chr5 | 79791522 | ||||||
| chr5:79791542
|
G | A | 16 | a0002c0106t0007g0029a0003c0003t0001g0192a0009c0009t0001g0346others(13): Show | 16 | HG01496.hp1 HG02055.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.11789+473G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 11/12 | chr5 | 79791542 | ||||||
| chr5:79791556
|
A | G | 2 | a0030c0095t0003g0271a0058c0092t0003g0263 | 2 | HG02451.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.11789+487A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 11/12 | chr5 | 79791556 | ||||||
| chr5:79791664
|
G | T | 1 | a0001c0001t0001g0285 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.11789+595G>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 11/12 | chr5 | 79791664 | ||||||
| chr5:79791713
|
C | CA | 13 | a0001c0001t0001g0013a0002c0002t0002g0143a0003c0003t0003g0105others(10): Show | 13 | HG01109.hp1 HG01167.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.11789+664dupA | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr5 | 79791713 | |||||
| chr5:79791713
|
CA | C | 45 | a0001c0001t0001g0064a0001c0001t0001g0235a0002c0002t0001g0222others(42): Show | 46 | HG00408.hp1 HG00609.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.11789+664delA | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr5 | 79791713 | |||||
| chr5:79791713
|
CAA | C | 25 | a0001c0001t0001g0246a0001c0001t0001g0292a0002c0002t0002g0054others(22): Show | 25 | HG02015.hp2 HG02145.hp2 HG02165.hp1 others(22): Show |
intron_variant | MODIFIER | c.11789+663_11789+66 others(6): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr5 | 79791713 | |||||
| chr5:79791713
|
CAAA | C | 7 | a0003c0003t0001g0153a0007c0008t0001g0168a0007c0008t0001g0340others(4): Show | 7 | HG01074.hp1 HG02717.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.11789+662_11789+66 others(7): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr5 | 79791713 | |||||
| chr5:79791713
|
CAAAAA | C | 157 | a0001c0001t0001g0063a0001c0001t0001g0102a0001c0001t0001g0124others(154): Show | 157 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.11789+660_11789+66 others(9): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr5 | 79791713 | |||||
| chr5:79791952
|
T | C | 2 | a0001c0033t0001g0139a0001c0055t0001g0116 | 2 | HG02080.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.11789+883T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 11/12 | chr5 | 79791952 | ||||||
| chr5:79791953
|
G | T | 5 | a0002c0002t0002g0066a0004c0006t0002g0210a0008c0007t0002g0111others(2): Show | 5 | NA18953.hp2 NA18963.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.11789+884G>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 11/12 | chr5 | 79791953 | ||||||
| chr5:79792109
|
T | A | 1 | a0010c0065t0002g0080 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.11789+1040T>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 11/12 | chr5 | 79792109 | ||||||
| chr5:79792249
|
T | C | 3 | a0003c0003t0008g0018a0023c0022t0008g0016a0023c0022t0008g0025 | 3 | HG02630.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.11789+1180T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 11/12 | chr5 | 79792249 | ||||||
| chr5:79792328
|
G | GA | 18 | a0001c0001t0001g0124a0001c0001t0001g0198a0001c0001t0001g0235others(15): Show | 18 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(15): Show |
intron_variant | MODIFIER | c.11790-1103dupA | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr5 | 79792328 | |||||
| chr5:79792409
|
G | A | 1 | a0066c0057t0003g0219 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.11790-1028G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 11/12 | chr5 | 79792409 | ||||||
| chr5:79792454
|
G | T | 1 | a0004c0011t0003g0251 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.11790-983G>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 11/12 | chr5 | 79792454 | ||||||
| chr5:79792493
|
A | G | 1 | a0002c0106t0007g0029 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.11790-944A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 11/12 | chr5 | 79792493 | ||||||
| chr5:79792573
|
A | G | 1 | a0008c0007t0002g0006 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.11790-864A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 11/12 | chr5 | 79792573 | ||||||
| chr5:79792664
|
A | G | 4 | a0019c0024t0017g0355a0028c0043t0001g0183a0028c0043t0001g0267others(1): Show | 4 | HG02809.hp2 HG02922.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.11790-773A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 11/12 | chr5 | 79792664 | ||||||
| chr5:79792790
|
T | C | 2 | a0014c0045t0002g0194a0014c0045t0002g0230 | 2 | NA19003.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.11790-647T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 11/12 | chr5 | 79792790 | ||||||
| chr5:79792978
|
C | G | 3 | a0003c0034t0012g0021a0015c0073t0015g0343a0029c0044t0012g0036 | 3 | HG03139.hp1 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.11790-459C>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 11/12 | chr5 | 79792978 | ||||||
| chr5:79793152
|
C | T | 47 | a0001c0001t0001g0097a0001c0001t0001g0166a0001c0013t0003g0087others(44): Show | 47 | HG00323.hp2 HG00621.hp1 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.11790-285C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 11/12 | chr5 | 79793152 | ||||||
