Item | Value |
---|---|
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 | MAARS others(577): Show |
chr8 | 97639184 | 97735260 |
a0002 | 0/0 | 582 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | MAARS others(577): Show |
chr8 | 97639184 | 97735260 |
a0003 | 0/0 | 582 | 5 | 0 | 3 | 0 | 0 | 2 | 0 | MTDH_chr8_97639184_97735260 | MTDH | MAARS others(577): Show |
chr8 | 97639184 | 97735260 |
a0004 | 0/0 | 582 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | MAARS others(577): Show |
chr8 | 97639184 | 97735260 |
a0005 | 0/0 | 582 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | MAARS others(577): Show |
chr8 | 97639184 | 97735260 |
a0006 | 0/0 | 582 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | MAARS others(577): Show |
chr8 | 97639184 | 97735260 |
a0007 | 0/0 | 582 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MTDH_chr8_97639184_97735260 | MTDH | MAARS others(577): Show |
chr8 | 97639184 | 97735260 |
a0008 | 0/0 | 582 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | MAARS others(577): Show |
chr8 | 97639184 | 97735260 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1746 | 299 | 81 | 45 | 136 | 6 | 29 | MTDH_chr8_97639184_97735260 | MTDH | ATGGC others(1741): Show |
chr8 | 97639184 | 97735260 | ||
a0001c0002 | 0/0 | 1746 | 49 | 1 | 10 | 31 | 0 | 7 | MTDH_chr8_97639184_97735260 | MTDH | ATGGC others(1741): Show |
chr8 | 97639184 | 97735260 | ||
a0001c0005 | 0/0 | 1746 | 3 | 3 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | ATGGC others(1741): Show |
chr8 | 97639184 | 97735260 | ||
a0001c0006 | 0/0 | 1746 | 2 | 0 | 0 | 1 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | ATGGC others(1741): Show |
chr8 | 97639184 | 97735260 | ||
a0001c0007 | 0/0 | 1746 | 2 | 2 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | ATGGC others(1741): Show |
chr8 | 97639184 | 97735260 | ||
a0002c0003 | 0/0 | 1746 | 5 | 4 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | ATGGC others(1741): Show |
chr8 | 97639184 | 97735260 | ||
a0003c0004 | 0/0 | 1746 | 5 | 0 | 3 | 0 | 0 | 2 | MTDH_chr8_97639184_97735260 | MTDH | ATGGC others(1741): Show |
chr8 | 97639184 | 97735260 | ||
a0004c0010 | 0/0 | 1746 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | ATGGC others(1741): Show |
chr8 | 97639184 | 97735260 | ||
a0005c0011 | 0/0 | 1746 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | ATGGC others(1741): Show |
chr8 | 97639184 | 97735260 | ||
a0006c0009 | 0/0 | 1746 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | ATGGC others(1741): Show |
chr8 | 97639184 | 97735260 | ||
a0007c0012 | 0/0 | 1746 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | ATGGC others(1741): Show |
chr8 | 97639184 | 97735260 | ||
a0008c0008 | 0/0 | 1746 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | ATGGC others(1741): Show |
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 | AAGCC others(7665): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0002 | 1/0 | 7662 | 59 | 2 | 14 | 32 | 3 | 7 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7657): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0003 | 0/0 | 7670 | 5 | 0 | 2 | 0 | 0 | 3 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7665): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0004 | 0/0 | 7661 | 27 | 5 | 6 | 15 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7656): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0005 | 0/0 | 7661 | 12 | 11 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7656): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0006 | 0/0 | 7668 | 10 | 10 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7663): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0007 | 0/0 | 7671 | 2 | 0 | 0 | 2 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7666): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0008 | 0/0 | 7671 | 8 | 7 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7666): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0009 | 0/0 | 7671 | 6 | 0 | 0 | 6 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7666): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0010 | 0/0 | 7662 | 6 | 0 | 1 | 4 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7657): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0011 | 0/0 | 7671 | 6 | 1 | 0 | 5 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7666): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0012 | 0/0 | 7661 | 6 | 6 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7656): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0013 | 0/0 | 7671 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7666): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0014 | 0/0 | 7663 | 5 | 0 | 0 | 5 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7658): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0016 | 0/0 | 7662 | 4 | 4 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7657): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0017 | 0/0 | 7671 | 3 | 0 | 0 | 3 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7666): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0018 | 0/0 | 7671 | 3 | 3 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7666): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0019 | 0/0 | 7663 | 3 | 3 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7658): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0020 | 0/0 | 7671 | 3 | 0 | 0 | 1 | 1 | 1 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7666): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0021 | 0/0 | 7671 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7666): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0022 | 0/0 | 7667 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7662): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0023 | 0/0 | 7671 | 3 | 3 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7666): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0024 | 0/0 | 7670 | 3 | 0 | 1 | 0 | 0 | 2 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7665): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0025 | 0/0 | 7662 | 2 | 0 | 2 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7657): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0026 | 0/0 | 7663 | 2 | 0 | 0 | 2 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7658): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0027 | 0/0 | 7671 | 2 | 0 | 0 | 2 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7666): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0028 | 0/0 | 7662 | 2 | 0 | 2 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7657): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0029 | 0/0 | 7661 | 2 | 0 | 0 | 0 | 0 | 2 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7656): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0030 | 0/0 | 7670 | 2 | 0 | 0 | 2 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7665): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0031 | 0/0 | 7672 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7667): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0032 | 0/0 | 7671 | 2 | 2 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7666): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0033 | 0/0 | 7662 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7657): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0034 | 0/0 | 7672 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7667): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0036 | 0/0 | 7671 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7666): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0037 | 0/0 | 7670 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7665): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0038 | 0/0 | 7672 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7667): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0039 | 0/0 | 7672 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7667): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0040 | 0/0 | 7672 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7667): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0041 | 0/0 | 7672 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7667): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0042 | 0/0 | 7662 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7657): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0043 | 0/0 | 7673 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7668): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0044 | 0/0 | 7671 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7666): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0045 | 0/0 | 7670 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7665): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0046 | 0/0 | 7670 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7665): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0047 | 0/0 | 7672 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7667): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0048 | 0/0 | 7669 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7664): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0050 | 0/0 | 7672 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7667): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0051 | 0/0 | 7670 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7665): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0052 | 0/0 | 7671 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7666): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0054 | 0/0 | 7669 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7664): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0055 | 0/0 | 7668 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7663): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0056 | 0/0 | 7668 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7663): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0057 | 0/0 | 7663 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7658): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0058 | 0/0 | 7663 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7658): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0059 | 0/0 | 7664 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7659): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0060 | 0/0 | 7661 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7656): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0061 | 0/0 | 7663 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7658): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0062 | 0/0 | 7664 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7659): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0064 | 0/0 | 7659 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7654): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0065 | 0/0 | 7663 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7658): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0066 | 0/0 | 7662 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7657): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0067 | 0/0 | 7661 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7656): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0068 | 0/0 | 7661 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7656): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0069 | 0/0 | 7663 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7658): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0071 | 0/0 | 7663 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7658): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0072 | 0/0 | 7669 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7664): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0073 | 0/0 | 7663 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7658): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0076 | 0/0 | 7670 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7665): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0079 | 0/0 | 7669 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7664): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0083 | 0/0 | 7662 | 1 | 0 | 0 | 0 | 1 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7657): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0084 | 0/0 | 7661 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7656): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0086 | 0/0 | 7671 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7666): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0087 | 0/1 | 7662 | 1 | 0 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7657): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0088 | 0/0 | 7668 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7663): Show |
chr8 | 97639184 | 97735260 |
a0001c0001t0091 | 0/0 | 7671 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7666): Show |
chr8 | 97639184 | 97735260 |
a0001c0002t0003 | 0/0 | 7670 | 31 | 1 | 3 | 22 | 0 | 5 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7665): Show |
chr8 | 97639184 | 97735260 |
a0001c0002t0007 | 0/0 | 7671 | 6 | 0 | 4 | 1 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7666): Show |
chr8 | 97639184 | 97735260 |
a0001c0002t0021 | 0/0 | 7671 | 2 | 0 | 0 | 2 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7666): Show |
chr8 | 97639184 | 97735260 |
a0001c0002t0031 | 0/0 | 7672 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7667): Show |
chr8 | 97639184 | 97735260 |
a0001c0002t0074 | 0/0 | 7673 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7668): Show |
chr8 | 97639184 | 97735260 |
a0001c0002t0075 | 0/0 | 7671 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7666): Show |
chr8 | 97639184 | 97735260 |
a0001c0002t0077 | 0/0 | 7671 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7666): Show |
chr8 | 97639184 | 97735260 |
a0001c0002t0078 | 0/0 | 7670 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7665): Show |
chr8 | 97639184 | 97735260 |
a0001c0002t0080 | 0/0 | 7663 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7658): Show |
chr8 | 97639184 | 97735260 |
a0001c0002t0081 | 0/0 | 7662 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7657): Show |
chr8 | 97639184 | 97735260 |
a0001c0002t0082 | 0/0 | 7662 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7657): Show |
chr8 | 97639184 | 97735260 |
a0001c0002t0089 | 0/0 | 7670 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7665): Show |
chr8 | 97639184 | 97735260 |
a0001c0002t0090 | 0/0 | 7671 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7666): Show |
chr8 | 97639184 | 97735260 |
a0001c0005t0022 | 0/0 | 7667 | 2 | 2 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7662): Show |
chr8 | 97639184 | 97735260 |
a0001c0005t0085 | 0/0 | 7660 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7655): Show |
chr8 | 97639184 | 97735260 |
a0001c0006t0004 | 0/0 | 7661 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7656): Show |
chr8 | 97639184 | 97735260 |
a0001c0006t0063 | 0/0 | 7661 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7656): Show |
chr8 | 97639184 | 97735260 |
a0001c0007t0003 | 0/0 | 7670 | 2 | 2 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7665): Show |
chr8 | 97639184 | 97735260 |
a0002c0003t0013 | 0/0 | 7671 | 4 | 3 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7666): Show |
chr8 | 97639184 | 97735260 |
a0002c0003t0035 | 0/0 | 7671 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7666): Show |
chr8 | 97639184 | 97735260 |
a0003c0004t0015 | 0/0 | 7670 | 3 | 0 | 1 | 0 | 0 | 2 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7665): Show |
chr8 | 97639184 | 97735260 |
a0003c0004t0049 | 0/0 | 7671 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7666): Show |
chr8 | 97639184 | 97735260 |
a0003c0004t0053 | 0/0 | 7669 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7664): Show |
chr8 | 97639184 | 97735260 |
a0004c0010t0092 | 0/0 | 7670 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7665): Show |
chr8 | 97639184 | 97735260 |
a0005c0011t0070 | 0/0 | 7669 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7664): Show |
chr8 | 97639184 | 97735260 |
a0006c0009t0003 | 0/0 | 7670 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7665): Show |
chr8 | 97639184 | 97735260 |
a0007c0012t0015 | 0/0 | 7670 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7665): Show |
chr8 | 97639184 | 97735260 |
a0008c0008t0002 | 0/0 | 7662 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | AAGCC others(7657): Show |
chr8 | 97639184 | 97735260 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0001g0037 | 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 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0001g0047 | 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 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0001g0053 | 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 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 1 | 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 | 1 | 0 | 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 |
a0001c0001t0001g0074 | 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 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0001g0083 | 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 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 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 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0002g0003 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 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 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0001t0002g0271 | 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 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0002g0279 | 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 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0002g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0002g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0002g0340 | 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 |
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 |
a0001c0001t0002g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0002g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0002g0351 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0002g0355 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0002g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0002g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 |
a0001c0001t0002g0360 | 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 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0003g0254 | 0/0 | 1 | 0 | 1 | 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 |
a0001c0001t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0004g0273 | 0/0 | 1 | 0 | 1 | 0 | 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 |
a0001c0001t0004g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0004g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0004g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0004g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0004g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0004g0306 | 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 |
a0001c0001t0004g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0004g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0004g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0004g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0004g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0004g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0004g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0004g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0004g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0004g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0004g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0005g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0005g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0005g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0005g0012 | 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 |
a0001c0001t0005g0016 | 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 |
a0001c0001t0005g0114 | 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 |
a0001c0001t0005g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0005g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0006g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0006g0181 | 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 |
a0001c0001t0006g0186 | 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 |
a0001c0001t0007g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0007g0173 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0001t0008g0158 | 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 |
a0001c0001t0008g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0008g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0008g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0008g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0009g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0009g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0009g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0009g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0009g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0009g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0010g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0010g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0010g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0010g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0010g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0010g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0011g0142 | 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 |
a0001c0001t0011g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0011g0147 | 0/0 | 1 | 1 | 0 | 0 | 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 |
a0001c0001t0011g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0012g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0012g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0012g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0012g0009 | 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 |
a0001c0001t0012g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0013g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0014g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0014g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0014g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0014g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0014g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0016g0120 | 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 |
a0001c0001t0016g0124 | 0/0 | 1 | 1 | 0 | 0 | 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 |
a0001c0001t0017g0040 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0001t0018g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0018g0136 | 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 |
