Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 92140 |
|---|---|
| ensemblid | ENSG00000147649.10 |
| hgncid | 29608 |
| symbol | MTDH |
| name | metadherin |
| refseq_nuc | NM_178812.4 |
| refseq_prot | NP_848927.2 |
| ensembl_nuc | ENST00000336273.8 |
| ensembl_prot | ENSP00000338235.3 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 97644184 |
| end | 97730260 |
| strand | + |
| ver | v1.2 |
| region | chr8:97644184-97730260 |
| region5000 | chr8:97639184-97735260 |
| regionname0 | MTDH_chr8_97644184_97730260 |
| regionname5000 | MTDH_chr8_97639184_97735260 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 582 | 355 | 87 | 55 | 168 | 6 | 37 | 135 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0002 | 0/0 | 582 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0003 | 0/0 | 582 | 5 | 0 | 3 | 0 | 0 | 2 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0004 | 0/0 | 582 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0005 | 0/0 | 582 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0006 | 0/0 | 582 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0007 | 0/0 | 582 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0008 | 0/0 | 582 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1749 | 299 | 81 | 45 | 136 | 6 | 29 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| c0002 | 0/0 | 1749 | 49 | 1 | 10 | 31 | 0 | 7 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| c0003 | 0/0 | 1749 | 5 | 4 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| c0004 | 0/0 | 1749 | 5 | 0 | 3 | 0 | 0 | 2 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| c0005 | 0/0 | 1749 | 3 | 3 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| c0006 | 0/0 | 1749 | 2 | 0 | 0 | 1 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| c0007 | 0/0 | 1749 | 2 | 2 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| c0008 | 0/0 | 1749 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| c0009 | 0/0 | 1749 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| c0010 | 0/0 | 1749 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| c0011 | 0/0 | 1749 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| c0012 | 0/0 | 1749 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 5922 | 63 | 7 | 8 | 40 | 1 | 7 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0002 | 1/0 | 5914 | 60 | 2 | 14 | 33 | 3 | 7 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0003 | 0/0 | 5922 | 39 | 3 | 5 | 23 | 0 | 8 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0004 | 0/0 | 5913 | 28 | 5 | 6 | 16 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0005 | 0/0 | 5913 | 12 | 11 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0006 | 0/0 | 5920 | 10 | 10 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0007 | 0/0 | 5923 | 8 | 0 | 4 | 3 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0008 | 0/0 | 5923 | 8 | 7 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0009 | 0/0 | 5923 | 6 | 0 | 0 | 6 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0010 | 0/0 | 5914 | 6 | 0 | 1 | 4 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0011 | 0/0 | 5923 | 6 | 1 | 0 | 5 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0012 | 0/0 | 5913 | 6 | 6 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0013 | 0/0 | 5923 | 5 | 3 | 1 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0014 | 0/0 | 5915 | 5 | 0 | 0 | 5 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0015 | 0/0 | 5922 | 4 | 0 | 1 | 0 | 0 | 3 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0016 | 0/0 | 5914 | 4 | 4 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0017 | 0/0 | 5923 | 3 | 0 | 0 | 3 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0018 | 0/0 | 5923 | 3 | 3 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0019 | 0/0 | 5915 | 3 | 3 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0020 | 0/0 | 5923 | 3 | 0 | 0 | 1 | 1 | 1 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0021 | 0/0 | 5923 | 3 | 1 | 0 | 2 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0022 | 0/0 | 5919 | 3 | 3 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0023 | 0/0 | 5923 | 3 | 3 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0024 | 0/0 | 5914 | 2 | 0 | 2 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0025 | 0/0 | 5915 | 2 | 0 | 0 | 2 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0026 | 0/0 | 5923 | 2 | 0 | 0 | 2 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0027 | 0/0 | 5914 | 2 | 0 | 2 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0028 | 0/0 | 5913 | 2 | 0 | 0 | 0 | 0 | 2 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0029 | 0/0 | 5922 | 2 | 0 | 0 | 2 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0030 | 0/0 | 5924 | 2 | 0 | 1 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0031 | 0/0 | 5923 | 2 | 2 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0032 | 0/0 | 5922 | 2 | 0 | 0 | 0 | 0 | 2 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0033 | 0/0 | 5914 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0034 | 0/0 | 5924 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0035 | 0/0 | 5923 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0036 | 0/0 | 5923 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0037 | 0/0 | 5922 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0038 | 0/0 | 5924 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0039 | 0/0 | 5924 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0040 | 0/0 | 5924 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0041 | 0/0 | 5924 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0042 | 0/0 | 5914 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0043 | 0/0 | 5925 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0044 | 0/0 | 5923 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0045 | 0/0 | 5922 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0046 | 0/0 | 5922 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0047 | 0/0 | 5924 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0048 | 0/0 | 5921 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0049 | 0/0 | 5923 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0050 | 0/0 | 5924 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0051 | 0/0 | 5922 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0052 | 0/0 | 5923 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0053 | 0/0 | 5921 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0054 | 0/0 | 5921 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0055 | 0/0 | 5920 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0056 | 0/0 | 5920 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0057 | 0/0 | 5915 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0058 | 0/0 | 5915 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0059 | 0/0 | 5916 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0060 | 0/0 | 5913 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0061 | 0/0 | 5915 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0062 | 0/0 | 5916 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0063 | 0/0 | 5913 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0064 | 0/0 | 5911 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0065 | 0/0 | 5915 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0066 | 0/0 | 5914 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0067 | 0/0 | 5913 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0068 | 0/0 | 5913 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0069 | 0/0 | 5915 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0070 | 0/0 | 5921 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0071 | 0/0 | 5915 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0072 | 0/0 | 5921 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0073 | 0/0 | 5915 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0074 | 0/0 | 5925 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0075 | 0/0 | 5923 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0076 | 0/0 | 5922 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0077 | 0/0 | 5923 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0078 | 0/0 | 5922 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0079 | 0/0 | 5921 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0080 | 0/0 | 5915 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0081 | 0/0 | 5914 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0082 | 0/0 | 5914 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0083 | 0/0 | 5914 | 1 | 0 | 0 | 0 | 1 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0084 | 0/0 | 5913 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0085 | 0/0 | 5912 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0086 | 0/0 | 5923 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0087 | 0/1 | 5914 | 1 | 0 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0088 | 0/0 | 5920 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0089 | 0/0 | 5922 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0090 | 0/0 | 5923 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0091 | 0/0 | 5923 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0092 | 0/0 | 5922 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| t0093 | 0/0 | 5922 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0298 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0317 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0354 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0358 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| g0370 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1749 | 299 | 81 | 45 | 136 | 6 | 29 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0002 | 0/0 | 1749 | 49 | 1 | 10 | 31 | 0 | 7 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0005 | 0/0 | 1749 | 3 | 3 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0006 | 0/0 | 1749 | 2 | 0 | 0 | 1 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0007 | 0/0 | 1749 | 2 | 2 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0002c0003 | 0/0 | 1749 | 5 | 4 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0003c0004 | 0/0 | 1749 | 5 | 0 | 3 | 0 | 0 | 2 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0004c0008 | 0/0 | 1749 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0005c0010 | 0/0 | 1749 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0006c0009 | 0/0 | 1749 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0007c0011 | 0/0 | 1749 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0008c0012 | 0/0 | 1749 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 7670 | 63 | 7 | 8 | 40 | 1 | 7 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0002 | 1/0 | 7662 | 59 | 2 | 14 | 32 | 3 | 7 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0003 | 0/0 | 7670 | 5 | 0 | 2 | 0 | 0 | 3 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0004 | 0/0 | 7661 | 27 | 5 | 6 | 15 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0005 | 0/0 | 7661 | 12 | 11 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0006 | 0/0 | 7668 | 10 | 10 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0007 | 0/0 | 7671 | 2 | 0 | 0 | 2 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0008 | 0/0 | 7671 | 8 | 7 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0009 | 0/0 | 7671 | 6 | 0 | 0 | 6 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0010 | 0/0 | 7662 | 6 | 0 | 1 | 4 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0011 | 0/0 | 7671 | 6 | 1 | 0 | 5 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0012 | 0/0 | 7661 | 6 | 6 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0013 | 0/0 | 7671 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0014 | 0/0 | 7663 | 5 | 0 | 0 | 5 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0016 | 0/0 | 7662 | 4 | 4 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0017 | 0/0 | 7671 | 3 | 0 | 0 | 3 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0018 | 0/0 | 7671 | 3 | 3 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0019 | 0/0 | 7663 | 3 | 3 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0020 | 0/0 | 7671 | 3 | 0 | 0 | 1 | 1 | 1 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0021 | 0/0 | 7671 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0022 | 0/0 | 7667 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0023 | 0/0 | 7671 | 3 | 3 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0024 | 0/0 | 7662 | 2 | 0 | 2 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0025 | 0/0 | 7663 | 2 | 0 | 0 | 2 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0026 | 0/0 | 7671 | 2 | 0 | 0 | 2 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0027 | 0/0 | 7662 | 2 | 0 | 2 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0028 | 0/0 | 7661 | 2 | 0 | 0 | 0 | 0 | 2 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0029 | 0/0 | 7670 | 2 | 0 | 0 | 2 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0030 | 0/0 | 7672 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0031 | 0/0 | 7671 | 2 | 2 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0032 | 0/0 | 7670 | 2 | 0 | 0 | 0 | 0 | 2 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0033 | 0/0 | 7662 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0034 | 0/0 | 7672 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0036 | 0/0 | 7671 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0037 | 0/0 | 7670 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0038 | 0/0 | 7672 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0039 | 0/0 | 7672 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0040 | 0/0 | 7672 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0041 | 0/0 | 7672 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0042 | 0/0 | 7662 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0043 | 0/0 | 7673 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0044 | 0/0 | 7671 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0045 | 0/0 | 7670 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0046 | 0/0 | 7670 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0047 | 0/0 | 7672 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0048 | 0/0 | 7669 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0050 | 0/0 | 7672 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0051 | 0/0 | 7670 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0052 | 0/0 | 7671 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0054 | 0/0 | 7669 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0055 | 0/0 | 7668 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0056 | 0/0 | 7668 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0057 | 0/0 | 7663 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0058 | 0/0 | 7663 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0059 | 0/0 | 7664 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0060 | 0/0 | 7661 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0061 | 0/0 | 7663 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0062 | 0/0 | 7664 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0064 | 0/0 | 7659 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0065 | 0/0 | 7663 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0066 | 0/0 | 7662 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0067 | 0/0 | 7661 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0068 | 0/0 | 7661 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0069 | 0/0 | 7663 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0071 | 0/0 | 7663 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0072 | 0/0 | 7669 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0073 | 0/0 | 7663 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0076 | 0/0 | 7670 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0079 | 0/0 | 7669 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0083 | 0/0 | 7662 | 1 | 0 | 0 | 0 | 1 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0084 | 0/0 | 7661 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0086 | 0/0 | 7671 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0087 | 0/1 | 7662 | 1 | 0 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0088 | 0/0 | 7668 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0091 | 0/0 | 7671 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0001t0093 | 0/0 | 7670 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0002t0003 | 0/0 | 7670 | 31 | 1 | 3 | 22 | 0 | 5 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0002t0007 | 0/0 | 7671 | 6 | 0 | 4 | 1 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0002t0021 | 0/0 | 7671 | 2 | 0 | 0 | 2 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0002t0030 | 0/0 | 7672 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0002t0074 | 0/0 | 7673 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0002t0075 | 0/0 | 7671 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0002t0077 | 0/0 | 7671 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0002t0078 | 0/0 | 7670 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0002t0080 | 0/0 | 7663 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0002t0081 | 0/0 | 7662 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0002t0082 | 0/0 | 7662 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0002t0089 | 0/0 | 7670 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0002t0090 | 0/0 | 7671 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0005t0022 | 0/0 | 7667 | 2 | 2 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0005t0085 | 0/0 | 7660 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0006t0004 | 0/0 | 7661 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0006t0063 | 0/0 | 7661 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0001c0007t0003 | 0/0 | 7670 | 2 | 2 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0002c0003t0013 | 0/0 | 7671 | 4 | 3 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0002c0003t0035 | 0/0 | 7671 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0003c0004t0015 | 0/0 | 7670 | 3 | 0 | 1 | 0 | 0 | 2 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0003c0004t0049 | 0/0 | 7671 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0003c0004t0053 | 0/0 | 7669 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0004c0008t0002 | 0/0 | 7662 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0005c0010t0092 | 0/0 | 7670 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0006c0009t0003 | 0/0 | 7670 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0007c0011t0070 | 0/0 | 7669 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| a0008c0012t0015 | 0/0 | 7670 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | copy fasta | chr8 | 97639184 | 97735260 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0298 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0354 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0358 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0002g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0004g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0004g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0004g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0004g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0004g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0004g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0004g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0004g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0004g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0004g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0004g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0004g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0004g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0004g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0004g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0004g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0004g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0004g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0004g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0004g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0004g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0004g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0005g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0005g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0005g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0005g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0005g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0005g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0005g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0005g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0005g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0005g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0005g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0005g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0006g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0006g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0006g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0006g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0006g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0006g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0006g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0006g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0006g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0006g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0007g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0007g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0008g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0008g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0008g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0008g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0008g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0008g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0008g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0008g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0009g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0009g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0009g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0009g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0009g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0009g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0010g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0010g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0010g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0010g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0010g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0010g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0011g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0011g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0011g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0011g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0011g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0011g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0012g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0012g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0012g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0012g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0012g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0012g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0013g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0014g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0014g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0014g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0014g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0014g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0016g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0016g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0016g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0016g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0017g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0017g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0017g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0018g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0018g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0018g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0019g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0019g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0019g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0020g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0020g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0020g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0021g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0022g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0023g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0023g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0023g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0024g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0024g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0025g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0025g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0026g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0026g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0027g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0027g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0028g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0028g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0029g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0029g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0030g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0031g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0031g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0032g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0032g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0033g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0034g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0036g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0037g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0038g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0039g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0040g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0041g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0042g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0043g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0044g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0045g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0046g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0047g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0048g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0050g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0051g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0052g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0054g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0055g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0056g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0057g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0058g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0059g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0060g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0061g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0062g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0064g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0065g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0066g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0067g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0068g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0069g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0071g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0072g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0073g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0076g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0079g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0083g0370 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0084g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0086g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0087g0317 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0088g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0091g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0001t0093g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0002t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0002t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0002t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0002t0003g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0002t0003g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0002t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0002t0003g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0002t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0002t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0002t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0002t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0002t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0002t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0002t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0002t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0002t0003g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0002t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0002t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0002t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0002t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0002t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0002t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0002t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0002t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0002t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0002t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0002t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0002t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0002t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0002t0003g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0002t0003g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0002t0007g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0002t0007g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0002t0007g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0002t0007g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0002t0007g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0002t0007g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0002t0021g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0002t0021g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0002t0030g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0002t0074g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0002t0075g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0002t0077g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0002t0078g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0002t0080g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0002t0081g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0002t0082g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0002t0089g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0002t0090g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0005t0022g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0005t0022g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0005t0085g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0006t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0006t0063g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0007t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0001c0007t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0002c0003t0013g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0002c0003t0013g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0002c0003t0013g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0002c0003t0013g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0002c0003t0035g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0003c0004t0015g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0003c0004t0015g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0003c0004t0015g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0003c0004t0049g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0003c0004t0053g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0004c0008t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0005c0010t0092g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0006c0009t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0007c0011t0070g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| a0008c0012t0015g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0322 | EUR | GBR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG00140 | hp2 | a0001 | c0001 | t0020 | g0021 | EUR | GBR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG00408 | hp1 | a0001 | c0002 | t0003 | g0203 | EAS | CHS | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG00408 | hp2 | a0001 | c0001 | t0004 | g0323 | EAS | CHS | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG00423 | hp2 | a0001 | c0002 | t0003 | g0207 | EAS | CHS | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | CHS | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG00558 | hp2 | a0001 | c0002 | t0003 | g0220 | EAS | CHS | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG00597 | hp1 | a0001 | c0001 | t0025 | g0365 | EAS | CHS | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG00597 | hp2 | a0001 | c0001 | t0043 | g0040 | EAS | CHS | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0302 | EAS | CHS | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG00609 | hp2 | a0001 | c0002 | t0003 | g0241 | EAS | CHS | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG00621 | hp2 | a0001 | c0002 | t0003 | g0222 | EAS | CHS | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0333 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG00642 | hp2 | a0001 | c0001 | t0004 | g0337 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG00673 | hp1 | a0001 | c0001 | t0011 | g0148 | EAS | CHS | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG00673 | hp2 | a0001 | c0006 | t0004 | g0261 | EAS | CHS | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG00733 | hp1 | a0001 | c0001 | t0024 | g0009 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG00733 | hp2 | a0002 | c0003 | t0013 | g0128 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG00735 | hp1 | a0001 | c0002 | t0003 | g0212 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG00735 | hp2 | a0001 | c0001 | t0076 | g0174 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG00738 | hp1 | a0001 | c0001 | t0084 | g0327 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG00738 | hp2 | a0001 | c0001 | t0024 | g0007 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG00741 | hp1 | a0005 | c0010 | t0092 | g0247 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0330 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG01070 | hp1 | a0001 | c0001 | t0027 | g0318 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG01070 | hp2 | a0001 | c0001 | t0004 | g0335 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG01074 | hp1 | a0001 | c0001 | t0027 | g0315 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0257 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG01081 | hp1 | a0001 | c0001 | t0045 | g0105 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG01081 | hp2 | a0001 | c0001 | t0008 | g0163 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0292 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG01099 | hp2 | a0001 | c0001 | t0091 | g0029 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG01109 | hp1 | a0001 | c0002 | t0074 | g0211 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG01109 | hp2 | a0001 | c0001 | t0005 | g0113 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0255 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0281 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG01168 | hp1 | a0003 | c0004 | t0053 | g0248 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0343 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0276 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0173 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0264 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0275 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG01243 | hp2 | a0001 | c0001 | t0040 | g0258 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0140 | AMR | CLM | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0286 | AMR | CLM | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG01258 | hp2 | a0001 | c0001 | t0004 | g0294 | AMR | CLM | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0296 | AMR | CLM | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG01361 | hp1 | a0003 | c0004 | t0049 | g0249 | AMR | CLM | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG01361 | hp2 | a0001 | c0001 | t0010 | g0287 | AMR | CLM | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG01496 | hp1 | a0003 | c0004 | t0015 | g0250 | AMR | CLM | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG01496 | hp2 | a0001 | c0002 | t0007 | g0198 | AMR | CLM | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0102 | EUR | IBS | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG01516 | hp2 | a0001 | c0001 | t0083 | g0370 | EUR | IBS | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG01884 | hp1 | a0002 | c0003 | t0035 | g0125 | AFR | ACB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0136 | AFR | ACB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG01891 | hp1 | a0007 | c0011 | t0070 | g0016 | AFR | ACB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0117 | AFR | ACB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG01934 | hp1 | a0001 | c0002 | t0030 | g0218 | AMR | PEL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG01934 | hp2 | a0001 | c0001 | t0004 | g0336 | AMR | PEL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG01952 | hp1 | a0001 | c0002 | t0003 | g0208 | AMR | PEL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG01978 | hp2 | a0001 | c0001 | t0093 | g0031 | AMR | PEL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG01981 | hp1 | a0001 | c0002 | t0007 | g0200 | AMR | PEL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0263 | AMR | PEL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02004 | hp1 | a0001 | c0002 | t0003 | g0213 | AMR | PEL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02004 | hp2 | a0001 | c0001 | t0079 | g0152 | AMR | PEL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02027 | hp1 | a0001 | c0002 | t0007 | g0232 | EAS | KHV | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0350 | EAS | KHV | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | KHV | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02040 | hp2 | a0001 | c0002 | t0003 | g0201 | EAS | KHV | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02055 | hp1 | a0001 | c0001 | t0016 | g0123 | AFR | ACB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02055 | hp2 | a0001 | c0001 | t0012 | g0002 | AFR | ACB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02056 | hp1 | a0001 | c0002 | t0077 | g0221 | EAS | KHV | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02056 | hp2 | a0001 | c0001 | t0047 | g0056 | EAS | KHV | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | KHV | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02132 | hp1 | a0001 | c0002 | t0003 | g0216 | EAS | KHV | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02132 | hp2 | a0001 | c0001 | t0020 | g0074 | EAS | KHV | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02145 | hp1 | a0001 | c0001 | t0042 | g0114 | AFR | ACB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02145 | hp2 | a0001 | c0005 | t0022 | g0195 | AFR | ACB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02148 | hp1 | a0001 | c0002 | t0075 | g0196 | AMR | PEL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0265 | AMR | PEL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | CDX | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02155 | hp2 | a0006 | c0009 | t0003 | g0233 | EAS | CDX | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | CDX | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | CDX | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02257 | hp2 | a0001 | c0001 | t0006 | g0183 | AFR | ACB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0014 | AFR | ACB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02258 | hp2 | a0001 | c0001 | t0008 | g0159 | AFR | ACB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0280 | AMR | PEL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02273 | hp2 | a0001 | c0002 | t0007 | g0217 | AMR | PEL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0283 | AFR | ACB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02280 | hp2 | a0001 | c0001 | t0006 | g0187 | AFR | ACB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02293 | hp1 | a0001 | c0002 | t0007 | g0199 | AMR | PEL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0266 | AMR | PEL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02451 | hp1 | a0001 | c0001 | t0057 | g0124 | AFR | ACB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0312 | AFR | ACB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02572 | hp1 | a0001 | c0007 | t0003 | g0153 | AFR | GWD | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02572 | hp2 | a0001 | c0001 | t0012 | g0011 | AFR | GWD | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0329 | SAS | PJL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02615 | hp1 | a0001 | c0001 | t0039 | g0126 | AFR | GWD | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02615 | hp2 | a0001 | c0001 | t0018 | g0135 | AFR | GWD | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02622 | hp1 | a0001 | c0001 | t0068 | g0328 | AFR | GWD | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02622 | hp2 | a0001 | c0001 | t0019 | g0108 | AFR | GWD | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02630 | hp1 | a0001 | c0001 | t0012 | g0015 | AFR | GWD | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02630 | hp2 | a0001 | c0001 | t0037 | g0131 | AFR | GWD | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02647 | hp1 | a0001 | c0005 | t0022 | g0193 | AFR | GWD | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02647 | hp2 | a0001 | c0001 | t0058 | g0120 | AFR | GWD | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02683 | hp1 | a0001 | c0001 | t0033 | g0342 | SAS | PJL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02683 | hp2 | a0001 | c0002 | t0078 | g0215 | SAS | PJL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02717 | hp1 | a0001 | c0001 | t0018 | g0133 | AFR | GWD | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02717 | hp2 | a0001 | c0001 | t0006 | g0185 | AFR | GWD | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02723 | hp1 | a0001 | c0001 | t0056 | g0111 | AFR | GWD | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02723 | hp2 | a0001 | c0001 | t0005 | g0013 | AFR | GWD | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02809 | hp1 | a0001 | c0001 | t0018 | g0132 | AFR | GWD | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02809 | hp2 | a0001 | c0001 | t0008 | g0160 | AFR | GWD | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02818 | hp2 | a0001 | c0001 | t0023 | g0158 | AFR | GWD | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0112 | AFR | GWD | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02895 | hp1 | a0002 | c0003 | t0013 | g0127 | AFR | GWD | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02896 | hp1 | a0001 | c0001 | t0016 | g0121 | AFR | GWD | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02896 | hp2 | a0001 | c0001 | t0031 | g0178 | AFR | GWD | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02897 | hp1 | a0002 | c0003 | t0013 | g0129 | AFR | GWD | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02897 | hp2 | a0001 | c0001 | t0016 | g0122 | AFR | GWD | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02922 | hp1 | a0001 | c0001 | t0022 | g0192 | AFR | ESN | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02922 | hp2 | a0001 | c0001 | t0054 | g0181 | AFR | ESN | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02965 | hp1 | a0001 | c0001 | t0016 | g0119 | AFR | ESN | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | ESN | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0006 | AFR | ESN | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0138 | AFR | ESN | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0115 | AFR | ESN | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02976 | hp2 | a0001 | c0001 | t0008 | g0161 | AFR | ESN | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0277 | SAS | PJL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG03017 | hp2 | a0001 | c0002 | t0003 | g0206 | SAS | PJL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0274 | AFR | GWD | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG03098 | hp1 | a0001 | c0001 | t0021 | g0168 | AFR | MSL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG03098 | hp2 | a0001 | c0001 | t0055 | g0186 | AFR | MSL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG03130 | hp1 | a0001 | c0005 | t0085 | g0194 | AFR | ESN | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG03130 | hp2 | a0001 | c0001 | t0008 | g0155 | AFR | ESN | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG03195 | hp1 | a0001 | c0001 | t0012 | g0003 | AFR | ESN | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG03195 | hp2 | a0001 | c0001 | t0008 | g0156 | AFR | ESN | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG03209 | hp1 | a0002 | c0003 | t0013 | g0130 | AFR | MSL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG03209 | hp2 | a0001 | c0001 | t0012 | g0010 | AFR | MSL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG03225 | hp1 | a0001 | c0001 | t0051 | g0251 | AFR | MSL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG03225 | hp2 | a0001 | c0001 | t0019 | g0109 | AFR | MSL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG03239 | hp1 | a0001 | c0001 | t0032 | g0030 | SAS | PJL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0321 | SAS | PJL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG03453 | hp1 | a0001 | c0001 | t0019 | g0110 | AFR | MSL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG03453 | hp2 | a0001 | c0001 | t0031 | g0177 | AFR | MSL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0190 | AFR | MSL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG03486 | hp2 | a0001 | c0001 | t0065 | g0167 | AFR | MSL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG03490 | hp1 | a0001 | c0001 | t0028 | g0326 | SAS | PJL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG03491 | hp2 | a0008 | c0012 | t0015 | g0246 | SAS | PJL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG03492 | hp1 | a0001 | c0001 | t0028 | g0306 | SAS | PJL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG03516 | hp1 | a0001 | c0001 | t0086 | g0166 | AFR | ESN | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0137 | AFR | ESN | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG03540 | hp1 | a0001 | c0001 | t0023 | g0165 | AFR | GWD | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG03540 | hp2 | a0001 | c0007 | t0003 | g0154 | AFR | GWD | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0353 | SAS | PJL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG03654 | hp2 | a0001 | c0002 | t0007 | g0219 | SAS | PJL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG03669 | hp1 | a0001 | c0002 | t0003 | g0204 | SAS | PJL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0352 | SAS | PJL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0289 | SAS | STU | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG03688 | hp2 | a0003 | c0004 | t0015 | g0244 | SAS | STU | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG03704 | hp1 | a0001 | c0002 | t0003 | g0225 | SAS | PJL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG03704 | hp2 | a0001 | c0001 | t0013 | g0259 | SAS | PJL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0179 | SAS | PJL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0316 | SAS | PJL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG03831 | hp1 | a0001 | c0001 | t0010 | g0345 | SAS | BEB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG03831 | hp2 | a0001 | c0001 | t0062 | g0349 | SAS | BEB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG03834 | hp1 | a0001 | c0002 | t0003 | g0254 | SAS | BEB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG03834 | hp2 | a0001 | c0006 | t0063 | g0332 | SAS | BEB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | BEB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0334 | SAS | BEB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | BEB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG03942 | hp2 | a0003 | c0004 | t0015 | g0245 | SAS | BEB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG04115 | hp1 | a0001 | c0001 | t0034 | g0118 | SAS | STU | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0172 | SAS | STU | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG04199 | hp1 | a0001 | c0001 | t0020 | g0047 | SAS | STU | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG04199 | hp2 | a0001 | c0001 | t0066 | g0357 | SAS | STU | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0175 | SAS | STU | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG04204 | hp2 | a0001 | c0001 | t0032 | g0093 | SAS | STU | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18522 | hp1 | a0001 | c0001 | t0012 | g0012 | AFR | YRI | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0180 | AFR | YRI | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | CHB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18612 | hp2 | a0001 | c0001 | t0010 | g0338 | EAS | CHB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18747 | hp2 | a0001 | c0001 | t0004 | g0291 | EAS | CHB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18906 | hp1 | a0001 | c0001 | t0006 | g0189 | AFR | YRI | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18906 | hp2 | a0001 | c0001 | t0008 | g0162 | AFR | YRI | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18939 | hp2 | a0001 | c0001 | t0048 | g0080 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18940 | hp1 | a0001 | c0001 | t0010 | g0290 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18940 | hp2 | a0001 | c0001 | t0050 | g0044 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18941 | hp1 | a0001 | c0001 | t0011 | g0147 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18941 | hp2 | a0001 | c0001 | t0010 | g0304 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18945 | hp1 | a0001 | c0001 | t0009 | g0086 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18946 | hp1 | a0001 | c0001 | t0064 | g0285 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18946 | hp2 | a0001 | c0001 | t0088 | g0019 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18947 | hp2 | a0001 | c0001 | t0011 | g0143 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18949 | hp1 | a0001 | c0001 | t0029 | g0150 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18949 | hp2 | a0001 | c0001 | t0026 | g0098 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18950 | hp1 | a0001 | c0001 | t0007 | g0171 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18950 | hp2 | a0001 | c0001 | t0009 | g0084 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18951 | hp2 | a0001 | c0001 | t0017 | g0038 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18952 | hp1 | a0001 | c0001 | t0004 | g0307 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18953 | hp1 | a0001 | c0002 | t0003 | g0238 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0363 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18956 | hp2 | a0001 | c0002 | t0090 | g0224 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18957 | hp1 | a0001 | c0002 | t0089 | g0197 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0341 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0359 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18961 | hp1 | a0001 | c0002 | t0021 | g0243 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18961 | hp2 | a0001 | c0001 | t0004 | g0305 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0344 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18965 | hp1 | a0001 | c0001 | t0030 | g0169 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18967 | hp1 | a0001 | c0001 | t0059 | g0262 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18970 | hp1 | a0001 | c0002 | t0003 | g0236 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18971 | hp2 | a0001 | c0002 | t0003 | g0229 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18972 | hp1 | a0001 | c0001 | t0061 | g0271 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18972 | hp2 | a0001 | c0002 | t0082 | g0223 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18973 | hp1 | a0001 | c0001 | t0014 | g0367 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18974 | hp1 | a0001 | c0001 | t0071 | g0145 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0361 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0366 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18975 | hp2 | a0001 | c0001 | t0004 | g0340 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18977 | hp2 | a0001 | c0001 | t0004 | g0267 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18980 | hp1 | a0001 | c0001 | t0004 | g0324 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18982 | hp1 | a0001 | c0002 | t0003 | g0228 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0319 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18984 | hp1 | a0001 | c0001 | t0004 | g0308 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18985 | hp1 | a0001 | c0001 | t0046 | g0028 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18985 | hp2 | a0004 | c0008 | t0002 | g0001 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18986 | hp1 | a0001 | c0001 | t0017 | g0039 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18986 | hp2 | a0001 | c0002 | t0081 | g0242 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18989 | hp1 | a0001 | c0001 | t0014 | g0360 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18990 | hp1 | a0001 | c0001 | t0004 | g0278 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18990 | hp2 | a0001 | c0002 | t0003 | g0209 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18991 | hp1 | a0001 | c0002 | t0021 | g0240 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18991 | hp2 | a0001 | c0001 | t0004 | g0284 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18992 | hp2 | a0001 | c0002 | t0003 | g0237 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18993 | hp1 | a0001 | c0001 | t0067 | g0348 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18993 | hp2 | a0001 | c0001 | t0011 | g0144 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18995 | hp1 | a0001 | c0001 | t0004 | g0346 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18998 | hp2 | a0001 | c0001 | t0036 | g0085 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0320 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19000 | hp1 | a0001 | c0002 | t0003 | g0239 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19000 | hp2 | a0001 | c0001 | t0069 | g0288 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19002 | hp1 | a0001 | c0001 | t0007 | g0170 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0362 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19007 | hp2 | a0001 | c0001 | t0011 | g0141 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19009 | hp2 | a0001 | c0002 | t0003 | g0202 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19010 | hp1 | a0001 | c0001 | t0009 | g0050 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19010 | hp2 | a0001 | c0001 | t0014 | g0368 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19011 | hp1 | a0001 | c0001 | t0026 | g0083 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0347 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19030 | hp1 | a0001 | c0001 | t0041 | g0134 | AFR | LWK | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19030 | hp2 | a0001 | c0001 | t0038 | g0023 | AFR | LWK | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19054 | hp1 | a0001 | c0001 | t0073 | g0149 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19056 | hp1 | a0001 | c0001 | t0009 | g0018 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19056 | hp2 | a0001 | c0002 | t0003 | g0234 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19058 | hp1 | a0001 | c0001 | t0014 | g0355 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19058 | hp2 | a0001 | c0001 | t0017 | g0037 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0331 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19062 | hp1 | a0001 | c0002 | t0003 | g0226 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19063 | hp1 | a0001 | c0001 | t0029 | g0151 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19063 | hp2 | a0001 | c0001 | t0009 | g0077 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19064 | hp2 | a0001 | c0002 | t0003 | g0227 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19065 | hp2 | a0001 | c0001 | t0004 | g0309 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19074 | hp2 | a0001 | c0002 | t0080 | g0205 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19079 | hp1 | a0001 | c0002 | t0003 | g0235 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19079 | hp2 | a0001 | c0001 | t0009 | g0052 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19080 | hp1 | a0001 | c0002 | t0003 | g0231 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19080 | hp2 | a0001 | c0001 | t0025 | g0364 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19081 | hp1 | a0001 | c0002 | t0003 | g0230 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19081 | hp2 | a0001 | c0001 | t0044 | g0082 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19083 | hp2 | a0001 | c0001 | t0010 | g0356 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19084 | hp2 | a0001 | c0001 | t0004 | g0325 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19085 | hp1 | a0001 | c0002 | t0003 | g0214 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19086 | hp2 | a0001 | c0001 | t0004 | g0351 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19088 | hp2 | a0001 | c0001 | t0004 | g0339 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19090 | hp1 | a0001 | c0001 | t0072 | g0142 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19090 | hp2 | a0001 | c0001 | t0014 | g0369 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0176 | AFR | YRI | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0004 | AFR | YRI | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0313 | AFR | ASW | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA20129 | hp2 | a0001 | c0001 | t0052 | g0252 | AFR | ASW | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0354 | EUR | TSI | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0358 | EUR | TSI | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | GIH | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA20905 | hp2 | a0001 | c0002 | t0003 | g0253 | SAS | GIH | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG01123 | hp2 | a0001 | c0001 | t0060 | g0282 | AMR | CLM | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0116 | AFR | ACB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0184 | AFR | ACB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02559 | hp1 | a0001 | c0001 | t0023 | g0164 | AFR | ACB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0008 | AFR | ACB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG03471 | hp1 | a0001 | c0001 | t0008 | g0157 | AFR | MSL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG03471 | hp2 | a0001 | c0001 | t0006 | g0191 | AFR | MSL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG06807 | hp1 | a0001 | c0001 | t0006 | g0182 | AFR | USA | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | USA | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA20300 | hp1 | a0001 | c0001 | t0011 | g0146 | AFR | USA | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA20300 | hp2 | a0001 | c0001 | t0006 | g0188 | AFR | USA | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | LWK | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| NA21309 | hp2 | a0001 | c0002 | t0003 | g0210 | AFR | LWK | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0087 | g0317 | REF | REF | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0298 | REF | REF | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:97644738
|
G | T | 2 | a0003a0008 | 6 | HG01168.hp1 HG01361.hp1 HG01496.hp1 others(3): Show |
missense_variant | MODERATE | c.232G>T | p.Ala78Ser | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/12 | 555/7662 | 232/1749 | 78/582 | chr8 | 97644738 | ||
| chr8:97644771
|
C | G | 1 | a0004 | 1 | NA18985.hp2 | missense_variant | MODERATE | c.265C>G | p.Arg89Gly | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/12 | 588/7662 | 265/1749 | 89/582 | chr8 | 97644771 | ||
| chr8:97644792
|
C | T | 1 | a0007 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.286C>T | p.Pro96Ser | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/12 | 609/7662 | 286/1749 | 96/582 | chr8 | 97644792 | ||
| chr8:97644813
|
C | G | 1 | a0002 | 5 | HG00733.hp2 HG01884.hp1 HG02895.hp1 others(2): Show |
missense_variant | MODERATE | c.307C>G | p.Leu103Val | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/12 | 630/7662 | 307/1749 | 103/582 | chr8 | 97644813 | ||
| chr8:97691089
|
A | G | 3 | a0003a0005a0008 | 7 | HG00741.hp1 HG01168.hp1 HG01361.hp1 others(4): Show |
missense_variant | MODERATE | c.949A>G | p.Thr317Ala | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/12 | 1272/7662 | 949/1749 | 317/582 | chr8 | 97691089 | ||
| chr8:97699799
|
A | G | 1 | a0006 | 1 | HG02155.hp2 | missense_variant | MODERATE | c.1094A>G | p.Gln365Arg | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 7/12 | 1417/7662 | 1094/1749 | 365/582 | chr8 | 97699799 | ||
| chr8:97699831
|
G | A | 1 | a0008 | 1 | HG03491.hp2 | missense_variant | MODERATE | c.1126G>A | p.Asp376Asn | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 7/12 | 1449/7662 | 1126/1749 | 376/582 | chr8 | 97699831 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:97644548
|
C | A | 1 | a0004c0008 | 1 | NA18985.hp2 | synonymous_variant | LOW | c.42C>A | p.Ala14Ala | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/12 | 365/7662 | 42/1749 | 14/582 | chr8 | 97644548 | ||
| chr8:97644560
|
G | A | 1 | a0001c0006 | 2 | HG00673.hp2 HG03834.hp2 |
synonymous_variant | LOW | c.54G>A | p.Ser18Ser | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/12 | 377/7662 | 54/1749 | 18/582 | chr8 | 97644560 | ||
| chr8:97644650
|
C | G | 1 | a0001c0007 | 2 | HG02572.hp1 HG03540.hp2 |
synonymous_variant | LOW | c.144C>G | p.Pro48Pro | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/12 | 467/7662 | 144/1749 | 48/582 | chr8 | 97644650 | ||
| chr8:97644734
|
C | G | 1 | a0001c0005 | 3 | HG02145.hp2 HG02647.hp1 HG03130.hp1 |
synonymous_variant | LOW | c.228C>G | p.Ala76Ala | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/12 | 551/7662 | 228/1749 | 76/582 | chr8 | 97644734 | ||
| chr8:97713742
|
G | A | 2 | a0001c0002a0006c0009 | 50 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(47): Show |
synonymous_variant | LOW | c.1353G>A | p.Lys451Lys | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/12 | 1676/7662 | 1353/1749 | 451/582 | chr8 | 97713742 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:97644202
|
C | G | 4 | a0001c0001t0032a0001c0001t0091a0001c0001t0093others(1): Show | 5 | HG00741.hp1 HG01099.hp2 HG01978.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-305C>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/12 | 305 | chr8 | 97644202 | |||||
| chr8:97644211
|
A | T | 2 | a0001c0002t0089a0001c0002t0090 | 2 | NA18956.hp2 NA18957.hp1 |
5_prime_UTR_variant | MODIFIER | c.-296A>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/12 | 296 | chr8 | 97644211 | |||||
| chr8:97644231
|
C | T | 1 | a0001c0001t0088 | 1 | NA18946.hp2 | 5_prime_UTR_variant | MODIFIER | c.-276C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/12 | 276 | chr8 | 97644231 | |||||
| chr8:97724879
|
G | T | 1 | a0001c0001t0087 | 1 | homoSapiens_chm13v2.hp1 | 3_prime_UTR_variant | MODIFIER | c.*209G>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 209 | chr8 | 97724879 | |||||
| chr8:97724902
|
T | C | 1 | a0001c0001t0033 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*232T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 232 | chr8 | 97724902 | |||||
| chr8:97724913
|
C | T | 1 | a0001c0001t0012 | 6 | HG02055.hp2 HG02572.hp2 HG02630.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*243C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 243 | chr8 | 97724913 | |||||
| chr8:97724997
|
G | T | 3 | a0001c0001t0008a0001c0001t0023a0001c0001t0086 | 12 | HG01081.hp2 HG02258.hp2 HG02559.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*327G>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 327 | chr8 | 97724997 | |||||
| chr8:97725002
|
A | G | 3 | a0001c0001t0022a0001c0005t0022a0001c0005t0085 | 4 | HG02145.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*332A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 332 | chr8 | 97725002 | |||||
| chr8:97725338
|
A | G | 1 | a0001c0001t0084 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*668A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 668 | chr8 | 97725338 | |||||
| chr8:97725521
|
C | T | 28 | a0001c0001t0003a0001c0001t0007a0001c0001t0011others(25): Show | 77 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*851C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 851 | chr8 | 97725521 | |||||
| chr8:97725681
|
A | G | 28 | a0001c0001t0003a0001c0001t0007a0001c0001t0011others(25): Show | 77 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*1011A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 1011 | chr8 | 97725681 | |||||
| chr8:97725839
|
T | G | 1 | a0001c0001t0034 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1169T>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 1169 | chr8 | 97725839 | |||||
| chr8:97726000
|
A | G | 1 | a0007c0011t0070 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1330A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 1330 | chr8 | 97726000 | |||||
| chr8:97726060
|
C | T | 1 | a0001c0001t0069 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1390C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 1390 | chr8 | 97726060 | |||||
| chr8:97726100
|
C | T | 1 | a0001c0001t0023 | 3 | HG02559.hp1 HG02818.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1430C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 1430 | chr8 | 97726100 | |||||
| chr8:97726133
|
T | C | 28 | a0001c0001t0003a0001c0001t0007a0001c0001t0011others(25): Show | 77 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*1463T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 1463 | chr8 | 97726133 | |||||
| chr8:97726206
|
G | A | 1 | a0002c0003t0035 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1536G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 1536 | chr8 | 97726206 | |||||
| chr8:97726346
|
G | C | 1 | a0001c0001t0036 | 1 | NA18998.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1676G>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 1676 | chr8 | 97726346 | |||||
| chr8:97726619
|
C | T | 1 | a0001c0001t0086 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1949C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 1949 | chr8 | 97726619 | |||||
| chr8:97726813
|
G | A | 3 | a0001c0001t0022a0001c0005t0022a0001c0005t0085 | 4 | HG02145.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2143G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 2143 | chr8 | 97726813 | |||||
| chr8:97726840
|
C | T | 1 | a0001c0001t0068 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2170C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 2170 | chr8 | 97726840 | |||||
| chr8:97726918
|
C | CA | 10 | a0001c0001t0013a0001c0001t0017a0001c0001t0018others(7): Show | 17 | HG00733.hp2 HG01243.hp2 HG01884.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2259dupA | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 2260 | INFO_REALIGN_3_PRIME | chr8 | 97726918 | ||||
| chr8:97726918
|
CA | C | 24 | a0001c0001t0003a0001c0001t0007a0001c0001t0021others(21): Show | 67 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*2259delA | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 2259 | INFO_REALIGN_3_PRIME | chr8 | 97726918 | ||||
| chr8:97727068
|
T | G | 4 | a0001c0001t0005a0001c0001t0012a0001c0001t0024others(1): Show | 21 | HG00733.hp1 HG00738.hp2 HG01109.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2398T>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 2398 | chr8 | 97727068 | |||||
| chr8:97727075
|
C | CA | 4 | a0001c0001t0019a0001c0001t0025a0001c0001t0042others(1): Show | 7 | HG00597.hp1 HG00597.hp2 HG02145.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2419dupA | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 2420 | INFO_REALIGN_3_PRIME | chr8 | 97727075 | ||||
| chr8:97727100
|
A | G | 2 | a0001c0002t0089a0001c0002t0090 | 2 | NA18956.hp2 NA18957.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2430A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 2430 | chr8 | 97727100 | |||||
| chr8:97727170
|
A | G | 1 | a0001c0001t0093 | 1 | HG01978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2500A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 2500 | chr8 | 97727170 | |||||
| chr8:97727172
|
T | A | 1 | a0001c0001t0071 | 1 | NA18974.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2502T>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 2502 | chr8 | 97727172 | |||||
| chr8:97727227
|
C | T | 1 | a0007c0011t0070 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2557C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 2557 | chr8 | 97727227 | |||||
| chr8:97727306
|
C | T | 23 | a0001c0001t0003a0001c0001t0007a0001c0001t0021others(20): Show | 66 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*2636C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 2636 | chr8 | 97727306 | |||||
| chr8:97727430
|
T | C | 1 | a0001c0001t0037 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2760T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 2760 | chr8 | 97727430 | |||||
| chr8:97727494
|
C | CAAAAAAA | 14 | a0001c0001t0006a0001c0001t0008a0001c0001t0011others(11): Show | 39 | HG00673.hp1 HG01081.hp2 HG01891.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*2830_*2836dupAAAA others(3): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 2837 | INFO_REALIGN_3_PRIME | chr8 | 97727494 | ||||
| chr8:97727494
|
C | CAAAAAAA others(1): Show |
26 | a0001c0001t0003a0001c0001t0007a0001c0001t0013others(23): Show | 73 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*2829_*2836dupAAAA others(4): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 2837 | INFO_REALIGN_3_PRIME | chr8 | 97727494 | ||||
| chr8:97727494
|
C | CAAAAAAA others(2): Show |
23 | a0001c0001t0001a0001c0001t0009a0001c0001t0017others(20): Show | 97 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*2828_*2836dupAAAA others(5): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 2837 | INFO_REALIGN_3_PRIME | chr8 | 97727494 | ||||
| chr8:97727494
|
C | CAAAAAAA others(3): Show |
3 | a0001c0001t0020a0001c0001t0043a0001c0001t0044 | 5 | HG00140.hp2 HG00597.hp2 HG02132.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2827_*2836dupAAAA others(6): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 2837 | INFO_REALIGN_3_PRIME | chr8 | 97727494 | ||||
| chr8:97727637
|
A | G | 1 | a0001c0001t0066 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2967A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 2967 | chr8 | 97727637 | |||||
| chr8:97727921
|
T | C | 1 | a0001c0001t0045 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3251T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 3251 | chr8 | 97727921 | |||||
| chr8:97728139
|
T | TA | 5 | a0001c0001t0013a0001c0001t0039a0001c0001t0040others(2): Show | 8 | HG00733.hp2 HG01243.hp2 HG01884.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3470dupA | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 3471 | INFO_REALIGN_3_PRIME | chr8 | 97728139 | ||||
| chr8:97728191
|
A | G | 28 | a0001c0001t0003a0001c0001t0007a0001c0001t0011others(25): Show | 77 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*3521A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 3521 | chr8 | 97728191 | |||||
| chr8:97728218
|
C | T | 74 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(71): Show | 222 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(219): Show |
3_prime_UTR_variant | MODIFIER | c.*3548C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 3548 | chr8 | 97728218 | |||||
| chr8:97728258
|
T | G | 1 | a0001c0001t0027 | 2 | HG01070.hp1 HG01074.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3588T>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 3588 | chr8 | 97728258 | |||||
| chr8:97728308
|
T | C | 1 | a0001c0002t0075 | 1 | HG02148.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3638T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 3638 | chr8 | 97728308 | |||||
| chr8:97728385
|
G | A | 1 | a0001c0001t0028 | 2 | HG03490.hp1 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3715G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 3715 | chr8 | 97728385 | |||||
| chr8:97728495
|
G | A | 81 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(78): Show | 249 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(246): Show |
3_prime_UTR_variant | MODIFIER | c.*3825G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 3825 | chr8 | 97728495 | |||||
| chr8:97728524
|
T | A | 3 | a0001c0001t0008a0001c0001t0023a0001c0001t0086 | 12 | HG01081.hp2 HG02258.hp2 HG02559.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3854T>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 3854 | chr8 | 97728524 | |||||
| chr8:97728578
|
T | G | 2 | a0001c0001t0044a0001c0001t0046 | 2 | NA18985.hp1 NA19081.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3908T>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 3908 | chr8 | 97728578 | |||||
| chr8:97728640
|
A | G | 1 | a0001c0002t0078 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3970A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 3970 | chr8 | 97728640 | |||||
| chr8:97728741
|
G | A | 1 | a0001c0002t0078 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4071G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 4071 | chr8 | 97728741 | |||||
| chr8:97728757
|
C | CA | 13 | a0001c0001t0010a0001c0001t0014a0001c0001t0018others(10): Show | 27 | HG01099.hp2 HG01361.hp2 HG01891.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*4105dupA | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 4106 | INFO_REALIGN_3_PRIME | chr8 | 97728757 | ||||
| chr8:97728757
|
C | CAA | 22 | a0001c0001t0003a0001c0001t0021a0001c0001t0029others(19): Show | 60 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*4104_*4105dupAA | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 4106 | INFO_REALIGN_3_PRIME | chr8 | 97728757 | ||||
| chr8:97728757
|
C | CAAA | 11 | a0001c0001t0007a0001c0001t0008a0001c0001t0011others(8): Show | 31 | HG00673.hp1 HG01081.hp2 HG01109.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*4103_*4105dupAAA | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 4106 | INFO_REALIGN_3_PRIME | chr8 | 97728757 | ||||
| chr8:97728757
|
CA | C | 5 | a0001c0001t0064a0003c0004t0015a0003c0004t0053others(2): Show | 7 | HG00741.hp1 HG01168.hp1 HG01496.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4105delA | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 4105 | INFO_REALIGN_3_PRIME | chr8 | 97728757 | ||||
| chr8:97728906
|
A | G | 75 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(72): Show | 223 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(220): Show |
3_prime_UTR_variant | MODIFIER | c.*4236A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 4236 | chr8 | 97728906 | |||||
| chr8:97728908
|
C | CT | 19 | a0001c0001t0001a0001c0001t0017a0001c0001t0020others(16): Show | 89 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*4251dupT | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 4252 | INFO_REALIGN_3_PRIME | chr8 | 97728908 | ||||
| chr8:97728908
|
C | CTT | 5 | a0001c0001t0009a0001c0001t0036a0001c0001t0043others(2): Show | 10 | HG00597.hp2 HG02056.hp2 NA18940.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4250_*4251dupTT | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 4252 | INFO_REALIGN_3_PRIME | chr8 | 97728908 | ||||
| chr8:97728928
|
A | G | 3 | a0001c0001t0016a0001c0001t0057a0001c0001t0058 | 6 | HG02055.hp1 HG02451.hp1 HG02647.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4258A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 4258 | chr8 | 97728928 | |||||
| chr8:97729005
|
G | A | 2 | a0001c0001t0051a0001c0001t0052 | 2 | HG03225.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4335G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 4335 | chr8 | 97729005 | |||||
| chr8:97729087
|
A | AT | 6 | a0001c0001t0052a0001c0001t0058a0001c0001t0059others(3): Show | 6 | HG02647.hp2 HG03831.hp2 NA18967.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4435dupT | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 4436 | INFO_REALIGN_3_PRIME | chr8 | 97729087 | ||||
| chr8:97729087
|
AT | A | 57 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(54): Show | 180 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(177): Show |
3_prime_UTR_variant | MODIFIER | c.*4435delT | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 4435 | INFO_REALIGN_3_PRIME | chr8 | 97729087 | ||||
| chr8:97729087
|
ATT | A | 22 | a0001c0001t0001a0001c0001t0009a0001c0001t0017others(19): Show | 96 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*4434_*4435delTT | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 4434 | INFO_REALIGN_3_PRIME | chr8 | 97729087 | ||||
| chr8:97729109
|
A | G | 1 | a0001c0001t0060 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4439A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 4439 | chr8 | 97729109 | |||||
| chr8:97729192
|
G | A | 3 | a0001c0001t0008a0001c0001t0023a0001c0001t0086 | 12 | HG01081.hp2 HG02258.hp2 HG02559.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*4522G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 4522 | chr8 | 97729192 | |||||
| chr8:97729198
|
G | A | 3 | a0001c0001t0032a0001c0001t0091a0001c0001t0093 | 4 | HG01099.hp2 HG01978.hp2 HG03239.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4528G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 4528 | chr8 | 97729198 | |||||
| chr8:97729276
|
C | T | 3 | a0001c0001t0006a0001c0001t0054a0001c0001t0055 | 12 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*4606C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 4606 | chr8 | 97729276 | |||||
| chr8:97729290
|
C | T | 83 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(80): Show | 253 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(250): Show |
3_prime_UTR_variant | MODIFIER | c.*4620C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 4620 | chr8 | 97729290 | |||||
| chr8:97729319
|
C | T | 1 | a0001c0001t0034 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4649C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 4649 | chr8 | 97729319 | |||||
| chr8:97729477
|
T | C | 75 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(72): Show | 223 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(220): Show |
3_prime_UTR_variant | MODIFIER | c.*4807T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 4807 | chr8 | 97729477 | |||||
| chr8:97729478
|
G | A | 1 | a0001c0002t0081 | 1 | NA18986.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4808G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 4808 | chr8 | 97729478 | |||||
| chr8:97729549
|
A | T | 1 | a0001c0001t0034 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4879A>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 4879 | chr8 | 97729549 | |||||
| chr8:97729693
|
C | T | 3 | a0001c0001t0076a0001c0001t0079a0001c0001t0083 | 3 | HG00735.hp2 HG01516.hp2 HG02004.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5023C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 5023 | chr8 | 97729693 | |||||
| chr8:97729694
|
G | A | 1 | a0001c0001t0055 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5024G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 5024 | chr8 | 97729694 | |||||
| chr8:97729931
|
C | T | 28 | a0001c0001t0003a0001c0001t0007a0001c0001t0011others(25): Show | 77 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*5261C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 12/12 | 5261 | chr8 | 97729931 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:97645057
|
G | A | 1 | a0004c0008t0002g0001 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.381+170G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97645057 | ||||||
| chr8:97645059
|
A | T | 1 | a0004c0008t0002g0001 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.381+172A>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97645059 | ||||||
| chr8:97645060
|
T | G | 1 | a0004c0008t0002g0001 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.381+173T>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97645060 | ||||||
| chr8:97645091
|
G | A | 15 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0006others(12): Show | 15 | HG00733.hp1 HG00738.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.381+204G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97645091 | ||||||
| chr8:97645329
|
G | C | 254 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(251): Show | 254 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(251): Show |
intron_variant | MODIFIER | c.381+442G>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97645329 | ||||||
| chr8:97645354
|
G | T | 1 | a0001c0001t0003g0255 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.381+467G>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97645354 | ||||||
| chr8:97645516
|
C | G | 2 | a0001c0002t0003g0253a0001c0002t0003g0254 | 2 | HG03834.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.381+629C>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97645516 | ||||||
| chr8:97645767
|
C | T | 2 | a0001c0001t0051g0251a0001c0001t0052g0252 | 2 | HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.381+880C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97645767 | ||||||
| chr8:97645806
|
T | G | 91 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(88): Show | 91 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.381+919T>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97645806 | ||||||
| chr8:97645864
|
A | G | 7 | a0003c0004t0015g0244a0003c0004t0015g0245a0003c0004t0015g0250others(4): Show | 7 | HG00741.hp1 HG01168.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.381+977A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97645864 | ||||||
| chr8:97645987
|
C | G | 50 | a0001c0002t0003g0201a0001c0002t0003g0202a0001c0002t0003g0203others(47): Show | 50 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.381+1100C>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97645987 | ||||||
| chr8:97646015
|
G | A | 3 | a0001c0001t0019g0108a0001c0001t0019g0109a0001c0001t0019g0110 | 3 | HG02622.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.381+1128G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97646015 | ||||||
| chr8:97646216
|
G | A | 91 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(88): Show | 91 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.381+1329G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97646216 | ||||||
| chr8:97646231
|
A | G | 91 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(88): Show | 91 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.381+1344A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97646231 | ||||||
| chr8:97646235
|
T | A | 1 | a0001c0001t0056g0111 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.381+1348T>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97646235 | ||||||
| chr8:97646245
|
A | G | 108 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0175others(105): Show | 108 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.381+1358A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97646245 | ||||||
| chr8:97646467
|
AAAG | A | 16 | a0001c0001t0006g0180a0001c0001t0006g0182a0001c0001t0006g0183others(13): Show | 16 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.381+1584_381+1586d others(5): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 97646467 | |||||
| chr8:97646508
|
A | G | 11 | a0001c0001t0002g0359a0001c0001t0002g0361a0001c0001t0002g0362others(8): Show | 11 | HG00597.hp1 NA18956.hp1 NA18960.hp1 others(8): Show |
intron_variant | MODIFIER | c.381+1621A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97646508 | ||||||
| chr8:97646574
|
CTTGAG | C | 12 | a0001c0001t0002g0256a0001c0001t0011g0141a0001c0001t0011g0143others(9): Show | 12 | HG00673.hp1 HG02155.hp1 NA18941.hp1 others(9): Show |
intron_variant | MODIFIER | c.381+1693_381+1697d others(7): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 97646574 | |||||
| chr8:97646661
|
G | A | 3 | a0001c0001t0019g0108a0001c0001t0019g0109a0001c0001t0019g0110 | 3 | HG02622.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.381+1774G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97646661 | ||||||
| chr8:97647094
|
C | A | 1 | a0001c0001t0002g0257 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.381+2207C>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97647094 | ||||||
| chr8:97647212
|
G | C | 6 | a0001c0001t0005g0112a0001c0001t0005g0113a0001c0001t0005g0115others(3): Show | 6 | HG01109.hp2 HG01891.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.381+2325G>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97647212 | ||||||
| chr8:97647244
|
TG | T | 3 | a0001c0001t0019g0108a0001c0001t0019g0109a0001c0001t0019g0110 | 3 | HG02622.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.381+2359delG | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 97647244 | |||||
| chr8:97647263
|
G | A | 249 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(246): Show | 249 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(246): Show |
intron_variant | MODIFIER | c.381+2376G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97647263 | ||||||
| chr8:97647398
|
C | T | 1 | a0001c0001t0002g0358 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.381+2511C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97647398 | ||||||
| chr8:97647422
|
G | A | 1 | a0001c0001t0002g0256 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.381+2535G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97647422 | ||||||
| chr8:97647466
|
G | A | 4 | a0003c0004t0015g0244a0003c0004t0015g0245a0005c0010t0092g0247others(1): Show | 4 | HG00741.hp1 HG03491.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.381+2579G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97647466 | ||||||
| chr8:97647762
|
C | G | 2 | a0003c0004t0015g0250a0003c0004t0049g0249 | 2 | HG01361.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.381+2875C>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97647762 | ||||||
| chr8:97647764
|
A | G | 1 | a0001c0001t0001g0107 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.381+2877A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97647764 | ||||||
| chr8:97647872
|
A | G | 13 | a0001c0001t0013g0259a0001c0001t0018g0132a0001c0001t0018g0133others(10): Show | 13 | HG00733.hp2 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.381+2985A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97647872 | ||||||
| chr8:97647879
|
C | T | 1 | a0001c0001t0057g0124 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.381+2992C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97647879 | ||||||
| chr8:97647880
|
G | A | 89 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(86): Show | 89 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.381+2993G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97647880 | ||||||
| chr8:97647893
|
A | G | 1 | a0001c0001t0066g0357 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.381+3006A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97647893 | ||||||
| chr8:97647933
|
G | A | 98 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(95): Show | 98 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.381+3046G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97647933 | ||||||
| chr8:97647950
|
G | GA | 6 | a0001c0001t0001g0017a0001c0001t0002g0260a0001c0001t0009g0018others(3): Show | 6 | HG00673.hp2 HG02004.hp2 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.381+3078dupA | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 97647950 | |||||
| chr8:97647950
|
GA | G | 8 | a0001c0001t0010g0356a0001c0001t0016g0119a0001c0001t0016g0121others(5): Show | 8 | HG02055.hp1 HG02451.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.381+3078delA | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 97647950 | |||||
| chr8:97648163
|
C | G | 1 | a0001c0001t0016g0123 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.381+3276C>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97648163 | ||||||
| chr8:97648275
|
C | G | 1 | a0001c0001t0005g0117 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.381+3388C>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97648275 | ||||||
| chr8:97648299
|
T | C | 255 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(252): Show | 255 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(252): Show |
intron_variant | MODIFIER | c.381+3412T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97648299 | ||||||
| chr8:97648300
|
A | G | 1 | a0001c0001t0014g0369 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.381+3413A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97648300 | ||||||
| chr8:97648418
|
G | A | 3 | a0001c0001t0002g0263a0001c0001t0002g0264a0001c0001t0002g0265 | 3 | HG01192.hp1 HG01981.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.381+3531G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97648418 | ||||||
| chr8:97648474
|
T | C | 1 | a0001c0001t0002g0260 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.381+3587T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97648474 | ||||||
| chr8:97648492
|
G | A | 1 | a0001c0001t0002g0266 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.381+3605G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97648492 | ||||||
| chr8:97648494
|
CT | C | 146 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0175others(143): Show | 146 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(143): Show |
