geneid | 3030 |
---|---|
ensemblid | ENSG00000084754.12 |
hgncid | 4801 |
symbol | HADHA |
name | hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha |
refseq_nuc | NM_000182.5 |
refseq_prot | NP_000173.2 |
ensembl_nuc | ENST00000380649.8 |
ensembl_prot | ENSP00000370023.3 |
mane_status | MANE Select |
chr | chr2 |
start | 26190635 |
end | 26244632 |
strand | - |
ver | v1.2 |
region | chr2:26190635-26244632 |
region5000 | chr2:26185635-26249632 |
regionname0 | HADHA_chr2_26190635_26244632 |
regionname5000 | HADHA_chr2_26185635_26249632 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 763 | 259 | 62 | 64 | 101 | 4 | 26 | 74 | HADHA_chr2_26185635_26249632 | HADHA | copy fasta | chr2 | 26185635 | 26249632 |
a0002 | 0/0 | 763 | 10 | 10 | 0 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | copy fasta | chr2 | 26185635 | 26249632 |
a0003 | 0/0 | 763 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | copy fasta | chr2 | 26185635 | 26249632 |
a0004 | 0/0 | 763 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | copy fasta | chr2 | 26185635 | 26249632 |
a0005 | 0/0 | 763 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | copy fasta | chr2 | 26185635 | 26249632 |
a0006 | 0/0 | 763 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | copy fasta | chr2 | 26185635 | 26249632 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2292 | 212 | 61 | 54 | 74 | 2 | 19 | HADHA_chr2_26185635_26249632 | HADHA | copy fasta | chr2 | 26185635 | 26249632 |
c0002 | 0/0 | 2292 | 44 | 1 | 9 | 25 | 2 | 7 | HADHA_chr2_26185635_26249632 | HADHA | copy fasta | chr2 | 26185635 | 26249632 |
c0003 | 0/0 | 2292 | 10 | 10 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | copy fasta | chr2 | 26185635 | 26249632 |
c0004 | 0/0 | 2292 | 2 | 2 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | copy fasta | chr2 | 26185635 | 26249632 |
c0005 | 0/0 | 2292 | 2 | 0 | 0 | 2 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | copy fasta | chr2 | 26185635 | 26249632 |
c0006 | 0/0 | 2292 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | copy fasta | chr2 | 26185635 | 26249632 |
c0007 | 0/0 | 2292 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | copy fasta | chr2 | 26185635 | 26249632 |
c0008 | 0/0 | 2292 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | copy fasta | chr2 | 26185635 | 26249632 |
c0009 | 0/0 | 2292 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | copy fasta | chr2 | 26185635 | 26249632 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 652 | 198 | 53 | 50 | 73 | 2 | 19 | HADHA_chr2_26185635_26249632 | HADHA | copy fasta | chr2 | 26185635 | 26249632 |
t0002 | 0/0 | 652 | 40 | 0 | 8 | 23 | 2 | 7 | HADHA_chr2_26185635_26249632 | HADHA | copy fasta | chr2 | 26185635 | 26249632 |
t0003 | 0/0 | 652 | 17 | 14 | 3 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | copy fasta | chr2 | 26185635 | 26249632 |
t0004 | 1/0 | 652 | 10 | 1 | 4 | 4 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | copy fasta | chr2 | 26185635 | 26249632 |
t0005 | 0/0 | 652 | 3 | 3 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | copy fasta | chr2 | 26185635 | 26249632 |
t0006 | 0/0 | 652 | 2 | 2 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | copy fasta | chr2 | 26185635 | 26249632 |
t0007 | 0/0 | 652 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | copy fasta | chr2 | 26185635 | 26249632 |
t0008 | 0/0 | 652 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | copy fasta | chr2 | 26185635 | 26249632 |
t0009 | 0/0 | 652 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | copy fasta | chr2 | 26185635 | 26249632 |
t0010 | 0/0 | 652 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | copy fasta | chr2 | 26185635 | 26249632 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 6 | 0 | 4 | 2 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0002 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0003 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0007 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0019 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0124 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2292 | 212 | 61 | 54 | 74 | 2 | 19 | HADHA_chr2_26185635_26249632 | HADHA | copy fasta | chr2 | 26185635 | 26249632 |
a0001c0002 | 0/0 | 2292 | 44 | 1 | 9 | 25 | 2 | 7 | HADHA_chr2_26185635_26249632 | HADHA | copy fasta | chr2 | 26185635 | 26249632 |
a0001c0005 | 0/0 | 2292 | 2 | 0 | 0 | 2 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | copy fasta | chr2 | 26185635 | 26249632 |
a0001c0007 | 0/0 | 2292 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | copy fasta | chr2 | 26185635 | 26249632 |
a0002c0003 | 0/0 | 2292 | 10 | 10 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | copy fasta | chr2 | 26185635 | 26249632 |
a0003c0004 | 0/0 | 2292 | 2 | 2 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | copy fasta | chr2 | 26185635 | 26249632 |
a0004c0008 | 0/0 | 2292 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | copy fasta | chr2 | 26185635 | 26249632 |
a0005c0006 | 0/0 | 2292 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | copy fasta | chr2 | 26185635 | 26249632 |
a0006c0009 | 0/0 | 2292 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | copy fasta | chr2 | 26185635 | 26249632 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2943 | 192 | 51 | 47 | 72 | 2 | 19 | HADHA_chr2_26185635_26249632 | HADHA | copy fasta | chr2 | 26185635 | 26249632 |
a0001c0001t0003 | 0/0 | 2943 | 7 | 4 | 3 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | copy fasta | chr2 | 26185635 | 26249632 |
a0001c0001t0004 | 1/0 | 2943 | 5 | 1 | 3 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | copy fasta | chr2 | 26185635 | 26249632 |
a0001c0001t0005 | 0/0 | 2943 | 3 | 3 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | copy fasta | chr2 | 26185635 | 26249632 |
a0001c0001t0006 | 0/0 | 2943 | 2 | 2 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | copy fasta | chr2 | 26185635 | 26249632 |
a0001c0001t0007 | 0/0 | 2943 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | copy fasta | chr2 | 26185635 | 26249632 |
a0001c0001t0008 | 0/0 | 2943 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | copy fasta | chr2 | 26185635 | 26249632 |
a0001c0001t0009 | 0/0 | 2943 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | copy fasta | chr2 | 26185635 | 26249632 |
a0001c0002t0002 | 0/0 | 2943 | 38 | 0 | 8 | 21 | 2 | 7 | HADHA_chr2_26185635_26249632 | HADHA | copy fasta | chr2 | 26185635 | 26249632 |
a0001c0002t0004 | 0/0 | 2943 | 5 | 0 | 1 | 4 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | copy fasta | chr2 | 26185635 | 26249632 |
a0001c0002t0010 | 0/0 | 2943 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | copy fasta | chr2 | 26185635 | 26249632 |
a0001c0005t0002 | 0/0 | 2943 | 2 | 0 | 0 | 2 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | copy fasta | chr2 | 26185635 | 26249632 |
a0001c0007t0001 | 0/0 | 2943 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | copy fasta | chr2 | 26185635 | 26249632 |
a0002c0003t0003 | 0/0 | 2943 | 10 | 10 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | copy fasta | chr2 | 26185635 | 26249632 |
a0003c0004t0001 | 0/0 | 2943 | 2 | 2 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | copy fasta | chr2 | 26185635 | 26249632 |
a0004c0008t0001 | 0/0 | 2943 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | copy fasta | chr2 | 26185635 | 26249632 |
a0005c0006t0001 | 0/0 | 2943 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | copy fasta | chr2 | 26185635 | 26249632 |
a0006c0009t0001 | 0/0 | 2943 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | copy fasta | chr2 | 26185635 | 26249632 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 6 | 0 | 4 | 2 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0007 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0003g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0004g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0004g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0004g0124 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0005g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0005g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0005g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0006g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0006g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0007g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0008g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0001t0009g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0002t0002g0002 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0002t0002g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0002t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0002t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0002t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0002t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0002t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0002t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0002t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0002t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0002t0004g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0002t0004g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0002t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0002t0010g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0005t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0001c0007t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0002c0003t0003g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0002c0003t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0002c0003t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0002c0003t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0002c0003t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0002c0003t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0002c0003t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0002c0003t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0002c0003t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0003c0004t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0003c0004t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0004c0008t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0005c0006t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
a0006c0009t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0002 | t0002 | g0225 | EUR | GBR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0092 | EUR | GBR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | CHS | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG00639 | hp2 | a0001 | c0001 | t0009 | g0112 | AMR | PUR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG00733 | hp2 | a0001 | c0001 | t0003 | g0034 | AMR | PUR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG00738 | hp1 | a0001 | c0002 | t0002 | g0217 | AMR | PUR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01069 | hp1 | a0001 | c0002 | t0004 | g0212 | AMR | PUR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01069 | hp2 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01071 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01074 | hp2 | a0001 | c0001 | t0003 | g0037 | AMR | PUR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01106 | hp2 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0035 | AMR | PUR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01175 | hp1 | a0001 | c0002 | t0002 | g0234 | AMR | PUR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01192 | hp1 | a0001 | c0002 | t0002 | g0209 | AMR | PUR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01255 | hp1 | a0006 | c0009 | t0001 | g0190 | AMR | CLM | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01358 | hp2 | a0005 | c0006 | t0001 | g0161 | AMR | CLM | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01884 | hp2 | a0002 | c0003 | t0003 | g0199 | AFR | ACB | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01981 | hp2 | a0001 | c0002 | t0002 | g0236 | AMR | PEL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02004 | hp1 | a0001 | c0002 | t0002 | g0211 | AMR | PEL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02004 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02015 | hp1 | a0001 | c0001 | t0007 | g0165 | EAS | KHV | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02015 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02040 | hp1 | a0001 | c0002 | t0002 | g0229 | EAS | KHV | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02055 | hp1 | a0001 | c0001 | t0005 | g0051 | AFR | ACB | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02055 | hp2 | a0001 | c0001 | t0006 | g0240 | AFR | ACB | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02074 | hp1 | a0001 | c0002 | t0004 | g0006 | EAS | KHV | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02080 | hp2 | a0001 | c0002 | t0002 | g0220 | EAS | KHV | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02129 | hp1 | a0004 | c0008 | t0001 | g0158 | EAS | KHV | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02129 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02135 | hp2 | a0001 | c0005 | t0002 | g0023 | EAS | KHV | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02155 | hp1 | a0001 | c0005 | t0002 | g0023 | EAS | CDX | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | CDX | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | ACB | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02300 | hp1 | a0001 | c0007 | t0001 | g0069 | AMR | PEL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02300 | hp2 | a0001 | c0002 | t0002 | g0222 | AMR | PEL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02622 | hp2 | a0002 | c0003 | t0003 | g0197 | AFR | GWD | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02630 | hp2 | a0002 | c0003 | t0003 | g0021 | AFR | GWD | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02717 | hp1 | a0002 | c0003 | t0003 | g0198 | AFR | GWD | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02717 | hp2 | a0003 | c0004 | t0001 | g0117 | AFR | GWD | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0138 | AFR | GWD | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02897 | hp2 | a0003 | c0004 | t0001 | g0116 | AFR | GWD | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ESN | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ESN | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | ESN | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02976 | hp1 | a0002 | c0003 | t0003 | g0196 | AFR | ESN | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02976 | hp2 | a0001 | c0001 | t0005 | g0050 | AFR | ESN | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG03017 | hp2 | a0001 | c0002 | t0002 | g0206 | SAS | PJL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | MSL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG03130 | hp1 | a0001 | c0001 | t0006 | g0239 | AFR | ESN | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG03139 | hp1 | a0001 | c0001 | t0005 | g0126 | AFR | ESN | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ESN | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ESN | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | MSL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | MSL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG03225 | hp1 | a0002 | c0003 | t0003 | g0026 | AFR | MSL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | MSL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | MSL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0031 | AFR | MSL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG03486 | hp1 | a0002 | c0003 | t0003 | g0027 | AFR | MSL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | MSL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG03490 | hp2 | a0001 | c0002 | t0002 | g0022 | SAS | PJL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG03492 | hp2 | a0001 | c0002 | t0002 | g0226 | SAS | PJL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0036 | AFR | ESN | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG03540 | hp2 | a0002 | c0003 | t0003 | g0021 | AFR | GWD | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG03654 | hp2 | a0001 | c0002 | t0002 | g0022 | SAS | PJL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG03669 | hp2 | a0001 | c0002 | t0002 | g0214 | SAS | PJL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG03710 | hp2 | a0001 | c0002 | t0002 | g0219 | SAS | PJL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | BEB | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | BEB | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG04184 | hp1 | a0001 | c0002 | t0002 | g0237 | SAS | BEB | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | BEB | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | STU | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | STU | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | STU | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | STU | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | YRI | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | YRI | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | CHB | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHB | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA18940 | hp1 | a0001 | c0002 | t0002 | g0231 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA18947 | hp1 | a0001 | c0002 | t0002 | g0228 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA18950 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA18954 | hp1 | a0001 | c0002 | t0004 | g0006 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA18965 | hp1 | a0001 | c0002 | t0002 | g0223 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA18974 | hp1 | a0001 | c0002 | t0002 | g0215 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA18979 | hp1 | a0001 | c0002 | t0002 | g0235 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA18982 | hp2 | a0001 | c0002 | t0004 | g0232 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA18988 | hp2 | a0001 | c0002 | t0002 | g0218 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA18991 | hp1 | a0001 | c0002 | t0002 | g0024 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA18993 | hp2 | a0001 | c0002 | t0002 | g0216 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA18994 | hp1 | a0001 | c0002 | t0002 | g0208 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA19002 | hp1 | a0001 | c0002 | t0004 | g0006 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA19003 | hp2 | a0001 | c0002 | t0002 | g0227 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA19011 | hp2 | a0001 | c0002 | t0002 | g0221 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | LWK | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | LWK | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA19057 | hp2 | a0001 | c0002 | t0002 | g0207 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA19058 | hp1 | a0001 | c0002 | t0002 | g0024 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA19067 | hp1 | a0001 | c0002 | t0002 | g0233 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA19067 | hp2 | a0001 | c0001 | t0008 | g0187 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA19070 | hp1 | a0001 | c0002 | t0002 | g0210 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA19090 | hp1 | a0001 | c0002 | t0002 | g0224 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0088 | EUR | TSI | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA20805 | hp2 | a0001 | c0002 | t0002 | g0230 | EUR | TSI | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01123 | hp1 | a0001 | c0002 | t0002 | g0213 | AMR | CLM | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0033 | AFR | ACB | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG03471 | hp1 | a0001 | c0001 | t0004 | g0032 | AFR | MSL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG03471 | hp2 | a0002 | c0003 | t0003 | g0108 | AFR | MSL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | USA | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | USA | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA20300 | hp1 | a0002 | c0003 | t0003 | g0200 | AFR | USA | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | USA | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA21309 | hp1 | a0001 | c0002 | t0010 | g0238 | AFR | LWK | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | LWK | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0007 | REF | REF | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0004 | g0124 | REF | REF | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:26197705
|
T | C | 1 | a0004 | 1 | HG02129.hp1 | missense_variant | MODERATE | c.1465A>G | p.Lys489Glu | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 14/20 | 1501/2943 | 1465/2292 | 489/763 | chr2 | 26197705 | ||
chr2:26197731
|
G | T | 1 | a0005 | 1 | HG01358.hp2 | missense_variant | MODERATE | c.1439C>A | p.Pro480Gln | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 14/20 | 1475/2943 | 1439/2292 | 480/763 | chr2 | 26197731 | ||
chr2:26209793
|
G | T | 1 | a0002 | 10 | HG01884.hp2 HG02622.hp2 HG02630.hp2 others(7): Show |
missense_variant | MODERATE | c.1072C>A | p.Gln358Lys | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 11/20 | 1108/2943 | 1072/2292 | 358/763 | chr2 | 26209793 | ||
chr2:26230279
|
C | A | 1 | a0003 | 2 | HG02717.hp2 HG02897.hp2 |
missense_variant | MODERATE | c.589G>T | p.Ala197Ser | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/20 | 625/2943 | 589/2292 | 197/763 | chr2 | 26230279 | ||
chr2:26239136
|
T | C | 1 | a0006 | 1 | HG01255.hp1 | missense_variant | MODERATE | c.75A>G | p.Ile25Met | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 2/20 | 111/2943 | 75/2292 | 25/763 | chr2 | 26239136 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:26192329
|
G | A | 1 | a0001c0007 | 1 | HG02300.hp1 | synonymous_variant | LOW | c.1981C>T | p.Leu661Leu | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 18/20 | 2017/2943 | 1981/2292 | 661/763 | chr2 | 26192329 | ||
chr2:26201257
|
G | A | 1 | a0001c0005 | 2 | HG02135.hp2 HG02155.hp1 |
synonymous_variant | LOW | c.1284C>T | p.Asn428Asn | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 13/20 | 1320/2943 | 1284/2292 | 428/763 | chr2 | 26201257 | ||
chr2:26232259
|
G | A | 2 | a0001c0002a0001c0005 | 46 | HG00140.hp1 HG00738.hp1 HG01069.hp1 others(43): Show |
synonymous_variant | LOW | c.474C>T | p.Tyr158Tyr | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 6/20 | 510/2943 | 474/2292 | 158/763 | chr2 | 26232259 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:26190688
|
G | A | 1 | a0001c0001t0007 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*562C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 20/20 | 562 | chr2 | 26190688 | |||||
chr2:26190689
|
G | A | 1 | a0001c0001t0005 | 3 | HG02055.hp1 HG02976.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*561C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 20/20 | 561 | chr2 | 26190689 | |||||
chr2:26190740
|
T | A | 3 | a0001c0001t0003a0001c0001t0006a0002c0003t0003 | 19 | HG00733.hp2 HG01074.hp2 HG01167.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*510A>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 20/20 | 510 | chr2 | 26190740 | |||||
chr2:26190847
|
G | A | 1 | a0001c0001t0008 | 1 | NA19067.hp2 | 3_prime_UTR_variant | MODIFIER | c.*403C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 20/20 | 403 | chr2 | 26190847 | |||||
chr2:26190948
|
C | T | 3 | a0001c0002t0002a0001c0002t0010a0001c0005t0002 | 41 | HG00140.hp1 HG00738.hp1 HG01123.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*302G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 20/20 | 302 | chr2 | 26190948 | |||||
chr2:26191038
|
T | C | 1 | a0001c0001t0009 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*212A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 20/20 | 212 | chr2 | 26191038 | |||||
chr2:26191048
|
C | T | 10 | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(7): Show | 204 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(201): Show |
3_prime_UTR_variant | MODIFIER | c.*202G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 20/20 | 202 | chr2 | 26191048 | |||||
chr2:26191224
|
C | A | 1 | a0001c0002t0010 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*26G>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 20/20 | 26 | chr2 | 26191224 | |||||
chr2:26244621
|
G | C | 1 | a0001c0001t0006 | 2 | HG02055.hp2 HG03130.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-25C>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/20 | chr2 | 26244621 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:26191664
|
G | A | 1 | a0001c0001t0001g0134 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2001-36C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 18/19 | chr2 | 26191664 | ||||||
chr2:26191741
|
T | A | 1 | a0001c0001t0001g0129 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2001-113A>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 18/19 | chr2 | 26191741 | ||||||
chr2:26191966
|
G | A | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.2001-338C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 18/19 | chr2 | 26191966 | ||||||
chr2:26191967
|
G | A | 1 | a0001c0002t0002g0215 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2001-339C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 18/19 | chr2 | 26191967 | ||||||
chr2:26191978
|
A | C | 35 | a0001c0002t0002g0002a0001c0002t0002g0022a0001c0002t0002g0024others(32): Show | 41 | HG00140.hp1 HG00738.hp1 HG01123.hp1 others(38): Show |
intron_variant | MODIFIER | c.2000+332T>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 18/19 | chr2 | 26191978 | ||||||
chr2:26192020
|
C | T | 8 | a0001c0001t0003g0033a0001c0001t0003g0034a0001c0001t0003g0035others(5): Show | 8 | HG00733.hp2 HG01074.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.2000+290G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 18/19 | chr2 | 26192020 | ||||||
chr2:26192129
|
A | G | 2 | a0001c0001t0001g0125a0001c0001t0005g0126 | 2 | HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2000+181T>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 18/19 | chr2 | 26192129 | ||||||
chr2:26192161
|
C | G | 2 | a0003c0004t0001g0116a0003c0004t0001g0117 | 2 | HG02717.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2000+149G>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 18/19 | chr2 | 26192161 | ||||||
chr2:26192219
|
T | TA | 19 | a0001c0001t0003g0031a0001c0001t0003g0033a0001c0001t0003g0034others(16): Show | 20 | HG00733.hp2 HG01074.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.2000+90dupT | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 18/19 | chr2 | 26192219 | ||||||
chr2:26192219
|
TA | T | 36 | a0001c0001t0001g0066a0001c0002t0002g0002a0001c0002t0002g0022others(33): Show | 42 | HG00140.hp1 HG00738.hp1 HG01123.hp1 others(39): Show |
intron_variant | MODIFIER | c.2000+90delT | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 18/19 | chr2 | 26192219 | ||||||
chr2:26192224
|
A | C | 88 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(85): Show | 103 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.2000+86T>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 18/19 | chr2 | 26192224 | ||||||
chr2:26192239
|
A | C | 10 | a0001c0001t0003g0138a0002c0003t0003g0021a0002c0003t0003g0026others(7): Show | 11 | HG01884.hp2 HG02622.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.2000+71T>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 18/19 | chr2 | 26192239 | ||||||
chr2:26192254
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2000+56G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 18/19 | chr2 | 26192254 | ||||||
chr2:26192558
|
G | A | 6 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0045others(3): Show | 6 | HG01884.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1886-134C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 17/19 | chr2 | 26192558 | ||||||
chr2:26192560
|
A | G | 203 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(200): Show | 231 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(228): Show |
intron_variant | MODIFIER | c.1886-136T>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 17/19 | chr2 | 26192560 | ||||||
chr2:26192692
|
G | C | 1 | a0001c0002t0002g0220 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1886-268C>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 17/19 | chr2 | 26192692 | ||||||
chr2:26192919
|
C | T | 1 | a0001c0001t0003g0031 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1886-495G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 17/19 | chr2 | 26192919 | ||||||
chr2:26192980
|
C | G | 2 | a0001c0001t0001g0139a0001c0001t0003g0138 | 2 | HG02723.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1886-556G>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 17/19 | chr2 | 26192980 | ||||||
chr2:26193028
|
A | G | 202 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(199): Show | 230 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(227): Show |
intron_variant | MODIFIER | c.1885+549T>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 17/19 | chr2 | 26193028 | ||||||
chr2:26193043
|
T | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(198): Show | 227 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.1885+534A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 17/19 | chr2 | 26193043 | ||||||
chr2:26193126
|
G | A | 1 | a0001c0001t0004g0004 | 3 | HG01069.hp2 HG01071.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.1885+451C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 17/19 | chr2 | 26193126 | ||||||
chr2:26193167
|
T | G | 203 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(200): Show | 231 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(228): Show |
intron_variant | MODIFIER | c.1885+410A>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 17/19 | chr2 | 26193167 | ||||||
chr2:26193288
|
G | T | 7 | a0002c0003t0003g0021a0002c0003t0003g0108a0002c0003t0003g0196others(4): Show | 8 | HG01884.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1885+289C>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 17/19 | chr2 | 26193288 | ||||||
chr2:26193293
|
C | CT | 4 | a0001c0001t0001g0078a0001c0001t0001g0205a0001c0001t0004g0004others(1): Show | 6 | HG01069.hp2 HG01071.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.1885+283dupA | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 17/19 | chr2 | 26193293 | ||||||
chr2:26193293
|
C | CTT | 92 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(89): Show | 101 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.1885+282_1885+283d others(4): Show |
HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 17/19 | chr2 | 26193293 | ||||||
chr2:26193293
|
C | CTTT | 96 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(93): Show | 111 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(108): Show |
intron_variant | MODIFIER | c.1885+281_1885+283d others(5): Show |
HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 17/19 | chr2 | 26193293 | ||||||
chr2:26193293
|
C | CTTTT | 10 | a0001c0001t0001g0125a0001c0001t0001g0143a0001c0001t0001g0149others(7): Show | 10 | HG02135.hp1 HG02818.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.1885+280_1885+283d others(6): Show |
HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 17/19 | chr2 | 26193293 | ||||||
chr2:26193432
|
A | G | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(198): Show | 227 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.1885+145T>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 17/19 | chr2 | 26193432 | ||||||
chr2:26193778
|
C | T | 2 | a0001c0001t0006g0239a0001c0001t0006g0240 | 2 | HG02055.hp2 HG03130.hp1 |
splice_region_variant&intron_variant | LOW | c.1690-6G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 16/19 | chr2 | 26193778 | ||||||
chr2:26193993
|
G | A | 8 | a0001c0001t0003g0033a0001c0001t0003g0034a0001c0001t0003g0035others(5): Show | 8 | HG00733.hp2 HG01074.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.1690-221C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 16/19 | chr2 | 26193993 | ||||||
chr2:26194031
|
G | T | 7 | a0002c0003t0003g0021a0002c0003t0003g0108a0002c0003t0003g0196others(4): Show | 8 | HG01884.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1690-259C>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 16/19 | chr2 | 26194031 | ||||||
chr2:26194093
|
C | T | 17 | a0001c0001t0003g0033a0001c0001t0003g0034a0001c0001t0003g0035others(14): Show | 18 | HG00733.hp2 HG01074.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.1690-321G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 16/19 | chr2 | 26194093 | ||||||