a0001c0001t0019g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0020g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0020g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0020g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0021g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0022g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0023g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0023g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0023g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0024g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0024g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0024g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0025g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0025g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0026g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0026g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0027g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0027g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0028g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0028g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0029g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0029g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0030g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0030g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0031g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0032g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0032g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0033g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0034g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0036g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0037g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0038g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0039g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0040g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0041g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0042g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0043g0041 | 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 |
a0001c0001t0045g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0046g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0047g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0048g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0050g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0051g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0052g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0054g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0055g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0056g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0057g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0058g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0059g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0060g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0061g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0062g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0064g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0065g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0066g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0067g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0068g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0069g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0071g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0072g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0073g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0076g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0079g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0083g0367 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0084g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0086g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0087g0327 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0088g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0001t0091g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0002t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0002t0003g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0002t0003g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0002t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0002t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0002t0003g0211 | 0/0 | 1 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0002t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0002t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0002t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0002t0003g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0002t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
a0001c0002t0003g0233 | 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 |
a0001c0002t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0002t0003g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
a0001c0002t0007g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 |
a0001c0002t0007g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0002t0007g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0002t0007g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0002t0021g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0002t0021g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0002t0031g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0002t0074g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0002t0075g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0002t0077g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0002t0078g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0002t0080g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0002t0081g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0002t0082g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0002t0089g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0002t0090g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0005t0022g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0005t0022g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0005t0085g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0006t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0001c0006t0063g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
a0001c0007t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0002c0003t0013g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0002c0003t0013g0129 | 0/0 | 1 | 0 | 1 | 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 |
a0002c0003t0013g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0002c0003t0035g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0003c0004t0015g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
a0003c0004t0015g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0003c0004t0049g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0003c0004t0053g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0004c0010t0092g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0005c0011t0070g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0006c0009t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0007c0012t0015g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
a0008c0008t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | g0003 | EUR | GBR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG00140 | hp2 | a0001 | c0001 | t0020 | g0024 | 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 | g0307 | EAS | CHS | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG00423 | hp2 | a0001 | c0002 | t0003 | g0202 | EAS | CHS | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | CHS | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG00558 | hp2 | a0001 | c0002 | t0003 | g0219 | EAS | CHS | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG00597 | hp1 | a0001 | c0001 | t0026 | g0364 | EAS | CHS | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG00597 | hp2 | a0001 | c0001 | t0043 | g0041 | EAS | CHS | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | CHS | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG00609 | hp2 | a0001 | c0002 | t0003 | g0240 | EAS | CHS | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG00621 | hp2 | a0001 | c0002 | t0003 | g0221 | EAS | CHS | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0326 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG00642 | hp2 | a0001 | c0001 | t0004 | g0334 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG00673 | hp1 | a0001 | c0001 | t0011 | g0149 | EAS | CHS | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG00673 | hp2 | a0001 | c0006 | t0004 | g0260 | EAS | CHS | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG00733 | hp1 | a0001 | c0001 | t0025 | g0017 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG00733 | hp2 | a0002 | c0003 | t0013 | g0129 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG00735 | hp1 | a0001 | c0002 | t0003 | g0211 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG00735 | hp2 | a0001 | c0001 | t0076 | g0175 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG00738 | hp1 | a0001 | c0001 | t0084 | g0312 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG00738 | hp2 | a0001 | c0001 | t0025 | g0013 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG00741 | hp1 | a0004 | c0010 | t0092 | g0246 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0319 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG01070 | hp1 | a0001 | c0001 | t0028 | g0321 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG01070 | hp2 | a0001 | c0001 | t0004 | g0333 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG01074 | hp1 | a0001 | c0001 | t0028 | g0320 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0256 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG01081 | hp1 | a0001 | c0001 | t0045 | g0106 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG01081 | hp2 | a0001 | c0001 | t0008 | g0165 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0291 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG01099 | hp2 | a0001 | c0001 | t0091 | g0033 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG01109 | hp1 | a0001 | c0002 | t0074 | g0210 | 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 | g0254 | 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 | g0247 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0340 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0275 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0174 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0263 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG01243 | hp1 | a0001 | c0001 | t0004 | g0273 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG01243 | hp2 | a0001 | c0001 | t0040 | g0257 | AMR | PUR | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0141 | AMR | CLM | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG01255 | hp2 | a0001 | c0001 | t0004 | g0285 | AMR | CLM | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG01258 | hp2 | a0001 | c0001 | t0004 | g0293 | AMR | CLM | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | CLM | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0295 | AMR | CLM | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG01361 | hp1 | a0003 | c0004 | t0049 | g0248 | AMR | CLM | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG01361 | hp2 | a0001 | c0001 | t0010 | g0286 | AMR | CLM | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG01496 | hp1 | a0003 | c0004 | t0015 | g0249 | AMR | CLM | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG01496 | hp2 | a0001 | c0002 | t0007 | g0197 | AMR | CLM | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0103 | EUR | IBS | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG01516 | hp2 | a0001 | c0001 | t0083 | g0367 | EUR | IBS | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG01884 | hp1 | a0002 | c0003 | t0035 | g0126 | AFR | ACB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG01884 | hp2 | a0001 | c0001 | t0004 | g0137 | AFR | ACB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG01891 | hp1 | a0005 | c0011 | t0070 | g0019 | AFR | ACB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG01891 | hp2 | a0001 | c0001 | t0005 | g0118 | AFR | ACB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG01934 | hp1 | a0001 | c0002 | t0031 | g0216 | AMR | PEL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG01934 | hp2 | a0001 | c0001 | t0004 | g0332 | AMR | PEL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG01952 | hp1 | a0001 | c0002 | t0003 | g0204 | AMR | PEL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG01978 | hp2 | a0001 | c0001 | t0024 | g0034 | AMR | PEL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG01981 | hp1 | a0001 | c0002 | t0007 | g0199 | AMR | PEL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0262 | AMR | PEL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02004 | hp1 | a0001 | c0002 | t0003 | g0212 | AMR | PEL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02004 | hp2 | a0001 | c0001 | t0079 | g0153 | AMR | PEL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02027 | hp1 | a0001 | c0002 | t0007 | g0231 | EAS | KHV | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0347 | EAS | KHV | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | KHV | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02040 | hp2 | a0001 | c0002 | t0003 | g0200 | EAS | KHV | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02055 | hp1 | a0001 | c0001 | t0016 | g0124 | AFR | ACB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02055 | hp2 | a0001 | c0001 | t0012 | g0006 | AFR | ACB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02056 | hp1 | a0001 | c0002 | t0077 | g0220 | EAS | KHV | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02056 | hp2 | a0001 | c0001 | t0047 | g0049 | EAS | KHV | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | KHV | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02132 | hp1 | a0001 | c0002 | t0003 | g0215 | EAS | KHV | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02132 | hp2 | a0001 | c0001 | t0020 | g0079 | EAS | KHV | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02145 | hp1 | a0001 | c0001 | t0042 | g0115 | AFR | ACB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02145 | hp2 | a0001 | c0005 | t0022 | g0192 | AFR | ACB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02148 | hp1 | a0001 | c0002 | t0075 | g0195 | AMR | PEL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0264 | AMR | PEL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | CDX | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02155 | hp2 | a0006 | c0009 | t0003 | g0232 | EAS | CDX | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | CDX | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | CDX | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02257 | hp2 | a0001 | c0001 | t0006 | g0181 | AFR | ACB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02258 | hp1 | a0001 | c0001 | t0005 | g0011 | AFR | ACB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02258 | hp2 | a0001 | c0001 | t0008 | g0160 | AFR | ACB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0279 | AMR | PEL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02273 | hp2 | a0001 | c0002 | t0007 | g0218 | AMR | PEL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02280 | hp1 | a0001 | c0001 | t0004 | g0282 | AFR | ACB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02280 | hp2 | a0001 | c0001 | t0006 | g0186 | AFR | ACB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02293 | hp1 | a0001 | c0002 | t0007 | g0198 | AMR | PEL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0265 | AMR | PEL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02451 | hp1 | a0001 | c0001 | t0057 | g0125 | AFR | ACB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0317 | AFR | ACB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02572 | hp1 | a0001 | c0007 | t0003 | g0154 | AFR | GWD | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02572 | hp2 | a0001 | c0001 | t0012 | g0008 | AFR | GWD | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0318 | SAS | PJL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02615 | hp1 | a0001 | c0001 | t0039 | g0127 | AFR | GWD | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02615 | hp2 | a0001 | c0001 | t0018 | g0136 | AFR | GWD | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02622 | hp1 | a0001 | c0001 | t0068 | g0314 | AFR | GWD | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02622 | hp2 | a0001 | c0001 | t0019 | g0109 | 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 | g0132 | AFR | GWD | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02647 | hp1 | a0001 | c0005 | t0022 | g0194 | AFR | GWD | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02647 | hp2 | a0001 | c0001 | t0058 | g0123 | AFR | GWD | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02683 | hp1 | a0001 | c0001 | t0033 | g0339 | SAS | PJL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02683 | hp2 | a0001 | c0002 | t0078 | g0214 | SAS | PJL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02717 | hp1 | a0001 | c0001 | t0018 | g0134 | AFR | GWD | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02717 | hp2 | a0001 | c0001 | t0006 | g0184 | AFR | GWD | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02723 | hp1 | a0001 | c0001 | t0056 | g0112 | AFR | GWD | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02723 | hp2 | a0001 | c0001 | t0005 | g0012 | AFR | GWD | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02809 | hp1 | a0001 | c0001 | t0018 | g0133 | AFR | GWD | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02809 | hp2 | a0001 | c0001 | t0008 | g0162 | AFR | GWD | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02818 | hp2 | a0001 | c0001 | t0023 | g0159 | AFR | GWD | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02886 | hp1 | a0001 | c0001 | t0005 | g0114 | AFR | GWD | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02895 | hp1 | a0002 | c0003 | t0013 | g0128 | AFR | GWD | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0108 | 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 | t0032 | g0179 | AFR | GWD | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02897 | hp1 | a0002 | c0003 | t0013 | g0130 | 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 | g0191 | AFR | ESN | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02922 | hp2 | a0001 | c0001 | t0054 | g0002 | AFR | ESN | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02965 | hp1 | a0001 | c0001 | t0016 | g0120 | AFR | ESN | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02965 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | ESN | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02970 | hp1 | a0001 | c0001 | t0005 | g0016 | AFR | ESN | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02970 | hp2 | a0001 | c0001 | t0004 | g0139 | AFR | ESN | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02976 | hp1 | a0001 | c0001 | t0005 | g0116 | AFR | ESN | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02976 | hp2 | a0001 | c0001 | t0008 | g0163 | AFR | ESN | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0276 | SAS | PJL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG03017 | hp2 | a0001 | c0002 | t0003 | g0207 | 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 | g0027 | AFR | GWD | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG03098 | hp1 | a0001 | c0001 | t0021 | g0169 | AFR | MSL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG03098 | hp2 | a0001 | c0001 | t0055 | g0185 | AFR | MSL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG03130 | hp1 | a0001 | c0005 | t0085 | g0193 | AFR | ESN | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG03130 | hp2 | a0001 | c0001 | t0008 | g0156 | AFR | ESN | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG03195 | hp1 | a0001 | c0001 | t0012 | g0005 | AFR | ESN | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG03195 | hp2 | a0001 | c0001 | t0008 | g0157 | AFR | ESN | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG03209 | hp1 | a0002 | c0003 | t0013 | g0131 | AFR | MSL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG03209 | hp2 | a0001 | c0001 | t0012 | g0018 | AFR | MSL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG03225 | hp1 | a0001 | c0001 | t0051 | g0250 | AFR | MSL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG03225 | hp2 | a0001 | c0001 | t0019 | g0110 | AFR | MSL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG03239 | hp1 | a0001 | c0001 | t0024 | g0032 | SAS | PJL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG03453 | hp1 | a0001 | c0001 | t0019 | g0111 | AFR | MSL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG03453 | hp2 | a0001 | c0001 | t0032 | g0178 | AFR | MSL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG03486 | hp1 | a0001 | c0001 | t0006 | g0189 | AFR | MSL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG03486 | hp2 | a0001 | c0001 | t0065 | g0168 | AFR | MSL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG03490 | hp1 | a0001 | c0001 | t0029 | g0304 | SAS | PJL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG03491 | hp2 | a0007 | c0012 | t0015 | g0245 | SAS | PJL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG03492 | hp1 | a0001 | c0001 | t0029 | g0305 | SAS | PJL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG03516 | hp1 | a0001 | c0001 | t0086 | g0167 | AFR | ESN | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG03516 | hp2 | a0001 | c0001 | t0004 | g0138 | AFR | ESN | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG03540 | hp1 | a0001 | c0001 | t0023 | g0166 | AFR | GWD | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG03540 | hp2 | a0001 | c0007 | t0003 | g0155 | AFR | GWD | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0350 | SAS | PJL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG03654 | hp2 | a0001 | c0002 | t0007 | g0217 | SAS | PJL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG03669 | hp1 | a0001 | c0002 | t0003 | g0205 | SAS | PJL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0349 | SAS | PJL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0288 | SAS | STU | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG03688 | hp2 | a0003 | c0004 | t0015 | g0243 | SAS | STU | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG03704 | hp1 | a0001 | c0002 | t0003 | g0224 | SAS | PJL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG03704 | hp2 | a0001 | c0001 | t0013 | g0258 | SAS | PJL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0180 | SAS | PJL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0324 | SAS | PJL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG03831 | hp1 | a0001 | c0001 | t0010 | g0342 | SAS | BEB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG03831 | hp2 | a0001 | c0001 | t0062 | g0346 | SAS | BEB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG03834 | hp1 | a0001 | c0002 | t0003 | g0253 | SAS | BEB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG03834 | hp2 | a0001 | c0006 | t0063 | g0323 | SAS | BEB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | BEB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG03927 | hp2 | a0001 | c0001 | t0004 | g0331 | SAS | BEB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | BEB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG03942 | hp2 | a0003 | c0004 | t0015 | g0244 | SAS | BEB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG04115 | hp1 | a0001 | c0001 | t0034 | g0119 | 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 | g0046 | SAS | STU | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG04199 | hp2 | a0001 | c0001 | t0066 | g0354 | SAS | STU | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0176 | SAS | STU | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG04204 | hp2 | a0001 | c0001 | t0024 | g0094 | SAS | STU | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18522 | hp1 | a0001 | c0001 | t0012 | g0009 | AFR | YRI | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18522 | hp2 | a0001 | c0001 | t0006 | g0002 | AFR | YRI | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | CHB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18612 | hp2 | a0001 | c0001 | t0010 | g0335 | EAS | CHB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | CHB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18747 | hp2 | a0001 | c0001 | t0004 | g0290 | EAS | CHB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18906 | hp1 | a0001 | c0001 | t0006 | g0188 | AFR | YRI | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18906 | hp2 | a0001 | c0001 | t0008 | g0164 | AFR | YRI | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18939 | hp2 | a0001 | c0001 | t0048 | g0078 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18940 | hp1 | a0001 | c0001 | t0010 | g0289 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18940 | hp2 | a0001 | c0001 | t0050 | g0045 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18941 | hp1 | a0001 | c0001 | t0011 | g0148 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18941 | hp2 | a0001 | c0001 | t0010 | g0303 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18945 | hp1 | a0001 | c0001 | t0009 | g0087 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18946 | hp1 | a0001 | c0001 | t0064 | g0284 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18946 | hp2 | a0001 | c0001 | t0088 | g0022 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18947 | hp2 | a0001 | c0001 | t0011 | g0145 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18949 | hp1 | a0001 | c0001 | t0030 | g0151 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18949 | hp2 | a0001 | c0001 | t0027 | g0099 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18950 | hp1 | a0001 | c0001 | t0007 | g0173 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18950 | hp2 | a0001 | c0001 | t0009 | g0085 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0271 | 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 | g0310 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18953 | hp1 | a0001 | c0002 | t0003 | g0237 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0360 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18956 | hp2 | a0001 | c0002 | t0090 | g0223 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18957 | hp1 | a0001 | c0002 | t0089 | g0196 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0338 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0356 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18961 | hp1 | a0001 | c0002 | t0021 | g0242 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18961 | hp2 | a0001 | c0001 | t0004 | g0313 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0341 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18965 | hp1 | a0001 | c0001 | t0031 | g0170 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18967 | hp1 | a0001 | c0001 | t0059 | g0261 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0325 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0090 | 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 | g0299 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18971 | hp2 | a0001 | c0002 | t0003 | g0228 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18972 | hp1 | a0001 | c0001 | t0061 | g0270 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18972 | hp2 | a0001 | c0002 | t0082 | g0222 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18973 | hp1 | a0001 | c0001 | t0014 | g0365 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18974 | hp1 | a0001 | c0001 | t0071 | g0146 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0358 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0362 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18975 | hp2 | a0001 | c0001 | t0004 | g0336 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18977 | hp2 | a0001 | c0001 | t0004 | g0266 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18980 | hp1 | a0001 | c0001 | t0004 | g0306 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18982 | hp1 | a0001 | c0002 | t0003 | g0227 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0329 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0302 | 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 | g0080 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18985 | hp1 | a0001 | c0001 | t0046 | g0031 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18985 | hp2 | a0008 | c0008 | t0002 | g0004 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18986 | hp1 | a0001 | c0001 | t0017 | g0040 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18986 | hp2 | a0001 | c0002 | t0081 | g0241 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18989 | hp1 | a0001 | c0001 | t0014 | g0357 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18990 | hp1 | a0001 | c0001 | t0004 | g0277 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18990 | hp2 | a0001 | c0002 | t0003 | g0208 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18991 | hp1 | a0001 | c0002 | t0021 | g0239 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18991 | hp2 | a0001 | c0001 | t0004 | g0283 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18992 | hp2 | a0001 | c0002 | t0003 | g0235 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18993 | hp1 | a0001 | c0001 | t0067 | g0345 | 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 | g0343 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18998 | hp2 | a0001 | c0001 | t0036 | g0086 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0330 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA19000 | hp1 | a0001 | c0002 | t0003 | g0238 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA19000 | hp2 | a0001 | c0001 | t0069 | g0287 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA19002 | hp1 | a0001 | c0001 | t0007 | g0171 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0359 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA19007 | hp2 | a0001 | c0001 | t0011 | g0142 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA19009 | hp2 | a0001 | c0002 | t0003 | g0201 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA19010 | hp1 | a0001 | c0001 | t0009 | g0054 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA19010 | hp2 | a0001 | c0001 | t0014 | g0363 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA19011 | hp1 | a0001 | c0001 | t0027 | g0084 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0344 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA19030 | hp1 | a0001 | c0001 | t0041 | g0135 | AFR | LWK | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA19030 | hp2 | a0001 | c0001 | t0038 | g0026 | AFR | LWK | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA19054 | hp1 | a0001 | c0001 | t0073 | g0150 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA19056 | hp1 | a0001 | c0001 | t0009 | g0021 | 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 | g0352 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA19058 | hp2 | a0001 | c0001 | t0017 | g0039 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0328 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0020 | 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 | g0268 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA19063 | hp1 | a0001 | c0001 | t0030 | g0152 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA19063 | hp2 | a0001 | c0001 | t0009 | g0081 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA19064 | hp2 | a0001 | c0002 | t0003 | g0225 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA19065 | hp2 | a0001 | c0001 | t0004 | g0311 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA19074 | hp2 | a0001 | c0002 | t0080 | g0206 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA19079 | hp1 | a0001 | c0002 | t0003 | g0233 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA19079 | hp2 | a0001 | c0001 | t0009 | g0056 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA19080 | hp1 | a0001 | c0002 | t0003 | g0230 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA19080 | hp2 | a0001 | c0001 | t0026 | g0361 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA19081 | hp1 | a0001 | c0002 | t0003 | g0229 | 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 | g0095 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA19083 | hp2 | a0001 | c0001 | t0010 | g0353 | 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 | g0309 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA19085 | hp1 | a0001 | c0002 | t0003 | g0213 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA19086 | hp2 | a0001 | c0001 | t0004 | g0348 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA19088 | hp2 | a0001 | c0001 | t0004 | g0337 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA19090 | hp1 | a0001 | c0001 | t0072 | g0143 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA19090 | hp2 | a0001 | c0001 | t0014 | g0366 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA19240 | hp1 | a0001 | c0001 | t0005 | g0177 | AFR | YRI | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA19240 | hp2 | a0001 | c0001 | t0005 | g0007 | AFR | YRI | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0322 | AFR | ASW | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA20129 | hp2 | a0001 | c0001 | t0052 | g0251 | AFR | ASW | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0351 | EUR | TSI | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0355 | EUR | TSI | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | GIH | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA20905 | hp2 | a0001 | c0002 | t0003 | g0252 | SAS | GIH | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG01123 | hp2 | a0001 | c0001 | t0060 | g0280 | AMR | CLM | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02109 | hp1 | a0001 | c0001 | t0005 | g0117 | AFR | ACB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02109 | hp2 | a0001 | c0001 | t0006 | g0183 | AFR | ACB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02559 | hp1 | a0001 | c0001 | t0023 | g0161 | AFR | ACB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG02559 | hp2 | a0001 | c0001 | t0005 | g0014 | AFR | ACB | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG03471 | hp1 | a0001 | c0001 | t0008 | g0158 | AFR | MSL | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
HG03471 | hp2 | a0001 | c0001 | t0006 | g0190 | 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 | g0036 | AFR | USA | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA20300 | hp1 | a0001 | c0001 | t0011 | g0147 | AFR | USA | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA20300 | hp2 | a0001 | c0001 | t0006 | g0187 | AFR | USA | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
NA21309 | hp2 | a0001 | c0002 | t0003 | g0209 | AFR | LWK | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
homoSapiens | chm13v2 | a0001 | c0001 | t0087 | g0327 | REF | REF | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0298 | REF | REF | MTDH_chr8_97639184_97735260 | MTDH | chr8 | 97639184 | 97735260 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:97644738 | G | T | 2 | a0003 a0007 |
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 | a0008 | 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 | a0005 | 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 | a0003 a0004 a0007 |
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 | a0007 | 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 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:97644548 | C | A | 1 | a0008c0008 | 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 | a0001c0002 a0006c0009 |
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 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:97644202 | C | G | 3 | a0001c0001t0024 a0001c0001t0091 a0004c0010t0092 |
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 | a0001c0002t0089 a0001c0002t0090 |
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 | ||||||
chr8:97724902 | 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 | a0001c0001t0008 a0001c0001t0023 a0001c0001t0086 |
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 | a0001c0001t0022 a0001c0005t0022 a0001c0005t0085 |
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 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0011 others(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 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0011 others(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 | a0005c0011t0070 | 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 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0011 others(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 | a0001c0001t0022 a0001c0005t0022 a0001c0005t0085 |
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 | a0001c0001t0013 a0001c0001t0017 a0001c0001t0018 others(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 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0021 others(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 | a0001c0001t0005 a0001c0001t0012 a0001c0001t0025 others(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 | a0001c0001t0019 a0001c0001t0026 a0001c0001t0042 others(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 | a0001c0002t0089 a0001c0002t0090 |
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 | a0001c0001t0024 | 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 | a0005c0011t0070 | 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 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0021 others(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 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0011 others(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 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0013 others(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 |
22 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0017 others(19): 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 | a0001c0001t0020 a0001c0001t0043 a0001c0001t0044 |
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 | a0001c0001t0013 a0001c0001t0039 a0001c0001t0040 others(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 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0011 others(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 | 73 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(70): 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 | a0001c0001t0028 | 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 | a0001c0001t0029 | 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 | 80 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(77): 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 | a0001c0001t0008 a0001c0001t0023 a0001c0001t0086 |
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 | a0001c0001t0044 a0001c0001t0046 |
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 | a0001c0001t0010 a0001c0001t0014 a0001c0001t0018 others(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 | a0001c0001t0003 a0001c0001t0021 a0001c0001t0030 others(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 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0011 others(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 | a0001c0001t0064 a0003c0004t0015 a0003c0004t0053 others(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 | 74 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(71): 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 | 18 | a0001c0001t0001 a0001c0001t0017 a0001c0001t0020 others(15): 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 | a0001c0001t0009 a0001c0001t0036 a0001c0001t0043 others(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 | a0001c0001t0016 a0001c0001t0057 a0001c0001t0058 |
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 | a0001c0001t0051 a0001c0001t0052 |
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 | a0001c0001t0052 a0001c0001t0058 a0001c0001t0059 others(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 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(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 | 21 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0017 others(18): 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 | a0001c0001t0008 a0001c0001t0023 a0001c0001t0086 |
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 | 2 | a0001c0001t0024 a0001c0001t0091 |
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 | a0001c0001t0006 a0001c0001t0054 a0001c0001t0055 |
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 | 82 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(79): 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 | 74 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(71): 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 | a0001c0001t0076 a0001c0001t0079 a0001c0001t0083 |
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 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0011 others(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 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:97645057 | G | A | 1 | a0008c0008t0002g0004 | 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 | a0008c0008t0002g0004 | 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 | a0008c0008t0002g0004 | 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 | a0001c0001t0005g0007 a0001c0001t0005g0010 a0001c0001t0005g0011 others(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 | 253 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(250): 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 | a0001c0001t0003g0254 | 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 | a0001c0002t0003g0252 a0001c0002t0003g0253 |
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 | a0001c0001t0051g0250 a0001c0001t0052g0251 |
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 | 90 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(87): 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 | a0003c0004t0015g0243 a0003c0004t0015g0244 a0003c0004t0015g0249 others(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 | a0001c0002t0003g0200 a0001c0002t0003g0201 a0001c0002t0003g0202 others(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 | a0001c0001t0019g0109 a0001c0001t0019g0110 a0001c0001t0019g0111 |
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 | 90 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(87): 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 | 90 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(87): 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 | a0001c0001t0056g0112 | 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 | a0001c0001t0003g0172 a0001c0001t0003g0174 a0001c0001t0003g0176 others(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 | a0001c0001t0006g0002 a0001c0001t0006g0181 a0001c0001t0006g0182 others(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 | a0001c0001t0002g0356 a0001c0001t0002g0358 a0001c0001t0002g0359 others(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 | a0001c0001t0002g0255 a0001c0001t0011g0142 a0001c0001t0011g0144 others(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 | a0001c0001t0019g0109 a0001c0001t0019g0110 a0001c0001t0019g0111 |
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 | a0001c0001t0002g0256 | 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 | a0001c0001t0005g0113 a0001c0001t0005g0114 a0001c0001t0005g0116 others(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 | a0001c0001t0019g0109 a0001c0001t0019g0110 a0001c0001t0019g0111 |
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 | 248 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(245): 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 | a0001c0001t0002g0355 | 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 | a0001c0001t0002g0255 | 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 | a0003c0004t0015g0243 a0003c0004t0015g0244 a0004c0010t0092g0246 others(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 | a0003c0004t0015g0249 a0003c0004t0049g0248 |
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 | a0001c0001t0001g0108 | 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 | a0001c0001t0013g0258 a0001c0001t0018g0133 a0001c0001t0018g0134 others(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 | a0001c0001t0057g0125 | 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 | 88 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(85): 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 | a0001c0001t0066g0354 | 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 | 97 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(94): 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 | a0001c0001t0001g0020 a0001c0001t0002g0259 a0001c0001t0009g0021 others(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 | a0001c0001t0010g0353 a0001c0001t0016g0120 a0001c0001t0016g0121 others(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 | a0001c0001t0016g0124 | 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 | a0001c0001t0005g0118 | 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 | 254 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(251): 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 | a0001c0001t0014g0366 | 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 | a0001c0001t0002g0262 a0001c0001t0002g0263 a0001c0001t0002g0264 |
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 | a0001c0001t0002g0259 | 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 | a0001c0001t0002g0265 | 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 | a0001c0001t0003g0172 a0001c0001t0003g0174 a0001c0001t0003g0176 others(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 | 254 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(251): 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 | a0001c0001t0002g0267 a0001c0001t0002g0268 a0001c0001t0002g0269 others(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 | 98 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(95): 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 | a0001c0001t0014g0352 a0001c0001t0059g0261 |
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 | a0001c0001t0003g0180 | 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 | a0001c0001t0004g0273 a0001c0001t0004g0274 |
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 | a0001c0002t0075g0195 | 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 | a0001c0001t0013g0258 a0001c0001t0018g0133 a0001c0001t0018g0134 others(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 | a0001c0007t0003g0154 a0001c0007t0003g0155 |
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 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(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 | a0001c0001t0011g0142 a0001c0001t0011g0144 a0001c0001t0011g0145 others(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 | a0001c0001t0022g0191 a0001c0005t0022g0192 a0001c0005t0022g0194 others(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 | a0001c0001t0016g0120 a0001c0001t0016g0121 a0001c0001t0016g0122 others(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 | a0001c0001t0013g0258 | 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 | a0001c0001t0006g0190 | 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 | a0001c0001t0002g0351 | 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 | a0005c0011t0070g0019 | 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 | a0001c0001t0002g0262 | 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 | a0001c0001t0051g0250 a0001c0001t0052g0251 |