intron_variant | MODIFIER | c.381+3621delT | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 97648494 | |||||
| chr8:97648574
|
T | G | 255 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(252): Show | 255 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(252): Show |
intron_variant | MODIFIER | c.381+3687T>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97648574 | ||||||
| chr8:97648640
|
T | C | 7 | a0001c0001t0002g0268a0001c0001t0002g0269a0001c0001t0002g0270others(4): Show | 7 | HG00544.hp2 NA18942.hp2 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.381+3753T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97648640 | ||||||
| chr8:97648927
|
CTT | C | 99 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(96): Show | 99 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.381+4042_381+4043d others(4): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 97648927 | |||||
| chr8:97649041
|
A | G | 2 | a0001c0001t0014g0355a0001c0001t0059g0262 | 2 | NA18967.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.381+4154A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97649041 | ||||||
| chr8:97649498
|
A | C | 1 | a0001c0001t0003g0179 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.381+4611A>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97649498 | ||||||
| chr8:97649555
|
T | C | 2 | a0001c0001t0004g0274a0001c0001t0004g0275 | 2 | HG01243.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.381+4668T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97649555 | ||||||
| chr8:97649645
|
C | A | 1 | a0001c0002t0075g0196 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.381+4758C>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97649645 | ||||||
| chr8:97649900
|
G | A | 13 | a0001c0001t0013g0259a0001c0001t0018g0132a0001c0001t0018g0133others(10): Show | 13 | HG00733.hp2 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.381+5013G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97649900 | ||||||
| chr8:97650061
|
G | A | 2 | a0001c0007t0003g0153a0001c0007t0003g0154 | 2 | HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.381+5174G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97650061 | ||||||
| chr8:97650108
|
C | G | 4 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(1): Show | 4 | HG00639.hp2 HG00642.hp1 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+5221C>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97650108 | ||||||
| chr8:97650112
|
A | G | 12 | a0001c0001t0011g0141a0001c0001t0011g0143a0001c0001t0011g0144others(9): Show | 12 | HG00673.hp1 HG04115.hp1 NA18941.hp1 others(9): Show |
intron_variant | MODIFIER | c.381+5225A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97650112 | ||||||
| chr8:97650148
|
G | A | 4 | a0001c0001t0022g0192a0001c0005t0022g0193a0001c0005t0022g0195others(1): Show | 4 | HG02145.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+5261G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97650148 | ||||||
| chr8:97650208
|
A | T | 6 | a0001c0001t0016g0119a0001c0001t0016g0121a0001c0001t0016g0122others(3): Show | 6 | HG02055.hp1 HG02451.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.381+5321A>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97650208 | ||||||
| chr8:97650293
|
G | T | 1 | a0001c0001t0013g0259 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.381+5406G>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97650293 | ||||||
| chr8:97650414
|
A | G | 1 | a0001c0001t0006g0191 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.381+5527A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97650414 | ||||||
| chr8:97650415
|
C | T | 1 | a0001c0001t0002g0354 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.381+5528C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97650415 | ||||||
| chr8:97650458
|
A | G | 1 | a0007c0011t0070g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.381+5571A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97650458 | ||||||
| chr8:97650467
|
G | A | 1 | a0001c0001t0002g0263 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.381+5580G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97650467 | ||||||
| chr8:97650649
|
C | T | 2 | a0001c0001t0051g0251a0001c0001t0052g0252 | 2 | HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.381+5762C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97650649 | ||||||
| chr8:97650739
|
A | G | 3 | a0001c0001t0019g0108a0001c0001t0019g0109a0001c0001t0019g0110 | 3 | HG02622.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.381+5852A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97650739 | ||||||
| chr8:97650823
|
A | T | 1 | a0001c0001t0034g0118 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.381+5936A>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97650823 | ||||||
| chr8:97650854
|
C | T | 1 | a0001c0001t0005g0116 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.381+5967C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97650854 | ||||||
| chr8:97650932
|
C | G | 4 | a0001c0001t0018g0132a0001c0001t0018g0133a0001c0001t0018g0135others(1): Show | 4 | HG02615.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+6045C>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97650932 | ||||||
| chr8:97650968
|
C | T | 2 | a0001c0007t0003g0153a0001c0007t0003g0154 | 2 | HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.381+6081C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97650968 | ||||||
| chr8:97651155
|
A | G | 252 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(249): Show | 252 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(249): Show |
intron_variant | MODIFIER | c.381+6268A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97651155 | ||||||
| chr8:97651242
|
A | T | 1 | a0001c0001t0006g0191 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.381+6355A>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97651242 | ||||||
| chr8:97651354
|
C | T | 1 | a0001c0001t0005g0117 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.381+6467C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97651354 | ||||||
| chr8:97651386
|
C | G | 1 | a0001c0001t0019g0110 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.381+6499C>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97651386 | ||||||
| chr8:97651455
|
T | C | 1 | a0001c0001t0001g0020 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.381+6568T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97651455 | ||||||
| chr8:97651534
|
C | T | 2 | a0001c0001t0005g0115a0001c0001t0005g0116 | 2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.381+6647C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97651534 | ||||||
| chr8:97651542
|
G | A | 1 | a0003c0004t0049g0249 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.381+6655G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97651542 | ||||||
| chr8:97651579
|
G | A | 252 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(249): Show | 252 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(249): Show |
intron_variant | MODIFIER | c.381+6692G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97651579 | ||||||
| chr8:97651639
|
T | C | 7 | a0003c0004t0015g0244a0003c0004t0015g0245a0003c0004t0015g0250others(4): Show | 7 | HG00741.hp1 HG01168.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.381+6752T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97651639 | ||||||
| chr8:97651753
|
G | T | 2 | a0001c0001t0031g0177a0001c0001t0031g0178 | 2 | HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.381+6866G>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97651753 | ||||||
| chr8:97651810
|
A | T | 1 | a0001c0002t0003g0241 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.381+6923A>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97651810 | ||||||
| chr8:97651846
|
T | C | 2 | a0001c0001t0002g0276a0001c0001t0002g0277 | 2 | HG01175.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.381+6959T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97651846 | ||||||
| chr8:97651997
|
A | G | 99 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(96): Show | 99 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.381+7110A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97651997 | ||||||
| chr8:97652125
|
G | A | 1 | a0001c0001t0020g0021 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.381+7238G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97652125 | ||||||
| chr8:97652161
|
G | A | 1 | a0002c0003t0035g0125 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.381+7274G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97652161 | ||||||
| chr8:97652223
|
G | A | 1 | a0001c0001t0019g0110 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.381+7336G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97652223 | ||||||
| chr8:97652239
|
G | C | 13 | a0001c0001t0008g0155a0001c0001t0008g0156a0001c0001t0008g0157others(10): Show | 13 | HG01081.hp2 HG02258.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.381+7352G>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97652239 | ||||||
| chr8:97652300
|
C | T | 84 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0026others(81): Show | 84 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.381+7413C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97652300 | ||||||
| chr8:97652425
|
G | A | 66 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0175others(63): Show | 66 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.381+7538G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97652425 | ||||||
| chr8:97652501
|
T | C | 1 | a0001c0001t0005g0117 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.381+7614T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97652501 | ||||||
| chr8:97652591
|
G | A | 1 | a0001c0001t0008g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.381+7704G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97652591 | ||||||
| chr8:97652625
|
A | G | 1 | a0001c0001t0056g0111 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.381+7738A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97652625 | ||||||
| chr8:97652872
|
A | C | 1 | a0001c0001t0002g0353 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.381+7985A>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97652872 | ||||||
| chr8:97652891
|
C | T | 1 | a0001c0001t0002g0352 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.381+8004C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97652891 | ||||||
| chr8:97652987
|
C | T | 1 | a0001c0001t0034g0118 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.382-8085C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97652987 | ||||||
| chr8:97652988
|
G | A | 1 | a0001c0001t0001g0026 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.382-8084G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97652988 | ||||||
| chr8:97653216
|
A | G | 11 | a0001c0001t0011g0141a0001c0001t0011g0143a0001c0001t0011g0144others(8): Show | 11 | HG00673.hp1 NA18941.hp1 NA18947.hp2 others(8): Show |
intron_variant | MODIFIER | c.382-7856A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97653216 | ||||||
| chr8:97653326
|
C | G | 1 | a0001c0001t0001g0100 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.382-7746C>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97653326 | ||||||
| chr8:97653365
|
C | G | 1 | a0001c0001t0010g0356 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.382-7707C>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97653365 | ||||||
| chr8:97653393
|
G | C | 8 | a0001c0001t0013g0259a0001c0001t0039g0126a0001c0001t0040g0258others(5): Show | 8 | HG00733.hp2 HG01243.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.382-7679G>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97653393 | ||||||
| chr8:97653480
|
C | T | 1 | a0001c0001t0004g0351 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.382-7592C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97653480 | ||||||
| chr8:97653519
|
C | G | 1 | a0001c0001t0010g0356 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.382-7553C>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97653519 | ||||||
| chr8:97653543
|
C | T | 1 | a0001c0001t0002g0256 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.382-7529C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97653543 | ||||||
| chr8:97653612
|
C | CAACA | 3 | a0001c0001t0019g0108a0001c0001t0019g0109a0001c0001t0019g0110 | 3 | HG02622.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.382-7458_382-7455d others(6): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 97653612 | |||||
| chr8:97653646
|
T | C | 1 | a0001c0001t0004g0278 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.382-7426T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97653646 | ||||||
| chr8:97653829
|
A | G | 1 | a0001c0001t0065g0167 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.382-7243A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97653829 | ||||||
| chr8:97653854
|
G | A | 1 | a0001c0001t0021g0168 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.382-7218G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97653854 | ||||||
| chr8:97653962
|
C | T | 7 | a0001c0001t0013g0259a0001c0001t0040g0258a0002c0003t0013g0127others(4): Show | 7 | HG00733.hp2 HG01243.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.382-7110C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97653962 | ||||||
| chr8:97653991
|
A | G | 1 | a0001c0001t0002g0140 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.382-7081A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97653991 | ||||||
| chr8:97653993
|
C | G | 1 | a0001c0001t0056g0111 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.382-7079C>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97653993 | ||||||
| chr8:97654099
|
A | C | 4 | a0001c0001t0016g0121a0001c0001t0016g0122a0001c0001t0057g0124others(1): Show | 4 | HG02451.hp1 HG02647.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-6973A>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97654099 | ||||||
| chr8:97654400
|
A | C | 8 | a0001c0001t0013g0259a0001c0001t0039g0126a0001c0001t0040g0258others(5): Show | 8 | HG00733.hp2 HG01243.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.382-6672A>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97654400 | ||||||
| chr8:97654477
|
T | C | 92 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(89): Show | 92 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.382-6595T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97654477 | ||||||
| chr8:97654517
|
G | A | 1 | a0001c0001t0034g0118 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.382-6555G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97654517 | ||||||
| chr8:97654554
|
CT | C | 6 | a0001c0001t0002g0268a0001c0001t0002g0279a0001c0001t0002g0280others(3): Show | 6 | HG02273.hp1 NA18942.hp2 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.382-6505delT | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 97654554 | |||||
| chr8:97654587
|
G | A | 66 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0175others(63): Show | 66 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.382-6485G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97654587 | ||||||
| chr8:97654608
|
A | G | 12 | a0001c0001t0008g0155a0001c0001t0008g0156a0001c0001t0008g0157others(9): Show | 12 | HG01081.hp2 HG02258.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.382-6464A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97654608 | ||||||
| chr8:97654649
|
G | A | 6 | a0001c0001t0006g0180a0001c0001t0006g0182a0001c0001t0006g0183others(3): Show | 6 | HG02109.hp2 HG02257.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.382-6423G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97654649 | ||||||
| chr8:97654752
|
T | C | 3 | a0001c0001t0019g0108a0001c0001t0019g0109a0001c0001t0019g0110 | 3 | HG02622.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.382-6320T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97654752 | ||||||
| chr8:97654754
|
C | T | 1 | a0001c0001t0057g0124 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.382-6318C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97654754 | ||||||
| chr8:97654872
|
G | C | 1 | a0003c0004t0049g0249 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.382-6200G>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97654872 | ||||||
| chr8:97654930
|
T | C | 1 | a0001c0001t0001g0101 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.382-6142T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97654930 | ||||||
| chr8:97654935
|
A | G | 11 | a0001c0001t0011g0141a0001c0001t0011g0143a0001c0001t0011g0144others(8): Show | 11 | HG00673.hp1 NA18941.hp1 NA18947.hp2 others(8): Show |
intron_variant | MODIFIER | c.382-6137A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97654935 | ||||||
| chr8:97655071
|
C | T | 1 | a0001c0001t0001g0099 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.382-6001C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97655071 | ||||||
| chr8:97655177
|
C | G | 6 | a0001c0001t0016g0119a0001c0001t0016g0121a0001c0001t0016g0122others(3): Show | 6 | HG02055.hp1 HG02451.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.382-5895C>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97655177 | ||||||
| chr8:97655219
|
A | G | 1 | a0001c0001t0034g0118 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.382-5853A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97655219 | ||||||
| chr8:97655423
|
C | T | 1 | a0001c0001t0003g0175 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.382-5649C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97655423 | ||||||
| chr8:97655462
|
A | T | 1 | a0001c0001t0065g0167 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.382-5610A>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97655462 | ||||||
| chr8:97655549
|
C | T | 50 | a0001c0002t0003g0201a0001c0002t0003g0202a0001c0002t0003g0203others(47): Show | 50 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.382-5523C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97655549 | ||||||
| chr8:97655612
|
T | C | 1 | a0001c0001t0001g0027 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.382-5460T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97655612 | ||||||
| chr8:97655669
|
G | A | 7 | a0003c0004t0015g0244a0003c0004t0015g0245a0003c0004t0015g0250others(4): Show | 7 | HG00741.hp1 HG01168.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.382-5403G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97655669 | ||||||
| chr8:97655670
|
G | T | 11 | a0001c0002t0003g0231a0001c0002t0003g0234a0001c0002t0003g0235others(8): Show | 11 | HG00609.hp2 HG02027.hp1 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.382-5402G>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97655670 | ||||||
| chr8:97655674
|
A | G | 5 | a0001c0002t0003g0226a0001c0002t0003g0227a0001c0002t0003g0228others(2): Show | 5 | NA18971.hp2 NA18982.hp1 NA19062.hp1 others(2): Show |
intron_variant | MODIFIER | c.382-5398A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97655674 | ||||||
| chr8:97655680
|
A | G | 3 | a0001c0001t0002g0266a0001c0001t0002g0280a0001c0001t0002g0354 | 3 | HG02273.hp1 HG02293.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.382-5392A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97655680 | ||||||
| chr8:97656124
|
A | G | 1 | a0007c0011t0070g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.382-4948A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97656124 | ||||||
| chr8:97656172
|
C | G | 1 | a0001c0001t0002g0140 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.382-4900C>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97656172 | ||||||
| chr8:97656301
|
C | CT | 25 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(22): Show | 25 | HG00673.hp1 HG01952.hp2 HG02027.hp2 others(22): Show |
intron_variant | MODIFIER | c.382-4749dupT | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 97656301 | |||||
| chr8:97656301
|
CT | C | 43 | a0001c0001t0001g0102a0001c0001t0002g0281a0001c0001t0004g0274others(40): Show | 43 | HG00733.hp2 HG01081.hp2 HG01123.hp2 others(40): Show |
intron_variant | MODIFIER | c.382-4749delT | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 97656301 | |||||
| chr8:97656301
|
CTT | C | 63 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0175others(60): Show | 63 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.382-4750_382-4749d others(4): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 97656301 | |||||
| chr8:97656323
|
T | G | 1 | a0001c0001t0056g0111 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.382-4749T>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97656323 | ||||||
| chr8:97656365
|
C | T | 4 | a0001c0001t0022g0192a0001c0005t0022g0193a0001c0005t0022g0195others(1): Show | 4 | HG02145.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-4707C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97656365 | ||||||
| chr8:97656484
|
G | A | 14 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0006others(11): Show | 14 | HG00733.hp1 HG00738.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.382-4588G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97656484 | ||||||
| chr8:97656523
|
G | A | 4 | a0001c0001t0032g0030a0001c0001t0032g0093a0001c0001t0091g0029others(1): Show | 4 | HG01099.hp2 HG01978.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-4549G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97656523 | ||||||
| chr8:97656625
|
A | G | 7 | a0003c0004t0015g0244a0003c0004t0015g0245a0003c0004t0015g0250others(4): Show | 7 | HG00741.hp1 HG01168.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.382-4447A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97656625 | ||||||
| chr8:97656781
|
C | T | 1 | a0001c0001t0002g0350 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.382-4291C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97656781 | ||||||
| chr8:97656828
|
G | A | 1 | a0001c0001t0034g0118 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.382-4244G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97656828 | ||||||
| chr8:97656981
|
C | CA | 21 | a0001c0001t0001g0094a0001c0001t0004g0136a0001c0001t0004g0137others(18): Show | 21 | HG00733.hp2 HG01243.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.382-4077dupA | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 97656981 | |||||
| chr8:97656981
|
CAAAA | C | 7 | a0001c0001t0006g0180a0001c0001t0006g0182a0001c0001t0006g0183others(4): Show | 7 | HG02109.hp2 HG02257.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.382-4080_382-4077d others(6): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 97656981 | |||||
| chr8:97656999
|
A | G | 1 | a0001c0001t0029g0151 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.382-4073A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97656999 | ||||||
| chr8:97657044
|
A | G | 1 | a0001c0001t0001g0025 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.382-4028A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97657044 | ||||||
| chr8:97657059
|
A | C | 252 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(249): Show | 252 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(249): Show |
intron_variant | MODIFIER | c.382-4013A>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97657059 | ||||||
| chr8:97657274
|
C | G | 1 | a0001c0001t0002g0140 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.382-3798C>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97657274 | ||||||
| chr8:97657549
|
G | A | 100 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(97): Show | 100 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.382-3523G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97657549 | ||||||
| chr8:97657555
|
G | A | 1 | a0001c0002t0082g0223 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.382-3517G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97657555 | ||||||
| chr8:97657708
|
A | G | 11 | a0001c0001t0006g0180a0001c0001t0006g0182a0001c0001t0006g0183others(8): Show | 11 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.382-3364A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97657708 | ||||||
| chr8:97657723
|
G | A | 1 | a0001c0001t0002g0140 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.382-3349G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97657723 | ||||||
| chr8:97657819
|
T | C | 2 | a0001c0001t0001g0032a0001c0001t0088g0019 | 2 | NA18946.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.382-3253T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97657819 | ||||||
| chr8:97657841
|
A | G | 1 | a0001c0001t0003g0179 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.382-3231A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97657841 | ||||||
| chr8:97657847
|
A | G | 12 | a0001c0001t0006g0180a0001c0001t0006g0182a0001c0001t0006g0183others(9): Show | 12 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.382-3225A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97657847 | ||||||
| chr8:97658011
|
C | T | 7 | a0003c0004t0015g0244a0003c0004t0015g0245a0003c0004t0015g0250others(4): Show | 7 | HG00741.hp1 HG01168.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.382-3061C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97658011 | ||||||
| chr8:97658240
|
C | T | 1 | a0001c0002t0003g0241 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.382-2832C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97658240 | ||||||
| chr8:97658304
|
G | A | 13 | a0001c0001t0008g0155a0001c0001t0008g0156a0001c0001t0008g0157others(10): Show | 13 | HG01081.hp2 HG02258.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.382-2768G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97658304 | ||||||
| chr8:97658384
|
G | C | 1 | a0001c0001t0064g0285 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.382-2688G>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97658384 | ||||||
| chr8:97658750
|
A | G | 4 | a0001c0001t0032g0030a0001c0001t0032g0093a0001c0001t0091g0029others(1): Show | 4 | HG01099.hp2 HG01978.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-2322A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97658750 | ||||||
| chr8:97658772
|
T | G | 1 | a0001c0001t0056g0111 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.382-2300T>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97658772 | ||||||
| chr8:97658833
|
G | A | 2 | a0001c0002t0089g0197a0001c0002t0090g0224 | 2 | NA18956.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.382-2239G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97658833 | ||||||
| chr8:97659003
|
C | T | 8 | a0001c0001t0013g0259a0001c0001t0039g0126a0001c0001t0040g0258others(5): Show | 8 | HG00733.hp2 HG01243.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.382-2069C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97659003 | ||||||
| chr8:97659065
|
T | A | 1 | a0001c0001t0006g0191 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.382-2007T>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97659065 | ||||||
| chr8:97659085
|
G | A | 5 | a0001c0001t0011g0141a0001c0001t0011g0143a0001c0001t0011g0144others(2): Show | 5 | NA18947.hp2 NA18974.hp1 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.382-1987G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97659085 | ||||||
| chr8:97659142
|
CA | C | 81 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0006others(78): Show | 81 | HG00673.hp1 HG00733.hp1 HG00733.hp2 others(78): Show |
intron_variant | MODIFIER | c.382-1916delA | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 97659142 | |||||
| chr8:97659187
|
G | A | 1 | a0001c0001t0004g0136 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.382-1885G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97659187 | ||||||
| chr8:97659256
|
C | T | 1 | a0001c0001t0004g0136 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.382-1816C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97659256 | ||||||
| chr8:97659298
|
A | AC | 111 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(108): Show | 111 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.382-1774_382-1773i others(3): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97659298 | ||||||
| chr8:97659696
|
A | G | 4 | a0001c0001t0022g0192a0001c0005t0022g0193a0001c0005t0022g0195others(1): Show | 4 | HG02145.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-1376A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97659696 | ||||||
| chr8:97659836
|
G | A | 1 | a0001c0001t0039g0126 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.382-1236G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97659836 | ||||||
| chr8:97660159
|
C | CA | 7 | a0003c0004t0015g0244a0003c0004t0015g0245a0003c0004t0015g0250others(4): Show | 7 | HG00741.hp1 HG01168.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.382-905dupA | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 97660159 | |||||
| chr8:97660325
|
T | G | 1 | a0001c0001t0055g0186 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.382-747T>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97660325 | ||||||
| chr8:97660387
|
T | C | 1 | a0001c0001t0008g0156 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.382-685T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97660387 | ||||||
| chr8:97660500
|
T | C | 4 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(1): Show | 4 | HG00140.hp2 HG01258.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-572T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97660500 | ||||||
| chr8:97660880
|
ATT | A | 66 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0175others(63): Show | 66 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.382-189_382-188del others(2): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 97660880 | |||||
| chr8:97660883
|
T | TTA | 106 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0024others(103): Show | 106 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.382-172_382-171dup others(2): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 97660883 | |||||
| chr8:97660883
|
T | TTATA | 11 | a0001c0001t0001g0020a0001c0001t0011g0141a0001c0001t0011g0143others(8): Show | 11 | HG00673.hp1 HG03927.hp1 NA18941.hp1 others(8): Show |
intron_variant | MODIFIER | c.382-174_382-171dup others(4): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 97660883 | |||||
| chr8:97660911
|
G | GATA | 252 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(249): Show | 252 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(249): Show |
intron_variant | MODIFIER | c.382-158_382-156dup others(3): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr8 | 97660911 | |||||
| chr8:97661022
|
C | T | 111 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(108): Show | 111 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.382-50C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 1/11 | chr8 | 97661022 | ||||||
| chr8:97661336
|
G | A | 1 | a0001c0001t0002g0350 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.483+163G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97661336 | ||||||
| chr8:97661409
|
C | T | 1 | a0001c0001t0004g0284 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.483+236C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97661409 | ||||||
| chr8:97661495
|
A | G | 2 | a0001c0001t0013g0259a0001c0001t0040g0258 | 2 | HG01243.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.483+322A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97661495 | ||||||
| chr8:97661764
|
G | A | 1 | a0001c0001t0001g0027 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.483+591G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97661764 | ||||||
| chr8:97661791
|
A | G | 1 | a0001c0001t0002g0344 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.483+618A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97661791 | ||||||
| chr8:97661918
|
C | CA | 111 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0107others(108): Show | 111 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.483+761dupA | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97661918 | |||||
| chr8:97661918
|
C | CAA | 104 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(101): Show | 104 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.483+760_483+761dup others(2): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97661918 | |||||
| chr8:97661918
|
CAAAAA | C | 7 | a0003c0004t0015g0244a0003c0004t0015g0245a0003c0004t0015g0250others(4): Show | 7 | HG00741.hp1 HG01168.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.483+757_483+761del others(5): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97661918 | |||||
| chr8:97661954
|
C | T | 80 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0175others(77): Show | 80 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.483+781C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97661954 | ||||||
| chr8:97662024
|
G | T | 1 | a0001c0001t0001g0090 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.483+851G>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97662024 | ||||||
| chr8:97662060
|
C | T | 2 | a0001c0001t0001g0089a0001c0001t0026g0098 | 2 | NA18949.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.483+887C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97662060 | ||||||
| chr8:97662143
|
A | G | 1 | a0001c0001t0002g0343 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.483+970A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97662143 | ||||||
| chr8:97662294
|
C | A | 1 | a0001c0001t0016g0123 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.483+1121C>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97662294 | ||||||
| chr8:97662306
|
G | C | 1 | a0001c0002t0007g0198 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.483+1133G>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97662306 | ||||||
| chr8:97662352
|
A | T | 17 | a0001c0001t0001g0088a0001c0001t0006g0180a0001c0001t0006g0182others(14): Show | 17 | HG00621.hp1 HG02109.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.483+1179A>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97662352 | ||||||
| chr8:97662495
|
G | A | 3 | a0001c0001t0017g0037a0001c0001t0017g0038a0001c0001t0017g0039 | 3 | NA18951.hp2 NA18986.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.483+1322G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97662495 | ||||||
| chr8:97662543
|
T | C | 1 | a0001c0001t0004g0286 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.483+1370T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97662543 | ||||||
| chr8:97662558
|
G | C | 15 | a0001c0001t0013g0259a0001c0001t0018g0132a0001c0001t0018g0133others(12): Show | 15 | HG00733.hp2 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.483+1385G>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97662558 | ||||||
| chr8:97662559
|
G | A | 1 | a0001c0001t0037g0131 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.483+1386G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97662559 | ||||||
| chr8:97662560
|
T | C | 225 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(222): Show | 225 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(222): Show |
intron_variant | MODIFIER | c.483+1387T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97662560 | ||||||
| chr8:97662675
|
A | G | 12 | a0001c0001t0008g0155a0001c0001t0008g0156a0001c0001t0008g0157others(9): Show | 12 | HG01081.hp2 HG02258.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.483+1502A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97662675 | ||||||
| chr8:97662679
|
G | A | 15 | a0001c0001t0013g0259a0001c0001t0018g0132a0001c0001t0018g0133others(12): Show | 15 | HG00733.hp2 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.483+1506G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97662679 | ||||||
| chr8:97662752
|
C | G | 1 | a0001c0001t0057g0124 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.483+1579C>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97662752 | ||||||
| chr8:97662783
|
C | CA | 10 | a0001c0002t0003g0241a0001c0007t0003g0153a0001c0007t0003g0154others(7): Show | 10 | HG00609.hp2 HG00741.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.483+1621dupA | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97662783 | |||||
| chr8:97662791
|
A | G | 2 | a0001c0001t0001g0087a0001c0001t0033g0342 | 2 | HG02683.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.483+1618A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97662791 | ||||||
| chr8:97662791
|
AAAAG | A | 13 | a0001c0001t0006g0180a0001c0001t0006g0182a0001c0001t0006g0183others(10): Show | 13 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.483+1638_483+1641d others(6): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97662791 | |||||
| chr8:97662958
|
A | G | 1 | a0001c0001t0023g0165 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.483+1785A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97662958 | ||||||
| chr8:97663282
|
C | T | 91 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(88): Show | 91 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.483+2109C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97663282 | ||||||
| chr8:97663430
|
G | A | 1 | a0001c0001t0011g0147 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.483+2257G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97663430 | ||||||
| chr8:97663610
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.483+2437G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97663610 | ||||||
| chr8:97663639
|
C | A | 1 | a0001c0001t0005g0115 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.483+2466C>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97663639 | ||||||
| chr8:97663680
|
T | C | 224 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(221): Show | 224 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(221): Show |
intron_variant | MODIFIER | c.483+2507T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97663680 | ||||||
| chr8:97663691
|
G | GT | 105 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0175others(102): Show | 105 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.483+2519dupT | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97663691 | |||||
| chr8:97663748
|
C | CA | 114 | a0001c0001t0002g0140a0001c0001t0002g0263a0001c0001t0002g0276others(111): Show | 114 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.483+2595dupA | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97663748 | |||||
| chr8:97663748
|
CA | C | 17 | a0001c0001t0002g0341a0001c0001t0005g0004a0001c0001t0005g0005others(14): Show | 17 | HG00733.hp1 HG00738.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.483+2595delA | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97663748 | |||||
| chr8:97663748
|
CAA | C | 6 | a0001c0001t0005g0112a0001c0001t0005g0113a0001c0001t0005g0115others(3): Show | 6 | HG01109.hp2 HG01891.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.483+2594_483+2595d others(4): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97663748 | |||||
| chr8:97663748
|
CAAAAA | C | 91 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(88): Show | 91 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.483+2591_483+2595d others(7): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97663748 | |||||
| chr8:97663760
|
A | AG | 4 | a0001c0001t0022g0192a0001c0005t0022g0193a0001c0005t0022g0195others(1): Show | 4 | HG02145.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.483+2587_483+2588i others(3): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97663760 | ||||||
| chr8:97663916
|
C | A | 1 | a0001c0001t0034g0118 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.483+2743C>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97663916 | ||||||
| chr8:97664034
|
G | A | 1 | a0001c0001t0018g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.483+2861G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97664034 | ||||||
| chr8:97664068
|
A | G | 1 | a0001c0001t0034g0118 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.483+2895A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97664068 | ||||||
| chr8:97664071
|
G | C | 2 | a0001c0002t0007g0199a0001c0002t0007g0200 | 2 | HG01981.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.483+2898G>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97664071 | ||||||
| chr8:97664114
|
G | C | 15 | a0001c0001t0013g0259a0001c0001t0018g0132a0001c0001t0018g0133others(12): Show | 15 | HG00733.hp2 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.483+2941G>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97664114 | ||||||
| chr8:97664240
|
C | CA | 103 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(100): Show | 103 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.483+3068dupA | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97664240 | |||||
| chr8:97664280
|
C | G | 1 | a0001c0001t0034g0118 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.483+3107C>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97664280 | ||||||
| chr8:97664355
|
CA | C | 12 | a0001c0001t0008g0155a0001c0001t0008g0156a0001c0001t0008g0157others(9): Show | 12 | HG01081.hp2 HG02258.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.483+3195delA | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97664355 | |||||
| chr8:97664398
|
C | T | 1 | a0001c0002t0003g0220 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.483+3225C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97664398 | ||||||
| chr8:97664480
|
G | A | 4 | a0001c0001t0022g0192a0001c0005t0022g0193a0001c0005t0022g0195others(1): Show | 4 | HG02145.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.483+3307G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97664480 | ||||||
| chr8:97664504
|
A | G | 3 | a0001c0001t0004g0339a0001c0001t0004g0340a0001c0001t0010g0290 | 3 | NA18940.hp1 NA18975.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.483+3331A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97664504 | ||||||
| chr8:97664609
|
A | G | 21 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0006others(18): Show | 21 | HG00733.hp1 HG00738.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.483+3436A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97664609 | ||||||
| chr8:97664619
|
G | A | 221 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(218): Show | 221 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(218): Show |
intron_variant | MODIFIER | c.483+3446G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97664619 | ||||||
| chr8:97664699
|
TTTTC | T | 4 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0107others(1): Show | 4 | HG02257.hp1 HG02895.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.483+3542_483+3545d others(6): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97664699 | |||||
| chr8:97664981
|
C | T | 1 | a0001c0001t0010g0338 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.483+3808C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97664981 | ||||||
| chr8:97665057
|
C | T | 7 | a0001c0002t0007g0198a0001c0002t0007g0199a0001c0002t0007g0200others(4): Show | 7 | HG01496.hp2 HG01934.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.483+3884C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97665057 | ||||||
| chr8:97665119
|
A | G | 3 | a0001c0001t0002g0263a0001c0001t0002g0264a0001c0001t0002g0265 | 3 | HG01192.hp1 HG01981.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.483+3946A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97665119 | ||||||
| chr8:97665432
|
A | G | 253 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(250): Show | 253 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(250): Show |
intron_variant | MODIFIER | c.483+4259A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97665432 | ||||||
| chr8:97665494
|
A | C | 4 | a0001c0001t0009g0018a0001c0001t0009g0084a0001c0001t0009g0086others(1): Show | 4 | NA18945.hp1 NA18950.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.483+4321A>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97665494 | ||||||
| chr8:97665673
|
A | G | 1 | a0001c0001t0062g0349 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.483+4500A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97665673 | ||||||
| chr8:97665807
|
T | G | 4 | a0001c0001t0022g0192a0001c0005t0022g0193a0001c0005t0022g0195others(1): Show | 4 | HG02145.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.483+4634T>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97665807 | ||||||
| chr8:97665897
|
C | A | 1 | a0001c0002t0003g0225 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.483+4724C>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97665897 | ||||||
| chr8:97665902
|
G | A | 12 | a0001c0001t0006g0180a0001c0001t0006g0182a0001c0001t0006g0183others(9): Show | 12 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.483+4729G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97665902 | ||||||
| chr8:97665918
|
G | A | 1 | a0001c0001t0001g0041 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.483+4745G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97665918 | ||||||
| chr8:97666127
|
C | CA | 48 | a0001c0001t0001g0042a0001c0001t0002g0292a0001c0001t0004g0284others(45): Show | 48 | HG00673.hp1 HG00733.hp2 HG01099.hp1 others(45): Show |
intron_variant | MODIFIER | c.483+4973dupA | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97666127 | |||||
| chr8:97666127
|
CA | C | 16 | a0001c0001t0001g0081a0001c0001t0001g0100a0001c0001t0002g0341others(13): Show | 16 | HG00642.hp2 HG00741.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.483+4973delA | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97666127 | |||||
| chr8:97666174
|
A | G | 1 | a0007c0011t0070g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.483+5001A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97666174 | ||||||
| chr8:97666271
|