chr2:26194172
|
C | G | 1 | a0001c0001t0001g0155 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1689+398G>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 16/19 | chr2 | 26194172 | ||||||
chr2:26194226
|
T | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(198): Show | 227 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.1689+344A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 16/19 | chr2 | 26194226 | ||||||
chr2:26194494
|
T | A | 3 | a0001c0001t0001g0014a0001c0001t0001g0163a0001c0001t0001g0164 | 4 | HG00408.hp2 NA18947.hp2 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.1689+76A>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 16/19 | chr2 | 26194494 | ||||||
chr2:26194664
|
C | A | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(198): Show | 227 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.1621-26G>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 15/19 | chr2 | 26194664 | ||||||
chr2:26194811
|
G | T | 1 | a0001c0001t0001g0159 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1621-173C>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 15/19 | chr2 | 26194811 | ||||||
chr2:26194960
|
G | A | 3 | a0001c0001t0001g0071a0001c0001t0001g0080a0001c0001t0001g0085 | 3 | HG01123.hp2 HG01258.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.1620+132C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 15/19 | chr2 | 26194960 | ||||||
chr2:26195081
|
C | G | 9 | a0001c0001t0003g0031a0001c0001t0003g0033a0001c0001t0003g0034others(6): Show | 9 | HG00733.hp2 HG01074.hp2 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.1620+11G>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 15/19 | chr2 | 26195081 | ||||||
chr2:26195545
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1480-313G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 14/19 | chr2 | 26195545 | ||||||
chr2:26195599
|
C | T | 2 | a0002c0003t0003g0026a0002c0003t0003g0027 | 2 | HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1480-367G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 14/19 | chr2 | 26195599 | ||||||
chr2:26195604
|
G | C | 2 | a0001c0002t0002g0208a0001c0002t0002g0227 | 2 | NA18994.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.1480-372C>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 14/19 | chr2 | 26195604 | ||||||
chr2:26195612
|
G | T | 1 | a0001c0001t0001g0155 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1480-380C>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 14/19 | chr2 | 26195612 | ||||||
chr2:26195673
|
C | T | 1 | a0001c0001t0001g0140 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1480-441G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 14/19 | chr2 | 26195673 | ||||||
chr2:26195919
|
A | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(198): Show | 227 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.1480-687T>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 14/19 | chr2 | 26195919 | ||||||
chr2:26196111
|
A | T | 1 | a0002c0003t0003g0200 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1480-879T>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 14/19 | chr2 | 26196111 | ||||||
chr2:26196174
|
G | C | 3 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030 | 3 | HG01167.hp2 HG01169.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1480-942C>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 14/19 | chr2 | 26196174 | ||||||
chr2:26196419
|
A | G | 9 | a0001c0001t0003g0031a0001c0001t0003g0033a0001c0001t0003g0034others(6): Show | 9 | HG00733.hp2 HG01074.hp2 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.1480-1187T>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 14/19 | chr2 | 26196419 | ||||||
chr2:26196601
|
C | G | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(198): Show | 227 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.1479+1090G>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 14/19 | chr2 | 26196601 | ||||||
chr2:26196605
|
C | T | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(180): Show | 208 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(205): Show |
intron_variant | MODIFIER | c.1479+1086G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 14/19 | chr2 | 26196605 | ||||||
chr2:26196613
|
C | T | 192 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(189): Show | 218 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.1479+1078G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 14/19 | chr2 | 26196613 | ||||||
chr2:26196641
|
T | C | 2 | a0001c0001t0001g0009a0001c0001t0001g0089 | 3 | HG03490.hp1 HG03492.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1479+1050A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 14/19 | chr2 | 26196641 | ||||||
chr2:26196727
|
G | T | 1 | a0001c0001t0001g0091 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1479+964C>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 14/19 | chr2 | 26196727 | ||||||
chr2:26196866
|
G | C | 1 | a0001c0001t0001g0195 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1479+825C>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 14/19 | chr2 | 26196866 | ||||||
chr2:26197401
|
T | C | 1 | a0001c0002t0002g0228 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1479+290A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 14/19 | chr2 | 26197401 | ||||||
chr2:26197801
|
A | G | 3 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111 | 3 | HG02809.hp2 HG03098.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1393-24T>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 13/19 | chr2 | 26197801 | ||||||
chr2:26197839
|
T | G | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(198): Show | 227 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.1393-62A>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 13/19 | chr2 | 26197839 | ||||||
chr2:26197916
|
A | C | 6 | a0002c0003t0003g0021a0002c0003t0003g0196a0002c0003t0003g0197others(3): Show | 7 | HG01884.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1393-139T>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 13/19 | chr2 | 26197916 | ||||||
chr2:26197940
|
G | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(198): Show | 227 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.1393-163C>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 13/19 | chr2 | 26197940 | ||||||
chr2:26197971
|
C | T | 9 | a0001c0001t0003g0031a0001c0001t0003g0033a0001c0001t0003g0034others(6): Show | 9 | HG00733.hp2 HG01074.hp2 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.1393-194G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 13/19 | chr2 | 26197971 | ||||||
chr2:26198185
|
T | C | 1 | a0001c0001t0001g0156 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1393-408A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 13/19 | chr2 | 26198185 | ||||||
chr2:26198227
|
C | T | 9 | a0001c0001t0003g0031a0001c0001t0003g0033a0001c0001t0003g0034others(6): Show | 9 | HG00733.hp2 HG01074.hp2 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.1393-450G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 13/19 | chr2 | 26198227 | ||||||
chr2:26198369
|
G | GT | 192 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(189): Show | 215 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(212): Show |
intron_variant | MODIFIER | c.1393-593dupA | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 13/19 | chr2 | 26198369 | ||||||
chr2:26198380
|
G | T | 7 | a0002c0003t0003g0021a0002c0003t0003g0108a0002c0003t0003g0196others(4): Show | 8 | HG01884.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1393-603C>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 13/19 | chr2 | 26198380 | ||||||
chr2:26198381
|
T | G | 7 | a0002c0003t0003g0021a0002c0003t0003g0108a0002c0003t0003g0196others(4): Show | 8 | HG01884.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1393-604A>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 13/19 | chr2 | 26198381 | ||||||
chr2:26198400
|
G | T | 1 | a0001c0001t0003g0031 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1393-623C>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 13/19 | chr2 | 26198400 | ||||||
chr2:26198661
|
T | TA | 200 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(197): Show | 226 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(223): Show |
intron_variant | MODIFIER | c.1393-885dupT | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 13/19 | chr2 | 26198661 | ||||||
chr2:26198749
|
T | C | 1 | a0001c0001t0001g0102 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1393-972A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 13/19 | chr2 | 26198749 | ||||||
chr2:26199031
|
A | G | 2 | a0003c0004t0001g0116a0003c0004t0001g0117 | 2 | HG02717.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1393-1254T>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 13/19 | chr2 | 26199031 | ||||||
chr2:26199050
|
A | G | 199 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(196): Show | 225 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(222): Show |
intron_variant | MODIFIER | c.1393-1273T>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 13/19 | chr2 | 26199050 | ||||||
chr2:26199126
|
G | A | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(198): Show | 227 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.1393-1349C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 13/19 | chr2 | 26199126 | ||||||
chr2:26199463
|
T | C | 2 | a0001c0001t0001g0005a0001c0001t0001g0180 | 4 | HG00408.hp1 HG02056.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.1392+1686A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 13/19 | chr2 | 26199463 | ||||||
chr2:26199568
|
C | T | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074 | 3 | HG00738.hp2 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1392+1581G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 13/19 | chr2 | 26199568 | ||||||
chr2:26199755
|
G | A | 1 | a0001c0002t0002g0228 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1392+1394C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 13/19 | chr2 | 26199755 | ||||||
chr2:26199792
|
C | G | 1 | a0001c0001t0001g0083 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1392+1357G>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 13/19 | chr2 | 26199792 | ||||||
chr2:26199853
|
A | T | 6 | a0001c0001t0003g0033a0001c0001t0003g0034a0001c0001t0003g0035others(3): Show | 6 | HG00733.hp2 HG01074.hp2 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.1392+1296T>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 13/19 | chr2 | 26199853 | ||||||
chr2:26199894
|
G | A | 1 | a0001c0001t0004g0004 | 3 | HG01069.hp2 HG01071.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.1392+1255C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 13/19 | chr2 | 26199894 | ||||||
chr2:26200122
|
A | G | 1 | a0001c0001t0001g0054 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1392+1027T>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 13/19 | chr2 | 26200122 | ||||||
chr2:26200135
|
ATGTT | A | 7 | a0002c0003t0003g0021a0002c0003t0003g0108a0002c0003t0003g0196others(4): Show | 8 | HG01884.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1392+1010_1392+101 others(8): Show |
HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 13/19 | chr2 | 26200135 | ||||||
chr2:26200171
|
G | A | 3 | a0001c0001t0001g0189a0002c0003t0003g0026a0002c0003t0003g0027 | 3 | HG03225.hp1 HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1392+978C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 13/19 | chr2 | 26200171 | ||||||
chr2:26200402
|
T | C | 1 | a0001c0001t0004g0004 | 3 | HG01069.hp2 HG01071.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.1392+747A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 13/19 | chr2 | 26200402 | ||||||
chr2:26200545
|
G | A | 170 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(167): Show | 193 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.1392+604C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 13/19 | chr2 | 26200545 | ||||||
chr2:26200735
|
CT | C | 199 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(196): Show | 225 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(222): Show |
intron_variant | MODIFIER | c.1392+413delA | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 13/19 | chr2 | 26200735 | ||||||
chr2:26200789
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1392+360C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 13/19 | chr2 | 26200789 | ||||||
chr2:26200794
|
G | A | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(180): Show | 208 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(205): Show |
intron_variant | MODIFIER | c.1392+355C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 13/19 | chr2 | 26200794 | ||||||
chr2:26200893
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1392+256G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 13/19 | chr2 | 26200893 | ||||||
chr2:26200894
|
G | A | 1 | a0001c0002t0002g0220 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1392+255C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 13/19 | chr2 | 26200894 | ||||||
chr2:26200974
|
C | T | 1 | a0001c0001t0001g0018 | 2 | HG02080.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1392+175G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 13/19 | chr2 | 26200974 | ||||||
chr2:26201096
|
CTG | C | 6 | a0001c0001t0003g0033a0001c0001t0003g0034a0001c0001t0003g0035others(3): Show | 6 | HG00733.hp2 HG01074.hp2 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.1392+51_1392+52del others(2): Show |
HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 13/19 | chr2 | 26201096 | ||||||
chr2:26201139
|
C | T | 9 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(6): Show | 9 | HG01167.hp2 HG01169.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.1392+10G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 13/19 | chr2 | 26201139 | ||||||
chr2:26201463
|
A | C | 1 | a0001c0001t0001g0121 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1221-143T>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 12/19 | chr2 | 26201463 | ||||||
chr2:26201515
|
G | A | 70 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(67): Show | 77 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.1221-195C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 12/19 | chr2 | 26201515 | ||||||
chr2:26201648
|
T | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(198): Show | 227 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.1221-328A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 12/19 | chr2 | 26201648 | ||||||
chr2:26201714
|
A | C | 173 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(170): Show | 198 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.1221-394T>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 12/19 | chr2 | 26201714 | ||||||
chr2:26201788
|
CT | C | 11 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0045others(8): Show | 11 | HG01884.hp1 HG02055.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1221-469delA | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 12/19 | chr2 | 26201788 | ||||||
chr2:26201850
|
A | G | 1 | a0001c0001t0001g0075 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1221-530T>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 12/19 | chr2 | 26201850 | ||||||
chr2:26201857
|
T | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(198): Show | 227 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.1221-537A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 12/19 | chr2 | 26201857 | ||||||
chr2:26201961
|
A | AT | 6 | a0001c0001t0001g0047a0001c0001t0001g0061a0001c0001t0001g0127others(3): Show | 6 | HG01123.hp1 HG01192.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1221-642dupA | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 12/19 | chr2 | 26201961 | ||||||
chr2:26201961
|
AT | A | 102 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(99): Show | 114 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(111): Show |
intron_variant | MODIFIER | c.1221-642delA | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 12/19 | chr2 | 26201961 | ||||||
chr2:26202121
|
A | C | 1 | a0002c0003t0003g0108 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1221-801T>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 12/19 | chr2 | 26202121 | ||||||
