Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | MVACR others(758): Show |
chr2 | 26185635 | 26249632 |
| a0002 | 0/0 | 763 | 10 | 10 | 0 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | MVACR others(758): Show |
chr2 | 26185635 | 26249632 |
| a0003 | 0/0 | 763 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | MVACR others(758): Show |
chr2 | 26185635 | 26249632 |
| a0004 | 0/0 | 763 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | MVACR others(758): Show |
chr2 | 26185635 | 26249632 |
| a0005 | 0/0 | 763 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | MVACR others(758): Show |
chr2 | 26185635 | 26249632 |
| a0006 | 0/0 | 763 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | MVACR others(758): Show |
chr2 | 26185635 | 26249632 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2289 | 212 | 61 | 54 | 74 | 2 | 19 | HADHA_chr2_26185635_26249632 | HADHA | ATGGT others(2284): Show |
chr2 | 26185635 | 26249632 | ||
| a0001c0002 | 0/0 | 2289 | 44 | 1 | 9 | 25 | 2 | 7 | HADHA_chr2_26185635_26249632 | HADHA | ATGGT others(2284): Show |
chr2 | 26185635 | 26249632 | ||
| a0001c0005 | 0/0 | 2289 | 2 | 0 | 0 | 2 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | ATGGT others(2284): Show |
chr2 | 26185635 | 26249632 | ||
| a0001c0007 | 0/0 | 2289 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | ATGGT others(2284): Show |
chr2 | 26185635 | 26249632 | ||
| a0002c0003 | 0/0 | 2289 | 10 | 10 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | ATGGT others(2284): Show |
chr2 | 26185635 | 26249632 | ||
| a0003c0004 | 0/0 | 2289 | 2 | 2 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | ATGGT others(2284): Show |
chr2 | 26185635 | 26249632 | ||
| a0004c0009 | 0/0 | 2289 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | ATGGT others(2284): Show |
chr2 | 26185635 | 26249632 | ||
| a0005c0006 | 0/0 | 2289 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | ATGGT others(2284): Show |
chr2 | 26185635 | 26249632 | ||
| a0006c0008 | 0/0 | 2289 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | ATGGT others(2284): Show |
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 | AGAGG others(2938): Show |
chr2 | 26185635 | 26249632 |
| a0001c0001t0003 | 0/0 | 2943 | 7 | 4 | 3 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | AGAGG others(2938): Show |
chr2 | 26185635 | 26249632 |
| a0001c0001t0004 | 1/0 | 2943 | 5 | 1 | 3 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | AGAGG others(2938): Show |
chr2 | 26185635 | 26249632 |
| a0001c0001t0005 | 0/0 | 2943 | 3 | 3 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | AGAGG others(2938): Show |
chr2 | 26185635 | 26249632 |
| a0001c0001t0006 | 0/0 | 2943 | 2 | 2 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | AGAGG others(2938): Show |
chr2 | 26185635 | 26249632 |
| a0001c0001t0007 | 0/0 | 2943 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | AGAGG others(2938): Show |
chr2 | 26185635 | 26249632 |
| a0001c0001t0008 | 0/0 | 2943 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | AGAGG others(2938): Show |
chr2 | 26185635 | 26249632 |
| a0001c0001t0009 | 0/0 | 2943 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | AGAGG others(2938): Show |
chr2 | 26185635 | 26249632 |
| a0001c0002t0002 | 0/0 | 2943 | 38 | 0 | 8 | 21 | 2 | 7 | HADHA_chr2_26185635_26249632 | HADHA | AGAGG others(2938): Show |
chr2 | 26185635 | 26249632 |
| a0001c0002t0004 | 0/0 | 2943 | 5 | 0 | 1 | 4 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | AGAGG others(2938): Show |
chr2 | 26185635 | 26249632 |
| a0001c0002t0010 | 0/0 | 2943 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | AGAGG others(2938): Show |
chr2 | 26185635 | 26249632 |
| a0001c0005t0002 | 0/0 | 2943 | 2 | 0 | 0 | 2 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | AGAGG others(2938): Show |
chr2 | 26185635 | 26249632 |
| a0001c0007t0001 | 0/0 | 2943 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | AGAGG others(2938): Show |
chr2 | 26185635 | 26249632 |
| a0002c0003t0003 | 0/0 | 2943 | 10 | 10 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | AGAGG others(2938): Show |
chr2 | 26185635 | 26249632 |
| a0003c0004t0001 | 0/0 | 2943 | 2 | 2 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | AGAGG others(2938): Show |
chr2 | 26185635 | 26249632 |
| a0004c0009t0001 | 0/0 | 2943 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | AGAGG others(2938): Show |
chr2 | 26185635 | 26249632 |
| a0005c0006t0001 | 0/0 | 2943 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | AGAGG others(2938): Show |
chr2 | 26185635 | 26249632 |
| a0006c0008t0001 | 0/0 | 2943 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | AGAGG others(2938): Show |
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 |
| a0001c0001t0001g0008 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 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 | 0 | 0 | 2 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0017 | 0/0 | 2 | 1 | 1 | 0 | 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 | 2 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 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 | 0 | 1 | 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 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 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 | 0 | 0 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0069 | 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 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 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 | 0 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 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 | 1 | 0 | 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 |
| a0001c0001t0001g0108 | 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 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0135 | 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 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 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 | 0 | 1 | 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 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 1 | 0 | 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 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0187 | 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 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 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 |
| a0001c0001t0003g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0003g0032 | 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 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0003g0136 | 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 |
| a0001c0001t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0004g0123 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0005g0049 | 0/0 | 1 | 1 | 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 |
| a0001c0001t0005g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0006g0238 | 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 |
| a0001c0001t0007g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0008g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0001t0009g0111 | 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 |
| a0001c0002t0002g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0002t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0002t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0002t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 1 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0002t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0002t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0002t0002g0236 | 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 |
| a0001c0002t0004g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0002t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0002t0010g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0005t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0001c0007t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0002c0003t0003g0022 | 0/0 | 2 | 2 | 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 |
| a0002c0003t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0002c0003t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0002c0003t0003g0195 | 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 |
| a0003c0004t0001g0115 | 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 |