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 | a0001c0001t0019g0109 a0001c0001t0019g0110 a0001c0001t0019g0111 |
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 | a0001c0001t0034g0119 | 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 | a0001c0001t0005g0117 | 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 | a0001c0001t0018g0133 a0001c0001t0018g0134 a0001c0001t0018g0136 others(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 | a0001c0007t0003g0154 a0001c0007t0003g0155 |
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 | 251 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(248): 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 | a0001c0001t0006g0190 | 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 | a0001c0001t0005g0118 | 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 | a0001c0001t0019g0111 | 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 | a0001c0001t0001g0023 | 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 | a0001c0001t0005g0116 a0001c0001t0005g0117 |
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 | a0003c0004t0049g0248 | 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 | 251 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(248): 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 | a0003c0004t0015g0243 a0003c0004t0015g0244 a0003c0004t0015g0249 others(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 | a0001c0001t0032g0178 a0001c0001t0032g0179 |
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 | a0001c0002t0003g0240 | 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 | a0001c0001t0002g0275 a0001c0001t0002g0276 |
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 | 98 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(95): 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 | a0001c0001t0020g0024 | 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 | a0002c0003t0035g0126 | 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 | a0001c0001t0019g0111 | 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 | a0001c0001t0008g0156 a0001c0001t0008g0157 a0001c0001t0008g0158 others(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 | 83 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(80): 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 | a0001c0001t0003g0172 a0001c0001t0003g0174 a0001c0001t0003g0176 others(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 | a0001c0001t0005g0118 | 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 | a0001c0001t0008g0156 | 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 | a0001c0001t0056g0112 | 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 | a0001c0001t0002g0350 | 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 | a0001c0001t0002g0349 | 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 | a0001c0001t0034g0119 | 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 | a0001c0001t0001g0029 | 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 | a0001c0001t0011g0142 a0001c0001t0011g0144 a0001c0001t0011g0145 others(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 | a0001c0001t0001g0101 | 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 | a0001c0001t0010g0353 | 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 | a0001c0001t0013g0258 a0001c0001t0039g0127 a0001c0001t0040g0257 others(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 | a0001c0001t0004g0348 | 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 | a0001c0001t0010g0353 | 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 | a0001c0001t0002g0255 | 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 | a0001c0001t0019g0109 a0001c0001t0019g0110 a0001c0001t0019g0111 |
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 | a0001c0001t0004g0277 | 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 | a0001c0001t0065g0168 | 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 | a0001c0001t0021g0169 | 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 | a0001c0001t0013g0258 a0001c0001t0040g0257 a0002c0003t0013g0128 others(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 | a0001c0001t0002g0141 | 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 | a0001c0001t0056g0112 | 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 | a0001c0001t0016g0121 a0001c0001t0016g0122 a0001c0001t0057g0125 others(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 | a0001c0001t0013g0258 a0001c0001t0039g0127 a0001c0001t0040g0257 others(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 | 91 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(88): 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 | a0001c0001t0034g0119 | 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 | a0001c0001t0002g0267 a0001c0001t0002g0278 a0001c0001t0002g0279 others(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 | a0001c0001t0003g0172 a0001c0001t0003g0174 a0001c0001t0003g0176 others(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 | a0001c0001t0008g0156 a0001c0001t0008g0157 a0001c0001t0008g0158 others(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 | a0001c0001t0006g0002 a0001c0001t0006g0181 a0001c0001t0006g0182 others(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 | a0001c0001t0019g0109 a0001c0001t0019g0110 a0001c0001t0019g0111 |
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 | a0001c0001t0057g0125 | 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 | a0003c0004t0049g0248 | 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 | a0001c0001t0001g0102 | 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 | a0001c0001t0011g0142 a0001c0001t0011g0144 a0001c0001t0011g0145 others(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 | a0001c0001t0001g0100 | 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 | a0001c0001t0016g0120 a0001c0001t0016g0121 a0001c0001t0016g0122 others(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 | a0001c0001t0034g0119 | 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 | a0001c0001t0003g0176 | 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 | a0001c0001t0065g0168 | 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 | a0001c0002t0003g0200 a0001c0002t0003g0201 a0001c0002t0003g0202 others(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 | a0001c0001t0001g0030 | 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 | a0003c0004t0015g0243 a0003c0004t0015g0244 a0003c0004t0015g0249 others(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 | a0001c0002t0003g0230 a0001c0002t0003g0233 a0001c0002t0003g0234 others(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 | a0001c0002t0003g0225 a0001c0002t0003g0226 a0001c0002t0003g0227 others(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 | a0001c0001t0002g0265 a0001c0001t0002g0279 a0001c0001t0002g0351 |
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 | a0005c0011t0070g0019 | 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 | a0001c0001t0002g0141 | 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 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(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 | a0001c0001t0001g0103 a0001c0001t0002g0281 a0001c0001t0004g0273 others(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 | a0001c0001t0003g0172 a0001c0001t0003g0174 a0001c0001t0003g0176 others(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 | a0001c0001t0056g0112 | 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 | a0001c0001t0022g0191 a0001c0005t0022g0192 a0001c0005t0022g0194 others(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 | a0001c0001t0005g0007 a0001c0001t0005g0010 a0001c0001t0005g0011 others(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 | a0001c0001t0024g0032 a0001c0001t0024g0034 a0001c0001t0024g0094 others(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 | a0003c0004t0015g0243 a0003c0004t0015g0244 a0003c0004t0015g0249 others(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 | a0001c0001t0002g0347 | 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 | a0001c0001t0034g0119 | 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 | a0001c0001t0001g0095 a0001c0001t0004g0137 a0001c0001t0004g0138 others(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 | a0001c0001t0006g0002 a0001c0001t0006g0181 a0001c0001t0006g0182 others(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 | a0001c0001t0030g0152 | 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 | a0001c0001t0001g0028 | 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 | 251 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(248): 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 | a0001c0001t0002g0141 | 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 | 99 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(96): 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 | a0001c0002t0082g0222 | 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 | a0001c0001t0006g0002 a0001c0001t0006g0181 a0001c0001t0006g0182 others(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 | a0001c0001t0002g0141 | 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 | a0001c0001t0001g0035 a0001c0001t0088g0022 |
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 | a0001c0001t0003g0180 | 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 | a0001c0001t0006g0002 a0001c0001t0006g0181 a0001c0001t0006g0182 others(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 | a0003c0004t0015g0243 a0003c0004t0015g0244 a0003c0004t0015g0249 others(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 | a0001c0002t0003g0240 | 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 | a0001c0001t0008g0156 a0001c0001t0008g0157 a0001c0001t0008g0158 others(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 | a0001c0001t0064g0284 | 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 | a0001c0001t0024g0032 a0001c0001t0024g0034 a0001c0001t0024g0094 others(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 | a0001c0001t0056g0112 | 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 | a0001c0002t0089g0196 a0001c0002t0090g0223 |
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 | a0001c0001t0013g0258 a0001c0001t0039g0127 a0001c0001t0040g0257 others(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 | a0001c0001t0006g0190 | 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 | a0001c0001t0011g0142 a0001c0001t0011g0144 a0001c0001t0011g0145 others(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 | a0001c0001t0005g0007 a0001c0001t0005g0010 a0001c0001t0005g0011 others(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 | a0001c0001t0004g0137 | 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 | a0001c0001t0004g0137 | 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 | 110 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(107): 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 | a0001c0001t0022g0191 a0001c0005t0022g0192 a0001c0005t0022g0194 others(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 | a0001c0001t0039g0127 | 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 | a0003c0004t0015g0243 a0003c0004t0015g0244 a0003c0004t0015g0249 others(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 | a0001c0001t0055g0185 | 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 | a0001c0001t0008g0157 | 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 | 3 | a0001c0001t0001g0001 a0001c0001t0001g0036 a0001c0001t0020g0024 |
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 | a0001c0001t0003g0172 a0001c0001t0003g0174 a0001c0001t0003g0176 others(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 | 105 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0025 others(102): 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 | a0001c0001t0001g0023 a0001c0001t0011g0142 a0001c0001t0011g0144 others(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 | 251 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(248): 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 | 110 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(107): 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 | a0001c0001t0002g0347 | 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 | a0001c0001t0004g0283 | 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 | a0001c0001t0013g0258 a0001c0001t0040g0257 |
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 | a0001c0001t0001g0030 | 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 | a0001c0001t0002g0341 | 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 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0108 others(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 | 103 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(100): 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 | a0003c0004t0015g0243 a0003c0004t0015g0244 a0003c0004t0015g0249 others(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 | a0001c0001t0003g0172 a0001c0001t0003g0174 a0001c0001t0003g0176 others(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 | a0001c0001t0001g0091 | 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 | a0001c0001t0001g0090 a0001c0001t0027g0099 |
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 | a0001c0001t0002g0340 | 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 | a0001c0001t0016g0124 | 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 | a0001c0002t0007g0197 | 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 | a0001c0001t0001g0089 a0001c0001t0006g0002 a0001c0001t0006g0181 others(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 | a0001c0001t0017g0038 a0001c0001t0017g0039 a0001c0001t0017g0040 |
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 | a0001c0001t0004g0285 | 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 | a0001c0001t0013g0258 a0001c0001t0018g0133 a0001c0001t0018g0134 others(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 | a0001c0001t0037g0132 | 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 | 224 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(221): 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 | a0001c0001t0008g0156 a0001c0001t0008g0157 a0001c0001t0008g0158 others(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 | a0001c0001t0013g0258 a0001c0001t0018g0133 a0001c0001t0018g0134 others(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 | a0001c0001t0057g0125 | 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 | a0001c0002t0003g0240 a0001c0007t0003g0154 a0001c0007t0003g0155 others(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 | a0001c0001t0001g0088 a0001c0001t0033g0339 |
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 | a0001c0001t0006g0002 a0001c0001t0006g0181 a0001c0001t0006g0182 others(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 | a0001c0001t0023g0166 | 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 | 90 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(87): 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 | a0001c0001t0011g0148 | 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 | a0001c0001t0001g0089 | 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 | a0001c0001t0005g0116 | 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 | 223 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(220): 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 | a0001c0001t0003g0172 a0001c0001t0003g0174 a0001c0001t0003g0176 others(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 | a0001c0001t0002g0141 a0001c0001t0002g0262 a0001c0001t0002g0275 others(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 | a0001c0001t0002g0338 a0001c0001t0005g0007 a0001c0001t0005g0010 others(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 | a0001c0001t0005g0113 a0001c0001t0005g0114 a0001c0001t0005g0116 others(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 | 90 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(87): 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 | a0001c0001t0022g0191 a0001c0005t0022g0192 a0001c0005t0022g0194 others(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 | a0001c0001t0034g0119 | 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 | a0001c0001t0018g0133 | 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 | a0001c0001t0034g0119 | 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 | a0001c0002t0007g0198 a0001c0002t0007g0199 |
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 | a0001c0001t0013g0258 a0001c0001t0018g0133 a0001c0001t0018g0134 others(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 | 102 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(99): 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 | a0001c0001t0034g0119 | 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 | a0001c0001t0008g0156 a0001c0001t0008g0157 a0001c0001t0008g0158 others(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 | a0001c0002t0003g0219 | 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 | a0001c0001t0022g0191 a0001c0005t0022g0192 a0001c0005t0022g0194 others(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 | a0001c0001t0004g0336 a0001c0001t0004g0337 a0001c0001t0010g0289 |
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 | a0001c0001t0005g0007 a0001c0001t0005g0010 a0001c0001t0005g0011 others(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 | 220 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(217): 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 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0108 others(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 | a0001c0001t0010g0335 | 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 | a0001c0002t0007g0197 a0001c0002t0007g0198 a0001c0002t0007g0199 others(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 | a0001c0001t0002g0262 a0001c0001t0002g0263 a0001c0001t0002g0264 |
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 | 252 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(249): 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 | a0001c0001t0009g0021 a0001c0001t0009g0085 a0001c0001t0009g0087 others(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 | a0001c0001t0062g0346 | 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 | a0001c0001t0022g0191 a0001c0005t0022g0192 a0001c0005t0022g0194 others(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 | a0001c0002t0003g0224 | 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 | a0001c0001t0006g0002 a0001c0001t0006g0181 a0001c0001t0006g0182 others(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 | a0001c0001t0001g0042 | 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 | a0001c0001t0001g0043 a0001c0001t0002g0291 a0001c0001t0004g0283 others(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 | a0001c0001t0001g0083 a0001c0001t0001g0101 a0001c0001t0002g0338 others(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 | a0005c0011t0070g0019 | 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 | a0001c0002t0003g0215 | 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 | a0001c0001t0004g0137 | 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 | a0001c0001t0004g0266 a0001c0001t0004g0343 |
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 | a0001c0001t0018g0136 | 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 | a0001c0001t0006g0190 | 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 | a0001c0001t0022g0191 a0001c0005t0022g0192 a0001c0005t0022g0194 others(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 | 98 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(95): 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 | 98 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(95): 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 | a0001c0001t0003g0176 a0001c0001t0003g0180 |
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 | a0001c0001t0016g0120 a0001c0001t0016g0121 a0001c0001t0016g0122 others(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 | a0001c0001t0019g0109 a0001c0001t0019g0110 a0001c0001t0019g0111 |
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 | a0001c0001t0001g0089 | 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 | a0001c0001t0004g0332 a0001c0001t0004g0333 |
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 | a0001c0001t0002g0292 | 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 | a0001c0001t0005g0007 a0001c0001t0005g0113 a0001c0001t0005g0114 others(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 | a0005c0011t0070g0019 | 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 | a0001c0001t0004g0293 | 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 | a0001c0001t0005g0007 a0001c0001t0005g0010 a0001c0001t0005g0011 others(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 | a0001c0002t0003g0237 | 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 | a0001c0001t0018g0133 a0001c0001t0018g0134 a0001c0001t0018g0136 others(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 | 99 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0025 others(96): 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 | a0001c0001t0001g0104 a0001c0001t0011g0142 a0001c0001t0011g0144 others(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 | a0001c0001t0003g0172 a0001c0001t0003g0174 a0001c0001t0003g0176 others(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 | a0001c0001t0021g0169 a0001c0001t0031g0170 a0001c0001t0034g0119 others(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 | a0001c0002t0003g0221 | 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 | a0001c0001t0013g0258 a0001c0001t0018g0133 a0001c0001t0018g0134 others(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 | a0001c0001t0019g0109 a0001c0001t0019g0110 a0001c0001t0019g0111 |
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 | 360 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(357): Show |
362 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(359): 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 | a0001c0001t0001g0068 | 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 | a0001c0001t0055g0185 | 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 | a0001c0001t0001g0044 | 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 | 98 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(95): 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 | a0001c0001t0037g0132 | 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 | a0001c0001t0039g0127 | 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 | a0001c0001t0002g0275 a0001c0001t0002g0276 |
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 | a0001c0001t0005g0007 a0001c0001t0005g0010 a0001c0001t0005g0011 others(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 | a0001c0001t0005g0007 a0001c0001t0005g0010 a0001c0001t0005g0011 others(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 | a0001c0001t0051g0250 a0001c0001t0052g0251 |
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 | a0001c0001t0076g0175 a0001c0001t0079g0153 a0001c0001t0083g0367 |