chr2:26202722
|
T | C | 1 | a0001c0001t0001g0181 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1220+1340A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 12/19 | chr2 | 26202722 | ||||||
chr2:26203003
|
G | T | 1 | a0001c0001t0001g0086 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1220+1059C>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 12/19 | chr2 | 26203003 | ||||||
chr2:26203067
|
G | A | 1 | a0001c0002t0002g0224 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1220+995C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 12/19 | chr2 | 26203067 | ||||||
chr2:26203140
|
A | G | 1 | a0001c0001t0001g0093 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1220+922T>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 12/19 | chr2 | 26203140 | ||||||
chr2:26203160
|
A | G | 1 | a0001c0001t0009g0112 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1220+902T>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 12/19 | chr2 | 26203160 | ||||||
chr2:26203170
|
C | A | 25 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0018others(22): Show | 29 | HG00408.hp1 HG00639.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1220+892G>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 12/19 | chr2 | 26203170 | ||||||
chr2:26203534
|
G | A | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(198): Show | 227 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.1220+528C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 12/19 | chr2 | 26203534 | ||||||
chr2:26203691
|
T | A | 2 | a0001c0001t0001g0141a0001c0001t0001g0142 | 2 | HG02132.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.1220+371A>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 12/19 | chr2 | 26203691 | ||||||
chr2:26203747
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1220+315C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 12/19 | chr2 | 26203747 | ||||||
chr2:26203856
|
C | T | 6 | a0001c0001t0003g0033a0001c0001t0003g0034a0001c0001t0003g0035others(3): Show | 6 | HG00733.hp2 HG01074.hp2 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.1220+206G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 12/19 | chr2 | 26203856 | ||||||
chr2:26204606
|
A | G | 3 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111 | 3 | HG02809.hp2 HG03098.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1086-410T>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 11/19 | chr2 | 26204606 | ||||||
chr2:26204718
|
G | A | 6 | a0001c0001t0001g0015a0001c0001t0001g0118a0001c0001t0001g0176others(3): Show | 7 | HG02615.hp1 HG02647.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1086-522C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 11/19 | chr2 | 26204718 | ||||||
chr2:26204798
|
G | C | 1 | a0001c0002t0002g0222 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1086-602C>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 11/19 | chr2 | 26204798 | ||||||
chr2:26204873
|
CCATCGTG others(8): Show |
C | 3 | a0001c0001t0001g0106a0001c0001t0001g0128a0001c0001t0001g0137 | 3 | HG02257.hp1 HG02895.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1086-692_1086-678d others(17): Show |
HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 11/19 | chr2 | 26204873 | ||||||
chr2:26205236
|
T | G | 6 | a0002c0003t0003g0021a0002c0003t0003g0196a0002c0003t0003g0197others(3): Show | 7 | HG01884.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1086-1040A>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 11/19 | chr2 | 26205236 | ||||||
chr2:26205263
|
C | T | 35 | a0001c0002t0002g0002a0001c0002t0002g0022a0001c0002t0002g0024others(32): Show | 43 | HG00140.hp1 HG00738.hp1 HG01123.hp1 others(40): Show |
intron_variant | MODIFIER | c.1086-1067G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 11/19 | chr2 | 26205263 | ||||||
chr2:26205337
|
C | T | 1 | a0001c0002t0002g0225 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1086-1141G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 11/19 | chr2 | 26205337 | ||||||
chr2:26205568
|
C | T | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0120others(5): Show | 10 | HG01069.hp2 HG01071.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.1086-1372G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 11/19 | chr2 | 26205568 | ||||||
chr2:26205665
|
T | G | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(198): Show | 227 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.1086-1469A>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 11/19 | chr2 | 26205665 | ||||||
chr2:26205688
|
C | T | 1 | a0001c0001t0004g0004 | 3 | HG01069.hp2 HG01071.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.1086-1492G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 11/19 | chr2 | 26205688 | ||||||
chr2:26205797
|
AT | A | 4 | a0001c0001t0001g0045a0001c0001t0001g0076a0002c0003t0003g0198others(1): Show | 4 | HG01884.hp2 HG02280.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1086-1602delA | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 11/19 | chr2 | 26205797 | ||||||
chr2:26205804
|
T | A | 16 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(13): Show | 17 | HG00733.hp2 HG01074.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.1086-1608A>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 11/19 | chr2 | 26205804 | ||||||
chr2:26205805
|
T | A | 195 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(192): Show | 219 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.1086-1609A>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 11/19 | chr2 | 26205805 | ||||||
chr2:26206029
|
G | C | 1 | a0001c0001t0001g0060 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1086-1833C>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 11/19 | chr2 | 26206029 | ||||||
chr2:26206080
|
C | T | 1 | a0001c0001t0001g0114 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1086-1884G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 11/19 | chr2 | 26206080 | ||||||
chr2:26206226
|
A | AT | 33 | a0001c0001t0001g0077a0001c0002t0002g0002a0001c0002t0002g0022others(30): Show | 41 | HG00140.hp1 HG00738.hp1 HG01123.hp1 others(38): Show |
intron_variant | MODIFIER | c.1086-2031dupA | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 11/19 | chr2 | 26206226 | ||||||
chr2:26206226
|
AT | A | 7 | a0001c0001t0001g0044a0001c0001t0001g0059a0001c0001t0001g0090others(4): Show | 7 | HG00642.hp2 HG00733.hp1 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.1086-2031delA | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 11/19 | chr2 | 26206226 | ||||||
chr2:26206286
|
C | T | 109 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(106): Show | 124 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(121): Show |
intron_variant | MODIFIER | c.1086-2090G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 11/19 | chr2 | 26206286 | ||||||
chr2:26206373
|
T | G | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1086-2177A>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 11/19 | chr2 | 26206373 | ||||||
chr2:26206375
|
C | G | 1 | a0001c0001t0001g0077 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1086-2179G>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 11/19 | chr2 | 26206375 | ||||||
chr2:26206421
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1086-2225C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 11/19 | chr2 | 26206421 | ||||||
chr2:26206582
|
C | G | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(198): Show | 227 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.1086-2386G>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 11/19 | chr2 | 26206582 | ||||||
chr2:26206659
|
T | C | 1 | a0001c0002t0010g0238 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1086-2463A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 11/19 | chr2 | 26206659 | ||||||
chr2:26206759
|
T | C | 6 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0045others(3): Show | 6 | HG01884.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1086-2563A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 11/19 | chr2 | 26206759 | ||||||
chr2:26206923
|
CATGGTGG others(42): Show |
C | 1 | a0001c0002t0002g0219 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1086-2776_1086-272 others(53): Show |
HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 11/19 | chr2 | 26206923 | ||||||
chr2:26206945
|
C | T | 2 | a0002c0003t0003g0026a0002c0003t0003g0027 | 2 | HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1086-2749G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 11/19 | chr2 | 26206945 | ||||||
chr2:26207031
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1085+2749G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 11/19 | chr2 | 26207031 | ||||||
chr2:26207163
|
A | G | 1 | a0002c0003t0003g0108 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1085+2617T>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 11/19 | chr2 | 26207163 | ||||||
chr2:26207319
|
GT | G | 5 | a0001c0001t0001g0044a0001c0001t0001g0184a0001c0001t0003g0037others(2): Show | 5 | HG01074.hp2 HG01169.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1085+2460delA | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 11/19 | chr2 | 26207319 | ||||||
chr2:26207319
|
GTT | G | 5 | a0001c0001t0003g0033a0001c0001t0003g0034a0001c0001t0003g0035others(2): Show | 5 | HG00733.hp2 HG01167.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1085+2459_1085+246 others(6): Show |
HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 11/19 | chr2 | 26207319 | ||||||
chr2:26207380
|
A | G | 2 | a0002c0003t0003g0026a0002c0003t0003g0027 | 2 | HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1085+2400T>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 11/19 | chr2 | 26207380 | ||||||
chr2:26207597
|
A | G | 1 | a0001c0002t0002g0233 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1085+2183T>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 11/19 | chr2 | 26207597 | ||||||
chr2:26207934
|
A | G | 2 | a0002c0003t0003g0026a0002c0003t0003g0027 | 2 | HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1085+1846T>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 11/19 | chr2 | 26207934 | ||||||
chr2:26208114
|
A | G | 194 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(191): Show | 220 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(217): Show |
intron_variant | MODIFIER | c.1085+1666T>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 11/19 | chr2 | 26208114 | ||||||
chr2:26208528
|
A | C | 1 | a0001c0001t0003g0031 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1085+1252T>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 11/19 | chr2 | 26208528 | ||||||
chr2:26208808
|
T | C | 4 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0107others(1): Show | 6 | HG01243.hp1 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1085+972A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 11/19 | chr2 | 26208808 | ||||||
chr2:26209103
|
T | C | 1 | a0002c0003t0003g0199 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1085+677A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 11/19 | chr2 | 26209103 | ||||||
chr2:26209182
|
G | A | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(180): Show | 208 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(205): Show |
intron_variant | MODIFIER | c.1085+598C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 11/19 | chr2 | 26209182 | ||||||
chr2:26209286
|
G | A | 1 | a0001c0001t0001g0014 | 2 | NA18947.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.1085+494C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 11/19 | chr2 | 26209286 | ||||||
chr2:26209350
|
T | G | 81 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(78): Show | 88 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(85): Show |
intron_variant | MODIFIER | c.1085+430A>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 11/19 | chr2 | 26209350 | ||||||
chr2:26209578
|
G | A | 2 | a0001c0002t0002g0206a0001c0002t0002g0229 | 2 | HG02040.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1085+202C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 11/19 | chr2 | 26209578 | ||||||
chr2:26210613
|
G | C | 1 | a0001c0001t0003g0031 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.976-724C>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 10/19 | chr2 | 26210613 | ||||||
chr2:26210699
|
T | C | 21 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(18): Show | 22 | HG00733.hp2 HG01074.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.976-810A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 10/19 | chr2 | 26210699 | ||||||
chr2:26210846
|
C | T | 3 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111 | 3 | HG02809.hp2 HG03098.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.976-957G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 10/19 | chr2 | 26210846 | ||||||
chr2:26210878
|
T | C | 8 | a0001c0001t0003g0033a0001c0001t0003g0034a0001c0001t0003g0035others(5): Show | 8 | HG00733.hp2 HG01074.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.976-989A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 10/19 | chr2 | 26210878 | ||||||
chr2:26210932
|
A | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(198): Show | 227 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.976-1043T>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 10/19 | chr2 | 26210932 | ||||||
chr2:26211153
|
C | A | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(198): Show | 227 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.976-1264G>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 10/19 | chr2 | 26211153 | ||||||
chr2:26211338
|
T | A | 1 | a0001c0001t0001g0162 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.975+1232A>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 10/19 | chr2 | 26211338 | ||||||
chr2:26211736
|
C | G | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(180): Show | 208 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(205): Show |
intron_variant | MODIFIER | c.975+834G>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 10/19 | chr2 | 26211736 | ||||||
chr2:26212145
|
C | T | 2 | a0001c0002t0004g0006a0001c0002t0004g0232 | 4 | HG02074.hp1 NA18954.hp1 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.975+425G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 10/19 | chr2 | 26212145 | ||||||
chr2:26212229
|
G | C | 1 | a0001c0001t0003g0031 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.975+341C>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 10/19 | chr2 | 26212229 | ||||||
chr2:26212258
|
T | C | 21 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(18): Show | 22 | HG00733.hp2 HG01074.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.975+312A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 10/19 | chr2 | 26212258 | ||||||
chr2:26212487
|
T | C | 1 | a0001c0001t0001g0078 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.975+83A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 10/19 | chr2 | 26212487 | ||||||
chr2:26212765
|
C | G | 1 | a0004c0008t0001g0158 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.919-139G>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 9/19 | chr2 | 26212765 | ||||||
chr2:26213352
|
T | C | 1 | a0001c0001t0001g0189 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.919-726A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 9/19 | chr2 | 26213352 | ||||||
chr2:26213618
|
G | A | 8 | a0001c0001t0003g0033a0001c0001t0003g0034a0001c0001t0003g0035others(5): Show | 8 | HG00733.hp2 HG01074.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.918+825C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 9/19 | chr2 | 26213618 | ||||||
chr2:26214303
|
C | T | 1 | a0001c0001t0001g0076 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.918+140G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 9/19 | chr2 | 26214303 | ||||||
chr2:26214361
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.918+82A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 9/19 | chr2 | 26214361 | ||||||
chr2:26214386
|
G | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0049a0001c0001t0001g0068 | 5 | HG00639.hp1 HG00642.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.918+57C>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 9/19 | chr2 | 26214386 | ||||||