| a0004c0009t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0005c0006t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| a0006c0008t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 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 | g0224 | EUR | GBR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0091 | 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 | g0162 | EAS | CHS | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG00639 | hp2 | a0001 | c0001 | t0009 | g0111 | 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 | g0112 | AMR | PUR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG00738 | hp1 | a0001 | c0002 | t0002 | g0216 | AMR | PUR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG01069 | hp1 | a0001 | c0002 | t0004 | g0211 | 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 | g0194 | AMR | PUR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0036 | AMR | PUR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0078 | 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 | g0061 | AMR | PUR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0034 | AMR | PUR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0233 | AMR | PUR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG01192 | hp1 | a0001 | c0002 | t0002 | g0208 | AMR | PUR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG01255 | hp1 | a0004 | c0009 | t0001 | g0189 | AMR | CLM | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0102 | 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 | g0103 | AMR | CLM | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG01358 | hp2 | a0005 | c0006 | t0001 | g0160 | 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 | g0166 | AMR | CLM | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG01884 | hp2 | a0002 | c0003 | t0003 | g0198 | AFR | ACB | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0083 | 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 | g0067 | AMR | PEL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG01981 | hp2 | a0001 | c0002 | t0002 | g0235 | AMR | PEL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02004 | hp1 | a0001 | c0002 | t0002 | g0210 | 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 | g0164 | 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 | g0228 | EAS | KHV | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0050 | AFR | ACB | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02055 | hp2 | a0001 | c0001 | t0006 | g0239 | AFR | ACB | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0181 | 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 | g0183 | EAS | KHV | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02080 | hp2 | a0001 | c0002 | t0002 | g0219 | EAS | KHV | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02129 | hp1 | a0006 | c0008 | t0001 | g0157 | 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 | g0086 | EAS | KHV | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02135 | hp2 | a0001 | c0005 | t0002 | g0024 | EAS | KHV | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0080 | 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 | g0024 | EAS | CDX | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | CDX | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | ACB | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02300 | hp1 | a0001 | c0007 | t0001 | g0068 | AMR | PEL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02300 | hp2 | a0001 | c0002 | t0002 | g0221 | AMR | PEL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02622 | hp2 | a0002 | c0003 | t0003 | g0196 | AFR | GWD | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02630 | hp2 | a0002 | c0003 | t0003 | g0022 | AFR | GWD | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02717 | hp1 | a0002 | c0003 | t0003 | g0197 | AFR | GWD | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02717 | hp2 | a0003 | c0004 | t0001 | g0116 | AFR | GWD | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0136 | AFR | GWD | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02897 | hp2 | a0003 | c0004 | t0001 | g0115 | AFR | GWD | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ESN | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ESN | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ESN | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02976 | hp1 | a0002 | c0003 | t0003 | g0195 | AFR | ESN | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0049 | AFR | ESN | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG03017 | hp2 | a0001 | c0002 | t0002 | g0205 | SAS | PJL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | MSL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | MSL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG03130 | hp1 | a0001 | c0001 | t0006 | g0238 | AFR | ESN | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0125 | AFR | ESN | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | ESN | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG03225 | hp1 | a0002 | c0003 | t0003 | g0027 | AFR | MSL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | MSL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | MSL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0032 | AFR | MSL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG03486 | hp1 | a0002 | c0003 | t0003 | g0028 | AFR | MSL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | MSL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG03490 | hp2 | a0001 | c0002 | t0002 | g0023 | SAS | PJL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG03492 | hp2 | a0001 | c0002 | t0002 | g0225 | SAS | PJL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ESN | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0035 | AFR | ESN | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG03540 | hp2 | a0002 | c0003 | t0003 | g0022 | AFR | GWD | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG03654 | hp2 | a0001 | c0002 | t0002 | g0023 | SAS | PJL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG03669 | hp2 | a0001 | c0002 | t0002 | g0213 | SAS | PJL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0020 | 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 | g0218 | SAS | PJL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | BEB | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | BEB | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0236 | SAS | BEB | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | BEB | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | STU | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | STU | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | STU | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | STU | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | YRI | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | YRI | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | CHB | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHB | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA18940 | hp1 | a0001 | c0002 | t0002 | g0230 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA18947 | hp1 | a0001 | c0002 | t0002 | g0227 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0064 | 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 | g0167 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0122 | 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 | g0222 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0145 | 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 | g0121 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA18974 | hp1 | a0001 | c0002 | t0002 | g0214 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA18979 | hp1 | a0001 | c0002 | t0002 | g0234 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA18982 | hp2 | a0001 | c0002 | t0004 | g0231 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA18988 | hp2 | a0001 | c0002 | t0002 | g0217 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA18991 | hp1 | a0001 | c0002 | t0002 | g0025 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA18993 | hp2 | a0001 | c0002 | t0002 | g0215 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA18994 | hp1 | a0001 | c0002 | t0002 | g0207 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0126 | 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 | g0146 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA19003 | hp2 | a0001 | c0002 | t0002 | g0226 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0170 | 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 | g0220 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | LWK | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | LWK | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0097 | 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 | g0206 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA19058 | hp1 | a0001 | c0002 | t0002 | g0025 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA19067 | hp1 | a0001 | c0002 | t0002 | g0232 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA19067 | hp2 | a0001 | c0001 | t0008 | g0186 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA19070 | hp1 | a0001 | c0002 | t0002 | g0209 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA19090 | hp1 | a0001 | c0002 | t0002 | g0223 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0087 | EUR | TSI | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA20805 | hp2 | a0001 | c0002 | t0002 | g0229 | EUR | TSI | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG01123 | hp1 | a0001 | c0002 | t0002 | g0212 | AMR | CLM | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | ACB | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0033 | AFR | MSL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG03471 | hp2 | a0002 | c0003 | t0003 | g0107 | AFR | MSL | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | USA | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | USA | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA20300 | hp1 | a0002 | c0003 | t0003 | g0199 | AFR | USA | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | USA | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA21309 | hp1 | a0001 | c0002 | t0010 | g0237 | AFR | LWK | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | LWK | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0008 | REF | REF | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0123 | REF | REF | HADHA_chr2_26185635_26249632 | HADHA | chr2 | 26185635 | 26249632 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:26197705 | T | C | 1 | a0006 | 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 | a0004 | 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 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0001c0002 a0001c0005 |
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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0001c0001t0003 a0001c0001t0006 a0002c0003t0003 |
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 | a0001c0002t0002 a0001c0002t0010 a0001c0005t0002 |
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 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(7): Show |
203 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(200): 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 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:26191664 | G | A | 1 | a0001c0001t0001g0133 | 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 | a0001c0001t0001g0128 | 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 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
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 | a0001c0002t0002g0214 | 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 | a0001c0002t0002g0002 a0001c0002t0002g0023 a0001c0002t0002g0025 others(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 | 7 | a0001c0001t0003g0007 a0001c0001t0003g0034 a0001c0001t0003g0035 others(4): 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 | a0001c0001t0001g0124 a0001c0001t0005g0125 |
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 | a0003c0004t0001g0115 a0003c0004t0001g0116 |
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 | 18 | a0001c0001t0003g0007 a0001c0001t0003g0032 a0001c0001t0003g0034 others(15): 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 | a0001c0001t0001g0065 a0001c0002t0002g0002 a0001c0002t0002g0023 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(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 | a0001c0001t0003g0136 a0002c0003t0003g0022 a0002c0003t0003g0027 others(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 | a0001c0001t0001g0158 | 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 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0044 others(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 | 202 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(199): Show |
230 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(227): 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 | a0001c0002t0002g0219 | 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 | a0001c0001t0003g0032 | 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 | a0001c0001t0001g0137 a0001c0001t0003g0136 |
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 | 201 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(198): Show |
229 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(226): Show |
intron_variant | MODIFIER | c.1885+549T>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 17/19 | chr2 | 26193028 | |||||||
| chr2:26193043 | T | C | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(197): Show |
226 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(223): 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 | 202 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(199): Show |
230 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(227): 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 | a0002c0003t0003g0022 a0002c0003t0003g0107 a0002c0003t0003g0195 others(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 | a0001c0001t0001g0077 a0001c0001t0001g0204 a0001c0001t0004g0004 others(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 | 91 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(88): Show |
100 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(97): 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 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0124 a0001c0001t0001g0141 a0001c0001t0001g0148 others(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 | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(197): Show |
226 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(223): 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 | a0001c0001t0006g0238 a0001c0001t0006g0239 |
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 | 7 | a0001c0001t0003g0007 a0001c0001t0003g0034 a0001c0001t0003g0035 others(4): 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 | a0002c0003t0003g0022 a0002c0003t0003g0107 a0002c0003t0003g0195 others(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 | 16 | a0001c0001t0003g0007 a0001c0001t0003g0034 a0001c0001t0003g0035 others(13): 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 | a0001c0001t0001g0154 | 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 | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(197): Show |
226 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(223): 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 | a0001c0001t0001g0015 a0001c0001t0001g0162 a0001c0001t0001g0163 |
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 | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(197): Show |
226 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(223): 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 | a0001c0001t0001g0158 | 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 | a0001c0001t0001g0070 a0001c0001t0001g0079 a0001c0001t0001g0084 |
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 | 8 | a0001c0001t0003g0007 a0001c0001t0003g0032 a0001c0001t0003g0034 others(5): 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 | a0001c0001t0001g0118 | 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 | a0002c0003t0003g0027 a0002c0003t0003g0028 |
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 | a0001c0002t0002g0207 a0001c0002t0002g0226 |
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 | a0001c0001t0001g0154 | 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 | a0001c0001t0001g0138 | 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 | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(197): Show |
226 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(223): 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 | a0002c0003t0003g0199 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 |
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 | 8 | a0001c0001t0003g0007 a0001c0001t0003g0032 a0001c0001t0003g0034 others(5): 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 | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(197): Show |
226 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(223): 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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(180): Show |
207 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(204): 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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(189): Show |
217 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(214): 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 | a0001c0001t0001g0010 a0001c0001t0001g0088 |
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 | a0001c0001t0001g0090 | 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 | a0001c0001t0001g0194 | 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 | a0001c0002t0002g0227 | 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 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 |