C | T | 1 | a0001c0002t0003g0216 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.483+5098C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97666271 | ||||||
| chr8:97666384
|
A | G | 1 | a0001c0001t0004g0136 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.483+5211A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97666384 | ||||||
| chr8:97666628
|
G | A | 2 | a0001c0001t0004g0267a0001c0001t0004g0346 | 2 | NA18977.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.483+5455G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97666628 | ||||||
| chr8:97666655
|
A | G | 1 | a0001c0001t0018g0135 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.483+5482A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97666655 | ||||||
| chr8:97666663
|
C | A | 1 | a0001c0001t0006g0191 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.483+5490C>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97666663 | ||||||
| chr8:97666944
|
G | A | 4 | a0001c0001t0022g0192a0001c0005t0022g0193a0001c0005t0022g0195others(1): Show | 4 | HG02145.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.483+5771G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97666944 | ||||||
| chr8:97666977
|
G | C | 99 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(96): Show | 99 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.483+5804G>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97666977 | ||||||
| chr8:97667007
|
G | A | 99 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(96): Show | 99 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.483+5834G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97667007 | ||||||
| chr8:97667068
|
G | A | 2 | a0001c0001t0003g0175a0001c0001t0003g0179 | 2 | HG03710.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.483+5895G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97667068 | ||||||
| chr8:97667097
|
CCTT | C | 6 | a0001c0001t0016g0119a0001c0001t0016g0121a0001c0001t0016g0122others(3): Show | 6 | HG02055.hp1 HG02451.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.483+5927_483+5929d others(5): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97667097 | |||||
| chr8:97667146
|
A | G | 3 | a0001c0001t0019g0108a0001c0001t0019g0109a0001c0001t0019g0110 | 3 | HG02622.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.483+5973A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97667146 | ||||||
| chr8:97667170
|
A | G | 1 | a0001c0001t0001g0088 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.483+5997A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97667170 | ||||||
| chr8:97667172
|
A | G | 2 | a0001c0001t0004g0335a0001c0001t0004g0336 | 2 | HG01070.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.483+5999A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97667172 | ||||||
| chr8:97667174
|
G | A | 1 | a0001c0001t0002g0293 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.483+6001G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97667174 | ||||||
| chr8:97667276
|
A | AT | 8 | a0001c0001t0005g0004a0001c0001t0005g0112a0001c0001t0005g0113others(5): Show | 8 | HG01109.hp2 HG01891.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.483+6109dupT | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97667276 | |||||
| chr8:97667401
|
A | G | 1 | a0007c0011t0070g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.483+6228A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97667401 | ||||||
| chr8:97667478
|
G | A | 1 | a0001c0001t0004g0294 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.483+6305G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97667478 | ||||||
| chr8:97667491
|
T | C | 21 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0006others(18): Show | 21 | HG00733.hp1 HG00738.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.483+6318T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97667491 | ||||||
| chr8:97667519
|
C | T | 1 | a0001c0002t0003g0238 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.483+6346C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97667519 | ||||||
| chr8:97667801
|
G | C | 5 | a0001c0001t0018g0132a0001c0001t0018g0133a0001c0001t0018g0135others(2): Show | 5 | HG02615.hp2 HG02630.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.483+6628G>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97667801 | ||||||
| chr8:97667831
|
T | TA | 100 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0025others(97): Show | 100 | HG00140.hp2 HG00544.hp1 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.483+6677dupA | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97667831 | |||||
| chr8:97667831
|
T | TAA | 26 | a0001c0001t0001g0103a0001c0001t0011g0141a0001c0001t0011g0143others(23): Show | 26 | HG00673.hp1 HG00733.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.483+6676_483+6677d others(4): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97667831 | |||||
| chr8:97667831
|
T | TAAA | 44 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0175others(41): Show | 44 | HG00609.hp2 HG00621.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.483+6675_483+6677d others(5): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97667831 | |||||
| chr8:97667831
|
T | TAAAA | 19 | a0001c0001t0021g0168a0001c0001t0030g0169a0001c0001t0034g0118others(16): Show | 19 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(16): Show |
intron_variant | MODIFIER | c.483+6674_483+6677d others(6): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97667831 | |||||
| chr8:97667896
|
C | T | 1 | a0001c0002t0003g0222 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.483+6723C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97667896 | ||||||
| chr8:97667920
|
A | C | 13 | a0001c0001t0013g0259a0001c0001t0018g0132a0001c0001t0018g0133others(10): Show | 13 | HG00733.hp2 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.483+6747A>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97667920 | ||||||
| chr8:97668005
|
C | T | 3 | a0001c0001t0019g0108a0001c0001t0019g0109a0001c0001t0019g0110 | 3 | HG02622.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.483+6832C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97668005 | ||||||
| chr8:97668006
|
C | G | 363 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(360): Show | 363 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(360): Show |
intron_variant | MODIFIER | c.483+6833C>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97668006 | ||||||
| chr8:97668013
|
C | T | 1 | a0001c0001t0001g0067 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.483+6840C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97668013 | ||||||
| chr8:97668015
|
C | T | 1 | a0001c0001t0055g0186 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.483+6842C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97668015 | ||||||
| chr8:97668104
|
G | A | 1 | a0001c0001t0001g0043 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.483+6931G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97668104 | ||||||
| chr8:97668189
|
A | G | 99 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(96): Show | 99 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.483+7016A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97668189 | ||||||
| chr8:97668211
|
C | T | 1 | a0001c0001t0037g0131 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.483+7038C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97668211 | ||||||
| chr8:97668239
|
A | G | 1 | a0001c0001t0039g0126 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.483+7066A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97668239 | ||||||
| chr8:97668256
|
C | T | 2 | a0001c0001t0002g0276a0001c0001t0002g0277 | 2 | HG01175.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.483+7083C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97668256 | ||||||
| chr8:97668560
|
C | CT | 22 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0006others(19): Show | 22 | HG00733.hp1 HG00738.hp2 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.483+7398dupT | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97668560 | |||||
| chr8:97668680
|
G | A | 21 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0006others(18): Show | 21 | HG00733.hp1 HG00738.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.483+7507G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97668680 | ||||||
| chr8:97668851
|
G | A | 2 | a0001c0001t0051g0251a0001c0001t0052g0252 | 2 | HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.483+7678G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97668851 | ||||||
| chr8:97668871
|
A | G | 3 | a0001c0001t0076g0174a0001c0001t0079g0152a0001c0001t0083g0370 | 3 | HG00735.hp2 HG01516.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.483+7698A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97668871 | ||||||
| chr8:97669143
|
A | G | 1 | a0001c0001t0002g0343 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.483+7970A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97669143 | ||||||
| chr8:97669172
|
G | A | 1 | a0001c0001t0052g0252 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.483+7999G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97669172 | ||||||
| chr8:97669212
|
G | C | 1 | a0001c0002t0078g0215 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.483+8039G>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97669212 | ||||||
| chr8:97669257
|
C | T | 1 | a0001c0001t0002g0361 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.483+8084C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97669257 | ||||||
| chr8:97669311
|
A | G | 66 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0175others(63): Show | 66 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.483+8138A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97669311 | ||||||
| chr8:97669329
|
A | G | 12 | a0001c0001t0006g0180a0001c0001t0006g0182a0001c0001t0006g0183others(9): Show | 12 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.483+8156A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97669329 | ||||||
| chr8:97669389
|
C | A | 1 | a0001c0001t0006g0187 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.483+8216C>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97669389 | ||||||
| chr8:97669543
|
C | G | 91 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0175others(88): Show | 91 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.483+8370C>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97669543 | ||||||
| chr8:97669582
|
CAAG | C | 91 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0175others(88): Show | 91 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.483+8410_483+8412d others(5): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97669582 | ||||||
| chr8:97669922
|
C | CA | 137 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(134): Show | 137 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(134): Show |
intron_variant | MODIFIER | c.483+8765dupA | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97669922 | |||||
| chr8:97669922
|
C | CAA | 111 | a0001c0001t0001g0027a0001c0001t0001g0103a0001c0001t0003g0172others(108): Show | 111 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.483+8764_483+8765d others(4): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97669922 | |||||
| chr8:97669922
|
C | CAAA | 6 | a0001c0001t0022g0192a0001c0001t0023g0158a0001c0001t0031g0177others(3): Show | 6 | HG02818.hp2 HG02896.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.483+8763_483+8765d others(5): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97669922 | |||||
| chr8:97669982
|
A | T | 252 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(249): Show | 252 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(249): Show |
intron_variant | MODIFIER | c.483+8809A>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97669982 | ||||||
| chr8:97670060
|
G | A | 8 | a0001c0001t0011g0141a0001c0001t0011g0143a0001c0001t0011g0144others(5): Show | 8 | HG00673.hp1 NA18941.hp1 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.483+8887G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97670060 | ||||||
| chr8:97670069
|
CT | C | 66 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0175others(63): Show | 66 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.483+8899delT | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97670069 | |||||
| chr8:97670084
|
A | G | 3 | a0001c0001t0019g0108a0001c0001t0019g0109a0001c0001t0019g0110 | 3 | HG02622.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.483+8911A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97670084 | ||||||
| chr8:97670188
|
C | T | 1 | a0001c0002t0003g0241 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.483+9015C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97670188 | ||||||
| chr8:97670247
|
C | T | 2 | a0001c0001t0002g0272a0001c0001t0002g0273 | 2 | NA18945.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.483+9074C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97670247 | ||||||
| chr8:97670485
|
G | A | 2 | a0002c0003t0013g0127a0002c0003t0013g0129 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.483+9312G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97670485 | ||||||
| chr8:97670617
|
C | T | 2 | a0001c0001t0051g0251a0001c0001t0052g0252 | 2 | HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.483+9444C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97670617 | ||||||
| chr8:97670886
|
A | G | 1 | a0001c0002t0003g0209 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.483+9713A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97670886 | ||||||
| chr8:97670901
|
C | T | 1 | a0001c0001t0029g0150 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.483+9728C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97670901 | ||||||
| chr8:97670937
|
T | G | 1 | a0001c0001t0002g0350 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.483+9764T>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97670937 | ||||||
| chr8:97670950
|
TTG | T | 6 | a0001c0001t0011g0141a0001c0001t0011g0143a0001c0001t0011g0146others(3): Show | 6 | NA18941.hp1 NA18947.hp2 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.483+9779_483+9780d others(4): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97670950 | |||||
| chr8:97670951
|
TG | T | 5 | a0001c0001t0011g0144a0001c0001t0011g0148a0001c0001t0029g0151others(2): Show | 5 | HG00673.hp1 NA18974.hp1 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.483+9779delG | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97670951 | ||||||
| chr8:97670952
|
G | GT | 76 | a0001c0001t0001g0043a0001c0001t0001g0066a0001c0001t0001g0097others(73): Show | 76 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.483+9803dupT | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97670952 | |||||
| chr8:97670952
|
G | GTT | 12 | a0001c0001t0004g0275a0001c0001t0006g0183a0001c0001t0006g0184others(9): Show | 12 | HG01123.hp2 HG01243.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.483+9802_483+9803d others(4): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97670952 | |||||
| chr8:97670952
|
GT | G | 68 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0025others(65): Show | 68 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.483+9803delT | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97670952 | |||||
| chr8:97670952
|
GTT | G | 47 | a0001c0001t0001g0048a0001c0001t0003g0175a0001c0001t0003g0255others(44): Show | 47 | HG00408.hp1 HG00558.hp2 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.483+9802_483+9803d others(4): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97670952 | |||||
| chr8:97670954
|
T | TG | 14 | a0001c0001t0008g0159a0001c0001t0013g0259a0001c0001t0018g0132others(11): Show | 14 | HG00733.hp2 HG01243.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.483+9781_483+9782i others(3): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97670954 | ||||||
| chr8:97670955
|
T | G | 6 | a0001c0001t0002g0303a0001c0001t0002g0353a0001c0001t0005g0115others(3): Show | 6 | HG01168.hp1 HG02976.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.483+9782T>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97670955 | ||||||
| chr8:97670956
|
T | G | 5 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0068others(2): Show | 5 | NA18952.hp2 NA18962.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.483+9783T>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97670956 | ||||||
| chr8:97670957
|
T | G | 7 | a0001c0001t0013g0259a0001c0001t0040g0258a0002c0003t0013g0127others(4): Show | 7 | HG00733.hp2 HG01243.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.483+9784T>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97670957 | ||||||
| chr8:97670960
|
T | G | 1 | a0002c0003t0035g0125 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.483+9787T>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97670960 | ||||||
| chr8:97671014
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.483+9841G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97671014 | ||||||
| chr8:97671049
|
T | C | 4 | a0003c0004t0015g0244a0003c0004t0015g0245a0005c0010t0092g0247others(1): Show | 4 | HG00741.hp1 HG03491.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.483+9876T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97671049 | ||||||
| chr8:97671052
|
G | A | 1 | a0001c0001t0001g0097 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.483+9879G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97671052 | ||||||
| chr8:97671059
|
G | A | 3 | a0001c0001t0019g0108a0001c0001t0019g0109a0001c0001t0019g0110 | 3 | HG02622.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.483+9886G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97671059 | ||||||
| chr8:97671121
|
G | A | 7 | a0001c0001t0001g0017a0001c0001t0001g0070a0001c0001t0001g0071others(4): Show | 7 | NA18983.hp1 NA18998.hp1 NA19003.hp2 others(4): Show |
intron_variant | MODIFIER | c.483+9948G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97671121 | ||||||
| chr8:97671141
|
A | G | 1 | a0003c0004t0015g0245 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.483+9968A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97671141 | ||||||
| chr8:97671190
|
C | T | 1 | a0001c0001t0008g0163 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.483+10017C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97671190 | ||||||
| chr8:97671262
|
C | T | 3 | a0001c0001t0008g0156a0001c0001t0008g0161a0001c0001t0008g0162 | 3 | HG02976.hp2 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.483+10089C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97671262 | ||||||
| chr8:97671265
|
T | A | 1 | a0001c0001t0043g0040 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.483+10092T>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97671265 | ||||||
| chr8:97671338
|
A | G | 30 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0006others(27): Show | 30 | HG00733.hp1 HG00738.hp2 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.483+10165A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97671338 | ||||||
| chr8:97671372
|
T | C | 24 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0006others(21): Show | 24 | HG00733.hp1 HG00738.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.483+10199T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97671372 | ||||||
| chr8:97671401
|
T | G | 1 | a0001c0001t0002g0279 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.483+10228T>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97671401 | ||||||
| chr8:97671486
|
C | T | 1 | a0001c0001t0002g0265 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.483+10313C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97671486 | ||||||
| chr8:97671792
|
C | T | 1 | a0001c0001t0004g0136 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.483+10619C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97671792 | ||||||
| chr8:97671988
|
T | C | 1 | a0007c0011t0070g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.483+10815T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97671988 | ||||||
| chr8:97672033
|
ATATC | A | 10 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0175others(7): Show | 10 | HG00735.hp2 HG01175.hp2 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.483+10862_483+1086 others(8): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97672033 | |||||
| chr8:97672040
|
CA | C | 10 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0175others(7): Show | 10 | HG00735.hp2 HG01175.hp2 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.483+10868delA | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97672040 | ||||||
| chr8:97672151
|
T | G | 3 | a0001c0001t0019g0108a0001c0001t0019g0109a0001c0001t0019g0110 | 3 | HG02622.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.483+10978T>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97672151 | ||||||
| chr8:97672216
|
T | C | 8 | a0001c0001t0013g0259a0001c0001t0039g0126a0001c0001t0040g0258others(5): Show | 8 | HG00733.hp2 HG01243.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.483+11043T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97672216 | ||||||
| chr8:97672533
|
A | G | 1 | a0001c0001t0034g0118 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.483+11360A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97672533 | ||||||
| chr8:97672732
|
C | T | 1 | a0001c0001t0034g0118 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.483+11559C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97672732 | ||||||
| chr8:97672887
|
G | A | 1 | a0001c0001t0002g0363 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.483+11714G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97672887 | ||||||
| chr8:97672894
|
A | T | 1 | a0001c0002t0003g0236 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.483+11721A>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97672894 | ||||||
| chr8:97672962
|
A | G | 1 | a0001c0001t0002g0299 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.483+11789A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97672962 | ||||||
| chr8:97672997
|
G | A | 1 | a0001c0001t0002g0297 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.483+11824G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97672997 | ||||||
| chr8:97673001
|
G | A | 1 | a0001c0001t0047g0056 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.483+11828G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97673001 | ||||||
| chr8:97673068
|
C | G | 3 | a0001c0001t0019g0108a0001c0001t0019g0109a0001c0001t0019g0110 | 3 | HG02622.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.483+11895C>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97673068 | ||||||
| chr8:97673154
|
T | C | 4 | a0001c0001t0022g0192a0001c0005t0022g0193a0001c0005t0022g0195others(1): Show | 4 | HG02145.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.483+11981T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97673154 | ||||||
| chr8:97673157
|
T | G | 1 | a0001c0002t0003g0225 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.483+11984T>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97673157 | ||||||
| chr8:97673162
|
C | T | 92 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(89): Show | 92 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.483+11989C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97673162 | ||||||
| chr8:97673169
|
G | A | 12 | a0001c0001t0006g0180a0001c0001t0006g0182a0001c0001t0006g0183others(9): Show | 12 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.483+11996G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97673169 | ||||||
| chr8:97673365
|
T | A | 2 | a0001c0001t0051g0251a0001c0001t0052g0252 | 2 | HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.483+12192T>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97673365 | ||||||
| chr8:97673387
|
G | A | 1 | a0001c0001t0004g0346 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.483+12214G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97673387 | ||||||
| chr8:97673431
|
G | C | 1 | a0001c0001t0001g0057 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.483+12258G>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97673431 | ||||||
| chr8:97673597
|
T | A | 9 | a0001c0002t0003g0201a0001c0002t0003g0202a0001c0002t0003g0203others(6): Show | 9 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(6): Show |
intron_variant | MODIFIER | c.483+12424T>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97673597 | ||||||
| chr8:97673600
|
C | T | 107 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0175others(104): Show | 107 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.483+12427C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97673600 | ||||||
| chr8:97673614
|
C | T | 15 | a0001c0001t0013g0259a0001c0001t0018g0132a0001c0001t0018g0133others(12): Show | 15 | HG00733.hp2 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.483+12441C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97673614 | ||||||
| chr8:97673664
|
C | T | 106 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(103): Show | 106 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.483+12491C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97673664 | ||||||
| chr8:97673665
|
G | A | 1 | a0001c0001t0011g0148 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.483+12492G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97673665 | ||||||
| chr8:97673906
|
C | T | 1 | a0001c0001t0034g0118 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.483+12733C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97673906 | ||||||
| chr8:97673946
|
G | C | 1 | a0001c0001t0004g0294 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.484-12722G>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97673946 | ||||||
| chr8:97673997
|
A | T | 1 | a0001c0001t0001g0089 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.484-12671A>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97673997 | ||||||
| chr8:97673998
|
T | A | 3 | a0001c0001t0004g0274a0001c0001t0004g0275a0001c0001t0012g0011 | 3 | HG01243.hp1 HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.484-12670T>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97673998 | ||||||
| chr8:97674300
|
C | T | 1 | a0001c0001t0009g0077 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.484-12368C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97674300 | ||||||
| chr8:97674534
|
A | G | 1 | a0001c0001t0034g0118 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.484-12134A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97674534 | ||||||
| chr8:97674573
|
G | A | 1 | a0001c0001t0023g0165 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.484-12095G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97674573 | ||||||
| chr8:97674814
|
C | CT | 32 | a0001c0001t0001g0099a0001c0001t0005g0004a0001c0001t0005g0005others(29): Show | 32 | HG00733.hp1 HG00738.hp2 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.484-11843dupT | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97674814 | |||||
| chr8:97674842
|
G | A | 3 | a0001c0001t0004g0339a0001c0001t0004g0340a0001c0001t0010g0290 | 3 | NA18940.hp1 NA18975.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.484-11826G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97674842 | ||||||
| chr8:97674904
|
G | A | 12 | a0001c0001t0006g0180a0001c0001t0006g0182a0001c0001t0006g0183others(9): Show | 12 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.484-11764G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97674904 | ||||||
| chr8:97674921
|
C | G | 1 | a0001c0001t0034g0118 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.484-11747C>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97674921 | ||||||
| chr8:97675230
|
A | G | 1 | a0001c0001t0002g0140 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.484-11438A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97675230 | ||||||
| chr8:97675558
|
T | A | 91 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(88): Show | 91 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.484-11110T>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97675558 | ||||||
| chr8:97675559
|
C | CA | 29 | a0001c0001t0001g0036a0001c0001t0001g0042a0001c0001t0001g0049others(26): Show | 29 | HG00423.hp1 HG00544.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.484-11089dupA | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97675559 | |||||
| chr8:97675559
|
C | CAA | 7 | a0001c0001t0018g0132a0001c0001t0018g0133a0001c0001t0018g0135others(4): Show | 7 | HG01884.hp1 HG02615.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.484-11090_484-1108 others(6): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97675559 | |||||
| chr8:97675559
|
CA | C | 22 | a0001c0001t0004g0335a0001c0001t0005g0004a0001c0001t0005g0005others(19): Show | 22 | HG00733.hp1 HG00738.hp2 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.484-11089delA | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97675559 | |||||
| chr8:97675578
|
AATTAC | A | 12 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0255others(9): Show | 12 | HG01167.hp1 HG01175.hp2 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.484-11086_484-1108 others(9): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97675578 | |||||
| chr8:97675725
|
A | T | 107 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0175others(104): Show | 107 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.484-10943A>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97675725 | ||||||
| chr8:97675747
|
C | T | 1 | a0001c0001t0004g0294 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.484-10921C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97675747 | ||||||
| chr8:97675765
|
C | T | 1 | a0001c0001t0056g0111 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.484-10903C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97675765 | ||||||
| chr8:97675820
|
C | T | 1 | a0001c0001t0041g0134 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.484-10848C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97675820 | ||||||
| chr8:97675927
|
A | G | 1 | a0001c0001t0004g0334 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.484-10741A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97675927 | ||||||
| chr8:97675939
|
GT | G | 65 | a0001c0001t0002g0358a0001c0001t0004g0138a0001c0001t0004g0267others(62): Show | 65 | HG00408.hp2 HG00642.hp2 HG00673.hp2 others(62): Show |
intron_variant | MODIFIER | c.484-10712delT | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97675939 | |||||
| chr8:97675940
|
T | TTA | 219 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(216): Show | 219 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(216): Show |
intron_variant | MODIFIER | c.484-10727_484-1072 others(6): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97675940 | |||||
| chr8:97675941
|
T | TA | 4 | a0001c0001t0001g0078a0001c0002t0003g0228a0001c0002t0003g0241others(1): Show | 4 | HG00609.hp2 HG01109.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.484-10727_484-1072 others(5): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97675941 | ||||||
| chr8:97675942
|
T | C | 219 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(216): Show | 219 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(216): Show |
intron_variant | MODIFIER | c.484-10726T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97675942 | ||||||
| chr8:97675943
|
T | C | 4 | a0001c0001t0001g0078a0001c0002t0003g0228a0001c0002t0003g0241others(1): Show | 4 | HG00609.hp2 HG01109.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.484-10725T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97675943 | ||||||
| chr8:97675964
|
A | G | 3 | a0001c0001t0001g0041a0001c0001t0001g0045a0001c0001t0001g0046 | 3 | NA18947.hp1 NA18952.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.484-10704A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97675964 | ||||||
| chr8:97676205
|
G | T | 7 | a0003c0004t0015g0244a0003c0004t0015g0245a0003c0004t0015g0250others(4): Show | 7 | HG00741.hp1 HG01168.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.484-10463G>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97676205 | ||||||
| chr8:97676741
|
T | C | 225 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(222): Show | 225 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(222): Show |
intron_variant | MODIFIER | c.484-9927T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97676741 | ||||||
| chr8:97676849
|
A | G | 16 | a0001c0001t0006g0180a0001c0001t0006g0182a0001c0001t0006g0183others(13): Show | 16 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.484-9819A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97676849 | ||||||
| chr8:97676963
|
C | T | 107 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0175others(104): Show | 107 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.484-9705C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97676963 | ||||||
| chr8:97677004
|
C | CAAAA | 7 | a0001c0001t0008g0157a0001c0001t0008g0159a0001c0001t0008g0160others(4): Show | 7 | HG02258.hp2 HG02559.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.484-9646_484-9643d others(6): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97677004 | |||||
| chr8:97677004
|
C | CAAAAA | 13 | a0001c0001t0001g0026a0001c0001t0001g0076a0001c0001t0008g0156others(10): Show | 13 | HG02451.hp1 HG02647.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.484-9647_484-9643d others(7): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97677004 | |||||
| chr8:97677004
|
C | CAAAAAA | 96 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0024others(93): Show | 96 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.484-9648_484-9643d others(8): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97677004 | |||||
| chr8:97677004
|
C | CAAAAAAA | 117 | a0001c0001t0001g0022a0001c0001t0001g0033a0001c0001t0001g0034others(114): Show | 117 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.484-9649_484-9643d others(9): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97677004 | |||||
| chr8:97677004
|
C | CAAAAAAA others(1): Show |
41 | a0001c0001t0002g0140a0001c0001t0002g0269a0001c0001t0002g0276others(38): Show | 41 | HG00140.hp2 HG00597.hp1 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.484-9650_484-9643d others(10): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97677004 | |||||
| chr8:97677004
|
C | CAAAAAAA others(2): Show |
58 | a0001c0001t0002g0310a0001c0001t0002g0362a0001c0001t0002g0366others(55): Show | 58 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.484-9651_484-9643d others(11): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97677004 | |||||
| chr8:97677004
|
C | CAAAAAAA others(3): Show |
21 | a0001c0001t0003g0172a0001c0001t0003g0175a0001c0001t0006g0180others(18): Show | 21 | HG00735.hp1 HG00735.hp2 HG01934.hp1 others(18): Show |
intron_variant | MODIFIER | c.484-9652_484-9643d others(12): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97677004 | |||||
| chr8:97677004
|
C | CAAAAAAA others(4): Show |
2 | a0001c0001t0006g0185a0001c0002t0090g0224 | 2 | HG02717.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.484-9653_484-9643d others(13): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97677004 | |||||
| chr8:97677004
|
CAA | C | 8 | a0001c0001t0013g0259a0001c0001t0039g0126a0001c0001t0040g0258others(5): Show | 8 | HG00733.hp2 HG01243.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.484-9644_484-9643d others(4): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97677004 | |||||
| chr8:97677052
|
G | A | 1 | a0005c0010t0092g0247 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.484-9616G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97677052 | ||||||
| chr8:97677102
|
G | C | 1 | a0002c0003t0035g0125 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.484-9566G>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97677102 | ||||||
| chr8:97677148
|
ACTCCAGC others(65): Show |
A | 91 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0175others(88): Show | 91 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.484-9518_484-9447d others(74): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97677148 | |||||
| chr8:97677180
|
C | CA | 46 | a0001c0001t0002g0139a0001c0001t0002g0140a0001c0001t0002g0260others(43): Show | 46 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.484-9457dupA | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97677180 | |||||
| chr8:97677180
|
C | CAA | 9 | a0001c0001t0002g0363a0001c0001t0002g0366a0001c0001t0004g0138others(6): Show | 9 | HG01884.hp1 HG02970.hp2 HG03927.hp2 others(6): Show |
intron_variant | MODIFIER | c.484-9458_484-9457d others(4): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97677180 | |||||
| chr8:97677180
|
CA | C | 36 | a0001c0001t0002g0321a0001c0001t0002g0322a0001c0001t0002g0333others(33): Show | 36 | HG00140.hp1 HG00639.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.484-9457delA | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97677180 | |||||
| chr8:97677180
|
CAAAAAAA others(5): Show |
C | 3 | a0001c0001t0019g0108a0001c0001t0019g0109a0001c0001t0019g0110 | 3 | HG02622.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.484-9468_484-9457d others(14): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97677180 | |||||
| chr8:97677180
|
CAAAAAAA others(6): Show |
C | 6 | a0001c0001t0001g0024a0001c0001t0001g0051a0001c0001t0001g0090others(3): Show | 6 | HG02027.hp2 HG03041.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.484-9469_484-9457d others(15): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97677180 | |||||
| chr8:97677180
|
CAAAAAAA others(7): Show |
C | 94 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(91): Show | 94 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.484-9470_484-9457d others(16): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97677180 | |||||
| chr8:97677321
|
G | A | 66 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0175others(63): Show | 66 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.484-9347G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97677321 | ||||||
| chr8:97677384
|
G | A | 3 | a0001c0001t0019g0108a0001c0001t0019g0109a0001c0001t0019g0110 | 3 | HG02622.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.484-9284G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97677384 | ||||||
| chr8:97677440
|
G | A | 4 | a0001c0001t0032g0030a0001c0001t0032g0093a0001c0001t0091g0029others(1): Show | 4 | HG01099.hp2 HG01978.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.484-9228G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97677440 | ||||||
| chr8:97677502
|
AAAG | A | 12 | a0001c0001t0006g0180a0001c0001t0006g0182a0001c0001t0006g0183others(9): Show | 12 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.484-9163_484-9161d others(5): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97677502 | |||||
| chr8:97677658
|
A | G | 91 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(88): Show | 91 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.484-9010A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97677658 | ||||||
| chr8:97677806
|
G | A | 252 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(249): Show | 252 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(249): Show |
intron_variant | MODIFIER | c.484-8862G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97677806 | ||||||
| chr8:97677991
|
C | T | 1 | a0001c0001t0002g0343 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.484-8677C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97677991 | ||||||
| chr8:97678331
|
G | A | 7 | a0001c0001t0002g0295a0001c0001t0002g0302a0001c0001t0002g0310others(4): Show | 7 | HG00609.hp1 NA18939.hp1 NA18967.hp1 others(4): Show |
intron_variant | MODIFIER | c.484-8337G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97678331 | ||||||
| chr8:97678431
|
G | A | 99 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(96): Show | 99 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.484-8237G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97678431 | ||||||
| chr8:97678503
|
A | G | 4 | a0001c0001t0022g0192a0001c0005t0022g0193a0001c0005t0022g0195others(1): Show | 4 | HG02145.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.484-8165A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97678503 | ||||||
| chr8:97678590
|
C | CTTTTTTT others(10): Show |
1 | a0001c0001t0011g0148 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.484-8078_484-8077i others(19): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97678590 | ||||||
| chr8:97678591
|
C | T | 1 | a0001c0001t0011g0148 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.484-8077C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97678591 | ||||||
| chr8:97678594
|
C | CT | 41 | a0001c0001t0002g0264a0001c0001t0002g0362a0001c0001t0002g0363others(38): Show | 41 | HG01081.hp2 HG01192.hp1 HG02055.hp1 others(38): Show |
intron_variant | MODIFIER | c.484-8050dupT | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97678594 | |||||
| chr8:97678594
|
C | CTTTTT | 76 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(73): Show | 76 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.484-8054_484-8050d others(7): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97678594 | |||||
| chr8:97678594
|
C | CTTTTTT | 16 | a0001c0001t0001g0026a0001c0001t0001g0054a0001c0001t0001g0055others(13): Show | 16 | HG00639.hp2 HG00642.hp1 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.484-8055_484-8050d others(8): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97678594 | |||||
| chr8:97678594
|
C | CTTTTTTT others(3): Show |
2 | a0001c0001t0034g0118a0001c0001t0039g0126 | 2 | HG02615.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.484-8059_484-8050d others(12): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97678594 | |||||
| chr8:97678594
|
C | CTTTTTTT others(4): Show |
1 | a0002c0003t0013g0128 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.484-8060_484-8050d others(13): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97678594 | |||||
| chr8:97678594
|
C | CTTTTTTT others(5): Show |
2 | a0001c0001t0018g0132a0001c0001t0018g0133 | 2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.484-8061_484-8050d others(14): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97678594 | |||||
| chr8:97678594
|
C | CTTTTTTT others(6): Show |
3 | a0001c0001t0018g0135a0001c0001t0037g0131a0001c0001t0041g0134 | 3 | HG02615.hp2 HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.484-8062_484-8050d others(15): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97678594 | |||||
| chr8:97678594
|
C | CTTTTTTT others(7): Show |
3 | a0001c0001t0051g0251a0001c0001t0052g0252a0007c0011t0070g0016 | 3 | HG01891.hp1 HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.484-8063_484-8050d others(16): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97678594 | |||||
| chr8:97678594
|
C | CTTTTTTT others(12): Show |
1 | a0001c0001t0029g0150 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.484-8068_484-8050d others(21): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97678594 | |||||
| chr8:97678594
|
C | CTTTTTTT others(13): Show |
2 | a0001c0001t0029g0151a0001c0001t0073g0149 | 2 | NA19054.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.484-8069_484-8050d others(22): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97678594 | |||||
| chr8:97678594
|
C | CTTTTTTT others(14): Show |
2 | a0001c0001t0011g0146a0001c0001t0011g0147 | 2 | NA18941.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.484-8070_484-8050d others(23): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97678594 | |||||
| chr8:97678594
|
C | CTTTTTTT others(17): Show |
1 | a0001c0001t0011g0143 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.484-8073_484-8050d others(26): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97678594 | |||||
| chr8:97678594
|
C | CTTTTTTT others(18): Show |
3 | a0001c0001t0011g0141a0001c0001t0011g0144a0001c0001t0071g0145 | 3 | NA18974.hp1 NA18993.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.484-8050_484-8049i others(27): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97678594 | |||||
| chr8:97678594
|
C | CTTTTTTT others(19): Show |
1 | a0001c0001t0072g0142 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.484-8050_484-8049i others(28): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97678594 | |||||
| chr8:97678594
|
C | T | 1 | a0001c0001t0011g0148 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.484-8074C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97678594 | ||||||
| chr8:97678594
|
CT | C | 62 | a0001c0001t0002g0297a0001c0001t0002g0343a0001c0001t0003g0172others(59): Show | 62 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.484-8050delT | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97678594 | |||||
| chr8:97678659
|
G | A | 1 | a0001c0001t0002g0353 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.484-8009G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97678659 | ||||||
| chr8:97678839
|
A | G | 1 | a0001c0001t0003g0175 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.484-7829A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97678839 | ||||||
| chr8:97678900
|
A | G | 2 | a0001c0002t0003g0253a0001c0002t0003g0254 | 2 | HG03834.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.484-7768A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97678900 | ||||||
| chr8:97679087
|
A | G | 1 | a0001c0001t0001g0053 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.484-7581A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97679087 | ||||||
| chr8:97679113
|
A | G | 1 | a0001c0001t0034g0118 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.484-7555A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97679113 | ||||||