chr2:26214675
|
C | G | 1 | a0001c0001t0001g0016 | 2 | HG01243.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.800-114G>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 8/19 | chr2 | 26214675 | ||||||
chr2:26214739
|
A | T | 3 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030 | 3 | HG01167.hp2 HG01169.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.800-178T>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 8/19 | chr2 | 26214739 | ||||||
chr2:26214822
|
A | C | 1 | a0002c0003t0003g0200 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.799+231T>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 8/19 | chr2 | 26214822 | ||||||
chr2:26215008
|
C | A | 1 | a0001c0001t0001g0142 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.799+45G>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 8/19 | chr2 | 26215008 | ||||||
chr2:26215384
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.677-209G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26215384 | ||||||
chr2:26215407
|
T | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(198): Show | 227 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.677-232A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26215407 | ||||||
chr2:26215706
|
C | T | 1 | a0001c0001t0001g0122 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.677-531G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26215706 | ||||||
chr2:26216122
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.677-947T>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26216122 | ||||||
chr2:26216201
|
T | C | 1 | a0001c0001t0001g0155 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.677-1026A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26216201 | ||||||
chr2:26216317
|
A | AT | 146 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(143): Show | 164 | HG00140.hp2 HG00621.hp1 HG00621.hp2 others(161): Show |
intron_variant | MODIFIER | c.677-1143dupA | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26216317 | ||||||
chr2:26216317
|
A | ATT | 10 | a0001c0001t0001g0047a0001c0001t0001g0061a0001c0001t0001g0096others(7): Show | 10 | HG02055.hp1 HG02132.hp2 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.677-1144_677-1143d others(4): Show |
HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26216317 | ||||||
chr2:26216317
|
AT | A | 5 | a0001c0001t0001g0020a0001c0001t0001g0107a0001c0001t0003g0035others(2): Show | 6 | HG01167.hp1 HG02004.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.677-1143delA | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26216317 | ||||||
chr2:26216389
|
T | C | 203 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(200): Show | 230 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(227): Show |
intron_variant | MODIFIER | c.677-1214A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26216389 | ||||||
chr2:26216488
|
A | T | 7 | a0002c0003t0003g0021a0002c0003t0003g0108a0002c0003t0003g0196others(4): Show | 8 | HG01884.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.677-1313T>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26216488 | ||||||
chr2:26216531
|
A | G | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(198): Show | 227 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.677-1356T>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26216531 | ||||||
chr2:26216572
|
C | T | 1 | a0004c0008t0001g0158 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.677-1397G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26216572 | ||||||
chr2:26216668
|
A | C | 4 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0107others(1): Show | 6 | HG01243.hp1 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.677-1493T>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26216668 | ||||||
chr2:26216803
|
C | A | 1 | a0001c0002t0002g0224 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.677-1628G>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26216803 | ||||||
chr2:26216960
|
G | A | 4 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0107others(1): Show | 6 | HG01243.hp1 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.677-1785C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26216960 | ||||||
chr2:26217001
|
C | T | 13 | a0001c0002t0002g0002a0001c0002t0002g0024a0001c0002t0002g0218others(10): Show | 20 | HG01981.hp2 HG02004.hp2 HG02015.hp2 others(17): Show |
intron_variant | MODIFIER | c.677-1826G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26217001 | ||||||
chr2:26217102
|
C | T | 1 | a0001c0001t0001g0123 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.677-1927G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26217102 | ||||||
chr2:26217126
|
T | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(198): Show | 227 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.677-1951A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26217126 | ||||||
chr2:26217564
|
C | T | 7 | a0001c0001t0003g0031a0001c0001t0003g0033a0001c0001t0003g0034others(4): Show | 7 | HG00733.hp2 HG01074.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.677-2389G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26217564 | ||||||
chr2:26217707
|
T | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(198): Show | 227 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.677-2532A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26217707 | ||||||
chr2:26217746
|
T | C | 6 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0045others(3): Show | 6 | HG01884.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.677-2571A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26217746 | ||||||
chr2:26217839
|
C | T | 3 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0121 | 3 | HG01257.hp2 HG01952.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.677-2664G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26217839 | ||||||
chr2:26218055
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.677-2880G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26218055 | ||||||
chr2:26218072
|
G | A | 1 | a0001c0002t0002g0217 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.677-2897C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26218072 | ||||||
chr2:26218074
|
G | A | 180 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(177): Show | 205 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.677-2899C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26218074 | ||||||
chr2:26218299
|
C | CA | 144 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(141): Show | 161 | HG00140.hp2 HG00408.hp1 HG00639.hp1 others(158): Show |
intron_variant | MODIFIER | c.677-3125dupT | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26218299 | ||||||
chr2:26218299
|
C | CAA | 57 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(54): Show | 66 | HG00408.hp2 HG00621.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.677-3126_677-3125d others(4): Show |
HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26218299 | ||||||
chr2:26218391
|
A | G | 1 | a0001c0001t0001g0067 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.677-3216T>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26218391 | ||||||
chr2:26218736
|
T | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(198): Show | 227 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.677-3561A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26218736 | ||||||
chr2:26218972
|
A | G | 2 | a0001c0001t0001g0075a0001c0001t0001g0102 | 2 | HG03831.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.677-3797T>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26218972 | ||||||
chr2:26219002
|
G | A | 180 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(177): Show | 205 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.677-3827C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26219002 | ||||||
chr2:26219006
|
C | CA | 161 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(158): Show | 183 | HG00140.hp2 HG00408.hp2 HG00621.hp1 others(180): Show |
intron_variant | MODIFIER | c.677-3832dupT | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26219006 | ||||||
chr2:26219006
|
C | CAA | 36 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0018others(33): Show | 40 | HG00408.hp1 HG00639.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.677-3833_677-3832d others(4): Show |
HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26219006 | ||||||
chr2:26219367
|
T | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(198): Show | 227 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.677-4192A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26219367 | ||||||
chr2:26219370
|
T | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(198): Show | 227 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.677-4195A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26219370 | ||||||
chr2:26219436
|
T | C | 1 | a0001c0001t0001g0049 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.677-4261A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26219436 | ||||||
chr2:26219525
|
C | G | 3 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030 | 3 | HG01167.hp2 HG01169.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.677-4350G>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26219525 | ||||||
chr2:26219890
|
C | T | 187 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(184): Show | 213 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(210): Show |
intron_variant | MODIFIER | c.677-4715G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26219890 | ||||||
chr2:26219990
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.677-4815G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26219990 | ||||||
chr2:26220024
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.677-4849G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26220024 | ||||||
chr2:26220043
|
T | C | 1 | a0001c0001t0001g0058 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.677-4868A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26220043 | ||||||
chr2:26220114
|
A | G | 1 | a0001c0001t0001g0068 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.677-4939T>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26220114 | ||||||
chr2:26220269
|
T | C | 15 | a0001c0001t0003g0033a0001c0001t0003g0034a0001c0001t0003g0035others(12): Show | 16 | HG00733.hp2 HG01074.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.677-5094A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26220269 | ||||||
chr2:26220463
|
G | A | 1 | a0001c0001t0008g0187 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.677-5288C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26220463 | ||||||
chr2:26220609
|
G | A | 3 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030 | 3 | HG01167.hp2 HG01169.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.677-5434C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26220609 | ||||||
chr2:26220668
|
G | A | 6 | a0001c0001t0003g0033a0001c0001t0003g0034a0001c0001t0003g0035others(3): Show | 6 | HG00733.hp2 HG01074.hp2 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.677-5493C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26220668 | ||||||
chr2:26220684
|
T | C | 1 | a0001c0001t0001g0058 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.677-5509A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26220684 | ||||||
chr2:26221293
|
T | C | 1 | a0001c0001t0001g0166 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.677-6118A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26221293 | ||||||
chr2:26221546
|
G | C | 187 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(184): Show | 213 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(210): Show |
intron_variant | MODIFIER | c.677-6371C>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26221546 | ||||||
chr2:26221988
|
G | T | 59 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(56): Show | 68 | HG00408.hp2 HG00621.hp1 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.677-6813C>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26221988 | ||||||
chr2:26222046
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.677-6871G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26222046 | ||||||
chr2:26222094
|
C | T | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(198): Show | 227 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.677-6919G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26222094 | ||||||
chr2:26222109
|
GAGGCCAT others(1): Show |
G | 5 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.677-6942_677-6935d others(10): Show |
HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26222109 | ||||||
chr2:26222127
|
C | CCTAAT | 5 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.677-6957_677-6953d others(7): Show |
HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26222127 | ||||||
chr2:26222160
|
GA | G | 5 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.677-6986delT | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26222160 | ||||||
chr2:26222377
|
T | C | 1 | a0001c0001t0005g0051 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.677-7202A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26222377 | ||||||
chr2:26222617
|
T | G | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(198): Show | 227 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.677-7442A>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26222617 | ||||||
chr2:26222682
|
A | G | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(198): Show | 227 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.677-7507T>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26222682 | ||||||
chr2:26223155
|
T | C | 6 | a0001c0001t0003g0033a0001c0001t0003g0034a0001c0001t0003g0035others(3): Show | 6 | HG00733.hp2 HG01074.hp2 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.676+7037A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26223155 | ||||||
chr2:26223277
|
T | C | 78 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(75): Show | 85 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.676+6915A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26223277 | ||||||
chr2:26223381
|
AC | A | 5 | a0001c0001t0003g0033a0001c0001t0003g0034a0001c0001t0003g0035others(2): Show | 5 | HG00733.hp2 HG01167.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.676+6810delG | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26223381 | ||||||
chr2:26223509
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.676+6683A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26223509 | ||||||
chr2:26223537
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.676+6655G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26223537 | ||||||
chr2:26223827
|
A | G | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(198): Show | 227 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.676+6365T>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26223827 | ||||||
chr2:26224129
|
T | C | 1 | a0001c0001t0009g0112 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.676+6063A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26224129 | ||||||
chr2:26224279
|
A | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(198): Show | 227 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.676+5913T>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26224279 | ||||||
chr2:26224409
|
T | G | 14 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(11): Show | 14 | HG00733.hp2 HG01074.hp2 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.676+5783A>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26224409 | ||||||
chr2:26224467
|
A | G | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(198): Show | 227 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.676+5725T>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26224467 | ||||||
chr2:26224513
|
A | C | 3 | a0001c0002t0002g0221a0001c0002t0002g0231a0001c0002t0002g0235 | 3 | NA18940.hp1 NA18979.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.676+5679T>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26224513 | ||||||
chr2:26224717
|
A | G | 1 | a0001c0002t0010g0238 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.676+5475T>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26224717 | ||||||
chr2:26225039
|