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 | a0001c0001t0002g0340 | 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 | a0001c0001t0052g0251 | 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 | a0001c0002t0078g0214 | 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 | a0001c0001t0002g0358 | 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 | a0001c0001t0003g0172 a0001c0001t0003g0174 a0001c0001t0003g0176 others(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 | a0001c0001t0006g0002 a0001c0001t0006g0181 a0001c0001t0006g0182 others(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 | a0001c0001t0006g0186 | 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 | a0001c0001t0003g0172 a0001c0001t0003g0174 a0001c0001t0003g0176 others(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 | a0001c0001t0003g0172 a0001c0001t0003g0174 a0001c0001t0003g0176 others(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 | 136 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(133): 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 | a0001c0001t0001g0030 a0001c0001t0001g0104 a0001c0001t0003g0172 others(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 | a0001c0001t0022g0191 a0001c0001t0023g0159 a0001c0001t0032g0178 others(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 | 251 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(248): 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 | a0001c0001t0011g0142 a0001c0001t0011g0144 a0001c0001t0011g0145 others(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 | a0001c0001t0003g0172 a0001c0001t0003g0174 a0001c0001t0003g0176 others(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 | a0001c0001t0019g0109 a0001c0001t0019g0110 a0001c0001t0019g0111 |
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 | a0001c0002t0003g0240 | 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 | a0001c0001t0002g0271 a0001c0001t0002g0272 |
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 | a0002c0003t0013g0128 a0002c0003t0013g0130 |
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 | a0001c0001t0051g0250 a0001c0001t0052g0251 |
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 | a0001c0002t0003g0208 | 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 | a0001c0001t0030g0151 | 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 | a0001c0001t0002g0347 | 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 | a0001c0001t0011g0142 a0001c0001t0011g0145 a0001c0001t0011g0147 others(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 | a0001c0001t0011g0144 a0001c0001t0011g0149 a0001c0001t0030g0152 others(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 | a0001c0001t0001g0044 a0001c0001t0001g0058 a0001c0001t0001g0096 others(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 | a0001c0001t0004g0273 a0001c0001t0006g0181 a0001c0001t0006g0183 others(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 | 67 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0001g0027 others(64): 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 | a0001c0001t0001g0063 a0001c0001t0003g0176 a0001c0001t0003g0254 others(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 | a0001c0001t0008g0160 a0001c0001t0013g0258 a0001c0001t0018g0133 others(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 | a0001c0001t0002g0302 a0001c0001t0002g0350 a0001c0001t0005g0116 others(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 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0069 others(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 | a0001c0001t0013g0258 a0001c0001t0040g0257 a0002c0003t0013g0128 others(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 | a0002c0003t0035g0126 | 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 | a0001c0001t0001g0025 | 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 | a0003c0004t0015g0243 a0003c0004t0015g0244 a0004c0010t0092g0246 others(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 | a0001c0001t0001g0096 | 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 | a0001c0001t0019g0109 a0001c0001t0019g0110 a0001c0001t0019g0111 |
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 | a0001c0001t0001g0020 a0001c0001t0001g0071 a0001c0001t0001g0072 others(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 | a0003c0004t0015g0244 | 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 | a0001c0001t0008g0165 | 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 | a0001c0001t0008g0157 a0001c0001t0008g0163 a0001c0001t0008g0164 |
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 | a0001c0001t0043g0041 | 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 | a0001c0001t0005g0007 a0001c0001t0005g0010 a0001c0001t0005g0011 others(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 | a0001c0001t0005g0007 a0001c0001t0005g0010 a0001c0001t0005g0011 others(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 | a0001c0001t0002g0278 | 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 | a0001c0001t0002g0264 | 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 | a0001c0001t0004g0137 | 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 | a0005c0011t0070g0019 | 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 | a0001c0001t0003g0172 a0001c0001t0003g0174 a0001c0001t0003g0176 others(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 | a0001c0001t0003g0172 a0001c0001t0003g0174 a0001c0001t0003g0176 others(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 | a0001c0001t0019g0109 a0001c0001t0019g0110 a0001c0001t0019g0111 |
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 | a0001c0001t0013g0258 a0001c0001t0039g0127 a0001c0001t0040g0257 others(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 | a0001c0001t0034g0119 | 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 | a0001c0001t0034g0119 | 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 | a0001c0001t0002g0360 | 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 | a0001c0001t0002g0300 | 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 | a0001c0001t0002g0296 | 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 | a0001c0001t0047g0049 | 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 | a0001c0001t0019g0109 a0001c0001t0019g0110 a0001c0001t0019g0111 |
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 | a0001c0001t0022g0191 a0001c0005t0022g0192 a0001c0005t0022g0194 others(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 | a0001c0002t0003g0224 | 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 | 91 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(88): 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 | a0001c0001t0006g0002 a0001c0001t0006g0181 a0001c0001t0006g0182 others(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 | a0001c0001t0051g0250 a0001c0001t0052g0251 |
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 | a0001c0001t0004g0343 | 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 | a0001c0001t0001g0050 | 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 | a0001c0002t0003g0200 a0001c0002t0003g0201 a0001c0002t0003g0202 others(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 | a0001c0001t0003g0172 a0001c0001t0003g0174 a0001c0001t0003g0176 others(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 | a0001c0001t0013g0258 a0001c0001t0018g0133 a0001c0001t0018g0134 others(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 | 105 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(102): 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 | a0001c0001t0011g0149 | 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 | a0001c0001t0034g0119 | 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 | a0001c0001t0004g0293 | 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 | a0001c0001t0001g0090 | 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 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0012g0008 |
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 | a0001c0001t0009g0081 | 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 | a0001c0001t0034g0119 | 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 | a0001c0001t0023g0166 | 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 | a0001c0001t0001g0100 a0001c0001t0005g0007 a0001c0001t0005g0010 others(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 | a0001c0001t0004g0336 a0001c0001t0004g0337 a0001c0001t0010g0289 |
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 | a0001c0001t0006g0002 a0001c0001t0006g0181 a0001c0001t0006g0182 others(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 | a0001c0001t0034g0119 | 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 | a0001c0001t0002g0141 | 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 | 90 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(87): 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 | a0001c0001t0001g0037 a0001c0001t0001g0043 a0001c0001t0001g0051 others(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 | a0001c0001t0018g0133 a0001c0001t0018g0134 a0001c0001t0018g0136 others(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 | a0001c0001t0004g0333 a0001c0001t0005g0007 a0001c0001t0005g0010 others(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 | a0001c0001t0003g0172 a0001c0001t0003g0174 a0001c0001t0003g0254 others(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 | a0001c0001t0003g0172 a0001c0001t0003g0174 a0001c0001t0003g0176 others(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 | a0001c0001t0004g0293 | 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 | a0001c0001t0056g0112 | 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 | a0001c0001t0041g0135 | 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 | a0001c0001t0004g0331 | 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 | a0001c0001t0002g0355 a0001c0001t0004g0139 a0001c0001t0004g0266 others(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 | 218 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(215): 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 | a0001c0001t0001g0071 a0001c0002t0003g0227 a0001c0002t0003g0240 others(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 | 218 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(215): 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 | a0001c0001t0001g0071 a0001c0002t0003g0227 a0001c0002t0003g0240 others(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 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0048 |
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 | a0003c0004t0015g0243 a0003c0004t0015g0244 a0003c0004t0015g0249 others(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 | 224 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(221): 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 | a0001c0001t0006g0002 a0001c0001t0006g0181 a0001c0001t0006g0182 others(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 | a0001c0001t0003g0172 a0001c0001t0003g0174 a0001c0001t0003g0176 others(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 | a0001c0001t0008g0158 a0001c0001t0008g0160 a0001c0001t0008g0162 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0080 a0001c0001t0008g0157 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0027 others(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 | 114 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0001g0036 others(111): Show |
116 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(113): 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 | a0001c0001t0002g0141 a0001c0001t0002g0268 a0001c0001t0002g0275 others(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 | a0001c0001t0002g0315 a0001c0001t0002g0359 a0001c0001t0002g0362 others(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 | a0001c0001t0003g0172 a0001c0001t0003g0176 a0001c0001t0006g0002 others(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 | a0001c0001t0006g0184 a0001c0002t0090g0223 |
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 | a0001c0001t0013g0258 a0001c0001t0039g0127 a0001c0001t0040g0257 others(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 | a0004c0010t0092g0246 | 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 | a0002c0003t0035g0126 | 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 | a0001c0001t0003g0172 a0001c0001t0003g0174 a0001c0001t0003g0176 others(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 | a0001c0001t0002g0140 a0001c0001t0002g0141 a0001c0001t0002g0259 others(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 | a0001c0001t0002g0360 a0001c0001t0002g0362 a0001c0001t0004g0139 others(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 | 35 | a0001c0001t0002g0003 a0001c0001t0002g0326 a0001c0001t0005g0007 others(32): 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 | a0001c0001t0019g0109 a0001c0001t0019g0110 a0001c0001t0019g0111 |
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 | a0001c0001t0001g0027 a0001c0001t0001g0059 a0001c0001t0001g0091 others(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 | 93 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(90): 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 | a0001c0001t0003g0172 a0001c0001t0003g0174 a0001c0001t0003g0176 others(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 | a0001c0001t0019g0109 a0001c0001t0019g0110 a0001c0001t0019g0111 |
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 | a0001c0001t0024g0032 a0001c0001t0024g0034 a0001c0001t0024g0094 others(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 | a0001c0001t0006g0002 a0001c0001t0006g0181 a0001c0001t0006g0182 others(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 | 90 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(87): 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 | 251 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(248): 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 | a0001c0001t0002g0340 | 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 | a0001c0001t0002g0294 a0001c0001t0002g0301 a0001c0001t0002g0315 others(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 | 98 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(95): 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 | a0001c0001t0022g0191 a0001c0005t0022g0192 a0001c0005t0022g0194 others(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 | a0001c0001t0011g0149 | 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 | a0001c0001t0011g0149 | 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 | a0001c0001t0002g0263 a0001c0001t0002g0359 a0001c0001t0002g0360 others(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 | 75 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(72): 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 | a0001c0001t0001g0029 a0001c0001t0001g0065 a0001c0001t0001g0066 others(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 | a0001c0001t0034g0119 a0001c0001t0039g0127 |
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 | a0002c0003t0013g0129 | 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 | a0001c0001t0018g0133 a0001c0001t0018g0134 |
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 | a0001c0001t0018g0136 a0001c0001t0037g0132 a0001c0001t0041g0135 |
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 | a0001c0001t0051g0250 a0001c0001t0052g0251 a0005c0011t0070g0019 |
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 | a0001c0001t0030g0151 | 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 | a0001c0001t0030g0152 a0001c0001t0073g0150 |
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 | a0001c0001t0011g0147 a0001c0001t0011g0148 |
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 | a0001c0001t0011g0145 | 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 | a0001c0001t0011g0142 a0001c0001t0011g0144 a0001c0001t0071g0146 |
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 | a0001c0001t0072g0143 | 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 | a0001c0001t0011g0149 | 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 | a0001c0001t0002g0296 a0001c0001t0002g0340 a0001c0001t0003g0172 others(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 | a0001c0001t0002g0350 | 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 | a0001c0001t0003g0176 | 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 | a0001c0002t0003g0252 a0001c0002t0003g0253 |
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 | a0001c0001t0001g0064 | 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 | a0001c0001t0034g0119 | 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 | a0001c0001t0002g0355 a0001c0001t0004g0266 a0001c0001t0004g0277 others(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 | a0001c0001t0019g0109 a0001c0001t0019g0110 a0001c0001t0019g0111 |
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 | a0001c0001t0011g0142 a0001c0001t0011g0144 a0001c0001t0011g0145 others(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 | a0001c0001t0003g0172 a0001c0001t0003g0174 a0001c0001t0003g0176 others(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 | 91 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(88): 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 | a0002c0003t0013g0128 a0002c0003t0013g0130 a0002c0003t0013g0131 |
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 | a0001c0001t0003g0172 a0001c0001t0003g0174 a0001c0001t0003g0176 others(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 | 252 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(249): 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 | a0001c0001t0002g0315 | 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 | a0001c0001t0006g0002 a0001c0001t0006g0181 a0001c0001t0006g0182 others(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 | a0001c0001t0001g0063 a0001c0001t0001g0083 a0001c0001t0047g0049 |
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 | a0001c0001t0016g0120 a0001c0001t0016g0121 a0001c0001t0016g0122 others(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 | a0001c0001t0005g0007 a0001c0001t0005g0010 a0001c0001t0005g0011 others(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 | a0001c0001t0019g0109 a0001c0001t0019g0110 a0001c0001t0019g0111 |
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 | 98 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(95): 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 | a0001c0001t0037g0132 | 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 | a0001c0001t0051g0250 | 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 | a0006c0009t0003g0232 | 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 | a0005c0011t0070g0019 | 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 | a0001c0001t0013g0258 a0001c0001t0018g0133 a0001c0001t0018g0134 others(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 | a0001c0001t0002g0288 | 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 | a0001c0001t0005g0007 a0001c0001t0005g0010 a0001c0001t0005g0011 others(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 | a0001c0001t0022g0191 a0001c0005t0022g0192 a0001c0005t0022g0194 others(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 | a0001c0001t0001g0075 a0001c0001t0001g0107 a0001c0001t0002g0294 others(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 | 132 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(129): 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 | a0001c0001t0001g0055 a0001c0001t0009g0081 a0001c0001t0012g0006 others(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 | a0001c0001t0002g0356 a0001c0001t0004g0138 a0001c0001t0004g0139 others(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 | a0001c0001t0051g0250 a0001c0001t0052g0251 |
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 | a0001c0001t0034g0119 | 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 | a0001c0001t0002g0255 | 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 | a0001c0002t0003g0207 | 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 | a0001c0001t0019g0109 a0001c0001t0019g0110 a0001c0001t0019g0111 |
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 | a0001c0001t0004g0293 | 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 | a0001c0001t0029g0304 a0001c0001t0029g0305 |
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 | a0001c0001t0002g0355 a0005c0011t0070g0019 |
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 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0001t0001g0075 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0102 a0001c0001t0002g0317 others(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 | a0001c0001t0001g0063 a0001c0001t0001g0069 a0001c0001t0002g0140 others(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 | a0001c0001t0001g0027 a0001c0001t0002g0003 a0001c0001t0002g0292 others(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 | 4 | a0001c0001t0001g0104 a0001c0001t0002g0291 a0001c0001t0006g0182 others(1): Show |
4 | HG01099.hp1 HG01123.hp1 HG02717.hp2 others(1): 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 | a0001c0001t0028g0321 | 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 | a0001c0001t0004g0282 a0002c0003t0013g0128 |
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 | a0001c0001t0013g0258 a0001c0001t0040g0257 |
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 | a0001c0001t0043g0041 | 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 | a0001c0001t0004g0273 a0001c0001t0004g0274 a0001c0001t0005g0011 others(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 | a0001c0001t0001g0044 a0001c0001t0001g0058 a0001c0001t0001g0091 others(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 | a0001c0001t0001g0035 a0001c0001t0001g0097 a0001c0001t0004g0277 others(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 | a0001c0001t0002g0318 | 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 | a0001c0001t0019g0109 a0001c0001t0019g0110 a0001c0001t0019g0111 |
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 | a0001c0001t0060g0280 | 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 | a0001c0002t0003g0233 a0001c0002t0003g0238 a0001c0002t0021g0239 |
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 | a0001c0002t0003g0230 a0001c0002t0003g0234 a0001c0002t0003g0236 others(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 | a0001c0001t0030g0152 a0001c0002t0007g0217 |
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 | a0001c0001t0011g0147 a0001c0001t0011g0148 a0001c0001t0030g0151 |
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 | a0001c0001t0004g0336 a0001c0001t0004g0337 a0001c0001t0010g0289 |
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 | a0001c0002t0003g0208 a0001c0002t0077g0220 |
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 | a0001c0002t0003g0201 a0001c0002t0003g0202 a0001c0002t0003g0203 others(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 | a0001c0001t0003g0174 a0001c0001t0076g0175 a0001c0002t0003g0200 others(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 | a0001c0001t0003g0172 a0001c0001t0003g0176 a0001c0001t0003g0180 others(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 | a0001c0001t0011g0142 a0001c0001t0011g0144 a0001c0001t0011g0145 others(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 | a0001c0001t0004g0313 | 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 | a0001c0001t0021g0169 a0001c0001t0031g0170 a0001c0002t0003g0204 others(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 | a0001c0001t0004g0309 | 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 | a0001c0001t0004g0306 a0001c0001t0004g0343 a0001c0001t0010g0342 |
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 | a0001c0001t0001g0030 a0001c0001t0004g0308 |
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 | a0001c0001t0023g0166 | 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 | a0001c0001t0032g0178 | 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 | a0001c0001t0032g0179 | 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 | a0001c0001t0010g0353 a0001c0006t0004g0260 |