| chr5:79793172
|
A | G | 28 | a0001c0001t0001g0124a0001c0001t0001g0198a0001c0001t0001g0235others(25): Show | 28 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.11790-265A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 11/12 | chr5 | 79793172 | ||||||
| chr5:79793230
|
T | C | 3 | a0007c0008t0011g0341a0019c0024t0017g0355a0035c0037t0011g0319 | 3 | HG02145.hp2 HG02809.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.11790-207T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 11/12 | chr5 | 79793230 | ||||||
| chr5:79793616
|
C | T | 1 | a0005c0005t0001g0270 | 1 | HG01243.hp2 | splice_region_variant&intron_variant | LOW | c.11963+6C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79793616 | ||||||
| chr5:79793688
|
A | T | 6 | a0007c0008t0001g0168a0009c0009t0001g0323a0010c0010t0001g0262others(3): Show | 6 | HG01074.hp1 HG02055.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.11963+78A>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79793688 | ||||||
| chr5:79793705
|
C | T | 47 | a0001c0001t0001g0097a0001c0001t0001g0166a0001c0013t0003g0087others(44): Show | 47 | HG00323.hp2 HG00621.hp1 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.11963+95C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79793705 | ||||||
| chr5:79793907
|
G | A | 1 | a0006c0004t0002g0199 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.11963+297G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79793907 | ||||||
| chr5:79793976
|
G | A | 1 | a0027c0042t0001g0134 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.11963+366G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79793976 | ||||||
| chr5:79794142
|
T | A | 2 | a0003c0069t0002g0310a0072c0071t0002g0191 | 2 | HG01109.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.11963+532T>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79794142 | ||||||
| chr5:79794144
|
G | A | 1 | a0020c0025t0001g0278 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.11963+534G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79794144 | ||||||
| chr5:79794206
|
A | T | 218 | a0001c0001t0001g0012a0001c0001t0001g0097a0001c0001t0001g0102others(215): Show | 219 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.11963+596A>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79794206 | ||||||
| chr5:79794212
|
G | A | 42 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0065others(39): Show | 42 | HG00735.hp2 HG00741.hp2 HG01106.hp2 others(39): Show |
intron_variant | MODIFIER | c.11963+602G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79794212 | ||||||
| chr5:79794464
|
T | G | 1 | a0057c0111t0002g0321 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.11963+854T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79794464 | ||||||
| chr5:79794573
|
T | G | 4 | a0003c0069t0002g0310a0015c0038t0002g0312a0072c0071t0002g0191others(1): Show | 4 | HG00642.hp2 HG01109.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.11963+963T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79794573 | ||||||
| chr5:79794781
|
G | A | 10 | a0001c0001t0002g0175a0001c0001t0002g0332a0004c0014t0002g0158others(7): Show | 10 | HG00438.hp2 HG00673.hp1 NA18941.hp2 others(7): Show |
intron_variant | MODIFIER | c.11963+1171G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79794781 | ||||||
| chr5:79795025
|
A | G | 2 | a0003c0003t0009g0313a0003c0034t0009g0320 | 2 | HG02896.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.11963+1415A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79795025 | ||||||
| chr5:79795027
|
A | C | 4 | a0001c0001t0001g0095a0020c0025t0001g0344a0031c0046t0001g0186others(1): Show | 4 | HG02976.hp2 HG03195.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.11963+1417A>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79795027 | ||||||
| chr5:79795180
|
G | C | 1 | a0020c0025t0001g0344 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.11963+1570G>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79795180 | ||||||
| chr5:79795250
|
C | T | 14 | a0001c0001t0001g0124a0001c0001t0001g0198a0001c0001t0001g0235others(11): Show | 14 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(11): Show |
intron_variant | MODIFIER | c.11963+1640C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79795250 | ||||||
| chr5:79795308
|
C | A | 13 | a0001c0001t0001g0012a0001c0001t0001g0102a0001c0001t0001g0239others(10): Show | 13 | HG01169.hp2 HG01516.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.11963+1698C>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79795308 | ||||||
| chr5:79795352
|
T | A | 14 | a0001c0001t0001g0124a0001c0001t0001g0198a0001c0001t0001g0235others(11): Show | 14 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(11): Show |
intron_variant | MODIFIER | c.11963+1742T>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79795352 | ||||||
| chr5:79795353
|
C | A | 14 | a0001c0001t0001g0124a0001c0001t0001g0198a0001c0001t0001g0235others(11): Show | 14 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(11): Show |
intron_variant | MODIFIER | c.11963+1743C>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79795353 | ||||||
| chr5:79795393
|
T | G | 1 | a0023c0022t0001g0185 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.11963+1783T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79795393 | ||||||
| chr5:79795420
|