C | G | 2 | a0001c0001t0001g0016a0001c0001t0001g0188 | 3 | HG01243.hp1 HG02559.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.676+5153G>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26225039 | ||||||
chr2:26225128
|
T | C | 1 | a0001c0001t0001g0059 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.676+5064A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26225128 | ||||||
chr2:26225397
|
CA | C | 6 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(3): Show | 6 | HG01167.hp2 HG01169.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.676+4794delT | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26225397 | ||||||
chr2:26225397
|
CAA | C | 193 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(190): Show | 219 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.676+4793_676+4794d others(4): Show |
HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26225397 | ||||||
chr2:26225517
|
CATG | C | 5 | a0001c0001t0003g0033a0001c0001t0003g0034a0001c0001t0003g0035others(2): Show | 5 | HG00733.hp2 HG01167.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.676+4672_676+4674d others(5): Show |
HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26225517 | ||||||
chr2:26225565
|
T | C | 1 | a0001c0001t0001g0181 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.676+4627A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26225565 | ||||||
chr2:26225962
|
T | A | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(198): Show | 227 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.676+4230A>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26225962 | ||||||
chr2:26226082
|
G | A | 180 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(177): Show | 205 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.676+4110C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26226082 | ||||||
chr2:26226086
|
A | G | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(198): Show | 227 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.676+4106T>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26226086 | ||||||
chr2:26226572
|
T | C | 3 | a0001c0001t0001g0156a0001c0001t0001g0168a0001c0001t0001g0169 | 3 | NA18944.hp2 NA18954.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.676+3620A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26226572 | ||||||
chr2:26226831
|
G | A | 1 | a0001c0001t0003g0037 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.676+3361C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26226831 | ||||||
chr2:26227082
|
G | C | 1 | a0001c0001t0001g0150 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.676+3110C>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26227082 | ||||||
chr2:26227112
|
C | A | 2 | a0002c0003t0003g0026a0002c0003t0003g0027 | 2 | HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.676+3080G>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26227112 | ||||||
chr2:26227511
|
CA | C | 198 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(195): Show | 224 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(221): Show |
intron_variant | MODIFIER | c.676+2680delT | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26227511 | ||||||
chr2:26227521
|
A | C | 6 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0045others(3): Show | 6 | HG01884.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.676+2671T>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26227521 | ||||||
chr2:26227712
|
G | A | 2 | a0001c0002t0002g0219a0001c0002t0002g0237 | 2 | HG03710.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.676+2480C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26227712 | ||||||
chr2:26228157
|
G | A | 1 | a0002c0003t0003g0200 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.676+2035C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26228157 | ||||||
chr2:26228195
|
A | G | 1 | a0001c0001t0001g0156 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.676+1997T>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26228195 | ||||||
chr2:26228230
|
A | C | 3 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030 | 3 | HG01167.hp2 HG01169.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.676+1962T>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26228230 | ||||||
chr2:26228348
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.676+1844C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26228348 | ||||||
chr2:26228807
|
G | A | 2 | a0001c0001t0001g0047a0001c0001t0001g0061 | 2 | HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.676+1385C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26228807 | ||||||
chr2:26228812
|
C | T | 5 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.676+1380G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26228812 | ||||||
chr2:26228815
|
G | A | 1 | a0001c0002t0002g0233 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.676+1377C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26228815 | ||||||
chr2:26228831
|
C | T | 6 | a0001c0001t0001g0007a0001c0001t0001g0044a0001c0001t0001g0055others(3): Show | 7 | HG01081.hp1 HG01109.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.676+1361G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26228831 | ||||||
chr2:26228948
|
A | G | 6 | a0001c0001t0001g0106a0001c0001t0001g0128a0001c0001t0001g0136others(3): Show | 6 | HG02257.hp1 HG02723.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.676+1244T>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26228948 | ||||||
chr2:26229054
|
A | G | 3 | a0001c0002t0002g0214a0001c0002t0002g0217a0001c0002t0002g0230 | 3 | HG00738.hp1 HG03669.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.676+1138T>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26229054 | ||||||
chr2:26229174
|
T | G | 5 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.676+1018A>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26229174 | ||||||
chr2:26229230
|
C | T | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0052others(1): Show | 4 | HG01934.hp1 HG02257.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.676+962G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26229230 | ||||||
chr2:26229329
|
C | A | 187 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(184): Show | 213 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(210): Show |
intron_variant | MODIFIER | c.676+863G>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26229329 | ||||||
chr2:26229341
|
T | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(198): Show | 227 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.676+851A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26229341 | ||||||
chr2:26229343
|
C | T | 9 | a0001c0001t0001g0038a0001c0001t0001g0154a0001c0001t0001g0155others(6): Show | 10 | HG01884.hp2 HG02155.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.676+849G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26229343 | ||||||
chr2:26229348
|
G | GCA | 9 | a0001c0001t0001g0039a0001c0001t0001g0152a0001c0001t0001g0174others(6): Show | 9 | HG01074.hp2 HG01192.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.676+842_676+843dup others(2): Show |
HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26229348 | ||||||
chr2:26229348
|
G | GCACA | 59 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(56): Show | 69 | HG00408.hp2 HG00621.hp1 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.676+840_676+843dup others(4): Show |
HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26229348 | ||||||
chr2:26229348
|
G | GCACACA | 88 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(85): Show | 97 | HG00140.hp2 HG00642.hp1 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.676+838_676+843dup others(6): Show |
HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26229348 | ||||||
chr2:26229348
|
G | GCACACAC others(1): Show |
26 | a0001c0001t0001g0005a0001c0001t0001g0018a0001c0001t0001g0045others(23): Show | 30 | HG00408.hp1 HG00639.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.676+836_676+843dup others(8): Show |
HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26229348 | ||||||
chr2:26229348
|
G | GCACACAC others(9): Show |
1 | a0001c0001t0004g0004 | 3 | HG01069.hp2 HG01071.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.676+828_676+843dup others(16): Show |
HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26229348 | ||||||
chr2:26229348
|
G | GCACACAC others(11): Show |
1 | a0001c0001t0001g0067 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.676+826_676+843dup others(18): Show |
HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26229348 | ||||||
chr2:26229348
|
G | GCGCA | 6 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(3): Show | 6 | HG01167.hp2 HG01169.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.676+843_676+844ins others(4): Show |
HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26229348 | ||||||
chr2:26229348
|
G | GCGCACAC others(1): Show |
3 | a0001c0001t0001g0015a0001c0001t0001g0113a0001c0001t0001g0186 | 4 | HG00642.hp2 HG02615.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.676+843_676+844ins others(8): Show |
HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26229348 | ||||||
chr2:26229348
|
G | GCGCACAC others(3): Show |
1 | a0001c0001t0001g0176 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.676+843_676+844ins others(10): Show |
HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26229348 | ||||||
chr2:26229429
|
T | C | 2 | a0002c0003t0003g0026a0002c0003t0003g0027 | 2 | HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.676+763A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26229429 | ||||||
chr2:26229522
|
A | T | 1 | a0001c0002t0010g0238 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.676+670T>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26229522 | ||||||
chr2:26229674
|
C | G | 2 | a0003c0004t0001g0116a0003c0004t0001g0117 | 2 | HG02717.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.676+518G>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26229674 | ||||||
chr2:26229725
|
G | T | 1 | a0002c0003t0003g0026 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.676+467C>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26229725 | ||||||
chr2:26229737
|
G | A | 38 | a0001c0002t0002g0002a0001c0002t0002g0022a0001c0002t0002g0024others(35): Show | 46 | HG00140.hp1 HG00738.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.676+455C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26229737 | ||||||
chr2:26229837
|
T | C | 1 | a0001c0001t0001g0043 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.676+355A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26229837 | ||||||
chr2:26229920
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.676+272G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26229920 | ||||||
chr2:26230603
|
T | G | 1 | a0001c0002t0002g0220 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.574-309A>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 6/19 | chr2 | 26230603 | ||||||
chr2:26230627
|
T | C | 6 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0045others(3): Show | 6 | HG01884.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.574-333A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 6/19 | chr2 | 26230627 | ||||||
chr2:26230979
|
T | C | 2 | a0003c0004t0001g0116a0003c0004t0001g0117 | 2 | HG02717.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.574-685A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 6/19 | chr2 | 26230979 | ||||||
chr2:26231177
|
A | G | 6 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0045others(3): Show | 6 | HG01884.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.574-883T>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 6/19 | chr2 | 26231177 | ||||||
chr2:26231303
|
T | C | 1 | a0001c0001t0001g0111 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.573+857A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 6/19 | chr2 | 26231303 | ||||||
chr2:26231757
|
G | C | 1 | a0001c0001t0001g0118 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.573+403C>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 6/19 | chr2 | 26231757 | ||||||
chr2:26231839
|
C | T | 38 | a0001c0002t0002g0002a0001c0002t0002g0022a0001c0002t0002g0024others(35): Show | 46 | HG00140.hp1 HG00738.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.573+321G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 6/19 | chr2 | 26231839 | ||||||
chr2:26231888
|
G | A | 2 | a0001c0001t0001g0039a0001c0001t0001g0040 | 2 | HG01884.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.573+272C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 6/19 | chr2 | 26231888 | ||||||
chr2:26231968
|
C | CA | 45 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0053others(42): Show | 55 | HG00140.hp1 HG00738.hp1 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.573+191dupT | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 6/19 | chr2 | 26231968 | ||||||
chr2:26231968
|
CA | C | 20 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0044others(17): Show | 24 | HG01069.hp2 HG01071.hp1 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.573+191delT | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 6/19 | chr2 | 26231968 | ||||||
chr2:26231968
|
CAA | C | 12 | a0001c0001t0001g0028a0001c0001t0001g0030a0001c0001t0003g0031others(9): Show | 12 | HG00733.hp2 HG01167.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.573+190_573+191del others(2): Show |
HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 6/19 | chr2 | 26231968 | ||||||
chr2:26232128
|
A | G | 79 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(76): Show | 86 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.573+32T>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 6/19 | chr2 | 26232128 | ||||||
chr2:26232134
|
C | G | 38 | a0001c0002t0002g0002a0001c0002t0002g0022a0001c0002t0002g0024others(35): Show | 46 | HG00140.hp1 HG00738.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.573+26G>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 6/19 | chr2 | 26232134 | ||||||
chr2:26232151
|
T | TA | 5 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.573+8dupT | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 6/19 | chr2 | 26232151 | ||||||
chr2:26232782
|
A | C | 1 | a0001c0001t0001g0073 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.454-503T>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 5/19 | chr2 | 26232782 | ||||||
chr2:26232837
|
C | T | 1 | a0001c0001t0004g0004 | 3 | HG01069.hp2 HG01071.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.454-558G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 5/19 | chr2 | 26232837 | ||||||
chr2:26232846
|
A | G | 3 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132 | 3 | HG00621.hp2 HG02523.hp1 NA18940.hp2 |
intron_variant | MODIFIER | c.454-567T>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 5/19 | chr2 | 26232846 | ||||||
chr2:26232941
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.454-662A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 5/19 | chr2 | 26232941 | ||||||
chr2:26232943
|
A | G | 143 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(140): Show | 163 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(160): Show |
intron_variant | MODIFIER | c.454-664T>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 5/19 | chr2 | 26232943 | ||||||
chr2:26233155
|
C | T | 1 | a0001c0001t0001g0189 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.454-876G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 5/19 | chr2 | 26233155 | ||||||
chr2:26233227
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.454-948G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 5/19 | chr2 | 26233227 | ||||||
chr2:26233871
|
A | G | 6 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(3): Show | 6 | HG01496.hp1 HG01934.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.453+346T>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 5/19 | chr2 | 26233871 | ||||||
chr2:26233974
|
G | C | 3 | a0001c0001t0001g0134a0001c0001t0001g0144a0006c0009t0001g0190 | 3 | HG01255.hp1 HG02071.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.453+243C>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 5/19 | chr2 | 26233974 | ||||||
chr2:26234399
|