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 | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(197): Show |
226 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(223): 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 | a0002c0003t0003g0022 a0002c0003t0003g0195 a0002c0003t0003g0196 others(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 | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(197): Show |
226 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(223): Show |
intron_variant | MODIFIER | c.1393-163C>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 13/19 | chr2 | 26197940 | |||||||
| chr2:26197971 | C | T | 8 | a0001c0001t0003g0007 a0001c0001t0003g0032 a0001c0001t0003g0034 others(5): 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 | a0001c0001t0001g0155 | 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 | 8 | a0001c0001t0003g0007 a0001c0001t0003g0032 a0001c0001t0003g0034 others(5): 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 | 191 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(188): Show |
214 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.1393-593dupA | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 13/19 | chr2 | 26198369 | |||||||
| chr2:26198380 | G | T | 7 | a0002c0003t0003g0022 a0002c0003t0003g0107 a0002c0003t0003g0195 others(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 | a0002c0003t0003g0022 a0002c0003t0003g0107 a0002c0003t0003g0195 others(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 | a0001c0001t0003g0032 | 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 | 199 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(196): Show |
225 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(222): Show |
intron_variant | MODIFIER | c.1393-885dupT | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 13/19 | chr2 | 26198661 | |||||||
| chr2:26198749 | T | C | 1 | a0001c0001t0001g0101 | 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 | a0003c0004t0001g0115 a0003c0004t0001g0116 |
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 | 198 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(195): Show |
224 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(221): Show |
intron_variant | MODIFIER | c.1393-1273T>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 13/19 | chr2 | 26199050 | |||||||
| chr2:26199126 | G | A | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(197): Show |
226 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(223): 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 | a0001c0001t0001g0005 a0001c0001t0001g0179 |
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 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 |
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 | a0001c0002t0002g0227 | 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 | a0001c0001t0001g0082 | 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 | 5 | a0001c0001t0003g0007 a0001c0001t0003g0034 a0001c0001t0003g0035 others(2): 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 | a0001c0001t0001g0053 | 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 | a0002c0003t0003g0022 a0002c0003t0003g0107 a0002c0003t0003g0195 others(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 | a0001c0001t0001g0188 a0002c0003t0003g0027 a0002c0003t0003g0028 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(167): Show |
192 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.1392+604C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 13/19 | chr2 | 26200545 | |||||||
| chr2:26200735 | CT | C | 198 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(195): Show |
224 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(221): Show |
intron_variant | MODIFIER | c.1392+413delA | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 13/19 | chr2 | 26200735 | |||||||
| chr2:26200789 | G | A | 1 | a0001c0001t0001g0204 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(180): Show |
207 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(204): 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 | a0001c0001t0001g0086 | 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 | a0001c0002t0002g0219 | 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 | a0001c0001t0001g0019 | 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 | 5 | a0001c0001t0003g0007 a0001c0001t0003g0034 a0001c0001t0003g0035 others(2): 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 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0120 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(67): Show |
76 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.1221-195C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 12/19 | chr2 | 26201515 | |||||||
| chr2:26201648 | T | C | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(197): Show |
226 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(223): 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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(170): Show |
197 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(194): 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 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0044 others(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 | a0001c0001t0001g0074 | 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 | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(197): Show |
226 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(223): 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 | a0001c0001t0001g0046 a0001c0001t0001g0060 a0001c0001t0001g0126 others(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 | 101 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(98): Show |
113 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(110): Show |
intron_variant | MODIFIER | c.1221-642delA | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 12/19 | chr2 | 26201961 | |||||||
| chr2:26202121 | A | C | 1 | a0002c0003t0003g0107 | 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 | a0001c0001t0001g0180 | 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 | a0001c0001t0001g0085 | 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 | a0001c0002t0002g0223 | 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 | a0001c0001t0001g0092 | 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 | a0001c0001t0009g0111 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(197): Show |
226 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(223): 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 | a0001c0001t0001g0139 a0001c0001t0001g0140 |
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 | a0001c0001t0001g0130 | 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 | 5 | a0001c0001t0003g0007 a0001c0001t0003g0034 a0001c0001t0003g0035 others(2): 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 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0117 a0001c0001t0001g0175 others(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 | a0001c0002t0002g0221 | 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 | a0001c0001t0001g0105 a0001c0001t0001g0127 a0001c0001t0001g0135 |
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 | a0002c0003t0003g0022 a0002c0003t0003g0195 a0002c0003t0003g0196 others(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 | a0001c0002t0002g0002 a0001c0002t0002g0023 a0001c0002t0002g0025 others(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 | a0001c0002t0002g0224 | 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 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0119 others(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 | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(197): Show |
226 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(223): 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 | a0001c0001t0001g0044 a0001c0001t0001g0075 a0002c0003t0003g0197 others(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 | 15 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(12): 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 | 194 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(191): Show |
218 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(215): 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 | a0001c0001t0001g0059 | 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 | a0001c0001t0001g0113 | 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 | a0001c0001t0001g0076 a0001c0002t0002g0002 a0001c0002t0002g0023 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0058 a0001c0001t0001g0089 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(106): Show |