C | T | 1 | a0001c0001t0002g0329 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.11963+1810C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79795420 | ||||||
| chr5:79795480
|
T | C | 1 | a0003c0003t0003g0352 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.11963+1870T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79795480 | ||||||
| chr5:79795653
|
A | T | 3 | a0009c0009t0014g0266a0028c0043t0001g0183a0028c0043t0001g0267 | 3 | HG03139.hp2 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.11963+2043A>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79795653 | ||||||
| chr5:79795691
|
G | T | 13 | a0001c0001t0001g0198a0001c0001t0001g0235a0001c0055t0001g0116others(10): Show | 13 | HG00323.hp1 HG00609.hp1 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.11963+2081G>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79795691 | ||||||
| chr5:79795848
|
G | A | 2 | a0005c0005t0004g0017a0006c0004t0001g0059 | 2 | HG03239.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.11963+2238G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79795848 | ||||||
| chr5:79795923
|
C | T | 23 | a0001c0013t0003g0087a0001c0013t0003g0205a0003c0003t0003g0081others(20): Show | 23 | HG00323.hp2 HG00621.hp1 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.11963+2313C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79795923 | ||||||
| chr5:79795945
|
G | C | 131 | a0001c0001t0002g0056a0001c0001t0002g0076a0001c0001t0002g0126others(128): Show | 132 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.11963+2335G>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79795945 | ||||||
| chr5:79796013
|
G | A | 2 | a0019c0024t0017g0355a0035c0037t0011g0319 | 2 | HG02809.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.11963+2403G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79796013 | ||||||
| chr5:79796092
|
TC | T | 149 | a0001c0001t0001g0124a0001c0001t0001g0198a0001c0001t0001g0235others(146): Show | 150 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.11963+2485delC | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr5 | 79796092 | |||||
| chr5:79796160
|
G | T | 1 | a0001c0001t0002g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.11963+2550G>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79796160 | ||||||
| chr5:79796200
|
A | G | 1 | a0008c0067t0001g0305 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.11963+2590A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79796200 | ||||||
| chr5:79796208
|
G | A | 1 | a0029c0044t0004g0026 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.11963+2598G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79796208 | ||||||
| chr5:79796274
|
A | G | 149 | a0001c0001t0001g0124a0001c0001t0001g0198a0001c0001t0001g0235others(146): Show | 150 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.11963+2664A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79796274 | ||||||
| chr5:79796324
|
A | AT | 39 | a0001c0013t0003g0087a0001c0013t0003g0205a0002c0106t0007g0029others(36): Show | 39 | HG00323.hp2 HG00621.hp1 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.11963+2725dupT | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr5 | 79796324 | |||||
| chr5:79796324
|
AT | A | 14 | a0001c0001t0001g0124a0001c0001t0001g0198a0001c0001t0001g0235others(11): Show | 14 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(11): Show |
intron_variant | MODIFIER | c.11963+2725delT | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr5 | 79796324 | |||||
| chr5:79796355
|
G | A | 2 | a0028c0043t0001g0183a0028c0043t0001g0267 | 2 | HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.11963+2745G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79796355 | ||||||
| chr5:79796394
|
A | G | 149 | a0001c0001t0001g0124a0001c0001t0001g0198a0001c0001t0001g0235others(146): Show | 150 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.11963+2784A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79796394 | ||||||
| chr5:79796547
|
C | T | 129 | a0001c0001t0002g0056a0001c0001t0002g0076a0001c0001t0002g0126others(126): Show | 130 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.11964-2823C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79796547 | ||||||
| chr5:79796573
|
G | A | 7 | a0017c0019t0001g0132a0017c0019t0001g0280a0017c0019t0001g0295others(4): Show | 7 | HG00642.hp1 HG01099.hp2 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.11964-2797G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79796573 | ||||||
| chr5:79796600
|
C | T | 17 | a0001c0001t0001g0012a0001c0001t0001g0102a0001c0001t0001g0239others(14): Show | 17 | HG01167.hp2 HG01169.hp2 HG01516.hp2 others(14): Show |
intron_variant | MODIFIER | c.11964-2770C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79796600 | ||||||
| chr5:79796823
|
A | G | 1 | a0029c0044t0012g0036 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.11964-2547A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79796823 | ||||||
| chr5:79796855
|
G | GTTAC | 220 | a0001c0001t0001g0012a0001c0001t0001g0097a0001c0001t0001g0102others(217): Show | 221 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.11964-2514_11964-2 others(10): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr5 | 79796855 | |||||
| chr5:79796910
|
G | GCC | 17 | a0001c0001t0001g0124a0001c0001t0001g0198a0001c0001t0001g0235others(14): Show | 17 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(14): Show |