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 | a0001c0001t0010g0303 | 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 | a0001c0001t0001g0036 | 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 | a0001c0001t0001g0100 | 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 | a0001c0001t0056g0112 | 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 | a0001c0001t0019g0111 | 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 | a0001c0001t0019g0110 | 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 | a0001c0001t0019g0109 | 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 | a0001c0001t0001g0096 a0001c0001t0012g0015 |
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 | a0001c0001t0001g0052 | 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 | a0001c0001t0025g0013 a0001c0001t0025g0017 |
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 | a0008c0008t0002g0004 | 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 | a0001c0001t0006g0190 a0001c0001t0061g0270 |
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 | a0001c0001t0002g0269 a0001c0001t0002g0271 a0001c0001t0002g0272 others(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 | a0001c0001t0002g0297 | 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 | a0001c0001t0037g0132 | 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 | a0001c0001t0084g0312 | 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 | a0001c0001t0065g0168 | 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 | a0001c0001t0001g0077 | 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 | a0001c0001t0004g0332 a0001c0001t0005g0016 a0001c0001t0041g0135 |
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 | a0001c0001t0005g0010 a0001c0001t0018g0133 a0001c0001t0018g0136 |
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 | a0001c0001t0005g0007 a0001c0001t0005g0113 a0001c0001t0005g0177 |
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 | a0001c0001t0018g0134 | 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 | a0001c0001t0005g0114 a0001c0001t0005g0118 |
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 | a0001c0001t0008g0162 | 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 | a0002c0003t0013g0129 | 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 | a0001c0001t0034g0119 | 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 | a0001c0001t0023g0166 | 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 | a0004c0010t0092g0246 a0007c0012t0015g0245 |
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 | a0001c0001t0001g0065 | 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 | a0001c0001t0001g0066 a0002c0003t0035g0126 |
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 | a0001c0001t0005g0116 a0001c0001t0005g0117 |
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 | a0001c0001t0042g0115 | 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 | a0001c0001t0001g0050 a0001c0001t0002g0003 a0002c0003t0013g0130 |
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 | a0001c0001t0008g0165 | 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 | a0001c0001t0001g0065 a0001c0001t0004g0309 |
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 | a0001c0001t0002g0279 | 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 | a0001c0001t0002g0355 | 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 | a0001c0001t0001g0042 | 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 | a0001c0001t0008g0158 a0001c0001t0008g0160 a0001c0001t0086g0167 |
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 | a0001c0001t0001g0065 a0001c0001t0004g0309 |
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 | a0001c0001t0001g0028 a0001c0001t0004g0331 a0001c0005t0022g0192 others(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 | a0003c0004t0015g0243 | 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 | a0002c0003t0013g0131 | 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 | a0001c0001t0002g0315 a0001c0001t0004g0137 |
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 | a0001c0001t0027g0099 | 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 | a0001c0001t0001g0048 a0001c0001t0001g0065 a0001c0001t0002g0319 others(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 | a0001c0001t0054g0002 | 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 | a0003c0004t0053g0247 | 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 | a0001c0001t0058g0123 | 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 | a0001c0001t0014g0365 a0001c0001t0014g0366 |
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 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0065 others(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 | a0001c0001t0002g0340 a0001c0001t0020g0024 a0001c0005t0085g0193 |
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 | a0001c0001t0051g0250 | 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 | a0001c0001t0001g0059 a0001c0001t0001g0092 a0001c0001t0024g0032 |
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 | a0001c0001t0001g0030 a0001c0001t0001g0047 a0001c0001t0001g0048 others(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 | a0001c0001t0002g0276 a0001c0001t0002g0278 a0001c0001t0002g0281 others(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 | a0001c0001t0002g0328 | 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 | a0001c0001t0001g0093 a0001c0001t0002g0358 a0001c0001t0024g0034 others(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 | a0001c0001t0001g0068 | 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 | a0001c0001t0001g0030 a0001c0001t0001g0044 a0001c0001t0001g0047 others(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 | a0001c0001t0001g0025 a0001c0001t0002g0275 a0001c0001t0002g0359 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0062 a0001c0001t0002g0141 others(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 | a0001c0001t0065g0168 | 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 | a0001c0001t0001g0103 | 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 | a0001c0001t0001g0029 | 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 | a0001c0001t0023g0159 | 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 | a0001c0001t0001g0030 a0001c0001t0001g0035 a0001c0001t0001g0044 others(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 | a0001c0001t0001g0043 a0001c0001t0002g0296 a0001c0001t0062g0346 others(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 | a0001c0001t0023g0159 | 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 | a0001c0001t0001g0088 a0001c0001t0008g0156 a0001c0001t0008g0157 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0043 a0001c0001t0002g0288 others(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 | a0001c0001t0002g0141 a0001c0001t0008g0156 a0001c0001t0008g0157 others(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 | a0001c0001t0002g0288 a0001c0001t0002g0325 a0001c0001t0086g0167 |
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 | a0001c0001t0008g0164 | 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 | a0003c0004t0049g0248 | 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 | a0001c0001t0002g0272 | 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 | 254 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(251): 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 | a0001c0001t0024g0094 | 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 | a0001c0001t0008g0156 a0001c0001t0008g0157 a0001c0001t0008g0158 others(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 | a0001c0001t0019g0109 a0001c0001t0019g0110 a0001c0001t0019g0111 |
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 | a0001c0001t0016g0124 | 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 | a0001c0001t0004g0282 a0001c0001t0068g0314 |
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 | a0001c0001t0002g0326 | 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 | a0001c0001t0071g0146 | 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 | a0001c0001t0034g0119 | 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 | a0001c0001t0002g0255 a0001c0001t0002g0262 a0001c0001t0002g0263 others(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 | a0001c0001t0002g0268 a0001c0001t0002g0288 a0001c0001t0002g0358 others(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 | a0001c0001t0001g0077 a0001c0001t0001g0088 a0001c0001t0002g0362 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0036 a0001c0001t0001g0047 others(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 | a0001c0001t0001g0023 a0001c0001t0001g0030 a0001c0001t0001g0035 others(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 | 10 | a0001c0001t0001g0001 a0001c0001t0001g0044 a0001c0001t0001g0052 others(7): 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 | a0001c0001t0001g0051 a0001c0001t0001g0053 a0001c0001t0001g0061 others(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 | a0001c0001t0001g0093 | 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 | a0001c0001t0001g0043 a0001c0001t0001g0062 a0001c0001t0001g0090 |
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 | a0001c0001t0045g0106 | 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 | a0001c0001t0002g0256 a0001c0001t0002g0296 a0001c0001t0002g0340 others(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 | a0001c0001t0004g0266 a0001c0001t0004g0306 a0001c0001t0004g0307 others(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 | a0001c0001t0008g0162 a0001c0001t0009g0056 a0001c0001t0013g0258 others(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 | a0001c0001t0006g0181 a0001c0001t0006g0183 a0001c0001t0006g0187 others(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 | a0001c0001t0006g0002 a0001c0001t0006g0182 a0001c0001t0006g0184 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0037 a0001c0001t0001g0055 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0028 a0001c0001t0001g0072 others(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 | a0001c0001t0001g0107 a0001c0001t0002g0141 |
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 | a0001c0001t0022g0191 a0001c0005t0022g0192 a0001c0005t0022g0194 others(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 | a0005c0011t0070g0019 | 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 | a0001c0001t0002g0292 | 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 | a0001c0002t0003g0215 | 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 | a0001c0001t0001g0025 | 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 | a0001c0001t0024g0032 | 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 | a0001c0001t0002g0301 | 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 | a0001c0002t0003g0227 | 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 | a0001c0001t0056g0112 | 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 | a0001c0001t0066g0354 | 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 | a0001c0001t0013g0258 a0001c0001t0039g0127 a0001c0001t0040g0257 others(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 | a0001c0005t0022g0192 a0001c0005t0085g0193 |
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 | a0003c0004t0049g0248 | 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 | a0001c0001t0006g0186 | 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 | a0001c0001t0006g0002 a0001c0001t0006g0181 a0001c0001t0006g0182 others(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 | a0001c0001t0026g0364 | 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 | a0001c0001t0024g0032 | 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 | a0001c0001t0001g0068 | 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 | a0001c0001t0002g0355 a0001c0001t0004g0266 a0001c0001t0004g0277 others(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 | a0001c0001t0012g0006 | 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 | 251 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(248): 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 | a0001c0002t0003g0221 | 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 | a0001c0001t0005g0007 a0001c0001t0005g0010 a0001c0001t0005g0011 others(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 | a0001c0001t0002g0347 | 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 | a0001c0001t0001g0067 | 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 | a0001c0001t0001g0028 a0001c0001t0001g0061 a0001c0001t0002g0360 others(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 | a0001c0002t0003g0208 | 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 | a0003c0004t0015g0243 a0003c0004t0015g0244 a0003c0004t0015g0249 others(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 | a0001c0001t0004g0332 a0001c0001t0004g0333 |
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 | a0001c0001t0002g0288 | 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 | a0001c0005t0022g0192 a0001c0005t0022g0194 a0001c0005t0085g0193 |
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 | 98 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(95): 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 | a0008c0008t0002g0004 | 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 | a0001c0001t0014g0365 a0001c0001t0014g0366 |
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 | a0001c0001t0005g0118 | 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 | a0001c0001t0009g0021 a0001c0001t0009g0054 a0001c0001t0009g0056 others(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 | a0001c0001t0005g0007 a0001c0001t0005g0010 a0001c0001t0005g0011 others(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 | a0003c0004t0015g0243 a0003c0004t0015g0244 a0003c0004t0015g0249 others(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 | a0001c0001t0008g0156 a0001c0001t0008g0157 a0001c0001t0008g0158 others(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 | a0003c0004t0015g0243 a0003c0004t0015g0244 a0003c0004t0015g0249 others(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 | a0001c0002t0003g0230 a0001c0002t0003g0233 a0001c0002t0003g0234 others(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 | a0001c0001t0056g0112 | 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 | a0001c0001t0003g0172 a0001c0001t0003g0174 a0001c0001t0003g0176 others(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 | a0001c0001t0013g0258 a0001c0001t0018g0133 a0001c0001t0018g0134 others(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 | a0001c0001t0002g0341 | 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 | a0001c0001t0006g0190 | 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 | a0001c0001t0034g0119 | 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 | a0001c0001t0002g0295 | 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 | a0001c0001t0004g0283 | 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 | a0001c0001t0006g0002 a0001c0001t0006g0181 a0001c0001t0006g0182 others(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 | a0001c0001t0001g0030 | 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 | a0001c0001t0002g0267 a0001c0001t0002g0268 a0001c0001t0002g0269 others(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 | a0001c0001t0013g0258 a0001c0001t0039g0127 a0001c0001t0040g0257 others(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 | a0001c0001t0002g0262 a0001c0001t0002g0263 a0001c0001t0002g0264 |
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 | a0001c0001t0004g0282 | 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 | a0001c0001t0003g0180 | 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 | a0001c0001t0003g0180 | 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 | a0001c0002t0007g0217 | 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 | a0001c0002t0007g0231 | 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 | a0001c0001t0006g0189 | 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 | a0001c0002t0003g0211 a0001c0002t0003g0212 a0001c0002t0003g0213 others(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 | a0001c0001t0002g0271 a0001c0001t0002g0272 a0001c0001t0002g0349 others(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 | a0001c0001t0003g0172 a0001c0001t0003g0174 a0001c0001t0003g0176 others(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 | a0001c0001t0034g0119 | 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 | a0001c0001t0002g0344 | 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 | a0001c0001t0002g0330 a0001c0001t0002g0344 a0001c0001t0004g0273 others(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 | 237 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(234): 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 | a0001c0001t0004g0138 a0001c0001t0004g0139 |
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 | a0001c0001t0033g0339 | 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 | 220 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(217): 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 | a0001c0001t0001g0074 a0001c0001t0002g0349 |
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 | a0001c0001t0003g0180 | 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 | a0001c0001t0002g0341 | 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 | 98 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(95): 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 | a0001c0001t0022g0191 a0001c0005t0022g0192 a0001c0005t0022g0194 others(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 | a0001c0001t0001g0069 a0001c0001t0027g0084 |
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 | a0001c0002t0003g0240 | 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 | 224 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(221): 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 | a0001c0001t0002g0317 | 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 | a0001c0001t0008g0156 a0001c0001t0008g0157 a0001c0001t0008g0158 others(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 | 98 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(95): 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 | a0001c0002t0007g0197 a0001c0002t0007g0198 a0001c0002t0007g0199 others(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 | a0001c0001t0002g0291 a0001c0001t0002g0295 a0001c0001t0002g0319 others(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 | a0001c0001t0001g0089 a0001c0001t0002g0355 a0001c0001t0004g0266 others(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 | a0001c0001t0006g0181 a0001c0001t0006g0183 |
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 | a0001c0001t0013g0258 a0001c0001t0018g0133 a0001c0001t0018g0134 others(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 | a0001c0002t0007g0197 a0001c0002t0007g0218 a0001c0002t0031g0216 others(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 | a0001c0002t0003g0252 a0001c0002t0003g0253 |
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 | a0001c0001t0001g0035 a0001c0001t0001g0044 a0001c0001t0001g0058 others(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 | a0001c0001t0051g0250 a0001c0001t0052g0251 |
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 | a0001c0001t0086g0167 | 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 | a0001c0001t0021g0169 | 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 | a0001c0001t0004g0336 a0001c0001t0004g0337 a0001c0001t0010g0289 |
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 | a0001c0001t0008g0156 a0001c0001t0008g0157 a0001c0001t0008g0158 others(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 | a0001c0001t0005g0007 a0001c0001t0005g0010 a0001c0001t0005g0011 others(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 | a0001c0001t0005g0007 a0001c0001t0005g0010 a0001c0001t0005g0011 others(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 | a0001c0001t0006g0002 a0001c0001t0006g0181 a0001c0001t0006g0182 others(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 | a0001c0001t0009g0056 | 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 | a0001c0001t0004g0309 a0001c0001t0004g0313 |
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 | a0001c0001t0019g0109 a0001c0001t0019g0110 a0001c0001t0019g0111 |
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 | a0001c0001t0008g0158 | 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 | a0001c0001t0030g0151 | 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 | a0001c0002t0003g0221 | 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 | 99 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(96): 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 | a0001c0001t0016g0120 | 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 | a0001c0001t0003g0172 a0001c0001t0003g0174 a0001c0001t0003g0176 others(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 | a0001c0001t0003g0172 a0001c0001t0003g0174 a0001c0001t0003g0176 others(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 | a0001c0001t0004g0137 | 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 | a0001c0001t0002g0347 | 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 | a0001c0001t0003g0172 a0001c0001t0003g0174 a0001c0001t0003g0176 others(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 | a0001c0001t0001g0025 a0001c0001t0006g0002 a0001c0001t0006g0181 others(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 | a0001c0001t0003g0172 a0001c0001t0003g0174 a0001c0001t0003g0176 others(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 | a0001c0001t0019g0109 a0001c0001t0019g0111 |
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 | a0001c0001t0004g0313 | 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 | a0001c0001t0038g0026 | 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 | a0001c0001t0001g0091 | 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 | a0001c0001t0056g0112 | 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 | a0001c0001t0034g0119 | 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 | a0001c0001t0076g0175 | 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 | a0001c0001t0004g0138 a0001c0001t0004g0139 |
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 | a0001c0001t0005g0010 a0001c0001t0005g0014 a0001c0001t0012g0005 others(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 | a0001c0001t0031g0170 | 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 | a0001c0001t0034g0119 | 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 | a0001c0001t0005g0007 a0001c0001t0005g0010 a0001c0001t0005g0011 others(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 | a0001c0001t0008g0156 a0001c0001t0008g0157 a0001c0001t0008g0158 others(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 | a0003c0004t0015g0243 a0003c0004t0015g0244 a0003c0004t0015g0249 others(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 | a0001c0001t0003g0172 a0001c0001t0003g0174 a0001c0001t0003g0176 others(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 | a0005c0011t0070g0019 | 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 | a0001c0001t0016g0120 a0001c0001t0016g0121 a0001c0001t0016g0122 others(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 | a0001c0001t0037g0132 | 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 | a0001c0001t0065g0168 | 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 | a0001c0001t0003g0172 a0001c0001t0003g0174 a0001c0001t0003g0176 others(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 | a0001c0001t0002g0328 | 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 | a0001c0001t0032g0178 | 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 | a0001c0001t0011g0149 | 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 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0012 others(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 | a0001c0001t0005g0114 a0001c0001t0005g0118 a0001c0001t0042g0115 |