123 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(120): 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 | a0001c0001t0001g0076 | 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 | a0001c0001t0001g0076 | 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 | a0001c0001t0001g0026 | 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 | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(197): Show |
226 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(223): 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 | a0001c0002t0010g0237 | 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 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0044 others(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 | a0001c0002t0002g0218 | 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 | a0002c0003t0003g0027 a0002c0003t0003g0028 |
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 | a0001c0001t0001g0118 | 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 | a0002c0003t0003g0107 | 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 | a0001c0001t0001g0043 a0001c0001t0001g0183 a0001c0001t0003g0036 others(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 | 4 | a0001c0001t0003g0007 a0001c0001t0003g0034 a0001c0001t0003g0035 others(1): 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 | a0002c0003t0003g0027 a0002c0003t0003g0028 |
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 | a0001c0002t0002g0232 | 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 | a0002c0003t0003g0027 a0002c0003t0003g0028 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(191): Show |
219 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(216): 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 | a0001c0001t0003g0032 | 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 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0106 others(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 | a0002c0003t0003g0198 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(180): Show |
207 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(204): 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 | a0001c0001t0001g0015 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(78): Show |
87 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(84): 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 | a0001c0002t0002g0205 a0001c0002t0002g0228 |
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 | a0001c0001t0003g0032 | 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 | 20 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(17): 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 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 |
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 | 7 | a0001c0001t0003g0007 a0001c0001t0003g0034 a0001c0001t0003g0035 others(4): 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 | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(197): Show |
226 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(223): Show |
intron_variant | MODIFIER | c.976-1043T>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 10/19 | chr2 | 26210932 | |||||||
| chr2:26211153 | C | A | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(197): Show |
226 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(223): 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 | a0001c0001t0001g0161 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(180): Show |
207 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(204): 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 | a0001c0002t0004g0006 a0001c0002t0004g0231 |
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 | a0001c0001t0003g0032 | 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 | 20 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(17): 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 | a0001c0001t0001g0077 | 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 | a0006c0008t0001g0157 | 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 | a0001c0001t0001g0188 | 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 | 7 | a0001c0001t0003g0007 a0001c0001t0003g0034 a0001c0001t0003g0035 others(4): 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 | a0001c0001t0001g0075 | 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 | a0001c0001t0001g0056 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0048 a0001c0001t0001g0067 |
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 | a0001c0001t0001g0017 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 |
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 | a0002c0003t0003g0199 | 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 | a0001c0001t0001g0140 | 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 | a0001c0001t0001g0147 | 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 | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(197): Show |
226 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(223): 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 | a0001c0001t0001g0121 | 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 | a0001c0001t0001g0179 | 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 | a0001c0001t0001g0154 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(143): Show |
163 | HG00140.hp2 HG00621.hp1 HG00621.hp2 others(160): Show |
intron_variant | MODIFIER | c.677-1143dupA | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26216317 | |||||||
| chr2:26216317 | A | ATT | 10 | a0001c0001t0001g0046 a0001c0001t0001g0060 a0001c0001t0001g0095 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0106 a0001c0001t0003g0034 others(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 | 202 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(199): Show |
229 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(226): 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 | a0002c0003t0003g0022 a0002c0003t0003g0107 a0002c0003t0003g0195 others(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 | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(197): Show |
226 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(223): 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 | a0006c0008t0001g0157 | 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 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0106 others(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 | a0001c0002t0002g0223 | 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 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0106 others(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 | a0001c0002t0002g0002 a0001c0002t0002g0025 a0001c0002t0002g0217 others(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 | a0001c0001t0001g0122 | 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 | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(197): Show |
226 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(223): Show |
intron_variant | MODIFIER | c.677-1951A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26217126 | |||||||
| chr2:26217564 | C | T | 6 | a0001c0001t0003g0007 a0001c0001t0003g0032 a0001c0001t0003g0034 others(3): 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 | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(197): Show |
226 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(223): 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 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0044 others(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 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0120 |
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 | a0001c0001t0001g0091 | 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 | a0001c0002t0002g0216 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(177): Show |
204 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(201): Show |
intron_variant | MODIFIER | c.677-2899C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26218074 | |||||||
| chr2:26218299 | C | CA | 143 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(140): Show |
160 | HG00140.hp2 HG00408.hp1 HG00639.hp1 others(157): Show |
intron_variant | MODIFIER | c.677-3125dupT | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26218299 | |||||||
| chr2:26218299 | C | CAA | 57 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(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 | a0001c0001t0001g0066 | 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 | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(197): Show |
226 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(223): 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 | a0001c0001t0001g0074 a0001c0001t0001g0101 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(177): Show |
204 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(201): 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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(158): Show |