| chr8:97679171
|
G | A | 35 | a0001c0001t0002g0358a0001c0001t0004g0267a0001c0001t0004g0278others(32): Show | 35 | HG00408.hp2 HG00642.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.484-7497G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97679171 | ||||||
| chr8:97679194
|
G | T | 3 | a0001c0001t0019g0108a0001c0001t0019g0109a0001c0001t0019g0110 | 3 | HG02622.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.484-7474G>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97679194 | ||||||
| chr8:97679198
|
C | T | 11 | a0001c0001t0011g0141a0001c0001t0011g0143a0001c0001t0011g0144others(8): Show | 11 | HG00673.hp1 NA18941.hp1 NA18947.hp2 others(8): Show |
intron_variant | MODIFIER | c.484-7470C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97679198 | ||||||
| chr8:97679242
|
A | G | 66 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0175others(63): Show | 66 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.484-7426A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97679242 | ||||||
| chr8:97679340
|
A | G | 92 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(89): Show | 92 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.484-7328A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97679340 | ||||||
| chr8:97679370
|
G | A | 3 | a0002c0003t0013g0127a0002c0003t0013g0129a0002c0003t0013g0130 | 3 | HG02895.hp1 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.484-7298G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97679370 | ||||||
| chr8:97679399
|
A | G | 66 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0175others(63): Show | 66 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.484-7269A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97679399 | ||||||
| chr8:97679490
|
G | A | 253 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(250): Show | 253 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(250): Show |
intron_variant | MODIFIER | c.484-7178G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97679490 | ||||||
| chr8:97679618
|
C | T | 1 | a0001c0001t0002g0310 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.484-7050C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97679618 | ||||||
| chr8:97679688
|
A | G | 28 | a0001c0001t0006g0180a0001c0001t0006g0182a0001c0001t0006g0183others(25): Show | 28 | HG01081.hp2 HG02109.hp2 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.484-6980A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97679688 | ||||||
| chr8:97679717
|
A | G | 3 | a0001c0001t0001g0048a0001c0001t0001g0081a0001c0001t0047g0056 | 3 | HG02056.hp2 HG02165.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.484-6951A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97679717 | ||||||
| chr8:97679765
|
T | C | 6 | a0001c0001t0016g0119a0001c0001t0016g0121a0001c0001t0016g0122others(3): Show | 6 | HG02055.hp1 HG02451.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.484-6903T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97679765 | ||||||
| chr8:97679767
|
A | G | 21 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0006others(18): Show | 21 | HG00733.hp1 HG00738.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.484-6901A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97679767 | ||||||
| chr8:97679820
|
AT | A | 3 | a0001c0001t0019g0108a0001c0001t0019g0109a0001c0001t0019g0110 | 3 | HG02622.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.484-6847delT | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97679820 | ||||||
| chr8:97679995
|
G | A | 99 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(96): Show | 99 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.484-6673G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97679995 | ||||||
| chr8:97680039
|
A | G | 1 | a0001c0001t0037g0131 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.484-6629A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97680039 | ||||||
| chr8:97680063
|
G | A | 1 | a0001c0001t0051g0251 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.484-6605G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97680063 | ||||||
| chr8:97680278
|
C | A | 1 | a0006c0009t0003g0233 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.484-6390C>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97680278 | ||||||
| chr8:97680358
|
C | G | 1 | a0007c0011t0070g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.484-6310C>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97680358 | ||||||
| chr8:97680358
|
C | T | 15 | a0001c0001t0013g0259a0001c0001t0018g0132a0001c0001t0018g0133others(12): Show | 15 | HG00733.hp2 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.484-6310C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97680358 | ||||||
| chr8:97681126
|
A | G | 1 | a0001c0002t0003g0236 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.484-5542A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97681126 | ||||||
| chr8:97681194
|
A | G | 1 | a0001c0001t0002g0289 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.484-5474A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97681194 | ||||||
| chr8:97681338
|
A | G | 30 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0006others(27): Show | 30 | HG00733.hp1 HG00738.hp2 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.484-5330A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97681338 | ||||||
| chr8:97681354
|
A | G | 4 | a0001c0001t0022g0192a0001c0005t0022g0193a0001c0005t0022g0195others(1): Show | 4 | HG02145.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.484-5314A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97681354 | ||||||
| chr8:97681407
|
G | GT | 9 | a0001c0001t0001g0079a0001c0001t0001g0106a0001c0001t0002g0295others(6): Show | 9 | HG00423.hp1 HG00733.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.484-5250dupT | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97681407 | |||||
| chr8:97681491
|
C | CT | 133 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(130): Show | 133 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.484-5158dupT | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97681491 | |||||
| chr8:97681491
|
C | CTT | 9 | a0001c0001t0001g0060a0001c0001t0009g0077a0001c0001t0012g0002others(6): Show | 9 | HG02055.hp2 HG02622.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.484-5159_484-5158d others(4): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97681491 | |||||
| chr8:97681491
|
CT | C | 16 | a0001c0001t0002g0359a0001c0001t0004g0137a0001c0001t0004g0138others(13): Show | 16 | HG00741.hp1 HG01168.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.484-5158delT | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97681491 | |||||
| chr8:97681491
|
CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0051g0251a0001c0001t0052g0252 | 2 | HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.484-5168_484-5158d others(13): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97681491 | |||||
| chr8:97681543
|
G | T | 1 | a0001c0001t0034g0118 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.484-5125G>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97681543 | ||||||
| chr8:97681719
|
C | T | 1 | a0001c0001t0002g0256 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.484-4949C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97681719 | ||||||
| chr8:97681829
|
C | T | 1 | a0001c0002t0003g0206 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.484-4839C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97681829 | ||||||
| chr8:97682128
|
G | A | 3 | a0001c0001t0019g0108a0001c0001t0019g0109a0001c0001t0019g0110 | 3 | HG02622.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.484-4540G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97682128 | ||||||
| chr8:97682228
|
CTTTATAT others(5): Show |
C | 1 | a0001c0001t0004g0294 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.484-4438_484-4427d others(14): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682228 | |||||
| chr8:97682228
|
CTTTATAT others(7): Show |
C | 2 | a0001c0001t0028g0306a0001c0001t0028g0326 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.484-4438_484-4425d others(16): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682228 | |||||
| chr8:97682230
|
T | A | 2 | a0001c0001t0002g0358a0007c0011t0070g0016 | 2 | HG01891.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.484-4438T>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97682230 | ||||||
| chr8:97682230
|
TTA | T | 14 | a0001c0001t0001g0045a0001c0001t0001g0049a0001c0001t0001g0073others(11): Show | 14 | HG00423.hp1 HG00621.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.484-4388_484-4387d others(4): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682230 | |||||
| chr8:97682230
|
TTATA | T | 6 | a0001c0001t0001g0036a0001c0001t0001g0101a0001c0001t0002g0312others(3): Show | 6 | HG00639.hp2 HG02451.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.484-4390_484-4387d others(6): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682230 | |||||
| chr8:97682230
|
TTATATA | T | 9 | a0001c0001t0001g0048a0001c0001t0001g0069a0001c0001t0002g0139others(6): Show | 9 | HG02040.hp1 HG02132.hp2 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.484-4392_484-4387d others(8): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682230 | |||||
| chr8:97682230
|
TTATATAT others(1): Show |
T | 10 | a0001c0001t0001g0024a0001c0001t0002g0293a0001c0001t0002g0296others(7): Show | 10 | HG00609.hp1 HG01358.hp2 HG02165.hp2 others(7): Show |
intron_variant | MODIFIER | c.484-4394_484-4387d others(10): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682230 | |||||
| chr8:97682230
|
TTATATAT others(3): Show |
T | 5 | a0001c0001t0001g0103a0001c0001t0002g0292a0001c0001t0006g0182others(2): Show | 5 | HG01099.hp1 HG01123.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.484-4396_484-4387d others(12): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682230 | |||||
| chr8:97682230
|
TTATATAT others(5): Show |
T | 1 | a0001c0001t0027g0318 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.484-4398_484-4387d others(14): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682230 | |||||
| chr8:97682230
|
TTATATAT others(7): Show |
T | 2 | a0001c0001t0004g0283a0002c0003t0013g0127 | 2 | HG02280.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.484-4400_484-4387d others(16): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682230 | |||||
| chr8:97682230
|
TTATATAT others(9): Show |
T | 2 | a0001c0001t0013g0259a0001c0001t0040g0258 | 2 | HG01243.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.484-4402_484-4387d others(18): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682230 | |||||
| chr8:97682230
|
TTATATAT others(13): Show |
T | 1 | a0001c0001t0043g0040 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.484-4406_484-4387d others(22): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682230 | |||||
| chr8:97682230
|
TTATATAT others(15): Show |
T | 4 | a0001c0001t0004g0274a0001c0001t0004g0275a0001c0001t0005g0008others(1): Show | 4 | HG01243.hp1 HG02258.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.484-4408_484-4387d others(24): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682230 | |||||
| chr8:97682230
|
TTATATAT others(17): Show |
T | 11 | a0001c0001t0001g0043a0001c0001t0001g0066a0001c0001t0001g0090others(8): Show | 11 | HG02055.hp2 HG02572.hp2 NA18522.hp1 others(8): Show |
intron_variant | MODIFIER | c.484-4410_484-4387d others(26): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682230 | |||||
| chr8:97682230
|
TTATATAT others(19): Show |
T | 15 | a0001c0001t0001g0032a0001c0001t0001g0096a0001c0001t0004g0278others(12): Show | 15 | HG00408.hp2 NA18612.hp2 NA18747.hp2 others(12): Show |
intron_variant | MODIFIER | c.484-4412_484-4387d others(28): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682230 | |||||
| chr8:97682230
|
TTATATAT others(25): Show |
T | 1 | a0001c0001t0002g0329 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.484-4418_484-4387d others(34): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682230 | |||||
| chr8:97682232
|
A | T | 3 | a0001c0001t0019g0108a0001c0001t0019g0109a0001c0001t0019g0110 | 3 | HG02622.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.484-4436A>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97682232 | ||||||
| chr8:97682240
|
ATATATAT others(37): Show |
A | 1 | a0001c0001t0060g0282 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.484-4426_484-4383d others(46): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682240 | |||||
| chr8:97682242
|
ATATATAT others(35): Show |
A | 3 | a0001c0002t0003g0235a0001c0002t0003g0239a0001c0002t0021g0240 | 3 | NA18991.hp1 NA19000.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.484-4424_484-4383d others(44): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682242 | |||||
| chr8:97682242
|
ATATATAT others(36): Show |
A | 7 | a0001c0002t0003g0231a0001c0002t0003g0234a0001c0002t0003g0236others(4): Show | 7 | HG00609.hp2 HG02027.hp1 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.484-4424_484-4382d others(45): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682242 | |||||
| chr8:97682242
|
ATATATAT others(37): Show |
A | 2 | a0001c0001t0029g0151a0001c0002t0007g0219 | 2 | HG03654.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.484-4424_484-4381d others(46): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682242 | |||||
| chr8:97682242
|
ATATATAT others(38): Show |
A | 3 | a0001c0001t0011g0146a0001c0001t0011g0147a0001c0001t0029g0150 | 3 | NA18941.hp1 NA18949.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.484-4424_484-4380d others(47): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682242 | |||||
| chr8:97682244
|
ATATATAT others(33): Show |
A | 3 | a0001c0001t0004g0339a0001c0001t0004g0340a0001c0001t0010g0290 | 3 | NA18940.hp1 NA18975.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.484-4422_484-4383d others(42): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682244 | |||||
| chr8:97682244
|
ATATATAT others(34): Show |
A | 2 | a0001c0002t0003g0209a0001c0002t0077g0221 | 2 | HG02056.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.484-4422_484-4382d others(43): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682244 | |||||
| chr8:97682244
|
ATATATAT others(35): Show |
A | 5 | a0001c0002t0003g0202a0001c0002t0003g0203a0001c0002t0003g0207others(2): Show | 5 | HG00408.hp1 HG00423.hp2 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.484-4422_484-4381d others(44): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682244 | |||||
| chr8:97682244
|
ATATATAT others(36): Show |
A | 22 | a0001c0001t0003g0173a0001c0001t0076g0174a0001c0002t0003g0201others(19): Show | 22 | HG00558.hp2 HG00621.hp2 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.484-4422_484-4380d others(45): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682244 | |||||
| chr8:97682244
|
ATATATAT others(37): Show |
A | 17 | a0001c0001t0003g0172a0001c0001t0003g0175a0001c0001t0003g0179others(14): Show | 17 | HG01109.hp1 HG01167.hp1 HG01516.hp2 others(14): Show |
intron_variant | MODIFIER | c.484-4422_484-4379d others(46): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682244 | |||||
| chr8:97682244
|
ATATATAT others(38): Show |
A | 7 | a0001c0001t0011g0141a0001c0001t0011g0143a0001c0001t0011g0144others(4): Show | 7 | HG00673.hp1 NA18947.hp2 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.484-4422_484-4378d others(47): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682244 | |||||
| chr8:97682244
|
ATATATAT others(41): Show |
A | 1 | a0001c0001t0004g0305 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.484-4422_484-4375d others(50): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682244 | |||||
| chr8:97682246
|
ATATATAT others(36): Show |
A | 8 | a0001c0001t0021g0168a0001c0001t0030g0169a0001c0002t0003g0208others(5): Show | 8 | HG01891.hp1 HG01952.hp1 HG02148.hp1 others(5): Show |
intron_variant | MODIFIER | c.484-4420_484-4378d others(45): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682246 | |||||
| chr8:97682247
|
TATATATA others(12): Show |
T | 1 | a0001c0001t0004g0325 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.484-4420_484-4402d others(21): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97682247 | ||||||
| chr8:97682247
|
TATATATA others(18): Show |
T | 3 | a0001c0001t0004g0324a0001c0001t0004g0346a0001c0001t0010g0345 | 3 | HG03831.hp1 NA18980.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.484-4420_484-4396d others(27): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97682247 | ||||||
| chr8:97682247
|
TATATATA others(20): Show |
T | 2 | a0001c0001t0001g0027a0001c0001t0004g0308 | 2 | NA18984.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.484-4420_484-4394d others(29): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97682247 | ||||||
| chr8:97682248
|
A | G | 1 | a0001c0001t0023g0165 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.484-4420A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97682248 | ||||||
| chr8:97682248
|
ATATATAT others(37): Show |
A | 1 | a0001c0001t0031g0177 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.484-4418_484-4375d others(46): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682248 | |||||
| chr8:97682248
|
ATATATAT others(38): Show |
A | 1 | a0001c0001t0031g0178 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.484-4418_484-4374d others(47): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682248 | |||||
| chr8:97682249
|
TATATATA others(18): Show |
T | 2 | a0001c0001t0010g0356a0001c0006t0004g0261 | 2 | HG00673.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.484-4418_484-4394d others(27): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97682249 | ||||||
| chr8:97682249
|
TATATATA others(20): Show |
T | 1 | a0001c0001t0010g0304 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.484-4418_484-4392d others(29): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97682249 | ||||||
| chr8:97682250
|
ATATATAT others(28): Show |
A | 1 | a0001c0001t0001g0035 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.484-4416_484-4382d others(37): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682250 | |||||
| chr8:97682251
|
TATATATA others(16): Show |
T | 1 | a0001c0001t0001g0099 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.484-4416_484-4394d others(25): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97682251 | ||||||
| chr8:97682251
|
TATATATA others(22): Show |
T | 1 | a0001c0001t0056g0111 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.484-4416_484-4388d others(31): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97682251 | ||||||
| chr8:97682252
|
ATATATAT others(29): Show |
A | 1 | a0001c0001t0019g0110 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.484-4414_484-4379d others(38): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682252 | |||||
| chr8:97682254
|
ATATATAT others(27): Show |
A | 1 | a0001c0001t0019g0109 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.484-4412_484-4379d others(36): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682254 | |||||
| chr8:97682254
|
ATATATAT others(29): Show |
A | 1 | a0001c0001t0019g0108 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.484-4412_484-4377d others(38): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682254 | |||||
| chr8:97682255
|
TATATATA others(18): Show |
T | 2 | a0001c0001t0001g0097a0001c0001t0012g0015 | 2 | HG02630.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.484-4412_484-4388d others(27): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97682255 | ||||||
| chr8:97682256
|
ATATATAT others(18): Show |
A | 1 | a0001c0001t0001g0059 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.484-4410_484-4386d others(27): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682256 | |||||
| chr8:97682256
|
ATATATAT others(34): Show |
A | 2 | a0001c0001t0024g0007a0001c0001t0024g0009 | 2 | HG00733.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.484-4410_484-4370d others(43): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682256 | |||||
| chr8:97682257
|
TATATATA others(16): Show |
T | 1 | a0004c0008t0002g0001 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.484-4410_484-4388d others(25): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97682257 | ||||||
| chr8:97682258
|
ATATATAT others(16): Show |
A | 2 | a0001c0001t0006g0191a0001c0001t0061g0271 | 2 | HG03471.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.484-4408_484-4386d others(25): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682258 | |||||
| chr8:97682258
|
ATATATAT others(17): Show |
A | 8 | a0001c0001t0002g0270a0001c0001t0002g0272a0001c0001t0002g0273others(5): Show | 8 | HG00544.hp2 HG01070.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.484-4408_484-4385d others(26): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682258 | |||||
| chr8:97682258
|
ATATATAT others(19): Show |
A | 1 | a0001c0001t0002g0300 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.484-4408_484-4383d others(28): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682258 | |||||
| chr8:97682258
|
ATATATAT others(20): Show |
A | 1 | a0001c0001t0037g0131 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.484-4408_484-4382d others(29): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682258 | |||||
| chr8:97682259
|
TATATATA others(6): Show |
T | 1 | a0001c0001t0084g0327 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.484-4408_484-4396d others(15): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97682259 | ||||||
| chr8:97682260
|
A | G | 1 | a0001c0001t0065g0167 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.484-4408A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97682260 | ||||||
| chr8:97682260
|
ATATATAT others(14): Show |
A | 1 | a0001c0001t0001g0075 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.484-4406_484-4386d others(23): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682260 | |||||
| chr8:97682260
|
ATATATAT others(15): Show |
A | 3 | a0001c0001t0004g0336a0001c0001t0005g0006a0001c0001t0041g0134 | 3 | HG01934.hp2 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.484-4406_484-4385d others(24): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682260 | |||||
| chr8:97682260
|
ATATATAT others(16): Show |
A | 3 | a0001c0001t0005g0005a0001c0001t0018g0132a0001c0001t0018g0135 | 3 | HG02615.hp2 HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.484-4406_484-4384d others(25): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682260 | |||||
| chr8:97682260
|
ATATATAT others(18): Show |
A | 3 | a0001c0001t0005g0004a0001c0001t0005g0113a0001c0001t0005g0176 | 3 | HG01109.hp2 NA19240.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.484-4406_484-4382d others(27): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682260 | |||||
| chr8:97682262
|
ATATATAT others(14): Show |
A | 1 | a0001c0001t0018g0133 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.484-4404_484-4384d others(23): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682262 | |||||
| chr8:97682262
|
ATATATAT others(18): Show |
A | 2 | a0001c0001t0005g0112a0001c0001t0005g0117 | 2 | HG01891.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.484-4404_484-4380d others(27): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682262 | |||||
| chr8:97682264
|
A | G | 1 | a0001c0001t0008g0160 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.484-4404A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97682264 | ||||||
| chr8:97682264
|
ATATATAT others(11): Show |
A | 1 | a0002c0003t0013g0128 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.484-4402_484-4385d others(20): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682264 | |||||
| chr8:97682264
|
ATATATAT others(12): Show |
A | 1 | a0001c0001t0034g0118 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.484-4402_484-4384d others(21): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682264 | |||||
| chr8:97682264
|
ATATATAT others(16): Show |
A | 1 | a0001c0001t0023g0165 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.484-4402_484-4380d others(25): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682264 | |||||
| chr8:97682265
|
TATATATA others(6): Show |
T | 2 | a0005c0010t0092g0247a0008c0012t0015g0246 | 2 | HG00741.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.484-4402_484-4390d others(15): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97682265 | ||||||
| chr8:97682266
|
A | T | 1 | a0001c0001t0001g0055 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.484-4402A>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97682266 | ||||||
| chr8:97682266
|
ATATATAT others(9): Show |
A | 2 | a0001c0001t0001g0065a0002c0003t0035g0125 | 2 | HG01884.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.484-4400_484-4385d others(18): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682266 | |||||
| chr8:97682266
|
ATATATAT others(14): Show |
A | 2 | a0001c0001t0005g0115a0001c0001t0005g0116 | 2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.484-4400_484-4380d others(23): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682266 | |||||
| chr8:97682266
|
ATATATAT others(16): Show |
A | 1 | a0001c0001t0042g0114 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.484-4400_484-4378d others(25): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682266 | |||||
| chr8:97682267
|
TATATATA others(6): Show |
T | 3 | a0001c0001t0001g0057a0001c0001t0002g0322a0002c0003t0013g0129 | 3 | HG00140.hp1 HG02897.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.484-4400_484-4388d others(15): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97682267 | ||||||
| chr8:97682268
|
A | G | 1 | a0001c0001t0008g0163 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.484-4400A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97682268 | ||||||
| chr8:97682268
|
A | T | 2 | a0001c0001t0001g0055a0001c0001t0004g0325 | 2 | NA18612.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.484-4400A>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97682268 | ||||||
| chr8:97682268
|
ATATATAT others(7): Show |
A | 1 | a0001c0001t0002g0280 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.484-4398_484-4385d others(16): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682268 | |||||
| chr8:97682268
|
ATATATAT others(8): Show |
A | 1 | a0001c0001t0002g0358 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.484-4398_484-4384d others(17): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682268 | |||||
| chr8:97682268
|
ATATATAT others(11): Show |
A | 1 | a0001c0001t0016g0121 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.484-4398_484-4381d others(20): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682268 | |||||
| chr8:97682268
|
ATATATAT others(12): Show |
A | 1 | a0001c0001t0016g0122 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.484-4398_484-4380d others(21): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682268 | |||||
| chr8:97682268
|
ATATATAT others(14): Show |
A | 1 | a0001c0001t0001g0041 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.484-4398_484-4378d others(23): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682268 | |||||
| chr8:97682270
|
A | G | 3 | a0001c0001t0008g0157a0001c0001t0008g0159a0001c0001t0086g0166 | 3 | HG02258.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.484-4398A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97682270 | ||||||
| chr8:97682270
|
A | T | 2 | a0001c0001t0001g0055a0001c0001t0004g0325 | 2 | NA18612.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.484-4398A>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97682270 | ||||||
| chr8:97682270
|
ATATATAT others(4): Show |
A | 4 | a0001c0001t0001g0025a0001c0001t0004g0334a0001c0005t0022g0195others(1): Show | 4 | HG02145.hp2 HG02257.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.484-4396_484-4386d others(13): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682270 | |||||
| chr8:97682270
|
ATATATAT others(5): Show |
A | 1 | a0003c0004t0015g0244 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.484-4396_484-4385d others(14): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682270 | |||||
| chr8:97682270
|
ATATATAT others(6): Show |
A | 1 | a0002c0003t0013g0130 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.484-4396_484-4384d others(15): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682270 | |||||
| chr8:97682270
|
ATATATAT others(7): Show |
A | 2 | a0001c0001t0002g0310a0001c0001t0004g0136 | 2 | HG01884.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.484-4396_484-4383d others(16): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682270 | |||||
| chr8:97682270
|
ATATATAT others(12): Show |
A | 1 | a0001c0001t0026g0098 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.484-4396_484-4378d others(21): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682270 | |||||
| chr8:97682272
|
A | T | 5 | a0001c0001t0001g0046a0001c0001t0001g0055a0001c0001t0002g0330others(2): Show | 5 | HG00741.hp2 HG03516.hp2 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.484-4396A>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97682272 | ||||||
| chr8:97682272
|
ATATATAT others(3): Show |
A | 1 | a0001c0001t0054g0181 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.484-4394_484-4385d others(12): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682272 | |||||
| chr8:97682272
|
ATATATAT others(4): Show |
A | 1 | a0003c0004t0053g0248 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.484-4394_484-4384d others(13): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682272 | |||||
| chr8:97682272
|
ATATATAT others(7): Show |
A | 1 | a0001c0001t0058g0120 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.484-4394_484-4381d others(16): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682272 | |||||
| chr8:97682273
|
T | C | 2 | a0001c0001t0014g0367a0001c0001t0014g0369 | 2 | NA18973.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.484-4395T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97682273 | ||||||
| chr8:97682274
|
A | T | 14 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0054others(11): Show | 14 | HG00738.hp1 HG00741.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.484-4394A>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97682274 | ||||||
| chr8:97682274
|
ATATATAT others(3): Show |
A | 3 | a0001c0001t0002g0343a0001c0001t0020g0021a0001c0005t0085g0194 | 3 | HG00140.hp2 HG01168.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.484-4392_484-4383d others(12): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682274 | |||||
| chr8:97682274
|
ATATATAT others(5): Show |
A | 1 | a0001c0001t0051g0251 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.484-4392_484-4381d others(14): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682274 | |||||
| chr8:97682275
|
TATA | T | 3 | a0001c0001t0001g0051a0001c0001t0001g0091a0001c0001t0032g0030 | 3 | HG03239.hp1 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.484-4392_484-4390d others(5): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97682275 | ||||||
| chr8:97682276
|
A | T | 38 | a0001c0001t0001g0027a0001c0001t0001g0045a0001c0001t0001g0046others(35): Show | 38 | HG00408.hp2 HG00673.hp2 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.484-4392A>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97682276 | ||||||
| chr8:97682276
|
ATATATT | A | 7 | a0001c0001t0002g0277a0001c0001t0002g0279a0001c0001t0002g0281others(4): Show | 7 | HG01167.hp2 HG03017.hp1 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.484-4390_484-4385d others(8): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682276 | |||||
| chr8:97682276
|
ATATATTT others(6): Show |
A | 1 | a0001c0001t0002g0331 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.484-4390_484-4378d others(15): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682276 | |||||
| chr8:97682277
|
TATA | T | 5 | a0001c0001t0001g0092a0001c0001t0002g0361a0001c0001t0025g0365others(2): Show | 5 | HG00597.hp1 HG01978.hp2 NA18939.hp2 others(2): Show |
intron_variant | MODIFIER | c.484-4390_484-4388d others(5): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97682277 | ||||||
| chr8:97682278
|
A | ATTTTTTT others(4): Show |
1 | a0001c0001t0001g0067 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.484-4389_484-4388i others(13): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682278 | |||||
| chr8:97682278
|
A | T | 46 | a0001c0001t0001g0027a0001c0001t0001g0043a0001c0001t0001g0045others(43): Show | 46 | HG00408.hp2 HG00621.hp1 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.484-4390A>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97682278 | ||||||
| chr8:97682278
|
ATATT | A | 6 | a0001c0001t0001g0022a0001c0001t0002g0276a0001c0001t0002g0362others(3): Show | 6 | HG01175.hp1 HG02886.hp2 NA18940.hp2 others(3): Show |
intron_variant | MODIFIER | c.484-4388_484-4385d others(6): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682278 | |||||
| chr8:97682278
|
ATATTT | A | 6 | a0001c0001t0001g0017a0001c0001t0001g0063a0001c0001t0002g0140others(3): Show | 6 | HG01255.hp1 NA18960.hp1 NA18999.hp1 others(3): Show |
intron_variant | MODIFIER | c.484-4388_484-4384d others(7): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682278 | |||||
| chr8:97682278
|
ATATTTTT others(3): Show |
A | 1 | a0001c0001t0065g0167 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.484-4388_484-4379d others(12): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682278 | |||||
| chr8:97682280
|
A | ATATATAT others(3): Show |
1 | a0001c0001t0001g0102 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.484-4387_484-4386i others(12): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682280 | |||||
| chr8:97682280
|
A | ATATATTT others(6): Show |
1 | a0001c0001t0001g0026 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.484-4387_484-4386i others(15): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682280 | |||||
| chr8:97682280
|
A | G | 1 | a0001c0001t0023g0158 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.484-4388A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97682280 | ||||||
| chr8:97682280
|
A | T | 75 | a0001c0001t0001g0027a0001c0001t0001g0032a0001c0001t0001g0043others(72): Show | 75 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.484-4388A>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97682280 | ||||||
| chr8:97682281
|
T | TA | 4 | a0001c0001t0001g0042a0001c0001t0002g0297a0001c0001t0062g0349others(1): Show | 4 | HG03516.hp1 HG03831.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.484-4387_484-4386i others(3): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97682281 | ||||||
| chr8:97682281
|
T | TATATATA others(4): Show |
1 | a0001c0001t0023g0158 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.484-4387_484-4386i others(13): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97682281 | ||||||
| chr8:97682282
|
T | A | 13 | a0001c0001t0001g0087a0001c0001t0008g0155a0001c0001t0008g0156others(10): Show | 13 | HG02258.hp2 HG02559.hp1 HG02922.hp1 others(10): Show |
intron_variant | MODIFIER | c.484-4386T>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97682282 | ||||||
| chr8:97682283
|
T | A | 7 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0002g0289others(4): Show | 7 | HG01258.hp1 HG02818.hp2 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.484-4385T>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97682283 | ||||||
| chr8:97682284
|
T | A | 10 | a0001c0001t0002g0140a0001c0001t0008g0155a0001c0001t0008g0156others(7): Show | 10 | HG01081.hp2 HG01255.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.484-4384T>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97682284 | ||||||
| chr8:97682285
|
T | A | 3 | a0001c0001t0002g0289a0001c0001t0002g0314a0001c0001t0086g0166 | 3 | HG03516.hp1 HG03688.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.484-4383T>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97682285 | ||||||
| chr8:97682286
|
T | A | 1 | a0001c0001t0008g0162 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.484-4382T>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97682286 | ||||||
| chr8:97682287
|
T | A | 1 | a0003c0004t0049g0249 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.484-4381T>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97682287 | ||||||
| chr8:97682443
|
C | T | 1 | a0001c0001t0002g0273 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.484-4225C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97682443 | ||||||
| chr8:97682552
|
T | C | 255 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(252): Show | 255 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(252): Show |
intron_variant | MODIFIER | c.484-4116T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97682552 | ||||||
| chr8:97682624
|
A | G | 1 | a0001c0001t0032g0093 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.484-4044A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97682624 | ||||||
| chr8:97682750
|
T | TA | 13 | a0001c0001t0008g0155a0001c0001t0008g0156a0001c0001t0008g0157others(10): Show | 13 | HG01081.hp2 HG02258.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.484-3909dupA | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97682750 | |||||
| chr8:97682861
|
A | G | 3 | a0001c0001t0019g0108a0001c0001t0019g0109a0001c0001t0019g0110 | 3 | HG02622.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.484-3807A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97682861 | ||||||
| chr8:97682868
|
G | A | 1 | a0001c0001t0016g0123 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.484-3800G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97682868 | ||||||
| chr8:97682932
|
A | G | 2 | a0001c0001t0004g0283a0001c0001t0068g0328 | 2 | HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.484-3736A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97682932 | ||||||
| chr8:97682975
|
A | G | 1 | a0001c0001t0002g0333 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.484-3693A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97682975 | ||||||
| chr8:97682981
|
A | G | 1 | a0001c0001t0071g0145 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.484-3687A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97682981 | ||||||
| chr8:97683001
|
T | A | 1 | a0001c0001t0034g0118 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.484-3667T>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97683001 | ||||||
| chr8:97683045
|
C | CT | 50 | a0001c0001t0002g0256a0001c0001t0002g0263a0001c0001t0002g0264others(47): Show | 50 | HG00597.hp1 HG00621.hp2 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.484-3586dupT | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97683045 | |||||
| chr8:97683045
|
C | CTT | 23 | a0001c0001t0002g0269a0001c0001t0002g0289a0001c0001t0002g0361others(20): Show | 23 | HG00408.hp1 HG00558.hp2 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.484-3587_484-3586d others(4): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97683045 | |||||
| chr8:97683045
|
C | CTTT | 8 | a0001c0001t0001g0075a0001c0001t0001g0087a0001c0001t0002g0366others(5): Show | 8 | HG00423.hp2 HG00558.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.484-3588_484-3586d others(5): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97683045 | |||||
| chr8:97683045
|
C | CTTTT | 20 | a0001c0001t0001g0026a0001c0001t0001g0035a0001c0001t0001g0045others(17): Show | 20 | HG00621.hp1 HG01099.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.484-3589_484-3586d others(6): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97683045 | |||||
| chr8:97683045
|
C | CTTTTT | 25 | a0001c0001t0001g0020a0001c0001t0001g0027a0001c0001t0001g0032others(22): Show | 25 | HG00140.hp2 HG00597.hp2 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.484-3590_484-3586d others(7): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97683045 | |||||
| chr8:97683045
|
C | CTTTTTT | 11 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0043others(8): Show | 11 | HG00544.hp1 HG00642.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.484-3591_484-3586d others(8): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97683045 | |||||
| chr8:97683045
|
C | CTTTTTTT others(3): Show |
4 | a0001c0001t0001g0049a0001c0001t0001g0058a0001c0001t0001g0064others(1): Show | 4 | HG01952.hp2 HG01978.hp1 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.484-3595_484-3586d others(12): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97683045 | |||||
| chr8:97683045
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0001g0092 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.484-3597_484-3586d others(14): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97683045 | |||||
| chr8:97683045
|
C | CTTTTTTT others(7): Show |
3 | a0001c0001t0001g0042a0001c0001t0001g0063a0001c0001t0001g0089 | 3 | NA18968.hp2 NA18977.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.484-3599_484-3586d others(16): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97683045 | |||||
| chr8:97683045
|
C | CTTTTTTT others(14): Show |
1 | a0001c0001t0045g0105 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.484-3606_484-3586d others(23): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97683045 | |||||
| chr8:97683045
|
CT | C | 29 | a0001c0001t0002g0257a0001c0001t0002g0297a0001c0001t0002g0343others(26): Show | 29 | HG01070.hp1 HG01074.hp1 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.484-3586delT | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97683045 | |||||
| chr8:97683045
|
CTT | C | 15 | a0001c0001t0004g0267a0001c0001t0004g0308a0001c0001t0004g0323others(12): Show | 15 | HG00408.hp2 HG00673.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.484-3587_484-3586d others(4): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97683045 | |||||
| chr8:97683045
|
CTTTT | C | 15 | a0001c0001t0008g0160a0001c0001t0009g0052a0001c0001t0013g0259others(12): Show | 15 | HG00733.hp2 HG01243.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.484-3589_484-3586d others(6): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97683045 | |||||
| chr8:97683045
|
CTTTTT | C | 14 | a0001c0001t0006g0183a0001c0001t0006g0184a0001c0001t0006g0188others(11): Show | 14 | HG00673.hp1 HG01081.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.484-3590_484-3586d others(7): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97683045 | |||||
| chr8:97683045
|
CTTTTTT | C | 22 | a0001c0001t0006g0180a0001c0001t0006g0182a0001c0001t0006g0185others(19): Show | 22 | HG02280.hp2 HG02717.hp2 HG02897.hp2 others(19): Show |
intron_variant | MODIFIER | c.484-3591_484-3586d others(8): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97683045 | |||||
| chr8:97683045
|
CTTTTTTT others(1): Show |
C | 10 | a0001c0001t0001g0024a0001c0001t0001g0036a0001c0001t0001g0055others(7): Show | 10 | HG00423.hp1 HG02970.hp1 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.484-3593_484-3586d others(10): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97683045 | |||||
| chr8:97683045
|
CTTTTTTT others(2): Show |
C | 20 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0070others(17): Show | 20 | HG00733.hp1 HG00738.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.484-3594_484-3586d others(11): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97683045 | |||||
| chr8:97683045
|
CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0001g0106a0001c0001t0002g0140 | 2 | HG01255.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.484-3597_484-3586d others(14): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97683045 | |||||
| chr8:97683045
|
CTTTTTTT others(7): Show |
C | 4 | a0001c0001t0022g0192a0001c0005t0022g0193a0001c0005t0022g0195others(1): Show | 4 | HG02145.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.484-3599_484-3586d others(16): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97683045 | |||||
| chr8:97683045
|
CTTTTTTT others(8): Show |
C | 1 | a0007c0011t0070g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.484-3600_484-3586d others(17): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97683045 | |||||
| chr8:97683045
|
CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0002g0293 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.484-3601_484-3586d others(18): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97683045 | |||||
| chr8:97683045
|
CTTTTTTT others(11): Show |
C | 1 | a0001c0002t0003g0216 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.484-3603_484-3586d others(20): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97683045 | |||||
| chr8:97683045
|
CTTTTTTT others(13): Show |
C | 1 | a0001c0001t0001g0022 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.484-3605_484-3586d others(22): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97683045 | |||||
| chr8:97683045
|
CTTTTTTT others(14): Show |
C | 1 | a0001c0001t0032g0030 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.484-3606_484-3586d others(23): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97683045 | |||||
| chr8:97683045
|
CTTTTTTT others(17): Show |
C | 1 | a0001c0001t0002g0302 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.484-3609_484-3586d others(26): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97683045 | |||||
| chr8:97683103
|
C | T | 1 | a0001c0002t0003g0228 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.484-3565C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97683103 | ||||||
| chr8:97683167
|
C | T | 1 | a0001c0001t0056g0111 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.484-3501C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97683167 | ||||||
| chr8:97683189
|
C | T | 1 | a0001c0001t0066g0357 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.484-3479C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97683189 | ||||||