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 | a0001c0001t0005g0116 a0001c0001t0005g0117 |
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 | a0001c0001t0011g0142 a0001c0001t0011g0144 a0001c0001t0011g0147 others(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 | a0001c0001t0011g0145 a0001c0001t0019g0109 a0001c0001t0019g0111 others(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 | a0001c0001t0001g0080 a0001c0001t0008g0160 a0001c0001t0030g0151 others(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 | a0001c0001t0008g0156 a0001c0001t0008g0163 a0001c0001t0008g0164 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0072 a0001c0001t0001g0073 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0071 a0001c0001t0001g0075 others(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 | a0001c0001t0051g0250 | 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 | a0001c0001t0052g0251 | 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 | a0001c0001t0056g0112 a0001c0001t0083g0367 |
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 | a0001c0001t0046g0031 | 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 | a0001c0001t0001g0027 | 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 | a0001c0001t0001g0107 | 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 | a0001c0001t0003g0174 | 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 | a0001c0001t0001g0065 a0001c0001t0001g0068 |
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 | a0001c0001t0001g0053 | 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 | a0001c0001t0009g0054 | 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 | a0001c0001t0001g0052 a0001c0001t0027g0084 |
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 | a0001c0001t0031g0170 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0064 others(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 | a0001c0001t0001g0028 | 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 | a0001c0001t0001g0101 a0001c0001t0020g0079 a0001c0001t0043g0041 |
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 | a0001c0001t0001g0108 a0001c0001t0009g0056 a0004c0010t0092g0246 |
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 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
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 | a0003c0004t0049g0248 | 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 | a0003c0004t0015g0249 | 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 | a0001c0001t0003g0176 a0001c0001t0003g0180 a0001c0001t0007g0171 others(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 | a0001c0001t0019g0110 a0001c0001t0076g0175 a0001c0001t0079g0153 others(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 | a0001c0001t0024g0034 a0001c0001t0024g0094 |
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 | a0001c0001t0001g0050 a0001c0001t0036g0086 a0001c0002t0074g0210 |
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 | a0001c0001t0001g0047 a0001c0001t0001g0089 a0001c0001t0001g0096 others(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 | a0001c0001t0001g0091 a0001c0001t0020g0024 |
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 | a0001c0001t0001g0025 a0001c0001t0021g0169 |
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 | a0001c0001t0001g0062 | 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 | a0001c0007t0003g0154 | 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 | a0001c0001t0001g0060 a0001c0002t0007g0199 a0001c0002t0031g0216 |
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 | a0001c0001t0001g0066 a0001c0001t0001g0090 a0001c0001t0027g0099 |
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 | a0001c0001t0001g0023 a0001c0001t0001g0036 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0055 a0001c0001t0001g0093 a0003c0004t0015g0243 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0030 a0001c0001t0001g0042 others(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 | a0001c0001t0001g0077 a0001c0001t0020g0046 |
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 | a0001c0001t0065g0168 | 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 | a0001c0001t0001g0043 a0001c0007t0003g0155 |
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 | a0001c0001t0024g0032 a0001c0001t0032g0178 a0001c0002t0003g0202 others(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 | a0001c0001t0032g0179 a0001c0002t0003g0207 |
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 | a0001c0001t0001g0088 | 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 | a0001c0001t0001g0048 a0001c0001t0001g0100 a0001c0001t0017g0039 others(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 | a0001c0001t0045g0106 a0003c0004t0015g0244 |
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 | a0001c0001t0013g0258 a0001c0001t0040g0257 a0002c0003t0013g0129 |
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 | a0001c0001t0037g0132 | 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 | a0001c0002t0003g0212 a0001c0002t0003g0225 a0001c0002t0003g0235 |
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 | a0001c0001t0034g0119 | 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 | a0001c0001t0001g0035 a0001c0002t0003g0240 a0001c0002t0007g0231 |
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 | a0001c0001t0001g0076 a0001c0001t0048g0078 a0001c0002t0003g0219 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0104 a0007c0012t0015g0245 |
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 | a0001c0001t0009g0021 | 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 | a0002c0003t0013g0128 a0002c0003t0013g0130 a0002c0003t0013g0131 |
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 | a0001c0001t0003g0254 a0001c0001t0018g0136 |
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 | a0001c0002t0003g0209 | 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 | a0001c0002t0003g0200 a0001c0002t0003g0201 a0001c0002t0003g0203 others(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 | a0001c0002t0003g0230 a0001c0002t0003g0238 a0001c0002t0078g0214 |
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 | a0001c0001t0088g0022 a0001c0002t0003g0208 a0001c0002t0003g0229 |
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 | a0001c0001t0023g0159 a0001c0001t0023g0166 |
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 | a0001c0001t0009g0085 a0001c0001t0009g0087 |
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 | a0002c0003t0035g0126 | 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 | a0001c0001t0018g0133 a0001c0001t0018g0134 |
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 | a0001c0002t0003g0224 a0001c0002t0003g0233 a0001c0002t0003g0234 others(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 | a0001c0001t0008g0162 a0001c0001t0023g0161 |
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 | a0001c0001t0041g0135 | 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 | a0001c0002t0003g0227 | 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 | a0001c0002t0003g0213 a0001c0002t0003g0215 |
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 | a0001c0002t0003g0237 | 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 | a0001c0002t0082g0222 | 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 | a0001c0002t0077g0220 | 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 | a0001c0002t0090g0223 a0001c0005t0022g0194 |
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 | a0001c0005t0022g0192 a0001c0005t0085g0193 |
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 | a0001c0002t0081g0241 a0001c0002t0089g0196 |
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 | a0001c0002t0003g0204 | 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 | a0001c0002t0021g0239 | 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 | a0001c0002t0080g0206 | 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 | a0001c0001t0022g0191 | 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 | a0001c0001t0005g0007 a0001c0001t0005g0177 |
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 | a0001c0001t0016g0124 | 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 | a0001c0001t0016g0120 | 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 | a0001c0001t0057g0125 | 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 | a0001c0001t0016g0121 a0001c0001t0016g0122 a0001c0001t0039g0127 |
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 | a0001c0001t0058g0123 | 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 | a0001c0001t0002g0326 a0001c0001t0004g0274 a0001c0001t0004g0332 others(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 | a0001c0002t0003g0252 a0001c0002t0003g0253 |
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 | a0001c0001t0002g0141 a0001c0001t0002g0267 a0001c0001t0002g0268 others(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 | a0001c0001t0006g0181 a0001c0001t0006g0182 a0001c0001t0006g0183 others(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 | a0001c0001t0006g0181 a0001c0001t0006g0182 a0001c0001t0006g0183 others(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 | a0001c0001t0006g0181 a0001c0001t0006g0182 a0001c0001t0006g0183 others(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 | a0001c0001t0006g0181 a0001c0001t0006g0182 a0001c0001t0006g0183 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0071 a0001c0001t0001g0072 others(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 | a0001c0001t0001g0080 | 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 | a0001c0001t0001g0020 a0001c0001t0001g0037 a0001c0001t0001g0071 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0037 a0001c0001t0001g0071 others(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 | a0001c0001t0008g0156 a0001c0001t0008g0157 a0001c0001t0008g0158 others(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 | a0001c0001t0011g0142 a0001c0001t0011g0144 a0001c0001t0011g0145 others(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 | a0001c0001t0005g0014 | 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 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0012 others(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 | a0001c0001t0012g0009 | 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 | a0001c0001t0001g0020 a0001c0001t0001g0037 a0001c0001t0001g0071 others(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 | a0005c0011t0070g0019 | 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 | a0001c0001t0042g0115 | 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 | a0001c0001t0019g0109 a0001c0001t0019g0111 |
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 | a0001c0001t0005g0116 a0001c0001t0005g0117 |
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 | a0001c0001t0005g0114 a0001c0001t0005g0118 |
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 | a0001c0001t0006g0181 a0001c0001t0006g0182 a0001c0001t0006g0183 others(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 | a0001c0001t0003g0174 a0001c0001t0003g0176 a0001c0001t0003g0180 others(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 | a0001c0001t0003g0254 a0001c0001t0052g0251 a0001c0001t0083g0367 others(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 | a0001c0001t0008g0160 a0001c0001t0008g0162 a0001c0001t0018g0133 others(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 | a0001c0001t0001g0088 a0001c0001t0021g0169 a0001c0001t0036g0086 others(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 |
9 | a0001c0001t0001g0001 a0001c0001t0016g0121 a0001c0001t0016g0122 others(6): 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 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0013g0258 others(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 | a0001c0001t0001g0091 a0001c0001t0001g0098 a0001c0001t0001g0104 others(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 | a0001c0001t0001g0053 a0001c0001t0001g0097 a0001c0001t0005g0007 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0035 others(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 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0059 others(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 | a0001c0001t0001g0023 a0001c0001t0001g0028 a0001c0001t0001g0069 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0057 a0001c0001t0001g0064 others(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 | a0001c0001t0001g0093 a0001c0001t0001g0101 |
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 | a0001c0001t0001g0020 a0001c0001t0001g0037 a0001c0001t0001g0071 others(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 | a0001c0001t0004g0348 | 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 | a0001c0001t0018g0133 a0001c0001t0018g0134 a0001c0001t0018g0136 others(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 | a0001c0001t0034g0119 | 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 | a0001c0001t0016g0120 | 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 | a0001c0001t0002g0259 a0001c0001t0002g0271 a0001c0001t0002g0278 others(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 | 137 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0027 others(134): 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 | a0001c0001t0051g0250 a0001c0001t0052g0251 |
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 | a0001c0001t0001g0063 | 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 | a0002c0003t0013g0128 a0002c0003t0013g0130 a0002c0003t0013g0131 |
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 | a0001c0002t0003g0209 | 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 | 251 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(248): 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 | a0001c0001t0011g0142 a0001c0001t0011g0144 a0001c0001t0011g0145 others(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 | a0001c0001t0034g0119 | 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 | a0001c0001t0001g0083 | 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 | a0001c0001t0003g0172 a0001c0001t0003g0174 a0001c0001t0003g0176 others(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 | a0001c0001t0002g0265 a0001c0001t0002g0279 a0001c0001t0002g0351 |
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 | a0001c0001t0050g0045 | 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 | a0001c0001t0005g0007 a0001c0001t0005g0010 a0001c0001t0005g0011 others(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 | a0001c0001t0025g0017 | 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 | 98 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(95): 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 | a0001c0001t0006g0002 a0001c0001t0006g0181 a0001c0001t0006g0182 others(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 | a0001c0001t0013g0258 a0001c0001t0018g0133 a0001c0001t0018g0134 others(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 | |||||||
chr8:97699436 | C | CA | 9 | a0001c0001t0001g0102 a0001c0001t0016g0120 a0001c0001t0016g0121 others(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 | a0001c0001t0006g0002 a0001c0001t0006g0181 a0001c0001t0006g0182 others(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 | a0001c0001t0006g0002 a0001c0001t0006g0181 a0001c0001t0006g0182 others(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 | a0001c0001t0009g0081 | 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 | a0001c0001t0001g0025 | 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 | a0001c0001t0004g0331 | 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 | a0001c0001t0039g0127 | 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 | a0003c0004t0015g0243 a0003c0004t0015g0244 a0003c0004t0015g0249 others(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 | 99 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(96): 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 | a0001c0001t0006g0190 | 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 | a0001c0001t0001g0053 | 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 | a0001c0001t0065g0168 | 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 | a0001c0001t0056g0112 | 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 | a0001c0001t0001g0023 | 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 | a0001c0001t0084g0312 | 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 | a0003c0004t0015g0243 a0003c0004t0015g0244 a0003c0004t0015g0249 others(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 | a0001c0001t0002g0355 | 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 | a0001c0001t0016g0120 | 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 | a0001c0002t0003g0204 | 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 | a0001c0001t0006g0002 a0001c0001t0006g0181 a0001c0001t0006g0182 others(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 | 223 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(220): 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 | a0001c0002t0003g0209 | 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 | a0001c0001t0002g0264 | 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 | a0001c0001t0056g0112 | 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 | a0001c0001t0012g0008 | 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 | a0001c0001t0006g0002 a0001c0001t0006g0181 a0001c0001t0006g0182 others(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 | a0001c0001t0004g0293 | 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 | a0001c0002t0003g0204 a0001c0002t0080g0206 a0001c0002t0081g0241 others(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 | a0001c0001t0002g0264 | 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 | a0001c0001t0002g0300 | 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 | a0001c0001t0039g0127 | 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 | a0001c0001t0002g0350 | 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 | a0003c0004t0015g0243 a0003c0004t0015g0244 a0003c0004t0015g0249 others(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 | a0001c0001t0003g0176 | 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 | a0001c0001t0013g0258 a0001c0001t0018g0133 a0001c0001t0018g0134 others(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 | a0001c0001t0038g0026 | 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 | a0001c0002t0003g0207 | 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 | a0001c0001t0002g0294 a0001c0001t0002g0316 a0001c0001t0069g0287 |
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 | a0001c0001t0008g0156 a0001c0001t0016g0121 a0001c0001t0016g0122 others(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 | a0001c0001t0002g0141 | 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 | a0001c0001t0016g0120 a0001c0001t0016g0121 a0001c0001t0016g0122 others(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 | a0001c0001t0004g0266 a0001c0001t0004g0277 a0001c0001t0004g0283 others(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 | a0001c0001t0002g0291 | 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 | a0001c0001t0004g0137 | 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 | a0001c0001t0037g0132 | 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 | a0001c0001t0016g0120 a0001c0001t0016g0121 a0001c0001t0016g0122 others(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 | a0001c0001t0006g0002 a0001c0001t0006g0181 a0001c0001t0006g0182 others(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 | a0001c0001t0001g0030 | 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 | a0005c0011t0070g0019 | 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 | a0001c0001t0051g0250 | 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 | a0003c0004t0015g0243 a0003c0004t0015g0244 a0003c0004t0015g0249 others(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 | a0001c0001t0002g0355 a0001c0001t0004g0293 a0001c0001t0029g0304 others(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 | a0001c0001t0002g0291 a0001c0001t0002g0295 a0001c0001t0002g0319 others(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 | a0001c0001t0004g0137 | 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 | a0001c0001t0001g0107 a0001c0001t0045g0106 |
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 | a0001c0001t0002g0140 a0001c0001t0002g0294 a0001c0001t0002g0301 others(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 | a0001c0001t0016g0120 a0001c0001t0016g0121 a0001c0001t0016g0122 others(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 | a0001c0001t0052g0251 | 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 | a0005c0011t0070g0019 | 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 | 251 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(248): 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 | a0001c0002t0003g0215 | 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 | a0001c0001t0008g0158 | 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 | a0001c0001t0002g0338 a0001c0001t0014g0357 |
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 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0002g0259 others(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 | a0001c0001t0003g0172 a0001c0001t0005g0016 a0001c0001t0006g0189 others(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 | a0001c0001t0006g0002 a0001c0001t0006g0181 a0001c0001t0006g0182 others(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 | a0001c0001t0013g0258 a0001c0001t0039g0127 a0001c0001t0040g0257 others(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 | a0001c0001t0008g0156 a0001c0001t0008g0157 a0001c0001t0008g0158 others(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 | a0001c0001t0001g0103 a0001c0001t0001g0105 a0001c0002t0003g0200 others(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 | a0001c0001t0002g0265 | 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 | a0001c0001t0030g0152 | 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 | a0001c0001t0001g0057 | 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 | a0001c0001t0002g0259 a0001c0001t0002g0264 a0001c0001t0002g0275 others(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 | a0001c0001t0002g0288 a0001c0001t0002g0355 a0001c0001t0004g0266 others(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 | a0001c0001t0004g0331 a0001c0001t0008g0157 a0001c0001t0008g0160 others(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 | a0001c0001t0006g0190 a0001c0001t0008g0158 a0001c0001t0008g0162 others(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 | a0001c0001t0011g0148 a0001c0002t0003g0202 a0001c0002t0003g0203 others(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 | a0001c0001t0003g0254 a0001c0001t0011g0149 a0001c0001t0030g0152 others(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 | a0001c0001t0003g0174 a0001c0001t0006g0184 a0001c0001t0006g0186 others(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 | a0001c0001t0003g0172 a0001c0001t0006g0002 a0001c0001t0006g0181 others(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 | a0001c0001t0003g0176 a0001c0001t0003g0180 a0001c0001t0006g0187 others(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 | a0001c0001t0022g0191 a0001c0001t0032g0179 a0001c0002t0078g0214 others(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 | a0001c0001t0032g0178 | 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 | a0001c0001t0072g0143 a0001c0002t0003g0215 |