T | G | 38 | a0001c0002t0002g0002a0001c0002t0002g0022a0001c0002t0002g0024others(35): Show | 46 | HG00140.hp1 HG00738.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.315-44A>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26234399 | ||||||
chr2:26234638
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.315-283G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26234638 | ||||||
chr2:26234639
|
G | A | 59 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(56): Show | 68 | HG00408.hp2 HG00621.hp1 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.315-284C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26234639 | ||||||
chr2:26234722
|
C | T | 6 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0045others(3): Show | 6 | HG01884.hp1 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.315-367G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26234722 | ||||||
chr2:26234765
|
CA | C | 36 | a0001c0001t0001g0048a0001c0002t0002g0002a0001c0002t0002g0022others(33): Show | 44 | HG00140.hp1 HG00738.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.315-411delT | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26234765 | ||||||
chr2:26235169
|
C | T | 2 | a0001c0001t0006g0239a0001c0001t0006g0240 | 2 | HG02055.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.315-814G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26235169 | ||||||
chr2:26235172
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.315-817C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26235172 | ||||||
chr2:26235201
|
C | T | 38 | a0001c0002t0002g0002a0001c0002t0002g0022a0001c0002t0002g0024others(35): Show | 46 | HG00140.hp1 HG00738.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.315-846G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26235201 | ||||||
chr2:26235317
|
A | G | 2 | a0001c0001t0001g0122a0001c0001t0001g0127 | 2 | NA18966.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.315-962T>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26235317 | ||||||
chr2:26235376
|
T | C | 3 | a0001c0002t0002g0214a0001c0002t0002g0217a0001c0002t0002g0230 | 3 | HG00738.hp1 HG03669.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.315-1021A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26235376 | ||||||
chr2:26235496
|
G | A | 38 | a0001c0002t0002g0002a0001c0002t0002g0022a0001c0002t0002g0024others(35): Show | 46 | HG00140.hp1 HG00738.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.315-1141C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26235496 | ||||||
chr2:26235504
|
T | C | 237 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(234): Show | 271 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.315-1149A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26235504 | ||||||
chr2:26235510
|
C | T | 6 | a0001c0001t0001g0015a0001c0001t0001g0118a0001c0001t0001g0176others(3): Show | 7 | HG02615.hp1 HG02647.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.315-1155G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26235510 | ||||||
chr2:26235643
|
G | A | 2 | a0001c0001t0001g0174a0001c0001t0001g0175 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.314+1212C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26235643 | ||||||
chr2:26235877
|
C | A | 1 | a0001c0001t0001g0204 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.314+978G>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26235877 | ||||||
chr2:26235878
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.314+977G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26235878 | ||||||
chr2:26236008
|
C | T | 2 | a0001c0001t0001g0047a0001c0001t0001g0061 | 2 | HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.314+847G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26236008 | ||||||
chr2:26236083
|
T | C | 1 | a0001c0002t0002g0231 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.314+772A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26236083 | ||||||
chr2:26236177
|
T | A | 1 | a0001c0001t0001g0184 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.314+678A>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26236177 | ||||||
chr2:26236203
|
T | C | 1 | a0001c0001t0001g0191 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.314+652A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26236203 | ||||||
chr2:26236339
|
A | ATG | 9 | a0001c0001t0001g0013a0001c0001t0001g0041a0001c0001t0001g0045others(6): Show | 10 | HG01258.hp1 HG02040.hp2 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.314+514_314+515dup others(2): Show |
HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26236339 | ||||||
chr2:26236339
|
A | ATGTG | 7 | a0001c0001t0001g0121a0001c0001t0001g0194a0001c0001t0006g0239others(4): Show | 9 | HG00738.hp1 HG02055.hp2 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.314+512_314+515dup others(4): Show |
HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26236339 | ||||||
chr2:26236339
|
A | ATGTGTG | 31 | a0001c0001t0003g0031a0001c0002t0002g0002a0001c0002t0002g0022others(28): Show | 37 | HG00140.hp1 HG01123.hp1 HG01175.hp1 others(34): Show |
intron_variant | MODIFIER | c.314+510_314+515dup others(6): Show |
HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26236339 | ||||||
chr2:26236359
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.314+496C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26236359 | ||||||
chr2:26236359
|
G | GTA | 57 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(54): Show | 62 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.314+494_314+495dup others(2): Show |
HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26236359 | ||||||
chr2:26236359
|
G | GTATA | 3 | a0001c0001t0001g0042a0001c0001t0001g0060a0001c0001t0001g0082 | 3 | HG01081.hp1 HG01934.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.314+492_314+495dup others(4): Show |
HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26236359 | ||||||
chr2:26236359
|
G | GTGTGTGT others(1): Show |
3 | a0001c0002t0002g0207a0001c0002t0002g0216a0001c0002t0004g0212 | 3 | HG01069.hp1 NA18993.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.314+495_314+496ins others(8): Show |
HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26236359 | ||||||
chr2:26236361
|
A | G | 20 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(17): Show | 22 | HG00733.hp2 HG00738.hp1 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.314+494T>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26236361 | ||||||
chr2:26236363
|
A | G | 8 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(5): Show | 8 | HG01167.hp2 HG01169.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.314+492T>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26236363 | ||||||
chr2:26236375
|
ATACT | A | 1 | a0001c0001t0004g0004 | 3 | HG01069.hp2 HG01071.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.314+476_314+479del others(4): Show |
HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26236375 | ||||||
chr2:26236376
|
T | C | 1 | a0001c0001t0001g0135 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.314+479A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26236376 | ||||||
chr2:26236377
|
A | T | 1 | a0001c0001t0001g0135 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.314+478T>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26236377 | ||||||
chr2:26236377
|
ACT | A | 3 | a0001c0001t0003g0033a0001c0001t0003g0036a0001c0001t0004g0032 | 3 | HG02109.hp2 HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.314+476_314+477del others(2): Show |
HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26236377 | ||||||
chr2:26236378
|
C | T | 10 | a0001c0001t0001g0003a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 14 | HG00639.hp1 HG00642.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.314+477G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26236378 | ||||||
chr2:26236378
|
CTCTGTGT others(1): Show |
C | 3 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0006g0240 | 3 | HG00733.hp2 HG01167.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.314+469_314+476del others(8): Show |
HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26236378 | ||||||
chr2:26236378
|
CTCTGTGT others(7): Show |
C | 1 | a0001c0001t0003g0031 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.314+463_314+476del others(14): Show |
HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26236378 | ||||||
chr2:26236379
|
T | A | 10 | a0001c0001t0001g0003a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 14 | HG00639.hp1 HG00642.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.314+476A>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26236379 | ||||||
chr2:26236380
|
C | CTG | 6 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0121others(3): Show | 6 | NA18964.hp1 NA18966.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.314+473_314+474dup others(2): Show |
HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26236380 | ||||||
chr2:26236380
|
C | CTGTGTG | 3 | a0001c0001t0001g0103a0001c0001t0001g0119a0001c0001t0001g0120 | 3 | HG01346.hp1 HG02523.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.314+469_314+474dup others(6): Show |
HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26236380 | ||||||
chr2:26236380
|
C | G | 39 | a0001c0001t0001g0135a0001c0001t0006g0239a0001c0002t0002g0002others(36): Show | 45 | HG00140.hp1 HG00738.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.314+475G>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26236380 | ||||||
chr2:26236380
|
CTG | C | 14 | a0001c0001t0001g0020a0001c0001t0001g0028a0001c0001t0001g0029others(11): Show | 15 | HG01167.hp2 HG01169.hp2 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.314+473_314+474del others(2): Show |
HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26236380 | ||||||
chr2:26236380
|
CTGTG | C | 8 | a0001c0001t0001g0188a0002c0003t0003g0021a0002c0003t0003g0108others(5): Show | 9 | HG01884.hp2 HG02622.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.314+471_314+474del others(4): Show |
HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26236380 | ||||||
chr2:26236380
|
CTGTGTGT others(3): Show |
C | 2 | a0001c0001t0005g0050a0001c0001t0005g0051 | 2 | HG02055.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.314+465_314+474del others(10): Show |
HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26236380 | ||||||
chr2:26236382
|
G | C | 6 | a0001c0001t0001g0003a0001c0001t0001g0049a0001c0001t0001g0067others(3): Show | 10 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.314+473C>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26236382 | ||||||
chr2:26236384
|
G | C | 1 | a0001c0001t0001g0043 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.314+471C>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26236384 | ||||||
chr2:26236416
|
G | A | 25 | a0001c0002t0002g0002a0001c0002t0002g0024a0001c0002t0002g0206others(22): Show | 32 | HG00140.hp1 HG00738.hp1 HG01981.hp2 others(29): Show |
intron_variant | MODIFIER | c.314+439C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26236416 | ||||||
chr2:26236416
|
G | GTA | 7 | a0001c0002t0002g0022a0001c0002t0002g0207a0001c0002t0002g0213others(4): Show | 8 | HG01123.hp1 HG01175.hp1 HG03490.hp2 others(5): Show |
intron_variant | MODIFIER | c.314+438_314+439ins others(2): Show |
HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26236416 | ||||||
chr2:26236418
|
G | A | 37 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(34): Show | 45 | HG00140.hp1 HG00738.hp1 HG01123.hp1 others(42): Show |
intron_variant | MODIFIER | c.314+437C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26236418 | ||||||
chr2:26236420
|
G | A | 105 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0015others(102): Show | 126 | HG00140.hp1 HG00408.hp1 HG00639.hp1 others(123): Show |
intron_variant | MODIFIER | c.314+435C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26236420 | ||||||
chr2:26236420
|
G | GTA | 47 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(44): Show | 56 | HG00408.hp2 HG00621.hp1 HG01081.hp1 others(53): Show |
intron_variant | MODIFIER | c.314+433_314+434dup others(2): Show |
HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26236420 | ||||||
chr2:26236420
|
G | GTATA | 7 | a0001c0001t0001g0010a0001c0001t0001g0094a0001c0001t0001g0095others(4): Show | 8 | NA18944.hp1 NA18971.hp1 NA18980.hp1 others(5): Show |
intron_variant | MODIFIER | c.314+431_314+434dup others(4): Show |
HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26236420 | ||||||
chr2:26236420
|
G | GTATATA | 4 | a0001c0002t0002g0210a0001c0002t0002g0211a0001c0002t0004g0212others(1): Show | 4 | HG01069.hp1 HG02004.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.314+429_314+434dup others(6): Show |
HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26236420 | ||||||
chr2:26236420
|
G | GTGTA | 37 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0044others(34): Show | 38 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.314+434_314+435ins others(4): Show |
HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26236420 | ||||||
chr2:26236420
|
G | GTGTGTA | 10 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0072others(7): Show | 12 | HG01074.hp1 HG01261.hp1 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.314+434_314+435ins others(6): Show |
HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26236420 | ||||||
chr2:26236420
|
G | GTGTGTGT others(3): Show |
2 | a0001c0001t0001g0079a0001c0001t0001g0113 | 2 | HG00642.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.314+434_314+435ins others(10): Show |
HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26236420 | ||||||
chr2:26236427
|
CT | C | 6 | a0001c0001t0003g0033a0001c0001t0003g0034a0001c0001t0003g0035others(3): Show | 6 | HG00733.hp2 HG01074.hp2 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.314+427delA | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26236427 | ||||||
chr2:26236487
|
C | T | 38 | a0001c0002t0002g0002a0001c0002t0002g0022a0001c0002t0002g0024others(35): Show | 46 | HG00140.hp1 HG00738.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.314+368G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26236487 | ||||||
chr2:26236528
|
C | T | 5 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.314+327G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26236528 | ||||||
chr2:26236720
|
C | T | 2 | a0001c0001t0001g0039a0001c0001t0001g0040 | 2 | HG01884.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.314+135G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26236720 | ||||||
chr2:26236802
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.314+53C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26236802 | ||||||
chr2:26236821
|
G | T | 1 | a0001c0001t0001g0118 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.314+34C>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 4/19 | chr2 | 26236821 | ||||||
chr2:26237089
|
C | T | 2 | a0001c0001t0001g0075a0001c0001t0001g0102 | 2 | HG03831.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.181-101G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 3/19 | chr2 | 26237089 | ||||||
chr2:26237090
|
G | A | 7 | a0002c0003t0003g0021a0002c0003t0003g0108a0002c0003t0003g0196others(4): Show | 8 | HG01884.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.181-102C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 3/19 | chr2 | 26237090 | ||||||
chr2:26237204
|
C | T | 79 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(76): Show | 86 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.181-216G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 3/19 | chr2 | 26237204 | ||||||
chr2:26237223
|
A | G | 5 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.181-235T>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 3/19 | chr2 | 26237223 | ||||||
chr2:26237232
|
C | T | 2 | a0003c0004t0001g0116a0003c0004t0001g0117 | 2 | HG02717.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.181-244G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 3/19 | chr2 | 26237232 | ||||||
chr2:26237339
|
C | A | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG02602.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.181-351G>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 3/19 | chr2 | 26237339 | ||||||
chr2:26237402
|