182 | HG00140.hp2 HG00408.hp2 HG00621.hp1 others(179): Show |
intron_variant | MODIFIER | c.677-3832dupT | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26219006 | |||||||
| chr2:26219006 | C | CAA | 35 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0019 others(32): 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 | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(197): Show |
226 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(223): Show |
intron_variant | MODIFIER | c.677-4192A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26219367 | |||||||
| chr2:26219370 | T | C | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(197): Show |
226 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(223): 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 | a0001c0001t0001g0048 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(184): Show |
212 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(209): 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 | a0001c0001t0001g0084 | 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 | a0001c0001t0001g0147 | 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 | a0001c0001t0001g0057 | 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 | a0001c0001t0001g0067 | 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 | 14 | a0001c0001t0003g0007 a0001c0001t0003g0034 a0001c0001t0003g0035 others(11): 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 | a0001c0001t0008g0186 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 |
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 | 5 | a0001c0001t0003g0007 a0001c0001t0003g0034 a0001c0001t0003g0035 others(2): 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 | a0001c0001t0001g0057 | 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 | a0001c0001t0001g0165 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(184): Show |
212 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(209): 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 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(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 | a0001c0001t0001g0132 | 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 | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(197): Show |
226 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(223): 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 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(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 | a0001c0001t0005g0050 | 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 | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(197): Show |
226 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(223): Show |
intron_variant | MODIFIER | c.677-7442A>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26222617 | |||||||
| chr2:26222682 | A | G | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(197): Show |
226 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(223): Show |
intron_variant | MODIFIER | c.677-7507T>C | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26222682 | |||||||
| chr2:26223155 | T | C | 5 | a0001c0001t0003g0007 a0001c0001t0003g0034 a0001c0001t0003g0035 others(2): 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 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(75): Show |
84 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.676+6915A>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26223277 | |||||||
| chr2:26223381 | AC | A | 4 | a0001c0001t0003g0007 a0001c0001t0003g0034 a0001c0001t0003g0035 others(1): 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 | a0001c0001t0001g0124 | 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 | a0001c0001t0001g0066 | 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 | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(197): Show |
226 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(223): 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 | a0001c0001t0009g0111 | 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 | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(197): Show |
226 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(223): Show |
intron_variant | MODIFIER | c.676+5913T>G | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26224279 | |||||||
| chr2:26224409 | T | G | 13 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(10): 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 | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(197): Show |
226 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(223): 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 | a0001c0002t0002g0220 a0001c0002t0002g0230 a0001c0002t0002g0234 |
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 | a0001c0002t0010g0237 | 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 | a0001c0001t0001g0017 a0001c0001t0001g0187 |
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 | a0001c0001t0001g0058 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(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 | 192 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(189): Show |
218 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(215): 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 | 4 | a0001c0001t0003g0007 a0001c0001t0003g0034 a0001c0001t0003g0035 others(1): 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 | a0001c0001t0001g0180 | 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 | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(197): Show |
226 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(223): 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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(177): Show |
204 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(201): Show |
intron_variant | MODIFIER | c.676+4110C>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26226082 | |||||||
| chr2:26226086 | A | G | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(197): Show |
226 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(223): 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 | a0001c0001t0001g0155 a0001c0001t0001g0167 a0001c0001t0001g0168 |
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 | a0001c0001t0003g0036 | 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 | a0001c0001t0001g0149 | 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 | a0002c0003t0003g0027 a0002c0003t0003g0028 |
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 | 197 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(194): Show |
223 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(220): Show |
intron_variant | MODIFIER | c.676+2680delT | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26227511 | |||||||
| chr2:26227521 | A | C | 6 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0044 others(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 | a0001c0002t0002g0218 a0001c0002t0002g0236 |
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 | a0002c0003t0003g0199 | 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 | a0001c0001t0001g0155 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 |
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 | a0001c0001t0001g0079 | 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 | a0001c0001t0001g0046 a0001c0001t0001g0060 |
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 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(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 | a0001c0002t0002g0232 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0043 a0001c0001t0001g0054 others(3): Show |
6 | HG01081.hp1 HG01109.hp1 HG01169.hp1 others(3): 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 | a0001c0001t0001g0105 a0001c0001t0001g0127 a0001c0001t0001g0134 others(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 | a0001c0002t0002g0213 a0001c0002t0002g0216 a0001c0002t0002g0229 |
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 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(184): Show |
212 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.676+863G>T | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 7/19 | chr2 | 26229329 | |||||||
| chr2:26229341 | T | C | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(197): Show |
226 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(223): 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 | a0001c0001t0001g0037 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0151 a0001c0001t0001g0173 others(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 | 58 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(55): 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 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(85): Show |