| chr8:97683226
|
G | C | 8 | a0001c0001t0013g0259a0001c0001t0039g0126a0001c0001t0040g0258others(5): Show | 8 | HG00733.hp2 HG01243.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.484-3442G>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97683226 | ||||||
| chr8:97683343
|
G | A | 2 | a0001c0005t0022g0195a0001c0005t0085g0194 | 2 | HG02145.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.484-3325G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97683343 | ||||||
| chr8:97683354
|
C | T | 1 | a0003c0004t0049g0249 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.484-3314C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97683354 | ||||||
| chr8:97683420
|
G | A | 1 | a0001c0001t0006g0187 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.484-3248G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97683420 | ||||||
| chr8:97683424
|
C | T | 12 | a0001c0001t0006g0180a0001c0001t0006g0182a0001c0001t0006g0183others(9): Show | 12 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.484-3244C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97683424 | ||||||
| chr8:97683533
|
C | T | 1 | a0001c0001t0025g0365 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.484-3135C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97683533 | ||||||
| chr8:97683569
|
T | C | 1 | a0001c0001t0032g0030 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.484-3099T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97683569 | ||||||
| chr8:97683622
|
G | C | 1 | a0001c0001t0001g0067 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.484-3046G>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97683622 | ||||||
| chr8:97683672
|
G | T | 35 | a0001c0001t0002g0358a0001c0001t0004g0267a0001c0001t0004g0278others(32): Show | 35 | HG00408.hp2 HG00642.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.484-2996G>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97683672 | ||||||
| chr8:97683878
|
G | A | 1 | a0001c0001t0012g0002 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.484-2790G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97683878 | ||||||
| chr8:97683901
|
T | C | 252 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(249): Show | 252 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(249): Show |
intron_variant | MODIFIER | c.484-2767T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97683901 | ||||||
| chr8:97683979
|
C | T | 1 | a0001c0002t0003g0222 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.484-2689C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97683979 | ||||||
| chr8:97684026
|
G | A | 28 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0006others(25): Show | 28 | HG00733.hp1 HG00738.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.484-2642G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97684026 | ||||||
| chr8:97684078
|
G | A | 1 | a0001c0001t0002g0350 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.484-2590G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97684078 | ||||||
| chr8:97684089
|
A | G | 1 | a0001c0001t0001g0054 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.484-2579A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97684089 | ||||||
| chr8:97684139
|
C | CA | 24 | a0001c0001t0001g0025a0001c0001t0001g0064a0001c0001t0002g0363others(21): Show | 24 | HG00741.hp1 HG01168.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.484-2513dupA | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97684139 | |||||
| chr8:97684149
|
A | C | 1 | a0001c0002t0003g0209 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.484-2519A>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97684149 | ||||||
| chr8:97684420
|
ACT | A | 7 | a0003c0004t0015g0244a0003c0004t0015g0245a0003c0004t0015g0250others(4): Show | 7 | HG00741.hp1 HG01168.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.484-2245_484-2244d others(4): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr8 | 97684420 | |||||
| chr8:97684677
|
A | G | 2 | a0001c0001t0004g0335a0001c0001t0004g0336 | 2 | HG01070.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.484-1991A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97684677 | ||||||
| chr8:97684840
|
C | T | 1 | a0001c0001t0002g0289 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.484-1828C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97684840 | ||||||
| chr8:97684877
|
C | A | 3 | a0001c0005t0022g0193a0001c0005t0022g0195a0001c0005t0085g0194 | 3 | HG02145.hp2 HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.484-1791C>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97684877 | ||||||
| chr8:97684993
|
G | C | 99 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(96): Show | 99 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.484-1675G>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97684993 | ||||||
| chr8:97685074
|
C | A | 1 | a0004c0008t0002g0001 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.484-1594C>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97685074 | ||||||
| chr8:97685075
|
C | T | 2 | a0001c0001t0014g0367a0001c0001t0014g0369 | 2 | NA18973.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.484-1593C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97685075 | ||||||
| chr8:97685193
|
T | A | 1 | a0001c0001t0005g0117 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.484-1475T>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97685193 | ||||||
| chr8:97685241
|
ATT | A | 7 | a0001c0001t0009g0018a0001c0001t0009g0050a0001c0001t0009g0052others(4): Show | 7 | HG00597.hp2 NA18940.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.484-1426_484-1425d others(4): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97685241 | ||||||
| chr8:97685853
|
T | C | 21 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0006others(18): Show | 21 | HG00733.hp1 HG00738.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.484-815T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97685853 | ||||||
| chr8:97685921
|
G | A | 7 | a0003c0004t0015g0244a0003c0004t0015g0245a0003c0004t0015g0250others(4): Show | 7 | HG00741.hp1 HG01168.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.484-747G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97685921 | ||||||
| chr8:97686025
|
T | C | 13 | a0001c0001t0008g0155a0001c0001t0008g0156a0001c0001t0008g0157others(10): Show | 13 | HG01081.hp2 HG02258.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.484-643T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97686025 | ||||||
| chr8:97686156
|
C | T | 7 | a0003c0004t0015g0244a0003c0004t0015g0245a0003c0004t0015g0250others(4): Show | 7 | HG00741.hp1 HG01168.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.484-512C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97686156 | ||||||
| chr8:97686208
|
T | A | 7 | a0001c0002t0003g0231a0001c0002t0003g0234a0001c0002t0003g0235others(4): Show | 7 | HG02027.hp1 HG02155.hp2 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.484-460T>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97686208 | ||||||
| chr8:97686282
|
G | A | 1 | a0001c0001t0056g0111 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.484-386G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 2/11 | chr8 | 97686282 | ||||||
| chr8:97686962
|
AT | A | 122 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0175others(119): Show | 122 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.568+213delT | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr8 | 97686962 | |||||
| chr8:97687059
|
T | C | 15 | a0001c0001t0013g0259a0001c0001t0018g0132a0001c0001t0018g0133others(12): Show | 15 | HG00733.hp2 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.568+307T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 3/11 | chr8 | 97687059 | ||||||
| chr8:97687270
|
A | G | 1 | a0001c0001t0002g0344 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.569-159A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 3/11 | chr8 | 97687270 | ||||||
| chr8:97687343
|
G | A | 1 | a0001c0001t0006g0191 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.569-86G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 3/11 | chr8 | 97687343 | ||||||
| chr8:97687673
|
T | C | 1 | a0001c0001t0034g0118 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.745+68T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 4/11 | chr8 | 97687673 | ||||||
| chr8:97687792
|
C | T | 1 | a0001c0001t0002g0296 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.745+187C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 4/11 | chr8 | 97687792 | ||||||
| chr8:97687840
|
T | C | 1 | a0001c0001t0004g0284 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.745+235T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 4/11 | chr8 | 97687840 | ||||||
| chr8:97688003
|
T | C | 12 | a0001c0001t0006g0180a0001c0001t0006g0182a0001c0001t0006g0183others(9): Show | 12 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.745+398T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 4/11 | chr8 | 97688003 | ||||||
| chr8:97688135
|
T | G | 1 | a0001c0001t0001g0027 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.745+530T>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 4/11 | chr8 | 97688135 | ||||||
| chr8:97688138
|
G | C | 7 | a0001c0001t0002g0268a0001c0001t0002g0269a0001c0001t0002g0270others(4): Show | 7 | HG00544.hp2 NA18942.hp2 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.745+533G>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 4/11 | chr8 | 97688138 | ||||||
| chr8:97688282
|
A | C | 8 | a0001c0001t0013g0259a0001c0001t0039g0126a0001c0001t0040g0258others(5): Show | 8 | HG00733.hp2 HG01243.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.745+677A>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 4/11 | chr8 | 97688282 | ||||||
| chr8:97688367
|
G | A | 3 | a0001c0001t0002g0263a0001c0001t0002g0264a0001c0001t0002g0265 | 3 | HG01192.hp1 HG01981.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.746-671G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 4/11 | chr8 | 97688367 | ||||||
| chr8:97688577
|
T | C | 1 | a0001c0001t0004g0283 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.746-461T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 4/11 | chr8 | 97688577 | ||||||
| chr8:97688649
|
T | C | 1 | a0001c0001t0003g0179 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.746-389T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 4/11 | chr8 | 97688649 | ||||||
| chr8:97688681
|
C | T | 1 | a0001c0001t0003g0179 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.746-357C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 4/11 | chr8 | 97688681 | ||||||
| chr8:97688715
|
A | G | 1 | a0001c0002t0007g0219 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.746-323A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 4/11 | chr8 | 97688715 | ||||||
| chr8:97688862
|
C | T | 1 | a0001c0002t0007g0232 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.746-176C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 4/11 | chr8 | 97688862 | ||||||
| chr8:97689290
|
C | A | 1 | a0001c0001t0006g0190 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.811+187C>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 5/11 | chr8 | 97689290 | ||||||
| chr8:97689297
|
C | T | 5 | a0001c0002t0003g0212a0001c0002t0003g0213a0001c0002t0003g0214others(2): Show | 5 | HG00621.hp2 HG00735.hp1 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.811+194C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 5/11 | chr8 | 97689297 | ||||||
| chr8:97689464
|
T | TA | 19 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0002g0352others(16): Show | 19 | HG01081.hp2 HG01891.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.811+374dupA | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr8 | 97689464 | |||||
| chr8:97689464
|
T | TAA | 62 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0175others(59): Show | 62 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.811+373_811+374dup others(2): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr8 | 97689464 | |||||
| chr8:97689690
|
C | T | 1 | a0001c0001t0034g0118 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.811+587C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 5/11 | chr8 | 97689690 | ||||||
| chr8:97689700
|
C | A | 1 | a0001c0001t0002g0347 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.811+597C>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 5/11 | chr8 | 97689700 | ||||||
| chr8:97689705
|
C | CT | 7 | a0001c0001t0002g0320a0001c0001t0002g0347a0001c0001t0004g0274others(4): Show | 7 | HG01243.hp1 HG01891.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.811+619dupT | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr8 | 97689705 | |||||
| chr8:97689705
|
CT | C | 238 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(235): Show | 238 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(235): Show |
intron_variant | MODIFIER | c.811+619delT | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr8 | 97689705 | |||||
| chr8:97689722
|
T | G | 2 | a0001c0001t0004g0137a0001c0001t0004g0138 | 2 | HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.811+619T>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 5/11 | chr8 | 97689722 | ||||||
| chr8:97689744
|
G | A | 1 | a0001c0001t0033g0342 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.811+641G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 5/11 | chr8 | 97689744 | ||||||
| chr8:97689995
|
CT | C | 221 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(218): Show | 221 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(218): Show |
intron_variant | MODIFIER | c.811+909delT | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr8 | 97689995 | |||||
| chr8:97690080
|
C | T | 2 | a0001c0001t0001g0072a0001c0001t0002g0352 | 2 | HG03669.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.812-872C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 5/11 | chr8 | 97690080 | ||||||
| chr8:97690090
|
G | A | 1 | a0001c0001t0003g0179 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.812-862G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 5/11 | chr8 | 97690090 | ||||||
| chr8:97690148
|
C | T | 1 | a0001c0001t0002g0344 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.812-804C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 5/11 | chr8 | 97690148 | ||||||
| chr8:97690324
|
A | C | 99 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(96): Show | 99 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.812-628A>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 5/11 | chr8 | 97690324 | ||||||
| chr8:97690365
|
A | G | 4 | a0001c0001t0022g0192a0001c0005t0022g0193a0001c0005t0022g0195others(1): Show | 4 | HG02145.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.812-587A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 5/11 | chr8 | 97690365 | ||||||
| chr8:97690390
|
A | G | 2 | a0001c0001t0001g0069a0001c0001t0026g0083 | 2 | NA19011.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.812-562A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 5/11 | chr8 | 97690390 | ||||||
| chr8:97690535
|
T | G | 1 | a0001c0002t0003g0241 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.812-417T>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 5/11 | chr8 | 97690535 | ||||||
| chr8:97690643
|
A | ATAAT | 225 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(222): Show | 225 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(222): Show |
intron_variant | MODIFIER | c.812-306_812-305ins others(4): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr8 | 97690643 | |||||
| chr8:97691237
|
T | A | 1 | a0001c0001t0002g0312 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1048+49T>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97691237 | ||||||
| chr8:97691267
|
AAAAC | A | 12 | a0001c0001t0008g0155a0001c0001t0008g0156a0001c0001t0008g0157others(9): Show | 12 | HG01081.hp2 HG02258.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1048+80_1048+83del others(4): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97691267 | ||||||
| chr8:97691319
|
T | G | 99 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(96): Show | 99 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.1048+131T>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97691319 | ||||||
| chr8:97691362
|
A | G | 6 | a0001c0002t0007g0198a0001c0002t0007g0199a0001c0002t0007g0200others(3): Show | 6 | HG01496.hp2 HG01934.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.1048+174A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97691362 | ||||||
| chr8:97691615
|
G | A | 5 | a0001c0001t0002g0292a0001c0001t0002g0296a0001c0001t0002g0313others(2): Show | 5 | HG00741.hp2 HG01099.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.1048+427G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97691615 | ||||||
| chr8:97691703
|
T | TTG | 63 | a0001c0001t0001g0088a0001c0001t0002g0358a0001c0001t0004g0267others(60): Show | 63 | HG00408.hp2 HG00621.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.1048+533_1048+534d others(4): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97691703 | |||||
| chr8:97691850
|
G | A | 2 | a0001c0001t0006g0183a0001c0001t0006g0184 | 2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1048+662G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97691850 | ||||||
| chr8:97691869
|
GT | G | 13 | a0001c0001t0013g0259a0001c0001t0018g0132a0001c0001t0018g0133others(10): Show | 13 | HG00733.hp2 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1048+687delT | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97691869 | |||||
| chr8:97691946
|
C | T | 4 | a0001c0002t0007g0198a0001c0002t0007g0217a0001c0002t0030g0218others(1): Show | 4 | HG01496.hp2 HG01934.hp1 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.1048+758C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97691946 | ||||||
| chr8:97691973
|
G | A | 2 | a0001c0002t0003g0253a0001c0002t0003g0254 | 2 | HG03834.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1048+785G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97691973 | ||||||
| chr8:97692041
|
T | G | 11 | a0001c0001t0001g0032a0001c0001t0001g0043a0001c0001t0001g0066others(8): Show | 11 | NA18946.hp2 NA18951.hp2 NA18953.hp2 others(8): Show |
intron_variant | MODIFIER | c.1048+853T>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97692041 | ||||||
| chr8:97692055
|
A | G | 2 | a0001c0001t0051g0251a0001c0001t0052g0252 | 2 | HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1048+867A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97692055 | ||||||
| chr8:97692099
|
G | A | 1 | a0001c0001t0086g0166 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1048+911G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97692099 | ||||||
| chr8:97692112
|
C | T | 1 | a0001c0001t0021g0168 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1048+924C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97692112 | ||||||
| chr8:97692146
|
G | A | 3 | a0001c0001t0004g0339a0001c0001t0004g0340a0001c0001t0010g0290 | 3 | NA18940.hp1 NA18975.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1048+958G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97692146 | ||||||
| chr8:97692188
|
TTTGC | T | 12 | a0001c0001t0008g0155a0001c0001t0008g0156a0001c0001t0008g0157others(9): Show | 12 | HG01081.hp2 HG02258.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1048+1003_1048+100 others(8): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97692188 | |||||
| chr8:97692378
|
C | CT | 21 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0006others(18): Show | 21 | HG00733.hp1 HG00738.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1048+1200dupT | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97692378 | |||||
| chr8:97692410
|
G | A | 21 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0006others(18): Show | 21 | HG00733.hp1 HG00738.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1048+1222G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97692410 | ||||||
| chr8:97692542
|
AT | A | 12 | a0001c0001t0006g0180a0001c0001t0006g0182a0001c0001t0006g0183others(9): Show | 12 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1048+1361delT | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97692542 | |||||
| chr8:97692567
|
G | A | 1 | a0001c0001t0009g0052 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1048+1379G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97692567 | ||||||
| chr8:97692663
|
C | T | 2 | a0001c0001t0004g0305a0001c0001t0004g0325 | 2 | NA18961.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1048+1475C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97692663 | ||||||
| chr8:97693142
|
AGTT | A | 3 | a0001c0001t0019g0108a0001c0001t0019g0109a0001c0001t0019g0110 | 3 | HG02622.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1048+1958_1048+196 others(7): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97693142 | |||||
| chr8:97693165
|
G | A | 1 | a0001c0001t0008g0157 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1048+1977G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97693165 | ||||||
| chr8:97693205
|
T | A | 1 | a0001c0001t0029g0150 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1048+2017T>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97693205 | ||||||
| chr8:97693254
|
G | A | 1 | a0001c0002t0003g0222 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1048+2066G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97693254 | ||||||
| chr8:97693287
|
G | A | 100 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(97): Show | 100 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.1048+2099G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97693287 | ||||||
| chr8:97693399
|
T | A | 1 | a0001c0001t0016g0119 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1048+2211T>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97693399 | ||||||
| chr8:97693475
|
A | G | 107 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0175others(104): Show | 107 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.1048+2287A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97693475 | ||||||
| chr8:97693773
|
T | C | 107 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0175others(104): Show | 107 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.1048+2585T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97693773 | ||||||
| chr8:97693988
|
T | C | 1 | a0001c0001t0004g0136 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1048+2800T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97693988 | ||||||
| chr8:97694114
|
A | T | 1 | a0001c0001t0002g0350 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1048+2926A>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97694114 | ||||||
| chr8:97694195
|
T | C | 77 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0175others(74): Show | 77 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.1048+3007T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97694195 | ||||||
| chr8:97694200
|
C | CT | 13 | a0001c0001t0001g0022a0001c0001t0006g0180a0001c0001t0006g0182others(10): Show | 13 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1048+3026dupT | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97694200 | |||||
| chr8:97694217
|
G | A | 66 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0175others(63): Show | 66 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.1048+3029G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97694217 | ||||||
| chr8:97694340
|
G | A | 2 | a0001c0001t0019g0108a0001c0001t0019g0110 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1048+3152G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97694340 | ||||||
| chr8:97694358
|
T | C | 1 | a0001c0001t0004g0305 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1048+3170T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97694358 | ||||||
| chr8:97694405
|
C | T | 1 | a0001c0001t0038g0023 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1048+3217C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97694405 | ||||||
| chr8:97694474
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1048+3286C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97694474 | ||||||
| chr8:97694796
|
G | A | 1 | a0001c0001t0056g0111 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1048+3608G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97694796 | ||||||
| chr8:97694857
|
A | T | 1 | a0001c0001t0034g0118 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1048+3669A>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97694857 | ||||||
| chr8:97695189
|
A | G | 1 | a0001c0001t0076g0174 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1048+4001A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97695189 | ||||||
| chr8:97695234
|
C | G | 2 | a0001c0001t0004g0137a0001c0001t0004g0138 | 2 | HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1048+4046C>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97695234 | ||||||
| chr8:97695347
|
C | G | 8 | a0001c0001t0005g0005a0001c0001t0005g0008a0001c0001t0012g0002others(5): Show | 8 | HG02055.hp2 HG02559.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1048+4159C>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97695347 | ||||||
| chr8:97695404
|
G | C | 1 | a0001c0001t0030g0169 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1048+4216G>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97695404 | ||||||
| chr8:97695722
|
T | C | 1 | a0001c0001t0034g0118 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1049-4032T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97695722 | ||||||
| chr8:97695804
|
T | C | 21 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0006others(18): Show | 21 | HG00733.hp1 HG00738.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1049-3950T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97695804 | ||||||
| chr8:97695984
|
T | C | 12 | a0001c0001t0008g0155a0001c0001t0008g0156a0001c0001t0008g0157others(9): Show | 12 | HG01081.hp2 HG02258.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1049-3770T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97695984 | ||||||
| chr8:97696112
|
A | G | 7 | a0003c0004t0015g0244a0003c0004t0015g0245a0003c0004t0015g0250others(4): Show | 7 | HG00741.hp1 HG01168.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.1049-3642A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97696112 | ||||||
| chr8:97696187
|
G | C | 122 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0175others(119): Show | 122 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.1049-3567G>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97696187 | ||||||
| chr8:97696392
|
A | G | 1 | a0007c0011t0070g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1049-3362A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97696392 | ||||||
| chr8:97696562
|
C | T | 7 | a0001c0001t0016g0119a0001c0001t0016g0121a0001c0001t0016g0122others(4): Show | 7 | HG02055.hp1 HG02451.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1049-3192C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97696562 | ||||||
| chr8:97696577
|
T | C | 1 | a0001c0001t0037g0131 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1049-3177T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97696577 | ||||||
| chr8:97696702
|
A | T | 1 | a0001c0001t0065g0167 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1049-3052A>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97696702 | ||||||
| chr8:97696793
|
A | G | 66 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0175others(63): Show | 66 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.1049-2961A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97696793 | ||||||
| chr8:97696873
|
G | A | 1 | a0001c0001t0002g0331 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1049-2881G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97696873 | ||||||
| chr8:97696972
|
A | G | 1 | a0001c0001t0031g0177 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1049-2782A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97696972 | ||||||
| chr8:97697111
|
CTGTCTCA others(41): Show |
C | 1 | a0001c0001t0011g0148 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1049-2639_1049-259 others(52): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697111 | |||||
| chr8:97697119
|
C | CAAAAAAA | 10 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0008others(7): Show | 10 | HG00733.hp1 HG00738.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1049-2630_1049-262 others(11): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697119 | |||||
| chr8:97697119
|
C | CAAAAAAA others(3): Show |
3 | a0001c0001t0005g0112a0001c0001t0005g0117a0001c0001t0042g0114 | 3 | HG01891.hp2 HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1049-2633_1049-262 others(14): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697119 | |||||
| chr8:97697119
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0005g0113 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1049-2634_1049-262 others(15): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697119 | |||||
| chr8:97697119
|
C | CAAAAAAA others(5): Show |
2 | a0001c0001t0005g0115a0001c0001t0005g0116 | 2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(16): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697119 | |||||
| chr8:97697119
|
C | CAAAAAAA others(7): Show |
6 | a0001c0001t0011g0141a0001c0001t0011g0144a0001c0001t0011g0146others(3): Show | 6 | NA18941.hp1 NA18974.hp1 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(18): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697119 | |||||
| chr8:97697119
|
C | CAAAAAAA others(8): Show |
4 | a0001c0001t0011g0143a0001c0001t0019g0108a0001c0001t0019g0110others(1): Show | 4 | HG01168.hp1 HG02622.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(19): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697119 | |||||
| chr8:97697119
|
C | CAAAAAAA others(9): Show |
5 | a0001c0001t0001g0076a0001c0001t0008g0159a0001c0001t0029g0150others(2): Show | 5 | HG02258.hp2 HG03516.hp1 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(20): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697119 | |||||
| chr8:97697119
|
C | CAAAAAAA others(10): Show |
5 | a0001c0001t0008g0155a0001c0001t0008g0161a0001c0001t0008g0162others(2): Show | 5 | HG01081.hp2 HG02976.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(21): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697119 | |||||
| chr8:97697119
|
C | CAAAAAAA others(11): Show |
7 | a0001c0001t0001g0036a0001c0001t0001g0070a0001c0001t0001g0071others(4): Show | 7 | HG03195.hp2 NA18983.hp1 NA18989.hp2 others(4): Show |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(22): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697119 | |||||
| chr8:97697119
|
C | CAAAAAAA others(12): Show |
5 | a0001c0001t0001g0017a0001c0001t0001g0078a0001c0001t0001g0079others(2): Show | 5 | HG00423.hp1 HG03471.hp1 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(23): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697119 | |||||
| chr8:97697129
|
A | AAAAAAAA others(44): Show |
1 | a0001c0001t0051g0251 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1049-2624_1049-262 others(55): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(45): Show |
1 | a0001c0001t0052g0252 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1049-2624_1049-262 others(56): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(19): Show |
2 | a0001c0001t0056g0111a0001c0001t0083g0370 | 2 | HG01516.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(30): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(23): Show |
1 | a0001c0001t0044g0082 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1049-2624_1049-262 others(34): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(27): Show |
1 | a0001c0001t0046g0028 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1049-2624_1049-262 others(38): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(29): Show |
1 | a0001c0001t0001g0024 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1049-2624_1049-262 others(40): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(18): Show |
1 | a0001c0001t0001g0106 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1049-2624_1049-262 others(29): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(20): Show |
1 | a0001c0001t0003g0173 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1049-2624_1049-262 others(31): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(24): Show |
2 | a0001c0001t0001g0055a0001c0001t0001g0067 | 2 | NA18612.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(35): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(28): Show |
1 | a0001c0001t0001g0049 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1049-2624_1049-262 others(39): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(30): Show |
1 | a0001c0001t0009g0050 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1049-2624_1049-262 others(41): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(32): Show |
2 | a0001c0001t0001g0059a0001c0001t0026g0083 | 2 | HG00544.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(43): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(19): Show |
1 | a0001c0001t0030g0169 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1049-2624_1049-262 others(30): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(23): Show |
6 | a0001c0001t0001g0026a0001c0001t0001g0053a0001c0001t0001g0054others(3): Show | 6 | HG00639.hp2 HG01192.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(34): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(25): Show |
1 | a0001c0001t0001g0025 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1049-2624_1049-262 others(36): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(27): Show |
3 | a0001c0001t0001g0100a0001c0001t0020g0074a0001c0001t0043g0040 | 3 | HG00597.hp2 HG02129.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(38): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(29): Show |
3 | a0001c0001t0001g0107a0001c0001t0009g0052a0005c0010t0092g0247 | 3 | HG00741.hp1 HG02895.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(40): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(31): Show |
2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | NA18971.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(42): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(33): Show |
1 | a0003c0004t0049g0249 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1049-2624_1049-262 others(44): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(37): Show |
1 | a0003c0004t0015g0250 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1049-2624_1049-262 others(48): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(18): Show |
4 | a0001c0001t0003g0175a0001c0001t0003g0179a0001c0001t0007g0170others(1): Show | 4 | HG03710.hp1 HG04204.hp1 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(29): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(20): Show |
4 | a0001c0001t0019g0109a0001c0001t0076g0174a0001c0001t0079g0152others(1): Show | 4 | HG00735.hp2 HG01099.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(31): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(22): Show |
2 | a0001c0001t0032g0093a0001c0001t0093g0031 | 2 | HG01978.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(33): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(24): Show |
3 | a0001c0001t0001g0057a0001c0001t0036g0085a0001c0002t0074g0211 | 3 | HG01109.hp1 NA18998.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(35): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(26): Show |
7 | a0001c0001t0001g0045a0001c0001t0001g0088a0001c0001t0001g0097others(4): Show | 7 | HG00621.hp1 HG01516.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(37): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(28): Show |
2 | a0001c0001t0001g0090a0001c0001t0020g0021 | 2 | HG00140.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(39): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(15): Show |
2 | a0001c0001t0001g0022a0001c0001t0021g0168 | 2 | HG02886.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(26): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(17): Show |
1 | a0001c0001t0001g0063 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1049-2624_1049-262 others(28): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(19): Show |
1 | a0001c0007t0003g0153 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1049-2624_1049-262 others(30): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(21): Show |
3 | a0001c0001t0001g0062a0001c0002t0007g0200a0001c0002t0030g0218 | 3 | HG01358.hp1 HG01934.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(32): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(23): Show |
3 | a0001c0001t0001g0065a0001c0001t0001g0089a0001c0001t0026g0098 | 3 | NA18949.hp2 NA18968.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(34): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(25): Show |
10 | a0001c0001t0001g0020a0001c0001t0001g0035a0001c0001t0001g0048others(7): Show | 10 | HG00642.hp1 HG02165.hp1 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(36): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(27): Show |
3 | a0001c0001t0001g0060a0001c0001t0001g0092a0003c0004t0015g0244 | 3 | HG03688.hp2 NA18942.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(38): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(29): Show |
6 | a0001c0001t0001g0027a0001c0001t0001g0034a0001c0001t0001g0041others(3): Show | 6 | HG01952.hp2 NA18940.hp2 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(40): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(31): Show |
2 | a0001c0001t0001g0075a0001c0001t0020g0047 | 2 | HG00558.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(42): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(16): Show |
1 | a0001c0001t0065g0167 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1049-2624_1049-262 others(27): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(18): Show |
2 | a0001c0001t0001g0042a0001c0007t0003g0154 | 2 | HG03540.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(29): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(20): Show |
8 | a0001c0001t0031g0177a0001c0001t0032g0030a0001c0002t0003g0204others(5): Show | 8 | HG00423.hp2 HG01496.hp2 HG02148.hp1 others(5): Show |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(31): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(22): Show |
2 | a0001c0001t0031g0178a0001c0002t0003g0206 | 2 | HG02896.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(33): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(24): Show |
1 | a0001c0001t0001g0087 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1049-2624_1049-262 others(35): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(26): Show |
5 | a0001c0001t0001g0046a0001c0001t0001g0099a0001c0001t0017g0037others(2): Show | 5 | HG02273.hp2 NA18952.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(37): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(38): Show |
2 | a0001c0001t0045g0105a0003c0004t0015g0245 | 2 | HG01081.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(49): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(11): Show |
3 | a0001c0001t0013g0259a0001c0001t0040g0258a0002c0003t0013g0128 | 3 | HG00733.hp2 HG01243.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(22): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(13): Show |
1 | a0001c0001t0037g0131 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1049-2624_1049-262 others(24): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(21): Show |
3 | a0001c0002t0003g0213a0001c0002t0003g0227a0001c0002t0003g0237 | 3 | HG02004.hp1 NA18992.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(32): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(23): Show |
1 | a0001c0001t0034g0118 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1049-2624_1049-262 others(34): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(25): Show |
3 | a0001c0001t0001g0032a0001c0002t0003g0241a0001c0002t0007g0232 | 3 | HG00609.hp2 HG02027.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(36): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(27): Show |
3 | a0001c0001t0001g0073a0001c0001t0048g0080a0001c0002t0003g0220 | 3 | HG00558.hp2 NA18939.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(38): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(29): Show |
3 | a0001c0001t0001g0033a0001c0001t0001g0103a0008c0012t0015g0246 | 3 | HG01123.hp1 HG01258.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(40): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(28): Show |
1 | a0001c0001t0009g0018 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1049-2624_1049-262 others(39): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(12): Show |
3 | a0002c0003t0013g0127a0002c0003t0013g0129a0002c0003t0013g0130 | 3 | HG02895.hp1 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(23): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(16): Show |
2 | a0001c0001t0003g0255a0001c0001t0018g0135 | 2 | HG01167.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(27): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(18): Show |
1 | a0001c0002t0003g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1049-2624_1049-262 others(29): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(20): Show |
7 | a0001c0002t0003g0201a0001c0002t0003g0202a0001c0002t0003g0203others(4): Show | 7 | HG00408.hp1 HG00621.hp2 HG00735.hp1 others(4): Show |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(31): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(22): Show |
3 | a0001c0002t0003g0231a0001c0002t0003g0239a0001c0002t0078g0215 | 3 | HG02683.hp2 NA19000.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(33): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(24): Show |
3 | a0001c0001t0088g0019a0001c0002t0003g0209a0001c0002t0003g0230 | 3 | NA18946.hp2 NA18990.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(35): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(9): Show |
2 | a0001c0001t0023g0158a0001c0001t0023g0165 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(20): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(27): Show |
2 | a0001c0001t0009g0084a0001c0001t0009g0086 | 2 | NA18945.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(38): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(11): Show |
1 | a0002c0003t0035g0125 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1049-2624_1049-262 others(22): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(13): Show |
2 | a0001c0001t0018g0132a0001c0001t0018g0133 | 2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(24): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(21): Show |
6 | a0001c0002t0003g0225a0001c0002t0003g0234a0001c0002t0003g0235others(3): Show | 6 | HG02155.hp2 HG03654.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(32): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(8): Show |
2 | a0001c0001t0008g0160a0001c0001t0023g0164 | 2 | HG02559.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(19): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(14): Show |
1 | a0001c0001t0041g0134 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1049-2624_1049-262 others(25): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(18): Show |
1 | a0001c0002t0003g0228 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1049-2624_1049-262 others(29): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(20): Show |
2 | a0001c0002t0003g0214a0001c0002t0003g0216 | 2 | HG02132.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(31): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(24): Show |
1 | a0001c0002t0003g0238 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1049-2624_1049-262 others(35): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(26): Show |
1 | a0001c0002t0082g0223 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1049-2624_1049-262 others(37): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(28): Show |
1 | a0001c0002t0077g0221 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1049-2624_1049-262 others(39): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(11): Show |
2 | a0001c0002t0090g0224a0001c0005t0022g0193 | 2 | HG02647.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(22): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(10): Show |
2 | a0001c0005t0022g0195a0001c0005t0085g0194 | 2 | HG02145.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(21): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(12): Show |
2 | a0001c0002t0081g0242a0001c0002t0089g0197 | 2 | NA18957.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(23): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(18): Show |
1 | a0001c0002t0003g0208 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1049-2624_1049-262 others(29): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(24): Show |
1 | a0001c0002t0021g0240 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1049-2624_1049-262 others(35): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(26): Show |
1 | a0001c0002t0080g0205 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1049-2624_1049-262 others(37): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(11): Show |
1 | a0001c0001t0022g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1049-2624_1049-262 others(22): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(7): Show |
2 | a0001c0001t0005g0004a0001c0001t0005g0176 | 2 | NA19240.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(18): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(6): Show |
1 | a0001c0001t0016g0123 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1049-2624_1049-262 others(17): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(8): Show |