intron_variant | MODIFIER | c.11964-2459_11964-2 others(8): Show |
CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr5 | 79796910 | |||||
| chr5:79796931
|
T | G | 21 | a0001c0001t0001g0124a0001c0001t0001g0198a0001c0001t0001g0235others(18): Show | 21 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(18): Show |
intron_variant | MODIFIER | c.11964-2439T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79796931 | ||||||
| chr5:79797173
|
C | A | 1 | a0023c0022t0001g0185 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.11964-2197C>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79797173 | ||||||
| chr5:79797437
|
G | A | 150 | a0001c0001t0001g0124a0001c0001t0001g0198a0001c0001t0001g0235others(147): Show | 151 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.11964-1933G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79797437 | ||||||
| chr5:79797753
|
C | T | 1 | a0054c0108t0001g0187 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.11964-1617C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79797753 | ||||||
| chr5:79797796
|
G | C | 218 | a0001c0001t0001g0012a0001c0001t0001g0097a0001c0001t0001g0102others(215): Show | 219 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.11964-1574G>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79797796 | ||||||
| chr5:79798025
|
T | C | 6 | a0003c0034t0012g0021a0009c0009t0014g0266a0015c0073t0015g0343others(3): Show | 6 | HG02970.hp1 HG02970.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.11964-1345T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79798025 | ||||||
| chr5:79798163
|
G | A | 1 | a0002c0106t0007g0029 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.11964-1207G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79798163 | ||||||
| chr5:79798196
|
T | C | 22 | a0001c0001t0001g0012a0001c0001t0001g0102a0001c0001t0001g0239others(19): Show | 22 | HG01099.hp1 HG01167.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.11964-1174T>C | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79798196 | ||||||
| chr5:79798238
|
A | G | 2 | a0003c0003t0001g0153a0007c0008t0001g0340 | 2 | HG02717.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.11964-1132A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79798238 | ||||||
| chr5:79798329
|
C | T | 3 | a0005c0005t0001g0039a0005c0089t0001g0348a0047c0105t0001g0042 | 3 | NA18983.hp2 NA18990.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.11964-1041C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79798329 | ||||||
| chr5:79798331
|
C | T | 14 | a0001c0001t0001g0012a0001c0001t0001g0102a0001c0001t0001g0239others(11): Show | 14 | HG01099.hp1 HG01169.hp2 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.11964-1039C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79798331 | ||||||
| chr5:79798335
|
C | T | 2 | a0004c0011t0003g0251a0004c0011t0003g0349 | 2 | HG00621.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.11964-1035C>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79798335 | ||||||
| chr5:79798402
|
C | A | 1 | a0001c0001t0001g0198 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.11964-968C>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79798402 | ||||||
| chr5:79798759
|
T | G | 33 | a0001c0001t0001g0064a0001c0001t0001g0124a0001c0001t0001g0171others(30): Show | 33 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.11964-611T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79798759 | ||||||
| chr5:79798773
|
G | T | 3 | a0009c0009t0002g0265a0009c0009t0002g0268a0012c0015t0016g0318 | 3 | HG00741.hp1 HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.11964-597G>T | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79798773 | ||||||
| chr5:79798791
|
C | A | 1 | a0013c0016t0007g0315 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.11964-579C>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79798791 | ||||||
| chr5:79798862
|
A | G | 207 | a0001c0001t0001g0064a0001c0001t0001g0124a0001c0001t0001g0171others(204): Show | 208 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.11964-508A>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79798862 | ||||||
| chr5:79799080
|
G | A | 23 | a0001c0001t0002g0142a0001c0001t0002g0175a0001c0001t0002g0197others(20): Show | 23 | HG00438.hp2 HG00673.hp1 HG02074.hp2 others(20): Show |
intron_variant | MODIFIER | c.11964-290G>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79799080 | ||||||
| chr5:79799227
|
G | GA | 54 | a0001c0001t0001g0012a0001c0001t0001g0102a0001c0001t0001g0239others(51): Show | 54 | HG00323.hp2 HG00621.hp1 HG01081.hp2 others(51): Show |
intron_variant | MODIFIER | c.11964-141dupA | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr5 | 79799227 | |||||
| chr5:79799296
|
T | A | 30 | a0001c0013t0003g0087a0001c0013t0003g0205a0002c0106t0007g0029others(27): Show | 30 | HG00323.hp2 HG00621.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.11964-74T>A | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79799296 | ||||||
| chr5:79799322
|
T | G | 24 | a0001c0001t0001g0124a0001c0001t0001g0198a0001c0001t0001g0235others(21): Show | 24 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.11964-48T>G | CMYA5 | ENSG00000164309.15 | transcript | ENST00000446378.3 | protein_coding | 12/12 | chr5 | 79799322 |