G | A | 37 | a0001c0002t0002g0002a0001c0002t0002g0022a0001c0002t0002g0024others(34): Show | 45 | HG00140.hp1 HG00738.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.181-414C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 3/19 | chr2 | 26237402 | ||||||
chr2:26237567
|
G | A | 1 | a0001c0001t0001g0189 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.181-579C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 3/19 | chr2 | 26237567 | ||||||
chr2:26237690
|
T | C | 1 | a0001c0001t0001g0102 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.181-702A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 3/19 | chr2 | 26237690 | ||||||
chr2:26237759
|
T | C | 1 | a0001c0001t0001g0204 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.181-771A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 3/19 | chr2 | 26237759 | ||||||
chr2:26237927
|
TCTTA | T | 7 | a0002c0003t0003g0021a0002c0003t0003g0108a0002c0003t0003g0196others(4): Show | 8 | HG01884.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.181-943_181-940del others(4): Show |
HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 3/19 | chr2 | 26237927 | ||||||
chr2:26237984
|
T | G | 1 | a0001c0001t0001g0067 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.180+950A>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 3/19 | chr2 | 26237984 | ||||||
chr2:26238194
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.180+740G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 3/19 | chr2 | 26238194 | ||||||
chr2:26238207
|
T | C | 1 | a0001c0001t0001g0067 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.180+727A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 3/19 | chr2 | 26238207 | ||||||
chr2:26238285
|
T | C | 2 | a0001c0001t0001g0052a0001c0001t0001g0053 | 2 | HG02257.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.180+649A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 3/19 | chr2 | 26238285 | ||||||
chr2:26238290
|
C | T | 1 | a0001c0001t0001g0025 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.180+644G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 3/19 | chr2 | 26238290 | ||||||
chr2:26238301
|
G | A | 9 | a0001c0001t0003g0031a0001c0001t0003g0033a0001c0001t0003g0034others(6): Show | 9 | HG00733.hp2 HG01074.hp2 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.180+633C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 3/19 | chr2 | 26238301 | ||||||
chr2:26238302
|
C | A | 9 | a0001c0001t0003g0031a0001c0001t0003g0033a0001c0001t0003g0034others(6): Show | 9 | HG00733.hp2 HG01074.hp2 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.180+632G>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 3/19 | chr2 | 26238302 | ||||||
chr2:26238303
|
C | T | 9 | a0001c0001t0003g0031a0001c0001t0003g0033a0001c0001t0003g0034others(6): Show | 9 | HG00733.hp2 HG01074.hp2 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.180+631G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 3/19 | chr2 | 26238303 | ||||||
chr2:26238864
|
A | ACATCTTT others(9): Show |
1 | a0001c0001t0001g0192 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.180+54_180+69dupCT others(14): Show |
HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 3/19 | chr2 | 26238864 | ||||||
chr2:26238865
|
C | G | 38 | a0001c0002t0002g0002a0001c0002t0002g0022a0001c0002t0002g0024others(35): Show | 46 | HG00140.hp1 HG00738.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.180+69G>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 3/19 | chr2 | 26238865 | ||||||
chr2:26239082
|
T | C | 7 | a0002c0003t0003g0021a0002c0003t0003g0108a0002c0003t0003g0196others(4): Show | 8 | HG01884.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.109+20A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 2/19 | chr2 | 26239082 | ||||||
chr2:26239225
|
A | T | 38 | a0001c0002t0002g0002a0001c0002t0002g0022a0001c0002t0002g0024others(35): Show | 46 | HG00140.hp1 HG00738.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.68-82T>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26239225 | ||||||
chr2:26239495
|
G | T | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | NA18971.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.68-352C>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26239495 | ||||||
chr2:26239734
|
A | G | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074 | 3 | HG00738.hp2 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.68-591T>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26239734 | ||||||
chr2:26239862
|
C | T | 78 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(75): Show | 85 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.68-719G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26239862 | ||||||
chr2:26240020
|
T | C | 3 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030 | 3 | HG01167.hp2 HG01169.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.68-877A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26240020 | ||||||
chr2:26240069
|
C | G | 138 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(135): Show | 154 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(151): Show |
intron_variant | MODIFIER | c.68-926G>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26240069 | ||||||
chr2:26240156
|
C | T | 38 | a0001c0002t0002g0002a0001c0002t0002g0022a0001c0002t0002g0024others(35): Show | 46 | HG00140.hp1 HG00738.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.68-1013G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26240156 | ||||||
chr2:26240400
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.68-1257G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26240400 | ||||||
chr2:26240613
|
A | T | 1 | a0001c0001t0001g0113 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.68-1470T>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26240613 | ||||||
chr2:26240655
|
ATTT | A | 8 | a0001c0001t0003g0033a0001c0001t0003g0034a0001c0001t0003g0035others(5): Show | 8 | HG00733.hp2 HG01074.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.68-1515_68-1513del others(3): Show |
HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26240655 | ||||||
chr2:26240723
|
A | G | 1 | a0001c0001t0001g0067 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.68-1580T>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26240723 | ||||||
chr2:26240727
|
T | C | 14 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(11): Show | 14 | HG00733.hp2 HG01074.hp2 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.68-1584A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26240727 | ||||||
chr2:26240921
|
C | G | 1 | a0001c0002t0002g0207 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.68-1778G>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26240921 | ||||||
chr2:26241084
|
A | C | 1 | a0001c0001t0001g0070 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.68-1941T>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26241084 | ||||||
chr2:26241123
|
C | T | 1 | a0001c0001t0009g0112 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.68-1980G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26241123 | ||||||
chr2:26241154
|
A | G | 14 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(11): Show | 14 | HG00733.hp2 HG01074.hp2 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.68-2011T>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26241154 | ||||||
chr2:26241190
|
C | T | 14 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(11): Show | 14 | HG00733.hp2 HG01074.hp2 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.68-2047G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26241190 | ||||||
chr2:26241191
|
G | A | 79 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(76): Show | 86 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.68-2048C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26241191 | ||||||
chr2:26241358
|
G | A | 1 | a0001c0001t0001g0054 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.68-2215C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26241358 | ||||||
chr2:26241445
|
C | T | 1 | a0001c0001t0001g0194 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.68-2302G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26241445 | ||||||
chr2:26241477
|
C | A | 4 | a0001c0001t0001g0011a0001c0001t0001g0103a0001c0001t0001g0104others(1): Show | 5 | HG01346.hp1 HG01358.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-2334G>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26241477 | ||||||
chr2:26241477
|
C | CA | 17 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0055others(14): Show | 20 | HG00642.hp1 HG01081.hp1 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.68-2335dupT | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26241477 | ||||||
chr2:26241480
|
A | C | 62 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(59): Show | 71 | HG00140.hp1 HG00733.hp2 HG00738.hp1 others(68): Show |
intron_variant | MODIFIER | c.68-2337T>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26241480 | ||||||
chr2:26241483
|
A | C | 5 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-2340T>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26241483 | ||||||
chr2:26241526
|
C | A | 5 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-2383G>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26241526 | ||||||
chr2:26241540
|
A | G | 139 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(136): Show | 157 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(154): Show |
intron_variant | MODIFIER | c.68-2397T>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26241540 | ||||||
chr2:26241595
|
G | C | 1 | a0001c0001t0001g0067 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.68-2452C>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26241595 | ||||||
chr2:26241651
|
C | CA | 11 | a0001c0001t0001g0030a0001c0001t0001g0068a0001c0001t0001g0192others(8): Show | 11 | HG01175.hp1 HG01981.hp1 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.68-2509dupT | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26241651 | ||||||
chr2:26241818
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.68-2675C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26241818 | ||||||
chr2:26242023
|
T | TC | 6 | a0002c0003t0003g0021a0002c0003t0003g0196a0002c0003t0003g0197others(3): Show | 7 | HG01884.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.67+2506dupG | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26242023 | ||||||
chr2:26242042
|
C | T | 1 | a0002c0003t0003g0196 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.67+2488G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26242042 | ||||||
chr2:26242071
|
C | T | 52 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(49): Show | 60 | HG00140.hp1 HG00733.hp2 HG00738.hp1 others(57): Show |
intron_variant | MODIFIER | c.67+2459G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26242071 | ||||||
chr2:26242159
|
G | C | 45 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(42): Show | 49 | HG00140.hp2 HG00733.hp1 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.67+2371C>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26242159 | ||||||
chr2:26242339
|
T | C | 1 | a0001c0001t0001g0105 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.67+2191A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26242339 | ||||||
chr2:26242364
|
A | C | 5 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.67+2166T>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26242364 | ||||||
chr2:26242409
|
A | C | 1 | a0001c0001t0001g0107 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.67+2121T>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26242409 | ||||||
chr2:26242410
|
A | AAACACAA others(3): Show |
1 | a0001c0001t0001g0106 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.67+2110_67+2119dup others(10): Show |
HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26242410 | ||||||
chr2:26242552
|
C | CCAGG | 79 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(76): Show | 86 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.67+1974_67+1977dup others(4): Show |
HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26242552 | ||||||
chr2:26242801
|
G | A | 9 | a0001c0001t0003g0031a0001c0001t0003g0033a0001c0001t0003g0034others(6): Show | 9 | HG00733.hp2 HG01074.hp2 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.67+1729C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26242801 | ||||||
chr2:26242813
|
G | A | 7 | a0001c0001t0001g0195a0002c0003t0003g0021a0002c0003t0003g0196others(4): Show | 8 | HG01071.hp2 HG01884.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.67+1717C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26242813 | ||||||
chr2:26242815
|
G | C | 6 | a0002c0003t0003g0021a0002c0003t0003g0196a0002c0003t0003g0197others(3): Show | 7 | HG01884.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.67+1715C>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26242815 | ||||||
chr2:26242821
|
G | C | 6 | a0002c0003t0003g0021a0002c0003t0003g0196a0002c0003t0003g0197others(3): Show | 7 | HG01884.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.67+1709C>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26242821 | ||||||
chr2:26242841
|
T | G | 1 | a0001c0001t0001g0201 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.67+1689A>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26242841 | ||||||
chr2:26242980
|
C | T | 52 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(49): Show | 60 | HG00140.hp1 HG00733.hp2 HG00738.hp1 others(57): Show |
intron_variant | MODIFIER | c.67+1550G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26242980 | ||||||
chr2:26243031
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.67+1499C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26243031 | ||||||
chr2:26243102
|
T | TCC | 9 | a0001c0001t0003g0031a0001c0001t0003g0033a0001c0001t0003g0034others(6): Show | 9 | HG00733.hp2 HG01074.hp2 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.67+1426_67+1427dup others(2): Show |
HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26243102 | ||||||
chr2:26243135
|
G | A | 1 | a0001c0001t0003g0037 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.67+1395C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26243135 | ||||||
chr2:26243331
|
C | A | 1 | a0001c0001t0001g0203 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.67+1199G>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26243331 | ||||||
chr2:26243403
|
GT | G | 37 | a0001c0002t0002g0002a0001c0002t0002g0022a0001c0002t0002g0024others(34): Show | 45 | HG00140.hp1 HG00738.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.67+1126delA | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26243403 | ||||||
chr2:26243501
|
A | T | 1 | a0001c0001t0001g0038 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.67+1029T>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26243501 | ||||||
chr2:26243662
|
G | A | 38 | a0001c0002t0002g0002a0001c0002t0002g0022a0001c0002t0002g0024others(35): Show | 46 | HG00140.hp1 HG00738.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.67+868C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26243662 | ||||||
chr2:26243662
|
G | C | 1 | a0001c0001t0001g0204 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.67+868C>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26243662 | ||||||
chr2:26243733
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.67+797C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26243733 | ||||||
chr2:26243904
|
C | T | 52 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(49): Show | 60 | HG00140.hp1 HG00733.hp2 HG00738.hp1 others(57): Show |
intron_variant | MODIFIER | c.67+626G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26243904 | ||||||
chr2:26244107
|
C | T | 37 | a0001c0002t0002g0002a0001c0002t0002g0022a0001c0002t0002g0024others(34): Show | 45 | HG00140.hp1 HG00738.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.67+423G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26244107 | ||||||
chr2:26244392
|
C | T | 1 | a0001c0001t0001g0025 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.67+138G>A | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26244392 | ||||||
chr2:26244479
|
C | A | 38 | a0001c0002t0002g0002a0001c0002t0002g0022a0001c0002t0002g0024others(35): Show | 46 | HG00140.hp1 HG00738.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.67+51G>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26244479 |