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 | a0001c0001t0065g0168 | 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 | 31 | a0001c0001t0002g0255 a0001c0001t0002g0265 a0001c0001t0002g0267 others(28): Show |
31 | HG00544.hp2 HG00609.hp1 HG00639.hp1 others(28): 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 | a0001c0001t0004g0274 a0001c0001t0012g0015 a0001c0001t0016g0120 others(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 | a0001c0001t0004g0137 a0001c0001t0005g0114 a0001c0001t0005g0116 others(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 | a0001c0001t0005g0007 a0001c0001t0005g0010 a0001c0001t0005g0011 others(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 | a0001c0001t0001g0023 a0001c0001t0001g0028 a0001c0001t0001g0029 others(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 | 72 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0025 others(69): 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 | a0001c0002t0003g0209 a0001c0002t0003g0252 a0001c0002t0003g0253 |
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 | a0001c0001t0007g0171 a0001c0001t0007g0173 |
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 | a0001c0001t0013g0258 a0001c0001t0018g0133 a0001c0001t0018g0134 others(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 | a0001c0001t0008g0156 a0001c0001t0008g0157 a0001c0001t0008g0158 others(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 | 98 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(95): 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 | a0001c0001t0003g0172 a0001c0001t0003g0174 a0001c0001t0003g0176 others(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 | |||||||
chr8:97708551 | G | T | 90 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(87): 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 | a0002c0003t0035g0126 | 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 | a0001c0001t0072g0143 | 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 | 45 | a0001c0001t0002g0003 a0001c0001t0002g0141 a0001c0001t0002g0256 others(42): Show |
45 | HG00140.hp1 HG00597.hp1 HG00673.hp2 others(42): 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 | a0001c0001t0002g0003 a0001c0001t0002g0264 a0001c0001t0002g0349 others(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 | a0001c0001t0002g0265 a0001c0001t0002g0279 a0001c0001t0002g0301 others(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 | a0001c0001t0004g0306 a0001c0001t0005g0012 a0001c0001t0005g0014 others(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 | a0001c0001t0006g0186 a0001c0001t0006g0190 |
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 | a0001c0001t0006g0183 | 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 | a0001c0001t0006g0189 | 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 | a0001c0001t0006g0002 | 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 | a0001c0001t0006g0184 | 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 | a0001c0001t0006g0188 | 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 | a0001c0001t0006g0181 a0001c0001t0006g0182 |
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 | a0001c0001t0054g0002 | 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 | a0001c0001t0058g0123 | 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 | a0001c0001t0006g0187 | 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 | a0001c0001t0055g0185 | 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 | a0001c0001t0005g0007 a0001c0001t0005g0177 a0001c0001t0016g0124 others(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 | a0001c0001t0005g0113 a0001c0001t0013g0258 a0001c0001t0018g0134 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0035 others(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 | 72 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(69): 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 | a0001c0001t0001g0073 a0001c0001t0001g0093 a0001c0001t0001g0107 others(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 | a0001c0001t0003g0176 a0001c0001t0004g0266 a0001c0001t0031g0170 others(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 | a0001c0001t0002g0269 a0001c0001t0002g0271 a0001c0001t0002g0272 others(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 | a0001c0001t0011g0147 a0001c0001t0011g0148 a0001c0001t0011g0149 others(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 | a0001c0001t0002g0338 a0001c0001t0016g0122 |
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 | a0001c0001t0002g0315 | 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 | a0001c0002t0003g0202 | 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 | a0001c0002t0003g0202 | 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 | a0001c0002t0003g0202 | 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 | a0007c0012t0015g0245 | 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 | a0001c0001t0065g0168 | 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 | a0001c0001t0001g0107 a0001c0001t0002g0292 a0001c0001t0004g0273 others(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 | a0001c0001t0001g0073 a0001c0001t0001g0083 a0001c0001t0006g0002 others(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 | a0001c0001t0019g0109 a0001c0001t0019g0110 a0001c0001t0019g0111 |
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 | a0001c0001t0052g0251 | 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 | a0007c0012t0015g0245 | 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 | 224 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(221): 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 | a0001c0001t0068g0314 | 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 | a0001c0001t0001g0071 | 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 | a0001c0001t0039g0127 | 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 | a0001c0001t0051g0250 a0001c0001t0052g0251 |
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 | a0001c0001t0006g0002 a0001c0001t0006g0181 a0001c0001t0006g0182 others(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 | 249 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(246): 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 | a0001c0001t0003g0172 a0001c0001t0003g0174 a0001c0001t0003g0176 others(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 | a0001c0001t0014g0352 a0001c0001t0059g0261 |
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 | a0001c0001t0002g0140 a0001c0001t0002g0259 a0001c0001t0002g0275 others(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 | a0001c0001t0002g0281 a0001c0001t0002g0295 a0001c0001t0002g0297 others(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 | a0001c0001t0001g0097 a0001c0001t0003g0172 a0001c0001t0003g0174 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0044 a0001c0001t0001g0076 others(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 | 87 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(84): 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 | a0001c0001t0034g0119 | 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 | a0001c0001t0001g0089 | 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 | a0001c0001t0034g0119 | 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 | a0001c0001t0068g0314 | 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 | a0001c0001t0006g0002 a0001c0001t0006g0181 a0001c0001t0006g0182 others(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 | a0001c0001t0016g0120 a0001c0001t0016g0121 a0001c0001t0016g0122 others(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 | 101 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(98): 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 | a0001c0001t0006g0002 a0001c0001t0006g0181 a0001c0001t0006g0182 others(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 | a0001c0001t0001g0107 a0001c0001t0045g0106 |
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 | a0001c0001t0001g0072 | 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 | a0001c0001t0002g0288 | 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 | a0001c0001t0004g0273 a0001c0001t0004g0274 |
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 | a0001c0001t0002g0360 | 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 | a0001c0001t0073g0150 | 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 | a0001c0001t0051g0250 a0001c0001t0052g0251 |
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 | a0001c0001t0004g0306 | 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 | a0001c0001t0006g0190 | 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 | a0003c0004t0015g0243 a0003c0004t0015g0244 a0003c0004t0015g0249 others(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 | a0001c0001t0006g0002 a0001c0001t0006g0181 a0001c0001t0006g0182 others(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 | a0001c0001t0013g0258 a0001c0001t0018g0133 a0001c0001t0018g0134 others(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 | a0001c0001t0001g0102 | 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 | a0001c0001t0013g0258 a0001c0001t0039g0127 a0001c0001t0040g0257 others(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 | a0001c0001t0016g0120 a0001c0001t0016g0121 a0001c0001t0016g0122 others(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 | a0001c0001t0002g0360 | 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 | a0001c0001t0004g0331 | 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 | a0001c0001t0004g0138 | 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 | a0001c0001t0039g0127 | 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 | a0001c0001t0004g0273 a0001c0001t0004g0274 |
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 | a0001c0002t0089g0196 a0001c0002t0090g0223 |
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 | a0001c0001t0025g0013 | 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 | a0001c0001t0006g0002 a0001c0001t0006g0181 a0001c0001t0006g0182 others(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 | a0001c0001t0002g0360 | 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 | a0001c0002t0003g0227 | 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 | a0001c0001t0051g0250 a0001c0001t0052g0251 |
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 | a0001c0001t0019g0109 a0001c0001t0019g0110 a0001c0001t0019g0111 |
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 | a0001c0001t0065g0168 | 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 | a0001c0001t0004g0137 | 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 | a0008c0008t0002g0004 | 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 | a0001c0001t0009g0056 | 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 | 98 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(95): 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 | 99 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(96): 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 | a0001c0001t0013g0258 a0001c0001t0018g0133 a0001c0001t0018g0134 others(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 | a0001c0001t0013g0258 a0001c0001t0018g0133 a0001c0001t0018g0134 others(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 | a0001c0001t0002g0265 | 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 | 90 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(87): 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 | a0001c0001t0001g0051 a0001c0001t0001g0061 |
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 | 224 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(221): 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 | a0001c0001t0033g0339 | 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 | a0001c0001t0002g0317 | 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 | a0001c0001t0006g0002 a0001c0001t0006g0181 a0001c0001t0006g0182 others(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 | a0001c0001t0008g0157 a0001c0001t0008g0163 a0001c0001t0008g0164 |
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 | a0001c0001t0034g0119 | 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 | 99 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(96): 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 | a0001c0001t0004g0266 a0001c0001t0004g0277 a0001c0001t0004g0283 others(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 | a0001c0001t0001g0101 a0001c0001t0011g0142 a0001c0001t0011g0144 others(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 | a0001c0001t0052g0251 | 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 | a0001c0001t0002g0291 a0001c0001t0002g0295 a0001c0001t0002g0319 others(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 | a0001c0001t0040g0257 | 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 | a0001c0001t0005g0011 | 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 | a0001c0002t0003g0235 a0001c0002t0003g0237 a0001c0002t0021g0239 |
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 | a0001c0001t0002g0302 | 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 | a0001c0001t0013g0258 a0001c0001t0018g0133 a0001c0001t0018g0134 others(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 | a0001c0001t0034g0119 | 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 | a0001c0001t0011g0142 a0001c0001t0011g0144 a0001c0001t0011g0145 others(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 | a0001c0001t0042g0115 | 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 | a0001c0001t0005g0010 a0001c0001t0005g0014 a0001c0001t0012g0005 others(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 | a0001c0001t0006g0002 a0001c0001t0006g0181 a0001c0001t0006g0182 others(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 | a0001c0001t0002g0140 a0001c0001t0002g0297 a0001c0001t0004g0331 others(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 | 201 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(198): 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 | a0001c0001t0008g0156 a0001c0001t0008g0158 a0001c0001t0008g0160 others(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 | a0001c0001t0018g0133 a0001c0001t0018g0134 a0001c0001t0018g0136 others(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 | a0001c0001t0034g0119 | 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 | a0001c0001t0008g0165 | 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 | a0001c0001t0001g0057 a0001c0001t0001g0064 |
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 | a0001c0001t0024g0094 | 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 | a0001c0001t0067g0345 | 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 | a0004c0010t0092g0246 a0007c0012t0015g0245 |
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 | a0001c0001t0002g0350 | 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 | a0003c0004t0015g0249 a0003c0004t0049g0248 |
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 | a0003c0004t0015g0243 a0003c0004t0015g0244 a0003c0004t0015g0249 others(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 | a0001c0001t0010g0286 | 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 | 242 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(239): 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 | a0005c0011t0070g0019 | 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 | a0001c0001t0023g0159 | 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 | a0001c0001t0001g0044 a0001c0001t0002g0275 a0001c0001t0002g0281 others(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 | a0001c0001t0051g0250 a0001c0001t0052g0251 |
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 | a0002c0003t0013g0131 | 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 | a0001c0001t0018g0133 a0001c0001t0018g0134 a0001c0001t0018g0136 others(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 | a0001c0001t0012g0005 a0001c0001t0012g0006 |
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 | a0001c0001t0006g0002 a0001c0001t0006g0181 a0001c0001t0006g0182 others(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 | a0001c0001t0004g0138 a0001c0001t0004g0139 |
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 | 92 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(89): 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 | a0001c0001t0002g0263 a0001c0001t0002g0322 a0001c0001t0002g0338 others(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 | a0001c0001t0005g0010 a0001c0001t0005g0011 a0001c0001t0005g0012 others(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 | a0001c0001t0005g0007 a0001c0001t0005g0113 a0001c0001t0005g0114 others(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 | a0001c0001t0001g0077 a0001c0001t0001g0093 a0001c0001t0002g0329 others(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 | a0001c0001t0003g0172 a0001c0001t0003g0174 a0001c0001t0003g0176 others(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 | a0003c0004t0015g0243 a0003c0004t0015g0244 a0004c0010t0092g0246 others(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 | 98 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(95): 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 | a0001c0001t0028g0320 a0001c0001t0028g0321 |
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 | 99 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(96): 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 | a0001c0001t0005g0007 a0001c0001t0005g0010 a0001c0001t0005g0011 others(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 | 251 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(248): 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 | a0001c0001t0006g0002 a0001c0001t0006g0181 a0001c0001t0006g0182 others(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 | 90 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(87): 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 | a0001c0001t0034g0119 | 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 | a0001c0001t0003g0172 a0001c0001t0003g0174 a0001c0001t0003g0176 others(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 | a0001c0001t0001g0102 | 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 | a0001c0001t0001g0059 a0001c0001t0001g0092 a0001c0001t0005g0007 others(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 | a0001c0001t0008g0156 a0001c0001t0008g0157 a0001c0001t0008g0158 others(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 | 251 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(248): 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 | a0001c0001t0014g0365 a0001c0001t0014g0366 |
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 | a0001c0001t0013g0258 a0001c0001t0018g0133 a0001c0001t0018g0134 others(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 | 210 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(207): 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 | a0001c0001t0001g0044 a0001c0001t0001g0071 a0001c0001t0013g0258 others(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 | a0001c0001t0001g0107 a0001c0001t0045g0106 |
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 | a0001c0001t0022g0191 a0001c0005t0022g0192 a0001c0005t0022g0194 others(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 | a0001c0001t0018g0133 a0001c0001t0018g0134 a0001c0001t0018g0136 others(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 | a0001c0001t0034g0119 | 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 | a0001c0002t0003g0225 a0001c0002t0003g0228 |
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 | a0001c0001t0067g0345 | 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 | a0001c0001t0013g0258 a0001c0001t0018g0133 a0001c0001t0018g0134 others(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 | a0001c0001t0064g0284 | 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 | a0003c0004t0015g0243 | 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 | a0001c0002t0003g0202 a0001c0002t0003g0208 |
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 | a0001c0001t0005g0007 a0001c0001t0005g0010 a0001c0001t0005g0011 others(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 | a0005c0011t0070g0019 | 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 | a0003c0004t0015g0243 a0003c0004t0015g0244 a0003c0004t0015g0249 others(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 | a0003c0004t0015g0244 | 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 | a0001c0001t0034g0119 | 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 | 222 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(219): 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 | a0001c0001t0002g0256 | 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 | a0001c0001t0006g0002 a0001c0001t0006g0181 a0001c0001t0006g0182 others(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 | a0001c0001t0051g0250 a0001c0001t0052g0251 |
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 | a0001c0001t0034g0119 | 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 | a0001c0005t0022g0192 a0001c0005t0022g0194 a0001c0005t0085g0193 |
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 | a0001c0001t0005g0007 a0001c0001t0005g0010 a0001c0001t0005g0011 others(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 | a0001c0001t0034g0119 | 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 | a0001c0001t0001g0061 a0001c0001t0002g0262 a0001c0001t0002g0294 others(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 | a0001c0001t0086g0167 | 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 | 89 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(86): 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 | 279 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0023 others(276): 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 | a0001c0001t0008g0156 a0001c0001t0008g0157 a0001c0001t0008g0158 others(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 | a0001c0001t0001g0070 a0001c0001t0008g0156 a0001c0001t0008g0157 others(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 | a0001c0001t0008g0156 a0001c0001t0008g0157 a0001c0001t0008g0158 others(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 | a0001c0001t0001g0071 | 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 | a0001c0001t0003g0172 a0001c0001t0003g0174 a0001c0001t0003g0176 others(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 | a0001c0001t0073g0150 | 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 | a0001c0001t0019g0109 a0001c0001t0019g0110 a0001c0001t0019g0111 others(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 | a0001c0001t0064g0284 | 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 | a0001c0001t0001g0074 | 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 | a0001c0001t0004g0285 | 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 | a0001c0001t0001g0050 | 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 | a0001c0001t0022g0191 a0001c0005t0022g0192 a0001c0005t0022g0194 others(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 | a0001c0001t0034g0119 | 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 | a0001c0001t0019g0109 a0001c0001t0019g0110 a0001c0001t0019g0111 |
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 | a0001c0001t0003g0172 a0001c0001t0003g0174 a0001c0001t0003g0176 others(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 | a0001c0001t0011g0142 a0001c0001t0011g0144 a0001c0001t0011g0145 others(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 |