96 | HG00140.hp2 HG00642.hp1 HG00733.hp1 others(93): 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 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0044 others(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 | a0001c0001t0001g0066 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0112 a0001c0001t0001g0185 |
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 | a0001c0001t0001g0175 | 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 | a0002c0003t0003g0027 a0002c0003t0003g0028 |
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 | a0001c0002t0010g0237 | 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 | a0003c0004t0001g0115 a0003c0004t0001g0116 |
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 | a0002c0003t0003g0027 | 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 | a0001c0002t0002g0002 a0001c0002t0002g0023 a0001c0002t0002g0025 others(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 | a0001c0001t0001g0042 | 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 | a0001c0001t0001g0061 | 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 | a0001c0002t0002g0219 | 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 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0044 others(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 | a0003c0004t0001g0115 a0003c0004t0001g0116 |
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 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0044 others(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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0117 | 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 | a0001c0002t0002g0002 a0001c0002t0002g0023 a0001c0002t0002g0025 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0039 |
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 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0052 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0042 a0001c0001t0001g0043 others(17): Show |
23 | HG01069.hp2 HG01071.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.573+191delT | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 6/19 | chr2 | 26231968 | |||||||
| chr2:26231968 | CAA | C | 11 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0003g0007 others(8): 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 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(76): Show |
85 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(82): 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 | a0001c0002t0002g0002 a0001c0002t0002g0023 a0001c0002t0002g0025 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0072 | 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 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 |
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 | a0001c0001t0001g0043 | 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 | 142 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(139): Show |
162 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(159): 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 | a0001c0001t0001g0188 | 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 | a0001c0001t0001g0149 | 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 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(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 | a0001c0001t0001g0133 a0001c0001t0001g0142 a0004c0009t0001g0189 |
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 | a0001c0002t0002g0002 a0001c0002t0002g0023 a0001c0002t0002g0025 others(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 | a0001c0001t0001g0112 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0044 others(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 | a0001c0001t0001g0047 a0001c0002t0002g0002 a0001c0002t0002g0023 others(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 | a0001c0001t0006g0238 a0001c0001t0006g0239 |
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 | a0001c0001t0001g0063 | 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 | a0001c0002t0002g0002 a0001c0002t0002g0023 a0001c0002t0002g0025 others(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 | a0001c0001t0001g0121 a0001c0001t0001g0126 |
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 | a0001c0002t0002g0213 a0001c0002t0002g0216 a0001c0002t0002g0229 |
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 | a0001c0002t0002g0002 a0001c0002t0002g0023 a0001c0002t0002g0025 others(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 | 236 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(233): Show |
270 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(267): 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 | a0001c0001t0001g0016 a0001c0001t0001g0117 a0001c0001t0001g0175 others(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 | a0001c0001t0001g0173 a0001c0001t0001g0174 |
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 | a0001c0001t0001g0203 | 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 | a0001c0001t0001g0203 | 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 | a0001c0001t0001g0046 a0001c0001t0001g0060 |
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 | a0001c0002t0002g0230 | 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 | a0001c0001t0001g0183 | 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 | a0001c0001t0001g0190 | 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 | a0001c0001t0001g0014 a0001c0001t0001g0040 a0001c0001t0001g0044 others(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 | a0001c0001t0001g0120 a0001c0001t0001g0193 a0001c0001t0006g0238 others(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 | a0001c0001t0003g0032 a0001c0002t0002g0002 a0001c0002t0002g0023 others(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 | a0001c0001t0001g0103 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(54): Show |
61 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(58): 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 | a0001c0001t0001g0041 a0001c0001t0001g0059 a0001c0001t0001g0081 |
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 | a0001c0002t0002g0206 a0001c0002t0002g0215 a0001c0002t0004g0211 |
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 | 19 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(16): 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 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0145 | 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 | a0001c0001t0001g0145 | 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 | a0001c0001t0003g0007 a0001c0001t0003g0035 a0001c0001t0004g0033 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0030 others(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 | a0001c0001t0003g0007 a0001c0001t0003g0034 a0001c0001t0006g0239 |
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 | a0001c0001t0003g0032 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0030 others(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 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0120 others(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 | a0001c0001t0001g0102 a0001c0001t0001g0118 a0001c0001t0001g0119 |
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 | a0001c0001t0001g0145 a0001c0001t0006g0238 a0001c0002t0002g0002 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0029 a0001c0001t0001g0030 others(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 | a0001c0001t0001g0187 a0002c0003t0003g0022 a0002c0003t0003g0107 others(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 | a0001c0001t0005g0049 a0001c0001t0005g0050 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0048 a0001c0001t0001g0066 others(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 | a0001c0001t0001g0042 | 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 | a0001c0002t0002g0002 a0001c0002t0002g0025 a0001c0002t0002g0205 others(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 | a0001c0002t0002g0023 a0001c0002t0002g0206 a0001c0002t0002g0212 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(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 | 104 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0016 others(101): 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 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(44): Show |
55 | HG00408.hp2 HG00621.hp1 HG01081.hp1 others(52): 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 | a0001c0001t0001g0011 a0001c0001t0001g0093 a0001c0001t0001g0094 others(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 | a0001c0002t0002g0209 a0001c0002t0002g0210 a0001c0002t0004g0211 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0026 a0001c0001t0001g0043 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0071 others(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 | a0001c0001t0001g0078 a0001c0001t0001g0112 |