1 | a0001c0001t0016g0119 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1049-2624_1049-262 others(19): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(10): Show |
1 | a0001c0001t0057g0124 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1049-2624_1049-262 others(21): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAA others(12): Show |
3 | a0001c0001t0016g0121a0001c0001t0016g0122a0001c0001t0039g0126 | 3 | HG02615.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(23): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | AAAAAAAT others(10): Show |
1 | a0001c0001t0058g0120 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1049-2624_1049-262 others(21): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697129 | |||||
| chr8:97697129
|
A | T | 4 | a0001c0001t0002g0333a0001c0001t0004g0274a0001c0001t0004g0335others(1): Show | 4 | HG00639.hp1 HG01070.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.1049-2625A>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97697129 | ||||||
| chr8:97697130
|
A | AAAAAAAA others(20): Show |
2 | a0001c0002t0003g0253a0001c0002t0003g0254 | 2 | HG03834.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1049-2624_1049-262 others(31): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97697130 | ||||||
| chr8:97697131
|
T | A | 23 | a0001c0001t0002g0140a0001c0001t0002g0268a0001c0001t0002g0269others(20): Show | 23 | HG00544.hp2 HG01255.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1049-2623T>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97697131 | ||||||
| chr8:97697133
|
T | A | 11 | a0001c0001t0006g0182a0001c0001t0006g0183a0001c0001t0006g0184others(8): Show | 11 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1049-2621T>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97697133 | ||||||
| chr8:97697135
|
T | A | 11 | a0001c0001t0006g0182a0001c0001t0006g0183a0001c0001t0006g0184others(8): Show | 11 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1049-2619T>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97697135 | ||||||
| chr8:97697137
|
T | A | 10 | a0001c0001t0006g0182a0001c0001t0006g0183a0001c0001t0006g0184others(7): Show | 10 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1049-2617T>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97697137 | ||||||
| chr8:97697139
|
T | A | 9 | a0001c0001t0006g0182a0001c0001t0006g0183a0001c0001t0006g0184others(6): Show | 9 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1049-2615T>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97697139 | ||||||
| chr8:97697142
|
A | ATTTTTTT others(1): Show |
7 | a0001c0001t0001g0036a0001c0001t0001g0070a0001c0001t0001g0071others(4): Show | 7 | HG00423.hp1 NA18983.hp1 NA18989.hp2 others(4): Show |
intron_variant | MODIFIER | c.1049-2611_1049-261 others(12): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697142 | |||||
| chr8:97697144
|
A | ATTTTTTT others(3): Show |
1 | a0001c0001t0001g0076 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1049-2609_1049-260 others(14): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697144 | |||||
| chr8:97697144
|
A | T | 9 | a0001c0001t0001g0017a0001c0001t0001g0036a0001c0001t0001g0070others(6): Show | 9 | HG00423.hp1 NA18983.hp1 NA18989.hp2 others(6): Show |
intron_variant | MODIFIER | c.1049-2610A>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97697144 | ||||||
| chr8:97697146
|
A | T | 10 | a0001c0001t0001g0017a0001c0001t0001g0036a0001c0001t0001g0070others(7): Show | 10 | HG00423.hp1 NA18983.hp1 NA18984.hp2 others(7): Show |
intron_variant | MODIFIER | c.1049-2608A>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97697146 | ||||||
| chr8:97697148
|
A | ATTTT | 6 | a0001c0001t0008g0155a0001c0001t0008g0156a0001c0001t0008g0157others(3): Show | 6 | HG01081.hp2 HG02976.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1049-2605_1049-260 others(8): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697148 | |||||
| chr8:97697148
|
A | ATTTTTTT others(1): Show |
7 | a0001c0001t0011g0141a0001c0001t0011g0143a0001c0001t0011g0144others(4): Show | 7 | NA18941.hp1 NA18947.hp2 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.1049-2605_1049-260 others(12): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697148 | |||||
| chr8:97697148
|
A | ATTTTTTT others(4): Show |
1 | a0001c0001t0005g0008 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1049-2605_1049-260 others(15): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697148 | |||||
| chr8:97697148
|
A | ATTTTTTT others(5): Show |
7 | a0001c0001t0005g0005a0001c0001t0005g0013a0001c0001t0005g0014others(4): Show | 7 | HG00733.hp1 HG00738.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1049-2605_1049-260 others(16): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697148 | |||||
| chr8:97697148
|
A | ATTTTTTT others(6): Show |
1 | a0001c0001t0012g0012 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1049-2605_1049-260 others(17): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697148 | |||||
| chr8:97697148
|
A | T | 12 | a0001c0001t0001g0017a0001c0001t0001g0036a0001c0001t0001g0070others(9): Show | 12 | HG00423.hp1 NA18949.hp1 NA18983.hp1 others(9): Show |
intron_variant | MODIFIER | c.1049-2606A>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97697148 | ||||||
| chr8:97697150
|
A | ATATATAT others(30): Show |
1 | a0007c0011t0070g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1049-2603_1049-260 others(41): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697150 | |||||
| chr8:97697150
|
A | ATATATAT others(25): Show |
1 | a0001c0001t0042g0114 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1049-2603_1049-260 others(36): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697150 | |||||
| chr8:97697150
|
A | ATATATAT others(21): Show |
2 | a0001c0001t0019g0108a0001c0001t0019g0110 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1049-2603_1049-260 others(32): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697150 | |||||
| chr8:97697150
|
A | ATATATAT others(17): Show |
2 | a0001c0001t0005g0115a0001c0001t0005g0116 | 2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1049-2603_1049-260 others(28): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697150 | |||||
| chr8:97697150
|
A | ATATATAT others(19): Show |
2 | a0001c0001t0005g0112a0001c0001t0005g0117 | 2 | HG01891.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1049-2603_1049-260 others(30): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697150 | |||||
| chr8:97697150
|
A | ATATATAT others(20): Show |
1 | a0001c0001t0005g0113 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1049-2603_1049-260 others(31): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697150 | |||||
| chr8:97697150
|
A | ATATTTTT | 11 | a0001c0001t0006g0182a0001c0001t0006g0183a0001c0001t0006g0184others(8): Show | 11 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1049-2603_1049-260 others(11): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697150 | |||||
| chr8:97697150
|
A | ATTT | 55 | a0001c0001t0003g0173a0001c0001t0003g0175a0001c0001t0003g0179others(52): Show | 55 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.1049-2596_1049-259 others(7): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697150 | |||||
| chr8:97697150
|
A | ATTTTT | 7 | a0001c0001t0003g0255a0001c0001t0052g0252a0001c0001t0083g0370others(4): Show | 7 | HG01167.hp1 HG01516.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.1049-2598_1049-259 others(9): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697150 | |||||
| chr8:97697150
|
A | ATTTTTT | 11 | a0001c0001t0008g0159a0001c0001t0008g0160a0001c0001t0018g0132others(8): Show | 11 | HG02258.hp2 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1049-2599_1049-259 others(10): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697150 | |||||
| chr8:97697150
|
A | ATTTTTTT | 9 | a0001c0001t0001g0087a0001c0001t0021g0168a0001c0001t0036g0085others(6): Show | 9 | HG01168.hp1 HG01496.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.1049-2600_1049-259 others(11): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697150 | |||||
| chr8:97697150
|
A | ATTTTTTT others(1): Show |
10 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0016g0121others(7): Show | 10 | HG00140.hp2 HG00733.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1049-2601_1049-259 others(12): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697150 | |||||
| chr8:97697150
|
A | ATTTTTTT others(2): Show |
7 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0013g0259others(4): Show | 7 | HG00544.hp1 HG01243.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1049-2602_1049-259 others(13): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697150 | |||||
| chr8:97697150
|
A | ATTTTTTT others(3): Show |
10 | a0001c0001t0001g0090a0001c0001t0001g0095a0001c0001t0001g0103others(7): Show | 10 | HG01081.hp1 HG01123.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1049-2603_1049-259 others(14): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697150 | |||||
| chr8:97697150
|
A | ATTTTTTT others(4): Show |
10 | a0001c0001t0001g0049a0001c0001t0001g0096a0001c0001t0005g0004others(7): Show | 10 | HG00741.hp1 HG01978.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1049-2594_1049-259 others(15): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697150 | |||||
| chr8:97697150
|
A | ATTTTTTT others(5): Show |
24 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0032others(21): Show | 24 | HG00597.hp2 HG01192.hp2 HG01516.hp1 others(21): Show |
intron_variant | MODIFIER | c.1049-2594_1049-259 others(16): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697150 | |||||
| chr8:97697150
|
A | ATTTTTTT others(6): Show |
11 | a0001c0001t0001g0043a0001c0001t0001g0046a0001c0001t0001g0058others(8): Show | 11 | HG00621.hp1 HG00642.hp1 HG02602.hp2 others(8): Show |
intron_variant | MODIFIER | c.1049-2594_1049-259 others(17): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697150 | |||||
| chr8:97697150
|
A | ATTTTTTT others(7): Show |
14 | a0001c0001t0001g0026a0001c0001t0001g0045a0001c0001t0001g0051others(11): Show | 14 | HG00639.hp2 HG01358.hp1 HG01978.hp2 others(11): Show |
intron_variant | MODIFIER | c.1049-2594_1049-259 others(18): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697150 | |||||
| chr8:97697150
|
A | ATTTTTTT others(8): Show |
10 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0068others(7): Show | 10 | HG02257.hp1 HG03195.hp1 HG03225.hp2 others(7): Show |
intron_variant | MODIFIER | c.1049-2594_1049-259 others(19): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697150 | |||||
| chr8:97697150
|
A | ATTTTTTT others(9): Show |
10 | a0001c0001t0001g0022a0001c0001t0001g0053a0001c0001t0001g0061others(7): Show | 10 | HG00558.hp1 HG01099.hp2 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.1049-2594_1049-259 others(20): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697150 | |||||
| chr8:97697150
|
A | ATTTTTTT others(10): Show |
2 | a0001c0001t0001g0092a0001c0001t0001g0100 | 2 | HG02129.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.1049-2594_1049-259 others(21): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697150 | |||||
| chr8:97697150
|
A | T | 41 | a0001c0001t0001g0017a0001c0001t0001g0036a0001c0001t0001g0070others(38): Show | 41 | HG00423.hp1 HG00733.hp1 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.1049-2604A>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97697150 | ||||||
| chr8:97697159
|
T | G | 1 | a0001c0001t0004g0351 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1049-2595T>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97697159 | ||||||
| chr8:97697191
|
G | A | 4 | a0001c0001t0018g0132a0001c0001t0018g0133a0001c0001t0018g0135others(1): Show | 4 | HG02615.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1049-2563G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97697191 | ||||||
| chr8:97697196
|
G | A | 1 | a0001c0001t0034g0118 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1049-2558G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97697196 | ||||||
| chr8:97697366
|
AATATTAT others(31): Show |
A | 1 | a0001c0001t0016g0119 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1049-2387_1049-235 others(42): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97697366 | ||||||
| chr8:97697381
|
G | GT | 46 | a0001c0001t0002g0260a0001c0001t0002g0272a0001c0001t0002g0279others(43): Show | 46 | HG00408.hp2 HG00609.hp2 HG01258.hp2 others(43): Show |
intron_variant | MODIFIER | c.1049-2350dupT | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697381 | |||||
| chr8:97697381
|
GT | G | 138 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0026others(135): Show | 138 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.1049-2350delT | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697381 | |||||
| chr8:97697381
|
GTTTTTTT others(3): Show |
G | 2 | a0001c0001t0051g0251a0001c0001t0052g0252 | 2 | HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1049-2359_1049-235 others(14): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697381 | |||||
| chr8:97697447
|
G | T | 1 | a0001c0001t0001g0048 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1049-2307G>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97697447 | ||||||
| chr8:97697543
|
AC | A | 3 | a0002c0003t0013g0127a0002c0003t0013g0129a0002c0003t0013g0130 | 3 | HG02895.hp1 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1049-2208delC | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97697543 | |||||
| chr8:97697546
|
C | T | 1 | a0001c0002t0003g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1049-2208C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97697546 | ||||||
| chr8:97697578
|
T | C | 252 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(249): Show | 252 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(249): Show |
intron_variant | MODIFIER | c.1049-2176T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97697578 | ||||||
| chr8:97697610
|
C | T | 11 | a0001c0001t0011g0141a0001c0001t0011g0143a0001c0001t0011g0144others(8): Show | 11 | HG00673.hp1 NA18941.hp1 NA18947.hp2 others(8): Show |
intron_variant | MODIFIER | c.1049-2144C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97697610 | ||||||
| chr8:97698029
|
T | C | 1 | a0001c0001t0034g0118 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1049-1725T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97698029 | ||||||
| chr8:97698242
|
A | G | 1 | a0001c0001t0001g0081 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1049-1512A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97698242 | ||||||
| chr8:97698315
|
C | T | 107 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0175others(104): Show | 107 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.1049-1439C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97698315 | ||||||
| chr8:97698526
|
C | T | 3 | a0001c0001t0002g0266a0001c0001t0002g0280a0001c0001t0002g0354 | 3 | HG02273.hp1 HG02293.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1049-1228C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97698526 | ||||||
| chr8:97698746
|
A | G | 1 | a0001c0001t0050g0044 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1049-1008A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97698746 | ||||||
| chr8:97698812
|
C | T | 21 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0006others(18): Show | 21 | HG00733.hp1 HG00738.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1049-942C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97698812 | ||||||
| chr8:97698989
|
A | T | 1 | a0001c0001t0024g0009 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1049-765A>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97698989 | ||||||
| chr8:97699106
|
T | A | 99 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(96): Show | 99 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.1049-648T>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97699106 | ||||||
| chr8:97699257
|
C | T | 12 | a0001c0001t0006g0180a0001c0001t0006g0182a0001c0001t0006g0183others(9): Show | 12 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1049-497C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97699257 | ||||||
| chr8:97699358
|
G | C | 14 | a0001c0001t0013g0259a0001c0001t0018g0132a0001c0001t0018g0133others(11): Show | 14 | HG00733.hp2 HG01243.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.1049-396G>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97699358 | ||||||
| chr8:97699406
|
C | G | 1 | a0001c0001t0087g0317 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1049-348C>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97699406 | ||||||
| chr8:97699436
|
C | CA | 9 | a0001c0001t0001g0101a0001c0001t0016g0119a0001c0001t0016g0121others(6): Show | 9 | HG00639.hp2 HG02055.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1049-305dupA | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97699436 | |||||
| chr8:97699436
|
CAA | C | 16 | a0001c0001t0006g0180a0001c0001t0006g0182a0001c0001t0006g0183others(13): Show | 16 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1049-306_1049-305d others(4): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97699436 | |||||
| chr8:97699443
|
A | G | 16 | a0001c0001t0006g0180a0001c0001t0006g0182a0001c0001t0006g0183others(13): Show | 16 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1049-311A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97699443 | ||||||
| chr8:97699465
|
G | A | 1 | a0001c0001t0009g0077 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1049-289G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97699465 | ||||||
| chr8:97699481
|
T | G | 1 | a0001c0001t0001g0022 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1049-273T>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97699481 | ||||||
| chr8:97699498
|
A | G | 1 | a0001c0001t0004g0334 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1049-256A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97699498 | ||||||
| chr8:97699656
|
T | G | 1 | a0001c0001t0039g0126 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1049-98T>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | chr8 | 97699656 | ||||||
| chr8:97699656
|
TA | T | 7 | a0003c0004t0015g0244a0003c0004t0015g0245a0003c0004t0015g0250others(4): Show | 7 | HG00741.hp1 HG01168.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.1049-93delA | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr8 | 97699656 | |||||
| chr8:97699879
|
AT | A | 100 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(97): Show | 100 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.1147+35delT | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr8 | 97699879 | |||||
| chr8:97700051
|
G | T | 1 | a0001c0001t0006g0191 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1147+199G>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 7/11 | chr8 | 97700051 | ||||||
| chr8:97700342
|
T | C | 1 | a0001c0001t0001g0049 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1147+490T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 7/11 | chr8 | 97700342 | ||||||
| chr8:97700447
|
T | C | 1 | a0001c0001t0065g0167 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1147+595T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 7/11 | chr8 | 97700447 | ||||||
| chr8:97700589
|
G | A | 1 | a0001c0001t0056g0111 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1147+737G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 7/11 | chr8 | 97700589 | ||||||
| chr8:97700680
|
A | G | 1 | a0001c0001t0001g0020 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1147+828A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 7/11 | chr8 | 97700680 | ||||||
| chr8:97700731
|
T | C | 1 | a0001c0001t0084g0327 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1147+879T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 7/11 | chr8 | 97700731 | ||||||
| chr8:97700960
|
T | C | 7 | a0003c0004t0015g0244a0003c0004t0015g0245a0003c0004t0015g0250others(4): Show | 7 | HG00741.hp1 HG01168.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.1147+1108T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 7/11 | chr8 | 97700960 | ||||||
| chr8:97701024
|
T | G | 1 | a0001c0001t0002g0358 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1147+1172T>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 7/11 | chr8 | 97701024 | ||||||
| chr8:97701066
|
G | A | 1 | a0001c0001t0016g0119 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1147+1214G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 7/11 | chr8 | 97701066 | ||||||
| chr8:97701118
|
G | A | 1 | a0001c0001t0002g0281 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1147+1266G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 7/11 | chr8 | 97701118 | ||||||
| chr8:97701308
|
A | G | 1 | a0001c0002t0003g0208 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1147+1456A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 7/11 | chr8 | 97701308 | ||||||
| chr8:97701679
|
G | A | 16 | a0001c0001t0006g0180a0001c0001t0006g0182a0001c0001t0006g0183others(13): Show | 16 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1147+1827G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 7/11 | chr8 | 97701679 | ||||||
| chr8:97701770
|
G | A | 224 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(221): Show | 224 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(221): Show |
intron_variant | MODIFIER | c.1147+1918G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 7/11 | chr8 | 97701770 | ||||||
| chr8:97701919
|
G | A | 1 | a0001c0002t0003g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1147+2067G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 7/11 | chr8 | 97701919 | ||||||
| chr8:97701994
|
T | C | 1 | a0001c0001t0002g0265 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1147+2142T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 7/11 | chr8 | 97701994 | ||||||
| chr8:97702017
|
T | C | 1 | a0001c0001t0056g0111 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1147+2165T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 7/11 | chr8 | 97702017 | ||||||
| chr8:97702107
|
A | G | 1 | a0001c0001t0012g0011 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1147+2255A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 7/11 | chr8 | 97702107 | ||||||
| chr8:97702221
|
C | T | 16 | a0001c0001t0006g0180a0001c0001t0006g0182a0001c0001t0006g0183others(13): Show | 16 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1147+2369C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 7/11 | chr8 | 97702221 | ||||||
| chr8:97702439
|
C | T | 1 | a0001c0001t0004g0294 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1147+2587C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 7/11 | chr8 | 97702439 | ||||||
| chr8:97702441
|
G | T | 6 | a0001c0002t0003g0208a0001c0002t0080g0205a0001c0002t0081g0242others(3): Show | 6 | HG01952.hp1 NA18956.hp2 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.1147+2589G>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 7/11 | chr8 | 97702441 | ||||||
| chr8:97702463
|
A | G | 1 | a0001c0001t0002g0265 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1147+2611A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 7/11 | chr8 | 97702463 | ||||||
| chr8:97702632
|
A | G | 1 | a0001c0001t0002g0299 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1147+2780A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 7/11 | chr8 | 97702632 | ||||||
| chr8:97702795
|
G | T | 1 | a0001c0001t0039g0126 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1147+2943G>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 7/11 | chr8 | 97702795 | ||||||
| chr8:97702807
|
G | A | 1 | a0001c0001t0002g0353 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1147+2955G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 7/11 | chr8 | 97702807 | ||||||
| chr8:97702842
|
G | A | 7 | a0003c0004t0015g0244a0003c0004t0015g0245a0003c0004t0015g0250others(4): Show | 7 | HG00741.hp1 HG01168.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.1147+2990G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 7/11 | chr8 | 97702842 | ||||||
| chr8:97703002
|
A | C | 1 | a0001c0001t0003g0175 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1147+3150A>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 7/11 | chr8 | 97703002 | ||||||
| chr8:97703138
|
A | T | 13 | a0001c0001t0013g0259a0001c0001t0018g0132a0001c0001t0018g0133others(10): Show | 13 | HG00733.hp2 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1147+3286A>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 7/11 | chr8 | 97703138 | ||||||
| chr8:97703474
|
T | G | 1 | a0001c0001t0038g0023 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1148-3152T>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 7/11 | chr8 | 97703474 | ||||||
| chr8:97703527
|
A | G | 1 | a0001c0002t0003g0206 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1148-3099A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 7/11 | chr8 | 97703527 | ||||||
| chr8:97703661
|
C | T | 3 | a0001c0001t0002g0295a0001c0001t0002g0311a0001c0001t0069g0288 | 3 | NA18939.hp1 NA19000.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1148-2965C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 7/11 | chr8 | 97703661 | ||||||
| chr8:97703784
|
C | A | 5 | a0001c0001t0008g0155a0001c0001t0016g0121a0001c0001t0016g0122others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1148-2842C>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 7/11 | chr8 | 97703784 | ||||||
| chr8:97703951
|
A | G | 1 | a0001c0001t0002g0140 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1148-2675A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 7/11 | chr8 | 97703951 | ||||||
| chr8:97704199
|
A | G | 6 | a0001c0001t0016g0119a0001c0001t0016g0121a0001c0001t0016g0122others(3): Show | 6 | HG02055.hp1 HG02451.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1148-2427A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 7/11 | chr8 | 97704199 | ||||||
| chr8:97704285
|
C | T | 22 | a0001c0001t0004g0267a0001c0001t0004g0278a0001c0001t0004g0284others(19): Show | 22 | HG00408.hp2 HG00673.hp2 HG03831.hp1 others(19): Show |
intron_variant | MODIFIER | c.1148-2341C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 7/11 | chr8 | 97704285 | ||||||
| chr8:97704780
|
T | G | 1 | a0001c0001t0002g0292 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1148-1846T>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 7/11 | chr8 | 97704780 | ||||||
| chr8:97704892
|
A | G | 1 | a0001c0001t0004g0136 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1148-1734A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 7/11 | chr8 | 97704892 | ||||||
| chr8:97705070
|
A | C | 1 | a0001c0001t0037g0131 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1148-1556A>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 7/11 | chr8 | 97705070 | ||||||
| chr8:97705221
|
C | T | 6 | a0001c0001t0016g0119a0001c0001t0016g0121a0001c0001t0016g0122others(3): Show | 6 | HG02055.hp1 HG02451.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1148-1405C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 7/11 | chr8 | 97705221 | ||||||
| chr8:97705222
|
G | A | 16 | a0001c0001t0006g0180a0001c0001t0006g0182a0001c0001t0006g0183others(13): Show | 16 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1148-1404G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 7/11 | chr8 | 97705222 | ||||||
| chr8:97705233
|
G | A | 1 | a0001c0001t0001g0027 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1148-1393G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 7/11 | chr8 | 97705233 | ||||||
| chr8:97705252
|
G | A | 1 | a0007c0011t0070g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1148-1374G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 7/11 | chr8 | 97705252 | ||||||
| chr8:97705340
|
G | A | 1 | a0001c0001t0044g0082 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1148-1286G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 7/11 | chr8 | 97705340 | ||||||
| chr8:97705403
|
C | T | 1 | a0001c0001t0051g0251 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1148-1223C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 7/11 | chr8 | 97705403 | ||||||
| chr8:97705406
|
C | G | 7 | a0003c0004t0015g0244a0003c0004t0015g0245a0003c0004t0015g0250others(4): Show | 7 | HG00741.hp1 HG01168.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.1148-1220C>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 7/11 | chr8 | 97705406 | ||||||
| chr8:97705503
|
G | A | 4 | a0001c0001t0002g0358a0001c0001t0004g0294a0001c0001t0028g0306others(1): Show | 4 | HG01258.hp2 HG03490.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.1148-1123G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 7/11 | chr8 | 97705503 | ||||||
| chr8:97705603
|
GA | G | 5 | a0001c0001t0002g0292a0001c0001t0002g0296a0001c0001t0002g0313others(2): Show | 5 | HG00741.hp2 HG01099.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.1148-1016delA | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr8 | 97705603 | |||||
| chr8:97705929
|
C | T | 1 | a0001c0001t0004g0136 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1148-697C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 7/11 | chr8 | 97705929 | ||||||
| chr8:97706212
|
G | T | 2 | a0001c0001t0001g0106a0001c0001t0045g0105 | 2 | HG01081.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1148-414G>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 7/11 | chr8 | 97706212 | ||||||
| chr8:97706261
|
A | G | 8 | a0001c0001t0002g0139a0001c0001t0002g0295a0001c0001t0002g0302others(5): Show | 8 | HG00609.hp1 HG02040.hp1 NA18939.hp1 others(5): Show |
intron_variant | MODIFIER | c.1148-365A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 7/11 | chr8 | 97706261 | ||||||
| chr8:97706488
|
T | TC | 6 | a0001c0001t0016g0119a0001c0001t0016g0121a0001c0001t0016g0122others(3): Show | 6 | HG02055.hp1 HG02451.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1148-137dupC | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr8 | 97706488 | |||||
| chr8:97706895
|
A | G | 1 | a0001c0001t0003g0172 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1272+145A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97706895 | ||||||
| chr8:97707030
|
T | C | 1 | a0001c0001t0052g0252 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1272+280T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97707030 | ||||||
| chr8:97707196
|
G | A | 1 | a0007c0011t0070g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1272+446G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97707196 | ||||||
| chr8:97707377
|
A | T | 252 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(249): Show | 252 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(249): Show |
intron_variant | MODIFIER | c.1272+627A>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97707377 | ||||||
| chr8:97707408
|
C | G | 1 | a0001c0002t0003g0216 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1272+658C>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97707408 | ||||||
| chr8:97707415
|
G | A | 1 | a0001c0001t0008g0157 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1272+665G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97707415 | ||||||
| chr8:97707430
|
G | T | 2 | a0001c0001t0002g0341a0001c0001t0014g0360 | 2 | NA18957.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.1272+680G>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97707430 | ||||||
| chr8:97707449
|
C | CT | 141 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0002g0260others(138): Show | 141 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.1272+723dupT | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97707449 | |||||
| chr8:97707449
|
C | CTT | 16 | a0001c0001t0003g0172a0001c0001t0005g0006a0001c0001t0006g0190others(13): Show | 16 | HG01081.hp2 HG01934.hp1 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.1272+722_1272+723d others(4): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97707449 | |||||
| chr8:97707482
|
GTCCTCAA others(2): Show |
G | 16 | a0001c0001t0006g0180a0001c0001t0006g0182a0001c0001t0006g0183others(13): Show | 16 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1272+737_1272+745d others(11): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97707482 | |||||
| chr8:97707595
|
A | C | 8 | a0001c0001t0013g0259a0001c0001t0039g0126a0001c0001t0040g0258others(5): Show | 8 | HG00733.hp2 HG01243.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1272+845A>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97707595 | ||||||
| chr8:97707713
|
G | C | 14 | a0001c0001t0008g0155a0001c0001t0008g0156a0001c0001t0008g0157others(11): Show | 14 | HG01081.hp2 HG01891.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1272+963G>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97707713 | ||||||
| chr8:97707962
|
C | CT | 10 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0002t0003g0201others(7): Show | 10 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(7): Show |
intron_variant | MODIFIER | c.1272+1224dupT | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97707962 | |||||
| chr8:97708100
|
T | C | 1 | a0001c0001t0002g0266 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1272+1350T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97708100 | ||||||
| chr8:97708129
|
G | A | 1 | a0001c0001t0029g0151 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1272+1379G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97708129 | ||||||
| chr8:97708209
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1272+1459C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97708209 | ||||||
| chr8:97708264
|
C | CT | 34 | a0001c0001t0002g0260a0001c0001t0002g0265a0001c0001t0002g0276others(31): Show | 34 | HG00597.hp1 HG00642.hp2 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.1272+1549dupT | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97708264 | |||||
| chr8:97708264
|
C | CTT | 11 | a0001c0001t0002g0289a0001c0001t0002g0358a0001c0001t0004g0267others(8): Show | 11 | HG00738.hp1 HG01081.hp2 HG03130.hp2 others(8): Show |
intron_variant | MODIFIER | c.1272+1548_1272+154 others(6): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97708264 | |||||
| chr8:97708264
|
C | CTTT | 8 | a0001c0001t0004g0334a0001c0001t0008g0156a0001c0001t0008g0159others(5): Show | 8 | HG01123.hp2 HG02258.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1272+1547_1272+154 others(7): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97708264 | |||||
| chr8:97708264
|
C | CTTTT | 18 | a0001c0001t0006g0191a0001c0001t0008g0157a0001c0001t0008g0160others(15): Show | 18 | HG00558.hp2 HG02809.hp2 HG02818.hp2 others(15): Show |
intron_variant | MODIFIER | c.1272+1546_1272+154 others(8): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97708264 | |||||
| chr8:97708264
|
C | CTTTTT | 27 | a0001c0001t0011g0147a0001c0002t0003g0203a0001c0002t0003g0204others(24): Show | 27 | HG00408.hp1 HG00423.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.1272+1545_1272+154 others(9): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97708264 | |||||
| chr8:97708264
|
C | CTTTTTT | 10 | a0001c0001t0003g0255a0001c0001t0011g0148a0001c0001t0029g0151others(7): Show | 10 | HG00673.hp1 HG01167.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.1272+1544_1272+154 others(10): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97708264 | |||||
| chr8:97708264
|
C | CTTTTTTT | 13 | a0001c0001t0003g0173a0001c0001t0006g0185a0001c0001t0006g0187others(10): Show | 13 | HG00735.hp2 HG01175.hp2 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.1272+1543_1272+154 others(11): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97708264 | |||||
| chr8:97708264
|
C | CTTTTTTT others(1): Show |
8 | a0001c0001t0003g0172a0001c0001t0006g0180a0001c0001t0006g0182others(5): Show | 8 | HG02109.hp2 HG02257.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.1272+1542_1272+154 others(12): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97708264 | |||||
| chr8:97708264
|
C | CTTTTTTT others(2): Show |
8 | a0001c0001t0003g0175a0001c0001t0003g0179a0001c0001t0006g0188others(5): Show | 8 | HG02572.hp1 HG03130.hp1 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1272+1541_1272+154 others(13): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97708264 | |||||
| chr8:97708264
|
C | CTTTTTTT others(3): Show |
5 | a0001c0001t0022g0192a0001c0001t0031g0178a0001c0002t0078g0215others(2): Show | 5 | HG02145.hp2 HG02647.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.1272+1540_1272+154 others(14): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97708264 | |||||
| chr8:97708264
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0031g0177 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1272+1539_1272+154 others(15): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97708264 | |||||
| chr8:97708264
|
C | CTTTTTTT others(5): Show |
2 | a0001c0001t0072g0142a0001c0002t0003g0216 | 2 | HG02132.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1272+1538_1272+154 others(16): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97708264 | |||||
| chr8:97708264
|
C | CTTTTTTT others(24): Show |
1 | a0001c0001t0065g0167 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1272+1519_1272+154 others(35): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97708264 | |||||
| chr8:97708264
|
CT | C | 32 | a0001c0001t0002g0256a0001c0001t0002g0266a0001c0001t0002g0268others(29): Show | 32 | HG00544.hp2 HG00609.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.1272+1549delT | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97708264 | |||||
| chr8:97708264
|
CTT | C | 6 | a0001c0001t0004g0274a0001c0001t0012g0015a0001c0001t0016g0119others(3): Show | 6 | HG02055.hp1 HG02615.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1272+1548_1272+154 others(6): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97708264 | |||||
| chr8:97708264
|
CTTT | C | 14 | a0001c0001t0004g0136a0001c0001t0005g0112a0001c0001t0005g0115others(11): Show | 14 | HG00738.hp2 HG01361.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1272+1547_1272+154 others(7): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97708264 | |||||
| chr8:97708264
|
CTTTT | C | 20 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0006others(17): Show | 20 | HG00733.hp1 HG00741.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1272+1546_1272+154 others(8): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97708264 | |||||
| chr8:97708264
|
CTTTTTTT | C | 16 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0026others(13): Show | 16 | HG00544.hp1 HG00621.hp1 HG00642.hp1 others(13): Show |
intron_variant | MODIFIER | c.1272+1543_1272+154 others(11): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97708264 | |||||
| chr8:97708264
|
CTTTTTTT others(1): Show |
C | 73 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0024others(70): Show | 73 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.1272+1542_1272+154 others(12): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97708264 | |||||
| chr8:97708264
|
CTTTTTTT others(3): Show |
C | 3 | a0001c0002t0003g0210a0001c0002t0003g0253a0001c0002t0003g0254 | 3 | HG03834.hp1 NA20905.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1272+1540_1272+154 others(14): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97708264 | |||||
| chr8:97708264
|
CTTTTTTT others(12): Show |
C | 2 | a0001c0001t0007g0170a0001c0001t0007g0171 | 2 | NA18950.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1272+1531_1272+154 others(23): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97708264 | |||||
| chr8:97708303
|
A | G | 13 | a0001c0001t0013g0259a0001c0001t0018g0132a0001c0001t0018g0133others(10): Show | 13 | HG00733.hp2 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1272+1553A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97708303 | ||||||
| chr8:97708368
|
CCCTCCCA others(311): Show |
C | 12 | a0001c0001t0008g0155a0001c0001t0008g0156a0001c0001t0008g0157others(9): Show | 12 | HG01081.hp2 HG02258.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1272+1678_1272+199 others(4): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97708368 | |||||
| chr8:97708512
|
G | C | 99 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(96): Show | 99 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.1272+1762G>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97708512 | ||||||
| chr8:97708529
|
A | G | 114 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0175others(111): Show | 114 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.1272+1779A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97708529 | ||||||
| chr8:97708544
|
A | G | 1 | a0001c0001t0087g0317 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1272+1794A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97708544 | ||||||
| chr8:97708551
|
G | T | 91 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(88): Show | 91 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.1272+1801G>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97708551 | ||||||
| chr8:97708556
|
A | G | 1 | a0002c0003t0035g0125 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1272+1806A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97708556 | ||||||
| chr8:97708580
|
CCTTTTTT others(7): Show |
C | 1 | a0001c0001t0072g0142 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1272+1831_1272+184 others(18): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97708580 | ||||||
| chr8:97708581
|
C | CT | 46 | a0001c0001t0002g0140a0001c0001t0002g0257a0001c0001t0002g0263others(43): Show | 46 | HG00140.hp1 HG00597.hp1 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.1272+1869dupT | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97708581 | |||||
| chr8:97708581
|
C | CTT | 14 | a0001c0001t0002g0265a0001c0001t0002g0321a0001c0001t0002g0352others(11): Show | 14 | HG00738.hp1 HG01884.hp2 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.1272+1868_1272+186 others(6): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97708581 | |||||
| chr8:97708581
|
C | CTTT | 8 | a0001c0001t0002g0266a0001c0001t0002g0280a0001c0001t0002g0302others(5): Show | 8 | HG00609.hp1 HG00642.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.1272+1867_1272+186 others(7): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97708581 | |||||
| chr8:97708581
|
C | CTTTTTT | 8 | a0001c0001t0004g0324a0001c0001t0005g0008a0001c0001t0005g0013others(5): Show | 8 | HG00733.hp1 HG00738.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.1272+1864_1272+186 others(10): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97708581 | |||||
| chr8:97708581
|
C | CTTTTTTT others(5): Show |
2 | a0001c0001t0006g0187a0001c0001t0006g0191 | 2 | HG02280.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1272+1858_1272+186 others(16): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97708581 | |||||
| chr8:97708581
|
C | CTTTTTTT others(9): Show |
1 | a0001c0001t0006g0184 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1272+1854_1272+186 others(20): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97708581 | |||||
| chr8:97708581
|
C | CTTTTTTT others(10): Show |
1 | a0001c0001t0006g0190 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1272+1853_1272+186 others(21): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97708581 | |||||
| chr8:97708581
|
C | CTTTTTTT others(13): Show |
1 | a0001c0001t0006g0180 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1272+1850_1272+186 others(24): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97708581 | |||||
| chr8:97708581
|
C | CTTTTTTT others(14): Show |
1 | a0001c0001t0006g0185 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1272+1849_1272+186 others(25): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97708581 | |||||
| chr8:97708581
|
C | CTTTTTTT others(15): Show |
1 | a0001c0001t0006g0189 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1272+1848_1272+186 others(26): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97708581 | |||||
| chr8:97708581
|
C | CTTTTTTT others(16): Show |
2 | a0001c0001t0006g0182a0001c0001t0006g0183 | 2 | HG02257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1272+1847_1272+186 others(27): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97708581 | |||||
| chr8:97708581
|
C | CTTTTTTT others(17): Show |
1 | a0001c0001t0054g0181 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1272+1846_1272+186 others(28): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97708581 | |||||
| chr8:97708581
|
C | CTTTTTTT others(18): Show |
1 | a0001c0001t0058g0120 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1272+1845_1272+186 others(29): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97708581 | |||||
| chr8:97708581
|
C | CTTTTTTT others(19): Show |
1 | a0001c0001t0006g0188 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1272+1844_1272+186 others(30): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97708581 | |||||
| chr8:97708581
|
C | CTTTTTTT others(20): Show |
1 | a0001c0001t0055g0186 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1272+1843_1272+186 others(31): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97708581 | |||||
| chr8:97708581
|
CTTTTTTT others(1): Show |
C | 8 | a0001c0001t0005g0004a0001c0001t0005g0176a0001c0001t0016g0123others(5): Show | 8 | HG01884.hp1 HG02055.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1272+1862_1272+186 others(12): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97708581 | |||||
| chr8:97708581
|
CTTTTTTT others(2): Show |
C | 7 | a0001c0001t0005g0113a0001c0001t0013g0259a0001c0001t0018g0133others(4): Show | 7 | HG00733.hp2 HG01109.hp2 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.1272+1861_1272+186 others(13): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97708581 | |||||