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 | 5 | a0001c0001t0003g0007 a0001c0001t0003g0034 a0001c0001t0003g0035 others(2): 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 | a0001c0002t0002g0002 a0001c0002t0002g0023 a0001c0002t0002g0025 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0039 |
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 | a0001c0001t0001g0065 | 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 | a0001c0001t0001g0117 | 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 | a0001c0001t0001g0074 a0001c0001t0001g0101 |
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 | a0002c0003t0003g0022 a0002c0003t0003g0107 a0002c0003t0003g0195 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(76): Show |
85 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(82): 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 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(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 | a0003c0004t0001g0115 a0003c0004t0001g0116 |
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 | a0001c0001t0001g0099 a0001c0001t0001g0100 |
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 | a0001c0002t0002g0002 a0001c0002t0002g0023 a0001c0002t0002g0025 others(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 | a0001c0001t0001g0188 | 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 | a0001c0001t0001g0101 | 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 | a0001c0001t0001g0203 | 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 | a0002c0003t0003g0022 a0002c0003t0003g0107 a0002c0003t0003g0195 others(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 | a0001c0001t0001g0066 | 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 | a0001c0001t0001g0054 | 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 | a0001c0001t0001g0066 | 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 | a0001c0001t0001g0051 a0001c0001t0001g0052 |
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 | a0001c0001t0001g0026 | 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 | 8 | a0001c0001t0003g0007 a0001c0001t0003g0032 a0001c0001t0003g0034 others(5): 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 | 8 | a0001c0001t0003g0007 a0001c0001t0003g0032 a0001c0001t0003g0034 others(5): 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 | 8 | a0001c0001t0003g0007 a0001c0001t0003g0032 a0001c0001t0003g0034 others(5): 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 | a0001c0001t0001g0191 | 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 | a0001c0002t0002g0002 a0001c0002t0002g0023 a0001c0002t0002g0025 others(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 | a0002c0003t0003g0022 a0002c0003t0003g0107 a0002c0003t0003g0195 others(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 | a0001c0002t0002g0002 a0001c0002t0002g0023 a0001c0002t0002g0025 others(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 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
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 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(75): Show |
84 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(81): 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 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 |
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 | 137 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(134): Show |
153 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(150): 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 | a0001c0002t0002g0002 a0001c0002t0002g0023 a0001c0002t0002g0025 others(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 | a0001c0001t0001g0070 | 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 | a0001c0001t0001g0112 | 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 | 7 | a0001c0001t0003g0007 a0001c0001t0003g0034 a0001c0001t0003g0035 others(4): 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 | a0001c0001t0001g0066 | 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 | 13 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(10): 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 | a0001c0002t0002g0206 | 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 | a0001c0001t0001g0069 | 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 | a0001c0001t0009g0111 | 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 | 13 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(10): 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 | 13 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(10): 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 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(76): Show |
85 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(82): 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 | a0001c0001t0001g0053 | 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 | a0001c0001t0001g0193 | 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 | a0001c0001t0001g0012 a0001c0001t0001g0102 a0001c0001t0001g0103 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0054 others(14): Show |
19 | HG00642.hp1 HG01081.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.68-2335dupT | HADHA | ENSG00000084754.12 | transcript | ENST00000380649.8 | protein_coding | 1/19 | chr2 | 26241477 | |||||||
| chr2:26241480 | A | C | 61 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(58): 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 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(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 | 138 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(135): Show |
156 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(153): 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 | a0001c0001t0001g0066 | 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 | a0001c0001t0001g0031 a0001c0001t0001g0067 a0001c0001t0001g0191 others(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 | a0001c0001t0001g0203 | 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 | a0002c0003t0003g0022 a0002c0003t0003g0195 a0002c0003t0003g0196 others(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 | a0002c0003t0003g0195 | 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 | 51 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(48): 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 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0104 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0106 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(76): Show |
85 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(82): 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 | 8 | a0001c0001t0003g0007 a0001c0001t0003g0032 a0001c0001t0003g0034 others(5): 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 | a0001c0001t0001g0194 a0002c0003t0003g0022 a0002c0003t0003g0195 others(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 | a0002c0003t0003g0022 a0002c0003t0003g0195 a0002c0003t0003g0196 others(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 | a0002c0003t0003g0022 a0002c0003t0003g0195 a0002c0003t0003g0196 others(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 | a0001c0001t0001g0200 | 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 | 51 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(48): 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 | a0001c0001t0001g0201 | 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 | 8 | a0001c0001t0003g0007 a0001c0001t0003g0032 a0001c0001t0003g0034 others(5): 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 | a0001c0001t0003g0036 | 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 | a0001c0001t0001g0202 | 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 | a0001c0002t0002g0002 a0001c0002t0002g0023 a0001c0002t0002g0025 others(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 | a0001c0001t0001g0037 | 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 | a0001c0002t0002g0002 a0001c0002t0002g0023 a0001c0002t0002g0025 others(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 | a0001c0001t0001g0203 | 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 | a0001c0001t0001g0204 | 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 | 51 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(48): 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 | a0001c0002t0002g0002 a0001c0002t0002g0023 a0001c0002t0002g0025 others(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 | a0001c0001t0001g0026 | 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 | a0001c0002t0002g0002 a0001c0002t0002g0023 a0001c0002t0002g0025 others(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 |