| chr8:97708581
|
CTTTTTTT others(3): Show |
C | 18 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0032others(15): Show | 18 | HG00544.hp1 HG00642.hp1 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.1272+1860_1272+186 others(14): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97708581 | |||||
| chr8:97708581
|
CTTTTTTT others(4): Show |
C | 73 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(70): Show | 73 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.1272+1859_1272+186 others(15): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97708581 | |||||
| chr8:97708581
|
CTTTTTTT others(5): Show |
C | 15 | a0001c0001t0001g0070a0001c0001t0001g0092a0001c0001t0001g0106others(12): Show | 15 | HG00741.hp1 HG01081.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.1272+1858_1272+186 others(16): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97708581 | |||||
| chr8:97708581
|
CTTTTTTT others(6): Show |
C | 7 | a0001c0001t0003g0175a0001c0001t0004g0267a0001c0001t0030g0169others(4): Show | 7 | HG00408.hp1 HG00558.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.1272+1857_1272+186 others(17): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97708581 | |||||
| chr8:97708581
|
CTTTTTTT others(7): Show |
C | 70 | a0001c0001t0002g0270a0001c0001t0002g0272a0001c0001t0002g0273others(67): Show | 70 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.1272+1856_1272+186 others(18): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97708581 | |||||
| chr8:97708581
|
CTTTTTTT others(8): Show |
C | 7 | a0001c0001t0011g0146a0001c0001t0011g0147a0001c0001t0011g0148others(4): Show | 7 | HG00621.hp2 HG00673.hp1 NA18941.hp1 others(4): Show |
intron_variant | MODIFIER | c.1272+1855_1272+186 others(19): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97708581 | |||||
| chr8:97708581
|
CTTTTTTT others(12): Show |
C | 2 | a0001c0001t0002g0341a0001c0001t0016g0122 | 2 | HG02897.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.1272+1851_1272+186 others(23): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97708581 | |||||
| chr8:97708581
|
CTTTTTTT others(13): Show |
C | 1 | a0001c0001t0016g0121 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1272+1850_1272+186 others(24): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97708581 | |||||
| chr8:97708581
|
CTTTTTTT others(14): Show |
C | 1 | a0001c0001t0002g0310 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1272+1849_1272+186 others(25): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97708581 | |||||
| chr8:97708774
|
G | A | 1 | a0001c0002t0003g0207 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1272+2024G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97708774 | ||||||
| chr8:97708784
|
C | G | 1 | a0001c0002t0003g0207 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1272+2034C>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97708784 | ||||||
| chr8:97708790
|
A | G | 1 | a0001c0002t0003g0207 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1272+2040A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97708790 | ||||||
| chr8:97708843
|
G | T | 1 | a0008c0012t0015g0246 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1272+2093G>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97708843 | ||||||
| chr8:97708858
|
C | A | 1 | a0001c0001t0065g0167 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1272+2108C>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97708858 | ||||||
| chr8:97709193
|
C | CA | 17 | a0001c0001t0001g0106a0001c0001t0002g0293a0001c0001t0004g0275others(14): Show | 17 | HG01243.hp1 HG01243.hp2 HG02056.hp2 others(14): Show |
intron_variant | MODIFIER | c.1272+2459dupA | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97709193 | |||||
| chr8:97709193
|
CA | C | 26 | a0001c0001t0001g0070a0001c0001t0001g0081a0001c0001t0006g0180others(23): Show | 26 | HG01081.hp2 HG02109.hp2 HG02257.hp2 others(23): Show |
intron_variant | MODIFIER | c.1272+2459delA | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97709193 | |||||
| chr8:97709200
|
A | C | 3 | a0001c0001t0019g0108a0001c0001t0019g0109a0001c0001t0019g0110 | 3 | HG02622.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1272+2450A>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97709200 | ||||||
| chr8:97709210
|
C | A | 1 | a0001c0001t0052g0252 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1272+2460C>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97709210 | ||||||
| chr8:97709231
|
G | T | 1 | a0008c0012t0015g0246 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1272+2481G>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97709231 | ||||||
| chr8:97709334
|
TAGA | T | 225 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(222): Show | 225 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(222): Show |
intron_variant | MODIFIER | c.1272+2587_1272+258 others(7): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97709334 | |||||
| chr8:97709501
|
A | C | 1 | a0001c0001t0068g0328 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1272+2751A>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97709501 | ||||||
| chr8:97709728
|
A | G | 1 | a0001c0001t0001g0078 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1272+2978A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97709728 | ||||||
| chr8:97710230
|
C | T | 1 | a0001c0001t0039g0126 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1273-3432C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97710230 | ||||||
| chr8:97710415
|
C | T | 2 | a0001c0001t0051g0251a0001c0001t0052g0252 | 2 | HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1273-3247C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97710415 | ||||||
| chr8:97710473
|
C | T | 12 | a0001c0001t0006g0180a0001c0001t0006g0182a0001c0001t0006g0183others(9): Show | 12 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1273-3189C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97710473 | ||||||
| chr8:97710534
|
CA | C | 250 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(247): Show | 250 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(247): Show |
intron_variant | MODIFIER | c.1273-3115delA | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97710534 | |||||
| chr8:97710582
|
C | T | 107 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0175others(104): Show | 107 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.1273-3080C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97710582 | ||||||
| chr8:97710654
|
C | G | 2 | a0001c0001t0014g0355a0001c0001t0059g0262 | 2 | NA18967.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.1273-3008C>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97710654 | ||||||
| chr8:97710683
|
C | CA | 20 | a0001c0001t0002g0139a0001c0001t0002g0260a0001c0001t0002g0276others(17): Show | 20 | HG00597.hp1 HG00741.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.1273-2952dupA | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97710683 | |||||
| chr8:97710683
|
CA | C | 42 | a0001c0001t0002g0281a0001c0001t0002g0296a0001c0001t0002g0300others(39): Show | 42 | HG00639.hp1 HG00733.hp1 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.1273-2952delA | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97710683 | |||||
| chr8:97710683
|
CAA | C | 106 | a0001c0001t0001g0096a0001c0001t0003g0172a0001c0001t0003g0173others(103): Show | 106 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.1273-2953_1273-295 others(6): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97710683 | |||||
| chr8:97710683
|
CAAA | C | 22 | a0001c0001t0001g0027a0001c0001t0001g0043a0001c0001t0001g0073others(19): Show | 22 | HG00597.hp2 HG01168.hp1 HG01361.hp1 others(19): Show |
intron_variant | MODIFIER | c.1273-2954_1273-295 others(7): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97710683 | |||||
| chr8:97710683
|
CAAAA | C | 88 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(85): Show | 88 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.1273-2955_1273-295 others(8): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97710683 | |||||
| chr8:97710683
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0034g0118 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1273-2962_1273-295 others(15): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97710683 | |||||
| chr8:97710722
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1273-2940G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97710722 | ||||||
| chr8:97710725
|
C | T | 1 | a0001c0001t0034g0118 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1273-2937C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97710725 | ||||||
| chr8:97710814
|
A | G | 1 | a0001c0001t0068g0328 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1273-2848A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97710814 | ||||||
| chr8:97711003
|
AAAAT | A | 12 | a0001c0001t0006g0180a0001c0001t0006g0182a0001c0001t0006g0183others(9): Show | 12 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1273-2653_1273-265 others(8): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97711003 | |||||
| chr8:97711098
|
A | C | 1 | a0001c0002t0003g0226 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1273-2564A>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97711098 | ||||||
| chr8:97711324
|
C | G | 6 | a0001c0001t0016g0119a0001c0001t0016g0121a0001c0001t0016g0122others(3): Show | 6 | HG02055.hp1 HG02451.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1273-2338C>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97711324 | ||||||
| chr8:97711337
|
T | TA | 102 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(99): Show | 102 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.1273-2309dupA | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97711337 | |||||
| chr8:97711491
|
AAAAC | A | 12 | a0001c0001t0006g0180a0001c0001t0006g0182a0001c0001t0006g0183others(9): Show | 12 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1273-2163_1273-216 others(8): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97711491 | |||||
| chr8:97711583
|
A | G | 2 | a0001c0001t0001g0106a0001c0001t0045g0105 | 2 | HG01081.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1273-2079A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97711583 | ||||||
| chr8:97711608
|
A | G | 1 | a0001c0001t0001g0071 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1273-2054A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97711608 | ||||||
| chr8:97711695
|
C | T | 1 | a0001c0001t0002g0289 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1273-1967C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97711695 | ||||||
| chr8:97711867
|
G | A | 2 | a0001c0001t0004g0274a0001c0001t0004g0275 | 2 | HG01243.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1273-1795G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97711867 | ||||||
| chr8:97711977
|
TATCGTTT others(5): Show |
T | 1 | a0001c0001t0002g0363 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1273-1682_1273-167 others(16): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97711977 | |||||
| chr8:97712031
|
A | G | 1 | a0001c0001t0073g0149 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1273-1631A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97712031 | ||||||
| chr8:97712495
|
C | T | 2 | a0001c0001t0051g0251a0001c0001t0052g0252 | 2 | HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1273-1167C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97712495 | ||||||
| chr8:97712585
|
T | C | 1 | a0001c0001t0004g0324 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1273-1077T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97712585 | ||||||
| chr8:97712614
|
A | G | 1 | a0001c0001t0006g0191 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1273-1048A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97712614 | ||||||
| chr8:97712616
|
C | A | 7 | a0003c0004t0015g0244a0003c0004t0015g0245a0003c0004t0015g0250others(4): Show | 7 | HG00741.hp1 HG01168.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.1273-1046C>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97712616 | ||||||
| chr8:97712675
|
C | A | 12 | a0001c0001t0006g0180a0001c0001t0006g0182a0001c0001t0006g0183others(9): Show | 12 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1273-987C>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97712675 | ||||||
| chr8:97712777
|
A | G | 13 | a0001c0001t0013g0259a0001c0001t0018g0132a0001c0001t0018g0133others(10): Show | 13 | HG00733.hp2 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1273-885A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97712777 | ||||||
| chr8:97712798
|
T | C | 1 | a0001c0001t0001g0101 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1273-864T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97712798 | ||||||
| chr8:97712856
|
T | C | 8 | a0001c0001t0013g0259a0001c0001t0039g0126a0001c0001t0040g0258others(5): Show | 8 | HG00733.hp2 HG01243.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1273-806T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97712856 | ||||||
| chr8:97712870
|
A | AT | 6 | a0001c0001t0016g0119a0001c0001t0016g0121a0001c0001t0016g0122others(3): Show | 6 | HG02055.hp1 HG02451.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1273-783dupT | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr8 | 97712870 | |||||
| chr8:97713001
|
A | T | 1 | a0001c0001t0002g0363 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1273-661A>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97713001 | ||||||
| chr8:97713108
|
G | A | 1 | a0001c0001t0004g0334 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1273-554G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97713108 | ||||||
| chr8:97713153
|
C | T | 1 | a0001c0001t0004g0137 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1273-509C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97713153 | ||||||
| chr8:97713268
|
G | A | 1 | a0001c0001t0039g0126 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1273-394G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97713268 | ||||||
| chr8:97713374
|
C | T | 2 | a0001c0001t0004g0274a0001c0001t0004g0275 | 2 | HG01243.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1273-288C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97713374 | ||||||
| chr8:97713416
|
C | T | 2 | a0001c0002t0089g0197a0001c0002t0090g0224 | 2 | NA18956.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.1273-246C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97713416 | ||||||
| chr8:97713504
|
T | C | 1 | a0001c0001t0024g0007 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1273-158T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 8/11 | chr8 | 97713504 | ||||||
| chr8:97713981
|
A | C | 12 | a0001c0001t0006g0180a0001c0001t0006g0182a0001c0001t0006g0183others(9): Show | 12 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1380+212A>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | chr8 | 97713981 | ||||||
| chr8:97714024
|
T | A | 1 | a0001c0001t0002g0363 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1380+255T>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | chr8 | 97714024 | ||||||
| chr8:97714025
|
A | C | 1 | a0001c0002t0003g0228 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1380+256A>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | chr8 | 97714025 | ||||||
| chr8:97714104
|
G | A | 2 | a0001c0001t0051g0251a0001c0001t0052g0252 | 2 | HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1380+335G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | chr8 | 97714104 | ||||||
| chr8:97714117
|
A | G | 3 | a0001c0001t0019g0108a0001c0001t0019g0109a0001c0001t0019g0110 | 3 | HG02622.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1380+348A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | chr8 | 97714117 | ||||||
| chr8:97714162
|
G | A | 1 | a0001c0001t0065g0167 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1380+393G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | chr8 | 97714162 | ||||||
| chr8:97714454
|
A | T | 1 | a0001c0001t0004g0136 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1380+685A>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | chr8 | 97714454 | ||||||
| chr8:97714466
|
C | T | 1 | a0004c0008t0002g0001 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1380+697C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | chr8 | 97714466 | ||||||
| chr8:97714476
|
C | T | 1 | a0001c0001t0009g0052 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1380+707C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | chr8 | 97714476 | ||||||
| chr8:97714489
|
AG | A | 99 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(96): Show | 99 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.1380+721delG | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | chr8 | 97714489 | ||||||
| chr8:97714596
|
A | C | 100 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(97): Show | 100 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.1380+827A>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | chr8 | 97714596 | ||||||
| chr8:97714604
|
C | CA | 13 | a0001c0001t0013g0259a0001c0001t0018g0132a0001c0001t0018g0133others(10): Show | 13 | HG00733.hp2 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1380+849dupA | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr8 | 97714604 | |||||
| chr8:97714619
|
G | A | 13 | a0001c0001t0013g0259a0001c0001t0018g0132a0001c0001t0018g0133others(10): Show | 13 | HG00733.hp2 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1380+850G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | chr8 | 97714619 | ||||||
| chr8:97714657
|
T | C | 1 | a0001c0001t0002g0266 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1380+888T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | chr8 | 97714657 | ||||||
| chr8:97714905
|
A | G | 91 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(88): Show | 91 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.1380+1136A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | chr8 | 97714905 | ||||||
| chr8:97715068
|
G | A | 2 | a0001c0001t0001g0058a0001c0001t0001g0064 | 2 | HG02602.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1380+1299G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | chr8 | 97715068 | ||||||
| chr8:97715190
|
T | C | 225 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(222): Show | 225 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(222): Show |
intron_variant | MODIFIER | c.1380+1421T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | chr8 | 97715190 | ||||||
| chr8:97715214
|
C | T | 1 | a0001c0001t0033g0342 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1380+1445C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | chr8 | 97715214 | ||||||
| chr8:97715222
|
G | T | 1 | a0001c0001t0002g0312 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1380+1453G>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | chr8 | 97715222 | ||||||
| chr8:97715363
|
G | A | 16 | a0001c0001t0006g0180a0001c0001t0006g0182a0001c0001t0006g0183others(13): Show | 16 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1380+1594G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | chr8 | 97715363 | ||||||
| chr8:97715421
|
G | A | 3 | a0001c0001t0008g0156a0001c0001t0008g0161a0001c0001t0008g0162 | 3 | HG02976.hp2 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1380+1652G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | chr8 | 97715421 | ||||||
| chr8:97715457
|
A | G | 1 | a0001c0001t0034g0118 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1380+1688A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | chr8 | 97715457 | ||||||
| chr8:97715598
|
A | G | 100 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(97): Show | 100 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.1380+1829A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | chr8 | 97715598 | ||||||
| chr8:97715845
|
C | T | 22 | a0001c0001t0004g0267a0001c0001t0004g0278a0001c0001t0004g0284others(19): Show | 22 | HG00408.hp2 HG00673.hp2 HG03831.hp1 others(19): Show |
intron_variant | MODIFIER | c.1380+2076C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | chr8 | 97715845 | ||||||
| chr8:97715988
|
A | AT | 13 | a0001c0001t0001g0100a0001c0001t0011g0141a0001c0001t0011g0143others(10): Show | 13 | HG00673.hp1 HG02129.hp1 NA18941.hp1 others(10): Show |
intron_variant | MODIFIER | c.1380+2231dupT | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr8 | 97715988 | |||||
| chr8:97715996
|
T | C | 1 | a0001c0001t0052g0252 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1380+2227T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | chr8 | 97715996 | ||||||
| chr8:97716023
|
G | A | 5 | a0001c0001t0002g0292a0001c0001t0002g0296a0001c0001t0002g0313others(2): Show | 5 | HG00741.hp2 HG01099.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.1380+2254G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | chr8 | 97716023 | ||||||
| chr8:97716119
|
G | A | 1 | a0001c0001t0040g0258 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1380+2350G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | chr8 | 97716119 | ||||||
| chr8:97716242
|
C | T | 1 | a0001c0001t0005g0014 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1380+2473C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | chr8 | 97716242 | ||||||
| chr8:97716404
|
A | T | 3 | a0001c0002t0003g0237a0001c0002t0003g0238a0001c0002t0021g0240 | 3 | NA18953.hp1 NA18991.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.1380+2635A>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | chr8 | 97716404 | ||||||
| chr8:97716525
|
T | C | 1 | a0001c0001t0002g0303 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1381-2524T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | chr8 | 97716525 | ||||||
| chr8:97716549
|
G | A | 13 | a0001c0001t0013g0259a0001c0001t0018g0132a0001c0001t0018g0133others(10): Show | 13 | HG00733.hp2 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1381-2500G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | chr8 | 97716549 | ||||||
| chr8:97716604
|
C | T | 1 | a0001c0001t0034g0118 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1381-2445C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | chr8 | 97716604 | ||||||
| chr8:97716793
|
C | T | 11 | a0001c0001t0011g0141a0001c0001t0011g0143a0001c0001t0011g0144others(8): Show | 11 | HG00673.hp1 NA18941.hp1 NA18947.hp2 others(8): Show |
intron_variant | MODIFIER | c.1381-2256C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | chr8 | 97716793 | ||||||
| chr8:97717125
|
A | G | 1 | a0001c0001t0042g0114 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1381-1924A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | chr8 | 97717125 | ||||||
| chr8:97717508
|
G | A | 8 | a0001c0001t0005g0005a0001c0001t0005g0008a0001c0001t0012g0002others(5): Show | 8 | HG02055.hp2 HG02559.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1381-1541G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | chr8 | 97717508 | ||||||
| chr8:97717580
|
C | T | 13 | a0001c0001t0006g0180a0001c0001t0006g0182a0001c0001t0006g0183others(10): Show | 13 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1381-1469C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | chr8 | 97717580 | ||||||
| chr8:97717622
|
T | TC | 17 | a0001c0001t0002g0139a0001c0001t0002g0300a0001c0001t0004g0334others(14): Show | 17 | HG00741.hp1 HG01168.hp1 HG02040.hp1 others(14): Show |
intron_variant | MODIFIER | c.1381-1415dupC | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr8 | 97717622 | |||||
| chr8:97717622
|
TC | T | 202 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0024others(199): Show | 202 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.1381-1415delC | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr8 | 97717622 | |||||
| chr8:97717631
|
C | G | 8 | a0001c0001t0008g0155a0001c0001t0008g0157a0001c0001t0008g0159others(5): Show | 8 | HG01081.hp2 HG02258.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1381-1418C>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | chr8 | 97717631 | ||||||
| chr8:97717632
|
C | G | 4 | a0001c0001t0018g0132a0001c0001t0018g0133a0001c0001t0018g0135others(1): Show | 4 | HG02615.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1381-1417C>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | chr8 | 97717632 | ||||||
| chr8:97717881
|
C | T | 1 | a0001c0001t0034g0118 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1381-1168C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | chr8 | 97717881 | ||||||
| chr8:97717926
|
T | G | 1 | a0001c0001t0008g0163 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1381-1123T>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | chr8 | 97717926 | ||||||
| chr8:97718028
|
G | A | 2 | a0001c0001t0001g0053a0001c0001t0001g0061 | 2 | HG03490.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1381-1021G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | chr8 | 97718028 | ||||||
| chr8:97718129
|
G | A | 1 | a0001c0001t0032g0093 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1381-920G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | chr8 | 97718129 | ||||||
| chr8:97718191
|
C | A | 1 | a0001c0001t0067g0348 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1381-858C>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | chr8 | 97718191 | ||||||
| chr8:97718191
|
C | T | 2 | a0005c0010t0092g0247a0008c0012t0015g0246 | 2 | HG00741.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1381-858C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | chr8 | 97718191 | ||||||
| chr8:97718262
|
C | G | 1 | a0001c0001t0002g0353 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1381-787C>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | chr8 | 97718262 | ||||||
| chr8:97718344
|
C | A | 2 | a0003c0004t0015g0250a0003c0004t0049g0249 | 2 | HG01361.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.1381-705C>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | chr8 | 97718344 | ||||||
| chr8:97718496
|
T | C | 7 | a0003c0004t0015g0244a0003c0004t0015g0245a0003c0004t0015g0250others(4): Show | 7 | HG00741.hp1 HG01168.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.1381-553T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | chr8 | 97718496 | ||||||
| chr8:97718499
|
T | G | 1 | a0001c0001t0010g0287 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1381-550T>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | chr8 | 97718499 | ||||||
| chr8:97718526
|
GT | G | 243 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(240): Show | 243 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(240): Show |
intron_variant | MODIFIER | c.1381-513delT | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr8 | 97718526 | |||||
| chr8:97718584
|
G | A | 1 | a0007c0011t0070g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1381-465G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | chr8 | 97718584 | ||||||
| chr8:97718624
|
A | G | 1 | a0001c0001t0023g0158 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1381-425A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | chr8 | 97718624 | ||||||
| chr8:97718708
|
G | GT | 23 | a0001c0001t0001g0043a0001c0001t0002g0276a0001c0001t0002g0281others(20): Show | 23 | HG01167.hp2 HG01175.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.1381-329dupT | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr8 | 97718708 | |||||
| chr8:97718711
|
T | G | 2 | a0001c0001t0051g0251a0001c0001t0052g0252 | 2 | HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1381-338T>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | chr8 | 97718711 | ||||||
| chr8:97718720
|
T | C | 1 | a0002c0003t0013g0130 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1381-329T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | chr8 | 97718720 | ||||||
| chr8:97718948
|
C | T | 5 | a0001c0001t0018g0132a0001c0001t0018g0133a0001c0001t0018g0135others(2): Show | 5 | HG02615.hp2 HG02630.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1381-101C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | chr8 | 97718948 | ||||||
| chr8:97719013
|
G | A | 2 | a0001c0001t0012g0002a0001c0001t0012g0003 | 2 | HG02055.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1381-36G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 9/11 | chr8 | 97719013 | ||||||
| chr8:97719350
|
G | A | 16 | a0001c0001t0006g0180a0001c0001t0006g0182a0001c0001t0006g0183others(13): Show | 16 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1521+161G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 10/11 | chr8 | 97719350 | ||||||
| chr8:97719442
|
G | A | 2 | a0001c0001t0004g0137a0001c0001t0004g0138 | 2 | HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1521+253G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 10/11 | chr8 | 97719442 | ||||||
| chr8:97719486
|
C | T | 93 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(90): Show | 93 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.1521+297C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 10/11 | chr8 | 97719486 | ||||||
| chr8:97719492
|
C | CA | 43 | a0001c0001t0002g0264a0001c0001t0002g0313a0001c0001t0002g0341others(40): Show | 43 | HG01081.hp2 HG01168.hp1 HG01192.hp1 others(40): Show |
intron_variant | MODIFIER | c.1521+323dupA | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr8 | 97719492 | |||||
| chr8:97719492
|
C | CAA | 46 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0008others(43): Show | 46 | HG00673.hp1 HG00733.hp1 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.1521+322_1521+323d others(4): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr8 | 97719492 | |||||
| chr8:97719492
|
C | CAAA | 12 | a0001c0001t0005g0004a0001c0001t0005g0112a0001c0001t0005g0113others(9): Show | 12 | HG00738.hp2 HG01109.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.1521+321_1521+323d others(5): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr8 | 97719492 | |||||
| chr8:97719492
|
CA | C | 6 | a0001c0001t0001g0075a0001c0001t0001g0092a0001c0001t0002g0319others(3): Show | 6 | HG00558.hp1 HG01168.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.1521+323delA | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr8 | 97719492 | |||||
| chr8:97719492
|
CAAAA | C | 66 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0175others(63): Show | 66 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.1521+320_1521+323d others(6): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr8 | 97719492 | |||||
| chr8:97719619
|
G | A | 4 | a0003c0004t0015g0244a0003c0004t0015g0245a0005c0010t0092g0247others(1): Show | 4 | HG00741.hp1 HG03491.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.1521+430G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 10/11 | chr8 | 97719619 | ||||||
| chr8:97719635
|
G | A | 99 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(96): Show | 99 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.1521+446G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 10/11 | chr8 | 97719635 | ||||||
| chr8:97719868
|
G | A | 2 | a0001c0001t0027g0315a0001c0001t0027g0318 | 2 | HG01070.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.1521+679G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 10/11 | chr8 | 97719868 | ||||||
| chr8:97720013
|
G | GT | 100 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(97): Show | 100 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.1521+825dupT | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr8 | 97720013 | |||||
| chr8:97720016
|
G | A | 21 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0006others(18): Show | 21 | HG00733.hp1 HG00738.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1521+827G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 10/11 | chr8 | 97720016 | ||||||
| chr8:97720053
|
A | G | 252 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(249): Show | 252 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(249): Show |
intron_variant | MODIFIER | c.1521+864A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 10/11 | chr8 | 97720053 | ||||||
| chr8:97720138
|
G | A | 12 | a0001c0001t0006g0180a0001c0001t0006g0182a0001c0001t0006g0183others(9): Show | 12 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1521+949G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 10/11 | chr8 | 97720138 | ||||||
| chr8:97720454
|
G | A | 91 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(88): Show | 91 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.1521+1265G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 10/11 | chr8 | 97720454 | ||||||
| chr8:97720522
|
G | A | 1 | a0001c0001t0034g0118 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1521+1333G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 10/11 | chr8 | 97720522 | ||||||
| chr8:97720552
|
G | A | 107 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0175others(104): Show | 107 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.1521+1363G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 10/11 | chr8 | 97720552 | ||||||
| chr8:97720576
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1521+1387G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 10/11 | chr8 | 97720576 | ||||||
| chr8:97720585
|
A | ATATT | 23 | a0001c0001t0001g0051a0001c0001t0001g0091a0001c0001t0005g0004others(20): Show | 23 | HG00733.hp1 HG00738.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1521+1399_1521+140 others(8): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr8 | 97720585 | |||||
| chr8:97720585
|
A | T | 14 | a0001c0001t0008g0155a0001c0001t0008g0156a0001c0001t0008g0157others(11): Show | 14 | HG01081.hp2 HG01891.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1521+1396A>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 10/11 | chr8 | 97720585 | ||||||
| chr8:97720589
|
A | T | 252 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(249): Show | 252 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(249): Show |
intron_variant | MODIFIER | c.1521+1400A>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 10/11 | chr8 | 97720589 | ||||||
| chr8:97720593
|
T | A | 2 | a0001c0001t0014g0367a0001c0001t0014g0369 | 2 | NA18973.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1521+1404T>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 10/11 | chr8 | 97720593 | ||||||
| chr8:97720609
|
G | A | 13 | a0001c0001t0013g0259a0001c0001t0018g0132a0001c0001t0018g0133others(10): Show | 13 | HG00733.hp2 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1521+1420G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 10/11 | chr8 | 97720609 | ||||||
| chr8:97720646
|
C | CT | 211 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(208): Show | 211 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(208): Show |
intron_variant | MODIFIER | c.1521+1474dupT | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr8 | 97720646 | |||||
| chr8:97720646
|
C | CTT | 21 | a0001c0001t0001g0043a0001c0001t0001g0078a0001c0001t0013g0259others(18): Show | 21 | HG00733.hp2 HG00741.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.1521+1473_1521+147 others(6): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr8 | 97720646 | |||||
| chr8:97720797
|
G | A | 2 | a0001c0001t0001g0106a0001c0001t0045g0105 | 2 | HG01081.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1521+1608G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 10/11 | chr8 | 97720797 | ||||||
| chr8:97720890
|
G | A | 4 | a0001c0001t0022g0192a0001c0005t0022g0193a0001c0005t0022g0195others(1): Show | 4 | HG02145.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1521+1701G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 10/11 | chr8 | 97720890 | ||||||
| chr8:97721053
|
G | C | 5 | a0001c0001t0018g0132a0001c0001t0018g0133a0001c0001t0018g0135others(2): Show | 5 | HG02615.hp2 HG02630.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1522-1826G>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 10/11 | chr8 | 97721053 | ||||||
| chr8:97721218
|
G | T | 1 | a0001c0001t0034g0118 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1522-1661G>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 10/11 | chr8 | 97721218 | ||||||
| chr8:97721232
|
A | G | 2 | a0001c0002t0003g0227a0001c0002t0003g0229 | 2 | NA18971.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1522-1647A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 10/11 | chr8 | 97721232 | ||||||
| chr8:97721327
|
C | G | 1 | a0001c0001t0067g0348 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1522-1552C>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 10/11 | chr8 | 97721327 | ||||||
| chr8:97721541
|
AT | A | 13 | a0001c0001t0013g0259a0001c0001t0018g0132a0001c0001t0018g0133others(10): Show | 13 | HG00733.hp2 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1522-1334delT | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr8 | 97721541 | |||||
| chr8:97722044
|
A | ACAAAAAT others(8): Show |
1 | a0001c0001t0064g0285 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1522-833_1522-819d others(17): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr8 | 97722044 | |||||
| chr8:97722072
|
G | A | 1 | a0003c0004t0015g0244 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1522-807G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 10/11 | chr8 | 97722072 | ||||||
| chr8:97722250
|
G | A | 2 | a0001c0002t0003g0207a0001c0002t0003g0209 | 2 | HG00423.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.1522-629G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 10/11 | chr8 | 97722250 | ||||||
| chr8:97722262
|
CAAAAA | C | 27 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0006others(24): Show | 27 | HG00733.hp1 HG00738.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.1522-615_1522-611d others(7): Show |
MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr8 | 97722262 | |||||
| chr8:97722307
|
A | T | 1 | a0007c0011t0070g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1522-572A>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 10/11 | chr8 | 97722307 | ||||||
| chr8:97722328
|
G | A | 1 | a0001c0002t0003g0203 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1522-551G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 10/11 | chr8 | 97722328 | ||||||
| chr8:97722386
|
A | G | 7 | a0003c0004t0015g0244a0003c0004t0015g0245a0003c0004t0015g0250others(4): Show | 7 | HG00741.hp1 HG01168.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.1522-493A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 10/11 | chr8 | 97722386 | ||||||
| chr8:97722463
|
G | T | 1 | a0003c0004t0015g0245 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1522-416G>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 10/11 | chr8 | 97722463 | ||||||
| chr8:97722533
|
C | T | 1 | a0001c0001t0034g0118 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1522-346C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 10/11 | chr8 | 97722533 | ||||||
| chr8:97722588
|
T | C | 223 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(220): Show | 223 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(220): Show |
intron_variant | MODIFIER | c.1522-291T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 10/11 | chr8 | 97722588 | ||||||
| chr8:97723164
|
C | T | 1 | a0001c0001t0002g0257 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1678+129C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 11/11 | chr8 | 97723164 | ||||||
| chr8:97723226
|
G | A | 15 | a0001c0001t0006g0180a0001c0001t0006g0182a0001c0001t0006g0183others(12): Show | 15 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1678+191G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 11/11 | chr8 | 97723226 | ||||||
| chr8:97723263
|
C | T | 2 | a0001c0001t0051g0251a0001c0001t0052g0252 | 2 | HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1678+228C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 11/11 | chr8 | 97723263 | ||||||
| chr8:97723279
|
T | A | 1 | a0001c0001t0034g0118 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1678+244T>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 11/11 | chr8 | 97723279 | ||||||
| chr8:97723310
|
A | G | 3 | a0001c0005t0022g0193a0001c0005t0022g0195a0001c0005t0085g0194 | 3 | HG02145.hp2 HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1678+275A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 11/11 | chr8 | 97723310 | ||||||
| chr8:97723323
|
G | A | 22 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0006others(19): Show | 22 | HG00733.hp1 HG00738.hp2 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1678+288G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 11/11 | chr8 | 97723323 | ||||||
| chr8:97723392
|
C | T | 1 | a0001c0001t0034g0118 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1678+357C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 11/11 | chr8 | 97723392 | ||||||
| chr8:97723397
|
C | CA | 24 | a0001c0001t0001g0064a0001c0001t0002g0263a0001c0001t0002g0295others(21): Show | 24 | HG00639.hp1 HG01081.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.1678+373dupA | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr8 | 97723397 | |||||
| chr8:97723515
|
G | A | 1 | a0001c0001t0086g0166 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1678+480G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 11/11 | chr8 | 97723515 | ||||||
| chr8:97723559
|
T | C | 90 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(87): Show | 90 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.1678+524T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 11/11 | chr8 | 97723559 | ||||||
| chr8:97723592
|
G | A | 280 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0022others(277): Show | 280 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(277): Show |
intron_variant | MODIFIER | c.1678+557G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 11/11 | chr8 | 97723592 | ||||||
| chr8:97723606
|
G | A | 12 | a0001c0001t0008g0155a0001c0001t0008g0156a0001c0001t0008g0157others(9): Show | 12 | HG01081.hp2 HG02258.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1678+571G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 11/11 | chr8 | 97723606 | ||||||
| chr8:97723612
|
A | G | 14 | a0001c0001t0001g0068a0001c0001t0008g0155a0001c0001t0008g0156others(11): Show | 14 | HG01081.hp2 HG02258.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.1678+577A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 11/11 | chr8 | 97723612 | ||||||
| chr8:97723616
|
A | G | 12 | a0001c0001t0008g0155a0001c0001t0008g0156a0001c0001t0008g0157others(9): Show | 12 | HG01081.hp2 HG02258.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1678+581A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 11/11 | chr8 | 97723616 | ||||||
| chr8:97723629
|
G | C | 1 | a0001c0001t0001g0078 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1678+594G>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 11/11 | chr8 | 97723629 | ||||||
| chr8:97723714
|
A | G | 66 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0175others(63): Show | 66 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.1678+679A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 11/11 | chr8 | 97723714 | ||||||
| chr8:97723716
|
C | T | 1 | a0001c0001t0073g0149 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1678+681C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 11/11 | chr8 | 97723716 | ||||||
| chr8:97723742
|
C | CA | 7 | a0001c0001t0019g0108a0001c0001t0019g0109a0001c0001t0019g0110others(4): Show | 7 | HG02145.hp2 HG02622.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1678+717dupA | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr8 | 97723742 | |||||
| chr8:97723766
|
A | T | 1 | a0001c0001t0064g0285 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1678+731A>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 11/11 | chr8 | 97723766 | ||||||
| chr8:97723837
|
G | A | 1 | a0001c0001t0001g0072 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1679-763G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 11/11 | chr8 | 97723837 | ||||||
| chr8:97723914
|
C | T | 1 | a0001c0001t0004g0286 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1679-686C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 11/11 | chr8 | 97723914 | ||||||
| chr8:97723928
|
C | T | 1 | a0001c0001t0001g0057 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1679-672C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 11/11 | chr8 | 97723928 | ||||||
| chr8:97723978
|
G | A | 4 | a0001c0001t0022g0192a0001c0005t0022g0193a0001c0005t0022g0195others(1): Show | 4 | HG02145.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1679-622G>A | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 11/11 | chr8 | 97723978 | ||||||
| chr8:97724155
|
C | T | 1 | a0001c0001t0034g0118 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1679-445C>T | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 11/11 | chr8 | 97724155 | ||||||
| chr8:97724375
|
A | G | 3 | a0001c0001t0019g0108a0001c0001t0019g0109a0001c0001t0019g0110 | 3 | HG02622.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1679-225A>G | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 11/11 | chr8 | 97724375 | ||||||
| chr8:97724448
|
T | C | 77 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0175others(74): Show | 77 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.1679-152T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 11/11 | chr8 | 97724448 | ||||||
| chr8:97724594
|
T | C | 11 | a0001c0001t0011g0141a0001c0001t0011g0143a0001c0001t0011g0144others(8): Show | 11 | HG00673.hp1 NA18941.hp1 NA18947.hp2 others(8): Show |
splice_region_variant&intron_variant | LOW | c.1679-6T>C | MTDH | ENSG00000147649.10 | transcript | ENST00000336273.8 | protein_coding | 11/11 | chr8 | 97724594 |